Synthesis, Biological, and Computational Evaluation of Novel 1,3,5-Substituted Indolin-2-one Derivatives as Inhibitors of Src Tyrosine Kinase-Reference-Cited by-同舟云学术

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Synthesis, Biological, and Computational Evaluation of Novel 1,3,5-Substituted Indolin-2-one Derivatives as Inhibitors of Src Tyrosine Kinase

Published:2015-08-11 Issue:10 Volume:348 Page:715-729
ISSN:0365-6233
Container-title:Archiv der Pharmazie
language:en
Short-container-title:Arch. Pharm. Chem. Life Sci.

Author:

Kilic-Kurt Zühal¹,Bakar Filiz²,Ölgen Süreyya¹³

Affiliation:

1. Department of Pharmaceutical Chemistry, Faculty of Pharmacy; Ankara University; Tandogan Ankara Turkey

2. Department of Biochemistry, Faculty of Pharmacy; Ankara University; Tandogan Ankara Turkey

3. Department of Pharmaceutical Chemistry, Faculty of Pharmacy; Istanbul Kemerburgaz University; Bagcılar Istanbul Turkey

Funder

Ankara University

Publisher

Wiley

Subject

Drug Discovery,Pharmaceutical Science

Reference50 articles.

1. Inhibition of Protein Kinase c-Src as a Therapeutic Approach for Cancer and Bone Metastases

2. Novel Insights Into c-Src

3. Role of Src expression and activation in human cancer

4. Mammary tumors expressing the neu proto-oncogene possess elevated c-Src tyrosine kinase activity.

5. Activation Of The Src Family Of Tyrosine Kinases In Mammary Tumorigenesis

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