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Bioorganic & Medicinal Chemistry Letters|April 14, 1999
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]thiophenesK Takeuchi, T J Kohn, D J Sall, et al.Bioorganic & Medicinal Chemistry Letters|March 26, 1999
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 chainJ A Bastian, N Chirgadze, M L Denney, et al.Journal of Medicinal Chemistry|October 27, 1995
Structure-activity study of tripeptide thrombin inhibitors using alpha-alkyl amino acids and other conformationally constrained amino acid substitutionsR T Shuman, R B Rothenberger, C S Campbell, et al.Contemporary Clinical Trials|November 19, 2021
Design and feasibility of a double-blind, randomized trial of peri-operative methylnaltrexone for postoperative ileus prevention after adult spinal arthrodesisConnor S Gifford, Benjamin G McGahan, Shelby D Miracle, et al.The Spine Journal : Official Journal of the North American Spine Society|August 22, 2021
Perioperative subcutaneous methylnaltrexone does not enhance gastrointestinal recovery after posterior short-segment spinal arthrodesis surgery: a randomized controlled trialConnor S Gifford, Benjamin G McGahan, Shelby D Miracle, et al.Bioorganic & Medicinal Chemistry Letters|June 24, 2000
Diamino benzo[b]thiophene derivatives as a novel class of active site directed thrombin inhibitors. Part 6: further focus on the contracted C4'-side chain analoguesK Takeuchi, T J Kohn, R W Harper, et al.Protein Science : a Publication of the Protein Society|July 1, 1997
The crystal structure of human alpha-thrombin complexed with LY178550, a nonpeptidyl, active site-directed inhibitorN Y Chirgadze, D J Sall, V J Klimkowski, et al.Bioorganic & Medicinal Chemistry Letters|January 5, 1999
Dibasic benzo[b]thiophene derivatives as a novel class of active site directed thrombin inhibitors. 2. Exploring interactions at the proximal (S2) binding siteD J Sall, S L Briggs, N Y Chirgadze, et al.Bioorganic & Medicinal Chemistry Letters|October 31, 2000
1,2-Disubstituted indole, azaindole and benzimidazole derivatives possessing amine moiety: a novel series of thrombin inhibitorsK Takeuchi, J A Bastian, D S Gifford-Moore, et al.Bioorganic & Medicinal Chemistry Letters|October 6, 1999
The design of potent, selective, non-covalent, peptide thrombin inhibitors utilizing imidazole as a S1 binding elementM R Wiley, L C Weir, S L Briggs, et al.Pageof 6