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Synthesis and in vitro anti-HIV activity of N-1,3-benzo[d]thiazol-2-yl-2-(2-oxo-2H-chromen-4-yl)acetamide derivatives using MTT method

Bhavsar, Dhairya, Trivedi, Jalpa, Parekh, Shrey, Savant, Mahesh, Thakrar, Shailesh, Bavishi, Abhay, Radadiya, Ashish, Vala, Hardevsinh, Lunagariya, Jignesh, Parmar, Manisha, Paresh, Ladwa, Loddo, Roberta and Shah, Anamik 2011. Synthesis and in vitro anti-HIV activity of N-1,3-benzo[d]thiazol-2-yl-2-(2-oxo-2H-chromen-4-yl)acetamide derivatives using MTT method. Biorganic and Medicinal Chemistry Letters 21 (11) , pp. 3443-3446. 10.1016/j.bmcl.2011.03.105

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Abstract

A series of novel N-1,3-benzo[d]thiazol-2-yl-2-(2-oxo-2H-chromen-4-yl)acetamide derivatives has been synthesized. All the newly synthesized compounds were evaluated for their anti-HIV activity using MTT method. Most of these compounds showed moderate to potent activity against wild-type HIV-1 with an EC50 ranging from >7 EC50 [μg/ml] to <100 EC50 [μg/ml]. Among them, N-1,3-benzo[d]thiazol-2-yl-2-(2-oxo-2H-chromen-4-yl)acetamide 6v was identified as the most promising compound (EC50 = <7 μg/ml). Among all the compounds, three compounds 6m, 6v and 6u have been exhibits potent anti-HIV activity against MT-4 cells.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Chemistry
Publisher: Elsevier
ISSN: 0960-894X
Date of Acceptance: 28 March 2011
Last Modified: 23 Mar 2018 11:08
URI: http://orca-mwe.cf.ac.uk/id/eprint/109868

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