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Discovery, SAR and X-ray structure of 1H-benzimidazole-5-carboxylic acid cyclohexyl-methyl-amides as inhibitors of inducible T-cell kinase (Itk)
- Source :
- Bioorganic & Medicinal Chemistry Letters. 18:5545-5549
- Publication Year :
- 2008
- Publisher :
- Elsevier BV, 2008.
-
Abstract
- A series of novel potent benzimidazole based inhibitors of interleukin-2 T-cell kinase (Itk) were prepared. In this report, we discuss the structure-activity relationship (SAR), selectivity, and cell-based activity for the series. We also discuss the SAR associated with an X-ray structure of one of the small-molecule inhibitors bound to ITK.
- Subjects :
- Benzimidazole
Molecular model
medicine.drug_class
Stereochemistry
Chemistry, Pharmaceutical
Carboxylic acid
Clinical Biochemistry
Carboxylic Acids
Molecular Conformation
Pharmaceutical Science
Carboxamide
Crystallography, X-Ray
Biochemistry
Chemical synthesis
Inhibitory Concentration 50
Mice
Structure-Activity Relationship
chemistry.chemical_compound
Drug Discovery
medicine
Animals
Enzyme Inhibitors
skin and connective tissue diseases
Molecular Biology
chemistry.chemical_classification
biology
Bicyclic molecule
Kinase
fungi
Organic Chemistry
Protein-Tyrosine Kinases
Amides
body regions
Models, Chemical
chemistry
Enzyme inhibitor
Drug Design
Microsomes, Liver
biology.protein
Molecular Medicine
Benzimidazoles
Subjects
Details
- ISSN :
- 0960894X
- Volume :
- 18
- Database :
- OpenAIRE
- Journal :
- Bioorganic & Medicinal Chemistry Letters
- Accession number :
- edsair.doi.dedup.....77216c0a135ce0c04945949b146cd09c
- Full Text :
- https://doi.org/10.1016/j.bmcl.2008.09.015