11-KETOANDROSTERONE

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C19H28O3
Molecular Weight	304.4238
Optical Activity	UNSPECIFIED
Defined Stereocenters	7 / 7
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of 11-KETOANDROSTERONE

Structure Search

SMILES

C[C@]12CC(=O)[C@H]3[C@@H](CC[C@H]4C[C@H](O)CC[C@]34C)[C@@H]1CCC2=O

InChI

InChIKey=IUNYGQONJQTULL-UFTZPVOZSA-N

InChI=1S/C19H28O3/c1-18-8-7-12(20)9-11(18)3-4-13-14-5-6-16(22)19(14,2)10-15(21)17(13)18/h11-14,17,20H,3-10H2,1-2H3/t11-,12+,13-,14-,17+,18-,19-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C19H28O3
Molecular Weight	304.4238
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	7 / 7
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

PubMed

PubMed

Title	Date	PubMed
Isotope ratio mass spectrometry analysis of the oxidation products of the main and minor metabolites of hydrocortisone and cortisone for antidoping controls.	2009-03	19056411
The effects of sex, age and commensal way of life on levels of fecal glucocorticoid metabolites in spiny mice (Acomys cahirinus).	2008-09-03	18586285
In vitro biosynthesis of novel 5beta-reduced steroids by the testis of the round goby, Neogobius melanostomus.	2005-01-01	15596066
Endogenous urinary steroids in premenopausal women with uterine leiomyomas.	2004-01	14698830
Glucocorticoid metabolites inhibit the metabolism of androstenedione in red blood cells of ruminants.	2003-03	12667200

Substance Class	Chemical Created by `admin` on `Mon Mar 31 20:53:44 GMT 2025` Edited by `admin` on `Mon Mar 31 20:53:44 GMT 2025`
Record UNII	3T4E87JT27
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

11-KETOANDROSTERONE

Common Name

English

NSC-56412

Preferred Name

English

5.ALPHA.-ANDROSTAN-3.ALPHA.-OL-11,17-DIONE

Common Name

English

11-OXOANDROSTERONE

Common Name

English

BA-2683

Common Name

English

5.ALPHA.-ANDROSTANE-3.ALPHA.-OL-11,17-DIONE

Common Name

English

3.ALPHA.-HYDROXY-5.ALPHA.-ANDROSTAN-11,17-DIONE

Systematic Name

English

Classification Tree Code System Code

LOINC

26943-1

Created by admin on Mon Mar 31 20:53:44 GMT 2025 , Edited by admin on Mon Mar 31 20:53:44 GMT 2025

LOINC

1661-8

Created by admin on Mon Mar 31 20:53:44 GMT 2025 , Edited by admin on Mon Mar 31 20:53:44 GMT 2025

LOINC

34214-7

Created by admin on Mon Mar 31 20:53:44 GMT 2025 , Edited by admin on Mon Mar 31 20:53:44 GMT 2025

LOINC

15005-2

Created by admin on Mon Mar 31 20:53:44 GMT 2025 , Edited by admin on Mon Mar 31 20:53:44 GMT 2025

LOINC

34213-9

Created by admin on Mon Mar 31 20:53:44 GMT 2025 , Edited by admin on Mon Mar 31 20:53:44 GMT 2025

LOINC

26944-9

Created by admin on Mon Mar 31 20:53:44 GMT 2025 , Edited by admin on Mon Mar 31 20:53:44 GMT 2025

LOINC

6702-5

Created by admin on Mon Mar 31 20:53:44 GMT 2025 , Edited by admin on Mon Mar 31 20:53:44 GMT 2025

LOINC

40814-6

Created by admin on Mon Mar 31 20:53:44 GMT 2025 , Edited by admin on Mon Mar 31 20:53:44 GMT 2025

LOINC

34215-4

Created by admin on Mon Mar 31 20:53:44 GMT 2025 , Edited by admin on Mon Mar 31 20:53:44 GMT 2025

Code System Code Type Description

WIKIPEDIA

11-Ketoandrosterone

Created by admin on Mon Mar 31 20:53:44 GMT 2025 , Edited by admin on Mon Mar 31 20:53:44 GMT 2025

PRIMARY

PUBCHEM

102029

Created by admin on Mon Mar 31 20:53:44 GMT 2025 , Edited by admin on Mon Mar 31 20:53:44 GMT 2025

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FDA UNII

3T4E87JT27

Created by admin on Mon Mar 31 20:53:44 GMT 2025 , Edited by admin on Mon Mar 31 20:53:44 GMT 2025

PRIMARY

CAS

1231-82-9

Created by admin on Mon Mar 31 20:53:44 GMT 2025 , Edited by admin on Mon Mar 31 20:53:44 GMT 2025

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EPA CompTox

DTXSID901043038

Created by admin on Mon Mar 31 20:53:44 GMT 2025 , Edited by admin on Mon Mar 31 20:53:44 GMT 2025

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NSC

56412

Created by admin on Mon Mar 31 20:53:44 GMT 2025 , Edited by admin on Mon Mar 31 20:53:44 GMT 2025

PRIMARY