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Volumn 33, Issue 6, 2010, Pages 821-830

Synthesis and antimicrobial and nitric oxide synthase inhibitory activities of novel isothiourea derivatives

Author keywords

Anti protozoal activity; Antibacterial activity; Antifungal activity; Isothiourea derivative; Nitric oxide synthase; Synthesis

Indexed keywords

(2 NITROBENZYL)ISOTHIOUREA; (2,3,4,5,6 PENTABROMOBENZYL)ISOTHIOUREA HYDROBROMIDE; (2,4 DINITROBENZYL)ISOTHIOUREA HYDROCHLORIDE; (3,4 DICHLOROBENZYL)ISOTHIOUREA HYDROCHLORIDE; 2 (5 NITROFURAN 2 YLMETHYL)ISOTHIOUREA; 4 NITROQUINOLINE 1 OXIDE; 7 NITROINDAZOLE; ANTIFUNGAL AGENT; ANTIINFECTIVE AGENT; ANTIPROTOZOAL AGENT; FLUCONAZOLE; METRONIDAZOLE; NITRIC OXIDE SYNTHASE; NITROFURANTOIN; THIOUREA DERIVATIVE; UNCLASSIFIED DRUG;

EID: 77954526783     PISSN: 02536269     EISSN: 19763786     Source Type: Journal    
DOI: 10.1007/s12272-010-0604-8     Document Type: Article
Times cited : (22)

References (41)
  • 1
    • 0032133353 scopus 로고    scopus 로고
    • Design of isoform-selective inhibitors of nitric oxide synthase
    • 10.1016/S1367-5931(98)80125-7 1:CAS:528:DyaK1cXmtFWnsr0%3D 9736922
    • B. R. Babu O. W. Griffith 1998 Design of isoform-selective inhibitors of nitric oxide synthase Curr. Opin. Chem. Biol. 2 491 500 10.1016/S1367-5931(98) 80125-7 1:CAS:528:DyaK1cXmtFWnsr0%3D 9736922
    • (1998) Curr. Opin. Chem. Biol. , vol.2 , pp. 491-500
    • Babu, B.R.1    Griffith, O.W.2
  • 2
    • 33645976903 scopus 로고    scopus 로고
    • The selective inhibition of inducible nitric oxide synthase prevents instestinal ischemia-reperfusion injury in mice
    • 10.1016/j.niox.2005.11.006 1:CAS:528:DC%2BD28XksVWmsrw%3D 16504557
    • E. Barocelli V. Ballabeni P. Ghizzardi F. Cattanuzza S. Bertoni C. A. M. Lagrasta M. Impiccatore 2006 The selective inhibition of inducible nitric oxide synthase prevents instestinal ischemia-reperfusion injury in mice Nitric Oxide 14 212 218 10.1016/j.niox.2005.11.006 1:CAS:528:DC%2BD28XksVWmsrw%3D 16504557
    • (2006) Nitric Oxide , vol.14 , pp. 212-218
    • Barocelli, E.1    Ballabeni, V.2    Ghizzardi, P.3    Cattanuzza, F.4    Bertoni, S.5    Lagrasta, C.A.M.6    Impiccatore, M.7
  • 4
    • 44449138081 scopus 로고    scopus 로고
    • Design, synthesis, and evaluation of potential inhibitors of nitric oxide synthase
    • DOI 10.1016/j.bmc.2008.04.036, PII S0968089608003647
    • T. Castano A. Encinas C. Perez A. Castro N. E. Campilo C. Gil 2008 Design, synthesis, and evaluation of potential inhibitors of nitric oxide synthase Bioorg. Med. Chem. 16 6193 6206 10.1016/j.bmc.2008.04.036 1:CAS:528:DC%2BD1cXmvFegtbg%3D 18477512 (Pubitemid 351758824)
    • (2008) Bioorganic and Medicinal Chemistry , vol.16 , Issue.11 , pp. 6193-6206
    • Castano, T.1    Encinas, A.2    Perez, C.3    Castro, A.4    Campillo, N.E.5    Gil, C.6
  • 5
    • 0026726032 scopus 로고
    • In vitro susceptibility of Giardia lamblia to albendazole, mebendazole and other chemotherapeutic agents
    • 10.1099/00222615-37-3-221 1:CAS:528:DyaK3sXlsF2mtg%3D%3D 1518040
    • R. Cedillo-Rivera O. Munoz 1992 In vitro susceptibility of Giardia lamblia to albendazole, mebendazole and other chemotherapeutic agents J. Med. Microbiol. 37 221 224 10.1099/00222615-37-3-221 1:CAS:528:DyaK3sXlsF2mtg%3D%3D 1518040
    • (1992) J. Med. Microbiol. , vol.37 , pp. 221-224
    • Cedillo-Rivera, R.1    Munoz, O.2
  • 6
    • 0031034723 scopus 로고    scopus 로고
    • In vitro susceptibility of Entamoeba histolytica to fluoroquinolones, nitrofurans and other antiamebic agents
    • 1:CAS:528:DyaK2sXhsVals7Y%3D 9033107
    • R. Cedillo-Rivera A. Tapia-Contreras J. Torres O. Munoz 1997 In vitro susceptibility of Entamoeba histolytica to fluoroquinolones, nitrofurans and other antiamebic agents Arch. Med. Res. 28 295 297 1:CAS:528:DyaK2sXhsVals7Y%3D 9033107
    • (1997) Arch. Med. Res. , vol.28 , pp. 295-297
    • Cedillo-Rivera, R.1    Tapia-Contreras, A.2    Torres, J.3    Munoz, O.4
  • 7
    • 33846702145 scopus 로고    scopus 로고
    • ClinicalLaboratory Standards Institute, Performance standards for antimicrobial disk susceptibility tests. CLSI document M2-A9 Wayne, PA, USA
    • Clinical and Laboratory Standards Institute, Performance standards for antimicrobial disk susceptibility tests. Approved standard - ninth edition. CLSI document M2-A9, Wayne, PA, USA (2006a).
    • (2006) Approved Standard - Ninth Edition
  • 8
    • 33846702145 scopus 로고    scopus 로고
    • ClinicalLaboratory Standards Institute, Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically. CLSI document M7-A7 Wayne, PA, USA
    • Clinical and Laboratory Standards Institute, Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically. Approved standard - seventh edition. CLSI document M7-A7, Wayne, PA, USA (2006b).
    • (2006) Approved Standard - Seventh Edition
  • 9
    • 3242679781 scopus 로고    scopus 로고
    • N-benzoyl-N′-alkylthioureas and their complexes with Ni(II), Co(III) and Pt(II) - Crystal structure of 3-benzoyl-1-butyl-1-methyl-thiourea: Activity against fungi and yeast
    • DOI 10.1016/j.jinorgbio.2004.03.019, PII S0162013404001102
    • R. del Campo J. J. Criado R. Gheorghe F. J. Gonzalez M. R. Hermosa F. Sanz J. L. Mazano E. Monte E. Rodriguez-Fernandez 2004 N-benzoyl-N′- alkylthioureas and their complexes with Ni(II), Co(III) and Pt(II) - crystal structure of 3-benzoyl-1-butyl-1-methyl-thiourea: activity against fungi and yeast J. Inorg. Biochem. 98 1307 1314 10.1016/j.jinorgbio.2004.03.019 15271506 (Pubitemid 38951051)
    • (2004) Journal of Inorganic Biochemistry , vol.98 , Issue.8 , pp. 1307-1314
    • Campo, R.D.1    Criado, J.J.2    Gheorghe, R.3    Gonzalez, F.J.4    Hermosa, M.R.5    Sanz, F.6    Manzano, J.L.7    Monte, E.8    Rodriguez-Fernandez, E.9
  • 10
    • 16644394243 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of novel tetrahydrobenzothienopyrimidines
    • 10.1007/BF02975838 1:CAS:528:DC%2BD2cXptFajtLo%3D 15473655
    • A. A. Eissa A. A. Moneer 2004 Synthesis and antimicrobial activity of novel tetrahydrobenzothienopyrimidines Arch. Pharm. Res. 27 885 892 10.1007/BF02975838 1:CAS:528:DC%2BD2cXptFajtLo%3D 15473655
    • (2004) Arch. Pharm. Res. , vol.27 , pp. 885-892
    • Eissa, A.A.1    Moneer, A.A.2
  • 11
    • 0028089793 scopus 로고
    • Potent and selective inhibition of human nitric oxide synthases. Inhibition by non-amino acid isothioureas
    • 1:CAS:528:DyaK2cXmt1Wjt7g%3D 7523409
    • E. P. Garvey J. A. Oplinger G. J. Tanoury P. A. Sherman M. Fowler S. Marshall M. F. Harmon J. E. Paith E. S. Furfine 1994 Potent and selective inhibition of human nitric oxide synthases. Inhibition by non-amino acid isothioureas J. Biol. Chem. 269 26669 26676 1:CAS:528:DyaK2cXmt1Wjt7g%3D 7523409
    • (1994) J. Biol. Chem. , vol.269 , pp. 26669-26676
    • Garvey, E.P.1    Oplinger, J.A.2    Tanoury, G.J.3    Sherman, P.A.4    Fowler, M.5    Marshall, S.6    Harmon, M.F.7    Paith, J.E.8    Furfine, E.S.9
  • 12
    • 0030272322 scopus 로고    scopus 로고
    • Inhibition of nitric oxide synthase by isothioureas: Cardiovascular and antinociceptive effects
    • DOI 10.1016/S0091-3057(96)00051-2, PII S0091305796000512
    • R. L. Handy P. Wallace P. K. Moore 1996 Inhibition of nitric oxide synthase by isothioureas: cardiovascular and antinociceptive effects Pharmacol. Biochem. Behav. 55 179 184 10.1016/S0091-3057(96)00051-2 1:CAS:528: DyaK28XntlClsbs%3D 8951952 (Pubitemid 26414098)
    • (1996) Pharmacology Biochemistry and Behavior , vol.55 , Issue.2 , pp. 179-184
    • Handy, R.L.C.1    Wallace, P.2    Moore, P.K.3
  • 13
    • 19544379712 scopus 로고    scopus 로고
    • Evaluation of 3-substituted arginine analogs as selective inhibitors of human nitric oxide synthase isozymes
    • DOI 10.1016/j.bmcl.2005.03.078, PII S0960894X05004014
    • R. Ijuin N. Umezawa S. Nagai T. Higuchi 2005 Evaluation of 3-substituted arginine analogs as selective inhibitors of human nitric oxide synthase isozymes Bioorg. Med. Chem. Lett. 15 2881 2885 10.1016/j.bmcl.2005.03.078 1:CAS:528:DC%2BD2MXks1WisLY%3D 15911272 (Pubitemid 40732239)
    • (2005) Bioorganic and Medicinal Chemistry Letters , vol.15 , Issue.11 , pp. 2881-2885
    • Ijuin, R.1    Umezawa, N.2    Nagai, S.-I.3    Higuchi, T.4
  • 14
    • 11144332075 scopus 로고    scopus 로고
    • Structure-activity relationship of S-benzylisothiourea derivatives to induce spherical cells in Escherichia coli
    • DOI 10.1271/bbb.68.2265
    • N. Iwai T. Ebata H. Nagura T. Kitazume K. Nagai M. Wachi 2004 Structure-activity relationship of S-benzylisothiourea derivatives to induce spherical cells in Escherichia coli. Biosci. Biotechnol. Biochem. 68 2265 2269 10.1271/bbb.68.2265 1:CAS:528:DC%2BD2cXhtVKlsbbF 15564663 (Pubitemid 40033499)
    • (2004) Bioscience, Biotechnology and Biochemistry , vol.68 , Issue.11 , pp. 2265-2269
    • Iwai, N.1    Ebata, T.2    Nagura, H.3    Kitazume, T.4    Nagai, K.5    Wachi, M.6
  • 15
    • 0041701451 scopus 로고    scopus 로고
    • Novel S-benzylisothiourea compound that induces spherical cells in Escherichia coli probably by acting on a rod-shape-determining protein(s) other than penicillin-binding protein 2
    • 10.1271/bbb.66.2658 1:CAS:528:DC%2BD3sXht1KjsQ%3D%3D 12596863
    • N. Iwai K. Nagai M. Wachi 2002 Novel S-benzylisothiourea compound that induces spherical cells in Escherichia coli probably by acting on a rod-shape-determining protein(s) other than penicillin-binding protein 2 Biosci. Biotechnol. Biochem. 66 2658 2662 10.1271/bbb.66.2658 1:CAS:528: DC%2BD3sXht1KjsQ%3D%3D 12596863
    • (2002) Biosci. Biotechnol. Biochem. , vol.66 , pp. 2658-2662
    • Iwai, N.1    Nagai, K.2    Wachi, M.3
  • 16
    • 0037333017 scopus 로고    scopus 로고
    • Activation of constitutive nitric oxide synthase(s) and absence of inducible isoform in aged rat brain
    • DOI 10.1016/S0197-0186(02)00098-0, PII S0197018602000980
    • H. A. Jesko M. Chalimoniuk J. B. Strosznajder 2003 Activation of constitutive nitric oxide synthase(s) and absence of inducible isoform in aged rat brain Neurochem. Int. 42 315 322 10.1016/S0197-0186(02)00098-0 1:CAS:528:DC%2BD38XptFGrs7w%3D 12470705 (Pubitemid 35447669)
    • (2003) Neurochemistry International , vol.42 , Issue.4 , pp. 315-322
    • Jesko, H.1    Chalimoniuk, M.2    Strosznajder, J.B.3
  • 17
    • 65149085044 scopus 로고    scopus 로고
    • Synthesis of phenylisothiourea derivatives as inhibitors of NO production in LPS activated macrophages
    • 10.1016/j.bmcl.2009.04.001 1:CAS:528:DC%2BD1MXmtVersL4%3D 19394216
    • G. H. Jin D. Y. Lee Y. J. Cheon H. J. Gim D. H. Kim H. D. Kim J. H. Ryu R. Jeon 2009 Synthesis of phenylisothiourea derivatives as inhibitors of NO production in LPS activated macrophages Bioorg. Med. Chem. Lett. 19 3088 3092 10.1016/j.bmcl.2009.04.001 1:CAS:528:DC%2BD1MXmtVersL4%3D 19394216
    • (2009) Bioorg. Med. Chem. Lett. , vol.19 , pp. 3088-3092
    • Jin, G.H.1    Lee, D.Y.2    Cheon, Y.J.3    Gim, H.J.4    Kim, D.H.5    Kim, H.D.6    Ryu, J.H.7    Jeon, R.8
  • 18
    • 0019238532 scopus 로고
    • Bacillus subtilis recassay test
    • F. E. de Sevres A. Hollaender (eds). Plenum Press New York
    • Kada, T., Hirano, K., and Shirasu, Y., Bacillus subtilis recassay test. In de Sevres, F. E. and Hollaender, A. (Eds.). Chemical Mutagens, vol. 6, Plenum Press, New York, pp. 149, (1980).
    • (1980) Chemical Mutagens , vol.6 , pp. 149
    • Kada, T.1    Hirano, K.2    Shirasu, Y.3
  • 19
    • 70449585521 scopus 로고    scopus 로고
    • Efficacy and mechanism of anti-tumor action of new potential CK2 inhibitors toward glioblastoma cells
    • 10.3892/ijo-00000424 1:CAS:528:DC%2BD1MXhtlCgurzM 19787263
    • B. Kaminska A. Ellert-Miklaszewska A. Oberbek P. Wisniewski B. Kaza M. Makowska M. Bretner Z. Kazimierczuk 2009 Efficacy and mechanism of anti-tumor action of new potential CK2 inhibitors toward glioblastoma cells Int. J. Oncol. 35 1091 1100 10.3892/ijo-00000424 1:CAS:528:DC%2BD1MXhtlCgurzM 19787263
    • (2009) Int. J. Oncol. , vol.35 , pp. 1091-1100
    • Kaminska, B.1    Ellert-Miklaszewska, A.2    Oberbek, A.3    Wisniewski, P.4    Kaza, B.5    Makowska, M.6    Bretner, M.7    Kazimierczuk, Z.8
  • 20
    • 62149108591 scopus 로고    scopus 로고
    • Design, synthesis, and anti-HCV activity of thiourea compounds
    • 10.1016/j.bmcl.2009.02.048 1:CAS:528:DC%2BD1MXjt1arsrc%3D 19251415
    • I. J. Kang L. W. Wang C. C. Lee Y. C. Lee Y. S. Chao T. A. Hsu J. H. Chern 2009 Design, synthesis, and anti-HCV activity of thiourea compounds Bioorg. Med. Chem. Lett. 19 1950 1955 10.1016/j.bmcl.2009.02.048 1:CAS:528:DC%2BD1MXjt1arsrc%3D 19251415
    • (2009) Bioorg. Med. Chem. Lett. , vol.19 , pp. 1950-1955
    • Kang, I.J.1    Wang, L.W.2    Lee, C.C.3    Lee, Y.C.4    Chao, Y.S.5    Hsu, T.A.6    Chern, J.H.7
  • 21
    • 53149151458 scopus 로고    scopus 로고
    • Synthesis, characterization and in vitro antibacterial activity of thiourea and urea derivatives of steroids
    • 10.1016/j.ejmech.2007.12.012 1:CAS:528:DC%2BD1cXht1CqsLfN 18294737
    • S. A. Khan N. Singh K. Saleem 2008 Synthesis, characterization and in vitro antibacterial activity of thiourea and urea derivatives of steroids Eur. J. Med. Chem. 43 2272 2277 10.1016/j.ejmech.2007.12.012 1:CAS:528: DC%2BD1cXht1CqsLfN 18294737
    • (2008) Eur. J. Med. Chem. , vol.43 , pp. 2272-2277
    • Khan, S.A.1    Singh, N.2    Saleem, K.3
  • 22
    • 67649774465 scopus 로고    scopus 로고
    • Urea derivatives as anticancer agents
    • 1:CAS:528:DC%2BD1MXlslOlsrc%3D 19442045
    • H. Q. Li P. C. Lv T. Yan H. L. Zhu 2009 Urea derivatives as anticancer agents Anticancer Agents Med. Chem. 9 471 480 1:CAS:528:DC%2BD1MXlslOlsrc%3D 19442045
    • (2009) Anticancer Agents Med. Chem. , vol.9 , pp. 471-480
    • Li, H.Q.1    Lv, P.C.2    Yan, T.3    Zhu, H.L.4
  • 23
    • 64049088223 scopus 로고    scopus 로고
    • Discovery of dual inhibitors targeting both HIV-1 capsid and human cyclophilin A to inhibit the assembly and uncoating of the viral capsid
    • 10.1016/j.bmc.2009.02.051 1:CAS:528:DC%2BD1MXksVWktrs%3D 19328002
    • J. Li Z. Tan S. Tang I. Hewlett R. Pang M. He S. He B. Tian K. Chen M. Yang 2009 Discovery of dual inhibitors targeting both HIV-1 capsid and human cyclophilin A to inhibit the assembly and uncoating of the viral capsid Bioorg. Med. Chem. 17 3177 3188 10.1016/j.bmc.2009.02.051 1:CAS:528:DC%2BD1MXksVWktrs%3D 19328002
    • (2009) Bioorg. Med. Chem. , vol.17 , pp. 3177-3188
    • Li, J.1    Tan, Z.2    Tang, S.3    Hewlett, I.4    Pang, R.5    He, M.6    He, S.7    Tian, B.8    Chen, K.9    Yang, M.10
  • 24
    • 77954489924 scopus 로고    scopus 로고
    • Antimicrobial activity of novel S-(benzyl) isothiourea derivatives against multiply resistant Pseudomonas aeruginosa and Burkholderia cepacia complex from patients with cystic fibrosis undergoing lung transplant assessment
    • 10.1016/j.healun.2008.11.276
    • A. Nicholson J. D. Perry A. L. James S. P. Stanforth A. De Soyza K. Gould 2009 Antimicrobial activity of novel S-(benzyl) isothiourea derivatives against multiply resistant Pseudomonas aeruginosa and Burkholderia cepacia complex from patients with cystic fibrosis undergoing lung transplant assessment J. Heart Lung Transplant. 28 S160 10.1016/j.healun.2008.11.276
    • (2009) J. Heart Lung Transplant. , vol.28 , pp. 160
    • Nicholson, A.1    Perry, J.D.2    James, A.L.3    Stanforth, S.P.4    De Soyza, A.5    Gould, K.6
  • 25
    • 12444284865 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 3-benzyl-1-methyl- and 1-methyl-3-phenyl-isothioureas as potential inhibitors of iNOS
    • 10.1016/j.bmcl.2004.11.047 1:CAS:528:DC%2BD2MXnsVKmtw%3D%3D 15664809
    • N. Paesano S. Marzocco C. Vicidomini C. Saturnino G. Autore G. De Martino G. Sbardella 2005 Synthesis and biological evaluation of 3-benzyl-1-methyl- and 1-methyl-3-phenyl-isothioureas as potential inhibitors of iNOS Bioorg. Med. Chem. Lett. 15 539 543 10.1016/j.bmcl.2004.11.047 1:CAS:528: DC%2BD2MXnsVKmtw%3D%3D 15664809
    • (2005) Bioorg. Med. Chem. Lett. , vol.15 , pp. 539-543
    • Paesano, N.1    Marzocco, S.2    Vicidomini, C.3    Saturnino, C.4    Autore, G.5    De Martino, G.6    Sbardella, G.7
  • 27
    • 64549110888 scopus 로고    scopus 로고
    • Novel isothiourea derivatives as potent neuroprotectors and cognition enhancers: Synthesis, biological and physicochemical properties
    • 10.1021/jm8012882 1:CAS:528:DC%2BD1MXjtFKhtrg%3D 19338354
    • G. L. Perlovich A. N. Proshin T. V. Volkova S. V. Kurkov V. V. Grigoriev L. N. Petrova S. O. Bachurin 2009 Novel isothiourea derivatives as potent neuroprotectors and cognition enhancers: synthesis, biological and physicochemical properties J. Med. Chem. 52 1845 1852 10.1021/jm8012882 1:CAS:528:DC%2BD1MXjtFKhtrg%3D 19338354
    • (2009) J. Med. Chem. , vol.52 , pp. 1845-1852
    • Perlovich, G.L.1    Proshin, A.N.2    Volkova, T.V.3    Kurkov, S.V.4    Grigoriev, V.V.5    Petrova, L.N.6    Bachurin, S.O.7
  • 28
    • 22844446396 scopus 로고    scopus 로고
    • Thiourea, triazole and thiadiazine compounds and their metal complexes as antifungal agents
    • DOI 10.1016/j.jinorgbio.2005.05.004, PII S0162013405001340
    • E. Rodriguez-Fernandez J. L. Mazano J. J. Benito M. R. Hermosa E. Monte J. J. Criado 2005 Thiourea, triazole and thiadiazine compounds and their metal complexes as antifungal agents J. Inorg. Biochem. 99 1558 1572 10.1016/j.jinorgbio.2005.05.004 1:CAS:528:DC%2BD2MXmvVCqtbg%3D 16005979 (Pubitemid 41039915)
    • (2005) Journal of Inorganic Biochemistry , vol.99 , Issue.8 , pp. 1558-1572
    • Rodriguez-Fernandez, E.1    Manzano, J.L.2    Benito, J.J.3    Hermosa, R.4    Monte, E.5    Criado, J.J.6
  • 29
    • 0017275314 scopus 로고
    • Recombination-deficient mutants of Bacillus subtilis
    • 1:STN:280:DyaE28%2FpsV2huw%3D%3D 812867
    • Y. Sadaie T. Kada 1976 Recombination-deficient mutants of Bacillus subtilis J. Bacteriol. 125 489 500 1:STN:280:DyaE28%2FpsV2huw%3D%3D 812867
    • (1976) J. Bacteriol. , vol.125 , pp. 489-500
    • Sadaie, Y.1    Kada, T.2
  • 30
    • 0036242431 scopus 로고    scopus 로고
    • Progress in the development of selective nitric oxide synthase (NOS) inhibitors
    • DOI 10.2174/1381612023396375
    • L. Salerno V. Sorrenti C. Di Giacomo G. Romeo M. A. Siracusa 2002 Progress in the development of selective nitric oxide synthase (NOS) inhibitors Curr. Pharm. Des. 8 177 200 10.2174/1381612023396375 1:CAS:528: DC%2BD38XhvFKmurg%3D 11812267 (Pubitemid 34449889)
    • (2002) Current Pharmaceutical Design , vol.8 , Issue.3 , pp. 177-200
    • Salerno, L.1    Sorrenti, V.2    Di Giacomo, C.3    Romeo, G.4    Siracusa, M.A.5
  • 31
    • 0030979486 scopus 로고    scopus 로고
    • Substituted N-phenylisothioureas: Potent inhibitors of human nitric oxide synthase with neuronal isoform selectivity
    • DOI 10.1021/jm960785c
    • B. G. Shearer S. Lee J. A. Oplinger L. W. Frick E. P. Garvey E. S. Furfine 1997 Substituted N-phenylisothioureas: potent inhibitors of human nitric oxide synthase with neuronal isoform selectivity J. Med. Chem. 40 1901 1905 10.1021/jm960785c 1:CAS:528:DyaK2sXjt1Sqs7c%3D 9191968 (Pubitemid 27251281)
    • (1997) Journal of Medicinal Chemistry , vol.40 , Issue.12 , pp. 1901-1905
    • Shearer, B.G.1    Lee, S.2    Oplinger, J.A.3    Frick, L.W.4    Garvey, E.P.5    Furfine, E.S.6
  • 32
    • 0030951938 scopus 로고    scopus 로고
    • Novel prodrugs of cyanamide that inhibit aldehyde dehydrogenase in vivo
    • DOI 10.1021/jm9606296
    • F. N. Shirota J. M. Stevens-Johnk E. G. DeMaster H. T. Nagasawa 1997 Novel prodrugs of cyanamide that inhibit aldehyde dehydrogenase in vivo J. Med. Chem. 40 1870 1875 10.1021/jm9606296 1:CAS:528:DyaK2sXjt1Sqs7g%3D 9191964 (Pubitemid 27251277)
    • (1997) Journal of Medicinal Chemistry , vol.40 , Issue.12 , pp. 1870-1875
    • Shirota, F.N.1    Stevens-Johnk, J.M.2    DeMaster, E.G.3    Nagasawa, H.T.4
  • 33
    • 0028848015 scopus 로고
    • Isothioureas: Potent inhibitors of nitric oxide synthases with variable isoform selectivity
    • 1:CAS:528:DyaK2MXjt12ltLc%3D 7533622
    • G. J. Southan C. Szabo C. Thiemermann 1995 Isothioureas: potent inhibitors of nitric oxide synthases with variable isoform selectivity Br. J. Pharmacol. 114 510 516 1:CAS:528:DyaK2MXjt12ltLc%3D 7533622
    • (1995) Br. J. Pharmacol. , vol.114 , pp. 510-516
    • Southan, G.J.1    Szabo, C.2    Thiemermann, C.3
  • 34
    • 0028577721 scopus 로고
    • Beneficial effects and improved survival in rodent models of septic shock with S-methylisothiourea sulfate, a potent and selective inhibitor of inducible nitric oxide synthase
    • 10.1073/pnas.91.26.12472 1:STN:280:DyaK2M7gsl2kuw%3D%3D 7528923
    • C. Szabo G. J. Southan C. Thiemermann 1994 Beneficial effects and improved survival in rodent models of septic shock with S-methylisothiourea sulfate, a potent and selective inhibitor of inducible nitric oxide synthase Proc. Natl. Acad. Sci. U.S.A. 91 12472 12476 10.1073/pnas.91.26.12472 1:STN:280:DyaK2M7gsl2kuw%3D%3D 7528923
    • (1994) Proc. Natl. Acad. Sci. U.S.A. , vol.91 , pp. 12472-12476
    • Szabo, C.1    Southan, G.J.2    Thiemermann, C.3
  • 35
    • 0025050899 scopus 로고
    • Carbamimidothioic acid phenylmethyl ester salts and their N, N′-tetramethyl derivatives as possible antimicrobial agents
    • 1:CAS:528:DyaK3MXpvVSitA%3D%3D 2148672
    • A. Tait M. Di Bella M. Bondi G. Quaglio U. Fabio 1990 Carbamimidothioic acid phenylmethyl ester salts and their N, N′-tetramethyl derivatives as possible antimicrobial agents Farmaco 45 617 630 1:CAS:528:DyaK3MXpvVSitA%3D%3D 2148672
    • (1990) Farmaco , vol.45 , pp. 617-630
    • Tait, A.1    Di Bella, M.2    Bondi, M.3    Quaglio, G.4    Fabio, U.5
  • 36
    • 0024912631 scopus 로고
    • S-Aryl(tetramethyl)isothiouronium salts as possible antimicrobial agents, IV
    • 1:CAS:528:DyaK3cXktVSiurY%3D 2517471
    • A. Tait M. G. Giovannini M. Di Bella M. Bondi G.P. Quaglio 1989 S-Aryl(tetramethyl)isothiouronium salts as possible antimicrobial agents, IV Farmaco 44 1129 1140 1:CAS:528:DyaK3cXktVSiurY%3D 2517471
    • (1989) Farmaco , vol.44 , pp. 1129-1140
    • Tait, A.1    Giovannini, M.G.2    Di Bella, M.3    Bondi, M.4    Quaglio, G.P.5
  • 37
    • 58149089159 scopus 로고    scopus 로고
    • Orally bioavailable isothioureas block function of the chemokine receptor CXCR4 in vitro and in vivo
    • 10.1021/jm801065q 1:CAS:528:DC%2BD1cXhsVWksrvF 19053768
    • G. Thoma M. B. Streiff J. Kovarik F. Glickman T. Wagner C. Beerli H. G. Zerwes 2008 Orally bioavailable isothioureas block function of the chemokine receptor CXCR4 in vitro and in vivo J. Med. Chem. 51 7915 7920 10.1021/jm801065q 1:CAS:528:DC%2BD1cXhsVWksrvF 19053768
    • (2008) J. Med. Chem. , vol.51 , pp. 7915-7920
    • Thoma, G.1    Streiff, M.B.2    Kovarik, J.3    Glickman, F.4    Wagner, T.5    Beerli, C.6    Zerwes, H.G.7
  • 38
    • 0032112928 scopus 로고    scopus 로고
    • Differential effect of 2-aminoethyl-isothiourea, an inhibitor of the inducible nitric oxide synthase, on microvascular blood flow and organ injury in models of hepatic ischemia-reperfusion and endotoxemia
    • 10.1097/00024382-199807000-00004 1:STN:280:DyaK1czltFeksA%3D%3D 9688086
    • Y. Wang J. A. Lawson H. Jaeschke 1998 Differential effect of 2-aminoethyl-isothiourea, an inhibitor of the inducible nitric oxide synthase, on microvascular blood flow and organ injury in models of hepatic ischemia-reperfusion and endotoxemia Shock 10 20 25 10.1097/00024382-199807000- 00004 1:STN:280:DyaK1czltFeksA%3D%3D 9688086
    • (1998) Shock , vol.10 , pp. 20-25
    • Wang, Y.1    Lawson, J.A.2    Jaeschke, H.3
  • 39
    • 2442568008 scopus 로고    scopus 로고
    • Synthesis and nNOS inhibitory activity of benzenealkyl isothiourea compounds
    • 1:CAS:528:DC%2BD2cXltVehsLg%3D 14628448
    • Y. G. Xu J. X. Zhang W. Y. Hua D. Y. Zhu 2003 Synthesis and nNOS inhibitory activity of benzenealkyl isothiourea compounds Yao Xue Xue Bao 38 586 591 1:CAS:528:DC%2BD2cXltVehsLg%3D 14628448
    • (2003) Yao Xue Xue Bao , vol.38 , pp. 586-591
    • Xu, Y.G.1    Zhang, J.X.2    Hua, W.Y.3    Zhu, D.Y.4
  • 40
    • 61349174765 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of sulfonylurea and thiourea derivatives substituted with benzenesulfonamide groups as potential hypoglycemic agents
    • 10.1016/j.bmcl.2009.01.082 1:CAS:528:DC%2BD1MXjtVSltL4%3D 19216076
    • H. B. Zhang Y. A. Zhang G. Z. Wu J. P. Zhou W. L. Huang X. W. Hu 2009 Synthesis and biological evaluation of sulfonylurea and thiourea derivatives substituted with benzenesulfonamide groups as potential hypoglycemic agents Bioorg. Med. Chem. Lett. 19 1740 1744 10.1016/j.bmcl.2009.01.082 1:CAS:528:DC%2BD1MXjtVSltL4%3D 19216076
    • (2009) Bioorg. Med. Chem. Lett. , vol.19 , pp. 1740-1744
    • Zhang, H.B.1    Zhang, Y.A.2    Wu, G.Z.3    Zhou, J.P.4    Huang, W.L.5    Hu, X.W.6
  • 41
    • 38649109136 scopus 로고    scopus 로고
    • Synthesis of acyl thiourea derivatives of chitosan and their antimicrobial activities in vitro
    • 10.1016/j.carres.2007.11.024 1:CAS:528:DC%2BD1cXhsFWqur4%3D 18083151
    • Z. Zhong R. Xing S. Liu L. Wang S. Cai P. Li 2008 Synthesis of acyl thiourea derivatives of chitosan and their antimicrobial activities in vitro Carbohydr. Res. 343 566 570 10.1016/j.carres.2007.11.024 1:CAS:528: DC%2BD1cXhsFWqur4%3D 18083151
    • (2008) Carbohydr. Res. , vol.343 , pp. 566-570
    • Zhong, Z.1    Xing, R.2    Liu, S.3    Wang, L.4    Cai, S.5    Li, P.6


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