Structural-Functional Analysis of 2,1,3-Benzoxadiazoles and Their N-oxides As HIV-1 Integrase Inhibitors
Human immunodeficiency virus type 1 integrase is one of the most attractive targets for the development of anti-HIV-1 inhibitors. The capacity of a series of 2,1,3-benzoxadiazoles (benzofurazans) and their N-oxides (benzofuroxans) selected using the PASS software to inhibit the catalytic activity of...
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Published in | Actanaturae Vol. 5; no. 1; pp. 63 - 72 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Russia (Federation)
A.I. Gordeyev
01.01.2013
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Subjects | |
Online Access | Get full text |
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