(PDF) Design, Synthesis, and Structure-Activity

Design, Synthesis, and Structure-Activity Relationships of Thieno[2, 3-B]pyridin-4-One Derivatives as a Novel Class of Potent, Orally Active, Non-Peptide Luteinizing Hormone-Releasing Hormone Receptor Antagonists

doi 10.1021/jm0512894.s001

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Design, Synthesis, and Structure-Activity Relationships of Thieno[2, 3-B]pyridin-4-One Derivatives as a Novel Class of Potent, Orally Active, Non-Peptide Luteinizing Hormone-Releasing Hormone Receptor Antagonists

doi 10.1021/jm0512894.s001

Full Text

Abstract

Date

Authors

Publisher

Related search

Design and Synthesis of Novel Potent Non-Peptide and Orally Active Renin Inhibitors

Antagonists of Bombesin/Gastrin-Releasing Peptide as Adjuncts to Agonists of Luteinizing Hormone–releasing Hormone in the Treatment of Experimental Prostate Cancer

Active Immunization of Heifers Against Luteinizing Hormone-Releasing Hormone, Human Chorionic Gonadotropin and Bovine Luteinizing Hormone

Potent, Selective, and Orally Efficacious Antagonists of Melanin-Concentrating Hormone Receptor 1

2-(3-Pyridyl)thiazolidine-4-Carboxamide Derivatives. II. Structure-Activity Relationships and Active Configuration of 2-(3-Pyridyl)thiazolidine-4-Carboxamides as Platelet-Activating Factor Receptor Antagonists.

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