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Details

Stereochemistry ABSOLUTE
Molecular Formula C18H24O2
Molecular Weight 272.382
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 19-NORANDROSTENEDIONE

SMILES

[H][C@@]12CCC(=O)[C@@]1(C)CC[C@]3([H])[C@@]4([H])CCC(=O)C=C4CC[C@@]23[H]

InChI

InChIKey=JRIZOGLBRPZBLQ-QXUSFIETSA-N
InChI=1S/C18H24O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h10,13-16H,2-9H2,1H3/t13-,14+,15+,16-,18-/m0/s1

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Searching for the physiological function of 17beta-hydroxysteroid dehydrogenase from the fungus Cochliobolus lunatus: studies of substrate specificity and expression analysis.
2001 Jan 22
[Urinary nandrolone metabolites in antidoping control].
2001 Sep
Effects of norandrostenedione and norandrostenediol in resistance-trained men.
2002 Sep
Analytical strategies for the detection of non-labelled anabolic androgenic steroids in nutritional supplements.
2004 Jul
Effect of multiple oral doses of androgenic anabolic steroids on endurance performance and serum indices of physical stress in healthy male subjects.
2006 Nov
Survey of nutritional supplements for selected illegal anabolic steroids and ephedrine using LC-MS/MS and GC-MS methods, respectively.
2007 Mar
Studies related to the origin of C18 neutral steroids isolated from extracts of urine from the male horse: the identification of urinary 19-oic acids and their decarboxylation to produce estr-4-en-17beta-ol-3-one (19-nortestosterone) and estr-4-ene-3,17-dione (19-norandrost-4-ene-3,17-dione) during sample processing.
2007 Mar 14
Doping in sport--2. Quantification of the impurity 19-norandrostenedione in pharmaceutical preparations of norethisterone.
2009 Mar
Steroid metabolism in chimeric mice with humanized liver.
2009 Nov
Influence of delivery mode on the urinary excretion of nandrolone metabolites.
2010 Apr
Novel steroid-sensing model and characterization of protein interactions based on fluorescence anisotropy decay.
2010 Apr 1
Name Type Language
19-NORANDROSTENEDIONE
Common Name English
19-NOR-4-ANDROSTENE-3,17-DION
Systematic Name English
19-NOR-4-ANDROSTENEDIONE
Code English
4-OESTREN-3,17-DIONE
Systematic Name English
NORETHISTERONE IMPURITY B [EP IMPURITY]
Common Name English
4-OESTRENDIONE
Common Name English
4-NORENDION
Common Name English
ESTR-4-ENE-3,17-DIONE
Systematic Name English
NORETHINDRONE RELATED COMPOUND B [USP-RS]
Common Name English
19-NOR-4-ANDROSTENE-3,17-DIONE
Systematic Name English
4-NORENDIONE
Common Name English
19-NORANDROST-4-ENE-3,17-DIONE
Common Name English
NORDIONE
Common Name English
NSC-12164
Code English
(+)-19-NORANDROST-4-EN-3,17-DIONE
Common Name English
19-NORANDROST-4-EN-3,17-DIONE
Systematic Name English
NORETHISTERONE ACETATE IMPURITY J [EP IMPURITY]
Common Name English
Classification Tree Code System Code
DEA NO. 4000
Created by admin on Fri Dec 15 15:47:53 GMT 2023 , Edited by admin on Fri Dec 15 15:47:53 GMT 2023
Code System Code Type Description
MESH
C002828
Created by admin on Fri Dec 15 15:47:53 GMT 2023 , Edited by admin on Fri Dec 15 15:47:53 GMT 2023
PRIMARY
CAS
734-32-7
Created by admin on Fri Dec 15 15:47:53 GMT 2023 , Edited by admin on Fri Dec 15 15:47:53 GMT 2023
PRIMARY
ECHA (EC/EINECS)
211-995-8
Created by admin on Fri Dec 15 15:47:53 GMT 2023 , Edited by admin on Fri Dec 15 15:47:53 GMT 2023
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DRUG BANK
DB01448
Created by admin on Fri Dec 15 15:47:53 GMT 2023 , Edited by admin on Fri Dec 15 15:47:53 GMT 2023
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SMS_ID
100000091511
Created by admin on Fri Dec 15 15:47:53 GMT 2023 , Edited by admin on Fri Dec 15 15:47:53 GMT 2023
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EVMPD
SUB25857
Created by admin on Fri Dec 15 15:47:53 GMT 2023 , Edited by admin on Fri Dec 15 15:47:53 GMT 2023
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WIKIPEDIA
19-NORANDROSTENEDIONE
Created by admin on Fri Dec 15 15:47:53 GMT 2023 , Edited by admin on Fri Dec 15 15:47:53 GMT 2023
PRIMARY
RS_ITEM_NUM
1470026
Created by admin on Fri Dec 15 15:47:53 GMT 2023 , Edited by admin on Fri Dec 15 15:47:53 GMT 2023
PRIMARY
FDA UNII
U90987PVU5
Created by admin on Fri Dec 15 15:47:53 GMT 2023 , Edited by admin on Fri Dec 15 15:47:53 GMT 2023
PRIMARY
NSC
12164
Created by admin on Fri Dec 15 15:47:53 GMT 2023 , Edited by admin on Fri Dec 15 15:47:53 GMT 2023
PRIMARY
PUBCHEM
92834
Created by admin on Fri Dec 15 15:47:53 GMT 2023 , Edited by admin on Fri Dec 15 15:47:53 GMT 2023
PRIMARY
EPA CompTox
DTXSID50862392
Created by admin on Fri Dec 15 15:47:53 GMT 2023 , Edited by admin on Fri Dec 15 15:47:53 GMT 2023
PRIMARY