Synthesis, molecular docking, and dynamic simulation targeting main protease (Mpro) of new, Thiazole clubbed pyridine scaffolds as potential COVID-19 inhibitors
Many biological activities of pyridine and thiazole derivatives have been reported, including
antiviral activity and, more recently, as COVID-19 inhibitors. Thus, in this paper, we …
antiviral activity and, more recently, as COVID-19 inhibitors. Thus, in this paper, we …
One-pot synthesis of novel thiazoles as potential anti-cancer agents
Background Thiazole and thiosemicarbazone derivatives are known to have potential
anticancer activity with a mechanism of action related to inhibition of matrix metallo …
anticancer activity with a mechanism of action related to inhibition of matrix metallo …
Mechanochemical synthesis and molecular docking studies of new azines bearing indole as anticancer agents
MS Ibrahim, B Farag, J Y. Al-Humaidi, MEA Zaki… - Molecules, 2023 - mdpi.com
The development of new approaches for the synthesis of new bioactive heterocyclic
derivatives is of the utmost importance for pharmaceutical industry. In this regard, the …
derivatives is of the utmost importance for pharmaceutical industry. In this regard, the …
A green synthesis, DFT calculations, and molecular docking study of some new indeno [2, 1-b] quinoxalines containing thiazole moiety
A series of new indenoquinoxaline-thiazole hybrids were synthesized by combining
indenoquinoxaline thiosemicarbazone with appropriate hydrazonoyl chlorides or α-halo …
indenoquinoxaline thiosemicarbazone with appropriate hydrazonoyl chlorides or α-halo …
Design, efficient synthesis and molecular docking of some novel thiazolyl-pyrazole derivatives as anticancer agents
Pyrazoles, thiazoles and fused thiazoles have been reported to possess many biological
activities. 3-Methyl-5-oxo-4-(2-arylhydrazono)-4, 5-dihydro-1 H-pyrazole-1-carbothioamides …
activities. 3-Methyl-5-oxo-4-(2-arylhydrazono)-4, 5-dihydro-1 H-pyrazole-1-carbothioamides …
Novel thiadiazole-thiazole hybrids: synthesis, molecular docking, and cytotoxicity evaluation against liver cancer cell lines
One of the worst diseases, cancer claims millions of lives each year throughout the world,
necessitating the creation of novel treatments. In this study, we designed a novel series of 1 …
necessitating the creation of novel treatments. In this study, we designed a novel series of 1 …
Design, synthesis, characterization, molecular docking studies and anticancer activity evaluation of novel hydrazinecarbothioamide, 1, 2, 4-triazole-3-thione, 4 …
ED Dincel, Ç Akdağ, T Kayra, ED Coşar… - Journal of Molecular …, 2022 - Elsevier
A series of novel hydrazinecarbothioamide, 1, 2, 4-triazole-3-thione, 4-thiazolidinone and 1,
3, 4-oxadiazole derivatives were synthesized and evaluated for their cytotoxic activity …
3, 4-oxadiazole derivatives were synthesized and evaluated for their cytotoxic activity …
[HTML][HTML] Synthesis, in-silico studies, and biological evaluation of some novel 3-thiazolyl-indoles as CDK2–inhibitors
The essential enzyme cyclin-dependent kinase 2 (CDK2) is a promising target for anticancer
drug development due to its pivotal role in regulating the cell cycle. This study aimed to …
drug development due to its pivotal role in regulating the cell cycle. This study aimed to …
Synthesis and biological evaluation of thiazolyl-ethylidene hydrazino-thiazole derivatives: a novel heterocyclic system
LA Al-Mutabagani, FM Abdelrazek, SM Gomha… - Applied Sciences, 2021 - mdpi.com
The reaction of 2-(1-(2-(2-(4-methoxybenzylidene) hydrazinyl)-4-methylthiazol-5-yl)
ethylidene) hydrazinecarbothioamide with a range of hydrazonoyl chlorides and α-halo …
ethylidene) hydrazinecarbothioamide with a range of hydrazonoyl chlorides and α-halo …
One‐pot synthesis of new thiadiazolyl‐pyridines as anticancer and antioxidant agents
SM Gomha, ZA Muhammad… - Journal of …, 2018 - Wiley Online Library
The reaction of one equivalents of 5‐acetylthiadiazole with one equivalent of aldehyde in
acetic acid and ammonium acetate yielded thiadiazolyl‐pyridine derivatives in a …
acetic acid and ammonium acetate yielded thiadiazolyl‐pyridine derivatives in a …