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Life Sciences|July 1, 1985
Active and inactive L-prolyl-L-leucyl glycinamide synthetic analogs in rat models of levodopa-treated Parkinson's diseaseT C Case, S R Snider, V J Hruby, et al.Biopolymers|July 1, 1991
Topographical requirements for delta-selective opioid peptidesG V Nikiforovich, V J Hruby, O Prakash, et al.Organic Letters|June 29, 2001
Asymmetric synthesis of alpha,beta-dialkyl-alpha-phenylalanines via direct alkylation of a chiral alanine derivative with racemic alpha-alkylbenzyl bromides. A case of high enantiomer differentiation at room temperatureV A Soloshonok, X Tang, V J Hruby, et al.Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|February 1, 1989
Structural characteristics of two highly selective opioid peptidesR J Knapp, W Kazmierski, V J Hruby, et al.The Journal of Pharmacology and Experimental Therapeutics|October 1, 1986
Design of oxytocin antagonists with prolonged action: potential tocolytic agents for the treatment of preterm laborW Y Chan, V J Hruby, T W Rockway, et al.The Journal of Peptide Research : Official Journal of the American Peptide Society|August 29, 2000
Evaluation of new base-labile 2-(4-nitrophenylsulfonyl) ethoxycarbonyl (Nsc)-amino acids for solid-phase peptide synthesisP M Balse, H J Kim, G Han, et al.Life Sciences|June 16, 1986
Cyclic somatostatin octapeptide analogues with high affinity and selectivity toward mu opioid receptorsK Gulya, J T Pelton, V J Hruby, et al.The Journal of Organic Chemistry|April 3, 2001
Solid-phase synthesis of O-linked glycopeptide analogues of enkephalinS A Mitchell, M R Pratt, V J Hruby, et al.Life Sciences|January 1, 1989
Melanin concentrating hormone analogues: contraction of the cyclic structure. II. Antagonist activityM Lebl, V J Hruby, A M Castrucci, et al.Life Sciences|January 1, 1992
Synthesis and binding characteristics of the highly delta-specific new tritiated opioid peptide, [3H]deltorphin IIB Búzás, G Tóth, S Cavagnero, et al.Pageof 72