Abstract
The synthesis of a series of proline derivatives (1a-e and 2a-b) as pure isomers is described. These compounds were evaluated in vitro for their ability to inhibit angiotensin converting enzyme (ACE) and compared to the potency of captopril taken as a reference drug. They showed only a weak ACE inhibitory activity.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Angiotensin-Converting Enzyme Inhibitors / chemistry*
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Angiotensin-Converting Enzyme Inhibitors / pharmacology
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Molecular Structure
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Oligopeptides / metabolism
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Proline / analogs & derivatives*
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Proline / pharmacology
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Structure-Activity Relationship
Substances
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Angiotensin-Converting Enzyme Inhibitors
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Oligopeptides
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hippuryl-histidyl-leucine
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Proline