The marine-derived pachycladin diterpenoids as novel inhibitors of wild-type and mutant EGFR-Reference-Cited by-同舟云学术

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The marine-derived pachycladin diterpenoids as novel inhibitors of wild-type and mutant EGFR

Published:2017-02 Issue: Volume:126 Page:51-68
ISSN:0006-2952
Container-title:Biochemical Pharmacology
language:en
Short-container-title:Biochemical Pharmacology

Author:

Mohyeldin Mohamed M.,Akl Mohamed R.,Siddique Abu Bakar,Hassan Hossam M.,El Sayed Khalid A.

Funder

National Cancer Institute of the National Institutes of Health

Publisher

Elsevier BV

Subject

Pharmacology,Biochemistry

Reference57 articles.

1. Epidermal growth factor receptor tyrosine kinase inhibitors: Current status and future perspectives in the development of novel irreversible inhibitors for the treatment of mutant non-small cell lung cancer;Galvani;Curr. Pharm. Des.,2013

2. Mechanisms of resistance to EGFR tyrosine kinase inhibitors;Huang;Acta Pharm. Sin. B,2015

3. Structure and clinical relevance of the epidermal growth factor receptor in human cancer;Kumar;J. Clin. Oncol.,2008

4. The ErbB/HER family of protein-tyrosine kinases and cancer;Roskoski;Pharmacol. Res.,2014

5. Second-generation irreversible epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs): a better mousetrap? A review of the clinical evidence;Ou;Crit. Rev. Oncol./Hematol.,2012

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