Synthesis, Antimicrobial and In Silico EGFR Inhibitory Activity Evaluation of Sulfonylamino Pyrrolidine Derivatives


如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅存取

详细

A series of novel sulfonylamino pyrrolidine derivatives were synthesized, characterized and evaluated for their antimicrobial activity. All compounds exhibited moderate activity against the microorganisms tested. The compounds were evaluated in silico for their ability to inhibit epidermal growth factor receptor (EGFR). Docking in silico demonstrated that the sulfonylamino pyrrolidine derivatives represent a new class of EGFR inhibitors and bind at the ATP binding pocket of the tyrosine kinase domain of EGFR. The free energy of binding and inhibition constant (ki) of the docked compounds were evaluated.

作者简介

B. Kumar

Sri Krishnadevaraya University

Email: guruprasadar@yahoo.co.in
印度, Anantapur, A. P.

A. Prasad

Faculty of Science and Technology, ICFAI Foundation for Higher Education

编辑信件的主要联系方式.
Email: guruprasadar@yahoo.co.in
印度, Hyderabad, Telangana

P. Reddy

Sri Krishnadevaraya University

Email: guruprasadar@yahoo.co.in
印度, Anantapur, A. P.

L. Ravindranath

Sri Krishnadevaraya University

Email: guruprasadar@yahoo.co.in
印度, Anantapur, A. P.


版权所有 © Springer Science+Business Media New York, 2016
##common.cookie##