Study of the reactivity of aminocyanopyrazoles and evaluation of the mitochondrial reductive function of some products
Author:
Affiliation:
1. Department of Chemistry, University of Sfax, Laboratory of Medicinal and Environmental Chemistry , 3018 Sfax , Tunisia
2. The School of Biosciences, The University of Birmingham, Edgbaston , Birmingham , B15 2TT , United Kingdom
Abstract
Publisher
Walter de Gruyter GmbH
Subject
Organic Chemistry
Link
https://www.degruyter.com/document/doi/10.1515/hc-2022-0001/pdf
Reference31 articles.
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3. Gupta S, Rodrigues LM, Esteves AP, Oliveira-Campos AMF, Jose’Nascimento MS, Nazareh N, et al. Synthesis of N-aryl-5-amino-4-cyanopyrazole derivatives as potent xanthine oxidase inhibitors. Eur J Med Chem. 2008;43:771–80.
4. Nepali K, Singh G, Turan A, Agarwal A, Sapra S, Kumar R, et al. A rational approach for the design and synthesis of 1-acetyl-3,5-diaryl-4,5-dihydro(1H)pyrazoles as a new class of potential non-purine xanthine oxidase inhibitors. Bioorg Med Chem. 2011;19(6):1950–8.
5. Rashad AE, Shamroukh AH, Abdel-Megeid RE, Ali HS. Synthesis and isomerization of some novel pyrazolopyrimidine and pyrazolotriazolopyrimidine derivatives. Molecules. 2014 25;19(5):5459–69.
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