A review on anticancer potentials of benzothiazole derivatives

N Pathak, E Rathi, N Kumar, SG Kini… - Mini reviews in …, 2020 - ingentaconnect.com
Benzothiazole is an organic compound bearing a heterocyclic nucleus (thiazole) which
imparts a broad spectrum of biological activities to it. The significant and potent activity of …

Thiazole and related heterocyclic systems as anticancer agents: A review on synthetic strategies, mechanisms of action and SAR Studies

Sahil, K Kaur, V Jaitak - Current medicinal chemistry, 2022 - benthamdirect.com
Background: Cancer is the second leading cause of death worldwide. Many anticancer
drugs are commercially available, but lack of selectivity, target specificity, cytotoxicity, and …

Naphthalene-based bis-N-salicylidene aniline dyes: Crystal structures, Hirshfeld surface analysis, computational study and molecular docking with the SARS-CoV-2 …

TM Burkhanova, MG Babashkina, T Taskin-Tok… - Journal of the Iranian …, 2022 - Springer
In this work, we report structural and computational studies of a series of naphthalene-based
bis-N-salicylidene aniline dyes, namely N, N′-bis-salicylidene-1, 5-diaminonaphthalene …

Novel Thiazolidine-2, 4-dione-trimethoxybenzene-thiazole Hybrids as Human Topoisomerases Inhibitors

MS Sinicropi, J Ceramella, P Vanelle, D Iacopetta… - Pharmaceuticals, 2023 - mdpi.com
Cancer is a complex and heterogeneous disease and is still one of the leading causes of
morbidity and mortality worldwide, mostly as the population ages. Despite the encouraging …

Comprehensive study of the interaction between Puerariae Radix flavonoids and DNA: From theoretical simulation to structural analysis to functional analysis

X Chen, Z He, X Wu, D Mao, C Feng, J Zhang… - … Acta Part A: Molecular …, 2020 - Elsevier
Puerariae Radix (PR) is a natural herb whose active ingredient is mainly flavonoids. To
explore the interaction between PR flavonoids and DNA not only has important biological …

Binding site feature description of 2-substituted benzothiazoles as potential AcrAB-TolC efflux pump inhibitors in E. coli

S Yilmaz, G Altinkanat-Gelmez, K Bolelli… - SAR and QSAR in …, 2015 - Taylor & Francis
The resistance-nodulation-division (RND) family efflux pumps are important in the antibiotic
resistance of Gram-negative bacteria. However, although a number of bacterial RND efflux …

Molecular docking-assisted investigation of Pd (II) complexes carrying “SNS” pincer-type pyridine-thioether ligand as potential drug candidates against COVID-19

HG Sogukomerogullari - Computers in Biology and Medicine, 2022 - Elsevier
Abstract The coronavirus disease 2019 (COVID-19) pandemic has posed a threat to public
health throughout the world since the Severe Acute Respiratory Syndrome Coronavirus 2 …

Anticancer drug—friend or foe

T Taşkın-Tok, S Gowder - Pharmacology and therapeutics, 2014 - books.google.com
Cancer is the third mostlethal disease in the world after cardiovascular,
parasiticandinfectious diseases, based on reports from American Cancer Society (ACS)[1 …

Synthesis and activity mechanism of some novel 2-substituted benzothiazoles as hGSTP1-1 enzyme inhibitors

K Bolelli, Y Musdal, E Aki-Yalcin… - SAR and QSAR in …, 2017 - Taylor & Francis
Human GSTP1-1 is one of the most important proteins, which overexpresses in a large
number of human tumours and is involved in the development of resistance to several …

[PDF][PDF] Possible mechanism of action of neurokinin-1 receptors (NK1R) antagonists

Ö Öztürk, E Aki-Yalcin, T Ertan-Bolelli… - Journal of Pharmacy …, 2017 - academia.edu
Recently, NK1R (Neurokinin-1 receptors) take attention as new and promising target in
anticancer drug development area. It has been proved that non-peptide NK1R antagonists L …