Synthesis and evaluation of heteroaryl substituted diazaspirocycles as scaffolds to probe the ATP-binding site of protein kinases-Reference-Cited by-同舟云学术

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Synthesis and evaluation of heteroaryl substituted diazaspirocycles as scaffolds to probe the ATP-binding site of protein kinases

Published:2013-09 Issue:18 Volume:21 Page:5707-5724
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Allen Charlotte E.,Chow Chiau L.,Caldwell John J.,Westwood Isaac M.,M. van Montfort Rob L.,Collins Ian

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference48 articles.

1. The Protein Kinase Complement of the Human Genome

2. Oncogenic kinase signalling

3. Hallmarks of Cancer: The Next Generation

4. Design and Development of Signal Transduction Inhibitors for Cancer Treatment: Experience and Challenges with Kinase Targets

5. Targeting the Human Kinome for Cancer Therapy: Current Perspectives

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2. Design and synthesis of novel 1,3,4‐oxadiazole based azaspirocycles catalyzed by NaI under mild condition and evaluated their antidiabetic and antibacterial activities;Journal of Heterocyclic Chemistry;2020-12-10

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4. 6-Substituted purines as ROCK inhibitors with anti-metastatic activity;Bioorganic Chemistry;2019-09

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