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Volumn 53, Issue 13, 2010, Pages 4949-4957

Phosphoramidate ProTides of 2′-C-methylguanosine as highly potent inhibitors of hepatitis C virus. Study of their in vitro and in vivo properties

Author keywords

[No Author keywords available]

Indexed keywords

2' C METHYLGUANOSINE; ALANINE; AMINO ACID; ESTER; GUANOSINE TRIPHOSPHATE; NUCLEOSIDE; PHOSPHORAMIDIC ACID DERIVATIVE; UNCLASSIFIED DRUG; VALINE;

EID: 77954347956     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/jm1003792     Document Type: Article
Times cited : (52)

References (17)
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    • Aryl phosphoramidate derivatives of d4T have improved anti-HIV efficacy in tissue culture and may act by the generation of a novel intracellular metabolite
    • McGuigan, C.; Cahard, D.; Sheeka, H. M.; De Clercq, E.; Balzarini, J. Aryl phosphoramidate derivatives of d4T have improved anti-HIV efficacy in tissue culture and may act by the generation of a novel intracellular metabolite J. Med. Chem. 1996, 39, 1748-1753
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    • McGuigan, C.1    Cahard, D.2    Sheeka, H.M.3    De Clercq, E.4    Balzarini, J.5
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    • The phosphoramidate ProTide approach greatly enhances the activity of beta-2′- C -methylpurines against Hepatitis C Virus
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    • McGuigan, C.1    Sutton, P.W.2    Cahard, D.3    Turner, K.4    Oleary, G.5    Wang, Y.6    Gumbleton, M.7    De Clercq, E.8    Balzarini, J.9
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    • ClogP values were calculated using ChemOffice Ultra 11.0
    • ClogP values were calculated using ChemOffice Ultra 11.0.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.