A New, Potent Urotensin II Receptor Peptide Agonist Containing a Pen Residue at the Disulfide Bridge-Reference-Cited by-同舟云学术

A New, Potent Urotensin II Receptor Peptide Agonist Containing a Pen Residue at the Disulfide Bridge

Published:2002-09-01 Issue:20 Volume:45 Page:4391-4394
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Grieco Paolo¹,Carotenuto Alfonso¹,Campiglia Pietro¹,Zampelli Enrico¹,Patacchini Riccardo¹,Maggi Carlo A.¹,Novellino Ettore¹,Rovero Paolo¹

Affiliation:

1. Department of Pharmaceutical and Toxicological Chemistry, University of Naples “Federico II”, I-80131 Naples, Italy, Department of Pharmaceutical Sciences, University of Salerno, Via Ponte Don Melillo 11C, I-84084 Fisciano, Italy, and Department of Pharmacology, Menarini Ricerche SpA, I-50131 Florence, Italy

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm025549i

Reference29 articles.

1. Cloning of the cDNA encoding the urotensin II precursor in frog and human reveals intense expression of the urotensin II gene in motoneurons of the spinal cord

2. Contraction of rat thoracic aorta strips induced by phorbol 12-myristate 13-acetate

3. A kinase-regulated PDZ-domain interaction controls endocytic sorting of the β2-adrenergic receptor

4. Identification of the natural ligand of an orphan G-protein-coupled receptor involved in the regulation of vasoconstriction

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