Design of Potent Dicyclic (4−10/5−8) Gonadotropin Releasing Hormone (GnRH) Antagonists-Reference-Cited by-同舟云学术

Design of Potent Dicyclic (4−10/5−8) Gonadotropin Releasing Hormone (GnRH) Antagonists

Published:2000-02-23 Issue:5 Volume:43 Page:784-796
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Rivier Jean E.¹,Struthers R. Scott¹,Porter John¹,Lahrichi Sabine L.¹,Jiang Guangcheng¹,Cervini Laura A.¹,Ibea Michel¹,Kirby Dean A.¹,Koerber Steven C.¹,Rivier Catherine L.¹

Affiliation:

1. The Clayton Foundation Laboratories for Peptide Biology, The Salk Institute, 10010 North Torrey Pines Road, La Jolla, California 92037, and Peptide Chemistry Department, Neurocrine Biosciences Inc., 10555 Science Center Drive, San Diego, California 92121

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm990115h

Reference59 articles.

1. Design of potent cyclic gonadotropin releasing hormone antagonists

2. Conformationally restrained cyclic peptides as antaconists of luteinizing hormone-releasing hormone

3. Structure of the porcine LH- and FSH-releasing hormone. I. The proposed amino acid sequence

4. Primary Structure of the Ovine Hypothalamic Luteinizing Hormone-Releasing Factor (LRF)

5. Antireproductive Effects of a Potent Gonadotropin-Releasing Hormone Antagonist in the Male Rat

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