2-Aminobenzothiazoles in anticancer drug design and discovery

G Huang, T Cierpicki, J Grembecka - Bioorganic chemistry, 2023 - Elsevier
Cancer is one of the major causes of mortality and morbidity worldwide. Substantial
research efforts have been made to develop new chemical entities with improved anticancer …

Significance of five-membered heterocycles in human histone deacetylase inhibitors

A Frühauf, M Behringer, FJ Meyer-Almes - Molecules, 2023 - mdpi.com
Five-membered heteroaromatic rings, in particular, have gained prominence in medicinal
chemistry as they offer enhanced metabolic stability, solubility and bioavailability, crucial …

Current status and future prospects of molecular hybrids with thiazolidinedione (TZD) scaffold in anticancer drug discovery

K Tilekar, O Shelke, N Upadhyay, A Lavecchia… - Journal of Molecular …, 2022 - Elsevier
Thiazolidinedione (TZD) containing derivatives have been proved to be promising
anticancer agents in preclinical and clinical evaluation phases. Hybrid molecules not just …

Mechanistic insights into binding of ligands with thiazolidinedione warhead to human histone deacetylase 4

M Schweipert, N Jänsch, N Upadhyay, K Tilekar… - Pharmaceuticals, 2021 - mdpi.com
Recently, we have reported that non-hydroxamate thiazolidinedione (TZD) analogs are
capable of inhibiting human deacetylase 4 (HDAC4). This study aims at the dissection of the …

Discovery of New 2-Phenylamino-3-acyl-1, 4-naphthoquinones as Inhibitors of Cancer Cells Proliferation: Searching for Intra-Cellular Targets Playing a Role in …

J Benites, JA Valderrama, Á Contreras, C Enríquez… - Molecules, 2023 - mdpi.com
A series of 2-phenylamino-3-acyl-1, 4-naphtoquinones were evaluated regarding their in
vitro antiproliferative activities using DU-145, MCF-7 and T24 cancer cells. Such activities …

Phenolic compounds as histone deacetylase inhibitors: binding propensity and interaction insights from molecular docking and dynamics simulations

AI Uba, G Zengin - Amino Acids, 2023 - Springer
Histone deacetylases are well-established target enzymes involved in the pathology of
different diseases including cancer and neurodegenerative disorders. The approved HDAC …

Design, in silico studies, synthesis, and in vitro anticancer assessment of new naphthylidene isoxazolidinedione derivatives

N Upadhyay, K Tilekar, A Oak… - Vietnam Journal of …, 2024 - Wiley Online Library
Cancer is the most destructive and fatal disease, representing an urgent medical challenge
to the world. The discovery of a new anticancer candidate may help reduce or eliminate this …

Recent review on selective histone deacetylase inhibitors in cancer therapy

A El-hameed, I Aya, MFA Mohamed… - Octahedron Drug …, 2024 - odr.journals.ekb.eg
Cancer is the most serious disease afflicting humans and a primary cause of death on a
global scale. Chemotherapy continues to be one of the most essential cancer treatments, in …

Histone deacetylase 4 (HDAC4), an epigenetic target for spinal muscular atrophy

N Tomašević - Biologia Serbica, 2023 - ojs.pmf.uns.ac.rs
Spinal muscular atrophy, a neurodegenerative recessive disease, is one of the leading
genetic causes of death in early infancy and childhood worldwide, having an etiology in a …

Synthesis of Polyamino-Carboxylate Scaffolds for Biological and Biomedical Applications

JB Concepcion - 2023 - search.proquest.com
Noninvasive techniques for disease imaging and targeted therapy allow for personalized
treatment regimens. Radiometal-based imaging and therapeutic agents are expanding due …