Structure–activity relationships of bioisosteric replacement of the carboxylic acid in novel androgen receptor pure antagonists-Reference-Cited by-同舟云学术

Structure–activity relationships of bioisosteric replacement of the carboxylic acid in novel androgen receptor pure antagonists

Published:2010-05 Issue:9 Volume:18 Page:3159-3168
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Yoshino Hitoshi,Sato Haruhiko,Tachibana Kazutaka,Shiraishi Takuya,Nakamura Mitsuaki,Ohta Masateru,Ishikura Nobuyuki,Nagamuta Masahiro,Onuma Etsuro,Nakagawa Toshito,Arai Shinichi,Ahn Koo-Hyeon,Jung Kyung-Yun,Kawata Hiromitsu

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference23 articles.

1. Phospholipids in liquid chromatography/mass spectrometry bioanalysis: comparison of three tandem mass spectrometric techniques for monitoring plasma phospholipids, the effect of mobile phase composition on phospholipids elution and the association of phospholipids with matrix effects

2. Current Drug Therapy for Prostate Cancer: An Overview

3. Use of the Nonsteroidal Anti-androgen Casodex in Advanced Prostatic Carcinoma

4. Clinical Progress with a New Antiandrogen, Casodex™ (Bicalutamide)

5. A Multicenter Randomized Trial Comparing the Luteinizing Hormone-Releasing Hormone Analogue Goserelin Acetate Alone and with Flutamide in the Treatment of Advanced Prostate Cancer

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