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

Details

Stereochemistry ABSOLUTE
Molecular Formula C17H20O5
Molecular Weight 304.3377
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of OLEOCANTHAL

SMILES

C\C=C(\C=O)[C@@H](CC=O)CC(=O)OCCC1=CC=C(O)C=C1

InChI

InChIKey=VPOVFCBNUOUZGG-VAKDEWRISA-N
InChI=1S/C17H20O5/c1-2-14(12-19)15(7-9-18)11-17(21)22-10-8-13-3-5-16(20)6-4-13/h2-6,9,12,15,20H,7-8,10-11H2,1H3/b14-2-/t15-/m0/s1

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Alzheimer's-associated Abeta oligomers show altered structure, immunoreactivity and synaptotoxicity with low doses of oleocanthal.
2009 Oct 15
Unusual pungency from extra-virgin olive oil is attributable to restricted spatial expression of the receptor of oleocanthal.
2011 Jan 19
Name Type Language
OLEOCANTHAL
MI  
INCI  
Official Name English
2-(4-HYDROXYPHENYL)ETHYL (3S,4E)-4-FORMYL-3-(2-OXOETHYL)HEX-4-ENOATE
Systematic Name English
OLEOCANTHAL, (-)-
Common Name English
(3S,4E)-4-FORMYL-3-(2-OXOETHYL)-4-HEXENOIC ACID 2-(4-HYDROXYPHENYL)ETHYL ESTER
Systematic Name English
DEACETOXY LIGSTROSIDE AGLYCON
Common Name English
(-)-OLEOCANTHAL
Common Name English
4-HEXENOIC ACID, 4-FORMYL-3-(2-OXOETHYL)-, 2-(4-HYDROXYPHENYL)ETHYL ESTER, (3S,4E)-
Systematic Name English
OLEOCANTHAL [MI]
Common Name English
OLEOCANTHAL [INCI]
Common Name English
Code System Code Type Description
CAS
289030-99-5
Created by admin on Sat Dec 16 20:18:38 GMT 2023 , Edited by admin on Sat Dec 16 20:18:38 GMT 2023
PRIMARY
WIKIPEDIA
OLEOCANTHAL
Created by admin on Sat Dec 16 20:18:38 GMT 2023 , Edited by admin on Sat Dec 16 20:18:38 GMT 2023
PRIMARY
MESH
C503534
Created by admin on Sat Dec 16 20:18:38 GMT 2023 , Edited by admin on Sat Dec 16 20:18:38 GMT 2023
PRIMARY
MERCK INDEX
m8192
Created by admin on Sat Dec 16 20:18:38 GMT 2023 , Edited by admin on Sat Dec 16 20:18:38 GMT 2023
PRIMARY Merck Index
CAS
1246025-97-7
Created by admin on Sat Dec 16 20:18:38 GMT 2023 , Edited by admin on Sat Dec 16 20:18:38 GMT 2023
ALTERNATIVE
PUBCHEM
11652416
Created by admin on Sat Dec 16 20:18:38 GMT 2023 , Edited by admin on Sat Dec 16 20:18:38 GMT 2023
PRIMARY
CHEBI
85673
Created by admin on Sat Dec 16 20:18:38 GMT 2023 , Edited by admin on Sat Dec 16 20:18:38 GMT 2023
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FDA UNII
AC7QO6038O
Created by admin on Sat Dec 16 20:18:38 GMT 2023 , Edited by admin on Sat Dec 16 20:18:38 GMT 2023
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EPA CompTox
DTXSID40183104
Created by admin on Sat Dec 16 20:18:38 GMT 2023 , Edited by admin on Sat Dec 16 20:18:38 GMT 2023
PRIMARY