Didanosine: Uses, Interactions, Mechanism of Action | DrugBank This compound belongs to the class of organic compounds known as purine 2',3'-dideoxyribonucleosides These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at positions 2 and 3
Didanosine - Wikipedia It is used in combination with other medications as part of highly active antiretroviral therapy (HAART) It is of the reverse-transcriptase inhibitor class Didanosine was first described in 1975 and approved for use in the United States in 1991 [2]
Didanosine | C10H12N4O3 | CID 135398739 - PubChem Didanosine is a purine 2',3'-dideoxyribonucleoside that is inosine in which the hydroxy groups at both the 2' and the 3' positions on the sugar moiety have been replaced by hydrogen An antiviral drug, it is used as a medication to treat HIV AIDS
Didanosine - UPMC Health Library Didanosine is used along with other medications to treat human immunodeficiency virus (HIV) infection Didanosine is in a class of medications called nucleoside reverse transcriptase inhibitors (NRTIs) It works by decreasing the amount of HIV in the blood
Didanosine - Laboratory Notes It belongs to a class of drugs called nucleoside reverse transcriptase inhibitors (NRTIs), which work by interfering with the reverse transcriptase enzyme—an essential component that HIV uses to replicate within human cells
Didanosine Overview - Active Ingredient - RxReasoner Didanosine belongs to a class of medicines called nucleoside analogues or nucleoside reversetranscriptase inhibitors (NRTIs) Intracellularly, didanosine is converted by cellular enzymes to the active metabolite, dideoxyadenosine 5'-triphosphate