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> Main
CHEBI:69083 - licorisoflavan A
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ChEBI Name
licorisoflavan A
ChEBI ID
CHEBI:69083
Definition
A member of the class of hydroxyisoflavans that is the 7-
O
-methyl derivative of licoricidin. Isolated from
Glycyrrhiza uralensis
, it exhibits antibacterial activity.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C27H34O5
Net Charge
0
Average Mass
438.55590
Monoisotopic Mass
438.24062
InChI
InChI=1S/C27H34O5/c1-
16(2)
7-
9-
20-
23(28)
12-
11-
19(26(20)
29)
18-
13-
22-
25(32-
15-
18)
14-
24(30-
5)
21(27(22)
31-
6)
10-
8-
17(3)
4/h7-
8,11-
12,14,18,28-
29H,9-
10,13,15H2,1-
6H3/t18-
/m0/s1
InChIKey
GDAAEAXMNLVRCZ-SFHVURJKSA-N
SMILES
COc1cc2OC[C@H](Cc2c(OC)c1CC=C(C)C)c1ccc(O)c(CC=C(C)C)c1O
Metabolite of Species
Details
Glycyrrhiza uralensis
(NCBI:txid74613)
Found in root
(BTO:0001188)
. Dried and ground roots extracted with supercritical CO2 with 5% EtOH as modifier See:
PubMed
Roles Classification
Biological Role
(s):
antibacterial agent
A substance (or active part thereof) that kills or slows the growth of bacteria.
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
licorisoflavan A (
CHEBI:69083
)
has functional parent
licoricidin (
CHEBI:69082
)
licorisoflavan A (
CHEBI:69083
)
has role
antibacterial agent (
CHEBI:33282
)
licorisoflavan A (
CHEBI:69083
)
has role
plant metabolite (
CHEBI:76924
)
licorisoflavan A (
CHEBI:69083
)
is a
aromatic ether (
CHEBI:35618
)
licorisoflavan A (
CHEBI:69083
)
is a
hydroxyisoflavans (
CHEBI:76250
)
licorisoflavan A (
CHEBI:69083
)
is a
methoxyisoflavan (
CHEBI:77002
)
IUPAC Name
4-
[(3
R
)-
5,7-
dimethoxy-
6-
(3-
methylbut-
2-
en-
1-
yl)-
3,4-
dihydro-
2
H
-
chromen-
3-
yl]-
2-
(3-
methylbut-
2-
en-
1-
yl)benzene-
1,3-
diol
Synonyms
Sources
(+)-2ʼ,4ʼ-dihydroxy-5,7-dimethoxy-6,3ʼ-diprenylisoflavan
LIPID MAPS
5-
O
-methyllicoricidin
ChemIDplus
7-
O
-methyllicoricidin
ChEBI
Manual Xrefs
Databases
HMDB0034184
HMDB
LMPK12080046
LIPID MAPS
View more database links
Registry Numbers
Types
Sources
129314-37-0
CAS Registry Number
ChemIDplus
5461708
Reaxys Registry Number
Reaxys
Citation
Type
Source
22074222
PubMed citation
Europe PMC
Last Modified
16 January 2014