Search Results - "Denney, Michael L."
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Use of Conformationally Restricted Benzamidines as Arginine Surrogates in the Design of Platelet GPIIb-IIIa Receptor Antagonists
Published in Journal of medicinal chemistry (29-08-1997)“…The use of 5,6-bicyclic amidines as arginine surrogates in the design of a novel class of potent platelet glycoprotein IIb-IIIa receptor (GPIIb-IIIa)…”
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Dibasic benzo[ b]thiophene derivatives as a novel class of active site directed thrombin inhibitors: 4. SAR studies on the conformationally restricted C3-side chain of hydroxybenzo[ b]thiophenes
Published in Bioorganic & medicinal chemistry letters (08-03-1999)“…A novel series of benzo[ b]thiophene diamine thrombin inhibitors with a conformationally restricted C3-side chain 3 was investigated. The constrained C3-side…”
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Diamino benzo[ b]thiophene derivatives as a novel class of active site directed thrombin inhibitors: 3. Enhancing activity by imposing conformational restriction in the C-4″ side chain 1
Published in Bioorganic & medicinal chemistry letters (1999)“…The preparation and biological evaluation of a series of benzo[ b]thiophene diamine thrombin inhibitors possessing conformationally restricted C-4″ linkers are…”
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Diamino benzo[b]thiophene derivatives as a novel class of active site directed thrombin inhibitors : 3. enhancing activity by imposing conformational restriction in the C-4 side chain
Published in Bioorganic & medicinal chemistry letters (08-02-1999)“…The preparation and biological evaluation of a series of benzo[b]thiophene diamine thrombin inhibitors possessing conformationally restricted C-4" linkers are…”
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Platelet glycoprotein IIb–IIIa receptor (GPIIb–IIIa) antagonists derived from amidinoindoles
Published in Bioorganic & medicinal chemistry letters (09-01-1996)“…A series of substituted amidinoindoles have been prepared as mimics of the RGD sequence and were studied as antagonists of the platelet glycoprotein IIb–IIIa…”
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A convenient synthesis of the thieno[3,2-c]pyridine nucleus
Published in Journal of heterocyclic chemistry (01-01-1993)“…The unsubstituted thieno[3,2‐c]pyridine ring system was prepared from thiophene‐3‐carboxaldehyde in 4 steps. The sequence is suitable for scale‐up…”
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