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

Details

Stereochemistry ABSOLUTE
Molecular Formula C21H29ClO3
Molecular Weight 364.906
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLOSTEBOL ACETATE

SMILES

CC(=O)O[C@H]1CC[C@H]2[C@@H]3CCC4=C(Cl)C(=O)CC[C@]4(C)[C@H]3CC[C@]12C

InChI

InChIKey=XYGMEFJSKQEBTO-KUJXMBTLSA-N
InChI=1S/C21H29ClO3/c1-12(23)25-18-7-6-14-13-4-5-16-19(22)17(24)9-11-20(16,2)15(13)8-10-21(14,18)3/h13-15,18H,4-11H2,1-3H3/t13-,14-,15-,18-,20+,21-/m0/s1

HIDE SMILES / InChI
Clostebol acetate (4-chloro-testosterone acetate), an anabolic androgenic agent used for fattening purposes in cattle breeding or applied topically in ophthalmological and dermatological treatments. The European Commission has prohibited its use since 1986.

Approval Year

PubMed

PubMed

TitleDatePubMed
Clostebol acetate.
2011-08-01
Transformations of steroid esters by Fusarium culmorum.
2007-02-14
Influence of Helix pomatia enzyme preparations on the oxidative conversion of some clostebol acetate metabolites in urine.
2002-03
Influence of the hapten conjugation site on the characteristics of antibodies generated against metabolites of clostebol acetate.
2000-08
Screening for the illegal use of clostebol acetate in cattle by identification of its urinary metabolites.
1994-02-19
Name Type Language
MACROBIN
Preferred Name English
CLOSTEBOL ACETATE
MART.   MI   WHO-DD  
Common Name English
4-CHLORO-17.BETA.-HYDROXYANDROST-4-EN-3-ONE ACETATE
Common Name English
CLOSTEBOL ACETATE [MART.]
Common Name English
NSC-72159
Code English
STERANABOL
Brand Name English
CLOSTEBOL ACETATE [MI]
Common Name English
4-CHLORO-3-OXOANDROST-4-EN-17.BETA.-YL ACETATE
Systematic Name English
Clostebol acetate [WHO-DD]
Common Name English
Code System Code Type Description
NSC
72159
Created by admin on Mon Mar 31 18:39:56 GMT 2025 , Edited by admin on Mon Mar 31 18:39:56 GMT 2025
PRIMARY
CAS
855-19-6
Created by admin on Mon Mar 31 18:39:56 GMT 2025 , Edited by admin on Mon Mar 31 18:39:56 GMT 2025
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EVMPD
SUB01375MIG
Created by admin on Mon Mar 31 18:39:56 GMT 2025 , Edited by admin on Mon Mar 31 18:39:56 GMT 2025
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RXCUI
236522
Created by admin on Mon Mar 31 18:39:56 GMT 2025 , Edited by admin on Mon Mar 31 18:39:56 GMT 2025
PRIMARY RxNorm
SMS_ID
100000087960
Created by admin on Mon Mar 31 18:39:56 GMT 2025 , Edited by admin on Mon Mar 31 18:39:56 GMT 2025
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ECHA (EC/EINECS)
212-720-4
Created by admin on Mon Mar 31 18:39:56 GMT 2025 , Edited by admin on Mon Mar 31 18:39:56 GMT 2025
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ChEMBL
CHEMBL2106571
Created by admin on Mon Mar 31 18:39:56 GMT 2025 , Edited by admin on Mon Mar 31 18:39:56 GMT 2025
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MERCK INDEX
m3667
Created by admin on Mon Mar 31 18:39:56 GMT 2025 , Edited by admin on Mon Mar 31 18:39:56 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID00234702
Created by admin on Mon Mar 31 18:39:56 GMT 2025 , Edited by admin on Mon Mar 31 18:39:56 GMT 2025
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PUBCHEM
13327
Created by admin on Mon Mar 31 18:39:56 GMT 2025 , Edited by admin on Mon Mar 31 18:39:56 GMT 2025
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DRUG CENTRAL
716
Created by admin on Mon Mar 31 18:39:56 GMT 2025 , Edited by admin on Mon Mar 31 18:39:56 GMT 2025
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FDA UNII
780ZZX4P14
Created by admin on Mon Mar 31 18:39:56 GMT 2025 , Edited by admin on Mon Mar 31 18:39:56 GMT 2025
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WIKIPEDIA
Clostebol acetate
Created by admin on Mon Mar 31 18:39:56 GMT 2025 , Edited by admin on Mon Mar 31 18:39:56 GMT 2025
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