Showing results (61-70 of 79) with videos related to
Sort By:
Pageof 8
Drug Design and Discovery|April 1, 1996
Hydrophobic D-amino acids in the design of peptide ligands for the pp60src SH2 domainM S Plummer, E A Lunney, K S Para, et al.Journal of Medicinal Chemistry|February 1, 1990
Renin inhibitors containing isosteric replacements of the amide bond connecting the P3 and P2 sitesJ S Kaltenbronn, J P Hudspeth, E A Lunney, et al.Psychological Services|October 10, 2018
Psychometric properties of a brief measure of posttraumatic stress disorder-related impairment: The Brief Inventory of Psychosocial FunctioningSarah E Kleiman, Michelle J Bovin, Shimrit K Black, et al.The Lancet. Public Health|May 25, 2026
Prevalence of adverse childhood experience items: a systematic review and meta-analysesSheri Madigan, Carole A Lunney, Anh Ly, et al.Bioorganic & Medicinal Chemistry Letters|March 31, 2009
Synthesis and SAR of 4-substituted-2-aminopyrimidines as novel c-Jun N-terminal kinase (JNK) inhibitorsPaul S Humphries, Jennifer A Lafontaine, Charles S Agree, et al.Journal of Medicinal Chemistry|August 4, 2006
4-Phenylpyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione inhibitors of the checkpoint kinase Wee1. Structure-activity relationships for chromophore modification and phenyl ring substitutionBrian D Palmer, Andrew M Thompson, R John Booth, et al.Bioorganic & Medicinal Chemistry Letters|October 10, 2001
Structure-based design of caspase-1 inhibitor containing a diphenyl ether sulfonamideA B Shahripour, M S Plummer, E A Lunney, et al.Biochemical and Biophysical Research Communications|April 25, 1996
Nonpeptidic HIV protease inhibitors: 4-hydroxy-pyran-2-one inhibitors with functional tethers to P1 phenyl ring to reach S3 pocket of the enzymeJ Vara Prasad, P J Tummino, D Ferguson, et al.Bioorganic & Medicinal Chemistry|December 12, 2001
Structure-based design of nonpeptide inhibitors of interleukin-1beta converting enzyme (ICE, caspase-1)Aurash B Shahripour, Mark S Plummer, Elizabeth A Lunney, et al.Journal of Medicinal Chemistry|June 29, 2001
4-Hydroxy-5,6-dihydropyrones as inhibitors of HIV protease: the effect of heterocyclic substituents at C-6 on antiviral potency and pharmacokinetic parametersS E Hagen, J Domagala, C Gajda, et al.Pageof 8