A multifaceted approach for the development of novel Hantzsch 1,4-dihydropyridines as anticancer agents: Rational design, parallel synthesis, analysis, cytotoxicity and EGFR/HER2 inhibition studies-Reference-Cited by-同舟云学术

A multifaceted approach for the development of novel Hantzsch 1,4-dihydropyridines as anticancer agents: Rational design, parallel synthesis, analysis, cytotoxicity and EGFR/HER2 inhibition studies

Published:2024-01 Issue: Volume:7 Page:101413
ISSN:2211-7156
Container-title:Results in Chemistry
language:en
Short-container-title:Results in Chemistry

Author:

Sruthi A.S.V.L.,Faizan Syed^ORCID,Vikram Hemant,Veena N.G.,Susil Aishwarya,Harindranath Haritha,Vasanth Kumar S.,Kumar Shivaraju Vasanth,Prashantha Kumar B.R.

Funder

JSS Academy of Higher Education and Research

Publisher

Elsevier BV

Reference57 articles.

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5. Synthesis of 4-(thiazol-2-ylamino)-benzenesulfonamides with carbonic anhydrase I, II and IX inhibitory activity and cytotoxic effects against breast cancer cell lines;Gawad;Bioorganic & Medicinal Chemistry.,2016

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1. N-Substituted dihydropyridines as promising EGFR tyrosine kinase inhibitors against breast cancer: Design, synthesis, biological evaluation, docking, and molecular dynamics simulations;Results in Chemistry;2024-01