Design and synthesis of isoquinolines and benzimidazoles as RAF kinase inhibitors-Reference-Cited by-同舟云学术

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Design and synthesis of isoquinolines and benzimidazoles as RAF kinase inhibitors

Published:2011-04 Issue:8 Volume:21 Page:2264-2269
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Buchstaller Hans-Peter,Burgdorf Lars,Finsinger Dirk,Stieber Frank,Sirrenberg Christian,Amendt Christiane,Grell Matthias,Zenke Frank,Krier Mireille

Publisher

Elsevier BV

Subject

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

Reference38 articles.

1. Protein Kinase A Blocks Raf-1 Activity by Stimulating 14-3-3 Binding and Blocking Raf-1 Interaction with Ras

2. The RAF proteins take centre stage

3. Targets for Cancer Chemotherapy Transcription Factors and Other Nuclear Proteins;Chiloeches,2002

4. Mitogenic signaling of Ras is regulated by differential interaction with Raf isozymes

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1. Recent development of multi-target VEGFR-2 inhibitors for the cancer therapy;Bioorganic Chemistry;2023-04

2. Ferroptosis‐modulating small molecules for targeting drug‐resistant cancer: Challenges and opportunities in manipulating redox signaling;Medicinal Research Reviews;2023-01-19

3. Synthesis of esters and amides of 2-aryl-1-hydroxy-4-methyl-1H-imidazole-5-carboxylic acids and study of their antiviral activity against orthopoxviruses;Bioorganic & Medicinal Chemistry Letters;2023-01

4. Design, synthesis and anticancer activity of novel 2-arylbenzimidazole/2-thiopyrimidines and 2-thioquinazolin-4(3H)-ones conjugates as targeted RAF and VEGFR-2 kinases inhibitors;Bioorganic Chemistry;2022-09

5. Benzimidazole‐based protein kinase inhibitors: Current perspectives in targeted cancer therapy;Chemical Biology & Drug Design;2022-08-19

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