A potent and selective agonist for NK-2 tachykinin receptor-Reference-Cited by-同舟云学术

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A potent and selective agonist for NK-2 tachykinin receptor

Published:1989-05 Issue:3 Volume:10 Page:593-595
ISSN:0196-9781
Container-title:Peptides
language:en
Short-container-title:Peptides

Author:

Rovero P.,Pestellini V.,Patacchini R.,Giuliani S.,Santicioli P.,Maggi C.A.,Meli A.,Giachetti A.

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Endocrinology,Physiology,Biochemistry

Reference17 articles.

1. Novel pharmacology of substance K binding sites: a third type of tachykinin receptor;Buck;Science,1984

2. Structure-activity studies on substance P;Couture;Can. J. Physiol. Pharmacol.,1979

3. Specific agonists for neurokinin B receptors;Drapeau;Eur. J. Pharmacol.,1987

4. Selective agonists for substance P and neurokinin receptors;Drapeau;Neuropeptides,1987

5. Characterization of a neurokinin B receptor site in rat brain using a highly selective radioligand;Laufer;J. Biol. Chem.,1986

Cited by 99 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Affinity, potency, efficacy, and selectivity of neurokinin A analogs at human recombinant NK2 and NK1 receptors;PLOS ONE;2018-10-25

2. Structure–activity relationship study of tachykinin peptides for the development of novel neurokinin-3 receptor selective agonists;Bioorganic & Medicinal Chemistry;2013-04

3. In vitro and in vivo pharmacological characterization of the novel NK1 receptor selective antagonist Netupitant;Peptides;2012-09

4. Tachykinins;Bioactive Peptides;2009-04-23

5. Analogues of the C-terminal fragments of neurokinins with modifications at their C-terminal methionyl residue;International Journal of Peptide and Protein Research;2009-01-12

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