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:3421 - carlinoside
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
carlinoside
ChEBI ID
CHEBI:3421
Definition
A
C
-glycosyl compound that is luteolin substituted at positions 8 and 6 by α-
L
-arabinopyranosyl and β-
D
-glucosyl residues respectively.
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
C26H28O15
Net Charge
0
Average Mass
580.49150
Monoisotopic Mass
580.14282
InChI
InChI=1S/C26H28O15/c27-
5-
13-
18(33)
21(36)
23(38)
26(41-
13)
15-
19(34)
14-
10(30)
4-
12(7-
1-
2-
8(28)
9(29)
3-
7)
40-
24(14)
16(20(15)
35)
25-
22(37)
17(32)
11(31)
6-
39-
25/h1-
4,11,13,17-
18,21-
23,25-
29,31-
38H,5-
6H2/t11-
,13+,17-
,18+,21-
,22+,23+,25-
,26-
/m0/s1
InChIKey
XBGYTZHKGMCEGE-VYUBKLCTSA-N
SMILES
OC[C@H]
1O[C@H]
([C@H]
(O)
[C@@H]
(O)
[C@@H]
1O)
c1c(O)
c([C@@H]
2OC[C@H]
(O)
[C@H]
(O)
[C@H]
2O)
c2oc(cc(=O)
c2c1O)
-
c1ccc(O)
c(O)
c1
Roles Classification
Chemical Role
(s):
antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Biological Role
(s):
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Application
(s):
anti-inflammatory agent
Any compound that has anti-inflammatory effects.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
carlinoside (
CHEBI:3421
)
has functional parent
luteolin (
CHEBI:15864
)
carlinoside (
CHEBI:3421
)
has role
anti-inflammatory agent (
CHEBI:67079
)
carlinoside (
CHEBI:3421
)
has role
antioxidant (
CHEBI:22586
)
carlinoside (
CHEBI:3421
)
has role
metabolite (
CHEBI:25212
)
carlinoside (
CHEBI:3421
)
is a
C
-glycosyl compound (
CHEBI:20857
)
carlinoside (
CHEBI:3421
)
is a
tetrahydroxyflavone (
CHEBI:38684
)
Synonyms
Sources
6-
C
-
β-
D
-
glucosyl-
8-
C
-
α-
L
-
arabinopyranosylluteolin
ChEBI
8-
C
-
α-
L
-
arabinopyranosyl-
6-
C
-
β-
D
-
glucosylluteolin
ChEBI
luteolin 6-
C
-
β-
D
-
glucopyranoside-
8-
C-
α-
L
-
arabinopyranoside
LIPID MAPS
luteolin 6-
C
-glucoside-8-
C
-arabinoside
ChEBI
Manual Xrefs
Databases
C00006184
KNApSAcK
C10026
KEGG COMPOUND
LMPK12110488
LIPID MAPS
View more database links
Registry Numbers
Types
Sources
59952-97-5
CAS Registry Number
KEGG COMPOUND
6563440
Reaxys Registry Number
Reaxys
Citations
Types
Sources
10820082
PubMed citation
Europe PMC
17981413
PubMed citation
Europe PMC
21801714
PubMed citation
Europe PMC
905416
PubMed citation
Europe PMC
Last Modified
28 July 2014