Abstract
4-(1,3-Benzothiazol-2-yl)thiophene-2-sulfonamide (4a) was found to be a moderately potent inhibitor of cyclin-dependent kinase 5 (cdk5) from a HTS screen. The synthesis and SAR around this hit is described. The X-ray coordinates of ligand 4a with cdk5 are also reported, showing an unusual binding mode to the hinge region via a water molecule.
Copyright © 2012 Elsevier Ltd. All rights reserved.
MeSH terms
-
Crystallography, X-Ray
-
Cyclin-Dependent Kinase 5 / antagonists & inhibitors*
-
Cyclin-Dependent Kinase 5 / metabolism
-
Dose-Response Relationship, Drug
-
Models, Molecular
-
Molecular Structure
-
Nerve Tissue Proteins / antagonists & inhibitors*
-
Nerve Tissue Proteins / metabolism
-
Protein Kinase Inhibitors / chemical synthesis*
-
Protein Kinase Inhibitors / chemistry
-
Protein Kinase Inhibitors / pharmacology*
-
Structure-Activity Relationship
-
Sulfonamides / chemical synthesis
-
Sulfonamides / chemistry*
-
Sulfonamides / pharmacology*
-
Thiophenes / chemical synthesis
-
Thiophenes / chemistry*
-
Thiophenes / pharmacology*
Substances
-
4-(1,3-benzothiazol-2-yl)thiophene-2-sulfonamide
-
Nerve Tissue Proteins
-
Protein Kinase Inhibitors
-
Sulfonamides
-
Thiophenes
-
neuronal Cdk5 activator (p25-p35)
-
Cyclin-Dependent Kinase 5