<i>In vitro</i> cytotoxicity and docking study of novel symmetric and asymmetric dihydropyridines and pyridines as EGFR tyrosine kinase inhibitors-Reference-Cited by-同舟云学术

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In vitro cytotoxicity and docking study of novel symmetric and asymmetric dihydropyridines and pyridines as EGFR tyrosine kinase inhibitors

Published:2022-05-02 Issue:1 Volume:100 Page:121-135
ISSN:1747-0277
Container-title:Chemical Biology & Drug Design
language:en
Short-container-title:Chem Biol Drug Des

Author:

Mansour Basem¹^ORCID,Bayoumi Waleed A.¹²^ORCID,El‐Sayed Magda A.²³,Abouzeid Laila A.¹²,Massoud Mohammed A. M.²

Affiliation:

1. Department of Pharmaceutical Chemistry Faculty of Pharmacy Delta University for Science and Technology Mansoura Egypt

2. Department of Pharmaceutical Organic Chemistry Faculty of Pharmacy Mansoura University Mansoura Egypt

3. Department of Pharmaceutical Chemistry Faculty of Pharmacy Horus University New Damietta Egypt

Publisher

Wiley

Subject

Molecular Medicine,Biochemistry,Drug Discovery,Pharmacology,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cbdd.14058

Reference75 articles.

1. Assessment of the Evolution of Cancer Treatment Therapies

2. Halogen bonds in biological molecules

3. Instability of calcium channel antagonists during sample preparation for LC–MS–MS analysis of serum samples

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5. Discovery of new symmetrical and asymmetrical nitrile-containing 1,4-dihydropyridine derivatives as dual kinases and P-glycoprotein inhibitors: synthesis, in vitro assays, and in silico studies;Journal of Enzyme Inhibition and Medicinal Chemistry;2022-09-12

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