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> Main
CHEBI:132653 - kadsurenin L
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ChEBI Name
kadsurenin L
ChEBI ID
CHEBI:132653
Definition
A neolignan with formula C
23
H
28
O
6
, originally isolated from
Piper kadsura
.
Stars
This entity has been manually annotated by the ChEBI Team.
Submitter
qingping liu
Supplier Information
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Formula
C23H28O6
Net Charge
0
Average Mass
400.466
Monoisotopic Mass
400.18859
InChI
InChI=1S/C23H28O6/c1-
7-
8-
16-
12-
23(28-
6)
13(2)
19(20(21(16)
25)
22(23)
29-
14(3)
24)
15-
9-
10-
17(26-
4)
18(11-
15)
27-
5/h7,9-
13,19-
20,22H,1,8H2,2-
6H3/t13-
,19+,20-
,22+,23+/m1/s1
InChIKey
TVDQUJSTRADHSU-WWDCKHPPSA-N
SMILES
O([C@@]12[C@@H]([C@H]([C@@]([C@@H]1OC(=O)C)(C(=O)C(=C2)CC=C)[H])C3=CC(OC)=C(OC)C=C3)C)C
Metabolite of Species
Details
Piper kadsura
(NCBI:txid54803)
See:
PubMed
Roles Classification
Biological Role
(s):
platelet-activating factor receptor antagonist
An antagonist that acts at the platelet-activating factor receptor.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
kadsurenin L (
CHEBI:132653
)
has role
plant metabolite (
CHEBI:76924
)
kadsurenin L (
CHEBI:132653
)
has role
platelet-activating factor receptor antagonist (
CHEBI:134182
)
kadsurenin L (
CHEBI:132653
)
is a
acetate ester (
CHEBI:47622
)
kadsurenin L (
CHEBI:132653
)
is a
bridged compound (
CHEBI:35990
)
kadsurenin L (
CHEBI:132653
)
is a
carbobicyclic compound (
CHEBI:36785
)
kadsurenin L (
CHEBI:132653
)
is a
cyclic ketone (
CHEBI:3992
)
kadsurenin L (
CHEBI:132653
)
is a
dimethoxybenzene (
CHEBI:51681
)
kadsurenin L (
CHEBI:132653
)
is a
enone (
CHEBI:51689
)
kadsurenin L (
CHEBI:132653
)
is a
neolignan (
CHEBI:25497
)
IUPAC Name
(1
R
,5
S
,6
R
,7
R
,8
S
)-
6-
(3,4-
dimethoxyphenyl)-
1-
methoxy-
7-
methyl-
4-
oxo-
3-
(prop-
2-
en-
1-
yl)bicyclo[3.2.1]oct-
2-
en-
8-
yl acetate
Synonym
Source
delta(8')-3,4,5'-Trimethoxy-4'-acetoxy-2',3',4',5'-tetrahydro-2'-oxo-7.3',8.5'-neolignan
ChemIDplus
Registry Numbers
Types
Sources
149438-61-9
CAS Registry Number
ChemIDplus
20034355
Reaxys Registry Number
Reaxys
Citation
Type
Source
8368081
PubMed citation
Europe PMC
Last Modified
15 December 2016