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Synthesis and molecular simulation study of furoic peptidomimetic derivatives as potent aminopeptodase N inhibitors.
- Source :
-
Die Pharmazie [Pharmazie] 2018 Mar 05; Vol. 73 (3), pp. 123-127. - Publication Year :
- 2018
-
Abstract
- The aminopeptidase N (APN) plays a critical role in angiogenesis and is over-expressed in tumor cells. In this paper, we report the synthesis and enzyme inhibition assay of furoic peptidomimetic compounds. These new compounds exhibit potent inhibitory ability toward APN with IC50 values lying in the micromolar level. The binding mode of inhibitors in APN active site was explained by a molecular simulation study. These data reveal that ligand coordinating with the catalytic Zn-ion is very important for inhibitory activities.
- Subjects :
- Animals
Binding Sites drug effects
Catalytic Domain drug effects
Indicators and Reagents
Ligands
Models, Molecular
Molecular Docking Simulation
Protein Binding
Structure-Activity Relationship
Swine
Zinc chemistry
CD13 Antigens antagonists & inhibitors
Enzyme Inhibitors chemical synthesis
Enzyme Inhibitors pharmacology
Peptidomimetics chemical synthesis
Peptidomimetics pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 0031-7144
- Volume :
- 73
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Die Pharmazie
- Publication Type :
- Academic Journal
- Accession number :
- 29544557
- Full Text :
- https://doi.org/10.1691/2018.7911