A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by an azido group. This modification prevents the formation of phosphodiester linkages which are needed for the completion of nucleic acid chains. The compound is a potent inhibitor of HIV replication, acting as a chain-terminator of viral DNA during reverse transcription. It improves immunologic function, partially reverses the HIV-induced neurological dysfunction, and improves certain other clinical abnormalities associated with AIDS. Its principal toxic effect is dose-dependent suppression of bone marrow, resulting in anemia and leukopenia. [PubChem]
Used in combination with other antiretroviral agents for the treatment of human immunovirus (HIV) infections.
Merck & Co Inc, Whitehouse Station, New Jersey, United States
San Francisco AIDS Clinic / San Francisco Gen Hosp, San Francisco, California, United States
New England Med Ctr, Boston, Massachusetts, United States
Univ of Washington, Seattle, Washington, United States
Phoenix Body Positive, Phoenix, Arizona, United States
Saint Vincent's AIDS Ctr, New York, New York, United States
George Washington Med Ctr, Washington, District of Columbia, United States
Chicago Ctr for Clinical Research, Chicago, Illinois, United States
Dr Bruce Rashbaum, Washington, District of Columbia, United States
Community Research Initiative of South Florida, Coral Gables, Florida, United States
ddC Coordinating Ctr, Wellesley Hills, Massachusetts, United States
UCLA Med Ctr, Los Angeles, California, United States
UCLA Med Ctr, Los Angeles, California, United States
Pharmacia & Upjohn, Peapack, New Jersey, United States
Univ of Miami School of Medicine, Miami, Florida, United States
Agouron Pharmaceuticals Inc, San Diego, California, United States
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