Novel pyrazolo[1,5-a]pyridines as PI3K inhibitors: variation of the central linker group-Reference-Cited by-同舟云学术

Novel pyrazolo[1,5-a]pyridines as PI3K inhibitors: variation of the central linker group

Published:2014 Issue:1 Volume:5 Page:41-46
ISSN:2040-2503
Container-title:Med. Chem. Commun.
language:en
Short-container-title:Med. Chem. Commun.

Author:

Kendall Jackie D.,Marshall Andrew J.,Giddens Anna C.,Tsang Kit Yee,Boyd Maruta,Frédérick Raphaël,Lill Claire L.,Lee Woo-Jeong,Kolekar Sharada,Chao Mindy,Malik Alisha,Yu Shuqiao,Chaussade Claire,Buchanan Christina M.,Rewcastle Gordon W.,Baguley Bruce C.,Flanagan Jack U.,Denny William A.,Shepherd Peter R.

Publisher

Royal Society of Chemistry (RSC)

Subject

Pharmaceutical Science,Biochemistry,Drug Discovery,Molecular Medicine,Pharmacology,Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/MD/C3MD00221G

Reference20 articles.

1. Progress in the Design and Development of Phosphoinositide 3-Kinase (PI3K) Inhibitors for the Treatment of Chronic Diseases

2. PTEN loss in the continuum of common cancers, rare syndromes and mouse models

3. Functional differences between two classes of oncogenic mutation in the PIK3CA gene

4. Development of Phosphoinositide-3 Kinase Pathway Inhibitors for Advanced Cancer

5. Targeting the phosphoinositide 3-kinase pathway in cancer

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