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epristeride
Known as:
17-N-t-butylcarboxamide androst-3,5-diene-3-carboxylic acid
National Institutes of Health
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Related topics
Related topics
4 relations
Broader (2)
5-alpha Reductase Inhibitors
Androstadienes
Narrower (2)
ONO-9302
SK&F-105657
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Design, synthesis and biological evaluation of novel androst-3,5-diene-3-carboxylic acid derivatives as inhibitors of 5α-reductase type 1 and 2
Kejing Lao
,
Jie Sun
,
+6 authors
H. Xiang
Steroids
2017
Corpus ID: 4436422
2002
2002
[The clinical efficacy of epristeride in the treatment of benign prostatic hyperplasia].
Xiao-bing Ju
,
Hong-fei Wu
,
Li-xin Hua
,
Wei Zhang
,
Jie Li
Zhonghua nan ke xue = National journal of…
2002
Corpus ID: 13003648
OBJECTIVES To estimate the clinical safety, efficacy of Epristeride in the treatment of benign prostatic hyperplasia (BPH…
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2001
2001
Inhibition of regrowth of prostatic glandular cells by epristeride.
L. Qian
,
X. L. Wang
,
Z. Tu
Acta Pharmacologica Sinica
2001
Corpus ID: 38420630
AIM To evaluate the ability of epristeride to inhibit the prostatic glandular regrowth. METHODS Normal rats were castrated…
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2001
2001
Inhibition of cultured rat prostatic epithelial cell growth by epristeride in vitro.
S. Wu
,
H. Z. Sun
,
Z. Tu
,
H. Y. Wu
Acta Pharmacologica Sinica
2001
Corpus ID: 26873360
AIM To study the molecular mechanism of rat prostate atrophy induced by epristeride. METHODS MTT test was used to determine the…
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2000
2000
[Pharmacokinetics of epristeride in rats and beagle dogs].
G. Wei
,
S. Xiao
,
C. X. Liu
Yao xue xue bao = Acta pharmaceutica Sinica
2000
Corpus ID: 30970215
AIM To study the pharmacokinetics of epristeride (EPR) in rats and Beagle dogs. METHODS The concentrations of EPR in biological…
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1999
1999
Reversible long-term toxicity of epristeride in beagle dogs.
Z. Sun
,
J. Feng
,
X. Qi
,
H. Y. Wu
,
W. Zheng
,
Z. Tu
Toxicology and Applied Pharmacology
1999
Corpus ID: 5908879
Epristeride (17beta-N-t-butylcarboxamide-androst-3, 5-diene-3-carboxylic acid) is an uncompetitive inhibitor of steroid 5alpha…
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1999
1999
A Novel Class of Inhibitors for Human Steroid 5α-Reductase : Phenoxybenzoic Acid Derivatives. I
S. Igarashi
,
Takenori Kimura
,
+5 authors
T. Mase
1999
Corpus ID: 22822940
In a search for novel nonsteroidal inhibitors of human prostatic 5α-reductase, we found a new series of phenoxybenzoic acid…
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1998
1998
Epristeride SmithKline Beecham.
Hedge Ss
1998
Corpus ID: 67942928
Epristeride is a transition-state, noncompetitive steroid 5-alpha-reductase inhibitor under development by SmithKline Beecham for…
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1998
1998
Mutagenicity tests on epristeride in vitro and in vivo.
X. L. Wang
,
W. J. Zhen
,
H. Y. Wu
,
J. Feng
,
Z. Tu
Zhongguo yao li xue bao = Acta pharmacologica…
1998
Corpus ID: 20589988
AIM To evaluate the genetic effects of epristeride (Epr), a new prospective drug for treating benign prostatic hyperplasia…
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1997
1997
Effects of steroid 5alpha-reductase inhibitor ONO-9302 and anti-androgen allylestrenol on the prostatic growth, and plasma and prostatic hormone levels in rats.
N. Yasuda
,
K. Fujino
,
T. Shiraji
,
F. Nambu
,
K. Kondo
Japanese Journal of Pharmacology
1997
Corpus ID: 19473782
ONO-9302 [epristeride; (-)-17beta-(tert-butylcarbamoyl)androsta-3,5-diene-3-carboxy lic acid] is a novel inhibitor of steroid…
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