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Christopher C. Jordan

University of Hertfordshire

22

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Synthesis of potent antagonists of substance P by modifying the methionyl and glutaminyl residues of its C‐terminal hexapeptide and without using d‐amino acids

2009 International Journal of Peptide and Protein Research
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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 relationships.

2009 International Journal of Peptide and Protein Research
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Low molecular weight neurokinin NK2 antagonists

1993 Bioorganic & Medicinal Chemistry Letters
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Anti-emetic profile of a non-peptide neurokinin NK1 receptor antagonist, CP-99,994, in ferrets

1993 European Journal of Pharmacology
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Highly potent and selective heptapeptide antagonists of the neurokinin NK-2 receptor

1992 Journal of Medicinal Chemistry
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Conformationally constrained tachykinin analogues: potent and highly selective neurokinin NK-2 receptor agonists.

1992 Journal of Medicinal Chemistry
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Effect of 5-HT3 receptor antagonists on responses to selective activation of mesolimbic dopaminergic pathways in the rat

1990 British Journal of Pharmacology
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Potent and highly selective neurokinin antagonists.

1990 Journal of Medicinal Chemistry
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Caerulein-induced antinociception: interaction with morphine and opioid antagonists in the rat.

1989 Neuropeptides
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Involvement of NK-1 receptors in neurokinin-induced plasma extravasation (PEV) in rat skin

1989 Regulatory Peptides
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