Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/54569
Title: Design, synthesis, computational and biological evaluation of novel hydroxamic and carboxylic acid derivatives as histone decaetylase inhibitors
Authors: Gharia, Bhavini
Suhagia, Bhanubhai N
Upadhyay, Jagatkumar
Champaneria, Richa
Lodha, Sandesh
Shah, Shailesh A
Keywords: Hydroxamic acid derivatives;Carboxylic acid derivatives;Anticancer agents;1,3,4-thiadiazoles;Computational study
Issue Date: May-2020
Publisher: NISCAIR-CSIR, India
Abstract: One of the recent targets is histone deacetylase (HDAC) which provide a very promising new approach for anticancer drugs, which may combine clinical efficacy with relatively mild toxicological side effects. Modification of histone acetylation level, promoted by histone acetylase (HAT) and HDAC enzyme, has been recognize to play an important role in epigenetic modulation of gene expression, so HDAC inhibitors are considered a new class of anticancer agents. A new series of hydroxamic and carboxylic acid analogues based on the 1,3,4-thiadiazole scaffold has been designed and synthesized with the aim of exploring its potential as new antitumor agents. Biological results have revealed that the structural modifications proposed significantly affected inhibitory potency as well as selectivity for HDAC inhibitors. Most target compounds are significantly more active, specifically 5a, 5b, 5e with IC50 values in the low micromolar or, the most active compounds in the series. Selected compounds have been tested on the viability of MDA-MB-231 (breast cancer cell) and K562 (chronic myelogenous leukemia cell), A549 (human lung cancer), PC3 (Prostate cancer cell lines) using MTT assay. Docking simulations suggested that the most active compounds can recognize the binding site (PDB Code 1w22 reference compound) using a similar interactions network. These results have allowed us to rationalize the observed structure–activity relationships.
Page(s): 690-699
URI: http://nopr.niscair.res.in/handle/123456789/54569
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.59B(05) [May 2020]

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