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ChEBI
> Main
CHEBI:78586 - aflatoxin B
1
endo
-8,9-oxide
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ChEBI Ontology
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ChEBI Name
aflatoxin B
1
endo
-8,9-oxide
ChEBI ID
CHEBI:78586
ChEBI ASCII Name
aflatoxin B1 endo-8,9-oxide
Definition
A member of the class of aflatoxins that is obtained by the formal epoxidation across the 8,9-double bond of aflatoxin B
1
.
Stars
This entity has been manually annotated by the ChEBI Team.
Submitter
Bijay
Supplier Information
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Formula
C17H12O7
Net Charge
0
Average Mass
328.27300
Monoisotopic Mass
328.05830
InChI
InChI=1S/C17H12O7/c1-
20-
7-
4-
8-
11(12-
14-
17(23-
14)
24-
16(12)
21-
8)
13-
10(7)
5-
2-
3-
6(18)
9(5)
15(19)
22-
13/h4,12,14,16-
17H,2-
3H2,1H3/t12-
,14+,16+,17-
/m1/s1
InChIKey
KHBXRZGALJGBPA-NQZOLGFYSA-N
SMILES
COc1cc2O[C@H]3O[C@H]4O[C@H]4[C@H]3c2c2oc(=O)c3C(=O)CCc3c12
Roles Classification
Biological Role
(s):
xenobiotic metabolite
Any metabolite produced by metabolism of a xenobiotic compound.
mycotoxin
Poisonous substance produced by fungi.
(via
aflatoxin
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
aflatoxin B
1
endo
-8,9-oxide (
CHEBI:78586
)
has functional parent
aflatoxin B
1
(
CHEBI:2504
)
aflatoxin B
1
endo
-8,9-oxide (
CHEBI:78586
)
has role
xenobiotic metabolite (
CHEBI:76206
)
aflatoxin B
1
endo
-8,9-oxide (
CHEBI:78586
)
is a
aflatoxin (
CHEBI:22271
)
aflatoxin B
1
endo
-8,9-oxide (
CHEBI:78586
)
is a
aromatic ether (
CHEBI:35618
)
aflatoxin B
1
endo
-8,9-oxide (
CHEBI:78586
)
is a
aromatic ketone (
CHEBI:76224
)
aflatoxin B
1
endo
-8,9-oxide (
CHEBI:78586
)
is a
cyclic ketal (
CHEBI:59779
)
aflatoxin B
1
endo
-8,9-oxide (
CHEBI:78586
)
is a
epoxide (
CHEBI:32955
)
IUPAC Name
(6a
S
,7a
R
,8a
S
,8b
R
)-
4-
methoxy-
2,3,6a,7a,8a,8b-
hexahydrocyclopenta[
c
]oxireno[4',5']furo[3',2':4,5]furo[2,3-
h
]chromene-
1,10-
dione
Synonyms
Sources
aflatoxin B
1
endo
-8,9-epoxide
ChEBI
AFNBO
SUBMITTER
Manual Xref
Database
C19595
KEGG COMPOUND
View more database links
Registry Numbers
Types
Sources
141899-13-0
CAS Registry Number
KEGG COMPOUND
141899-13-0
CAS Registry Number
ChemIDplus
6852034
Reaxys Registry Number
Reaxys
Citation
Type
Source
7766804
PubMed citation
Europe PMC
Last Modified
11 August 2014