Design of novel SHP2 inhibitors using Topomer CoMFA, HQSAR analysis, and molecular docking-Reference-Cited by-同舟云学术

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Design of novel SHP2 inhibitors using Topomer CoMFA, HQSAR analysis, and molecular docking

Published:2020-11-24 Issue:3 Volume:32 Page:1061-1076
ISSN:1040-0400
Container-title:Structural Chemistry
language:en
Short-container-title:Struct Chem

Author:

Tong Jian-Bo,Luo Ding,Zhang Xing,Bian Shuai

Funder

National Natural Science Foundation of China

Natural Science Foundation of Shaanxi Province

Shaanxi University of Science and Technology

Publisher

Springer Science and Business Media LLC

Subject

Physical and Theoretical Chemistry,Condensed Matter Physics

Link

https://link.springer.com/content/pdf/10.1007/s11224-020-01677-8.pdf

Reference38 articles.

1. Frankson R, Yu Z-H, Bai Y, Li Q, Zhang R-Y, Zhang Z-Y (2017) Therapeutic targeting of oncogenic tyrosine phosphatases. Cancer Res 77:5701–5705

2. Barford D, Neel BG (1998) Revealing mechanisms for SH2 domain mediated regulation of the protein tyrosine phosphatase SHP-2. Structure 6:249–254

3. Hui E, Cheung J, Zhu J, Su X, Taylor MJ, Wallweber HA et al (2017) T cell costimulatory receptor CD28 is a primary target for PD-1-mediated inhibition. Science (80-) 355:1428-+

4. Pluskey S, Wandless TJ, Walsh CT, Shoelson SE (1995) Potent stimulation of SH-PTP2 phosphatase activity by simultaneous occupancy of both SH2 domains. J Biol Chem 270:2897–2900

5. Tartaglia M, Mehler EL, Goldberg R, Zampino G, Brunner HG, Kremer H et al (2001) Correction: mutations in the protein tyrosine kinase gene, PTPN11, cause Noonan syndrome. Nat Genet 29:491–491

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