Synthesis, molecular docking, and dynamic simulation targeting main protease (Mpro) of new, Thiazole clubbed pyridine scaffolds as potential COVID-19 inhibitors

A Alghamdi, AS Abouzied, A Alamri, S Anwar… - Current Issues in …, 2023 - mdpi.com
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 …

One-pot synthesis of novel thiazoles as potential anti-cancer agents

AR Sayed, SM Gomha, EA Taher… - Drug design …, 2020 - Taylor & Francis
Background Thiazole and thiosemicarbazone derivatives are known to have potential
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 …

A green synthesis, DFT calculations, and molecular docking study of some new indeno [2, 1-b] quinoxalines containing thiazole moiety

AM Abdallah, SM Gomha, MEA Zaki… - Journal of Molecular …, 2023 - Elsevier
A series of new indenoquinoxaline-thiazole hybrids were synthesized by combining
indenoquinoxaline thiosemicarbazone with appropriate hydrazonoyl chlorides or α-halo …

Design, efficient synthesis and molecular docking of some novel thiazolyl-pyrazole derivatives as anticancer agents

AR Sayed, SM Gomha, FM Abdelrazek, MS Farghaly… - BMC chemistry, 2019 - Springer
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 …

Novel thiadiazole-thiazole hybrids: synthesis, molecular docking, and cytotoxicity evaluation against liver cancer cell lines

GF Aljohani, TZ Abolibda, M Alhilal… - Journal of Taibah …, 2022 - Taylor & Francis
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 …

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 …

[HTML][HTML] Synthesis, in-silico studies, and biological evaluation of some novel 3-thiazolyl-indoles as CDK2–inhibitors

SM Gomha, MEA Zaki, D Maliwal, RRS Pissurlenkar… - Results in …, 2023 - Elsevier
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 …

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 …

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 …