Nonpeptide Luteinizing Hormone-Releasing Hormone Antagonists Derived from Erythromycin A: Design, Synthesis, and Biological Activity of Cladinose Replacement Analogues-Reference-Cited by-同舟云学术

Nonpeptide Luteinizing Hormone-Releasing Hormone Antagonists Derived from Erythromycin A: Design, Synthesis, and Biological Activity of Cladinose Replacement Analogues

Published:2004-02-01 Issue:5 Volume:47 Page:1085-1097
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Randolph John T.¹,Waid Philip¹,Nichols Charles¹,Sauer Daryl¹,Haviv Fortuna¹,Diaz Gilbert¹,Bammert Gary¹,Besecke Leslie M.¹,Segreti Jason A.¹,Mohning Kurt M.¹,Bush Eugene N.¹,Wegner Craig D.¹,Greer Jonathan¹

Affiliation:

1. Global Pharmaceutical Research & Development, Abbott Laboratories, Abbott Park, Illinois 60064 and TAP Pharmaceutical Products Inc., Lake Forest, Illinois 60045

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm030418i

Reference23 articles.

1. Pharmacokinetic/Pharmacodynamic Modeling of Luteinizing Hormone (LH) Suppression and LH Surge Delay by Cetrorelix after Single and Multiple Doses in Healthy Premenopausal Women

2. Obstetrical and neonatal outcome after controlled ovarian stimulation for IVF using the GnRH antagonist ganirelix

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