N-substituted 2′-(aminoaryl)benzothiazoles as kinase inhibitors: Hit identification and scaffold hopping-Reference-Cited by-同舟云学术

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N-substituted 2′-(aminoaryl)benzothiazoles as kinase inhibitors: Hit identification and scaffold hopping

Published:2009-03 Issue:5 Volume:19 Page:1349-1356
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Tasler Stefan,Müller Oliver,Wieber Tanja,Herz Thomas,Krauss Rolf,Totzke Frank,Kubbutat Michael H.G.,Schächtele Christoph

Publisher

Elsevier BV

Subject

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

Reference56 articles.

1. Oncogenic kinase signalling

2. Cellular Targets for Anticancer Strategies

3. The ErbB Receptors and their Ligands in Cancer: An Overview

4. Drugging Cell Cycle Kinases in Cancer Therapy

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