Inhibitor repurposing reveals ALK, LTK, FGFR, RET and TRK kinases as the targets of AZD1480-Reference-Cited by-同舟云学术

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Inhibitor repurposing reveals ALK, LTK, FGFR, RET and TRK kinases as the targets of AZD1480

Published:2017-11-27 Issue:65 Volume:8 Page:109319-109331
ISSN:1949-2553
Container-title:Oncotarget
language:en
Short-container-title:Oncotarget

Author:

Gudernova Iva¹,Balek Lukas¹,Varecha Miroslav¹²,Kucerova Jana Fialova¹,Kunova Bosakova Michaela¹,Fafilek Bohumil¹²,Palusova Veronika¹,Uldrijan Stjepan¹²,Trantirek Lukas³,Krejci Pavel¹²

Affiliation:

1. Department of Biology, Faculty of Medicine, 62500 Brno, Czech Republic

2. International Clinical Research Center, St. Anne’s University Hospital, 65691 Brno, Czech Republic

3. Central European Institute of Technology, Masaryk University, 62500 Brno, Czech Republic

Publisher

Impact Journals, LLC

Subject

Oncology

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Discovery of 9H-pyrimido[4,5-b]indole derivatives as dual RET/TRKA inhibitors;Bioorganic & Medicinal Chemistry;2024-05

2. The Application of Artificial Intelligence and Drug Repositioning for the Identification of Fibroblast Growth Factor Receptor Inhibitors: A Review;Advanced Biomedical Research;2024-01

3. 3-hydroxy-3-(1H-indol-3-yl)-5-nitrooxindole and derivative;AIP Conference Proceedings;2024

4. Anti-Tumor Activity of AZD4547 Against NTRK1 Fusion Positive Cancer Cells Through Inhibition of NTRKs;Frontiers in Oncology;2021-11-01

5. Pyrazoloadenine Inhibitors of the RET Lung Cancer Oncoprotein Discovered by a Fragment Optimization Approach;ChemMedChem;2021-03-08

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