Discovery of novel dual VEGFR2 and Src inhibitors using a multistep virtual screening approach.

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Discovery of novel dual VEGFR2 and Src inhibitors using a multistep virtual screening approach.

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

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Discovery of novel dual VEGFR2 ...... ep virtual screening approach.

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Discovery of novel dual VEGFR2 ...... ep virtual screening approach.

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Discovery of novel dual VEGFR2 ...... ep virtual screening approach.

@ast

Discovery of novel dual VEGFR2 ...... ep virtual screening approach.

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Discovery of novel dual VEGFR2 ...... ep virtual screening approach.

@ast

Discovery of novel dual VEGFR2 ...... ep virtual screening approach.

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P1476

Discovery of novel dual VEGFR2 ...... ep virtual screening approach.

@en

P2093

Cheng Zhang

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Chu Qin

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Chun Mei Gao

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Jia En Sin

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Lin Tao

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Peng Zhang

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Shangying Chen

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Wai Keung Chui

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Xian Zeng

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Xuan Yang

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Equally Potent Inhibition of c-Src and Abl by Compounds that Recognize Inactive Kinase Conformations

Protein tyrosine kinase structure and function

Surflex: fully automatic flexible molecular docking using a molecular similarity-based search engine

ChEMBL web services: streamlining access to drug discovery data and utilities

Virtual exploration of the chemical universe up to 11 atoms of C, N, O, F: assembly of 26.4 million structures (110.9 million stereoisomers) and analysis for new ring systems, stereochemistry, physicochemical properties, compound classes, and drug d

Drug resistance by evasion of antiangiogenic targeting of VEGF signaling in late-stage pancreatic islet tumors

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7-24

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P31

scholarly article

P356

10.4155/FMC-2016-0162

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P433

http://www.w3.org/2001/XMLSchema#string

P478

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P50

Yu Zong Chen

P577

2016-12-20T00:00:00Z

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P698

27995811

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