Discovery of octahydropyrrolo [3,2‐b] pyridin derivative as a highly selective Type I inhibitor of FGFR3 over VEGFR2 by high‐throughput virtual screening-Reference-Cited by-同舟云学术

Discovery of octahydropyrrolo [3,2‐b] pyridin derivative as a highly selective Type I inhibitor of FGFR3 over VEGFR2 by high‐throughput virtual screening

Published:2022-12-11 Issue:2 Volume:124 Page:221-238
ISSN:0730-2312
Container-title:Journal of Cellular Biochemistry
language:en
Short-container-title:J of Cellular Biochemistry

Author:

Wang Xin¹,Ye Cheng‐hao¹,Li En‐min²,Xu Li‐yan²,Lin Wang‐qiang¹,Chen Guang‐hui¹^ORCID

Affiliation:

1. Department of Chemistry Shantou University Shantou China

2. Medical Informatics Research Center Shantou University Medical College Shantou China

Publisher

Wiley

Subject

Cell Biology,Molecular Biology,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcb.30357

Reference67 articles.

1. Targeting FGFR pathway in breast cancer

2. Roles of Fibroblast Growth Factor Receptors in Carcinogenesis

3. Fibroblast growth factor signalling: from development to cancer

4. Structure-based drug design of 1,3,5-triazine and pyrimidine derivatives as novel FGFR3 inhibitors with high selectivity over VEGFR2

5. In search of novel inhibitors of anti-cancer drug target fibroblast growth factor receptors: Insights from virtual screening, molecular docking, and molecular dynamics

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