Abstract
A series of prolyl-N-isonicotinoyl-(L)-4-aminophenylalanine derivatives substituted at the proline 4-position with cyclic amines was evaluated as VLA-4 antagonists. The ring size and presence or absence of fluorine affected potency and receptor occupancy. The analog with 3,3-difluoropiperidine at the proline 4-position (13) was the most potent compound and had very good duration of receptor occupancy in vitro. The ethyl ester prodrug of 13 demonstrated excellent receptor occupancy after oral dosing in rats.
MeSH terms
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Administration, Oral
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Animals
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Dipeptides / administration & dosage
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Dipeptides / chemical synthesis
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Dipeptides / chemistry*
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Drug Discovery
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Integrin alpha4beta1 / antagonists & inhibitors*
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Integrin alpha4beta1 / metabolism
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Phenylalanine / administration & dosage
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Phenylalanine / analogs & derivatives*
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Phenylalanine / chemical synthesis
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Prodrugs / administration & dosage
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Prodrugs / chemical synthesis
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Prodrugs / chemistry*
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Rats
Substances
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Dipeptides
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Integrin alpha4beta1
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N-(N-((3-cyanobenzene)sulfonyl)-4-(3,3-difluoropiperidin-1-yl)prolyl)-4-((3',5'-dichloroisonicotinoyl)amino)-phenylalanine
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Prodrugs
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Phenylalanine