Conformational Comparisons of a Series of Tachykinin Peptide Analogs
Author:
Affiliation:
1. Department of Chemistry, Mississippi State University, Mississippi State, Mississippi 39762, and Department of Physiology and Pharmacology, Northeastern Ohio Universities College of Medicine, Rootstown, Ohio 44272
Publisher
American Chemical Society (ACS)
Subject
Drug Discovery,Molecular Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/jm070577s
Reference31 articles.
1. Iverson, L. l.; Watling, K. J.; McKnight, A. T.; Williams, B. J.; Lee, C. M.Multiple Receptors for Subtance P and Related Tachykinins.Topics in Medicinal Chemistry, Proceedings of the 4th SCI-RSC Medicinal Chemistry Symposium; Royal Society of Chemistry: London, U.K., 1988.
2. Substance P causes direct depolarisation of neurones of guinea pig interpeduncular nucleus in vitro
3. Substance P as a Transmitter Candidate
4. Substance P Causes Pain—But Also Heals
5. Conformationally constrained tachykinin analogs: potent and highly selective neurokinin NK-2 receptor agonists
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