11-DEHYDROCORTICOSTERONE

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

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C21H28O4
Molecular Weight	344.4446
Optical Activity	UNSPECIFIED
Defined Stereocenters	6 / 6
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of 11-DEHYDROCORTICOSTERONE

Structure Search

SMILES

[H][C@@]12CC[C@H](C(=O)CO)[C@@]1(C)CC(=O)[C@@]3([H])[C@@]2([H])CCC4=CC(=O)CC[C@]34C

InChI

InChIKey=FUFLCEKSBBHCMO-KJQYFISQSA-N

InChI=1S/C21H28O4/c1-20-8-7-13(23)9-12(20)3-4-14-15-5-6-16(18(25)11-22)21(15,2)10-17(24)19(14)20/h9,14-16,19,22H,3-8,10-11H2,1-2H3/t14-,15-,16+,19+,20-,21-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C21H28O4
Molecular Weight	344.4446
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	6 / 6
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

PubMed

PubMed

Title	Date	PubMed
Cross talk between corticosteroids and alpha-adrenergic signalling augments cardiomyocyte hypertrophy: a possible role for SGK1.	2006 Jun 1	16533503
Resveratrol inhibits 11β-hydroxysteroid dehydrogenase type 1 activity in rat adipose microsomes.	2013 Sep	23814014

Patents

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 15:01:49 UTC 2023` Edited by `admin` on `Fri Dec 15 15:01:49 UTC 2023`
Record UNII	FO4V44A3G3
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

11-DEHYDROCORTICOSTERONE

Common Name

English

17-(1-KETO-2-HYDROXYETHYL)-.DELTA.4-ANDROSTEN-3,11-DIONE

Common Name

English

.DELTA.4-PREGNEN-21-OL-3,11,20-TRIONE

Common Name

English

DEHYDROCORTICOSTERONE

Common Name

English

KENDALL'S COMPOUND A

Common Name

English

NSC-9702

Code

English

21-HYDROXYPREGN-4-ENE-3,11,20-TRIONE

Systematic Name

English

Dehydrocorticosteron [WHO-DD]

Common Name

English

DEHYDROCORTICOSTERON

Common Name

English

11-DEHYDROCORTICOSTERONE [MI]

Common Name

English

Classification Tree Code System Code

LOINC

82846-7

Created by admin on Fri Dec 15 15:01:49 UTC 2023 , Edited by admin on Fri Dec 15 15:01:49 UTC 2023

LOINC

82849-1

Created by admin on Fri Dec 15 15:01:49 UTC 2023 , Edited by admin on Fri Dec 15 15:01:49 UTC 2023

LOINC

82848-3

Created by admin on Fri Dec 15 15:01:49 UTC 2023 , Edited by admin on Fri Dec 15 15:01:49 UTC 2023

LOINC

82847-5

Created by admin on Fri Dec 15 15:01:49 UTC 2023 , Edited by admin on Fri Dec 15 15:01:49 UTC 2023

Code System Code Type Description

SMS_ID

100000126063

Created by admin on Fri Dec 15 15:01:49 UTC 2023 , Edited by admin on Fri Dec 15 15:01:49 UTC 2023

PRIMARY

CHEBI

78600

Created by admin on Fri Dec 15 15:01:49 UTC 2023 , Edited by admin on Fri Dec 15 15:01:49 UTC 2023

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FDA UNII

FO4V44A3G3

Created by admin on Fri Dec 15 15:01:49 UTC 2023 , Edited by admin on Fri Dec 15 15:01:49 UTC 2023

PRIMARY

MESH

C003552

Created by admin on Fri Dec 15 15:01:49 UTC 2023 , Edited by admin on Fri Dec 15 15:01:49 UTC 2023

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EVMPD

SUB32794

Created by admin on Fri Dec 15 15:01:49 UTC 2023 , Edited by admin on Fri Dec 15 15:01:49 UTC 2023

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NSC

9702

Created by admin on Fri Dec 15 15:01:49 UTC 2023 , Edited by admin on Fri Dec 15 15:01:49 UTC 2023

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MERCK INDEX

m4143

Created by admin on Fri Dec 15 15:01:49 UTC 2023 , Edited by admin on Fri Dec 15 15:01:49 UTC 2023

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Merck Index

EPA CompTox

DTXSID40861617

Created by admin on Fri Dec 15 15:01:49 UTC 2023 , Edited by admin on Fri Dec 15 15:01:49 UTC 2023

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PUBCHEM

5311364

Created by admin on Fri Dec 15 15:01:49 UTC 2023 , Edited by admin on Fri Dec 15 15:01:49 UTC 2023

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CAS

72-23-1

Created by admin on Fri Dec 15 15:01:49 UTC 2023 , Edited by admin on Fri Dec 15 15:01:49 UTC 2023

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ECHA (EC/EINECS)

200-776-2

Created by admin on Fri Dec 15 15:01:49 UTC 2023 , Edited by admin on Fri Dec 15 15:01:49 UTC 2023

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WIKIPEDIA

11-Dehydrocorticosterone

Created by admin on Fri Dec 15 15:01:49 UTC 2023 , Edited by admin on Fri Dec 15 15:01:49 UTC 2023

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Related Record Type Details


					33M0S99YTT

MINERALOCORTICOID RECEPTOR

TARGET -> AGONIST

Comments:

Potent mineralocorticoid, with generally greater such activity than that of corticosterone.