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April 1, 1995Bioorganic & Medicinal Chemistry LettersOpen Access

Anti-human immunodeficiency virus type-1 (HIV-1) and anti-hepatitis B virus (HBV) activities of (2,3-dideoxy-2-fluoro-β-L-threo-pentofuranosyl)nucleosides

Yuejun Xiang Sócrates C.H. Cavalcanti Chung K. Chu Raymond F. Schinazi S. Balakrishna Pai Young-Lian Zhu Yung‐Chi Cheng

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Abstract

1-or-9-(2,3-Dideoxy-2-fluoro-β-L-threo-pentofuranosyl)- cytosine (F-β-L-ara-ddC) and-adenine (F-β-L-ara-ddA) were synthesized and their anti-HIV and anti-HBV activities were evaluated.

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Cite This Study

Xiang et al. (1995) studied this question.

synapsesocial.com/papers/6aa87a3d5422c01e0cfed712 https://doi.org/10.1016/0960-894x(95)00133-e

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1(-)-2'-deoxy-3'-thiacytidine is a potent, highly selective inhibitor of human immunodeficiency virus type 1 and type 2 replication in vitroIn Vitro Study · 1992 · 240 citations
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