메뉴 건너뛰기




Volumn 14, Issue 10, 2008, Pages 1001-1047

Recent developments in the chemistry and in the biological applications of amidoximes

Author keywords

Amidines; Amidoximes; Biological activities; NO donors; Prodrugs

Indexed keywords

1 METHYLIMIDAZOLE 5 AMIDOXIME; 1,2,4 OXADIAZOLE DERIVATIVE; 2 ETHOXY 2 NAPHTHYLACETAMIDOXIME; 2 ETHOXY 2 PHENYLACETAMIDOXIME; 2 HYDROXYACETAMIDOXIME; 4 CHLOROBENZAMIDOXIME; [2 (2 PHENYLTHIO)PHENYL]ACETAMIDOXIME; ACETAMIDOXIME; ACETYLSALICYLIC ACID; AMIDINE; AMIDOXIME DERIVATIVE; BENZAMIDINE; BENZAMIDOXIME; BENZYLAMIDOXIME; BISAMIDOXIME; DIMINAZENE ACETURATE; FLUNITRAZEPAM; FORMAMIDE OXIME; GLYCERYL TRINITRATE; IMIPRAMINE; INDAN DERIVATIVE; LAMIFIBAN; MELAGATRAN; OXIME; OXIME DERIVATIVE; PENTAMIDINE; PIRACETAM; SIBRAFIBAN; UNINDEXED DRUG; XIMELAGATRAN;

EID: 44449086440     PISSN: 13816128     EISSN: None     Source Type: Journal    
DOI: 10.2174/138161208784139675     Document Type: Review
Times cited : (79)

References (360)
  • 1
    • 44449118345 scopus 로고    scopus 로고
    • Nicolaides DN, Varella EA. In: Patai S Ed., Interscience, the chemistry of acid derivatives; the chemistry of amidoximes. New York, 1992; 2(Suppl. B, Pt 2): 875-966.
    • Nicolaides DN, Varella EA. In: Patai S Ed., Interscience, the chemistry of acid derivatives; the chemistry of amidoximes. New York, 1992; 2(Suppl. B, Pt 2): 875-966.
  • 2
    • 33947478356 scopus 로고
    • The chemistry of amidoximes and related compounds
    • Eloy F, Lenaers R. The chemistry of amidoximes and related compounds. Chem Rev 1962; 62:155-83.
    • (1962) Chem Rev , vol.62 , pp. 155-183
    • Eloy, F.1    Lenaers, R.2
  • 3
    • 0022851286 scopus 로고
    • Untersuchungen in der reihe der N1-hydroxyamidine: Synthesen und umsetzungen mit isocyanaten und 1,1′-carbonyl-diimidazol
    • Zinner G, Perner M, Grünefeld J, Schecker HG. Untersuchungen in der reihe der N1-hydroxyamidine: Synthesen und umsetzungen mit isocyanaten und 1,1′-carbonyl-diimidazol. Arch Pharm 1986; 319: 1073-9.
    • (1986) Arch Pharm , vol.319 , pp. 1073-1079
    • Zinner, G.1    Perner, M.2    Grünefeld, J.3    Schecker, H.G.4
  • 4
    • 0345021247 scopus 로고
    • Reaction of amidoximes with a-chloroalkanoic acid chlorides: Novel synthesis of 1,2,4-oxadiazin-5-ones
    • Hussein AC. Reaction of amidoximes with a-chloroalkanoic acid chlorides: novel synthesis of 1,2,4-oxadiazin-5-ones. Heterocycles 1987; 26: 163-73.
    • (1987) Heterocycles , vol.26 , pp. 163-173
    • Hussein, A.C.1
  • 5
    • 0027598092 scopus 로고
    • Hydroxyamidines as new extracting reagents for spectrophotometric determination of cadmium with 4-(2-pyridylazo)naphthol in industrial effluents, coal, and fly ash
    • Chakravarty S, Deb MK, Mishra RK. Hydroxyamidines as new extracting reagents for spectrophotometric determination of cadmium with 4-(2-pyridylazo)naphthol in industrial effluents, coal, and fly ash. J AOAC Int 1993; 76(3): 604-8.
    • (1993) J AOAC Int , vol.76 , Issue.3 , pp. 604-608
    • Chakravarty, S.1    Deb, M.K.2    Mishra, R.K.3
  • 6
    • 0026058489 scopus 로고
    • Sensitive spectrophotometric determination of osmium with pyrocatechol and hydroxyamidine
    • Deb MK, Mishra N, Patel KS, Mishra RK. Sensitive spectrophotometric determination of osmium with pyrocatechol and hydroxyamidine. Analyst 1991; 116: 323-5.
    • (1991) Analyst , vol.116 , pp. 323-325
    • Deb, M.K.1    Mishra, N.2    Patel, K.S.3    Mishra, R.K.4
  • 9
    • 0035952991 scopus 로고    scopus 로고
    • An improved synthesis of 1,2,4-oxadiazoles on solid support
    • Rice KD, Nuss JM. An improved synthesis of 1,2,4-oxadiazoles on solid support. Bioorg Med Chem Lett 2001; 11: 753-5.
    • (2001) Bioorg Med Chem Lett , vol.11 , pp. 753-755
    • Rice, K.D.1    Nuss, J.M.2
  • 10
    • 0037013933 scopus 로고    scopus 로고
    • Palladium-catalyzed N-arylation of O-methylamidoximes
    • Anbazhagan M, Stephens CE, Boykin DW. Palladium-catalyzed N-arylation of O-methylamidoximes. Tetrahedron Lett 2002; 43: 4221-4.
    • (2002) Tetrahedron Lett , vol.43 , pp. 4221-4224
    • Anbazhagan, M.1    Stephens, C.E.2    Boykin, D.W.3
  • 11
    • 0037049227 scopus 로고    scopus 로고
    • Regioselective cleavage of O-benzyl-N-arylamidoximes: Synthesis of N-aryl amidines and amidoximes
    • Anbazhagan M, Boykin DW, Stephens CE. Regioselective cleavage of O-benzyl-N-arylamidoximes: Synthesis of N-aryl amidines and amidoximes. Tetrahedron Lett 2002; 43: 9089-92.
    • (2002) Tetrahedron Lett , vol.43 , pp. 9089-9092
    • Anbazhagan, M.1    Boykin, D.W.2    Stephens, C.E.3
  • 12
    • 10044254490 scopus 로고    scopus 로고
    • Efficient conversion of o-substituted 3-hydroxy-4-imino-oxazolidin-2-ones into O-substituted α-hydroxyamidoximes
    • Kurz T, Widyan K. Efficient conversion of o-substituted 3-hydroxy-4-imino-oxazolidin-2-ones into O-substituted α-hydroxyamidoximes. Org Lett 2004; 6: 4403-5.
    • (2004) Org Lett , vol.6 , pp. 4403-4405
    • Kurz, T.1    Widyan, K.2
  • 13
    • 0029046233 scopus 로고
    • Synthesis of 1,2,4-oxadiazole-, 1,3,4-oxadiazole-, and 1,2,4-triazole-derived dipeptidomimetics
    • and references therein
    • Borg S, Estenne-Bouhtou G, Luthman K, Csoregh I, Hesselink W, Haeksell U. Synthesis of 1,2,4-oxadiazole-, 1,3,4-oxadiazole-, and 1,2,4-triazole-derived dipeptidomimetics. J Org Chem 1995; 60: 3112-20 and references therein.
    • (1995) J Org Chem , vol.60 , pp. 3112-3120
    • Borg, S.1    Estenne-Bouhtou, G.2    Luthman, K.3    Csoregh, I.4    Hesselink, W.5    Haeksell, U.6
  • 14
    • 0024465527 scopus 로고    scopus 로고
    • Novel benzodiazepine receptor partial agonists: Oxadiazolylimidazobenzodiazepines
    • Watjcn F, Baker R, Engelstoff M, Herbert R, Macleod A, Knight A, et al. Novel benzodiazepine receptor partial agonists: oxadiazolylimidazobenzodiazepines. J Med Chem 1999; 32: 2282-91.
    • (1999) J Med Chem , vol.32 , pp. 2282-2291
    • Watjcn, F.1    Baker, R.2    Engelstoff, M.3    Herbert, R.4    Macleod, A.5    Knight, A.6
  • 16
    • 0025955501 scopus 로고
    • Comparison of azabicyclic esters and oxadiazoles as ligands for the muscarinic receptor
    • Orlek BS, Blaney FE, Brown F, Clark MSG, Hadley MS, Hatcher J, et al. Comparison of azabicyclic esters and oxadiazoles as ligands for the muscarinic receptor. J Med Chem 1991; 34: 2726-35.
    • (1991) J Med Chem , vol.34 , pp. 2726-2735
    • Orlek, B.S.1    Blaney, F.E.2    Brown, F.3    Clark, M.S.G.4    Hadley, M.S.5    Hatcher, J.6
  • 17
    • 0028037925 scopus 로고
    • Oxadiazoles as ester bioisosteric replacements in compounds related to disoxaril. antirhinovirus activity
    • Diana GD, Volkots DL, Hitz TJ, Bailey TR, Long MA, Vescio N, et al. Oxadiazoles as ester bioisosteric replacements in compounds related to disoxaril. antirhinovirus activity. J Med Chem 1994; 37: 2421-36.
    • (1994) J Med Chem , vol.37 , pp. 2421-2436
    • Diana, G.D.1    Volkots, D.L.2    Hitz, T.J.3    Bailey, T.R.4    Long, M.A.5    Vescio, N.6
  • 19
    • 0032482498 scopus 로고    scopus 로고
    • Novel synthesis of oxadiazoles via palladium catalysis
    • Young JR, DeVita RJ. Novel synthesis of oxadiazoles via palladium catalysis. Tetrahedron Lett 1998; 39: 3931-4.
    • (1998) Tetrahedron Lett , vol.39 , pp. 3931-3934
    • Young, J.R.1    DeVita, R.J.2
  • 20
    • 0033601459 scopus 로고    scopus 로고
    • Solid-phase synthesis of 1,2,4-oxadiazoles
    • Sams CK, Lau J. Solid-phase synthesis of 1,2,4-oxadiazoles. Tetrahedron Lett 1999; 40: 9359-62.
    • (1999) Tetrahedron Lett , vol.40 , pp. 9359-9362
    • Sams, C.K.1    Lau, J.2
  • 21
    • 0033584066 scopus 로고    scopus 로고
    • Oxadiazole synthesis on solid supports
    • Liang GB, Qian X. Oxadiazole synthesis on solid supports. Bioorg Med Chem Lett 1999; 9: 2101-4.
    • (1999) Bioorg Med Chem Lett , vol.9 , pp. 2101-2104
    • Liang, G.B.1    Qian, X.2
  • 23
    • 15044363597 scopus 로고    scopus 로고
    • Rapid and efficient synthesis of 1,2,4-oxadiazoles utilizing polymer-supported reagents under microwave heating
    • Wang Y, Miller RI, Sauer DR, Djuric SW. Rapid and efficient synthesis of 1,2,4-oxadiazoles utilizing polymer-supported reagents under microwave heating. Org Lett 2005; 7: 925-8.
    • (2005) Org Lett , vol.7 , pp. 925-928
    • Wang, Y.1    Miller, R.I.2    Sauer, D.R.3    Djuric, S.W.4
  • 24
    • 33646508517 scopus 로고    scopus 로고
    • A 'one-pot' synthesis of α-1,2,4-oxadiazollo esters from malonic diesters and amidoximes under solvent-free conditions
    • Du W, Hagmann WK, Hale JJ. A 'one-pot' synthesis of α-1,2,4-oxadiazollo esters from malonic diesters and amidoximes under solvent-free conditions. Tetrahedron Lett 2006; 47: 4271-4.
    • (2006) Tetrahedron Lett , vol.47 , pp. 4271-4274
    • Du, W.1    Hagmann, W.K.2    Hale, J.J.3
  • 26
    • 44449105453 scopus 로고    scopus 로고
    • Method for producing amidines
    • WO 0061574, P282087
    • Zierke T, Mack H. Method for producing amidines. WO 0061574, 2000; Chem Abstr 2000; 133, P282087.
    • (2000) Chem Abstr , vol.133
    • Zierke, T.1    Mack, H.2
  • 29
    • 0027910386 scopus 로고
    • Ruthenium complex-catalyzed sencitive deoxygenation of amidoximes to amidines and its application to the facile synthesis of pyrimidines
    • Akazome M, Kondo T, Watanabe Y. Ruthenium complex-catalyzed sencitive deoxygenation of amidoximes to amidines and its application to the facile synthesis of pyrimidines. J Mol Catal 1993; 80: 383-93.
    • (1993) J Mol Catal , vol.80 , pp. 383-393
    • Akazome, M.1    Kondo, T.2    Watanabe, Y.3
  • 30
    • 4444356920 scopus 로고    scopus 로고
    • Solid-phase synthesis of amidines. by the reduction of amidoximes
    • Cesar J, Nadrah K, Dolenc MS. Solid-phase synthesis of amidines. by the reduction of amidoximes. Tetrahedron Lett 2004; 45: 7445-9.
    • (2004) Tetrahedron Lett , vol.45 , pp. 7445-7449
    • Cesar, J.1    Nadrah, K.2    Dolenc, M.S.3
  • 31
    • 0344442256 scopus 로고    scopus 로고
    • Direct conversion of amidoximes to amidines via transfer hydrogenation
    • Anbazhagan M, Boykin DW, Stephens CE. Direct conversion of amidoximes to amidines via transfer hydrogenation. Synthesis 2003; 2467-9.
    • (2003) Synthesis , pp. 2467-2469
    • Anbazhagan, M.1    Boykin, D.W.2    Stephens, C.E.3
  • 32
    • 0012281465 scopus 로고    scopus 로고
    • Oxidation of arylamidoximes by various chemical and biomimetic systems: Comparison with their oxidations by hemeproteins
    • Vadon-Le Goff S. Boucher JI, Mansuy DC Oxidation of arylamidoximes by various chemical and biomimetic systems: Comparison with their oxidations by hemeproteins. R Acad Sci Paris Série IIe Chimie/ Chemistry 2000; 3: 785-92.
    • (2000) R Acad Sci Paris Série IIe Chimie/ Chemistry , vol.3 , pp. 785-792
    • Vadon-Le Goff, S.1    Boucher, J.I.2    Mansuy, D.C.3
  • 33
    • 0032497909 scopus 로고    scopus 로고
    • Microsomal cytochrome P450 dependent oxidation of N-hydroxyguanidines, amidoximes, and ketoximes: Mechanism of the oxidative cleavage of their C=N(OH) bond with formation of nitrogen oxides
    • Jousserandot A, Boucher JL, Henry Y, Niklaus B, Clement B, Mansuy D. Microsomal cytochrome P450 dependent oxidation of N-hydroxyguanidines, amidoximes, and ketoximes: Mechanism of the oxidative cleavage of their C=N(OH) bond with formation of nitrogen oxides. Biochemistry 1998; 37: 17179-91.
    • (1998) Biochemistry , vol.37 , pp. 17179-17191
    • Jousserandot, A.1    Boucher, J.L.2    Henry, Y.3    Niklaus, B.4    Clement, B.5    Mansuy, D.6
  • 35
    • 0035898817 scopus 로고    scopus 로고
    • Oxidative cleavage of the C=N bond during singlet oxygenations of amidoximes
    • Öcal N, Erden I. Oxidative cleavage of the C=N bond during singlet oxygenations of amidoximes. Tetrahedron Lett 2001; 42: 4765-7.
    • (2001) Tetrahedron Lett , vol.42 , pp. 4765-4767
    • Öcal, N.1    Erden, I.2
  • 38
    • 0024369941 scopus 로고
    • Biosynthesis of nitric oxide from L-arginine: A pathway for the regulation of cell function and communication
    • Moncada S, Palmer RMJ, Higgs EA. Biosynthesis of nitric oxide from L-arginine: A pathway for the regulation of cell function and communication. Biochem Pharm. 1989; 38: 1709-15.
    • (1989) Biochem Pharm , vol.38 , pp. 1709-1715
    • Moncada, S.1    Palmer, R.M.J.2    Higgs, E.A.3
  • 39
    • 0023685375 scopus 로고
    • Mammallian synthesis of nitrite, nitrate, nitric oxide, and N-nitrosating agents
    • Marietta MA. Mammallian synthesis of nitrite, nitrate, nitric oxide, and N-nitrosating agents. Chem Res Toxicol 1988; 1: 249-57.
    • (1988) Chem Res Toxicol , vol.1 , pp. 249-257
    • Marietta, M.A.1
  • 40
    • 0025883342 scopus 로고
    • Nitric-oxide: Physiology, pathophysiology, and pharmacology
    • Moncada S, Palmer R, Higgs EA. Nitric-oxide: Physiology, pathophysiology, and pharmacology. Pharmacol Rev 1991: 43: 109-42.
    • (1991) Pharmacol Rev , vol.43 , pp. 109-142
    • Moncada, S.1    Palmer, R.2    Higgs, E.A.3
  • 41
    • 0028863627 scopus 로고
    • Molecular mechanisms and therapeutic strategies related to nitric oxide
    • Moncada S, Higgs EA. Molecular mechanisms and therapeutic strategies related to nitric oxide. FASEB J 1995; 9: 1319-30.
    • (1995) FASEB J , vol.9 , pp. 1319-1330
    • Moncada, S.1    Higgs, E.A.2
  • 42
    • 0029781820 scopus 로고    scopus 로고
    • The importance of superoxide in nitric oxide-dependent toxicity: Evidence for peroxynitrite-mediated injury
    • Crow JP, Beckman JS. The importance of superoxide in nitric oxide-dependent toxicity: Evidence for peroxynitrite-mediated injury. Adv Exp Med Biol 1996; 387: 147-61.
    • (1996) Adv Exp Med Biol , vol.387 , pp. 147-161
    • Crow, J.P.1    Beckman, J.S.2
  • 43
    • 0029805172 scopus 로고    scopus 로고
    • Nitric oxide, superoxide, and peroxynitrite: The good, the-bad, and ugly
    • Beckman JS, Koppenol WH. Nitric oxide, superoxide, and peroxynitrite: the good, the-bad, and ugly. Am J Physiol 1996; 271: C1424-37.
    • (1996) Am J Physiol , vol.271
    • Beckman, J.S.1    Koppenol, W.H.2
  • 44
    • 0028847858 scopus 로고
    • The comparative toxicity of nitric oxide and peroxynitrite to Escherichia coli
    • Brunelli L, Crow J, Beckman J. The comparative toxicity of nitric oxide and peroxynitrite to Escherichia coli. Arch Biochem Biophys 1995; 316: 327-34.
    • (1995) Arch Biochem Biophys , vol.316 , pp. 327-334
    • Brunelli, L.1    Crow, J.2    Beckman, J.3
  • 45
    • 0030203367 scopus 로고    scopus 로고
    • The role of peroxynitrite in the pathophysiology of shock, inflammation and ischemia-reperfusion injury
    • Szabó C. The role of peroxynitrite in the pathophysiology of shock, inflammation and ischemia-reperfusion injury. Shock 1996; 6: 79-88.
    • (1996) Shock , vol.6 , pp. 79-88
    • Szabó, C.1
  • 46
    • 0032533731 scopus 로고    scopus 로고
    • Hydroxyquanidines inhibit peroxynitrite-induced oxidation
    • Southan GJ, Salzman AL, Szabó C. Hydroxyquanidines inhibit peroxynitrite-induced oxidation. Free Rad Biol Med 1998; 25: 914-25
    • (1998) Free Rad Biol Med , vol.25 , pp. 914-925
    • Southan, G.J.1    Salzman, A.L.2    Szabó, C.3
  • 47
    • 0036525943 scopus 로고    scopus 로고
    • Nitric oxide donors: Chemical activities and biological applications
    • Wang PG, Xian M, Tang X, Wu X, Wen Z, Cai T, et al. Nitric oxide donors: Chemical activities and biological applications. Chem Rev 2002; 102: 1091-134.
    • (2002) Chem Rev , vol.102 , pp. 1091-1134
    • Wang, P.G.1    Xian, M.2    Tang, X.3    Wu, X.4    Wen, Z.5    Cai, T.6
  • 49
    • 0035425503 scopus 로고    scopus 로고
    • Nitric oxide synthases: Structure, function and inhibition
    • Alderton WK, Cooper CE, Knowles RG. Nitric oxide synthases: Structure, function and inhibition. Biochem J 2001; 357: 593-615.
    • (2001) Biochem J , vol.357 , pp. 593-615
    • Alderton, W.K.1    Cooper, C.E.2    Knowles, R.G.3
  • 50
    • 0033553802 scopus 로고    scopus 로고
    • Nitric oxide: Chemical puzzles posed by a biological messenger
    • Pfeiffer S, Mayer B, Hemmens B. Nitric oxide: Chemical puzzles posed by a biological messenger. Angew Chem Int Ed 1999; 38: 1714-31.
    • (1999) Angew Chem Int Ed , vol.38 , pp. 1714-1731
    • Pfeiffer, S.1    Mayer, B.2    Hemmens, B.3
  • 51
    • 0025892441 scopus 로고
    • N omega-hydroxy-L-arginine is an intermediate in the biosynthesis of nitric oxide from L-arginine
    • Stuehr DJ, Kwon NS, Nathan CF, Griffith OW, Feldman PL, Wiseman J. N omega-hydroxy-L-arginine is an intermediate in the biosynthesis of nitric oxide from L-arginine. J Biol Chem 1991; 266: 6259-63.
    • (1991) J Biol Chem , vol.266 , pp. 6259-6263
    • Stuehr, D.J.1    Kwon, N.S.2    Nathan, C.F.3    Griffith, O.W.4    Feldman, P.L.5    Wiseman, J.6
  • 52
    • 0027325255 scopus 로고
    • Nitric oxide synthase structure and mechanism
    • Marietta MA. Nitric oxide synthase structure and mechanism. J Biol Chem 1993; 268: 12231-34.
    • (1993) J Biol Chem , vol.268 , pp. 12231-12234
    • Marietta, M.A.1
  • 54
    • 0027292075 scopus 로고
    • Multiple catalytic functions of brain nitric oxide synthase: Biochemical characterization, cofactor-requirement, and the role of Nω-hydroxy-L-arginine as an intermediate
    • Klatt P, Schmidt K, Uray G, Mayer B. Multiple catalytic functions of brain nitric oxide synthase: Biochemical characterization, cofactor-requirement, and the role of Nω-hydroxy-L-arginine as an intermediate. J Biol Chem 1993; 268: 14781-7.
    • (1993) J Biol Chem , vol.268 , pp. 14781-14787
    • Klatt, P.1    Schmidt, K.2    Uray, G.3    Mayer, B.4
  • 55
    • 0028821761 scopus 로고
    • On the mechanism of nitric oxide formation upon oxidative cleavage of C=N(OH) bonds by NO-synthases and cytochromes P450
    • Mansuy D, Boucher JL, Clement B. On the mechanism of nitric oxide formation upon oxidative cleavage of C=N(OH) bonds by NO-synthases and cytochromes P450. Biochimie 1995; 77: 661-7.
    • (1995) Biochimie , vol.77 , pp. 661-667
    • Mansuy, D.1    Boucher, J.L.2    Clement, B.3
  • 57
    • 0026773733 scopus 로고
    • Formation of nitrogen-oxides and citrulline upon oxidation of N-omega-hydroxy-L-arginine by hemeproteins
    • Boucher JL, Genet A, Vadom S, Delaforge M, Mansuy D. Formation of nitrogen-oxides and citrulline upon oxidation of N-omega-hydroxy-L-arginine by hemeproteins. Biochem Biophys Res Commun 1992; 184: 1158-64.
    • (1992) Biochem Biophys Res Commun , vol.184 , pp. 1158-1164
    • Boucher, J.L.1    Genet, A.2    Vadom, S.3    Delaforge, M.4    Mansuy, D.5
  • 58
    • 0026735580 scopus 로고
    • Nitric oxide synthase is a cytochrome P450 type hemoprotein
    • White KA, Marietta MA. Nitric oxide synthase is a cytochrome P450 type hemoprotein. Biochemistry 1992; 31: 6627-31.
    • (1992) Biochemistry , vol.31 , pp. 6627-6631
    • White, K.A.1    Marietta, M.A.2
  • 59
    • 0026660191 scopus 로고
    • Spectral characterization of brain and macrophage nitric oxide synthases
    • Stuehr DJ, Saito MI. Spectral characterization of brain and macrophage nitric oxide synthases. J Biol Chem 1992; 267: 20547-50.
    • (1992) J Biol Chem , vol.267 , pp. 20547-20550
    • Stuehr, D.J.1    Saito, M.I.2
  • 60
    • 0026471538 scopus 로고
    • Cloned, expessed rat cerebellar nitric oxide synthase contains stoichiometric amounds of heme which binds carbon monoxide
    • McMillan K, Bredt DS, Hirsh DJ, Snyder SH, Clark JE, Masters BSS. Cloned, expessed rat cerebellar nitric oxide synthase contains stoichiometric amounds of heme which binds carbon monoxide. Proc Natl Acad Sci USA 1992; 89: 11141-5.
    • (1992) Proc Natl Acad Sci USA , vol.89 , pp. 11141-11145
    • McMillan, K.1    Bredt, D.S.2    Hirsh, D.J.3    Snyder, S.H.4    Clark, J.E.5    Masters, B.S.S.6
  • 61
    • 4644372669 scopus 로고    scopus 로고
    • Alternative nitric oxide-producing substrates for NO synthesis
    • Mansuy D, Boucher JL. Alternative nitric oxide-producing substrates for NO synthesis. Free Rad Biol Med 2004; 37: 1105-21.
    • (2004) Free Rad Biol Med , vol.37 , pp. 1105-1121
    • Mansuy, D.1    Boucher, J.L.2
  • 62
    • 0027320848 scopus 로고
    • Particular ability of liver P450s3A to catalyze the oxidation of Nω hydroxyarginine to citrulline and nitrogen oxides and occurrence in NO synthases of a sequence very similar to the home binding sequence in P450s
    • Renaud JP, Boucher JL, Vadon S, Delaforge M, Mansuy D. Particular ability of liver P450s3A to catalyze the oxidation of Nω hydroxyarginine to citrulline and nitrogen oxides and occurrence in NO synthases of a sequence very similar to the home binding sequence in P450s. Biochem Biophys Res Commun 1993; 192: 53-60.
    • (1993) Biochem Biophys Res Commun , vol.192 , pp. 53-60
    • Renaud, J.P.1    Boucher, J.L.2    Vadon, S.3    Delaforge, M.4    Mansuy, D.5
  • 63
    • 0021057712 scopus 로고
    • The oxidation of benzamidines in vitro
    • Clement B. The oxidation of benzamidines in vitro. Xenobiotica 1983; 13: 467-73.
    • (1983) Xenobiotica , vol.13 , pp. 467-473
    • Clement, B.1
  • 64
    • 0028278433 scopus 로고
    • N-hydroxylation of antiprotozoal drug pentamidine catalyzed by rabbit liver cytochrome P450 2C3 or human liver microsomes, microsomal retroreduction, and further oxidative transformation of the formed amidoximes
    • Clement B, Jung F. N-hydroxylation of antiprotozoal drug pentamidine catalyzed by rabbit liver cytochrome P450 2C3 or human liver microsomes, microsomal retroreduction, and further oxidative transformation of the formed amidoximes. Drug Metab Disp 1994; 22: 486-97.
    • (1994) Drug Metab Disp , vol.22 , pp. 486-497
    • Clement, B.1    Jung, F.2
  • 65
    • 0027141919 scopus 로고
    • Cytochrome P450-dependent N-hydroxylation of a guanidine (debrisoquine), microsomal catolyzed reduction and further oxidation of the N-hydroxyguanidine metabolite to the urea derivative
    • Clement B, Schultze-Mosgau MH, Wohlers H. Cytochrome P450-dependent N-hydroxylation of a guanidine (debrisoquine), microsomal catolyzed reduction and further oxidation of the N-hydroxyguanidine metabolite to the urea derivative. Biochem Pharmacol 1993; 46: 2249-67.
    • (1993) Biochem Pharmacol , vol.46 , pp. 2249-2267
    • Clement, B.1    Schultze-Mosgau, M.H.2    Wohlers, H.3
  • 66
    • 0005260048 scopus 로고    scopus 로고
    • Oxidation and reduction of nitrogen via CYP450: Importance of the reduction of genotoxic N-hydroxylated functional groups
    • IOS Press: Amsterdam
    • Clement B. Oxidation and reduction of nitrogen via CYP450: Importance of the reduction of genotoxic N-hydroxylated functional groups. Drug metabolism: Towards the new millenium; IOS Press: Amsterdam, 1998; 59-71.
    • (1998) Drug metabolism: Towards the new millenium , pp. 59-71
    • Clement, B.1
  • 67
    • 0035077590 scopus 로고    scopus 로고
    • Phase 2 metabolites of N-hydroxylated amidines (amidoximes): Synthesis, in vitro formation by pig hepatocytes, and mutagenicity testing
    • Clement B, Christiansen K, Girreser U. Phase 2 metabolites of N-hydroxylated amidines (amidoximes): Synthesis, in vitro formation by pig hepatocytes, and mutagenicity testing. Chem Res Toxicol 2001; 14: 319-26.
    • (2001) Chem Res Toxicol , vol.14 , pp. 319-326
    • Clement, B.1    Christiansen, K.2    Girreser, U.3
  • 68
    • 16244387932 scopus 로고    scopus 로고
    • Metabolism of benzamidoxime (N-hydroxyamidine) in human hepatocytes and role of UDP-glucuronosyltransferases
    • Fröhlich AK, Girreser U, Clement B. Metabolism of benzamidoxime (N-hydroxyamidine) in human hepatocytes and role of UDP-glucuronosyltransferases. Xenobiotica 2005; 35: 17-25.
    • (2005) Xenobiotica , vol.35 , pp. 17-25
    • Fröhlich, A.K.1    Girreser, U.2    Clement, B.3
  • 73
    • 0026565809 scopus 로고
    • Reduction of amidoxime derivatives to pentamidine in vivo
    • Clement B, Immel M, Terlinden R, Winger FJ. Reduction of amidoxime derivatives to pentamidine in vivo. Arch Pharm 1992; 325: 61-2
    • (1992) Arch Pharm , vol.325 , pp. 61-62
    • Clement, B.1    Immel, M.2    Terlinden, R.3    Winger, F.J.4
  • 75
    • 0029072182 scopus 로고
    • N-hydroxylation and N-Dealkylation by P450 of N-methylbenzamidine: N-oxygenation and N-oxidative dealkylation of one functional group
    • Clement B, Jung F. N-hydroxylation and N-Dealkylation by P450 of N-methylbenzamidine: N-oxygenation and N-oxidative dealkylation of one functional group. Xenobiotica 1995; 25: 443-55.
    • (1995) Xenobiotica , vol.25 , pp. 443-455
    • Clement, B.1    Jung, F.2
  • 79
    • 44449109484 scopus 로고    scopus 로고
    • Ortiz de Montellano PR, Reich N. O. In: Ortiz de Montellano PR Ed, Cytochrome P-450, structure, mechanism and biochemistry; Plenum Press, New York, 1986; pp. 273-314.
    • Ortiz de Montellano PR, Reich N. O. In: Ortiz de Montellano PR Ed, Cytochrome P-450, structure, mechanism and biochemistry; Plenum Press, New York, 1986; pp. 273-314.
  • 80
    • 0028924114 scopus 로고
    • Formation of nitrogen oxides including NO from oxidative cleavage of C=N(OH) bonds: A general cytochrome P450-dependent reaction
    • Jousserandot A, Boucher JL, Desseaux C, Delaforge M, Mansuy D. Formation of nitrogen oxides including NO from oxidative cleavage of C=N(OH) bonds: A general cytochrome P450-dependent reaction. Bioorg Med Chem Lett 1995; 5: 423-6.
    • (1995) Bioorg Med Chem Lett , vol.5 , pp. 423-426
    • Jousserandot, A.1    Boucher, J.L.2    Desseaux, C.3    Delaforge, M.4    Mansuy, D.5
  • 81
    • 0029156528 scopus 로고
    • Superoxide anion efficiently performs the oxidative cleavage of C=NOH bonds of amidoximes and N-hydroxyguanidines with formation of nitrogen oxides
    • Sennequier N, Boucher JL, Battioni P, Mansuy D. Superoxide anion efficiently performs the oxidative cleavage of C=NOH bonds of amidoximes and N-hydroxyguanidines with formation of nitrogen oxides. Tetrahedron Lett 1995; 34: 6059-62.
    • (1995) Tetrahedron Lett , vol.34 , pp. 6059-6062
    • Sennequier, N.1    Boucher, J.L.2    Battioni, P.3    Mansuy, D.4
  • 83
    • 0036038490 scopus 로고    scopus 로고
    • Reduction of N-hydroxylated compounds: Amidoximes (N-hydroxyamidines) as pro-drugs of amidines
    • Clement B. Reduction of N-hydroxylated compounds: Amidoximes (N-hydroxyamidines) as pro-drugs of amidines. Drug Metab Rev 2002; 34: 565-79.
    • (2002) Drug Metab Rev , vol.34 , pp. 565-579
    • Clement, B.1
  • 84
    • 0028176705 scopus 로고
    • G-hydroxy-L-arginine causes nitrite production in vascular smooth muscle cells in the absence of nitric oxide synthase activity
    • G-hydroxy-L-arginine causes nitrite production in vascular smooth muscle cells in the absence of nitric oxide synthase activity. FEBS Lett 1994; 341: 203-7.
    • (1994) FEBS Lett , vol.341 , pp. 203-207
    • Schott1    Bogen, C.M.2    Vetrovsky, P.3    Berton, C.C.4    Stoclet, J.C.5
  • 85
    • 0031764558 scopus 로고    scopus 로고
    • Nitric oxide synthesis by tracheal smooth muscle cells by a nitric oxide synthase-independent pathway
    • Jia Y, Zacour M, Tolloczko B, Martin JG. Nitric oxide synthesis by tracheal smooth muscle cells by a nitric oxide synthase-independent pathway. Am J Physiol 1998; 275: L895-901.
    • (1998) Am J Physiol , vol.275
    • Jia, Y.1    Zacour, M.2    Tolloczko, B.3    Martin, J.G.4
  • 87
    • 0034898074 scopus 로고    scopus 로고
    • Oxidation of the ketoxime acetoxime to nitric oxide by oxygen radical generating systems
    • Caro AA, Cederbaum AI, Stoyanovsky DA. Oxidation of the ketoxime acetoxime to nitric oxide by oxygen radical generating systems. Nitric Oxide 2001; 5: 413-24.
    • (2001) Nitric Oxide , vol.5 , pp. 413-424
    • Caro, A.A.1    Cederbaum, A.I.2    Stoyanovsky, D.A.3
  • 88
    • 0035928820 scopus 로고    scopus 로고
    • Lefevre-Groboillot D, Dijols S, Boucher JL, Mahy JP, Ricoux R, Desbois A, et al. N-hydroxyguanidines as new heme ligands: UV-visible, EPR, and resonance Raman studies of the interaction of various compounds bearing a C=NOH function with microperoxidase-8. Biochemistry 2001; 40: 9909-17.
    • Lefevre-Groboillot D, Dijols S, Boucher JL, Mahy JP, Ricoux R, Desbois A, et al. N-hydroxyguanidines as new heme ligands: UV-visible, EPR, and resonance Raman studies of the interaction of various compounds bearing a C=NOH function with microperoxidase-8. Biochemistry 2001; 40: 9909-17.
  • 89
    • 0023696576 scopus 로고
    • Genotoxic activities of benzamidine and its N-hydroxylated metabolite benzamidoxime in S. typhimurium and in mammalian cells
    • Clement B, Schmezer P, Weber H, Schlehofer JR, Schmidt S, Pool BL. Genotoxic activities of benzamidine and its N-hydroxylated metabolite benzamidoxime in S. typhimurium and in mammalian cells. J Cancer Res Clin Oncol 1988; 114: 363-8.
    • (1988) J Cancer Res Clin Oncol , vol.114 , pp. 363-368
    • Clement, B.1    Schmezer, P.2    Weber, H.3    Schlehofer, J.R.4    Schmidt, S.5    Pool, B.L.6
  • 90
    • 0029967158 scopus 로고    scopus 로고
    • Microsomal catalyzed N-hydroxylation of guanabenz and reduction of the N-hydroxylated metabolite: Characterization of the two reactions and genotoxic potential of guanabenz
    • Clement B, Demesmaeker M, Linne S. Microsomal catalyzed N-hydroxylation of guanabenz and reduction of the N-hydroxylated metabolite: Characterization of the two reactions and genotoxic potential of guanabenz. Chem Res Toxicol 1996; 9: 682-8
    • (1996) Chem Res Toxicol , vol.9 , pp. 682-688
    • Clement, B.1    Demesmaeker, M.2    Linne, S.3
  • 91
    • 0024260683 scopus 로고
    • Enzymatic reduction of benzamidoxime to benzamidine
    • Clement B, Schmidt S, Zimmerman M. Enzymatic reduction of benzamidoxime to benzamidine. Arch Pharm 1988; 321: 955-6.
    • (1988) Arch Pharm , vol.321 , pp. 955-956
    • Clement, B.1    Schmidt, S.2    Zimmerman, M.3
  • 92
    • 0024066886 scopus 로고
    • Reduction of benzamidoxime derivative to the corresponding benzamidine in vivo and in vitro
    • Hautpmann J, Paintz M, Kaiser B, Richter M. Reduction of benzamidoxime derivative to the corresponding benzamidine in vivo and in vitro. Pharmazie 1988; 43: 559-60.
    • (1988) Pharmazie , vol.43 , pp. 559-560
    • Hautpmann, J.1    Paintz, M.2    Kaiser, B.3    Richter, M.4
  • 93
    • 0024698562 scopus 로고
    • Biotransformation des benzamidins und des benzamidoxims durch mikrosomale enzyme von kaninchen.
    • Clement B, Zimmerman M, Schmidt S. Biotransformation des benzamidins und des benzamidoxims durch mikrosomale enzyme von kaninchen. Arch Pharm 1989; 322: 431-6.
    • (1989) Arch Pharm , vol.322 , pp. 431-436
    • Clement, B.1    Zimmerman, M.2    Schmidt, S.3
  • 94
    • 0027330146 scopus 로고
    • Biotransformations of benzamidine and benzamidoxime in vivo
    • Clement B, Immel M, Schmidt S, Steinmann U. Biotransformations of benzamidine and benzamidoxime in vivo. Arch Pharm 1993; 326: 807-12.
    • (1993) Arch Pharm , vol.326 , pp. 807-812
    • Clement, B.1    Immel, M.2    Schmidt, S.3    Steinmann, U.4
  • 96
    • 0028170321 scopus 로고
    • Cytochrome P450 dependent N-hydroxylation of an aminoguanidine (amidinohydrazone) and microsomal retroreduction of the N-hydroxylated product
    • Clement B, Schultze-Mosgau MH, Richter M, Besch A. Cytochrome P450 dependent N-hydroxylation of an aminoguanidine (amidinohydrazone) and microsomal retroreduction of the N-hydroxylated product. Xenobiotica, 1994; 24: 671-88.
    • (1994) Xenobiotica , vol.24 , pp. 671-688
    • Clement, B.1    Schultze-Mosgau, M.H.2    Richter, M.3    Besch, A.4
  • 97
    • 0030726786 scopus 로고    scopus 로고
    • Formation of guanoxabenz from guanabenz in human liver: A new metabolic marker for CYP1A2
    • Clement B, Demesmaeker M. Formation of guanoxabenz from guanabenz in human liver: A new metabolic marker for CYP1A2. Drug Metab Dispos 1997; 25: 1266-71.
    • (1997) Drug Metab Dispos , vol.25 , pp. 1266-1271
    • Clement, B.1    Demesmaeker, M.2
  • 98
    • 0037403707 scopus 로고    scopus 로고
    • Characterization of in vitro biotransformation of new, orally active, direct thrombin inhibitor ximelagatran, an amidoxime and ester prodrug
    • Clement B, Lopian K. Characterization of in vitro biotransformation of new, orally active, direct thrombin inhibitor ximelagatran, an amidoxime and ester prodrug. Drug Metab Disp 2003; 31: 645-51.
    • Drug Metab Disp 2003; 31: 645-51
    • Clement, B.1    Lopian, K.2
  • 99
    • 0035251672 scopus 로고    scopus 로고
    • The direct thrombin inhibitor melagatran and its oral prodrug H376/95: Intestinal absorption properties, biochemical and pharmacodynamic effects
    • Gustafsson D, Nyström JF. Carlsson S, Bredberg U, Eriksson U, Gyzander E, et al. The direct thrombin inhibitor melagatran and its oral prodrug H376/95: Intestinal absorption properties, biochemical and pharmacodynamic effects. Thromb Res 2001; 101: 171-81.
    • (2001) Thromb Res , vol.101 , pp. 171-181
    • Gustafsson, D.1    Nyström, J.F.2    Carlsson, S.3    Bredberg, U.4    Eriksson, U.5    Gyzander, E.6
  • 100
    • 0002439865 scopus 로고    scopus 로고
    • Pharmacodynamic properties of H376/95, a prodrug of the direct thrombin inhibitor melagatran, intended for oral use
    • Pt 1, 102
    • Gustafsson D, Nyström JE, Carlsson S, Bredberg U, Elg M, Gyzander E, et al. Pharmacodynamic properties of H376/95, a prodrug of the direct thrombin inhibitor melagatran, intended for oral use. Blood 1999; 94(Suppl 1, Pt 1): 102.
    • (1999) Blood , vol.94 , Issue.SUPPL. 1
    • Gustafsson, D.1    Nyström, J.E.2    Carlsson, S.3    Bredberg, U.4    Elg, M.5    Gyzander, E.6
  • 103
    • 29144492135 scopus 로고    scopus 로고
    • Heberling S, Girreser U, Wolf s, Clement B. Oxygen-insensitive enzymatic reduction of oximes to imines. Biochem Pharmacol 2006; 71: 354-65.
    • Heberling S, Girreser U, Wolf s, Clement B. Oxygen-insensitive enzymatic reduction of oximes to imines. Biochem Pharmacol 2006; 71: 354-65.
  • 105
    • 27544492348 scopus 로고    scopus 로고
    • Clement U, Mau S, Deters S, Havemeyer A. Hepatic, extrahepatic, microsomal, and mitochondrial activation of the N-hydroxylation prodrugs benzamidoxime, guanobenz, and Ro 48-3656. Drug Metab Dispos 2005; 33: 1740-7.
    • Clement U, Mau S, Deters S, Havemeyer A. Hepatic, extrahepatic, microsomal, and mitochondrial activation of the N-hydroxylation prodrugs benzamidoxime, guanobenz, and Ro 48-3656. Drug Metab Dispos 2005; 33: 1740-7.
  • 106
    • 0028986887 scopus 로고
    • N4-hydroxylation of sulfamethoxazole by cytochrome P450 of the cytochrome P4502C subfamily and reduction of sulfamethoxazole hydroxylamine in human and rat hepatic microsomes
    • Cribb AE, Spielberg SP, Griffin GP. N4-hydroxylation of sulfamethoxazole by cytochrome P450 of the cytochrome P4502C subfamily and reduction of sulfamethoxazole hydroxylamine in human and rat hepatic microsomes. Drug Metab Dispos 1995; 23: 406-14.
    • (1995) Drug Metab Dispos , vol.23 , pp. 406-414
    • Cribb, A.E.1    Spielberg, S.P.2    Griffin, G.P.3
  • 107
    • 0029959134 scopus 로고    scopus 로고
    • N-oxygenation of primary amines and hydroxylamines and retroreduction of hydroxylamines by adult human liver microsomes and adult human flavin-containing monooxygenase 3
    • Lin J, Berkman CE, Cashman JR. N-oxygenation of primary amines and hydroxylamines and retroreduction of hydroxylamines by adult human liver microsomes and adult human flavin-containing monooxygenase 3. Chem Res Toxicol 1996; 9:1183-93.
    • (1996) Chem Res Toxicol , vol.9 , pp. 1183-1193
    • Lin, J.1    Berkman, C.E.2    Cashman, J.R.3
  • 108
    • 0034452953 scopus 로고    scopus 로고
    • NADH-dependent reduction of sulphamethoxazole hydroxylamine in dog and human liver microsomes
    • Trepanier LA, Miller JL. NADH-dependent reduction of sulphamethoxazole hydroxylamine in dog and human liver microsomes. Xenobiotica 2000; 30: 1111-21.
    • (2000) Xenobiotica , vol.30 , pp. 1111-1121
    • Trepanier, L.A.1    Miller, J.L.2
  • 109
    • 15344340048 scopus 로고    scopus 로고
    • Characterization and partial purification of the rat and human enzyme systems active in the reduction of N-hydroxymelagatran and benzamidoxime
    • Andersson S, Hofmann Y, Nordling A, Li XQ, Nivelius S, Andersson TB, et al. Characterization and partial purification of the rat and human enzyme systems active in the reduction of N-hydroxymelagatran and benzamidoxime. Drug Metab Dispos 2005; 33: 570-8.
    • (2005) Drug Metab Dispos , vol.33 , pp. 570-578
    • Andersson, S.1    Hofmann, Y.2    Nordling, A.3    Li, X.Q.4    Nivelius, S.5    Andersson, T.B.6
  • 110
    • 29144493153 scopus 로고    scopus 로고
    • Identification of stearoyl CoA desaturase as the enzyme responsible for the reduction of ximelagatran/N-hydroxymelagatran and benzamidoxime in adipocytes
    • Johansson I, Thelin A, Hofmann Y, Andersson S, Nordling Å, Li QX, et al. Identification of stearoyl CoA desaturase as the enzyme responsible for the reduction of ximelagatran/N-hydroxymelagatran and benzamidoxime in adipocytes. Drug Metab Rev 2005; 37(Suppl. 1): 48-9.
    • (2005) Drug Metab Rev , vol.37 , Issue.SUPPL. 1 , pp. 48-49
    • Johansson, I.1    Thelin, A.2    Hofmann, Y.3    Andersson, S.4    Nordling, A.5    Li, Q.X.6
  • 112
    • 0026558347 scopus 로고
    • Conjunctive enhancement of enzymatic thrombolysis and prevention of thrombotic reocclusion with the selective factor Xa inhibitor, tick anticoangulant peptide-comparison to hirudin and heparin in a canine model of acute coronary-artery thrombosis
    • Sikto GR, Ramijit DR, Stabilito II, Lehman D, Lynch JJ, Vlasuk GP. Conjunctive enhancement of enzymatic thrombolysis and prevention of thrombotic reocclusion with the selective factor Xa inhibitor, tick anticoangulant peptide-comparison to hirudin and heparin in a canine model of acute coronary-artery thrombosis. Circulation 1992; 85: 805-15.
    • (1992) Circulation , vol.85 , pp. 805-815
    • Sikto, G.R.1    Ramijit, D.R.2    Stabilito, I.I.3    Lehman, D.4    Lynch, J.J.5    Vlasuk, G.P.6
  • 113
    • 0030727965 scopus 로고    scopus 로고
    • Anti-thrombotic and hemorrhagic effects of DX-9065a, a direct and selective factor Xa inhibitor: Comparison with a direct thrombin inhibitor and antithrombin III-dependent anticoagulants
    • Morishima Y, Tanabe K, Terada Y, Hara T, Kunitada S. Anti-thrombotic and hemorrhagic effects of DX-9065a, a direct and selective factor Xa inhibitor: Comparison with a direct thrombin inhibitor and antithrombin III-dependent anticoagulants. Thromb Haemost 1997; 78: 1366-71.
    • (1997) Thromb Haemost , vol.78 , pp. 1366-1371
    • Morishima, Y.1    Tanabe, K.2    Terada, Y.3    Hara, T.4    Kunitada, S.5
  • 114
    • 0034681376 scopus 로고    scopus 로고
    • Antithrombotic efficacy of RPR208566, a novel factor Xa inhibitor, in a rat model of carotid artery thrombosis
    • Heran C, Morgan S, Kasiewski C, Bostwick J, Bentley R, Klein S, et al. Antithrombotic efficacy of RPR208566, a novel factor Xa inhibitor, in a rat model of carotid artery thrombosis. Eur J Pharmacol 2000; 389: 201-7.
    • (2000) Eur J Pharmacol , vol.389 , pp. 201-207
    • Heran, C.1    Morgan, S.2    Kasiewski, C.3    Bostwick, J.4    Bentley, R.5    Klein, S.6
  • 115
    • 0031588348 scopus 로고    scopus 로고
    • YM-60828, a novel factor Xa inhibitor: Separation of its antithrombotic effects from its prolongation of blooding time
    • Sato K, Kawasaki T, Taniuchi Y, Hirayama F, Koshio H, Matsumoto Y. YM-60828, a novel factor Xa inhibitor: Separation of its antithrombotic effects from its prolongation of blooding time. Eur J Pharmacol 1997; 339: 141-6.
    • (1997) Eur J Pharmacol , vol.339 , pp. 141-146
    • Sato, K.1    Kawasaki, T.2    Taniuchi, Y.3    Hirayama, F.4    Koshio, H.5    Matsumoto, Y.6
  • 116
    • 0031957619 scopus 로고    scopus 로고
    • Effect of a synthetic factor Xa inhibitor, YM-60828, on blood vessel patency in combination with a thrombolytic agent and on blood loss from the operation site in a rat model of arterial thrombosis
    • Kawasaki T, Sato K, Hirayama F, Koshio H, Taniuchi Y, Matsumoto Y. Effect of a synthetic factor Xa inhibitor, YM-60828, on blood vessel patency in combination with a thrombolytic agent and on blood loss from the operation site in a rat model of arterial thrombosis. Thromb Haemost 1998; 79: 859-64.
    • (1998) Thromb Haemost , vol.79 , pp. 859-864
    • Kawasaki, T.1    Sato, K.2    Hirayama, F.3    Koshio, H.4    Taniuchi, Y.5    Matsumoto, Y.6
  • 117
    • 0031964032 scopus 로고    scopus 로고
    • Antithrombotic effects of YM-60828, a newly synthesized factor Xa inhibitor, in rat thrombosis models and its effects on bleeding time
    • Sato K, Kawasaki T, Hisamichi N, Taniuchi Y, Hirayama F, Koshio H, et al. Antithrombotic effects of YM-60828, a newly synthesized factor Xa inhibitor, in rat thrombosis models and its effects on bleeding time. J Pharmacol 1998; 123: 92-6.
    • (1998) J Pharmacol , vol.123 , pp. 92-96
    • Sato, K.1    Kawasaki, T.2    Hisamichi, N.3    Taniuchi, Y.4    Hirayama, F.5    Koshio, H.6
  • 118
    • 4544228404 scopus 로고    scopus 로고
    • Orally active factor Xa inhibitor: Synthesis and biological activity of masked amidines as prodrugs of novel 1,4-diazepane derivatives
    • Koshio H, Hirayama F, Ishihara T, Kaizawa H, Shigenaga T, Taniuchi Y, et al. Orally active factor Xa inhibitor: Synthesis and biological activity of masked amidines as prodrugs of novel 1,4-diazepane derivatives. Bioorg Med Chem 2004; 12: 5415-26.
    • (2004) Bioorg Med Chem , vol.12 , pp. 5415-5426
    • Koshio, H.1    Hirayama, F.2    Ishihara, T.3    Kaizawa, H.4    Shigenaga, T.5    Taniuchi, Y.6
  • 120
    • 0029984412 scopus 로고    scopus 로고
    • Antithrombotic and antilesion benefits without hemorrhagic risks by inhibiting tissue factor pathway
    • Harker LA, Hanson SR, Wilcox JN, Kelly AB. Antithrombotic and antilesion benefits without hemorrhagic risks by inhibiting tissue factor pathway. Haemostasis 1996; 26: 76-82.
    • (1996) Haemostasis , vol.26 , pp. 76-82
    • Harker, L.A.1    Hanson, S.R.2    Wilcox, J.N.3    Kelly, A.B.4
  • 121
    • 0030824413 scopus 로고    scopus 로고
    • Dissociation of antithrombotic effect and bleeding time prolongation in rabbits by inhibiting tissue factor function
    • Himber J, Kirchhofer D, Riederer M, Tschopp TB, Steiner B, Roux SP. Dissociation of antithrombotic effect and bleeding time prolongation in rabbits by inhibiting tissue factor function. Thromb Haemostasis 1997; 78: 1142-9.
    • (1997) Thromb Haemostasis , vol.78 , pp. 1142-1149
    • Himber, J.1    Kirchhofer, D.2    Riederer, M.3    Tschopp, T.B.4    Steiner, B.5    Roux, S.P.6
  • 122
    • 0041932150 scopus 로고    scopus 로고
    • Pharmacological interruption of acute thrombus formation with minimal hemorrhagic complications by a small molecule tissue factor/ factor VIIa inhibitor: Comparison to factor Xa and thrombin inhibition in a nonhuman primate thrombosis model
    • Suleymanov OD, Szalony JA, Salyers AK, Lachance RM, Parlow JJ, South MS, et al. Pharmacological interruption of acute thrombus formation with minimal hemorrhagic complications by a small molecule tissue factor/ factor VIIa inhibitor: Comparison to factor Xa and thrombin inhibition in a nonhuman primate thrombosis model. J Pharmool Exp Ther 2003; 306: 1115-21.
    • (2003) J Pharmool Exp Ther , vol.306 , pp. 1115-1121
    • Suleymanov, O.D.1    Szalony, J.A.2    Salyers, A.K.3    Lachance, R.M.4    Parlow, J.J.5    South, M.S.6
  • 123
    • 20144389170 scopus 로고    scopus 로고
    • A Selective, slow binding inhibitor of factor VIIa binds to a nonstandard active site conformation and attenuates thrombus formation in vivo
    • Olivero AG, Eigenbrot C, Goldsmith R, Robarge K, Artis DR, Flygare J, et al. A Selective, slow binding inhibitor of factor VIIa binds to a nonstandard active site conformation and attenuates thrombus formation in vivo. J Biol Chem 2005; 280: 9160-9.
    • (2005) J Biol Chem , vol.280 , pp. 9160-9169
    • Olivero, A.G.1    Eigenbrot, C.2    Goldsmith, R.3    Robarge, K.4    Artis, D.R.5    Flygare, J.6
  • 125
    • 0023664558 scopus 로고
    • Structure of the platelet membrane glycoprotein IIb. Homology to the alpha subunits of the vitronectin and fibronectin membrane receptors
    • Poncz M, Eisman R, Heidenreich R, Silver SM, Surrey S, Schwartz E, et al. Structure of the platelet membrane glycoprotein IIb. Homology to the alpha subunits of the vitronectin and fibronectin membrane receptors. J Biol Chem 1987; 262: 8476-82.
    • (1987) J Biol Chem , vol.262 , pp. 8476-8482
    • Poncz, M.1    Eisman, R.2    Heidenreich, R.3    Silver, S.M.4    Surrey, S.5    Schwartz, E.6
  • 126
    • 0023613707 scopus 로고
    • The platelet membrane glycoprotein IIb/IIIa complex. Structure, function, and relationship to adhesive protein receptors in nucleated cells
    • Phillips DR, Fitzgerald LA, Charo IF, Parise LV. The platelet membrane glycoprotein IIb/IIIa complex. Structure, function, and relationship to adhesive protein receptors in nucleated cells. Ann N Y Acad Sci 1987; 509: 177-87.
    • (1987) Ann N Y Acad Sci , vol.509 , pp. 177-187
    • Phillips, D.R.1    Fitzgerald, L.A.2    Charo, I.F.3    Parise, L.V.4
  • 128
    • 0027373464 scopus 로고
    • The effects of two synthetic glycoprotein IIb/IIIa antagonists, Ro 43-8857 and L-700,462, on platelet aggregation and bleeding in guinea pigs and dogs: Evidence that Ro 43-8857 is orally active
    • Cook NS, Bruttger O, Pally C, Hagenbach A. The effects of two synthetic glycoprotein IIb/IIIa antagonists, Ro 43-8857 and L-700,462, on platelet aggregation and bleeding in guinea pigs and dogs: Evidence that Ro 43-8857 is orally active. Thromb Haemostasis 1993; 70: 838-47.
    • (1993) Thromb Haemostasis , vol.70 , pp. 838-847
    • Cook, N.S.1    Bruttger, O.2    Pally, C.3    Hagenbach, A.4
  • 129
    • 9344236530 scopus 로고    scopus 로고
    • Orally active fibrinogen receptor antagonists. 2. amidoximes as prodrugs of amidines
    • Weller T, Alig L, Beresini M, Blackburn B, Bunting S, Hadváry P, et al. Orally active fibrinogen receptor antagonists. 2. amidoximes as prodrugs of amidines. J Med Chem 1996; 39: 3139-47.
    • (1996) J Med Chem , vol.39 , pp. 3139-3147
    • Weller, T.1    Alig, L.2    Beresini, M.3    Blackburn, B.4    Bunting, S.5    Hadváry, P.6
  • 130
    • 0031974072 scopus 로고    scopus 로고
    • Pharmacogenetics, pharmacodynamics and tolerability of a potent, non-peptidic, GP IIb/IIIa receptor antagonist following multiple oral administrations of a prodrug form
    • Refino CJ, Modi NB, Bullens S, Pater C, Lipari MT, Robarge K, et al. Pharmacogenetics, pharmacodynamics and tolerability of a potent, non-peptidic, GP IIb/IIIa receptor antagonist following multiple oral administrations of a prodrug form. Thromb Haemost 1998; 79: 169-76.
    • (1998) Thromb Haemost , vol.79 , pp. 169-176
    • Refino, C.J.1    Modi, N.B.2    Bullens, S.3    Pater, C.4    Lipari, M.T.5    Robarge, K.6
  • 131
    • 0035087137 scopus 로고    scopus 로고
    • Orally active GPIIb/IIIa antagonists: Synthesis and biological activities of masked amidines as prodrugs of 2-[(3S)-4-[2S)-2-(4-amidinobenzoylamino)-3-(4-methoxyphenyl) propanoyl]-3-(2-methoxy-2-oxoethyl)-2-oxopiperazinyl]acetic acid
    • Kitamura S, Fukushi H, Miyawaki T, Kawamura M, Terashita ZI, Naka T. Orally active GPIIb/IIIa antagonists: Synthesis and biological activities of masked amidines as prodrugs of 2-[(3S)-4-[2S)-2-(4-amidinobenzoylamino)-3-(4-methoxyphenyl) propanoyl]-3-(2-methoxy-2-oxoethyl)-2-oxopiperazinyl]acetic acid. Chem Pharm Bull 2001; 49: 268-77.
    • (2001) Chem Pharm Bull , vol.49 , pp. 268-277
    • Kitamura, S.1    Fukushi, H.2    Miyawaki, T.3    Kawamura, M.4    Terashita, Z.I.5    Naka, T.6
  • 132
    • 0031468133 scopus 로고    scopus 로고
    • New NO-donors with antithrombic and vasodilating activities, part 17. Arylazoamidoximes and 3-arylazo-1,2,4-oxadiazol-5-ones
    • Rehse K, Bade S, Harsdorf A, Clement B. New NO-donors with antithrombic and vasodilating activities, part 17. Arylazoamidoximes and 3-arylazo-1,2,4-oxadiazol-5-ones. Arch Pharm Pharm Med Chem 1997; 392-8.
    • (1997) Arch Pharm Pharm Med Chem , pp. 392-398
    • Rehse, K.1    Bade, S.2    Harsdorf, A.3    Clement, B.4
  • 133
    • 0032411249 scopus 로고    scopus 로고
    • New NO-donors with antithrombic and vasodilating activities, part 26. amidoximes and their prodrugs
    • Rehse K, Brehme F. New NO-donors with antithrombic and vasodilating activities, part 26. amidoximes and their prodrugs. Arch Pharm Pharm Med Chem 1998; 375-9.
    • (1998) Arch Pharm Pharm Med Chem , pp. 375-379
    • Rehse, K.1    Brehme, F.2
  • 134
    • 0015417053 scopus 로고
    • Utilization of operational schemes for analog synthesis in drug design
    • Topliss JG. Utilization of operational schemes for analog synthesis in drug design. J Med Chem 1972; 15: 1006-11.
    • (1972) J Med Chem , vol.15 , pp. 1006-1011
    • Topliss, J.G.1
  • 135
    • 0028913789 scopus 로고
    • Vorstellungen zur freisetzung von stickstoffmonoxid aus NO-pharmaka. modellreaktionen in gegenwart von licht und übergangsmetallkomplexen, 1. Mitt
    • Duchstein HJ, Riederer S. Vorstellungen zur freisetzung von stickstoffmonoxid aus NO-pharmaka. modellreaktionen in gegenwart von licht und übergangsmetallkomplexen, 1. Mitt Arch Pharm (Weinheim) 1995; 328: 317-24.
    • (1995) Arch Pharm (Weinheim) , vol.328 , pp. 317-324
    • Duchstein, H.J.1    Riederer, S.2
  • 136
    • 0024957314 scopus 로고
    • New quinoxaline and pyrimido[4,5-b]quinoxaline derivatives-potential antihypertensive and blood-platelet antiaggregating agents
    • Monge A, Palop J, Urbasos I, Fernandezalverez E. New quinoxaline and pyrimido[4,5-b]quinoxaline derivatives-potential antihypertensive and blood-platelet antiaggregating agents. J Heterocycl Chem 1989; 26: 1623-6.
    • (1989) J Heterocycl Chem , vol.26 , pp. 1623-1626
    • Monge, A.1    Palop, J.2    Urbasos, I.3    Fernandezalverez, E.4
  • 138
    • 0029744548 scopus 로고    scopus 로고
    • Ciofalo M, Petruso S, Schillaci D. Quantitative assay of photoinduced antibiotic activities of naturally-occurring 2,2′:5′,2″-terthiophenes. Planta Med 1996; 62: 374-5.
    • Ciofalo M, Petruso S, Schillaci D. Quantitative assay of photoinduced antibiotic activities of naturally-occurring 2,2′:5′,2″-terthiophenes. Planta Med 1996; 62: 374-5.
  • 139
    • 0028856199 scopus 로고
    • New antifungal bithienylacetylenes from Blumea obliqua
    • Ahmad VU, Alam N. New antifungal bithienylacetylenes from Blumea obliqua. J Nat Prod 1995; 58: 1426-9.
    • (1995) J Nat Prod , vol.58 , pp. 1426-1429
    • Ahmad, V.U.1    Alam, N.2
  • 140
    • 0028723245 scopus 로고
    • Photoactive terthiophenes-the influence of serum on anti-HIV (Human-Immunodeficiency-virus) activities
    • Hudson JB, Marles RJ, Soucy-Breau C, Harris L, Amason JT. Photoactive terthiophenes-the influence of serum on anti-HIV (Human-Immunodeficiency-virus) activities. Photochem Photobiol 1994; 60: 591-3.
    • (1994) Photochem Photobiol , vol.60 , pp. 591-593
    • Hudson, J.B.1    Marles, R.J.2    Soucy-Breau, C.3    Harris, L.4    Amason, J.T.5
  • 141
    • 0029363151 scopus 로고
    • Isolation of the insecticidal components of tagetes minuta (compositae) against mosquito larvae and adults
    • Perich MJ, Wells C, Bertsch W, Tredway KE. Isolation of the insecticidal components of tagetes minuta (compositae) against mosquito larvae and adults. J Am Mosq Control Assoc 1995; 11: 307-10.
    • (1995) J Am Mosq Control Assoc , vol.11 , pp. 307-310
    • Perich, M.J.1    Wells, C.2    Bertsch, W.3    Tredway, K.E.4
  • 142
    • 0034143210 scopus 로고    scopus 로고
    • Synergistic insecticidal mode of action between sesquiterpene lactones and a phototoxin, alpha-terthienyl
    • Guillet G, Harmatha J, Waddell TG, Philogene BJ, Arnason JT. Synergistic insecticidal mode of action between sesquiterpene lactones and a phototoxin, alpha-terthienyl. Photochem Photobiol 2000; 71: 111-5.
    • (2000) Photochem Photobiol , vol.71 , pp. 111-115
    • Guillet, G.1    Harmatha, J.2    Waddell, T.G.3    Philogene, B.J.4    Arnason, J.T.5
  • 144
    • 44449133055 scopus 로고
    • Nitrogen-containing organosilicon compounds. CXIX. Synthesis and biological activity of 5-trimethylsilylfuran derivatives containing azomethine and vinyl groups in the ring
    • Lukevics E, Erchak NP, Castro I, Zidermane AA, Dauvarte A. Nitrogen-containing organosilicon compounds. CXIX. Synthesis and biological activity of 5-trimethylsilylfuran derivatives containing azomethine and vinyl groups in the ring. Zh Izv Akad Nauk Latv SSR Ser Khim 1983; 735-8.
    • (1983) Zh Izv Akad Nauk Latv SSR Ser Khim , pp. 735-738
    • Lukevics, E.1    Erchak, N.P.2    Castro, I.3    Zidermane, A.A.4    Dauvarte, A.5
  • 145
    • 0030861099 scopus 로고    scopus 로고
    • Nitric oxide in the eye: Multi-faceted roles and diverse outcomes
    • Becquet F, Courtois Y, Goureau O. Nitric oxide in the eye: Multi-faceted roles and diverse outcomes. Surv Ophthalmol 1997; 42: 71-82.
    • (1997) Surv Ophthalmol , vol.42 , pp. 71-82
    • Becquet, F.1    Courtois, Y.2    Goureau, O.3
  • 148
    • 0025293775 scopus 로고
    • Footprinting studies on the sequence-selective binding of pentamidine to DNA
    • Fox KR, Sansom. CE, Stevens MPG. Footprinting studies on the sequence-selective binding of pentamidine to DNA. FEBS Lett 1990; 266: 150-4.
    • (1990) FEBS Lett , vol.266 , pp. 150-154
    • Fox, K.R.1    Sansom, C.E.2    Stevens, M.P.G.3
  • 149
    • 0026707681 scopus 로고
    • Crystal-structure of a pentamidine oligonucleotide complex - Implications for DNA-binding properties
    • Edwards KJ, Jenkins TC, Neidle S. Crystal-structure of a pentamidine oligonucleotide complex - Implications for DNA-binding properties. Biochemistry 1992; 31: 7104-9.
    • (1992) Biochemistry , vol.31 , pp. 7104-7109
    • Edwards, K.J.1    Jenkins, T.C.2    Neidle, S.3
  • 150
    • 0025272657 scopus 로고
    • Crystal-structare of a berenil dodecanucleotide complex - the role of water in sequence-specific ligand binding
    • Brown DG, Sanderson MR, Skelly JV, Jenkins TC, Brown T, Garman E. et al. Crystal-structare of a berenil dodecanucleotide complex - the role of water in sequence-specific ligand binding. EMBO J 1990; 9:1329-34.
    • (1990) EMBO J , vol.9 , pp. 1329-1334
    • Brown, D.G.1    Sanderson, M.R.2    Skelly, J.V.3    Jenkins, T.C.4    Brown, T.5    Garman, E.6
  • 151
    • 0026654185 scopus 로고
    • Crystal-structure of a berenil-D(CGCAAATTTGCG) complex - an example of a drug DNA recognition based on sequence-dependent structural features
    • Brown DG, Sanderson MR, Garman E, Neidle S. Crystal-structure of a berenil-D(CGCAAATTTGCG) complex - an example of a drug DNA recognition based on sequence-dependent structural features. J Mol Biol 1992, 226: 481-90.
    • (1992) J Mol Biol , vol.226 , pp. 481-490
    • Brown, D.G.1    Sanderson, M.R.2    Garman, E.3    Neidle, S.4
  • 152
    • 0027728591 scopus 로고
    • Amidines and guanidines in medicinal chemistry
    • Greenhill JV, Lue P. Amidines and guanidines in medicinal chemistry. Prog Med Chem 1993; 30: 203-326.
    • (1993) Prog Med Chem , vol.30 , pp. 203-326
    • Greenhill, J.V.1    Lue, P.2
  • 153
    • 84974972484 scopus 로고
    • Chemotherapy. XIX. Further report on new trypanocidal substances
    • King H, Lourie E, Yorke W. Chemotherapy. XIX. Further report on new trypanocidal substances. Ann Trop Med Parasitol 1938; 32: 177-92.
    • (1938) Ann Trop Med Parasitol , vol.32 , pp. 177-192
    • King, H.1    Lourie, E.2    Yorke, W.3
  • 154
    • 84975016422 scopus 로고
    • Studies in chemotherapy. XXI. The trypanocidal action of certain aromatic diamidines
    • Lourie EM, Yorke W. Studies in chemotherapy. XXI. The trypanocidal action of certain aromatic diamidines. Ann Trop Med 1939; 33: 289-304.
    • (1939) Ann Trop Med , vol.33 , pp. 289-304
    • Lourie, E.M.1    Yorke, W.2
  • 155
    • 33751543062 scopus 로고    scopus 로고
    • CYP4F enzymes are the major enzymes in human liver microsomes that catalyze the O-demethylation of the antiparasitic pro-drug DB289 [2,5-bis(4-amidinophenyl)furan-bis-O-methylamidoxime]
    • Wang MZ, Saulter JY, Usuki I, Cheung YL, Hall M, Bridges AS, et al. CYP4F enzymes are the major enzymes in human liver microsomes that catalyze the O-demethylation of the antiparasitic pro-drug DB289 [2,5-bis(4-amidinophenyl)furan-bis-O-methylamidoxime]. Drug Metab Dispos 2006; 34:1985-94.
    • (2006) Drug Metab Dispos , vol.34 , pp. 1985-1994
    • Wang, M.Z.1    Saulter, J.Y.2    Usuki, I.3    Cheung, Y.L.4    Hall, M.5    Bridges, A.S.6
  • 156
    • 0019198428 scopus 로고
    • Present status of chemotherapy and chemoprohylaxis of human trypanosomiasis in the Eastern Hemisphere
    • Apted FIC. Present status of chemotherapy and chemoprohylaxis of human trypanosomiasis in the Eastern Hemisphere. Pharmacol Ther 1980; 11: 391-413.
    • (1980) Pharmacol Ther , vol.11 , pp. 391-413
    • Apted, F.I.C.1
  • 157
    • 0022242790 scopus 로고
    • Visceral leishmaniasis unresponsive to antimonial drugs II. Response to high dosage sodium stibogluconate or prolonged treatment with pentamidine
    • Bryceson ADM, Chulay JD, Mugambi M, Were JB, Gachihi G, Chunge CN, et al, Visceral leishmaniasis unresponsive to antimonial drugs II. Response to high dosage sodium stibogluconate or prolonged treatment with pentamidine. Trans Roy Soc Trop Med Hyg 1985; 79: 705-14.
    • (1985) Trans Roy Soc Trop Med Hyg , vol.79 , pp. 705-714
    • Bryceson, A.D.M.1    Chulay, J.D.2    Mugambi, M.3    Were, J.B.4    Gachihi, G.5    Chunge, C.N.6
  • 158
    • 0016040773 scopus 로고
    • Efficacy of trimethoprim and sulfamethoxazole in prevention and treatment of pneumocystis-carinii pneumonitis
    • Hughes WT, McNabb PC, Makres TD, Feldman S. Efficacy of trimethoprim and sulfamethoxazole in prevention and treatment of pneumocystis-carinii pneumonitis. Antimicrob Agents Chemother 1974; 5: 289-93.
    • (1974) Antimicrob Agents Chemother , vol.5 , pp. 289-293
    • Hughes, W.T.1    McNabb, P.C.2    Makres, T.D.3    Feldman, S.4
  • 160
    • 0021882303 scopus 로고
    • Amidoximes of pentamidine: Synthesis, trypanocidal and leishimaniacidal activity
    • Clement B, Raether W. Amidoximes of pentamidine: Synthesis, trypanocidal and leishimaniacidal activity. Arzneim-Forsch 1995; 35: 1009-14.
    • (1995) Arzneim-Forsch , vol.35 , pp. 1009-1014
    • Clement, B.1    Raether, W.2
  • 161
    • 44449112601 scopus 로고
    • Benzamidoxime derivatives for treatment of protozoal infections
    • Ger. Offen DE 4321444;, 151361g
    • Clement B. Benzamidoxime derivatives for treatment of protozoal infections. Ger. Offen DE 4321444; Chem Abstrs 1995; 122: 151361g.
    • (1995) Chem Abstrs , vol.122
    • Clement, B.1
  • 162
    • 37049161803 scopus 로고
    • Some amidines and amidoximes with trypanocidal activity
    • Lamb ID, White AC. Some amidines and amidoximes with trypanocidal activity. J Chem Soc 1939; 1253-7.
    • (1939) J Chem Soc , pp. 1253-1257
    • Lamb, I.D.1    White, A.C.2
  • 163
    • 84948507547 scopus 로고
    • Experimental chemotherapy of typhus. Anti-rickettsial action of p-sulphonamidobenzamidine and related compounds
    • Andrewes CH, King H, Walker J. Experimental chemotherapy of typhus. Anti-rickettsial action of p-sulphonamidobenzamidine and related compounds. Proc R Soc Lond Ser B 1946; 133: 20-62.
    • (1946) Proc R Soc Lond Ser B , vol.133 , pp. 20-62
    • Andrewes, C.H.1    King, H.2    Walker, J.3
  • 164
  • 165
    • 8344223918 scopus 로고
    • Nouvelles recherches sur les rapports entre structure chimique, activite antibacterienne, antifungique et toxicite, dans la serie des esters de l'acide dithiocarbamique Ndisubstitue.
    • Chabrier P, Maillard G, Quevauviller A. Nouvelles recherches sur les rapports entre structure chimique, activite antibacterienne, antifungique et toxicite, dans la serie des esters de l'acide dithiocarbamique Ndisubstitue. Ann Pharm Fr 1956; 14: 720-8.
    • (1956) Ann Pharm Fr , vol.14 , pp. 720-728
    • Chabrier, P.1    Maillard, G.2    Quevauviller, A.3
  • 166
    • 37049161963 scopus 로고
    • Chemotherapeutic agents of the sulphone type. II. Sulphones related to benzamidine and benzylamine
    • Fuller AT, Tonkin IM, Walker J. Chemotherapeutic agents of the sulphone type. II. Sulphones related to benzamidine and benzylamine. J Chem Soc 1945; 633-7.
    • (1945) J Chem Soc , pp. 633-637
    • Fuller, A.T.1    Tonkin, I.M.2    Walker, J.3
  • 167
    • 0036985973 scopus 로고    scopus 로고
    • Antimicrobial Activity of the DNA Minor Groove Binders Furamidine and Analogues
    • Boykin DW. Antimicrobial Activity of the DNA Minor Groove Binders Furamidine and Analogues. J Braz Chem Soc 2002; 13: 763-71.
    • (2002) J Braz Chem Soc , vol.13 , pp. 763-771
    • Boykin, D.W.1
  • 170
    • 0011338502 scopus 로고
    • Pentamidine and related compounds in the treatment of Pneumocystis carinii infection
    • Watzer P Ed, 2nd ed. Marcel Dekker, New York, N.Y
    • Tidwell RR, Bell CA. Pentamidine and related compounds in the treatment of Pneumocystis carinii infection. In: Watzer P Ed, Pneumocystis carinii, 2nd ed. Marcel Dekker, New York, N.Y. 1993, pp. 561-83.
    • (1993) Pneumocystis carinii , pp. 561-583
    • Tidwell, R.R.1    Bell, C.A.2
  • 172
    • 0017576850 scopus 로고
    • Synthesis and antiprotozoal activity of 2,5-bis(4-guanylphenyl)furans
    • Das BP, Boykin DW. Synthesis and antiprotozoal activity of 2,5-bis(4-guanylphenyl)furans. J Med Chem 1977; 20: 531-6.
    • (1977) J Med Chem , vol.20 , pp. 531-536
    • Das, B.P.1    Boykin, D.W.2
  • 173
    • 0020024466 scopus 로고
    • Trypanosoma-rhodesiense - evaluation of the antitrypanosomal action of 2,5-bis(4-guanylphenyl)furan dihydrochloride
    • Steck EA, Kinnamon KE, Davidson DE, Duxbury RE, Johnson AJ, Masters RE. Trypanosoma-rhodesiense - evaluation of the antitrypanosomal action of 2,5-bis(4-guanylphenyl)furan dihydrochloride. Exp Parasitol 1982; 3: 133-44.
    • (1982) Exp Parasitol , vol.3 , pp. 133-144
    • Steck, E.A.1    Kinnamon, K.E.2    Davidson, D.E.3    Duxbury, R.E.4    Johnson, A.J.5    Masters, R.E.6
  • 174
    • 0346666412 scopus 로고    scopus 로고
    • Dicationic furans inhibit development of Cryptosporidium parvum in HSD/ICR suckling Swiss mice
    • Blagburn BL, Drain KL, Land TM, Moore PH, Lindsay DS, Kumar A, et al. Dicationic furans inhibit development of Cryptosporidium parvum in HSD/ICR suckling Swiss mice. J Parasitol 1999; 84: 851-6.
    • (1999) J Parasitol , vol.84 , pp. 851-856
    • Blagburn, B.L.1    Drain, K.L.2    Land, T.M.3    Moore, P.H.4    Lindsay, D.S.5    Kumar, A.6
  • 176
    • 0033468605 scopus 로고    scopus 로고
    • Palladium catalyzed cross-coupling reactions for the synthesis of 2,5-disubstituted furans
    • Kumar A, Stephens CE, Boykin DW. Palladium catalyzed cross-coupling reactions for the synthesis of 2,5-disubstituted furans. Heterocycl Comm 1999; 5: 301-4.
    • (1999) Heterocycl Comm , vol.5 , pp. 301-304
    • Kumar, A.1    Stephens, C.E.2    Boykin, D.W.3
  • 177
  • 178
    • 3843134198 scopus 로고    scopus 로고
    • O-Alkoxyamidine prodrugs of furamidine: In vitro transport and microsomal metabolism as indicators of in vivo efficacy in a mouse model of trypanosoma brucei rhodesiense infection
    • Ansede JH, Anbazhagan M, Brun R, Easterbrook JD, Hall JE, Boykin DW. O-Alkoxyamidine prodrugs of furamidine: in vitro transport and microsomal metabolism as indicators of in vivo efficacy in a mouse model of trypanosoma brucei rhodesiense infection. J Med Chem 2004; 47: 4335-9.
    • (2004) J Med Chem , vol.47 , pp. 4335-4339
    • Ansede, J.H.1    Anbazhagan, M.2    Brun, R.3    Easterbrook, J.D.4    Hall, J.E.5    Boykin, D.W.6
  • 179
    • 0036845742 scopus 로고    scopus 로고
    • Enhanced permeability of the antimicrobial agent 2,5-bis(4-amidinophenyl)furan across Caco-2 cell monolayers via its methylamidoxime prodrug
    • Zhou L, Lee K, Thakker DR, Boykin DW, Tidwell RR, Hall JE. Enhanced permeability of the antimicrobial agent 2,5-bis(4-amidinophenyl)furan across Caco-2 cell monolayers via its methylamidoxime prodrug. Pharm Res 2002; 19: 1689-95.
    • (2002) Pharm Res , vol.19 , pp. 1689-1695
    • Zhou, L.1    Lee, K.2    Thakker, D.R.3    Boykin, D.W.4    Tidwell, R.R.5    Hall, J.E.6
  • 180
    • 0035101948 scopus 로고    scopus 로고
    • Synthesis of deuterium-labelled. 2,5-Bis(4-amidinophenyl)furan, 2,5-Bis[4-(methoxyamidino) phenyl]furan, and 2,7-diamidinocarbazole
    • Stephens CE, Patrick DA, Chen H, Tidwell RR, Boykin DW. Synthesis of deuterium-labelled. 2,5-Bis(4-amidinophenyl)furan, 2,5-Bis[4-(methoxyamidino) phenyl]furan, and 2,7-diamidinocarbazole. J Label Compd Radiopharm. 2001; 44: 197-208.
    • (2001) J Label Compd Radiopharm , vol.44 , pp. 197-208
    • Stephens, C.E.1    Patrick, D.A.2    Chen, H.3    Tidwell, R.R.4    Boykin, D.W.5
  • 183
    • 0034616955 scopus 로고    scopus 로고
    • Large hydrophobic contributions are involved in DNA minor-groove complex formation with a series of diphenylfuran dications: Surface plasmon resonance and isothermal titration calorimetry studies
    • Mazur S, Tanious F, Ding D, Kumar A, Boykin DW, Neidle S, et al. Large hydrophobic contributions are involved in DNA minor-groove complex formation with a series of diphenylfuran dications: Surface plasmon resonance and isothermal titration calorimetry studies. J Mol Biol 2000; 300: 321-37.
    • (2000) J Mol Biol , vol.300 , pp. 321-337
    • Mazur, S.1    Tanious, F.2    Ding, D.3    Kumar, A.4    Boykin, D.W.5    Neidle, S.6
  • 185
    • 0001316659 scopus 로고
    • Plasmodium falciparum malaria parasite cultures and their use in immunology
    • Lefkovits I, Pernis B. Eds, Academic Press: San Diego
    • Matile H, Pink JRL. Plasmodium falciparum malaria parasite cultures and their use in immunology. In: Lefkovits I, Pernis B. Eds, Immunological Methods; Academic Press: San Diego 1990; pp. 221-34.
    • (1990) Immunological Methods , pp. 221-234
    • Matile, H.1    Pink, J.R.L.2
  • 186
    • 1942437514 scopus 로고    scopus 로고
    • Synthesis of deuterium-labelled 6-[5-(4-amidinophenyl) furan-2-yl]nicotinamidine and N-alkoxy-6-{5-[4-(N-alkoxyamidino) phenyl]-furan-2-yl}-nicotinamidines
    • Ismail MA, Boykin DW. Synthesis of deuterium-labelled 6-[5-(4-amidinophenyl) furan-2-yl]nicotinamidine and N-alkoxy-6-{5-[4-(N-alkoxyamidino) phenyl]-furan-2-yl}-nicotinamidines. J Label Compd Radiopharm 2004; 47: 233-42.
    • (2004) J Label Compd Radiopharm , vol.47 , pp. 233-242
    • Ismail, M.A.1    Boykin, D.W.2
  • 187
    • 3042552194 scopus 로고    scopus 로고
    • Ismail MA, Brun R, Wenzler T, Tanious FA, Wilson WD, Boykin DW. Novel dicationic imidazo[1,2-a]pyridines and 5,6,7,8-tetrahydro-imidazo [1,2-apyridines as antiprotozoal agents. J Med Chem 2004; 47: 3658-64.
    • Ismail MA, Brun R, Wenzler T, Tanious FA, Wilson WD, Boykin DW. Novel dicationic imidazo[1,2-a]pyridines and 5,6,7,8-tetrahydro-imidazo [1,2-apyridines as antiprotozoal agents. J Med Chem 2004; 47: 3658-64.
  • 188
    • 0033552891 scopus 로고    scopus 로고
    • 2- Amino-3-substituted-6-[(E)-1-phenyl-2-(N- methylcarbamoyl)vinyl]imidazo[1,2-a]pyridines as a novel class of inhibitors of human rhinovirus: Stereospecific synthesis and antiviral activity
    • Hamdouchi C, Blas J, Prado M, Gruber J, Heinz BA, Vance L. 2- Amino-3-substituted-6-[(E)-1-phenyl-2-(N- methylcarbamoyl)vinyl]imidazo[1,2-a]pyridines as a novel class of inhibitors of human rhinovirus: Stereospecific synthesis and antiviral activity. J Med Chem 1999; 42: 50-9.
    • (1999) J Med Chem , vol.42 , pp. 50-59
    • Hamdouchi, C.1    Blas, J.2    Prado, M.3    Gruber, J.4    Heinz, B.A.5    Vance, L.6
  • 189
    • 0037194280 scopus 로고    scopus 로고
    • Chemistry of bicyclic pyridines containing a ring-junction nitrogen
    • Hamama WS, Zoorob HH. Chemistry of bicyclic pyridines containing a ring-junction nitrogen. Tetrahedron 2002; 58: 6143-62.
    • (2002) Tetrahedron , vol.58 , pp. 6143-6162
    • Hamama, W.S.1    Zoorob, H.H.2
  • 190
    • 0032561411 scopus 로고    scopus 로고
    • Bis-cationic heteroaromatics as macrofilaricides: Synthesis of bis-amidine and bis-guanylhydrazone derivatives of substituted imidazo-[1,2-a]pyridines
    • Sundberg RJ, Biswas S, Murthi KK, Rowe D. Bis-cationic heteroaromatics as macrofilaricides: Synthesis of bis-amidine and bis-guanylhydrazone derivatives of substituted imidazo-[1,2-a]pyridines. J Med Chem 1998; 41: 4317-28.
    • (1998) J Med Chem , vol.41 , pp. 4317-4328
    • Sundberg, R.J.1    Biswas, S.2    Murthi, K.K.3    Rowe, D.4
  • 192
    • 33747498433 scopus 로고    scopus 로고
    • Synthesis, DNA affinity, and antiprotozoal activity of linear dicationios: Terphenyl diamidines and analogues
    • Ismail MA, Arafa RK, Brun R, Wenzler T, Miao Y, Wilson WD, et al. Synthesis, DNA affinity, and antiprotozoal activity of linear dicationios: Terphenyl diamidines and analogues. J Med Chem 2006; 49: 5324-32.
    • (2006) J Med Chem , vol.49 , pp. 5324-5332
    • Ismail, M.A.1    Arafa, R.K.2    Brun, R.3    Wenzler, T.4    Miao, Y.5    Wilson, W.D.6
  • 193
    • 0032728386 scopus 로고    scopus 로고
    • Dicationic dibenzofuran as anti-Pneumocystis carinii pneumonia agents: Synthesis, DNA binding, and anti-P.carinii activity in an immunosuppressed rat model
    • Wang S, Hall JE, Tanious FA, Wilson WD, Patrick DA, McCurdy DR, et al. Dicationic dibenzofuran as anti-Pneumocystis carinii pneumonia agents: Synthesis, DNA binding, and anti-P.carinii activity in an immunosuppressed rat model. Eur J Med Chem 1999; 34: 215-24.
    • (1999) Eur J Med Chem , vol.34 , pp. 215-224
    • Wang, S.1    Hall, J.E.2    Tanious, F.A.3    Wilson, W.D.4    Patrick, D.A.5    McCurdy, D.R.6
  • 194
    • 0032710064 scopus 로고    scopus 로고
    • Synthesis and anti-Pneumocystis carinii pneumonia activity of the novel dicationic dibenzothiophenes and orally active prodrugs
    • Patrick DA, Hall JE, Bender BC, McCurdy DR, Wilson WD, Tanious FA, et al. Synthesis and anti-Pneumocystis carinii pneumonia activity of the novel dicationic dibenzothiophenes and orally active prodrugs. Eur J Med Chem 1999; 34: 575-83.
    • (1999) Eur J Med Chem , vol.34 , pp. 575-583
    • Patrick, D.A.1    Hall, J.E.2    Bender, B.C.3    McCurdy, D.R.4    Wilson, W.D.5    Tanious, F.A.6
  • 196
    • 0023446039 scopus 로고
    • Molecular architecture of rabbit skeletal-muscle aldolase at 2.7 - a resolution
    • Sygusch J, Beaudry D, Allaire M. Molecular architecture of rabbit skeletal-muscle aldolase at 2.7 - a resolution. Proc Natl Acad Sci USA 1987; 84: 7846-50.
    • (1987) Proc Natl Acad Sci USA , vol.84 , pp. 7846-7850
    • Sygusch, J.1    Beaudry, D.2    Allaire, M.3
  • 197
    • 0033605891 scopus 로고    scopus 로고
    • The crystal structure of Escherichia coli class II fructose-1,6- bisphosphate aldolase in complex with phosphoglycolohydroxamate reveals details of mechanism and specificity
    • Hall DR, Leonard GA, Reed CD, Watt CI, Berry A, Hunter WN. The crystal structure of Escherichia coli class II fructose-1,6- bisphosphate aldolase in complex with phosphoglycolohydroxamate reveals details of mechanism and specificity. J Mol Biol 1999; 287: 383-94.
    • (1999) J Mol Biol , vol.287 , pp. 383-394
    • Hall, D.R.1    Leonard, G.A.2    Reed, C.D.3    Watt, C.I.4    Berry, A.5    Hunter, W.N.6
  • 198
    • 0025955197 scopus 로고
    • The Escherichia coli ts8 mutation is an allele of fda, the gene encoding fructose-1,6-diphosphate aldolase
    • Singer M, Rossmiesse P, Cali BM, Liebke H, Gross CA. The Escherichia coli ts8 mutation is an allele of fda, the gene encoding fructose-1,6-diphosphate aldolase. J Bacteriol 1991; 173: 6242-8.
    • (1991) J Bacteriol , vol.173 , pp. 6242-6248
    • Singer, M.1    Rossmiesse, P.2    Cali, B.M.3    Liebke, H.4    Gross, C.A.5
  • 199
    • 0005533813 scopus 로고
    • Properties of a mutant of Escherichia coli with a temperature-sensitive fructose-1,6-diphosphate aldolase
    • Böck A, Neidhart FC. Properties of a mutant of Escherichia coli with a temperature-sensitive fructose-1,6-diphosphate aldolase. J Bacteriol 1966; 92: 470-6.
    • (1966) J Bacteriol , vol.92 , pp. 470-476
    • Böck, A.1    Neidhart, F.C.2
  • 200
    • 2342471437 scopus 로고    scopus 로고
    • New highly selective inhibitors of class II fructose-1,6-bisphosphate aldolases
    • Fonvielle M, Weber P, Dabkowska K, Therisod M. New highly selective inhibitors of class II fructose-1,6-bisphosphate aldolases. Bioorg Med Chem Lett 2004; 14: 2923-6.
    • (2004) Bioorg Med Chem Lett , vol.14 , pp. 2923-2926
    • Fonvielle, M.1    Weber, P.2    Dabkowska, K.3    Therisod, M.4
  • 201
    • 0028517063 scopus 로고
    • Amidoxime resins based on poly(acrylonitrile-co-vinilidene chloride-co-divinylbenzene) and their behavior in uptake of uranium from sea water
    • Kabay N, Hayashi T, Jyo A, Egawa HJ. Amidoxime resins based on poly(acrylonitrile-co-vinilidene chloride-co-divinylbenzene) and their behavior in uptake of uranium from sea water. J Appl Polym Sci 1994; 54: 333-8.
    • (1994) J Appl Polym Sci , vol.54 , pp. 333-338
    • Kabay, N.1    Hayashi, T.2    Jyo, A.3    Egawa, H.J.4
  • 202
    • 0027909880 scopus 로고
    • Extraction of gold from Au(III) ion containing solution by a reactive fiber
    • Lin W, Lu Y, Zeng H. Extraction of gold from Au(III) ion containing solution by a reactive fiber J Appl Polym Sci 1993; 49: 1635-8.
    • (1993) J Appl Polym Sci , vol.49 , pp. 1635-1638
    • Lin, W.1    Lu, Y.2    Zeng, H.3
  • 203
    • 0034158815 scopus 로고    scopus 로고
    • Adsorption of copper(II) and chromium(III) ions onto amidoximated cellulose
    • Saliba R, Gauthier R, Petit-Ramel M. Adsorption of copper(II) and chromium(III) ions onto amidoximated cellulose. J Appl Polym Sci 2000; 75: 1624-31.
    • (2000) J Appl Polym Sci , vol.75 , pp. 1624-1631
    • Saliba, R.1    Gauthier, R.2    Petit-Ramel, M.3
  • 204
    • 0026819251 scopus 로고
    • Column studies on metal-ion removal by dyed cellulosic materials
    • Shukla SR, Sakhardande VD. Column studies on metal-ion removal by dyed cellulosic materials. J Appl Polym Sci 1992; 44: 903-10.
    • (1992) J Appl Polym Sci , vol.44 , pp. 903-910
    • Shukla, S.R.1    Sakhardande, V.D.2
  • 205
    • 17444419654 scopus 로고    scopus 로고
    • Radiation polymerization of 4-N-Acryloylamidobenzonitrile: Amidoximation, complexation and biological activity
    • Ali AAM, El-Sawy NM, Al Sagheer FA. Radiation polymerization of 4-N-Acryloylamidobenzonitrile: Amidoximation, complexation and biological activity. Intern J Polymer Mater 2005; 54: 359-73.
    • (2005) Intern J Polymer Mater , vol.54 , pp. 359-373
    • Ali, A.A.M.1    El-Sawy, N.M.2    Al Sagheer, F.A.3
  • 206
    • 0035208833 scopus 로고    scopus 로고
    • Radiation-induced graft polymerization of acrylic acid onto poly(tetrafluoroethylene-perfluorovinyl ether) copolymer films: Complexation with some transition metals and biological activity
    • El-Sawy NM, Al Sagheer FA. Radiation-induced graft polymerization of acrylic acid onto poly(tetrafluoroethylene-perfluorovinyl ether) copolymer films: Complexation with some transition metals and biological activity. Eur Polym J 2001; 37: 161-6.
    • (2001) Eur Polym J , vol.37 , pp. 161-166
    • El-Sawy, N.M.1    Al Sagheer, F.A.2
  • 207
    • 0032165062 scopus 로고    scopus 로고
    • Antibacterial activities of acrylic acid-grafted polypropylene fabric and its metallic salt
    • Park JS, Kim JH, Nho YC, Kwon OH. Antibacterial activities of acrylic acid-grafted polypropylene fabric and its metallic salt. J Appl Polym Sci 1998; 69: 2213-20.
    • (1998) J Appl Polym Sci , vol.69 , pp. 2213-2220
    • Park, J.S.1    Kim, J.H.2    Nho, Y.C.3    Kwon, O.H.4
  • 208
    • 44449150194 scopus 로고    scopus 로고
    • Buo-Hoï N, Lecocq J. New derivatives of p-mercaptobenzoic acid. Bull Chem Soc France 1946; 13: 139-47.
    • Buo-Hoï N, Lecocq J. New derivatives of p-mercaptobenzoic acid. Bull Chem Soc France 1946; 13: 139-47.
  • 209
    • 0010170843 scopus 로고
    • 5-nitro-2-furylamidoximes. US 1347874
    • Eloy F, Mirocha CJ. 5-nitro-2-furylamidoximes. US 1347874; Chem Abstr 1968; 68: 87139c.
    • (1968) Chem Abstr , vol.68
    • Eloy, F.1    Mirocha, C.J.2
  • 210
    • 0010121292 scopus 로고
    • 5-nitro-2-furoylamidoximes. US 3272828
    • Von Esch AM, Crovetti AJ. 5-nitro-2-furoylamidoximes. US 3272828; Chem Abstr 1966; 65: 18560c.
    • (1966) Chem Abstr , vol.65
    • Von Esch, A.M.1    Crovetti, A.J.2
  • 211
    • 0010119751 scopus 로고
    • Antibacterial and antifungal substituted 5-nitro-2-furylamidoximes. US 3660390
    • Von Esch AM, Crovetti AJ. Antibacterial and antifungal substituted 5-nitro-2-furylamidoximes. US 3660390; Chem Abstr 1972; 77: 61794y.
    • (1972) Chem Abstr , vol.77
    • Von Esch, A.M.1    Crovetti, A.J.2
  • 212
    • 44449133535 scopus 로고    scopus 로고
    • Saiwaka I, Wada T. β-(5-Nitro-2-furyl)acrylamide oxime. Japan 9334 (1967); Chem Abstr 1968; 68: 95663j.
    • Saiwaka I, Wada T. β-(5-Nitro-2-furyl)acrylamide oxime. Japan 9334 (1967); Chem Abstr 1968; 68: 95663j.
  • 213
    • 44449104066 scopus 로고    scopus 로고
    • Saiwaka I, Wada T. β-(5-Nitro-2-furylacrylamide oxime derivatives. Japan 9335 (1967); Chem Abstr 1968; 68: 95664k.
    • Saiwaka I, Wada T. β-(5-Nitro-2-furylacrylamide oxime derivatives. Japan 9335 (1967); Chem Abstr 1968; 68: 95664k.
  • 214
    • 44449139382 scopus 로고    scopus 로고
    • Netherlands 6500124
    • Norwich Pharmacal Co. N-(Methylcarbamyl)-5-nitrofuran-2-carboxamidoxime
    • Norwich Pharmacal Co. N-(Methylcarbamyl)-5-nitrofuran-2-carboxamidoxime. Netherlands 6500124; Chem Abstr 1996; 64: 8135d.
    • (1996) Chem Abstr , vol.64
  • 215
    • 44449165382 scopus 로고    scopus 로고
    • Leandri G, Maioli L, Ruzzier L. Synthesis and antibacterial activity of aromatic amidoxime and diazafuran derivatives. Boll Sci Fac Chim Ind Bologna 1957; 15: 57-62; Chem Abstr 1958; 52: 7291.
    • Leandri G, Maioli L, Ruzzier L. Synthesis and antibacterial activity of aromatic amidoxime and diazafuran derivatives. Boll Sci Fac Chim Ind Bologna 1957; 15: 57-62; Chem Abstr 1958; 52: 7291.
  • 216
    • 44449154225 scopus 로고    scopus 로고
    • Von Esch AM, Sherman WR. 5-nitro-2-furylamidoxime. US 3097214; Chem Abstr 1963; 59: 13950d
    • Von Esch AM, Sherman WR. 5-nitro-2-furylamidoxime. US 3097214; Chem Abstr 1963; 59: 13950d
  • 217
    • 44449146387 scopus 로고
    • 5-Nitro-2-thiazolecarboxamide oxime derivatives. Ger. Offen 2225434
    • Treuner U, Breuer H. 5-Nitro-2-thiazolecarboxamide oxime derivatives. Ger. Offen 2225434; Chem Abstr 1973; 78: 84396e.
    • (1973) Chem Abstr , vol.78
    • Treuner, U.1    Breuer, H.2
  • 219
    • 0347003669 scopus 로고    scopus 로고
    • Pyridine Oximes: Synthesis, Reactions, and Biological Activity
    • Abele E, Abele R, Lukevics E. Pyridine Oximes: Synthesis, Reactions, and Biological Activity. Chem Heterocyclic Comp 2003; 39: 825-65.
    • (2003) Chem Heterocyclic Comp , vol.39 , pp. 825-865
    • Abele, E.1    Abele, R.2    Lukevics, E.3
  • 220
    • 0348081315 scopus 로고
    • Notes - Pyridineamidoximes
    • Bernasek E. Notes - Pyridineamidoximes. J Org Chem 1957; 22: 1263.
    • (1957) J Org Chem , vol.22 , pp. 1263
    • Bernasek, E.1
  • 222
    • 44449160304 scopus 로고    scopus 로고
    • Spasov A, Golovinskii E. Syntheses in the pyridine series. I. Nicotinic and isonicotinic acid nitriles and amidoximes. Compt Rend Acad Bulg Sci 1958; 11: 287-89; Chem Abstr 1959; 53: 18026.
    • Spasov A, Golovinskii E. Syntheses in the pyridine series. I. Nicotinic and isonicotinic acid nitriles and amidoximes. Compt Rend Acad Bulg Sci 1958; 11: 287-89; Chem Abstr 1959; 53: 18026.
  • 223
    • 44449166489 scopus 로고    scopus 로고
    • Yoshitomi Pharmaceutical Industries, Ltd. Pyridinecarboxamide oximes. Jpn Tokkyo Koho JP 82 13542; Chem Abstr. 1982; 97: 182215g.
    • Yoshitomi Pharmaceutical Industries, Ltd. Pyridinecarboxamide oximes. Jpn Tokkyo Koho JP 82 13542; Chem Abstr. 1982; 97: 182215g.
  • 224
    • 0347547220 scopus 로고
    • Aromatic glyoxylonitrile oximes
    • US 3209008;, 18041g
    • Poziomek EJ, Melvin AR. Aromatic glyoxylonitrile oximes. US 3209008; Chem Abstr 1965; 63: 18041g.
    • (1965) Chem Abstr , vol.63
    • Poziomek, E.J.1    Melvin, A.R.2
  • 225
    • 0018070450 scopus 로고
    • Potential acetylcholinesterase reactivators - pyridine oxime derivatives. 1
    • Majewski M, Serafin B, Faff J, Borkowska G. Potential acetylcholinesterase reactivators - pyridine oxime derivatives. 1. Eur J Med Chem - Chim Ther 1978; 13: 403-5.
    • (1978) Eur J Med Chem - Chim Ther , vol.13 , pp. 403-405
    • Majewski, M.1    Serafin, B.2    Faff, J.3    Borkowska, G.4
  • 226
    • 0008781023 scopus 로고
    • Thiohydroximic ethers. 2. pyridine-4-thiohydroxime S-diethylaminoethylate and its physiological activity
    • Krivenchuk VE, Kokshareva NV, Sasinovich LM, Petrun'kin VE, Kagan YS. Thiohydroximic ethers. 2. pyridine-4-thiohydroxime S-diethylaminoethylate and its physiological activity. Khim-Farm Zh 1975; 9: 18-20.
    • (1975) Khim-Farm Zh , vol.9 , pp. 18-20
    • Krivenchuk, V.E.1    Kokshareva, N.V.2    Sasinovich, L.M.3    Petrun'kin, V.E.4    Kagan, Y.S.5
  • 227
    • 0348176841 scopus 로고
    • Isolation and reactions of pyridine-3-nitrile oxide
    • Majewski M, Serafin B, Oklesinska T. Isolation and reactions of pyridine-3-nitrile oxide. Rocz Chem 1977; 51: 975-8.
    • (1977) Rocz Chem , vol.51 , pp. 975-978
    • Majewski, M.1    Serafin, B.2    Oklesinska, T.3
  • 228
    • 44449167500 scopus 로고    scopus 로고
    • Kocevar M, Perdih M, Petric A, Polanc S, Sollner M, Vercek B. Transformations starting from pyridinecarboxamide oximes. Vestn Slov Kem Drus 1990; 37: 373-82; Chem Abstr 1991; 114: 228687.
    • Kocevar M, Perdih M, Petric A, Polanc S, Sollner M, Vercek B. Transformations starting from pyridinecarboxamide oximes. Vestn Slov Kem Drus 1990; 37: 373-82; Chem Abstr 1991; 114: 228687.
  • 229
    • 0346286004 scopus 로고
    • The action of nicotinic acid nitrites and amidoximes as growth factors for proteus vulgaris and Staphylococcus aureus
    • Golowinsky E, Markov KIZ. The action of nicotinic acid nitrites and amidoximes as growth factors for proteus vulgaris and Staphylococcus aureus. Naturforsch 1958; 13B: 725-6.
    • (1958) Naturforsch , vol.13 B , pp. 725-726
    • Golowinsky, E.1    Markov, K.I.Z.2
  • 230
    • 0347547080 scopus 로고
    • Pyridineamide oxime derivatives. Jpn Kokai 73 10075
    • Nakanishi M, Tsuda Y. Pyridineamide oxime derivatives. Jpn Kokai 73 10075; Chem Abstr 1973; 78, 111133a.
    • (1973) Chem Abstr , vol.78
    • Nakanishi, M.1    Tsuda, Y.2
  • 234
    • 44449131297 scopus 로고
    • Synthesis of dipyridinium mono-4-amidoxime iodides
    • Chen BH, Jiao KF, Song HQ. Synthesis of dipyridinium mono-4-amidoxime iodides. Acta Chim Sin 1986; 44: 417-20.
    • (1986) Acta Chim Sin , vol.44 , pp. 417-420
    • Chen, B.H.1    Jiao, K.F.2    Song, H.Q.3
  • 235
    • 0022746477 scopus 로고
    • 2,2′-bipyridyl-6-carboxamidoximes with potential antitumor and antimicrobial properties
    • Cristalli G, Frachetti P, Grifantini M, Ripa S. 2,2′-bipyridyl-6-carboxamidoximes with potential antitumor and antimicrobial properties. Pharmaco Ed Sci 1986; 41: 499-507.
    • (1986) Pharmaco Ed Sci , vol.41 , pp. 499-507
    • Cristalli, G.1    Frachetti, P.2    Grifantini, M.3    Ripa, S.4
  • 236
    • 0023607892 scopus 로고
    • Synthesis and antifungal activity of some allylamine derivatives
    • Bandiera T, Marinone F, Albini E. Synthesis and antifungal activity of some allylamine derivatives. J Heterocycl Chem 1987; 24: 1597-8.
    • (1987) J Heterocycl Chem , vol.24 , pp. 1597-1598
    • Bandiera, T.1    Marinone, F.2    Albini, E.3
  • 237
    • 0022995754 scopus 로고
    • Thiosemicarbazones of N-arylacetylformamidoximes and their tuberculostatic properties
    • Khalilova S, Poplevskaya I, Blonskaya LI, Blagodarny YA. Thiosemicarbazones of N-arylacetylformamidoximes and their tuberculostatic properties. Khim-Farm Zh 1986; 26: 1469-72.
    • (1986) Khim-Farm Zh , vol.26 , pp. 1469-1472
    • Khalilova, S.1    Poplevskaya, I.2    Blonskaya, L.I.3    Blagodarny, Y.A.4
  • 238
    • 0018178241 scopus 로고
    • Antitumor activity of amidoximes (hydroxyurea analoques) in murine tumor systems
    • Flora K, van't Riet B, Wampler G. Antitumor activity of amidoximes (hydroxyurea analoques) in murine tumor systems. Cancer Res 1978; 38: 1291-5.
    • (1978) Cancer Res , vol.38 , pp. 1291-1295
    • Flora, K.1    van't Riet, B.2    Wampler, G.3
  • 239
    • 0015239095 scopus 로고
    • Studies with hydroxyurea: The biologic and metabolic properties of formamidoxime. Biochim
    • Rosenkranz HS, Hjiorth R, Carr HS. Studies with hydroxyurea: The biologic and metabolic properties of formamidoxime. Biochim Biophys Acta 1971; 232: 48-60.
    • (1971) Biophys Acta , vol.232 , pp. 48-60
    • Rosenkranz, H.S.1    Hjiorth, R.2    Carr, H.S.3
  • 240
    • 0343764795 scopus 로고
    • Amidoximes of halogenated o- and p-hydroxybenzoic acids
    • Buu-Hoï N, Xuong W, Thang NV. Amidoximes of halogenated o- and p-hydroxybenzoic acids. Bull Soc Chim France 1954; 294-6.
    • (1954) Bull Soc Chim France , pp. 294-296
    • Buu-Hoï, N.1    Xuong, W.2    Thang, N.V.3
  • 241
    • 0030021757 scopus 로고    scopus 로고
    • 1-Methyl-1H-2-imidazo[4,5-b]pyridine-carboxylic acid and some of ist derivatives with suspected antituberculotic activity
    • Bukowski L, Janowier M. 1-Methyl-1H-2-imidazo[4,5-b]pyridine-carboxylic acid and some of ist derivatives with suspected antituberculotic activity. Pharmazie 1996; 51: 27-30.
    • (1996) Pharmazie , vol.51 , pp. 27-30
    • Bukowski, L.1    Janowier, M.2
  • 242
    • 0000953375 scopus 로고
    • Effects of PF1022A on developing larvae of Angiostrongylus costariciensis in mice, with special reference to route, dose and formulation
    • Terada M, Ishih A, Tungtrongchitr A, Sano M, Shomura T. Effects of PF1022A on developing larvae of Angiostrongylus costariciensis in mice, with special reference to route, dose and formulation. Jpn J Parasitol 1993; 42: 199-210.
    • (1993) Jpn J Parasitol , vol.42 , pp. 199-210
    • Terada, M.1    Ishih, A.2    Tungtrongchitr, A.3    Sano, M.4    Shomura, T.5
  • 243
    • 0031689882 scopus 로고    scopus 로고
    • Effects of amorphous and polymorphs of PF1022A, a new antinematode drug, on angiostrongylus costaricensis in mice
    • Kachi S, Terada M, Hashimoto H. H. Effects of amorphous and polymorphs of PF1022A, a new antinematode drug, on angiostrongylus costaricensis in mice. Jpn J Parasitol 1998; 77: 235-45.
    • (1998) Jpn J Parasitol , vol.77 , pp. 235-245
    • Kachi, S.1    Terada, M.2    Hashimoto, H.H.3
  • 247
    • 85007991332 scopus 로고
    • Total synthesis of the anthelmintic cyclodepsipeptide, PF1022A
    • Ohyama M, Iinuma K, Isogai A, Suzuki A. Total synthesis of the anthelmintic cyclodepsipeptide, PF1022A. Biosci Biotech Biochem. 1994; 58: 1193-4.
    • (1994) Biosci Biotech Biochem , vol.58 , pp. 1193-1194
    • Ohyama, M.1    Iinuma, K.2    Isogai, A.3    Suzuki, A.4
  • 248
    • 0002280019 scopus 로고
    • Synthesis and anthelmintic activity of the cyclodepsipeptide, PF1022A
    • Kobayashi M, Nanba T, Toyama T, Saito A. Synthesis and anthelmintic activity of the cyclodepsipeptide, PF1022A. Annu Rep Sankyo Res Lab 1994; 46: 67-75.
    • (1994) Annu Rep Sankyo Res Lab , vol.46 , pp. 67-75
    • Kobayashi, M.1    Nanba, T.2    Toyama, T.3    Saito, A.4
  • 249
    • 0028033957 scopus 로고
    • Synthesis of PF1022A, an anthelmintic cyclodepsipeptide
    • Dutton FE, Nelson SJ. Synthesis of PF1022A, an anthelmintic cyclodepsipeptide. J Antibiotics 1994; 47: 1322-7.
    • (1994) J Antibiotics , vol.47 , pp. 1322-1327
    • Dutton, F.E.1    Nelson, S.J.2
  • 250
    • 0035348158 scopus 로고    scopus 로고
    • Latrophilin-like receptor from the parasitic nematode Haemonchus contortus as target for the anthelmintic depsipeptide PF1022A
    • Saeger B, Schmitt-Wrede HP, Dehnhardt M, Benten WPM, Krucken J, Harder A, et al. Latrophilin-like receptor from the parasitic nematode Haemonchus contortus as target for the anthelmintic depsipeptide PF1022A. FASEB J 2001; 15: 1332-4.
    • (2001) FASEB J , vol.15 , pp. 1332-1334
    • Saeger, B.1    Schmitt-Wrede, H.P.2    Dehnhardt, M.3    Benten, W.P.M.4    Krucken, J.5    Harder, A.6
  • 251
    • 0036022148 scopus 로고    scopus 로고
    • Cyclooctadepsipeptides-a new class of anthelmintically active compounds
    • Harder A, von Samson-Himmelstjerna G. Cyclooctadepsipeptides-a new class of anthelmintically active compounds Parasitol Res 2002; 88: 481-8.
    • (2002) Parasitol Res , vol.88 , pp. 481-488
    • Harder, A.1    von Samson-Himmelstjerna, G.2
  • 253
    • 0011812798 scopus 로고
    • The solution conformation of chemotactic peptides and their backbonemodified analogs. Nuclear magnetic resonance and computermodeling studies with active amidoxime analogs of formylmethionyl-leucyl-phenylalanine
    • Rao VS, Sauve G, Lajoie G, Belleau B. The solution conformation of chemotactic peptides and their backbonemodified analogs. Nuclear magnetic resonance and computermodeling studies with active amidoxime analogs of formylmethionyl-leucyl-phenylalanine. Spectroscopy (Ottawa) 1995; 4: 153-70.
    • (1995) Spectroscopy (Ottawa) , vol.4 , pp. 153-170
    • Rao, V.S.1    Sauve, G.2    Lajoie, G.3    Belleau, B.4
  • 254
    • 44449114592 scopus 로고    scopus 로고
    • Jeschke P, Harder A, von Samson-Himmelstjerna G, Bonse G. Cyclo-imino depsipeptides and their utilization in controlling endoparasites (Bayer AG), PCT Application 0 076 985, 2000.
    • Jeschke P, Harder A, von Samson-Himmelstjerna G, Bonse G. Cyclo-imino depsipeptides and their utilization in controlling endoparasites (Bayer AG), PCT Application 0 076 985, 2000.
  • 255
    • 0030466249 scopus 로고    scopus 로고
    • Anthelmintic actions of the cyclic depsipeptide PF1022A and its electrophysiological effects on muscle cells of Ascaris suum
    • Martin RJ, Harder A, Londershausen M, Jeschke P. Anthelmintic actions of the cyclic depsipeptide PF1022A and its electrophysiological effects on muscle cells of Ascaris suum. Pestic Sci 1996; 48: 343-9.
    • (1996) Pestic Sci , vol.48 , pp. 343-349
    • Martin, R.J.1    Harder, A.2    Londershausen, M.3    Jeschke, P.4
  • 256
    • 0023260841 scopus 로고
    • Improved detection of anthelmintic activity in an in vitro screen utilizing adult Nippostrongylus brasiliensis
    • Rapson EB, Jenkins DC, Chilwan AS. Improved detection of anthelmintic activity in an in vitro screen utilizing adult Nippostrongylus brasiliensis. Z Parasitenkd 1987; 73: 190-1.
    • (1987) Z Parasitenkd , vol.73 , pp. 190-191
    • Rapson, E.B.1    Jenkins, D.C.2    Chilwan, A.S.3
  • 257
    • 0034763130 scopus 로고    scopus 로고
    • Synthesis and anthelmintic activity of thioamide analogues of cyclic octadepsipeptides such as PF1022A
    • Jeschke P, Harder A, Etzel W, Gau W, Thielking G, Bonse G, et al. Synthesis and anthelmintic activity of thioamide analogues of cyclic octadepsipeptides such as PF1022A. Pest Manag Sci 2001; 57: 1000-6.
    • (2001) Pest Manag Sci , vol.57 , pp. 1000-1006
    • Jeschke, P.1    Harder, A.2    Etzel, W.3    Gau, W.4    Thielking, G.5    Bonse, G.6
  • 259
    • 44449159749 scopus 로고    scopus 로고
    • Gutman AD. 2,6-Dichlorophenyl-substituted phenyl-nitroazones and their use as herbicides. US Patent 4425271, 1984
    • Gutman AD. 2,6-Dichlorophenyl-substituted phenyl-nitroazones and their use as herbicides. US Patent 4425271, 1984.
  • 260
    • 44449160303 scopus 로고    scopus 로고
    • Gutman AD. α-(Phenylazo)-2,6-dichlorobenzaldimino esters and their use as herbicides. US 4270947; Chem Abstr 1981; 95, 115055a
    • Gutman AD. α-(Phenylazo)-2,6-dichlorobenzaldimino esters and their use as herbicides. US 4270947; Chem Abstr 1981; 95, 115055a.
  • 262
    • 0035262127 scopus 로고    scopus 로고
    • Furan and thiophene oximes: Synthesis, reactions and biological activity
    • Abele E, Lukevics E. Furan and thiophene oximes: Synthesis, reactions and biological activity. Chem Heterocycl Comp 2001; 37: 141-69.
    • (2001) Chem Heterocycl Comp , vol.37 , pp. 141-169
    • Abele, E.1    Lukevics, E.2
  • 263
    • 0010114673 scopus 로고
    • Thiophene carboxamidoxime derivatives and their use in phytohormonal and herbicidal compositions. Ger Offen 2831983
    • Farge D, Leboul J, Le Goff Y, Poiget G. Thiophene carboxamidoxime derivatives and their use in phytohormonal and herbicidal compositions. Ger Offen 2831983; Chem Abstr 1979; 90: 181591v.
    • (1979) Chem Abstr , vol.90
    • Farge, D.1    Leboul, J.2    Le Goff, Y.3    Poiget, G.4
  • 264
    • 0010218282 scopus 로고
    • Thiophene amidoxime derivatives, and phytohormonal and herbicidal compositions containing them. IL 55228
    • Philagro SA., Thiophene amidoxime derivatives, and phytohormonal and herbicidal compositions containing them. IL 55228; Chem Abstr 1995; 99: 175584q
    • (1995) Chem Abstr , vol.99
    • Philagro, S.A.1
  • 265
    • 44449109949 scopus 로고    scopus 로고
    • N-disubstituted amidoxime and pyridazinyl O,N-disubstituted amidoxime derivatives useful as plant fungicides and for control of fungal attack on materials, e.g. wood
    • German Patent No 19837794 A1, 2000
    • Rheinheimer J, Rose I, Grote T, Lorenz G, Strathmann S. New pyridyl O,N-disubstituted amidoxime and pyridazinyl O,N-disubstituted amidoxime derivatives useful as plant fungicides and for control of fungal attack on materials, e.g. wood German Patent No 19837794 A1, 2000.
    • Rheinheimer, J.1    Rose, I.2    Grote, T.3    Lorenz, G.4    Strathmann, S.5    New pyridyl, O.6
  • 266
    • 44449096520 scopus 로고    scopus 로고
    • Benn FR, Charlton PT, Harmer GLM. Antihistaminic amino acetamidoximes. British Patent 895495; Chem Abstr 1962; 57: 13673b
    • Benn FR, Charlton PT, Harmer GLM. Antihistaminic amino acetamidoximes. British Patent 895495; Chem Abstr 1962; 57: 13673b.
  • 268
    • 0014179978 scopus 로고    scopus 로고
    • Larocca J, Gibson C N-Arylglyoxylohydroxamyl derivatives of nitrogen mustard. J Pharm Sci 1976; 56: 1683-4.
    • Larocca J, Gibson C N-Arylglyoxylohydroxamyl derivatives of nitrogen mustard. J Pharm Sci 1976; 56: 1683-4.
  • 269
    • 44449173427 scopus 로고    scopus 로고
    • Poplavskaya IA, Abdullin KA. Symposium on the synthesis of pharmaceutically active compounds, Odessa, 1976; Abstracts p. 100.
    • Poplavskaya IA, Abdullin KA. Symposium on the synthesis of pharmaceutically active compounds, Odessa, 1976; Abstracts p. 100.
  • 270
    • 44449157590 scopus 로고    scopus 로고
    • Poplavskaya IA, Abdullin KA. Symposium on problems in experimental chemotherapy, Cernogolovka, 1980; Abstracts, p. 120.
    • Poplavskaya IA, Abdullin KA. Symposium on problems in experimental chemotherapy, Cernogolovka, 1980; Abstracts, p. 120.
  • 271
    • 44449172386 scopus 로고    scopus 로고
    • Poplevskaya IA, Kurmangalieva RG, Khalilova. SF, Abdullin KA, Kudrina IK, Kabiev OK, Acetylformamidoxime derivatives and their antiblastic properties. Akad Nauk Kaz SSR. 1980; 52: 114-27; Chem Abstr 1981; 94: 174593b.
    • Poplevskaya IA, Kurmangalieva RG, Khalilova. SF, Abdullin KA, Kudrina IK, Kabiev OK, Acetylformamidoxime derivatives and their antiblastic properties. Akad Nauk Kaz SSR. 1980; 52: 114-27; Chem Abstr 1981; 94: 174593b.
  • 272
    • 44449115550 scopus 로고    scopus 로고
    • Poplavskaya IA, Kurmangaliyeva RG, Khalilova S, Abdullin KA, Kudrina IK. Derivatives of acetylformamide oxime and their cytostatic properties. Khim-Farm Zh 1981; 15: 16-21; Chem Abstr 1981; 95: 73413h.
    • Poplavskaya IA, Kurmangaliyeva RG, Khalilova S, Abdullin KA, Kudrina IK. Derivatives of acetylformamide oxime and their cytostatic properties. Khim-Farm Zh 1981; 15: 16-21; Chem Abstr 1981; 95: 73413h.
  • 273
    • 0016795206 scopus 로고
    • Synthesis and antiarrhythmic activity of substituted (2-pyrimidinylthio)acetamidoximes
    • Scotese A, Santilli A, Nelson G. Synthesis and antiarrhythmic activity of substituted (2-pyrimidinylthio)acetamidoximes. J Med Chem 1975; 18: 852-4.
    • (1975) J Med Chem , vol.18 , pp. 852-854
    • Scotese, A.1    Santilli, A.2    Nelson, G.3
  • 274
    • 44449158067 scopus 로고
    • 4-Phenoxy-3-hydroxybutyramidoxime derivatives, and their therapeutic use. Fr. Demande FR 2503147
    • Lafon L. 4-Phenoxy-3-hydroxybutyramidoxime derivatives, and their therapeutic use. Fr. Demande FR 2503147; Chem Abstr 1983; 98, 178973f.
    • (1983) Chem Abstr , vol.98
    • Lafon, L.1
  • 275
    • 44449173957 scopus 로고
    • Acetamidoxime derivatives. Belg. 866163
    • 103986p
    • Lafon L. Acetamidoxime derivatives. Belg. 866163; Chem Abstr 1979; 90, 103986p.
    • (1979) Chem Abstr , vol.90
    • Lafon, L.1
  • 276
    • 44449132011 scopus 로고
    • 2-(N-Phenylcarbamoyl)acetamide oximes. Ger. Offen 2607764
    • Fauran C, Bourgéry G, Gouret C. 2-(N-Phenylcarbamoyl)acetamide oximes. Ger. Offen 2607764; Chem Abstr 1977; 86, 5191y.
    • (1977) Chem Abstr , vol.86
    • Fauran, C.1    Bourgéry, G.2    Gouret, C.3
  • 277
    • 44449085752 scopus 로고
    • Propionamidoxime derivatives. Fr. Demande FR 2422630
    • Najer H, Obitz D. Propionamidoxime derivatives. Fr. Demande FR 2422630; Chem Abstr 1980,,93: 7898c.
    • (1980) Chem Abstr , vol.93
    • Najer, H.1    Obitz, D.2
  • 278
    • 44449084765 scopus 로고
    • Amidoxime derivatives and their therapeutic use.Fr. Demande FR 2485006
    • Menin J, Mangane M. Amidoxime derivatives and their therapeutic use.Fr. Demande FR 2485006; Chem Abstr 1982; 96, 199332v.
    • (1982) Chem Abstr , vol.96
    • Menin, J.1    Mangane, M.2
  • 279
    • 0019418619 scopus 로고
    • Neurotropic and psychotropic agents. 169. Synthesis of arylthioacetamidoximes as potential anti-depressants
    • Cervená I, Hrubantová M, Bartosová M, Protiva M. Neurotropic and psychotropic agents. 169. Synthesis of arylthioacetamidoximes as potential anti-depressants. Collect Czech Chem Comm 1981; 46: 1188-98.
    • (1981) Collect Czech Chem Comm , vol.46 , pp. 1188-1198
    • Cervená, I.1    Hrubantová, M.2    Bartosová, M.3    Protiva, M.4
  • 280
    • 44449142328 scopus 로고    scopus 로고
    • Protiva M, Cervená I. Hrunantova M, Bartosova M. Arylthio-acetamidoximes. Czech. CS 213038; Chem Abstr 1984; 101: 72455d.
    • Protiva M, Cervená I. Hrunantova M, Bartosova M. Arylthio-acetamidoximes. Czech. CS 213038; Chem Abstr 1984; 101: 72455d.
  • 281
    • 44449158571 scopus 로고
    • Heterocyclic amidoximes, derivatives, and their therapeutic uses. Eur
    • Pat Appl EP 67094;, 179232a
    • Obitz D. Heterocyclic amidoximes, derivatives, and their therapeutic uses. Eur Pat Appl EP 67094; Chem Abstr 1983; 98: 179232a.
    • (1983) Chem Abstr , vol.98
    • Obitz, D.1
  • 282
    • 0037558151 scopus 로고
    • Amidoxime derivatives and their use in therapy. Fr. Demande M 2506764
    • Najer H, Obitz D, Kaplan JP. Amidoxime derivatives and their use in therapy. Fr. Demande M 2506764; Chem Abstr 1983; 99: 38360z.
    • (1983) Chem Abstr , vol.99
    • Najer, H.1    Obitz, D.2    Kaplan, J.P.3
  • 284
    • 0037567394 scopus 로고    scopus 로고
    • Indole and isatin oxidimes: Synthesis, reactions and biological activity
    • Abele E. Abele R, Dzenitis O, Lukevics E. Indole and isatin oxidimes: synthesis, reactions and biological activity. Chem Heterocycl Comp 2003; 39: 3-35.
    • (2003) Chem Heterocycl Comp , vol.39 , pp. 3-35
    • Abele, E.1    Abele, R.2    Dzenitis, O.3    Lukevics, E.4
  • 285
    • 0010208685 scopus 로고
    • Jr. 5-Phenyl-2-furamidoximes
    • US 3946049;, 21083z
    • Pelosi SS Jr. 5-Phenyl-2-furamidoximes. US 3946049; Chem Abstr 1976; 85: 21083z.
    • (1976) Chem Abstr , vol.85
    • Pelosi, S.S.1
  • 286
    • 0028277874 scopus 로고
    • Oxadiazoles as bioisosteric transformations of carboxylic functionalities. Part I
    • Andersen KF, Jorgensen AS, Bræmstrup C. Oxadiazoles as bioisosteric transformations of carboxylic functionalities. Part I. Eur J Med Chem 1994; 29: 393-9.
    • (1994) Eur J Med Chem , vol.29 , pp. 393-399
    • Andersen, K.F.1    Jorgensen, A.S.2    Bræmstrup, C.3
  • 288
    • 0344282508 scopus 로고
    • Antihypertensive activity of hexahydro-1-azepin-azepinepropionamidoxime
    • Mull RP, Maxwell R, Plummer A. Antihypertensive activity of hexahydro-1-azepin-azepinepropionamidoxime. Nature 1957; 180: 1200-1.
    • (1957) Nature , vol.180 , pp. 1200-1201
    • Mull, R.P.1    Maxwell, R.2    Plummer, A.3
  • 289
    • 0010128550 scopus 로고
    • Amidoximes, amidines, and guanidines for medical use. Belg. 659467
    • Bell MR. Amidoximes, amidines, and guanidines for medical use. Belg. 659467; Chem Abstr 1966; 64: 2098h.
    • (1966) Chem Abstr , vol.64
    • Bell, M.R.1
  • 290
    • 44449140871 scopus 로고
    • Antihypertensive N-methylalkanamide oxime carbamates. Ger Offen 2318960
    • Henderson RM. Antihypertensive N-methylalkanamide oxime carbamates. Ger Offen 2318960; Chem Abstr 1974; 80: 27006v.
    • (1974) Chem Abstr , vol.80
    • Henderson, R.M.1
  • 291
    • 44449124514 scopus 로고    scopus 로고
    • Bailey DM. 2-Alkoxy-2-(naphthyl)alkanamidoximes. US 3720714; Chem Abstr 1973; 78: 14767On
    • Bailey DM. 2-Alkoxy-2-(naphthyl)alkanamidoximes. US 3720714; Chem Abstr 1973; 78: 14767On.
  • 296
    • 44449152938 scopus 로고    scopus 로고
    • Nishimura A, Shimizu M, Uno H, Hirooka T. Masuda Y, Kurokawa M. Amidoximes. Japan Kokai 75 50371; Chem Abstr 1975; 83: 206232z.
    • Nishimura A, Shimizu M, Uno H, Hirooka T. Masuda Y, Kurokawa M. Amidoximes. Japan Kokai 75 50371; Chem Abstr 1975; 83: 206232z.
  • 301
    • 0010219432 scopus 로고
    • Benzofuran-derived amidoximes and process for preparing the same. Brit. 1508210
    • Areschka A, Descamps M. Benzofuran-derived amidoximes and process for preparing the same. Brit. 1508210; Chem Abstr 1978; 89: 163390d.
    • (1978) Chem Abstr , vol.89
    • Areschka, A.1    Descamps, M.2
  • 302
    • 44449178666 scopus 로고    scopus 로고
    • Areschka A, Makauh J, Verbruggen F, Houben C, Descamps M, Heyndrickx JP, et al. Benzofurans. 61. Potential antihypertensive 3-benzo-furanylacetamidoximes. Eur J Med Chem 1977; 12; 37-91.
    • Areschka A, Makauh J, Verbruggen F, Houben C, Descamps M, Heyndrickx JP, et al. Benzofurans. 61. Potential antihypertensive 3-benzo-furanylacetamidoximes. Eur J Med Chem 1977; 12; 37-91.
  • 303
    • 0026391208 scopus 로고
    • Investigation on synthesis, hypotensive activity and highly selective adrenergic antagonistic activity of some simple and substituted indane derivatives
    • Ray SM, Lahiri SC. Investigation on synthesis, hypotensive activity and highly selective adrenergic antagonistic activity of some simple and substituted indane derivatives. J Indian Chem Soc 1991; 68: 549-55.
    • (1991) J Indian Chem Soc , vol.68 , pp. 549-555
    • Ray, S.M.1    Lahiri, S.C.2
  • 304
    • 0032413633 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of several coumarin-4-carboxamidoxime and 3-(coumarin-4-yl)-1,2,4-oxadiazole derivatives
    • Nicolaides D, Fylaktakidou KC, Litinas KE, Hadjipavlou-Litina D. Synthesis and biological evaluation of several coumarin-4-carboxamidoxime and 3-(coumarin-4-yl)-1,2,4-oxadiazole derivatives. Eur J Med Chem 1998; 33: 715-24.
    • (1998) Eur J Med Chem , vol.33 , pp. 715-724
    • Nicolaides, D.1    Fylaktakidou, K.C.2    Litinas, K.E.3    Hadjipavlou-Litina, D.4
  • 306
    • 0020415376 scopus 로고
    • Analgesic and antiinflammatory prorerties of 2-benzofuran amidoximes
    • Riffaud JP, Dupont C, Rene L, Royer R. Analgesic and antiinflammatory prorerties of 2-benzofuran amidoximes. Eur J Med Chem-Chim Ther 1982; 17: 577-81.
    • (1982) Eur J Med Chem-Chim Ther , vol.17 , pp. 577-581
    • Riffaud, J.P.1    Dupont, C.2    Rene, L.3    Royer, R.4
  • 307
    • 44449124513 scopus 로고
    • β-Triazolinonylpropionamidoximes and their derivatives
    • Somasekhara S, Upadhyaya NV. β-Triazolinonylpropionamidoximes and their derivatives. J Ind Chem Soc 1972; 49: 201-2.
    • (1972) J Ind Chem Soc , vol.49 , pp. 201-202
    • Somasekhara, S.1    Upadhyaya, N.V.2
  • 308
    • 0348176721 scopus 로고
    • Antiviral thiazolo [5,4-b] pyridine compounds
    • US 4443606;, 23468b
    • Wei PHL, Bell SC. Antiviral thiazolo [5,4-b] pyridine compounds. US 4443606; Chem Abstr 1984; 101: 23468b.
    • (1984) Chem Abstr , vol.101
    • Wei, P.H.L.1    Bell, S.C.2
  • 309
    • 0001367771 scopus 로고    scopus 로고
    • Inhibitors of carbohydrate-processing enzymes: Design and synthesis of sugar-shaped heterocycles
    • Ganem B. Inhibitors of carbohydrate-processing enzymes: Design and synthesis of sugar-shaped heterocycles. Acc Chem Res 1996; 29: 340-7
    • (1996) Acc Chem Res , vol.29 , pp. 340-347
    • Ganem, B.1
  • 310
    • 2542631521 scopus 로고
    • Amidines. 4. structure- basicity relation in monosubstituted N,N-(alkylene-alpha, omega)-N'-phenylformamidines
    • Oszczapowicz J, Orlinski R, Walczynska H. Amidines. 4. structure- basicity relation in monosubstituted N,N-(alkylene-alpha, omega)-N'-phenylformamidines. Pol J Chem 1979; 53: 2531-7.
    • (1979) Pol J Chem , vol.53 , pp. 2531-2537
    • Oszczapowicz, J.1    Orlinski, R.2    Walczynska, H.3
  • 311
    • 0034101163 scopus 로고    scopus 로고
    • Glycosidase inhibitors and their chemotherapeutic value, part 3
    • El Ashry ESH, Rashed N, Shobier AHS. Glycosidase inhibitors and their chemotherapeutic value, part 3. Pharmazie 2000; 55: 403-15.
    • (2000) Pharmazie , vol.55 , pp. 403-415
    • El Ashry, E.S.H.1    Rashed, N.2    Shobier, A.H.S.3
  • 312
    • 0027750880 scopus 로고
    • Amidine, amidrazone, and amidoxime derivatives of monosaccharide aldonolactams: Synthesis and evaluation as glyosidase inhibitors
    • Papandreou G, Tong MK, Ganem B. Amidine, amidrazone, and amidoxime derivatives of monosaccharide aldonolactams: Synthesis and evaluation as glyosidase inhibitors. J Am Chem Soc 1993; 115: 11682-90.
    • (1993) J Am Chem Soc , vol.115 , pp. 11682-11690
    • Papandreou, G.1    Tong, M.K.2    Ganem, B.3
  • 313
    • 84989580263 scopus 로고
    • Mimicking the glucosidase transition state: Shape/ charge considerations
    • Ganem B, Papandreou G. Mimicking the glucosidase transition state: Shape/ charge considerations. J Am Chem Soc 1991; 113: 8984-5.
    • (1991) J Am Chem Soc , vol.113 , pp. 8984-8985
    • Ganem, B.1    Papandreou, G.2
  • 314
    • 0025005239 scopus 로고
    • Potent, broad-spectrum inhibition of glycosidases by an amidine derivative of D-glucose
    • Tong MK, Papandreou G, Ganem B. Potent, broad-spectrum inhibition of glycosidases by an amidine derivative of D-glucose. J Am Chem Soc 1990; 112: 6137-9.
    • (1990) J Am Chem Soc , vol.112 , pp. 6137-6139
    • Tong, M.K.1    Papandreou, G.2    Ganem, B.3
  • 315
    • 12044254693 scopus 로고
    • Enzymatic cyclization of squalene and oxidosqualene to sterols and triterpenes
    • Abe I, Rohmer M, Prestwich GD. Enzymatic cyclization of squalene and oxidosqualene to sterols and triterpenes. Chem Rev 1993; 93: 2189-206
    • (1993) Chem Rev , vol.93 , pp. 2189-2206
    • Abe, I.1    Rohmer, M.2    Prestwich, G.D.3
  • 317
    • 0023515798 scopus 로고
    • Prokaryotic hopanoids and other polyterpenoid sterol surrogates
    • Ourisson G, Rohmer M, Poralla K. Prokaryotic hopanoids and other polyterpenoid sterol surrogates. Annu Rev Microbiol 1987; 41: 301-33
    • (1987) Annu Rev Microbiol , vol.41 , pp. 301-333
    • Ourisson, G.1    Rohmer, M.2    Poralla, K.3
  • 318
    • 0033597723 scopus 로고    scopus 로고
    • Amidrazone and amidoxime inhibitors of squalene hopene cyclase
    • Ganem B, Dong Y, Feng Zheng Y, Prestwich G. D. Amidrazone and amidoxime inhibitors of squalene hopene cyclase. J Org Chem 1999; 64: 5441-6.
    • (1999) J Org Chem , vol.64 , pp. 5441-5446
    • Ganem, B.1    Dong, Y.2    Feng Zheng, Y.3    Prestwich, G.D.4
  • 319
    • 44449151471 scopus 로고    scopus 로고
    • Drud design of radioactive metal complexes for nuclear medical diagnosis
    • Saji H, Horiuchi KS, Mukai T. Drud design of radioactive metal complexes for nuclear medical diagnosis. Biomed Res Trace Elements 2001; 12: 141-51.
    • (2001) Biomed Res Trace Elements , vol.12 , pp. 141-151
    • Saji, H.1    Horiuchi, K.S.2    Mukai, T.3
  • 320
    • 0035999836 scopus 로고    scopus 로고
    • 99mTc radiopharmaceuticals
    • 99mTc radiopharmaceuticals. Ann Nucl Med 2002; 16: 79-93.
    • (2002) Ann Nucl Med , vol.16 , pp. 79-93
    • Arano, Y.1
  • 324
    • 0001309714 scopus 로고
    • Internal of metal ion with amidoximes
    • Pearce GA Jr, Pflaum RT. Internal of metal ion with amidoximes. J Am Chem Soc 1959; 81: 6505-8.
    • (1959) J Am Chem Soc , vol.81 , pp. 6505-6508
    • Pearce Jr, G.A.1    Pflaum, R.T.2
  • 325
    • 44449142820 scopus 로고    scopus 로고
    • A new hydroxamamide-based ligand system for 99mTc labeling of proteins and polypeptides
    • Nakayama M, Ono M, Haratake M. A new hydroxamamide-based ligand system for 99mTc labeling of proteins and polypeptides. Biomed Res Trace Elements 2003; 14: 29-33.
    • (2003) Biomed Res Trace Elements , vol.14 , pp. 29-33
    • Nakayama, M.1    Ono, M.2    Haratake, M.3
  • 326
    • 15944368136 scopus 로고    scopus 로고
    • Facile synthesis of bis(hydroxamamide)-based tetradentate ligands for 99mTc-radiopharmaceutical
    • Xu H, Chu T, Wang X, Liu X. Facile synthesis of bis(hydroxamamide)-based tetradentate ligands for 99mTc-radiopharmaceutical. Appl Radiat Isot 2005; 62: 919-22.
    • (2005) Appl Radiat Isot , vol.62 , pp. 919-922
    • Xu, H.1    Chu, T.2    Wang, X.3    Liu, X.4
  • 329
    • 1642452629 scopus 로고    scopus 로고
    • Synthesis and biological results of the technetium-99m-labeled 4-nitroimidazole for imaging tumor hypoxia
    • Chu TW, Hu SW, Wei B, Wang Y, Liu XQ, Wang XY. Synthesis and biological results of the technetium-99m-labeled 4-nitroimidazole for imaging tumor hypoxia. Bioorg Med Chem Lett 2004; 14: 747-9.
    • (2004) Bioorg Med Chem Lett , vol.14 , pp. 747-749
    • Chu, T.W.1    Hu, S.W.2    Wei, B.3    Wang, Y.4    Liu, X.Q.5    Wang, X.Y.6
  • 330
    • 1542315602 scopus 로고    scopus 로고
    • Preparation and biodistribution of technetium-99m-labeled 1-(2-nitroimidazole-1-yl)-propanhydroxy-iminoamide (N2IPA) as a tumor hypoxia marker
    • Chu TW, Li RJ, Hu SW, Liu XQ, Wang XY. Preparation and biodistribution of technetium-99m-labeled 1-(2-nitroimidazole-1-yl)-propanhydroxy-iminoamide (N2IPA) as a tumor hypoxia marker. Nucl Med Biol 2004; 31: 199-203.
    • (2004) Nucl Med Biol , vol.31 , pp. 199-203
    • Chu, T.W.1    Li, R.J.2    Hu, S.W.3    Liu, X.Q.4    Wang, X.Y.5
  • 331
    • 0034650511 scopus 로고    scopus 로고
    • Synthesis of N-acetylxylos-amidoxime, a potensial transition state analog inhibitor of glycosyl-transferase
    • Devel L, Vidal-Cros A, Thellend A. Synthesis of N-acetylxylos-amidoxime, a potensial transition state analog inhibitor of glycosyl-transferase. Tetrahedron Lett 2000; 41: 299-301
    • (2000) Tetrahedron Lett , vol.41 , pp. 299-301
    • Devel, L.1    Vidal-Cros, A.2    Thellend, A.3
  • 332
    • 33845282544 scopus 로고
    • The synthesis and configurational stability of differentially protected beta-hydroxy-alpha.-amino aldehydes
    • Garner P, Park JM. The synthesis and configurational stability of differentially protected beta-hydroxy-alpha.-amino aldehydes. J Org Chem 1987; 52:2361-4.
    • (1987) J Org Chem , vol.52 , pp. 2361-2364
    • Garner, P.1    Park, J.M.2
  • 333
    • 11944267365 scopus 로고
    • Antisense oligonucleotides: A new therapeutic principle
    • Uhlmann E, Peyman A. Antisense oligonucleotides: A new therapeutic principle. Chem Rev 1990; 90: 543-84.
    • (1990) Chem Rev , vol.90 , pp. 543-584
    • Uhlmann, E.1    Peyman, A.2
  • 340
    • 0037421032 scopus 로고    scopus 로고
    • New and efficient synthesis of 5′-amino-5′-(S)-methyl-2′,5′- dideoxy-nucleosides
    • and references cited therein
    • Jung PMJ, Beaudegnies R, De Mesmaeker A, Wendeborn S. New and efficient synthesis of 5′-amino-5′-(S)-methyl-2′,5′- dideoxy-nucleosides. Tetrahedron Lett 2003; 44: 293-7 and references cited therein.
    • (2003) Tetrahedron Lett , vol.44 , pp. 293-297
    • Jung, P.M.J.1    Beaudegnies, R.2    De Mesmaeker, A.3    Wendeborn, S.4
  • 341
    • 0029787933 scopus 로고    scopus 로고
    • Association of short-strand DNA oligomers with guanidinium-linked nucleosides. A kinetic and thermodynamic study
    • Blaskó A, Dempcy RO, Minyat EE, Bruice TC. Association of short-strand DNA oligomers with guanidinium-linked nucleosides. A kinetic and thermodynamic study. J Am Chem Soc 1996; 118: 7892-9.
    • (1996) J Am Chem Soc , vol.118 , pp. 7892-7899
    • Blaskó, A.1    Dempcy, R.O.2    Minyat, E.E.3    Bruice, T.C.4
  • 342
    • 0030818901 scopus 로고    scopus 로고
    • Blaskó A, Dempcy RO, Minyat EE, Bruice TC. Fidelity of binding of the guanidinium nucleic acid (DNG) d(Tg)4-T-azido with short strand DNA oligomers A5G3A5, GA4G3A4G, G2A3 G3A3G2,G2A2 G5A2G2, A kinetic and thermodynamic study. Biochemistry 1997; 36:7821-31
    • 2). A kinetic and thermodynamic study. Biochemistry 1997; 36:7821-31.
  • 343
    • 0032542519 scopus 로고    scopus 로고
    • Nanosecond molecular dynamics of hybrid triplex and duplex of polycation deoxyribonucleic guanidine strands with a complimentary DNA strand
    • Luo J, Bruice TC. Nanosecond molecular dynamics of hybrid triplex and duplex of polycation deoxyribonucleic guanidine strands with a complimentary DNA strand. J Am Chem Soc 1998; 120: 1115-23.
    • (1998) J Am Chem Soc , vol.120 , pp. 1115-1123
    • Luo, J.1    Bruice, T.C.2
  • 344
    • 0033612014 scopus 로고    scopus 로고
    • Solid-phase synthesis of deoxynucleic guanidine (DNG) oligomers and melting point and circular dichroism analysis of binding fidelity of octameric thymidyl oligomers with DNA oligomers
    • Linkletter BA, Szabo IE, Bruice TC. Solid-phase synthesis of deoxynucleic guanidine (DNG) oligomers and melting point and circular dichroism analysis of binding fidelity of octameric thymidyl oligomers with DNA oligomers. J Am Chem Soc 1999; 121: 3888-96.
    • (1999) J Am Chem Soc , vol.121 , pp. 3888-3896
    • Linkletter, B.A.1    Szabo, I.E.2    Bruice, T.C.3
  • 345
    • 0033658462 scopus 로고    scopus 로고
    • Replacement of the phosphorodiester linkages of RNA with guanidinium linkages: The solid-phase synthesis of ribonucleic guanidine
    • Kojima N, Bruice TC. Replacement of the phosphorodiester linkages of RNA with guanidinium linkages: the solid-phase synthesis of ribonucleic guanidine. Org Lett 2000; 2: 81-4.
    • (2000) Org Lett , vol.2 , pp. 81-84
    • Kojima, N.1    Bruice, T.C.2
  • 346
    • 0037185355 scopus 로고    scopus 로고
    • Synthesis of ribonucleic guanidine: Replacement of the negative phosphodiester linkages of RNA with positive guanidinium linkages
    • Kojima N, Szabo IE, Bruice T. C. Synthesis of ribonucleic guanidine: replacement of the negative phosphodiester linkages of RNA with positive guanidinium linkages. Tetrahedron 2002; 58: 867-9.
    • (2002) Tetrahedron , vol.58 , pp. 867-869
    • Kojima, N.1    Szabo, I.E.2    Bruice, T.C.3
  • 347
    • 0038505291 scopus 로고    scopus 로고
    • Synthegis of dinucleotides containing nitrone, hydroxylamine and amidoxime linkages
    • Gallos JK, Dellios CC. Synthegis of dinucleotides containing nitrone, hydroxylamine and amidoxime linkages. Tetrahedron Lett 2003; 44:5679-81.
    • (2003) Tetrahedron Lett , vol.44 , pp. 5679-5681
    • Gallos, J.K.1    Dellios, C.C.2
  • 348
    • 0029033428 scopus 로고
    • Structure and dynamics of MMI linked nucleotides
    • Mohan V, Griffey RH, Davis DR. Structure and dynamics of MMI linked nucleotides. Tetrahedron 1995; 51: 6855-8.
    • (1995) Tetrahedron , vol.51 , pp. 6855-6858
    • Mohan, V.1    Griffey, R.H.2    Davis, D.R.3
  • 349
    • 44449167993 scopus 로고    scopus 로고
    • Bailey DM. 2-Alkoxy-2-phenylalkane amidoximes. US 3607941; Chem Abstr 1971; 75, 129556p
    • Bailey DM. 2-Alkoxy-2-phenylalkane amidoximes. US 3607941; Chem Abstr 1971; 75, 129556p.
  • 350
    • 44449116039 scopus 로고
    • (Arylsulfonyl)formamidoximes. Ger Offen 2248941
    • Treuner UD. (Arylsulfonyl)formamidoximes. Ger Offen 2248941; Chem Abstr 1973; 79, 18435m.
    • (1973) Chem Abstr , vol.79
    • Treuner, U.D.1
  • 351
    • 0346286126 scopus 로고
    • Jpn. Tokkyo Koho JP 82 13542;
    • Yoshitomi Pharmaceutical Industries Ltd. Pyridinecarboxamide oximes
    • Yoshitomi Pharmaceutical Industries Ltd. Pyridinecarboxamide oximes. Jpn. Tokkyo Koho JP 82 13542; Chem Abstr 1982; 97: 182215g.
    • (1982) Chem Abstr , vol.97
  • 352
    • 0024437955 scopus 로고
    • Synthesis and pharmacologic activity of amidoximes of (2-oxopirrolidino)alkane acids and relevant O-acyl derivatives
    • Glozman O, Orlove E, Voronina T. Synthesis and pharmacologic activity of amidoximes of (2-oxopirrolidino)alkane acids and relevant O-acyl derivatives. Khim-Farin Zh 1989; 23: 1147-52.
    • (1989) Khim-Farin Zh , vol.23 , pp. 1147-1152
    • Glozman, O.1    Orlove, E.2    Voronina, T.3
  • 354
    • 0022412803 scopus 로고
    • Backbone-modified oligopeptidic bioregulators - The synthesis and configuration of thiomide, amidoxime, cyanoamidine and amidrazone analogues of the chemotactic peptide N-formyl-methionyl-leucyl-phenylalanine (F-MET-LEU-PHE-OR)
    • Sauvé G, Rao V, Lajoie G, Belleau B. Backbone-modified oligopeptidic bioregulators - The synthesis and configuration of thiomide, amidoxime, cyanoamidine and amidrazone analogues of the chemotactic peptide N-formyl-methionyl-leucyl-phenylalanine (F-MET-LEU-PHE-OR). Canad J Chem 1985; 63: 3089-101.
    • (1985) Canad J Chem , vol.63 , pp. 3089-3101
    • Sauvé, G.1    Rao, V.2    Lajoie, G.3    Belleau, B.4
  • 355
    • 0000179987 scopus 로고
    • Synthesis and effects on arginase and nitric oxide synthase of two novel analogs of N ω-hydroxyarginine, Nω-hydroxyindospicine and p-hydroxyamidino-phenylalanine
    • Vadon S, Custot J, Bouche JI, Mansuy D. Synthesis and effects on arginase and nitric oxide synthase of two novel analogs of N ω-hydroxyarginine, Nω-hydroxyindospicine and p-hydroxyamidino-phenylalanine. J Chem Soc Perkin Trans 1966; 645-8.
    • (1966) J Chem Soc Perkin Trans , pp. 645-648
    • Vadon, S.1    Custot, J.2    Bouche, J.I.3    Mansuy, D.4
  • 356
    • 44449154705 scopus 로고
    • Imidamides derived from 2-oxo-3-benzothiazoline acetic acid, and their use as plant growth regulants. Eur
    • Pat Appl 24889;, 115525d
    • d'Amico JJ, Marvel JT. Imidamides derived from 2-oxo-3-benzothiazoline acetic acid, and their use as plant growth regulants. Eur Pat Appl 24889; Chem Abstr 1981; 95: 115525d.
    • (1981) Chem Abstr , vol.95
    • d'Amico, J.J.1    Marvel, J.T.2
  • 357
    • 44449176986 scopus 로고    scopus 로고
    • Hiller H, Fischer A. Alkylaminooxanil oximes. US Patent 3766270, 1973
    • Hiller H, Fischer A. Alkylaminooxanil oximes. US Patent 3766270, 1973.
  • 358
    • 44449111620 scopus 로고
    • substituted N-phenylformamidoxime. Ger Offen 2717437
    • Sinharay A, Bonin W. substituted N-phenylformamidoxime. Ger Offen 2717437; Chem Abstr 1979; 90:54644q.
    • (1979) Chem Abstr , vol.90
    • Sinharay, A.1    Bonin, W.2
  • 359
    • 44449158570 scopus 로고
    • Phosphorus esters of amidoximes, and compositions for and methods of controlling insects using them
    • US 4479946;, 57850f
    • Hodakowski LE, Bushey DF. Phosphorus esters of amidoximes, and compositions for and methods of controlling insects using them. US 4479946; Chem Abstr 1985; 102: 57850f.
    • (1985) Chem Abstr , vol.102
    • Hodakowski, L.E.1    Bushey, D.F.2
  • 360
    • 44449175462 scopus 로고
    • Aryloxyphenoxypropionamide oximes. Jpn
    • Kokai Tokkyo Koho JP 57169455;, 107168m
    • Mitsui Toatsu Chemicals, Inc. Aryloxyphenoxypropionamide oximes. Jpn Kokai Tokkyo Koho JP 57169455; Chem Abstr 1983 ; 98: 107168m.
    • (1983) Chem Abstr , vol.98


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.