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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

✍ Scribed by Jan Balzarini; Johannes Kruining; Orson Wedgwood; Christophe Pannecouque; Stefano Aquaro; Carlo-Federico Perno; Lieve Naesens; Myriam Witvrouw; Rudolf Heijtink; Erik De Clercq; Christopher McGuigan

Book ID: 117107737
Publisher: Elsevier Science
Year: 1997
Tongue: English
Weight: 563 KB
Volume: 410
Category: Article
ISSN: 0014-5793
DOI: 10.1016/s0014-5793(97)00616-9

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