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Details

Stereochemistry ABSOLUTE
Molecular Formula C19H32O2
Molecular Weight 292.4562
Optical Activity UNSPECIFIED
Defined Stereocenters 8 / 8
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3.ALPHA.-ANDROSTANEDIOL

SMILES

[H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@@]3([H])[C@@]2([H])CC[C@@]4([H])C[C@H](O)CC[C@]34C

InChI

InChIKey=CBMYJHIOYJEBSB-KHOSGYARSA-N
InChI=1S/C19H32O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12-17,20-21H,3-11H2,1-2H3/t12-,13+,14-,15-,16-,17-,18-,19-/m0/s1

HIDE SMILES / InChI

Molecular Formula C19H32O2
Molecular Weight 292.4562
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 8 / 8
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 20:18:52 UTC 2023
Edited
by admin
on Fri Dec 15 20:18:52 UTC 2023
Record UNII
J34MX0M30Y
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3.ALPHA.-ANDROSTANEDIOL
Common Name English
ANDROSTANE-3,17-DIOL, (3.ALPHA.,5.ALPHA.,17.BETA.)-
Systematic Name English
3ALPHA,17BETA-DIHYDROXY-5ALPHA-ANDROSTANE
Systematic Name English
DIHYDROANDROSTERONE
Common Name English
ETIOCHOLANE-3.ALPHA,17.BETA.-DIOL
Common Name English
5.ALPHA.-ADIOL
Common Name English
3.ALPHA.,17.BETA.-DIHYDROXY-5.ALPHA.-ANDROSTANE
Systematic Name English
5.ALPHA.-ANDROSTANE-3.ALPHA.,17.BETA.-DIOL
Systematic Name English
5 .ALPHA.-ANDROSTANE-3 .ALPHA.,17 .BETA.-DIOL
Systematic Name English
ANDROSTANE-3.ALPHA,17.BETA.-DIOL
Common Name English
5.ALPHA.-AND-3.ALPHA.,17.BETA.-DIOL
Common Name English
ANDROSTANEDIOL, 3.ALPHA.-
Common Name English
17.BETA.-DIHYDROANDROSTERONE
Common Name English
HOMBREOL
Common Name English
3.ALPHA.,5.ALPHA.-TETRAHYDROTESTOSTERONE
Common Name English
NSC-9899
Code English
Classification Tree Code System Code
DEA NO. 4000
Created by admin on Fri Dec 15 20:18:52 UTC 2023 , Edited by admin on Fri Dec 15 20:18:52 UTC 2023
Code System Code Type Description
NSC
9899
Created by admin on Fri Dec 15 20:18:52 UTC 2023 , Edited by admin on Fri Dec 15 20:18:52 UTC 2023
PRIMARY
CAS
1852-53-5
Created by admin on Fri Dec 15 20:18:52 UTC 2023 , Edited by admin on Fri Dec 15 20:18:52 UTC 2023
PRIMARY
CHEBI
36713
Created by admin on Fri Dec 15 20:18:52 UTC 2023 , Edited by admin on Fri Dec 15 20:18:52 UTC 2023
PRIMARY
ECHA (EC/EINECS)
217-447-4
Created by admin on Fri Dec 15 20:18:52 UTC 2023 , Edited by admin on Fri Dec 15 20:18:52 UTC 2023
PRIMARY
PUBCHEM
15818
Created by admin on Fri Dec 15 20:18:52 UTC 2023 , Edited by admin on Fri Dec 15 20:18:52 UTC 2023
PRIMARY
WIKIPEDIA
3α-Androstanediol
Created by admin on Fri Dec 15 20:18:52 UTC 2023 , Edited by admin on Fri Dec 15 20:18:52 UTC 2023
PRIMARY
FDA UNII
J34MX0M30Y
Created by admin on Fri Dec 15 20:18:52 UTC 2023 , Edited by admin on Fri Dec 15 20:18:52 UTC 2023
PRIMARY
DRUG BANK
DB01530
Created by admin on Fri Dec 15 20:18:52 UTC 2023 , Edited by admin on Fri Dec 15 20:18:52 UTC 2023
PRIMARY
EPA CompTox
DTXSID3022378
Created by admin on Fri Dec 15 20:18:52 UTC 2023 , Edited by admin on Fri Dec 15 20:18:52 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> METABOLITE
In reproductive tissues, dihydrotestosterone is further metabolized to 3-alpha and 3-beta androstanediol