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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:81485 - osthenol
Main
ChEBI Ontology
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ChEBI Name
osthenol
ChEBI ID
CHEBI:81485
Definition
A hydroxycoumarin that is umbelliferone in which the hydrogen at position 8 has been replaced by a prenyl group.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C14H14O3
Net Charge
0
Average Mass
230.260
Monoisotopic Mass
230.09429
InChI
InChI=1S/C14H14O3/c1-9(2)3-6-11-12(15)7-4-10-5-8-13(16)17-14(10)11/h3-5,7-8,15H,6H2,1-2H3
InChIKey
RAKJVIPCCGXHHS-UHFFFAOYSA-N
SMILES
C1=C(C(=C2C(=C1)C=CC(O2)=O)CC=C(C)C)O
Metabolite of Species
Details
Pastinaca sativa
(NCBI:txid4041)
Found in root
(BTO:0001188)
. See:
PubMed
Petroselinum crispum
(NCBI:txid4043)
See:
PubMed
Angelica dahurica
(NCBI:txid48101)
Found in root
(BTO:0001188)
. See:
PubMed
Angelica dahurica
var.
formosana
(NCBI:txid714446)
Found in root
(BTO:0001188)
. See:
PubMed
Cnidium monnieri
(NCBI:txid94007)
Found in fruit
(BTO:0000486)
. See:
PubMed
Roles Classification
Biological Role
(s):
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
antifungal agent
An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
osthenol (
CHEBI:81485
)
has functional parent
umbelliferone (
CHEBI:27510
)
osthenol (
CHEBI:81485
)
has role
antifungal agent (
CHEBI:35718
)
osthenol (
CHEBI:81485
)
has role
plant metabolite (
CHEBI:76924
)
osthenol (
CHEBI:81485
)
is a
hydroxycoumarin (
CHEBI:37912
)
IUPAC Name
7-hydroxy--2
H
-1-benzopyran-2-one
Synonyms
Sources
7-hydroxy-8-(3-methyl-but-2-enyl)coumarin
ChEBI
7-hydroxy-8-prenylcoumarin
ChEBI
8-(3-methylbut-2-en-1-yl)umbelliferone
ChEBI
8-prenylumbelliferone
ChEBI
osthenol
UniProt
Manual Xrefs
Databases
C00030900
KNApSAcK
C18080
KEGG COMPOUND
CN101362768
Patent
CPD-9838
MetaCyc
HMDB0034130
HMDB
View more database links
Registry Numbers
Types
Sources
190526
Reaxys Registry Number
Reaxys
484-14-0
CAS Registry Number
KEGG COMPOUND
484-14-0
CAS Registry Number
ChemIDplus
Citations
Types
Sources
18386483
PubMed citation
Europe PMC
20931624
PubMed citation
Europe PMC
24354545
PubMed citation
Europe PMC
26552172
PubMed citation
Europe PMC
26918393
PubMed citation
Europe PMC
26983206
PubMed citation
Europe PMC
28822155
PubMed citation
Europe PMC
Last Modified
10 April 2018