Discovery of an Orally-Active Nonsteroidal Androgen Receptor Pure Antagonist and the Structure–Activity Relationships of Its Derivatives

Chemical and Pharmaceutical Bulletin- Japan

doi 10.1248/cpb.56.1555

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January 1, 2008

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Pharmaceutical Society of Japan

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Discovery of an Orally-Active Nonsteroidal Androgen Receptor Pure Antagonist and the Structure–Activity Relationships of Its Derivatives

Chemical and Pharmaceutical Bulletin- Japan

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

Errata: Discovery of an Orally-Active Nonsteroidal Androgen Receptor Pure Antagonist and the Structure–Activity Relationships of Its Derivatives [Chem. Pharm. Bull. 56(11): 1555-1561 (2008)]

Discovery of Potent, Orally-Active, and Muscle-Selective Androgen Receptor Modulators Based on an N-Aryl-Hydroxybicyclohydantoin Scaffold

Structure–Activity Relationships of the Peptide Kappa Opioid Receptor Antagonist Zyklophin

Synthesis and Pharmacological Evaluation of Novel Arylpiperazine Derivatives as Nonsteroidal Androgen Receptor Antagonists

Structure-Activity Relationships of Xanthocillin Derivatives as Thrombopoietin Receptor Agonist

A Receptor-Grounded Approach to Teaching Nonsteroidal Antiinflammatory Drug Chemistry and Structure-Activity Relationships

An Orally Active Chemokine Receptor CCR2 Antagonist Prevents Glomerulosclerosis and Renal Failure in Type 2 Diabetes

Studies on Orally Active Cephalosporins. I. Synthesis and Structure-Activity Relationships of New 3-Substituted Carbamoyloxymethyl Cephalosporins.

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