Syntheses, in vitro evaluation and molecular docking studies of 5-bromo-2-aryl benzimidazoles as α-glucosidase inhibitors-Reference-Cited by-同舟云学术

Syntheses, in vitro evaluation and molecular docking studies of 5-bromo-2-aryl benzimidazoles as α-glucosidase inhibitors

Published:2016-07-22 Issue:9 Volume:25 Page:2058-2069
ISSN:1054-2523
Container-title:Medicinal Chemistry Research
language:en
Short-container-title:Med Chem Res

Author:

Arshad Tanzila,Khan Khalid Mohammed,Rasool Najma,Salar Uzma,Hussain Shafqat,Tahir Tehreem,Ashraf Mohammed,Wadood Abdul,Riaz Muhammad,Perveen Shahnaz,Taha Muhammad,Ismail Nor Hadiani

Funder

Higher Education Commission (HEC)

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics

Link

http://link.springer.com/content/pdf/10.1007/s00044-016-1614-y.pdf

Reference48 articles.

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3. Bansal Y, Silakari O (2012) The therapeutic journey of benzimidazole: a review. Bioorg Med Chem 20:6208–6236

4. Błaszczak-Świątkiewicz K, Olszewska P, Mikiciuk-Olasik E (2014) Biological approach of anticancer activity of new benzimidazole derivatives. Pharma Rep 66:100–106

5. Brink NG, Folkers K (1949) Vitamin B12. VI. 5,6-Dimethylbenzimidazole, a degradation product of vitamin B12. J Am Chem Soc 71:2951–2951

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