Novel Analogues of Degarelix Incorporating Hydroxy-, Methoxy-, and Pegylated-Urea Moieties at Positions 3, 5, 6 and the N-Terminus. Part III-Reference-Cited by-同舟云学术

Novel Analogues of Degarelix Incorporating Hydroxy-, Methoxy-, and Pegylated-Urea Moieties at Positions 3, 5, 6 and the N-Terminus. Part III

Published:2006-05-23 Issue:12 Volume:49 Page:3536-3543
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Samant Manoj P.¹,Hong Doley J.¹,Croston Glenn¹,Rivier Catherine¹,Rivier Jean¹

Affiliation:

1. The Clayton Foundation Laboratories for Peptide Biology, The Salk Institute, 10010 N. Torrey Pines Road, La Jolla, California 92037, and Ferring Research Institute Inc., 3550 General Atomics Court, Building 2, Room 442, San Diego, California 92121

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm060240a

Reference44 articles.

1. GnRH Antagonists: A New Generation of Long Acting Analogues Incorporating p-Ureido-phenylalanines at Positions 5 and 6

2. Iterative Approach to the Discovery of Novel Degarelix Analogues: Substitutions at Positions 3, 7, and 8. Part II

3. Gonadotropin-Releasing Hormone Antagonists: Novel Members of the Azaline B Family

4. Novel gonadotropin-releasing hormone antagonists: peptides incorporating modified N.omega.-cyanoguanidino moieties

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

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