Identification of an Indazole-Based Pharmacophore for the Inhibition of FGFR Kinases Using Fragment-Led de Novo Design.

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Identification of an Indazole-Based Pharmacophore for the Inhibition of FGFR Kinases Using Fragment-Led de Novo Design.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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name

Identification of an Indazole- ...... g Fragment-Led de Novo Design.

@en

Identification of an Indazole- ...... g Fragment-Led de Novo Design.

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type

Item

label

Identification of an Indazole- ...... g Fragment-Led de Novo Design.

@en

Identification of an Indazole- ...... g Fragment-Led de Novo Design.

@nl

prefLabel

Identification of an Indazole- ...... g Fragment-Led de Novo Design.

@en

Identification of an Indazole- ...... g Fragment-Led de Novo Design.

@nl

P1154

2-s2.0-85038407720

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P1433

ACS Medicinal Chemistry Letters

P1476

Identification of an Indazole- ...... ng Fragment-Led de Novo Design

@en

P2093

Abbey J Summers

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Laura O Johnson

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Lewis D Turner

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Margaret A Knowles

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P2860

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Design, synthesis and biological evaluation of novel FGFR inhibitors bearing an indazole scaffold

Protein structure-based de novo design and synthesis of aldose reductase inhibitors.

FGFR3 protein expression and its relationship to mutation status and prognostic variables in bladder cancer

Structure-based discovery of antibacterial drugs.

The Fibroblast Growth Factor signaling pathway

Recent advances in de novo design strategy for practical lead identification.

Fibroblast growth factor receptor 1 promotes proliferation and survival via activation of the mitogen-activated protein kinase pathway in bladder cancer.

A Decade of FGF Receptor Research in Bladder Cancer: Past, Present, and Future Challenges.

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1264-1268

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scholarly article

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10.1021/ACSMEDCHEMLETT.7B00349

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Colin W G Fishwick

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28838399

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2017-11-11T00:00:00Z

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1092650838

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29259745

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5733262

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125729/