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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H30O2
Molecular Weight 302.451
Optical Activity ( - )
Defined Stereocenters 7 / 7
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BNN-20

SMILES

[H][C@@]12CC[C@@]3(CO3)[C@@]1(C)CC[C@@]4([H])[C@@]2([H])CC=C5C[C@@H](O)CC[C@]45C

InChI

InChIKey=LKDLANDMNIFZOI-IJMQKCTASA-N
InChI=1S/C20H30O2/c1-18-8-5-14(21)11-13(18)3-4-15-16(18)6-9-19(2)17(15)7-10-20(19)12-22-20/h3,14-17,21H,4-12H2,1-2H3/t14-,15+,16-,17-,18-,19-,20+/m0/s1

HIDE SMILES / InChI

Molecular Formula C20H30O2
Molecular Weight 302.451
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 7 / 7
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 18:38:38 UTC 2023
Edited
by admin
on Sat Dec 16 18:38:38 UTC 2023
Record UNII
5WM22TG224
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BNN-20
Code English
BNN-50
Code English
17.BETA.-SPIRO(5-ANDROSTEN-17,2'-OXIRAN)-3.BETA.-OL
Systematic Name English
ANDROST-5-EN-3.BETA.-OL, 17.BETA.,171-EPOXY-17-METHYL-
Systematic Name English
17.BETA.-SPIRO-(ANDROST-5-EN-17,2'-OXIRAN)-3.BETA.-OL
Systematic Name English
SPIRO(ANDROST-5-ENE-17,2'-OXIRAN)-3-OL, (3.BETA.,17.BETA.)-
Systematic Name English
(-)-(3.BETA.,17.BETA.)-SPIRO(ANDROST-5-ENE-17,2'-OXIRAN)-3-OL
Systematic Name English
SPIRO(ANDROST-5-ENE-17,2'-OXIRAN)-3.BETA.-OL, (17S)-
Systematic Name English
(3.BETA.,17.BETA.)-SPIRO(ANDROST-5-ENE-17,2'-OXIRAN)-3-OL
Systematic Name English
Code System Code Type Description
CAS
847-75-6
Created by admin on Sat Dec 16 18:38:39 UTC 2023 , Edited by admin on Sat Dec 16 18:38:39 UTC 2023
PRIMARY
FDA UNII
5WM22TG224
Created by admin on Sat Dec 16 18:38:39 UTC 2023 , Edited by admin on Sat Dec 16 18:38:39 UTC 2023
PRIMARY
PUBCHEM
44542342
Created by admin on Sat Dec 16 18:38:39 UTC 2023 , Edited by admin on Sat Dec 16 18:38:39 UTC 2023
PRIMARY
WIKIPEDIA
BNN-20
Created by admin on Sat Dec 16 18:38:39 UTC 2023 , Edited by admin on Sat Dec 16 18:38:39 UTC 2023
PRIMARY
EPA CompTox
DTXSID201337173
Created by admin on Sat Dec 16 18:38:39 UTC 2023 , Edited by admin on Sat Dec 16 18:38:39 UTC 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY