Design of fructose-2,6-bisphosphatase inhibitors: A novel virtual screening approach
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Computer Graphics and Computer-Aided Design,Physical and Theoretical Chemistry,Spectroscopy
Reference54 articles.
1. Overexpression of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase in mouse liver lowers blood glucose by suppressing hepatic glucose production
2. Overexpression of fructose 2,6-bisphosphatase decreases glycolysis and delays cell cycle progression
3. Mechanism of activation of fructose-2,6-bisphosphatase by cAMP-dependent protein kinase.
4. An enzyme that catalyzes hydrolysis of fructose-2,6-bisphosphate
5. Purification and Characterization of a Novel Xylulose 5-Phosphate-activated Protein Phosphatase Catalyzing Dephosphorylation of Fructose-6-phosphate,2-kinase:Fructose-2,6-bisphosphatase
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2. The Discovery of Potentially Selective Human Neuronal Nitric Oxide Synthase (nNOS) Inhibitors: A Combination of Pharmacophore Modelling, CoMFA, Virtual Screening and Molecular Docking Studies;International Journal of Molecular Sciences;2014-05-14
3. Ligand-based designing, in silico screening, and biological evaluation of new potent fructose-1,6-bisphosphatase (FBPase) inhibitors;European Journal of Medicinal Chemistry;2012-10
4. Discovery of Heterocyclic Phosphonic Acids as Novelampmimics that are Potent and Selective Fructose-1,6-Bisphosphatase Inhibitors and Elicit Potent Glucose-Lowering Effects in Diabetic Animals and Humans;Case Studies in Modern Drug Discovery and Development;2012-05-21
5. Oxazole phosphonic acids as fructose 1,6-bisphosphatase inhibitors with potent glucose-lowering activity;MedChemComm;2011
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