ISSN: 0973-7510

E-ISSN: 2581-690X

Mohamed M. Abdalla1 , Abd El-Galil E. Amr2,3, Mohamed G. Assy4 and Zainab M. Ramadan4
1Research Unit, Saco Pharm. Co., 6th October City 11632, Egypt.
2Pharmaceutical Chemistry Department, Drug Exploration & Development Chair (DEDC),
College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.
3Applied Organic Chemistry Department, National Research Center, Dokki, Cairo, Egypt.
4Chemistry Department, Faculty of Science, Zagazig University, Zagazig, Egypt.
J Pure Appl Microbiol. 2014;8(5):3773-3780
© The Author(s). 2014
Received: 06/08/2014 | Accepted: 20/09/2014 | Published: 31/10/2014
Abstract

In our previous work, some of thienopyrimidine, benzoxazine, quinazoline and azole moieties 1-18 were synthesized before. We herein report the calcium channel blocking and anti-arrhythmic activities. Nineteen of these compounds were screened for their calcium channel blocking and anti-arrhythmic activities using of Nifedipine as the reference drug. The newly synthesized compounds showed potent calcium channel blocking and anti-arrhythmic activities with low toxicity (LD50) comparable to Nifedipine as reference drug.

Keywords

Thienopyrimidinoyl chloride, Thienopyrimidine, Benzamidazole, Calcium channel blocking, Anti-arrhythmic activities

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