Abstract
Use of a chlorophenoxyacetamide P1 group with a pyridinone acetamide P2/P3 gave an exceptionally potent thrombin inhibitor (K(i)=40 pM). Truncation of the molecule at the N-terminus gave unique, low nanomolar, non-covalent thrombin inhibitors which do not have a group to fill thrombin's 'distal binding pocket'. A co-crystal structure indicates the importance of an intramolecular hydrogen bond between the P1 side chain and P1/P2 amide link in this series.
MeSH terms
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Acetamides / chemical synthesis*
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Acetamides / pharmacology*
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Binding Sites
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Crystallization
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Crystallography, X-Ray
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Enzyme Inhibitors / chemical synthesis*
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Enzyme Inhibitors / chemistry
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Enzyme Inhibitors / pharmacology*
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Humans
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Models, Molecular
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Molecular Conformation
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Pyridones / chemical synthesis*
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Pyridones / pharmacology*
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Thrombin / antagonists & inhibitors*
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Thrombin / chemistry
Substances
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Acetamides
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Enzyme Inhibitors
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Pyridones
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Thrombin