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Volumn 44, Issue 18, 2001, Pages 3014-3021

New 3′-azido-3′-deoxythymidin-5′-yl O-(4-hydroxyalkyl or -alkenyl or -alkylepoxide) carbonate prodrugs: Synthesis and anti-HIV evaluation

Author keywords

[No Author keywords available]

Indexed keywords

3' AZIDO 3' DEOXYTHYMIDIN 5' YL O (4 HYDROXYEPOXIDE)CARBONATE; ALKENYL GROUP; ALKYL GROUP; CARBONIC ACID DERIVATIVE; EPOXIDE; PRODRUG; THYMIDINE DERIVATIVE; UNCLASSIFIED DRUG; ZIDOVUDINE; ZIDOVUDINE DERIVATIVE; ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT; DRUG DERIVATIVE;

EID: 0035974621     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm010863i     Document Type: Article
Times cited : (31)

References (50)
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    • Yarchoan, R.1    Broder, S.2
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    • On the therapeutic use of nucleosides and the penetrability of phosphorylated compounds
    • (1975) Biochem. Pharmacol. , vol.24 , pp. 1929-1932
    • Cohen, S.S.1
  • 28
    • 0033819409 scopus 로고    scopus 로고
    • 3′-Azido-3′-deoxythymidine (AZT) and AZT-resistant reverse transcriptase can increase the in vivo mutation rate of human immunodeficiency virus type 1
    • (2000) J. Virol. , vol.74 , pp. 9532-9539
    • Mansky, L.M.1    Bernard, L.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.