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Details

Stereochemistry ABSOLUTE
Molecular Formula C27H40O8
Molecular Weight 492.6017
Optical Activity UNSPECIFIED
Defined Stereocenters 11 / 11
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DESOXYCORTICOSTERONE GLUCOSIDE

SMILES

[H][C@@]12CC[C@H](C(=O)CO[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@]1(C)CC[C@@]4([H])[C@@]2([H])CCC5=CC(=O)CC[C@]45C

InChI

InChIKey=SMSMUZPFFJLROV-LARVYCNESA-N
InChI=1S/C27H40O8/c1-26-9-7-15(29)11-14(26)3-4-16-17-5-6-19(27(17,2)10-8-18(16)26)20(30)13-34-25-24(33)23(32)22(31)21(12-28)35-25/h11,16-19,21-25,28,31-33H,3-10,12-13H2,1-2H3/t16-,17-,18-,19+,21+,22+,23-,24+,25+,26-,27-/m0/s1

HIDE SMILES / InChI
Desoxycorticosterone glucoside was studied in human in 1950th, where was shown, that intravenous injection of this compound did not narrow arterial-cerebral venous glucose difference. In no instance did cerebral venous blood sugar content surpass or approach arterial levels.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Effect of intravenous injections of desoxycorticosterone glucoside upon blood glucose of adrenalectomized dogs.
1951 Dec
Effect of desoxycorticosterone glucoside upon cerebral blood flow and metabolism of human subjects.
1951 Feb

Sample Use Guides

Single injection of 50 mg of desoxycorticosterone glucoside.
Route of Administration: Intravenous
In Vitro Use Guide
Unknown
Name Type Language
DESOXYCORTICOSTERONE GLUCOSIDE
Common Name English
DESOXYCORTONE GLUCOSIDE
Common Name English
11-DEOXYCORTICOSTERONE 21-GLUCOSIDE
Common Name English
PREGN-4-ENE-3,20-DIONE, 21-(.BETA.-D-GLUCOPYRANOSYLOXY)-
Systematic Name English
11-DEOXYCORTICOSTERONE GLUCOSIDE
Common Name English
DEOXYCORTICOSTERONE .BETA.-D-GLUCOPYRANOSIDE
Common Name English
DEOXYCORTICOSTERONE 21-GLUCOSIDE
Common Name English
CORTICOSTERONE, DEOXY-, .BETA.-D-GLUCOPYRANOSIDE
Systematic Name English
DEOXYCORTICOSTERONE GLUCOSIDE
Common Name English
Code System Code Type Description
CAS
4319-56-6
Created by admin on Fri Dec 15 15:23:57 GMT 2023 , Edited by admin on Fri Dec 15 15:23:57 GMT 2023
PRIMARY
ECHA (EC/EINECS)
224-349-5
Created by admin on Fri Dec 15 15:23:57 GMT 2023 , Edited by admin on Fri Dec 15 15:23:57 GMT 2023
PRIMARY
PUBCHEM
9983130
Created by admin on Fri Dec 15 15:23:57 GMT 2023 , Edited by admin on Fri Dec 15 15:23:57 GMT 2023
PRIMARY
FDA UNII
629B2BG9GA
Created by admin on Fri Dec 15 15:23:57 GMT 2023 , Edited by admin on Fri Dec 15 15:23:57 GMT 2023
PRIMARY
EPA CompTox
DTXSID601235870
Created by admin on Fri Dec 15 15:23:57 GMT 2023 , Edited by admin on Fri Dec 15 15:23:57 GMT 2023
PRIMARY