Tuberculosis (TB) has been considered as the highly chronic, contagious and infectious disorder caused by Mycobacterium tuberculosis (Mtb). Every year more than 10 million …
TA Farghaly, EMH Abbas, AM Al-Soliemy, R Sabour… - Bioorganic …, 2022 - Elsevier
New hydrazonoyl-sulfonylthiazoles were designed and synthesized as EGFR inhibitors. The new sulfonylthiazole derivatives were assessed in vitro to measure their effect on EGFR …
Based on the structural study of previously known CDK2 inhibitors, a new series of pyrazolo [1, 5-a] pyrimidine derivatives was designed and synthesized. The target compounds were …
Introduction Several viral infections cause life-threatening consequences in humans, making them the most serious public health concerns. Despite the fact that several antiviral …
B Pakamwong, P Thongdee, B Kamsri… - Journal of Chemical …, 2024 - ACS Publications
Mycobacterium tuberculosis is the single most important global infectious disease killer and a World Health Organization critical priority pathogen for development of new antimicrobials …
P Bhaumick, R Kumar, SS Acharya… - The Journal of …, 2022 - ACS Publications
Herein, we report an efficient multicomponent reaction for the synthesis of trisubstituted thiazoles involving a one-pot C–C, C–N, and C–S bond-forming process from the readily …
AY Khormi, TA Farghaly, A Bayazeed, YO Al-Ghamdi… - RSC …, 2022 - pubs.rsc.org
Novel thiazole derivatives possessing phenyl sulfonyl moiety were designed and synthesized as B-RAFV600E kinase inhibitors based on the clinically-approved anticancer …
MS Abusaif, A Ragab, EA Fayed, YA Ammar… - Bioorganic …, 2025 - Elsevier
Hepatocellular carcinoma (HCC) ranks as the third most prevalent reason for cancer-related death on a global scale. Tyrosine kinase inhibitors (TKIs) continue to be the primary …
Abstract New 6, 7-dimethylquinoxalin-2 (1H)-one and hydrazineylidene thiazol-4-one derivatives were synthesized, and evaluated for their in vitro antimicrobial activity. The …