curcumin has been researched along with depsidone* in 1 studies
1 review(s) available for curcumin and depsidone
| Article | Year |
|---|---|
Design and development of integrase inhibitors as anti-HIV agents.
A review is presented on different categories of compounds that have been studied for the inhibition of the HIV-1 integrase to develop anti-HIV agents. These compounds are: oligonucleotides (double-stranded, triplex, and G-quartet), curcumin analogues, polyhydroxylated aromatic compounds, diketo acids, caffeoyl- and galloyl - based compounds, hydrazides and amides, tetracyclines, and depsides and depsidones. For all these compounds, the important structural features essential for the inhibition of the integrase are pointed out. Topics: Amides; Anti-HIV Agents; Caffeic Acids; Curcumin; Depsides; Drug Design; HIV Integrase; HIV Integrase Inhibitors; HIV-1; Humans; Hydrazines; Hydroxybenzoates; Keto Acids; Lactones; Molecular Structure; Oligonucleotides; Polycyclic Aromatic Hydrocarbons; Tetracyclines | 2003 |