Biologically Driven Synthesis of Pyrazolo[3,4-d]pyrimidines As Protein Kinase Inhibitors: An Old Scaffold As a New Tool for Medicinal Chemistry and Chemical Biology Studies-Reference-Cited by-同舟云学术

Biologically Driven Synthesis of Pyrazolo[3,4-d]pyrimidines As Protein Kinase Inhibitors: An Old Scaffold As a New Tool for Medicinal Chemistry and Chemical Biology Studies

Published:2014-05-29 Issue:14 Volume:114 Page:7189-7238
ISSN:0009-2665
Container-title:Chemical Reviews
language:en
Short-container-title:Chem. Rev.

Author:

Schenone Silvia¹,Radi Marco²,Musumeci Francesca¹,Brullo Chiara¹,Botta Maurizio³⁴

Affiliation:

1. Dipartimento di Farmacia, Università degli Studi di Genova Viale Benedetto XV, 3, 16132 Genova, Italy

2. Dipartimento di Farmacia, Università degli Studi di Parma Viale delle Scienze, 27/A, 43124 Parma, Italy

3. Dipartimento di Biotecnologie, Chimica e Farmacia, Università degli Studi di Siena Via Aldo Moro, 2, 53100 Siena, Italy

4. Sbarro Institute for Cancer Research and Molecular Medicine, Center for Biotechnology, College of Science and Technology, Temple University, BioLife Science Building, Suite 333, 1900 N 12th Street, Philadelphia, Pennsylvania 19122, United States

Publisher

American Chemical Society (ACS)

Subject

General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/cr400270z

Reference251 articles.

1. Evidence for a Negative-Feedback Mechanism in the Biosynthesis of Isoleucine

2. Potential Purine Antagonists. I. Synthesis of Some 4,6-Substituted Pyrazolo [3,4-d] pyrimidines1

3. Potential Purine Antagonists. VI. Synthesis of 1-Alkyl- and 1-Aryl-4-substituted Pyrazolo[3,4-d]pyrimidines1,2

4. Katritzky, A. R.; Rees, C. W.Comprehensive Heterocyclic Chemistry;Pergamon Press:New York, 1984; Vol.5, p278.

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