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dc.contributor.author정낙신-
dc.date.accessioned2016-08-28T11:08:36Z-
dc.date.available2016-08-28T11:08:36Z-
dc.date.issued2001-
dc.identifier.issn0960-894X-
dc.identifier.otherOAK-616-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/218750-
dc.description.abstractNovel D- and L-2′-azido-2′,3′-dideoxyribofuranosyl-4′- thiopyrimidines and purines have been synthesized starting from L-xylose and D-xylose, respectively. Among synthesized compounds tested against several viruses such as HIV-1, HSV-1, HSV-2, and HCMV, D-β-N6-methyladenine (ent-22a) and D-α-N6-methyladenine (ent-22b) analogues were found to exhibit significant anti-HCMV activity. © 2001 Elsevier Science Ltd.-
dc.languageEnglish-
dc.titleSynthesis and antiviral activity of novel D- and L-2′-azido-2′,3′-dideoxyribofuranosyl-4′- thiopyrimidines and purines-
dc.typeArticle-
dc.relation.issue4-
dc.relation.volume11-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage599-
dc.relation.lastpage603-
dc.relation.journaltitleBioorganic and Medicinal Chemistry Letters-
dc.identifier.doi10.1016/S0960-894X(01)00006-3-
dc.identifier.wosidWOS:000167022200039-
dc.identifier.scopusid2-s2.0-0035952288-
dc.author.googleKim H.O.-
dc.author.googleKim Y.H.-
dc.author.googleSuh H.-
dc.author.googleJeong L.S.-
dc.contributor.scopusid정낙신(16028528200)-
dc.date.modifydate20211210153610-
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약학대학 > 약학과 > Journal papers
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