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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:132452 - parasiloxanthin
Main
ChEBI Ontology
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ChEBI Name
parasiloxanthin
ChEBI ID
CHEBI:132452
Definition
A carotenol that is 7,8-dihydro-β,β-carotene carrying two hydroxy substituents at positions 3 and 3'.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C40H58O2
Net Charge
0
Average Mass
570.889
Monoisotopic Mass
570.44368
InChI
InChI=1S/C40H58O2/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-
21,23,35-
36,41-
42H,22,24-
28H2,1-
10H3/b12-
11+,17-
13+,18-
14+,23-
21+,29-
15+,30-
16+,31-
19+,32-
20+/t35-
,36-
/m1/s1
InChIKey
ZAYHYNGKERKFHJ-DRCJTWAYSA-N
SMILES
[C@@H]
1(CC(C(\C=C\C(=C\C=C\C(=C\C=C\C=C(\C=C\C=C(\CCC=2C(C)
(C[C@@H]
(CC2C)
O)
C)
/C)
/C)
\C)
\C)
=C(C1)
C)
(C)
C)
O
Metabolite of Species
Details
Calanus helgolandicus
(NCBI:txid114068)
See:
PubMed
Calanus helgolandicus
(NCBI:txid114068)
See:
MetaboLights Study
Silurus asotus
(NCBI:txid30991)
See:
PubMed
Plotosidae
(NCBI:txid30997)
See:
PubMed
Malapteruridae
(NCBI:txid31001)
See:
PubMed
Clariidae
(NCBI:txid31009)
See:
PubMed
Callichthyidae
(NCBI:txid31012)
See:
PubMed
Bagridae
(NCBI:txid31013)
See:
PubMed
Amblycipitidae
(NCBI:txid31019)
See:
PubMed
Escherichia coli
(NCBI:txid562)
See:
PubMed
Lota lota
(NCBI:txid69944)
See:
PubMed
Ictaluridae
(NCBI:txid7996)
See:
PubMed
Roles Classification
Biological Role
(s):
marine metabolite
Any metabolite produced during a metabolic reaction in marine macro- and microorganisms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
parasiloxanthin (
CHEBI:132452
)
has role
marine metabolite (
CHEBI:76507
)
parasiloxanthin (
CHEBI:132452
)
is a
carotenol (
CHEBI:23045
)
parasiloxanthin (
CHEBI:132452
)
is a
diol (
CHEBI:23824
)
IUPAC Name
(3
R
,3'
R
)-7,8-dihydro-β,β-carotene-3,3'-diol
Synonyms
Sources
7,8-Dihydro-beta,beta-carotene-3,3'-diol
KNApSAcK
7,8-Dihydrozeaxanthin
LIPID MAPS
Manual Xrefs
Databases
C00022866
KNApSAcK
HMDB0036915
HMDB
LMPR01070092
LIPID MAPS
View more database links
Registry Numbers
Types
Sources
21132410
Reaxys Registry Number
Reaxys
62994-48-3
CAS Registry Number
KNApSAcK
Citations
Types
Sources
10754789
PubMed citation
Europe PMC
12431401
PubMed citation
Europe PMC
21212565
PubMed citation
Europe PMC
26364855
PubMed citation
Europe PMC
9470222
PubMed citation
Europe PMC
Last Modified
12 January 2017