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

Details

Stereochemistry ABSOLUTE
Molecular Formula C19H28O5S
Molecular Weight 368.488
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PRASTERONE SULFATE

SMILES

[H][C@@]12CCC(=O)[C@@]1(C)CC[C@@]3([H])[C@@]2([H])CC=C4C[C@H](CC[C@]34C)OS(O)(=O)=O

InChI

InChIKey=CZWCKYRVOZZJNM-USOAJAOKSA-N
InChI=1S/C19H28O5S/c1-18-9-7-13(24-25(21,22)23)11-12(18)3-4-14-15-5-6-17(20)19(15,2)10-8-16(14)18/h3,13-16H,4-11H2,1-2H3,(H,21,22,23)/t13-,14-,15-,16-,18-,19-/m0/s1

HIDE SMILES / InChI

Molecular Formula C19H28O5S
Molecular Weight 368.488
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 6 / 6
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:24:43 UTC 2023
Edited
by admin
on Fri Dec 15 15:24:43 UTC 2023
Record UNII
57B09Q7FJR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PRASTERONE SULFATE
MART.   WHO-DD  
Common Name English
ANDROST-5-EN-17-ONE, 3-(SULFOOXY)-, (3.BETA.)-
Systematic Name English
Prasterone sulfate [WHO-DD]
Common Name English
PRASTERONE SULPHATE
Common Name English
DEHYDROEPIANDROSTERONE SULFATE
MI  
Common Name English
GENAFLOW
Brand Name English
PRASTERONE SULFATE [MART.]
Common Name English
ANDROST-5-EN-17-ONE, 3.BETA.-HYDROXY-, HYDROGEN SULFATE
Systematic Name English
DEHYDROANDROSTERONE SULFATE
Common Name English
DEHYDROEPIANDROSTERONE SULFATE [MI]
Common Name English
DHEA SULFATE
Common Name English
Classification Tree Code System Code
CFR 21 CFR 862.1245
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
LOINC 16721-3
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
LOINC 34282-4
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
LOINC 76347-4
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
LOINC 15053-2
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
LOINC 34280-8
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
LOINC 2192-3
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
LOINC 2191-5
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
LOINC 34281-6
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
LOINC 2190-7
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
LOINC 14688-6
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
LOINC 35205-4
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
Code System Code Type Description
DRUG BANK
DB05804
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
PRIMARY
PUBCHEM
12594
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
PRIMARY
DRUG CENTRAL
4049
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
PRIMARY
CAS
651-48-9
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
PRIMARY
MERCK INDEX
m4145
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
PRIMARY Merck Index
CHEBI
16814
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
PRIMARY
EPA CompTox
DTXSID8040228
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
PRIMARY
EVMPD
SUB34548
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
PRIMARY
WIKIPEDIA
DEHYDROEPIANDROSTERONE SULFATE
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
PRIMARY
FDA UNII
57B09Q7FJR
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
PRIMARY
SMS_ID
100000128006
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
PRIMARY
MESH
D019314
Created by admin on Fri Dec 15 15:24:43 UTC 2023 , Edited by admin on Fri Dec 15 15:24:43 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
TRANSPORTER -> SUBSTRATE
TRANSPORTER -> SUBSTRATE
TRANSPORTER -> SUBSTRATE
SALT/SOLVATE -> PARENT
TRANSPORTER -> INHIBITOR
Related Record Type Details
PARENT -> METABOLITE
Oral prasterone is sulfated to 5-DHEAS ester in the intestine and liver by sulfotransferases
Related Record Type Details
ACTIVE MOIETY