Design of a novel dipeptide substance P antagonist FK888-Reference-Cited by-同舟云学术

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Design of a novel dipeptide substance P antagonist FK888

Published:1993-07 Issue:1-2 Volume:46 Page:332-334
ISSN:0167-0115
Container-title:Regulatory Peptides
language:en
Short-container-title:Regulatory Peptides

Author:

Hagiwara Daijiro,Miyake Hiroshi,Igari Norihiro,Murano Kenji,Morimoto Hiroshi,Murai Masako,Fujii Takashi,Matsuo Masaaki

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Clinical Biochemistry,Endocrinology,Physiology,Biochemistry

Reference4 articles.

1. Asthma as an axon reflex;Barnes;Lancet,1986

2. Undeca- and octa-peptide antagonists for substance P, a study on the guinea pig trachea;Mizrahi;Eur. J. Pharmacol.,1984

3. Studies on neurokinin antagonists. 1. The design of novel tripeptides possessing the glutaminyl-d-tryptophylphenylalanine sequence as substance P antagonists;Hagiwara;J. Med. Chem.,1992

4. Studies on neurokinin antagonists. 2. Design and structure-activity relationships of novel tripeptide substance P antagonists, Nα-[Nα-(Nα-acetyl-l-threonyl)-N1-formyl-d-tryptophyl]-N-methyl-N-(phenylmethyl)-l- phenylalaninamide and its related compounds;Hagiwara;J. Med. Chem.,1992

Cited by 12 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. The Neurokinins: Peptidomimetic Ligand Design and Therapeutic Applications;Current Medicinal Chemistry;2020-03-27

2. Tachykinin NK1 Receptor Antagonists;Handbook of Experimental Pharmacology;2004

3. New substance P receptor antagonists. Conception, synthesis and biological evaluation of spirolactam derivatives and their tripeptide Cbz-Pro-Leu-Trp-OBzl(CF3)(2) and lactam pseudopeptide derivatives;Letters in Peptide Science;2000

4. A spectroscopic and molecular modeling study on novel pseudopeptides exhibiting biological activity;The Journal of Peptide Research;1999-10

5. Conformational analysis of pseudo-peptides: The case of FK888, a potent and selective substance P receptor antagonist;Letters in Peptide Science;1998-05

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