Abstract
The synthesis and SAR of a new class of piperidine-based alphavbeta3/alphavbeta5 integrin antagonists is described. Replacement of an amide bond in a prototype isonipecotamide by a C-C isostere, and adjustment of the spacer length between the carboxylic acid and basic moieties, led to low nanomolar antagonists of alphavbeta3 and/or alphavbeta5 integrins with excellent selectivity versus alpha(IIb)beta3.
MeSH terms
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Administration, Oral
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Animals
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Biological Availability
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Humans
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Integrin alphaVbeta3 / antagonists & inhibitors*
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Integrin alphaVbeta3 / metabolism
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Integrins / antagonists & inhibitors*
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Integrins / metabolism
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Piperidines / chemical synthesis*
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Piperidines / chemistry
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Piperidines / pharmacology
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Propionates / chemical synthesis*
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Propionates / chemistry
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Propionates / pharmacology
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Protein Binding
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Rats
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Receptors, Vitronectin / antagonists & inhibitors*
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Receptors, Vitronectin / metabolism
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Structure-Activity Relationship
Substances
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Integrin alphaVbeta3
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Integrins
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Piperidines
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Propionates
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Receptors, Vitronectin
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integrin alphaVbeta5