Functionalized 1,3-teraryls as a new class of hepatoprotectants: Part V

DOI: 10.1016/S0960-894X(98)00061-4

Source and publish data:

Bioorganic and Medicinal Chemistry Letters p. 469 - 472 (1998)

Update date:2022-07-30

Topics:

Authors:

Ram, Vishnu J.

Goel, Atul

Patnaik Patnaik

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Article abstract of DOI:10.1016/S0960-894X(98)00061-4

Functionalized 1,3-teraryls, synthesized through ring transformation of 6-aryl-3-carbomethoxy-4-methylthio-2H-pyran-2-one from arylketone have been screened for their hepatoprotective activity and some of them have demonstrated significant protection in animal model.

Full text of DOI:10.1016/S0960-894X(98)00061-4

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Product name:2H-Pyran-3-carboxylic acid, 6-(3-chloro-4-fluorophenyl)-4-(methylthio)-2-oxo-, methyl ester

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