A one-pot multicomponent facile synthesis of dihydropyrimidin-2(1H)-thione derivatives using triphenylgermane as a catalyst and its binding pattern validation
Author:
Affiliation:
1. Department of Chemistry
2. Quaid-i-Azam University
3. Islamabad-45320
4. Pakistan
5. Computational Biology Lab
6. National Center for Bioinformatics
7. Department of Physics
8. University of Sargodha
9. Sargodha
Abstract
A series of substituted dihydropyrimidin-2(1H)-thione derivatives (1–8) have been synthesized and docked against enzymes human topoisomerase II alpha (4FM9) and Helicobacter pylori urease (1E9Y) for binding mode validation.
Funder
Higher Education Commission, Pakistan
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2016/RA/C6RA19162B
Reference50 articles.
1. Silica sulfuric acid: an efficient and reusable catalyst for the one-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones
2. Synthesis and biological evaluation of novel pyrimidine-2(1H)-ones/thiones as potent anti-inflammatory and anticancer agents
3. Biologically active dihydropyrimidones of the Biginelli-type — a literature survey
4. An Efficient and Clean One-Pot Synthesis of 3,4-Dihydropyrimidine-2-(1H)-ones Catalyzed by SrCl2.6H2O-HCl in Solvent or Solvent-Free Conditions
5. Dihydropyrimidine calcium channel blockers: 2-heterosubstituted 4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridines
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