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ChEBI
> Main
CHEBI:78696 - cercosporamide
Main
ChEBI Ontology
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ChEBI Name
cercosporamide
ChEBI ID
CHEBI:78696
Definition
A member of the class of dibenzofurans that is a potent broad spectrum antifungal agent isolated from the fungus
Cercosporidium henningsii
.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C16H13NO7
Net Charge
0
Average Mass
331.27690
Monoisotopic Mass
331.06920
InChI
InChI=1S/C16H13NO7/c1-
5(18)
10-
7(20)
4-
9-
16(2,14(10)
22)
12-
8(21)
3-
6(19)
11(15(17)
23)
13(12)
24-
9/h3-
4,19-
21H,1-
2H3,(H2,17,23)
/t16-
/m1/s1
InChIKey
GEWLYFZWVLXQME-MRXNPFEDSA-N
SMILES
CC(=O)C1=C(O)C=C2Oc3c(c(O)cc(O)c3C(N)=O)[C@]2(C)C1=O
Roles Classification
Biological Role
(s):
antifungal agent
An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
phytotoxin
Any toxin produced by a plant.
fungal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor
An EC 2.7.11.* (protein-serine/threonine kinase) inhibitor that interferes with the action of mitogen-activated protein kinase (EC 2.7.11.24).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
cercosporamide (
CHEBI:78696
)
has role
antifungal agent (
CHEBI:35718
)
cercosporamide (
CHEBI:78696
)
has role
EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor (
CHEBI:79091
)
cercosporamide (
CHEBI:78696
)
has role
fungal metabolite (
CHEBI:76946
)
cercosporamide (
CHEBI:78696
)
has role
phytotoxin (
CHEBI:38231
)
cercosporamide (
CHEBI:78696
)
is a
dibenzofurans (
CHEBI:38922
)
cercosporamide (
CHEBI:78696
)
is a
methyl ketone (
CHEBI:51867
)
cercosporamide (
CHEBI:78696
)
is a
monocarboxylic acid amide (
CHEBI:29347
)
cercosporamide (
CHEBI:78696
)
is a
polyphenol (
CHEBI:26195
)
IUPAC Name
(9a
S
)-
8-
acetyl-
1,3,7-
trihydroxy-
9a-
methyl-
9-
oxo-
9,9a-
dihydrodibenzo[
b
,
d
]furan-
4-
carboxamide
Manual Xrefs
Databases
CN101292039
Patent
EP1914313
Patent
JP2008214336
Patent
KR20080033345
Patent
US2010152467
Patent
WO2007018194
Patent
View more database links
Registry Numbers
Types
Sources
131436-22-1
CAS Registry Number
ChemIDplus
5485233
Reaxys Registry Number
Reaxys
Citations
Types
Sources
15302826
PubMed citation
Europe PMC
21814808
PubMed citation
Europe PMC
23509154
PubMed citation
Europe PMC
8289782
PubMed citation
Europe PMC
Last Modified
04 June 2014