메뉴 건너뛰기




Volumn 67, Issue , 2013, Pages 1189-1203

Adenosine, its analogues and conjugates;Adenozyna, jej analogi i koniugaty

Author keywords

Adenosine; Adenosine analogues; Adenosine conjugates; Biological activity; Purine nucleosides

Indexed keywords

ADENOSINE; ANTIARRHYTHMIC AGENT; DRUG DERIVATIVE;

EID: 84892607300     PISSN: 00325449     EISSN: 17322693     Source Type: Journal    
DOI: 10.5604/17322693.1078588     Document Type: Article
Times cited : (10)

References (55)
  • 1
    • 79959966626 scopus 로고    scopus 로고
    • Clofarabine 5'-di and-triphosphates inhibit human ribonucleotide reductase by altering the quaternary structure of its large subunit
    • Aye Y., Stubbe J.: Clofarabine 5'-di and -triphosphates inhibit human ribonucleotide reductase by altering the quaternary structure of its large subunit. Proc. Natl. Acad. Sci. USA, 2011;108:9815-9820
    • (2011) Proc. Natl. Acad. Sci. USA , vol.108 , pp. 9815-9820
    • Aye, Y.1    Stubbe, J.2
  • 2
    • 84867884697 scopus 로고    scopus 로고
    • Effect of adenosine modified with a boron cluster pharmacophore on reactive oxygen species production by human neutrophils
    • Bednarska K., Olejniczak A. B., Piskala A., Klink M., Sulowska Z., Lesnikowski Z. J.: Effect of adenosine modified with a boron cluster pharmacophore on reactive oxygen species production by human neutrophils. Bioorg. Med. Chem., 2012;20:6621-6629
    • (2012) Bioorg. Med. Chem. , vol.20 , pp. 6621-6629
    • Bednarska, K.1    Olejniczak, A.B.2    Piskala, A.3    Klink, M.4    Sulowska, Z.5    Lesnikowski, Z.J.6
  • 5
    • 38049083924 scopus 로고    scopus 로고
    • 5'-Carbamoyl derivatives of 2'-C-methyl-purine nucleosides as selective A (1) adenosine receptor agonists: Affinity, efficacy, and selectivity for A (1) receptor from different species
    • Cappellacci L., Franchetti P., Vita P., Petrelli R., Lavecchia A., Costa B., Spinetti F., Martini C., Klotz K. N., Grifantini M.: 5'-Carbamoyl derivatives of 2'-C-methyl-purine nucleosides as selective A (1) adenosine receptor agonists: Affinity, efficacy, and selectivity for A (1) receptor from different species. Bioorg. Med. Chem., 2008;16:336-353
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 336-353
    • Cappellacci, L.1    Franchetti, P.2    Vita, P.3    Petrelli, R.4    Lavecchia, A.5    Costa, B.6    Spinetti, F.7    Martini, C.8    Klotz, K.N.9    Grifantini, M.10
  • 7
    • 79851507336 scopus 로고    scopus 로고
    • 2'-Deoxy-2'-α-C-(hydroxymethyl) adenosine as potential anti-HCV agent
    • Chavain N., Herdewijn P.: 2'-Deoxy-2'-α-C-(hydroxymethyl) adenosine as potential anti-HCV agent. Eur. J. Org. Chem., 2011;2011:1140-1147
    • (2011) Eur. J. Org. Chem. , vol.2011 , pp. 1140-1147
    • Chavain, N.1    Herdewijn, P.2
  • 8
    • 48449098290 scopus 로고    scopus 로고
    • Bis (sulfonamide) isosters of mycophenolic adenine dinucleotide analogues: Inhibition of inosine monophosphate dehydrogenase
    • Chen L., Petrelli R., Olesiak M., Wilson D. J., Labello N. P., Pankiewicz K. W.: Bis (sulfonamide) isosters of mycophenolic adenine dinucleotide analogues: inhibition of inosine monophosphate dehydrogenase. Bioorg. Med. Chem., 2008;16:7462-7469
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 7462-7469
    • Chen, L.1    Petrelli, R.2    Olesiak, M.3    Wilson, D.J.4    Labello, N.P.5    Pankiewicz, K.W.6
  • 9
    • 0028960866 scopus 로고
    • Detection of single-strand breaks and formamidopyrimidine-dna glycosylase-sensitive sites in dna of cultured human fibroblasts
    • Czene S, Harms-Ringdahl M.: Detection of single-strand breaks and formamidopyrimidine-dna glycosylase-sensitive sites in dna of cultured human fibroblasts. Mutat. Res., 1995;336:235-242
    • (1995) Mutat. Res. , vol.336 , pp. 235-242
    • Czene, S.1    Harms-Ringdahl, M.2
  • 11
    • 78650408267 scopus 로고    scopus 로고
    • Diadenosine 5', 5"-(boranated) polyphosphonate analogues as selective nucleotide pyrophosphatase/phosphodiesterase inhibitors
    • Eliahu S., Lecka J., Reiser G., Haas M., Bigonnesse F., Levesque S. A., Pelletier J., Sevigny J., Fischer B.: Diadenosine 5', 5"-(boranated) polyphosphonate analogues as selective nucleotide pyrophosphatase/ phosphodiesterase inhibitors. J. Med. Chem., 2010;53:8485-8497
    • (2010) J. Med. Chem. , vol.53 , pp. 8485-8497
    • Eliahu, S.1    Lecka, J.2    Reiser, G.3    Haas, M.4    Bigonnesse, F.5    Levesque, S.A.6    Pelletier, J.7    Sevigny, J.8    Fischer, B.9
  • 12
    • 79958760220 scopus 로고    scopus 로고
    • Synthesis and antiviral activity of cyclopropyl-spirocarbocyclic adenosine, (4R, 5S, 6R, 7R)-4-(6-amino-9H-purin-9-yl)-7-(hydroxymethyl) spiro [2. 4] heptane-5, 6-diol against hepatitis C virus
    • Gadthula S., Rawal R. K., Sharon A., Wu D., Korba B., Chu C. K.: Synthesis and antiviral activity of cyclopropyl-spirocarbocyclic adenosine, (4R, 5S, 6R, 7R)-4-(6-amino-9H-purin-9-yl)-7-(hydroxymethyl) spiro [2. 4] heptane-5, 6-diol against hepatitis C virus. Bioorg. Med. Chem. Lett., 2011;21:3982-3985
    • (2011) Bioorg. Med. Chem. Lett. , vol.21 , pp. 3982-3985
    • Gadthula, S.1    Rawal, R.K.2    Sharon, A.3    Wu, D.4    Korba, B.5    Chu, C.K.6
  • 13
  • 14
    • 0026456852 scopus 로고
    • The measurement of oxidative damage to DNA by HPLC and GC/MS techniques
    • Halliwell B., Dizdaroglu M.: The measurement of oxidative damage to DNA by HPLC and GC/MS techniques. Free Radic. Res. Commun., 1992;16:75-87
    • (1992) Free Radic. Res. Commun. , vol.16 , pp. 75-87
    • Halliwell, B.1    Dizdaroglu, M.2
  • 15
    • 84865640480 scopus 로고    scopus 로고
    • Adenosine A2A antagonists in Parkinson's disease: What's next?
    • Hickey P., Stacy M.: Adenosine A2A antagonists in Parkinson's disease: what's next? Curr. Neurol. Neurosci. Rep., 2012;12:376-385
    • (2012) Curr. Neurol. Neurosci. Rep. , vol.12 , pp. 376-385
    • Hickey, P.1    Stacy, M.2
  • 16
    • 79251469106 scopus 로고    scopus 로고
    • The role of adenosine receptor agonists in regulation of hematopoiesis
    • Hofer M., Pospisil M., Weiterowa L., Hoferova Z.: The role of adenosine receptor agonists in regulation of hematopoiesis. Molecules, 2011;16:675-685
    • (2011) Molecules , vol.16 , pp. 675-685
    • Hofer, M.1    Pospisil, M.2    Weiterowa, L.3    Hoferova, Z.4
  • 17
    • 80051826503 scopus 로고    scopus 로고
    • Mutagenicity of secondary oxidation products of 8-oxo-7, 8-dihydro-2'-deoxyguanosine 5'-triphosphate (8-hydroxy-2'-deoxyguanosine 5'-triphosphate)
    • Hori M., Suzuki T., Minakawa N., Matsuda A., Harashima H., Kamiya H.: Mutagenicity of secondary oxidation products of 8-oxo-7, 8-dihydro-2'- deoxyguanosine 5'-triphosphate (8-hydroxy-2'-deoxyguanosine 5'-triphosphate). Mutat. Res. - Fund. Mol. M, 2011;714:11-16
    • (2011) Mutat. Res. - Fund. Mol. M , vol.714 , pp. 11-16
    • Hori, M.1    Suzuki, T.2    Minakawa, N.3    Matsuda, A.4    Harashima, H.5    Kamiya, H.6
  • 18
    • 79953776648 scopus 로고    scopus 로고
    • Coumarin-purine ribofuranoside conjugates as new agents against hepatitis C virus
    • Hwu J. R., Lin S. Y., Tsay S. C., De Clercq E., Leyssen P., Neyts J.: Coumarin-purine ribofuranoside conjugates as new agents against hepatitis C virus. J. Med. Chem., 2011;54:2114-2126
    • (2011) J. Med. Chem. , vol.54 , pp. 2114-2126
    • Hwu, J.R.1    Lin, S.Y.2    Tsay, S.C.3    De Clercq, E.4    Leyssen, P.5    Neyts, J.6
  • 19
    • 0035038033 scopus 로고    scopus 로고
    • Sugar-modified nucleosides in past 10 years, a review
    • Ichikawa E., Kato K.: Sugar-modified nucleosides in past 10 years, a review. Curr. Med. Chem., 2001;8:385-423
    • (2001) Curr. Med. Chem. , vol.8 , pp. 385-423
    • Ichikawa, E.1    Kato, K.2
  • 20
    • 33644770260 scopus 로고    scopus 로고
    • Adenosine receptors as therapeutic targets
    • Jacobson K., Gao Z. G.: Adenosine receptors as therapeutic targets. Nat. Rev. Drug Discov, 2006;5:247-264
    • (2006) Nat. Rev. Drug Discov , vol.5 , pp. 247-264
    • Jacobson, K.1    Gao, Z.G.2
  • 22
    • 0034730498 scopus 로고    scopus 로고
    • A novel pharmacological approach to treating cardiac ischemia. Binary conjugates of A1 and A3 adenosine receptor agonists
    • Jacobson K. A., Xie R. Y., Young L., Chang L., Liang B. T.: A novel pharmacological approach to treating cardiac ischemia. Binary conjugates of A1 and A3 adenosine receptor agonists. J. Biol. Chem., 2000;275:30272-30279
    • (2000) J. Biol. Chem. , vol.275 , pp. 30272-30279
    • Jacobson, K.A.1    Xie, R.Y.2    Young, L.3    Chang, L.4    Liang, B.T.5
  • 23
    • 79957465550 scopus 로고    scopus 로고
    • Mechanism of action of pentostatin and cladribine in hairy cell leukemia
    • Johnston J. B.: Mechanism of action of pentostatin and cladribine in hairy cell leukemia. Leuk. Lymphoma, 2011;52, Suppl. 2:43-45
    • (2011) Leuk. Lymphoma , vol.52 , Issue.SUPPL. 2 , pp. 43-45
    • Johnston, J.B.1
  • 24
    • 84861017463 scopus 로고    scopus 로고
    • Rapid measurement of 8-oxo-7, 8-dihydro-2 '-deoxyguanosine in human biological matrices using ultra-high-performance liquid chromatography-tandem mass spectrometry
    • Lam P. M., Mistry V., Marczylo T. H., Konje J. C., Evans M. D., Cooke M. S.: Rapid measurement of 8-oxo-7, 8-dihydro-2 '-deoxyguanosine in human biological matrices using ultra-high-performance liquid chromatography-tandem mass spectrometry. Free Radic. Biol. Med., 2012;52:2057-2063
    • (2012) Free Radic. Biol. Med. , vol.52 , pp. 2057-2063
    • Lam, P.M.1    Mistry, V.2    Marczylo, T.H.3    Konje, J.C.4    Evans, M.D.5    Cooke, M.S.6
  • 25
    • 33646550489 scopus 로고    scopus 로고
    • Pharmacological and clinical studies on purine nucleoside analogs - New anticancer agents
    • Lech-Maranda E., Korycka A., Robak T.: Pharmacological and clinical studies on purine nucleoside analogs - new anticancer agents. Mini Rev. Med. Chem., 2006;6:575-581
    • (2006) Mini Rev. Med. Chem. , vol.6 , pp. 575-581
    • Lech-Maranda, E.1    Korycka, A.2    Robak, T.3
  • 26
    • 79957519264 scopus 로고    scopus 로고
    • Synthesis and binding affinity of homologated adenosine analogues as A3 adenosine receptor ligands
    • Lee W. H., Choi W. J. Jacobson K. A., Jeong L. S.: Synthesis and binding affinity of homologated adenosine analogues as A3 adenosine receptor ligands. Bull. Korean Chem. Soc, 2011;32:1620-1624
    • (2011) Bull. Korean Chem. Soc , vol.32 , pp. 1620-1624
    • Lee, W.H.1    Choi, W.J.2    Jacobson, K.A.3    Jeong, L.S.4
  • 27
    • 79959228146 scopus 로고    scopus 로고
    • Design, synthesis, and evaluation of 2-diethanolamino-4, 8-diheptamethyleneimino-2-(N-aminoethyl-N-ethanol amino)-6-(N, N-diethanolamino) pyrimido [5, 4-d]pyrimidine-fluorescein (8MDP-fluor), as a novel equilibrative nucleoside transporter probe
    • Lin W., Buolamwini K.: Design, synthesis, and evaluation of 2-diethanolamino-4, 8-diheptamethyleneimino-2-(N-aminoethyl-N-ethanol amino)-6-(N, N-diethanolamino) pyrimido [5, 4-d]pyrimidine-fluorescein (8MDP-fluor), as a novel equilibrative nucleoside transporter probe. Bioconjug. Chem., 2011;22:1221-1227
    • (2011) Bioconjug. Chem. , vol.22 , pp. 1221-1227
    • Lin, W.1    Buolamwini, K.2
  • 28
    • 0038243600 scopus 로고    scopus 로고
    • Intravenous adenosine alleviates neuropathic pain: A double blind placebo controlled crossover trial using an enriched enrolment design
    • Lynch M. E., Clark A. J., Sawynok J.: Intravenous adenosine alleviates neuropathic pain: a double blind placebo controlled crossover trial using an enriched enrolment design. Pain, 2003;103:111-117
    • (2003) Pain , vol.103 , pp. 111-117
    • Lynch, M.E.1    Clark, A.J.2    Sawynok, J.3
  • 30
    • 78650151809 scopus 로고    scopus 로고
    • Synthesis of cyclic adenosine 5'-diphosphate ribose analogues: A C2' endo/syn "southern" ribose confirmation underlies activity at the sea urchin cADPR receptor
    • Moreau C, Ashamu G. A., Bailey V. C., Galione A., Guse A. H., Potter B. V.: Synthesis of cyclic adenosine 5'-diphosphate ribose analogues: a C2' endo/syn "southern" ribose confirmation underlies activity at the sea urchin cADPR receptor. Org. Biomol. Chem., 2011;9:278-290
    • (2011) Org. Biomol. Chem. , vol.9 , pp. 278-290
    • Moreau, C.1    Ashamu, G.A.2    Bailey, V.C.3    Galione, A.4    Guse, A.H.5    Potter, B.V.6
  • 31
    • 8144226085 scopus 로고    scopus 로고
    • Boranophosphate salts as an excellent mimic of phosphate salts: Preparation, characterization, and properties
    • Nahum V., Fischer B.: Boranophosphate salts as an excellent mimic of phosphate salts: preparation, characterization, and properties. Eur. J. Inorg. Chem., 2004;2004:4124-4131
    • (2004) Eur. J. Inorg. Chem. , vol.2004 , pp. 4124-4131
    • Nahum, V.1    Fischer, B.2
  • 34
    • 49749093968 scopus 로고    scopus 로고
    • Synthesis of 3 '-C-hydroxymethyl-substituted pyrimidine and purine nucleosides as potential anti-hepatitis C virus (HCV) agents
    • Pei X., Choi W. J., Kim Y. M., Zhao L. X., Jeong L. S.: Synthesis of 3 '-C-hydroxymethyl-substituted pyrimidine and purine nucleosides as potential anti-hepatitis C virus (HCV) agents. Arch. Pharmacol. Res., 2008;31:843-849
    • (2008) Arch. Pharmacol. Res. , vol.31 , pp. 843-849
    • Pei, X.1    Choi, W.J.2    Kim, Y.M.3    Zhao, L.X.4    Jeong, L.S.5
  • 35
    • 31544467281 scopus 로고    scopus 로고
    • Recent advances in studies on biochemical and structural properties of equilibrative and concentrative nucleoside transporters
    • Podgórska M., Kocbuch K., Pawełczyk T.: Recent advances in studies on biochemical and structural properties of equilibrative and concentrative nucleoside transporters. Acta Biochim. Pol., 2005;52:749-758
    • (2005) Acta Biochim. Pol. , vol.52 , pp. 749-758
    • Podgórska, M.1    Kocbuch, K.2    Pawełczyk, T.3
  • 36
    • 84867575872 scopus 로고    scopus 로고
    • Synthesis and in vitro antitumour screening of 2-(β-d-xylofuranosyl) thiazole-4-carboxamide and two novel tiazofurin analogues with substituted tetrahydrofurodioxol moiety as a sugar mimic
    • Popsavin M., Spaić S., Svirčev M., Kojić V., Bogdanović G., Popsavin V.: Synthesis and in vitro antitumour screening of 2-(β-d-xylofuranosyl) thiazole-4-carboxamide and two novel tiazofurin analogues with substituted tetrahydrofurodioxol moiety as a sugar mimic. Bioorg. Med. Chem. Lett., 2012;22:6700-6704
    • (2012) Bioorg. Med. Chem. Lett. , vol.22 , pp. 6700-6704
    • Popsavin, M.1    Spaić, S.2    Svirčev, M.3    Kojić, V.4    Bogdanović, G.5    Popsavin, V.6
  • 37
    • 0031833150 scopus 로고    scopus 로고
    • Adenosine receptors: New opportunities for future drugs
    • Poulsen S. A., Quinn R. J.: Adenosine receptors: new opportunities for future drugs. Bioorg. Med. Chem., 1998;6:619-641
    • (1998) Bioorg. Med. Chem. , vol.6 , pp. 619-641
    • Poulsen, S.A.1    Quinn, R.J.2
  • 39
    • 50549090633 scopus 로고    scopus 로고
    • Adenosine-oligoarginine conjugate, a novel bisubstrate inhibitor, effectively dissociates the actin cytoskeleton
    • Raagel H., Lust M., Uri A., Pooga M.: Adenosine-oligoarginine conjugate, a novel bisubstrate inhibitor, effectively dissociates the actin cytoskeleton. FEBS Lett., 2008;275:3608-3624
    • (2008) FEBS Lett. , vol.275 , pp. 3608-3624
    • Raagel, H.1    Lust, M.2    Uri, A.3    Pooga, M.4
  • 40
    • 0028889564 scopus 로고
    • Determination of 8-oxoguanine in dna by gas-chromatography mass-spectrometry and hplc-electrochemical detection - Overestimation of the background level of the oxidized base by the gas-chromatography mass-spectrometry assay
    • Ravanat J. L., Turesky R. J., Gremaud E., Trudel L. J., Stadler R. H.: Determination of 8-oxoguanine in dna by gas-chromatography mass-spectrometry and hplc-electrochemical detection - overestimation of the background level of the oxidized base by the gas-chromatography mass-spectrometry assay. Chem. Res. Toxicol., 1995;8:1039-1045
    • (1995) Chem. Res. Toxicol. , vol.8 , pp. 1039-1045
    • Ravanat, J.L.1    Turesky, R.J.2    Gremaud, E.3    Trudel, L.J.4    Stadler, R.H.5
  • 41
    • 23844481419 scopus 로고    scopus 로고
    • Purine nucleoside analogues for the treatment of hematological malignancies: Pharmacology and clinical applications
    • Robak T., Korycka A., Kasznicki M., Wrzesien-Kus A., Smolewski P.: Purine nucleoside analogues for the treatment of hematological malignancies: pharmacology and clinical applications. Curr. Cancer Drug Tar., 2005;5:421-444
    • (2005) Curr. Cancer Drug Tar. , vol.5 , pp. 421-444
    • Robak, T.1    Korycka, A.2    Kasznicki, M.3    Wrzesien-Kus, A.4    Smolewski, P.5
  • 42
    • 63449116519 scopus 로고    scopus 로고
    • Current status o folder and new purine nucleoside analogues in the treatment of lymphoproliferative diseases
    • Robak T., Korycka A., Lech-Maranda E., Robak P.: Current status o folder and new purine nucleoside analogues in the treatment of lymphoproliferative diseases. Molecules, 2009;14:1183-1226
    • (2009) Molecules , vol.14 , pp. 1183-1226
    • Robak, T.1    Korycka, A.2    Lech-Maranda, E.3    Robak, P.4
  • 43
    • 80051495803 scopus 로고    scopus 로고
    • Therapeutic potential of adenosine analogues and conjugates
    • Samsel M., Dzierzbicka K.: Therapeutic potential of adenosine analogues and conjugates. Pharmacol. Rep., 2011;63:601-617
    • (2011) Pharmacol. Rep. , vol.63 , pp. 601-617
    • Samsel, M.1    Dzierzbicka, K.2
  • 44
    • 0025981359 scopus 로고
    • Insertion of specific bases during DNA-synthesis past the oxidation-damaged base 8-oxoDG
    • Shibutani S., Takeshita M., Grollaman A. P.: Insertion of specific bases during DNA-synthesis past the oxidation-damaged base 8-oxoDG. Nature, 1991;349:431-434
    • (1991) Nature , vol.349 , pp. 431-434
    • Shibutani, S.1    Takeshita, M.2    Grollaman, A.P.3
  • 47
    • 79953764331 scopus 로고    scopus 로고
    • Receptor desensitization and blockade of the suppressive effects of prostaglandin E (2) and adenosine on the cytotoxic activity of human melanoma-infiltrating T lymphocytes
    • Su Y. Y., Jackson E. K., Gorelik E.: Receptor desensitization and blockade of the suppressive effects of prostaglandin E (2) and adenosine on the cytotoxic activity of human melanoma-infiltrating T lymphocytes. Cancer Immunol. Immunother., 2011;60:111-122
    • (2011) Cancer Immunol. Immunother. , vol.60 , pp. 111-122
    • Su, Y.Y.1    Jackson, E.K.2    Gorelik, E.3
  • 48
    • 79955907006 scopus 로고    scopus 로고
    • Adenosine-1, 3-diazaphenoxazine derivative for selective base pair formation with 8-oxo-2'-deoxyguanosine in DNA
    • Taniguchi Y., Kawaguchi R., Sasaki S.: Adenosine-1, 3-diazaphenoxazine derivative for selective base pair formation with 8-oxo-2'-deoxyguanosine in DNA. J. Am. Chem. Soc., 2011;133:7272-7275
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 7272-7275
    • Taniguchi, Y.1    Kawaguchi, R.2    Sasaki, S.3
  • 49
    • 79953167994 scopus 로고    scopus 로고
    • Normal and abnormal functions of adenosine receptors in the central nervous system revealed by genetic knockout studies
    • Wei C. J., Li W., Chen J. F.: Normal and abnormal functions of adenosine receptors in the central nervous system revealed by genetic knockout studies. Biochim. Biophys. Acta, 2011;1808:1358-1379
    • (2011) Biochim. Biophys. Acta , vol.1808 , pp. 1358-1379
    • Wei, C.J.1    Li, W.2    Chen, J.F.3
  • 51
    • 34250198261 scopus 로고    scopus 로고
    • Facile quantification of lesions derived from 2'-deoxyguanosine in DNA
    • Xue L., Greenberg M. M.: Facile quantification of lesions derived from 2'-deoxyguanosine in DNA. J. Am. Chem. Soc., 2007;129:7010-7011
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 7010-7011
    • Xue, L.1    Greenberg, M.M.2
  • 52
    • 33745727138 scopus 로고    scopus 로고
    • Synthesis of 2-C-hydroxymethylribofuranosylpurines as potent anti-hepatitis C virus (HCV) agents
    • Yoo B. N., Kim H. O., Moon H. R., Seol S. K., Jang S. K., Lee K. M., Jeong L. S.: Synthesis of 2-C-hydroxymethylribofuranosylpurines as potent anti-hepatitis C virus (HCV) agents. Bioorg. Med. Chem. Lett., 2006;16:4190-4194
    • (2006) Bioorg. Med. Chem. Lett. , vol.16 , pp. 4190-4194
    • Yoo, B.N.1    Kim, H.O.2    Moon, H.R.3    Seol, S.K.4    Jang, S.K.5    Lee, K.M.6    Jeong, L.S.7
  • 53
    • 79957619755 scopus 로고    scopus 로고
    • Synthesis of a novel benzoyl adenosine analog containing a 1, 4-dioxane sugar analog and the synthesis of a corresponding uracil adenine dinucleotide
    • Yu Q., Carlsen P.: Synthesis of a novel benzoyl adenosine analog containing a 1, 4-dioxane sugar analog and the synthesis of a corresponding uracil adenine dinucleotide. Molecules, 2011;16:3985-3998
    • (2011) Molecules , vol.16 , pp. 3985-3998
    • Yu, Q.1    Carlsen, P.2
  • 54
    • 78650674078 scopus 로고    scopus 로고
    • Safety and pharmacokinetics of IDX184, a liver-targeted nucleotide polymerase inhibitor of hepatitis C virus, in healthy subjects
    • Zhou X. J., Pietropaolo K., Chen J., Khan S., Sullivan-Bolyai J., Mayers D.: Safety and pharmacokinetics of IDX184, a liver-targeted nucleotide polymerase inhibitor of hepatitis C virus, in healthy subjects. Antimicrob. Agents Chemother., 2011;55:76-81
    • (2011) Antimicrob. Agents Chemother. , vol.55 , pp. 76-81
    • Zhou, X.J.1    Pietropaolo, K.2    Chen, J.3    Khan, S.4    Sullivan-Bolyai, J.5    Mayers, D.6
  • 55
    • 33644985973 scopus 로고    scopus 로고
    • N-6-Ethyl-2-alkynyl NECAs, selective human A (3) adenosine receptor agonists
    • Zhu R., Frazier C. R., Linden J., Macdonald T. L.: N-6-Ethyl-2-alkynyl NECAs, selective human A (3) adenosine receptor agonists. Bioorg. Med. Chem. Lett., 2006;16:2416-2418
    • (2006) Bioorg. Med. Chem. Lett. , vol.16 , pp. 2416-2418
    • Zhu, R.1    Frazier, C.R.2    Linden, J.3    Macdonald, T.L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.