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1-Aminomethylisoquinoline-4-carboxylates as novel dipeptidylpeptidase IV inhibitors
- Source :
- Bioorganic & Medicinal Chemistry Letters. 10:1555-1558
- Publication Year :
- 2000
- Publisher :
- Elsevier BV, 2000.
-
Abstract
- Structure–activity relationship within a series of 1-aminoalkylisoquinoline-4-carboxylates as inhibitors of DPP-IV is described. A primary aminomethyl group is required to maintain biological activity. Substitution of the isoquinoline at the 6- and 8-positions with methoxy groups increases potency to 53 times that of the lead compound SDZ 029-576.
- Subjects :
- Stereochemistry
Dipeptidyl Peptidase 4
Clinical Biochemistry
Carboxylic Acids
Pharmaceutical Science
Biochemistry
Chemical synthesis
Structure-Activity Relationship
chemistry.chemical_compound
Drug Discovery
Tumor Cells, Cultured
Humans
Potency
Protease Inhibitors
Isoquinoline
Molecular Biology
chemistry.chemical_classification
Molecular Structure
Bicyclic molecule
biology
Organic Chemistry
Biological activity
Isoquinolines
Kinetics
Enzyme
chemistry
Enzyme inhibitor
Colonic Neoplasms
biology.protein
Molecular Medicine
Indicators and Reagents
Lead compound
Subjects
Details
- ISSN :
- 0960894X
- Volume :
- 10
- Database :
- OpenAIRE
- Journal :
- Bioorganic & Medicinal Chemistry Letters
- Accession number :
- edsair.doi.dedup.....56b2bdedfd819bd475630e43c7617ef9
- Full Text :
- https://doi.org/10.1016/s0960-894x(00)00286-9