Anticancer potential of indirubins in medicinal chemistry: Biological activity, structural modification, and structure-activity relationship

H Wang, Z Wang, C Wei, J Wang, Y Xu, G Bai… - European Journal of …, 2021 - Elsevier
Indirubin is the crucial ingredient of Danggui Longhui Wan and Qing-Dai, traditional
Chinese medicine herbal formulas used for the therapy of chronic myelocytic leukemia in …

[HTML][HTML] The fundamental role of oxime and oxime ether moieties in improving the physicochemical and anticancer properties of structurally diverse scaffolds

J Fotie, CM Matherne, JB Mather… - International Journal of …, 2023 - mdpi.com
The present review explores the critical role of oxime and oxime ether moieties in enhancing
the physicochemical and anticancer properties of structurally diverse molecular frameworks …

Pinpointing top inhibitors for GSK3β from pool of indirubin derivatives using rigorous computational workflow and their validation using molecular dynamics (MD) …

V Pandya, P Rao, J Prajapati, RM Rawal… - Scientific Reports, 2024 - nature.com
Glycogen synthase kinase-3β (GSK3β) is a pivotal protein kinase implicated in a spectrum of
debilitating diseases, encompassing cancer, diabetes, and neurodegenerative disorders …

Design, synthesis, in vitro and in silico evaluation of anti-colorectal cancer activity of curcumin analogues containing 1, 3-diphenyl-1H-pyrazole targeting EGFR …

NQH Doan, NTK Nguyen, NB Nguyen, TT Tran… - … et Biophysica Acta (BBA …, 2023 - Elsevier
Recent studies have shown that monocarbonyl analogues of curcumin (MACs) and 1H-
pyrazole heterocycle both demonstrated promising anticancer activities, in which several …

Binding of inhibitors to the monomeric and dimeric SARS-CoV-2 Mpro

NM Tam, PC Nam, DT Quang, NT Tung, VV Vu… - RSC …, 2021 - pubs.rsc.org
SARS-CoV-2 rapidly infects millions of people worldwide since December 2019. There is
still no effective treatment for the virus, resulting in the death of more than one million …

Design, synthesis, and evaluation of anti-breast cancer activity of colchicine-combretastatin A-4 analogues containing quinoline as microtubule-targeting agents

NQH Doan, HN Tran, NTM Nguyen… - Journal of Molecular …, 2024 - Elsevier
Research on compounds derived from, or inspired by, natural compounds as novel
anticancer agents has been a significantly focus in recent years. In this study, we reported …

Drug delivery of 6-bromoindirubin-3'-glycerol-oxime ether employing poly(d,l-lactide-co-glycolide)-based nanoencapsulation techniques with sustainable solvents

A Czapka, C Grune, P Schädel, V Bachmann… - Journal of …, 2022 - Springer
Background Insufficient solubility and stability of bioactive small molecules as well as poor
biocompatibility may cause low bioavailability and are common obstacles in drug …

[HTML][HTML] Design, Synthesis, anticancer evaluation and in silico studies of 2, 4, 6-trimethoxychalcone derivatives

T Li, W Li, X Yang, G Chen, X **, W Chen… - Saudi Pharmaceutical …, 2023 - Elsevier
Chalcone, a common chemical scaffold of many naturally occurring compounds, has been
widely used as an effective template for drug discovery due to its broad biological activities …

Target design of novel histone deacetylase 6 selective inhibitors with 2-mercaptoquinazolinone as the cap moiety

HTB Bui, PH Nguyen, QM Pham, HP Tran, DQ Tran… - Molecules, 2022 - mdpi.com
Epigenetic alterations found in all human cancers are promising targets for anticancer
therapy. In this sense, histone deacetylase inhibitors (HDACIs) are interesting anticancer …

[HTML][HTML] 1, 5-Benzothiazepine Derivatives: Green synthesis, in silico and in vitro evaluation as anticancer agents

M Haroun, SS Chobe, RR Alavala, SM Mathure… - Molecules, 2022 - mdpi.com
Considering the importance of benzothiazepine pharmacophore, an attempt was carried out
to synthesize novel 1, 5-benzothiazepine derivatives using polyethylene glycol-400 (PEG …