Dual Targeting of VEGFR2 and C-Met Kinases via the Design and Synthesis of Substituted 3-(Triazolo-thiadiazin-3-yl)indolin-2-one Derivatives as Angiogenesis Inhibitors-Reference-Cited by-同舟云学术

Dual Targeting of VEGFR2 and C-Met Kinases via the Design and Synthesis of Substituted 3-(Triazolo-thiadiazin-3-yl)indolin-2-one Derivatives as Angiogenesis Inhibitors

Published:2020-07-24 Issue:30 Volume:5 Page:18872-18886
ISSN:2470-1343
Container-title:ACS Omega
language:en
Short-container-title:ACS Omega

Author:

Mohamady Samy¹^ORCID,Galal Mahmoud²,Eldehna Wagdy M.³,Gutierrez David C.⁴,Ibrahim Hany S.⁵,Elmazar Mohey M.⁶,Ali Hamed I.⁴^ORCID

Affiliation:

1. Department of Pharmaceutical Chemistry, Faculty of Pharmacy, The British University in Egypt (BUE), El Sherouk City, Cairo 11837, Egypt

2. Department of Pharmacology, Faculty of Pharmacy, Helwan University, Helwan, Cairo, Egypt

3. Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Kafrelsheikh University, P.O. Box 33516, Kafrelsheikh, Egypt

4. Department of Pharmaceutical Sciences, Rangel College of Pharmacy, Health Science Center, Texas A&M University, Kingsville, Kingsville, Texas 78363, United States

5. Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Egyptian Russian University, Badr City, Cairo 11829, Egypt

6. Department of Pharmacology and Biochemistry, Faculty of Pharmacy, The British University in Egypt (BUE), El Sherouk City, Cairo 11837, Egypt

Funder

Texas A and M University

British University in Egypt

Publisher

American Chemical Society (ACS)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acsomega.0c02038

Reference59 articles.