Services
Research
Training
Industry
About us
ChEBI
Examples:
iron*
,
InChI=1S/CH4O/c1-2/h2H,1H3
,
caffeine
Advanced
Home
Advanced Search
Browse
Documentation
Download
Tools
About ChEBI
Submit
Contact us
DiNA
Statistics
Entity of the Month
Periodic Table
Ontology
Train online
User Manual
Annotation Manual
Developer Manual
FAQ's
BiNChE
libChEBI
Web Services
ChEBI
> Main
CHEBI:35326 - tunaxanthin
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
tunaxanthin
ChEBI ID
CHEBI:35326
Definition
A carotenol isolated from the white tuna, or albacore tuna (
Thunnus albacares
).
Stars
This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download
Molfile
XML
SDF
Find compounds which contain this structure
Find compounds which resemble this structure
Take structure to the Advanced Search
Formula
C40H56O2
Net Charge
0
Average Mass
568.87144
Monoisotopic Mass
568.42803
InChI
InChI=1S/C40H56O2/c1-
29(17-
13-
19-
31(3)
21-
23-
37-
33(5)
25-
35(41)
27-
39(37,7)
8)
15-
11-
12-
16-
30(2)
18-
14-
20-
32(4)
22-
24-
38-
34(6)
26-
36(42)
28-
40(38,9)
10/h11-
26,35-
38,41-
42H,27-
28H2,1-
10H3/b12-
11+,17-
13+,18-
14+,23-
21+,24-
22+,29-
15+,30-
16+,31-
19+,32-
20+
InChIKey
BIPAHAFBQLWRMC-DKLMTRRASA-N
SMILES
CC(\C=C\C=C(C)\C=C\C1C(C)=CC(O)CC1(C)C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1C(C)=CC(O)CC1(C)C
Roles Classification
Biological Role
(s):
marine metabolite
Any metabolite produced during a metabolic reaction in marine macro- and microorganisms.
animal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in animals that include diverse creatures from sponges, insects to mammals.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
tunaxanthin (
CHEBI:35326
)
has role
animal metabolite (
CHEBI:75767
)
tunaxanthin (
CHEBI:35326
)
has role
marine metabolite (
CHEBI:76507
)
tunaxanthin (
CHEBI:35326
)
is a
carotenol (
CHEBI:23045
)
Incoming
lactucaxanthin (
CHEBI:6357
)
is a
tunaxanthin (
CHEBI:35326
)
IUPAC Name
ε,ε-carotene-3,3'-diol
Registry Numbers
Types
Sources
2031575
Reaxys Registry Number
Reaxys
2031575
Beilstein Registry Number
Beilstein
Citations
Types
Sources
7141323
PubMed citation
Europe PMC
716757
PubMed citation
Europe PMC
Last Modified
08 May 2014