Conversion of 2′,3′-dideoxyadenosine (ddA) and 2′,3′-didehydro-2′,3′-dideoxyadenosine (d4A) to their corresponding aryloxyphosphoramidate derivatives markedly potentiates their activity against human immunodeficiency virus and hepatitis B virus
Open Access
- 30 June 1997
- journal article
- Published by Wiley in FEBS Letters
- Vol. 410 (2-3) , 324-328
- https://doi.org/10.1016/s0014-5793(97)00616-9
Abstract
No abstract availableKeywords
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