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International Journal of Peptide and Protein Research|December 1, 1993
Synthesis of a potent antagonist of substance P by replacing the CH2SCH3 and the alpha-carboxamide groups of the methionine at [Orn6]-SP6-11 by benzyl ester groupsK Karagiannis, G Stavropoulos, C Poulos, et al.
British Journal of Pharmacology|January 1, 1986
An examination of the pharmacology of two substance P antagonists and the evidence for tachykinin receptor subtypesS J Bailey, R L Featherstone, C C Jordan, et al.
International Journal of Peptide and Protein Research|April 1, 1993
Synthesis of potent antagonists of substance P by modifying the methionyl and glutaminyl residues of its C-terminal hexapeptide and without using D-amino acidsA Manolopoulou, K Karagiannis, G Stavropoulos, et al.
International Journal of Peptide and Protein Research|October 1, 1991
Synthesis of a potent agonist of substance P by modifying the methionyl and glutaminyl residues of the C-terminal hexapeptide of substance P. Structure-activity relationshipsK Karagiannis, A Manolopoulou, G Stavropoulos, et al.
British Journal of Pharmacology|June 1, 1988
Pharmacological properties of GR38032F, a novel antagonist at 5-HT3 receptorsA Butler, J M Hill, S J Ireland, et al.
Alimentary Pharmacology & Therapeutics|May 4, 2006
Efficacy and safety of bisacodyl in the acute treatment of constipation: a double-blind, randomized, placebo-controlled studyS Kienzle-Horn, J-M Vix, C Schuijt, et al.
The Journal of Physiology|September 1, 1982
The effects of substance P on histamine and 5-hydroxytryptamine release in the ratC M Fewtrell, J C Foreman, C C Jordan, et al.
British Journal of Pharmacology|June 1, 1991
Receptors mediating tachykinin-induced contractile responses in guinea-pig tracheaS J Ireland, F Bailey, A Cook, et al.
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