Design and synthesis of 2',3'-dideoxy-2',3'-didehydro-beta-L-cytidine (beta-L-d4C) and 2',3'-dideoxy 2',3'-didehydro-beta-L-5-fluorocytidine (beta-L-Fd4C), two exceptionally potent inhibitors of human hepatitis B virus (HBV) and potent inhibitors of human immunodeficiency virus (HIV) in vitro
- J Med Chem. 1996 Apr 26;39(9):1757-9. doi: 10.1021/jm950836q.
Affiliations
- 1. Department of Pharmacology, Yale University School of Medicine, New Haven, Connecticut 06520-8066, USA.
PMID: 8627596
DOI: 10.1021/jm950836q
Products
-
Cat. No.Product NameDescriptionTargetResearch Area
-
target: Nucleoside Antimetabolite/AnalogResearch Areas: Infection