Abstract
Probing with tool molecules, and by modeling and X-ray crystallography the binding modes of two structurally distinct series of DPP-4 inhibitors led to the discovery of a rare aromatic fluorine H-bond and the spatial requirement for better biaryl binding in the DPP-4 enzyme active site. These newly found binding elements were successfully incorporated into novel DPP-4 inhibitors.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Binding Sites
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Chemistry, Pharmaceutical / methods
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Crystallography, X-Ray / methods
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Dipeptidyl Peptidase 4 / chemistry*
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Dipeptidyl-Peptidase IV Inhibitors
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Drug Design
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Fluorine / chemistry
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Glycine / chemistry
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Humans
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Hydrogen Bonding
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Inhibitory Concentration 50
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Models, Chemical
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Models, Theoretical
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Molecular Conformation
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Software
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beta-Alanine / chemistry
Substances
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Dipeptidyl-Peptidase IV Inhibitors
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beta-Alanine
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Fluorine
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DPP4 protein, human
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Dipeptidyl Peptidase 4
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Glycine