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Details

Stereochemistry MIXED
Molecular Formula C20H30O2
Molecular Weight 302.451
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 2
E/Z Centers 4
Charge 0

SHOW SMILES / InChI
Structure of HEPAXANTHIN

SMILES

CC(=C/CO)\C=C\C=C(C)\C=C\C12OC1(C)CCCC2(C)C

InChI

InChIKey=XLRQASJLHKRLKG-JVSJJYLASA-N
InChI=1S/C20H30O2/c1-16(8-6-9-17(2)11-15-21)10-14-20-18(3,4)12-7-13-19(20,5)22-20/h6,8-11,14,21H,7,12-13,15H2,1-5H3/b9-6+,14-10+,16-8+,17-11+

HIDE SMILES / InChI

Molecular Formula C20H30O2
Molecular Weight 302.451
Charge 0
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 2
E/Z Centers 4
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 08:10:05 GMT 2023
Edited
by admin
on Sat Dec 16 08:10:05 GMT 2023
Record UNII
1YG3QZU2Z2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HEPAXANTHIN
MI  
Common Name English
2,4,6,8-NONATETRAEN-1-OL, 3,7-DIMETHYL-9-(2,2,6-TRIMETHYL-7-OXABICYCLO(4.1.0)HEPT-1-YL)-, (ALL-E)-
Systematic Name English
VITAMIN A 5,6-EPOXIDE, ALL-TRANS-
Common Name English
VITAMIN A EPOXIDE
Common Name English
VITAMIN A 5,6-EPOXIDE
Common Name English
5,6-EPOXY-5,6-DIHYDRORETINOL
Common Name English
5,6-EPOXYRETINOL
Common Name English
574-CHROMOGEN
Common Name English
HEPAXANTHIN [MI]
Common Name English
5,6-MONOEPOXYVITAMIN A
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID401318137
Created by admin on Sat Dec 16 08:10:05 GMT 2023 , Edited by admin on Sat Dec 16 08:10:05 GMT 2023
PRIMARY
CAS
512-39-0
Created by admin on Sat Dec 16 08:10:05 GMT 2023 , Edited by admin on Sat Dec 16 08:10:05 GMT 2023
PRIMARY
PUBCHEM
6438471
Created by admin on Sat Dec 16 08:10:05 GMT 2023 , Edited by admin on Sat Dec 16 08:10:05 GMT 2023
PRIMARY
MERCK INDEX
m756
Created by admin on Sat Dec 16 08:10:05 GMT 2023 , Edited by admin on Sat Dec 16 08:10:05 GMT 2023
PRIMARY Merck Index
FDA UNII
1YG3QZU2Z2
Created by admin on Sat Dec 16 08:10:05 GMT 2023 , Edited by admin on Sat Dec 16 08:10:05 GMT 2023
PRIMARY