Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 정낙신 | - |
dc.date.accessioned | 2016-08-28T11:08:03Z | - |
dc.date.available | 2016-08-28T11:08:03Z | - |
dc.date.issued | 2002 | - |
dc.identifier.issn | 0960-894X | - |
dc.identifier.other | OAK-1156 | - |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/219041 | - |
dc.description.abstract | Novel D-2′-azido-2′,3′-dideoxyarabinofuranosyl-4′- thiopyrimidines and purines have been synthesized, starting from L-xylose via azidation at the 2′-position as a key step. Most of the final nucleosides exhibited toxicity-dependent anti-HIV-1 activity, among which D-α-adenine analogue 3h was found to be the most cytotoxic. © 2002 Elsevier Science Ltd. All rights reserved. | - |
dc.language | English | - |
dc.title | Synthesis and biological evaluation of novel D-2′-azido-2′,3′-dideoxyarabinofuranosyl-4′- thiopyrimidines and purines | - |
dc.type | Article | - |
dc.relation.issue | 17 | - |
dc.relation.volume | 12 | - |
dc.relation.index | SCI | - |
dc.relation.index | SCIE | - |
dc.relation.index | SCOPUS | - |
dc.relation.startpage | 2403 | - |
dc.relation.lastpage | 2406 | - |
dc.relation.journaltitle | Bioorganic and Medicinal Chemistry Letters | - |
dc.identifier.doi | 10.1016/S0960-894X(02)00394-3 | - |
dc.identifier.wosid | WOS:000177603200032 | - |
dc.identifier.scopusid | 2-s2.0-1842853496 | - |
dc.author.google | Kim H.O. | - |
dc.author.google | Park Y.H. | - |
dc.author.google | Moon H.R. | - |
dc.author.google | Jeong L.S. | - |
dc.contributor.scopusid | 정낙신(16028528200) | - |
dc.date.modifydate | 20211210153610 | - |