Search Results - "SWISTOK, Joseph"
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The N-terminal Domain of RGS4 Confers Receptor-selective Inhibition of G Protein Signaling
Published in The Journal of biological chemistry (25-12-1998)“…Regulators of heterotrimeric G protein signaling (RGS) proteins are GTPase-activating proteins (GAPs) that accelerate GTP hydrolysis by G q and G i α…”
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A predictive pharmacophore model of human melanocortin-4 receptor as derived from the solution structures of cyclic peptides
Published in Bioorganic & medicinal chemistry (15-05-2004)“…A predictive pharmacophore model of human melanocortin-4 receptor (hMC4R) was derived from the NMR structures of a series of rigidified MT-II related cyclic…”
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Discovery of 1-amino-4-phenylcyclohexane-1-carboxylic acid and its influence on agonist selectivity between human melanocortin-4 and -1 receptors in linear pentapeptides
Published in Bioorganic & medicinal chemistry letters (15-11-2005)“…A design and synthesis of cis-Apc as new histidine surrogate and its incorporation into linear pentapeptides (Penta- cis-Apc-DPhe-Arg-Trp-Gly-NH 2) and related…”
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Preparation of human Melanocortin-4 receptor agonist libraries : Linear peptides X-Y-DPhe7-Arg8-Trp(or 2-Nal)9-Z-NH2
Published in Bioorganic & medicinal chemistry letters (15-12-2005)“…Two libraries of hMC4R agonists, X-Y-DPhe(7)-Arg(8)-2-Nal(9)-Z-NH(2) and X-Y-DPhe(7)-Arg(8)-Trp(9)-Z-NH(2), totaling 185 peptides were prepared using Irori…”
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Structure-activity relationship of linear peptide Bu-His6-DPhe7-Arg8-Trp9-Gly10-NH2 at the human melanocortin-1 and -4 receptors : DPhe7 and Trp9 substitution
Published in Bioorganic & medicinal chemistry letters (24-02-2003)“…A series of pentapeptides, based on hMC4R pentapeptide agonist (Bu-His(6)-DPhe(7)-Arg(8)-Trp(9)-Gly(10)-NH(2)), was prepared in which either DPhe(7) or Trp(9)…”
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Opportunities and challenges of developing peptide drugs in the pharmaceutical industry
Published in Advances in experimental medicine and biology (2009)Get more information
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Carboxylic acids and tetrazoles as isosteric replacements for sulfate in cholecystokinin analogs
Published in Journal of medicinal chemistry (01-03-1991)“…A series of analogues of the satiety-inducing peptide cholecystokinin (CCK-8) was prepared in which the sulfated tyrosine required for activation of peripheral…”
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Structure activity studies of tryptophan30 modified analogs of Ac-CCK-7
Published in International journal of peptide and protein research (01-04-1992)“…Cholecystokinin represents a family of gut hormones which among other activities, have been proposed to participate in satiety signaling…”
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Preparation of human Melanocortin-4 receptor agonist libraries: Linear peptides X-Y-DPhe 7-Arg 8-Trp(or 2-Nal) 9-Z-NH 2
Published in Bioorganic & medicinal chemistry letters (2005)“…Two libraries of hMC4R agonists, X- Y-DPhe 7-Arg 8-2-Nal 9- Z-NH 2 and X- Y-DPhe 7-Arg 8-Trp 9- Z-NH 2, totaling 185 peptides were prepared using Irori tagging…”
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Structure–Activity relationship of linear peptide Bu-His 6-DPhe 7-Arg 8-Trp 9-Gly 10-NH 2 at the human melanocortin-1 and -4 receptors: DPhe 7 and Trp 9 substitution
Published in Bioorganic & medicinal chemistry letters (2003)“…A series of pentapeptides, based on hMC4R pentapeptide agonist (Bu-His 6-DPhe 7-Arg 8-Trp 9-Gly 10-NH 2), was prepared in which either DPhe 7 or Trp 9 residue…”
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Structure-activity relationship of linear peptide Bu-His-DPhe-Arg-Trp-Gly-NH(2) at the human melanocortin-1 and -4 receptors: arginine substitution
Published in Bioorganic & medicinal chemistry letters (02-09-2002)“…A series of pentapeptides, based on Bu-His(6)-DPhe(7)-Arg(8)-Trp(9)-Gly(10)-NH(2) and modified at the Arg(8) position, was prepared and pharmacologically…”
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Structure-activity relationship of cyclic peptide penta-c[Asp-His(6)-DPhe(7)-Arg(8)-Trp(9)-Lys]-NH(2) at the human melanocortin-1 and -4 receptors: His(6) substitution
Published in Bioorganic & medicinal chemistry letters (07-04-2003)“…A series of MT-II related cyclic peptides, based on potent but non-selective hMC4R agonist (Penta-c[Asp-His(6)-DPhe(7)-Arg(8)-Trp(9)-Lys]-NH(2)) was prepared…”
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Structure-activity relationship of linear peptide Bu-His-DPhe-Arg-Trp-Gly-NH(2) at the human melanocortin-1 and -4 receptors: histidine substitution
Published in Bioorganic & medicinal chemistry letters (06-01-2003)“…Systematic substitution of His(6) residue using non-selective hMC4R pentapeptide agonist (Bu-His(6)-DPhe(7)-Arg(8)-Trp(9)-Gly(10)-NH(2)) as the template led to…”
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Structure–Activity relationship of linear peptide Bu-His-DPhe-Arg-Trp-Gly-NH 2 at the human melanocortin-1 and -4 receptors: histidine substitution
Published in Bioorganic & medicinal chemistry letters (2003)“…Systematic substitution of His 6 residue using non-selective hMC4R pentapeptide agonist (Bu-His 6-DPhe 7-Arg 8-Trp 9-Gly 10-NH 2) as the template led to the…”
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Structure–activity relationship of cyclic peptide penta-c[Asp-His 6-DPhe 7-Arg 8-Trp 9-Lys]-NH 2 at the human melanocortin-1 and -4 receptors: His 6 substitution
Published in Bioorganic & medicinal chemistry letters (2003)“…A series of MT-II related cyclic peptides, based on potent but non-selective hMC4R agonist (Penta-c[Asp-His 6-DPhe 7-Arg 8-Trp 9-Lys]-NH 2) was prepared in…”
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Structure–Activity relationship of linear peptide Bu-His-DPhe-Arg-Trp-Gly-NH 2 at the human melanocortin-1 and -4 receptors: arginine substitution
Published in Bioorganic & medicinal chemistry letters (2002)“…A series of pentapeptides, based on Bu-His 6-DPhe 7-Arg 8-Trp 9-Gly 10-NH 2 and modified at the Arg 8 position, was prepared and pharmacologically…”
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Analogs of CCK incorporating conformationally constrained replacements for Asp32
Published in Journal of medicinal chemistry (30-10-1992)Get full text
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