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all-trans-violaxanthin (CHEBI:35288)

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ChEBI Name all-trans-violaxanthin
ChEBI ID CHEBI:35288
ChEBI ASCII Name all-trans-violaxanthin
Definition The all-trans-stereoisomer of violaxanthin.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:46568, CHEBI:9993, CHEBI:22351
Supplier Information
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Formula Source
C40H56O4 KEGG COMPOUND
Net Charge 0
Average Mass 600.87024
InChI
InChI=1S/C40H56O4/c1-29(17-13-19-31(3)21-23-39-35(5,6)25-33(41)27-37(39,9)43-39)15-11-12-16-30(2)18-14-20-32(4)22-24-40-36(7,8)26-34(42)28-38(40,10)44-40/h11-24,33-34,41-42H,25-28H2,1-10H3/b12-11+,17-13+,18-14+,23-21+,24-22+,29-15+,30-16+,31-19+,32-20+/t33-,34-,37+,38+,39-,40-/m0/s1
InChIKey
SZCBXWMUOPQSOX-WVJDLNGLSA-N
SMILES
CC(\C=C\C=C(C)\C=C\[C@@]12O[C@]1(C)C[C@@H](O)CC2(C)C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/[C@@]12O[C@]1(C)C[C@@H](O)CC2(C)C
Roles Classification
Biological Role(s): plant secondary metabolite
Any plant metabolite that is not directly involved in the normal growth, development or reproduction of plants.
(via violaxanthin )
Application(s): food colouring
A food additive that imparts colour to food. In European countries, E-numbers for permitted food colours are from E 100 to E 199, divided into yellows (E 100-109), oranges (E 110-119), reds (E 120-129), blues and violets (E 130-139), greens (E 140-149), browns and blacks (E 150-159), and others (E 160-199).
View more on the ChEBI Ontology
ChEBI Ontology
Outgoing all-trans-violaxanthin (CHEBI:35288) has role food colouring (CHEBI:77182)
all-trans-violaxanthin (CHEBI:35288) is a violaxanthin (CHEBI:27295)
IUPAC Name
(3S,3'S,5R,5'R,6S,6'S)-5,5',6,6'-tetrahydro-5,6:5',6'-diepoxy-β,β-carotene-3,3'-diol
Synonyms Sources
(3S,3'S,5R,5'R,6S,6'S)-5,6:5',6'-diepoxy-5,5',6,6'-tetrahydro-β,β-carotene-3,3'-diol ChemIDplus
(3S,5R,6S,3'S,5'R,6'S)-5,6,5',6'-DIEPOXY-5,6,5',6'-TETRAHYDRO-BETA,BETA-CAROTENE-3,3'-DIOL PDBeChem
all-trans-Violaxanthin KEGG COMPOUND
E 161e ChEBI
Violaxanthin KEGG COMPOUND
Database Links Databases
C08614 KEGG COMPOUND
CPD1F-133 MetaCyc
HMDB03101 HMDB
LMPR01070282 LIPID MAPS
MOL000096 COMe
Violaxanthin Wikipedia
XAT PDBeChem
View more database links
Registry Numbers Types Sources
101269 Reaxys Registry Number Reaxys
101269 Beilstein Registry Number Beilstein
126-29-4 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
23820691 PubMed citation CiteXplore
24032717 PubMed citation CiteXplore
24506237 PubMed citation CiteXplore
Last Modified
27 March 2014

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