Original articleSynthesis, anti-HIV-1 integrase, and cytotoxic activities of 4-chloro-N-(4-oxopyrimidin-2-yl)-2-mercaptobenzenesulfonamide derivatives
-
Add time:08/24/2019 Source:sciencedirect.com
Several 4-chloro-N-(4-oxopyrimidin-2-yl)-2-mercaptobenzenesulfonamide derivatives 13–28 and 35–44 have been synthesized and tested as potential HIV-1 integrase (IN) inhibitors. Compounds 15–17, 19, 21–28, 36 and 41 inhibited IN with IC50 values in the range of 3.3–63.0 μM. The compounds 13, 15, 16, 21–24 and 26–28 were further tested at the US National Cancer Institute for their in vitro activity against a panel of 53–57 human tumor cell lines. The compounds 26–28 were inactive, whereas the other compounds exhibited high or reasonable activity (GI50 < 0.01–20.0 μM) against one or more human tumor cell lines.
We also recommend Trading Suppliers and Manufacturers of 4-[(3,4-Dihydro-6-chloro-2-methyl-4-oxoquinazolin)-3-yl]-2-hydroxybenzohydrazide (cas 19581-46-5). Pls Click Website Link as below: cas 19581-46-5 suppliers
Prev:Heterocyclic analogues of l-citrulline as inhibitors of the isoforms of nitric oxide synthase (NOS) and identification of Nδ-(4,5-dihydrothiazol-2-yl)ornithine as a potent inhibitor
Next:On the nature of the active intermediates in iron-catalyzed oxidation of cycloalkanes with hydrogen peroxide and peracids) - 【Back】【Close 】【Print】【Add to favorite 】


