Functionally substituted derivatives of novel thiourea and phenylthiourea as potent aldose reductase, α-amylase, and α-glycosidase inhibitors: in vitro and in silico studies-Reference-Cited by-同舟云学术

Functionally substituted derivatives of novel thiourea and phenylthiourea as potent aldose reductase, α-amylase, and α-glycosidase inhibitors: in vitro and in silico studies

Published:2024-02-19 Issue:6 Volume:32 Page:565-579
ISSN:1598-5032
Container-title:Macromolecular Research
language:en
Short-container-title:Macromol. Res.

Author:

Sujayev Afsun,Sadeghian Nastaran,Taslimi Parham^ORCID,Kılınç Namık,Akkuş Musa,Özçelik Burak,Farzaliyev Vagif,Alwasel Saleh H.,Gülçin İlhami

Funder

Science Development Fund under the President of the Republic of Azerbaijan

King Saud University

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s13233-024-00247-9.pdf

Reference48 articles.

1. G. Jenner, Effect of high pressure on Biginelli reactions. Steric hindrance and mechanistic considerations. Tetrahedron Lett. 45, 6195–6198 (2004)

2. J.-T. Li, J.-F. Han, J.-H. Yang, T.-S. Li, An efficient synthesis of 3,4-dihydropyrimidin-2-ones catalyzed by NH2SO3H under ultrasound irradiation. Ultrason. Sonochem. 10, 119–122 (2003)

3. A. Sudzhaev, R. Najafova, I. Rzayeva, Yu. Safarov, M. Allahverdiev, Study of the antioxidant properties of thiocarbamide derivatives of some amino alcohols. J. Appl. Chem. 84(8), 1329–1332 (2011)

4. V. Farzaliyev, A. Shuriberko, A. Sujayev, S. Osmanova, S. Gojayeva, K. Gahramanova, Synthesis, computational and biological activity of heteroatomic compounds based on phenylthiourea and acetophenone. J. Mol. Struct. 1221(9), 128844–128853 (2020)

5. L. Wang, C. Qian, H. Tian, M. Yun, Lanthanide triflate catalyzed one-pot synthesis of dihydropyrimidin-2(1H)-thiones by a three-component of 1,3-dicarbonyl compounds, Aldehydes, and thiourea using a solvent-free Biginelli condensation. Synth. Commun. 33, 1459–1468 (2003)