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Synthesis and glycosidase inhibitory activity of novel (2-phenyl-4H-benzopyrimedo[2,1-b]-thiazol-4-yliden)acetonitrile derivatives

journal contribution
posted on 2024-11-01, 12:42 authored by Vijay Patil, Kamalakar Nandre, Sougata Ghosh, Vaidya Rao, Balu Chopade, Sheshanath Bhosale, Sidhanath Bhosale
A series of (2-phenyl-4H-benzopyrimodo[2,1-b] [1,3]thiazol-4-yliden-4-yliden)acetonitrile derivatives have been prepared by ring transformation reaction of 4-(methylthio)- 2-oxo-6-aryl-2H-pyrane-3-carbonitriles. The yield of ring transformation product is moderate to good. Furthermore the glycosidase inhibitory activities were tested by using α-amylase and α-glucosidase pancreatic, intestinal and liver enzymes, responsible for hyperglycemia in type II diabetes. The results revealed that all compounds exhibit significant glycosidase inhibitory activity.

History

Related Materials

  1. 1.
    DOI - Is published in 10.1016/j.bmcl.2012.10.025
  2. 2.
    ISSN - Is published in 0960894X

Journal

Bioorganic and Medicinal Chemistry Letters

Volume

22

Issue

23

Start page

7011

End page

7014

Total pages

4

Publisher

Pergamon

Place published

United Kingdom

Language

English

Copyright

© 2012 Elsevier

Former Identifier

2006038312

Esploro creation date

2020-06-22

Fedora creation date

2012-12-10