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03. Biological Effects of Specific Chemicals
03. Biological Effects of Specific Chemicals
1,7-bis-(4-hydroxyphenyl)-2,4,6-heptatrienone [CHEBI:65503] (1)
08. Chemical Category
08. Chemical Category
1,7-bis-(4-hydroxyphenyl)-2,4,6-heptatrienone [CHEBI:65503] (1)
1,7-bis-(4-hydroxyphenyl)-2,4,6-heptatrienone [CHEBI:65503] (1)
1,7-bis-(4-hydroxyphenyl)-2,4,6-heptatrienone [CHEBI:65503] (1)
1,7-bis-(4-hydroxyphenyl)-2,4,6-heptatrienone [CHEBI:65503] (1)
1,7-bis-(4-hydroxyphenyl)-2,4,6-heptatrienone [CHEBI:65503] (1)
1,7-bis-(4-hydroxyphenyl)-2,4,6-heptatrienone [CHEBI:65503] (1)
1,7-bis-(4-hydroxyphenyl)-2,4,6-heptatrienone [CHEBI:65503] (1)
1,7-bis-(4-hydroxyphenyl)-2,4,6-heptatrienone [CHEBI:65503] (1)
1,7-bis-(4-hydroxyphenyl)-2,4,6-heptatrienone [CHEBI:65503] (1)
1,7-bis-(4-hydroxyphenyl)-2,4,6-heptatrienone [CHEBI:65503] (1)
1,7-bis-(4-hydroxyphenyl)-2,4,6-heptatrienone [CHEBI:65503] (1)
1,7-bis-(4-hydroxyphenyl)-2,4,6-heptatrienone [CHEBI:65503] (1)
1,7-bis-(4-hydroxyphenyl)-2,4,6-heptatrienone [CHEBI:65503] (1)
09. Chemical Capabilities
09. Chemical Capabilities
1,7-bis-(4-hydroxyphenyl)-2,4,6-heptatrienone [CHEBI:65503] (1)
ChEBI Compound Accession Identifier :
[CHEBI:65503]
ChEBI Compound Description :
An enone that consists of 7-oxohepta-1,3,5-triene-1,7-diyl moiety substituted by a 4-hydroxyphenyl substituent at C-1 and at C-7. It is isolated from the rhizomes of Etlingera elatior and has been found to inhibit lipid peroxidation.
ChEBI Compound Identification Number :
65503
ChEBI InChI Value :
InChI=1S/C19H16O3/c20-17-11-7-15(8-12-17)5-3-1-2-4-6-19(22)16-9-13-18(21)14-10-16/h1-14,20-21H/b2-1+,5-3+,6-4+
ChEBI InChIKey Value :
WRCGSWXFJPRBPO-CRQXNEITSA-N
ChEBI Compound Name :
1,7-bis-(4-hydroxyphenyl)-2,4,6-heptatrienone
ChEBI SMILES Value :
Oc1ccc(cc1)\C=C\C=C\C=C\C(=O)c1ccc(O)cc1
ChEBI Substance ID :
160645021
ChEBI URL :
ChEBI:65503
ChemSpider ID :
9452770
Ontomatica Chemical Accession Key (OnChAKey) :
WRCGSWXFJPRBPO_CRQXNEITSA_N_000_000000
PubChem Compound ID :
11277770