Search Results - "Menard, P R"
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New 4-Point Pharmacophore Method for Molecular Similarity and Diversity Applications: Overview of the Method and Applications, Including a Novel Approach to the Design of Combinatorial Libraries Containing Privileged Substructures
Published in Journal of medicinal chemistry (26-08-1999)“…A new 4-point pharmacophore method for molecular similarity and diversity that rapidly calculates all potential pharmacophores/pharmacophoric shapes for a…”
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Angiotensin-converting enzyme inhibitors: new orally active 1,4-thiazepine-2,5-diones, 1,4-thiazine-2,5-diones, and 1,4-benzothiazepine-2,5-diones possessing antihypertensive activity
Published in Journal of medicinal chemistry (01-05-1986)“…The preparation of a series of 1,4-thiazepine-2,5-diones, 1,4-thiazine-2,5-diones, and 1,4-benzothiazepine-2,5-diones and their ability in inhibiting the…”
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Angiotensin converting enzyme inhibitors. (Mercaptoaroyl)amino acids
Published in Journal of medicinal chemistry (01-03-1985)“…A series of (mercaptoaroyl)amino acids and related compounds was synthesized and tested for ability to inhibit angiotensin converting enzyme (ACE). The most…”
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Chemistry Space Metrics in Diversity Analysis, Library Design, and Compound Selection
Published in Journal of Chemical Information and Computer Sciences (23-11-1998)“…DiverseSolutions software was used to generate a “universal” chemistry space that can be used as a standard for profiling most structural sets of interest. A…”
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Rational Screening Set Design and Compound Selection: Cascaded Clustering
Published in Journal of Chemical Information and Computer Sciences (18-05-1998)“…The use of cascaded clustering is reported. This technique was developed to permit the application of Jarvis-Patrick clustering based on structural…”
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Synthesis and diversity analysis of lead discovery piperazine-2-carboxamide libraries
Published in Molecular diversity (01-01-1998)“…A Lead Discovery Library of piperazine-2-carboxamide derivatives was produced for general screening. This paper discloses two novel solid phase synthetic…”
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Angiotensin converting enzyme inhibitors. 9. Novel [[N-(1-carboxyl-3-phenylpropyl)amino]acyl]glycine derivatives with diuretic activity
Published in Journal of medicinal chemistry (01-06-1990)“…A series of molecules 1 having sulfonamide diuretic moieties covalently linked to non-sulfhydryl angiotensin-converting enzyme inhibitors (ACEI) were prepared…”
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Angiotensin converting enzyme inhibitors. 10. Aryl sulfonamide substituted N-[1-carboxy-3-phenylpropyl]-L-alanyl-L-proline derivatives as novel antihypertensives
Published in Journal of medicinal chemistry (01-06-1990)“…Compounds 1a-g consisting of enalaprilat covalently bonded to aryl sulfonamides, including several known thiazide diuretics, were synthesized and tested for…”
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Angiotensin-converting enzyme inhibitors. 9. Novel ((N-(-carboxy-3-phenylpropyl)-amino)acyl)glycine derivatives with diuretic activity
Published in Journal of medicinal chemistry (01-01-1990)“…A series of molecules 1 having sulfonamide diuretic moieties covalently linked to non-sulfhydryl angiotensin-converting enzyme inhibitors (ACEI) were prepared…”
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Angiotensin converting inhibitors. (Mercaptoaroyl)amino acids
Published in Journal of medicinal chemistry (01-01-1985)“…A series of (mercaptoaroyl)amino acids and related compounds was synthesized and tested for ability to inhibit angiotensin converting enzyme (ACE). The most…”
Get full text
Journal Article