U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C25H37NO3
Molecular Weight 399.5662
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of EPRISTERIDE

SMILES

[H][C@@]12CC[C@H](C(=O)NC(C)(C)C)[C@@]1(C)CC[C@@]3([H])[C@@]2([H])CC=C4C=C(CC[C@]34C)C(O)=O

InChI

InChIKey=VAPSMQAHNAZRKC-PQWRYPMOSA-N
InChI=1S/C25H37NO3/c1-23(2,3)26-21(27)20-9-8-18-17-7-6-16-14-15(22(28)29)10-12-24(16,4)19(17)11-13-25(18,20)5/h6,14,17-20H,7-13H2,1-5H3,(H,26,27)(H,28,29)/t17-,18-,19-,20+,24-,25-/m0/s1

HIDE SMILES / InChI
Epristeride is a steroid 5-alpha-reductase inhibitor developed for the treatment of prostatic hyperplasia and acne. The drug reached phase III clinical trial for hyperplasia in the UK, the US and Japan, however, the current status of the drug is unknown.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P31213
Gene ID: 6716.0
Gene Symbol: SRD5A2
Target Organism: Homo sapiens (Human)
11.0 nM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Mutagenicity tests on epristeride in vitro and in vivo.
1998 Nov
Inhibition of cultured rat prostatic epithelial cell growth by epristeride in vitro.
2001 Mar
Atrophy and apoptosis in ventral prostate of rats induced by 5alpha-reductase inhibitor, epristeride.
2001 May
Inhibition of regrowth of prostatic glandular cells by epristeride.
2001 Sep
Patents

Sample Use Guides

Epristeride tablets, 5 mg p.o., twice daily for 120 days.
Route of Administration: Oral
In Vitro Use Guide
Stromal cell proliferation in response to testosterone was dose-dependently inhibited by epristeride (1 x 10(-9) -3 x 10(-7) M, P < 0.05).
Name Type Language
EPRISTERIDE
INN   JAN   MI   USAN   WHO-DD  
USAN   INN  
Official Name English
Epristeride [WHO-DD]
Common Name English
EPRISTERIDE [MI]
Common Name English
ANDROSTA-3,5-DIENE-3-CARBOXYLIC ACID, 17-(((1,1-DIMETHYLETHYL)AMINO)CARBONYL)-, (17.BETA.)-
Common Name English
SK&F-105657
Code English
SK&F 105657
Code English
17β-(tert-Butylcarbamoyl)androsta-3,5-diene-3-carboxylic acid
Systematic Name English
EPRISTERIDE [JAN]
Common Name English
epristeride [INN]
Common Name English
EPRISTERIDE [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C2319
Created by admin on Fri Dec 15 15:52:21 GMT 2023 , Edited by admin on Fri Dec 15 15:52:21 GMT 2023
Code System Code Type Description
PUBCHEM
68741
Created by admin on Fri Dec 15 15:52:21 GMT 2023 , Edited by admin on Fri Dec 15 15:52:21 GMT 2023
PRIMARY
SMS_ID
100000084573
Created by admin on Fri Dec 15 15:52:21 GMT 2023 , Edited by admin on Fri Dec 15 15:52:21 GMT 2023
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WIKIPEDIA
Epristeride
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CAS
119169-78-7
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EVMPD
SUB06584MIG
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MERCK INDEX
m4960
Created by admin on Fri Dec 15 15:52:21 GMT 2023 , Edited by admin on Fri Dec 15 15:52:21 GMT 2023
PRIMARY Merck Index
NCI_THESAURUS
C81621
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EPA CompTox
DTXSID9048643
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USAN
EE-23
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INN
7054
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MESH
C072547
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ChEMBL
CHEMBL138225
Created by admin on Fri Dec 15 15:52:21 GMT 2023 , Edited by admin on Fri Dec 15 15:52:21 GMT 2023
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FDA UNII
39517A04PS
Created by admin on Fri Dec 15 15:52:21 GMT 2023 , Edited by admin on Fri Dec 15 15:52:21 GMT 2023
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