Thiazole: A versatile standalone moiety contributing to the development of various drugs and biologically active agents

MF Arshad, A Alam, AA Alshammari, MB Alhazza… - Molecules, 2022 - mdpi.com
For many decades, the thiazole moiety has been an important heterocycle in the world of
chemistry. The thiazole ring consists of sulfur and nitrogen in such a fashion that the pi (π) …

Development of novel pyridine-thiazole hybrid molecules as potential anticancer agents

I Ivasechko, I Yushyn, P Roszczenko, J Senkiv… - Molecules, 2022 - mdpi.com
Novel pyridine-thiazole hybrid molecules were synthesized and subjected to physico-
chemical characterization and screening of their cytotoxic action towards a panel of cell lines …

Blockage of the monoamine oxidase by a natural compound to overcome parkinson's disease via computational biology

M Sherafatizangeneh, C Farshadfar… - Journal of …, 2022 - World Scientific
The dopamine (DA) metabolism changes are significant in Parkinson's disease (PD). Levels
of monoamine oxidases (MAOs) play a critical role in DA metabolism and oxidative damage …

In-silico evaluations of the isolated phytosterols from polygonum hydropiper L against BACE1 and MAO drug targets

M Ayaz, A Wadood, A Sadiq, F Ullah… - Journal of …, 2022 - Taylor & Francis
Our previous anti-Alzheimer's studies on crude extracts, essential oils and isolated
compounds including β-sitostrol from Polygonum hydropiper L, motivated us for further …

[HTML][HTML] Development of Escherichia coli asparaginase II for the treatment of acute lymphocytic leukemia: In silico reduction of asparaginase II side effects by a novel …

N Ardalan, AA Sepahi… - Asian Pacific Journal of …, 2021 - ncbi.nlm.nih.gov
Acute lymphoblastic leukemia (ALL) is a common blood disease in children that is
accountable for many deaths. Due to major improvements in treatment procedures in the …

[HTML][HTML] The SARS-Cov-2 Proliferation blocked by a novel and potent main protease inhibitor via computer-aided drug design

S Shayan, S Jamaran, RH Askandar… - Iranian Journal of …, 2021 - ncbi.nlm.nih.gov
The recent prevalence of novel “coronavirus disease 2019” has expanded quickly globally,
causing a universal pandemic. Herein, an effort was constructed to design a potent drug to …

Prevention of SARS-CoV-2 proliferation with a novel and potent main protease inhibitor by docking, ADMET, MM-PBSA, and molecular dynamics simulation

A Noorbakhsh, RH Askandar, MS Alhagh… - Journal of …, 2021 - World Scientific
COVID-19 is the last disease caused by SARS-CoV-2 associated with a severe immune
response and lung damage. The main protease (Mpro) has a vital role in SARS-CoV-2 …

UM-164, a dual inhibitor of c-Src and p38 MAPK, suppresses proliferation of glioma by reducing YAP activity

H Xu, Y Zhang, J Liu, J Cui, Y Gan, Z Wu, Y Chang… - Cancers, 2022 - mdpi.com
Simple Summary UM-164, as a high-potency c-Src inhibitor, is the original lead compound
to be developed for targeting triple-negative breast cancer. Here we validated the fact that …

Early Blockage of Mycobacterium Tuberculosis Cell-wall Synthesis via EchA\6 Inhibition to Overcome Resistance Strain: Insights from Umbrella Sampling Simulations

RH Askandar, F Sharifi, S Shayan… - Current Bioactive …, 2023 - ingentaconnect.com
Background: Tuberculosis (TB) has long been the major infectious cause of mortality,
ranking higher than HIV/AIDS as the most common cause of death from a single infectious …

A consequence of drug targeting of aminoacyl‐tRNA synthetases in Mycobacteriumtuberculosis

U Ndagi, HM Kumalo… - Chemical Biology & Drug …, 2021 - Wiley Online Library
Drug‐resistant Mycobacterium tuberculosis poses a great threat to public health and
remains one of the red‐flag tagged infectious diseases, with the tendency of comorbidity …