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ChEBI
> Main
CHEBI:47802 - 5
H
-dibenzo[
b
,
f
]azepine
Main
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ChEBI Name
5
H
-dibenzo[
b
,
f
]azepine
ChEBI ID
CHEBI:47802
ChEBI ASCII Name
5H-dibenzo[b,f]azepine
Definition
A mancude organic heterotricyclic parent that consists of a seven-membered nitrogen hetrocycle fused with two benzene rings.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C14H11N
Net Charge
0
Average Mass
193.249
Monoisotopic Mass
193.08915
InChI
InChI=1S/C14H11N/c1-3-7-13-11(5-1)9-10-12-6-2-4-8-14(12)15-13/h1-10,15H
InChIKey
LCGTWRLJTMHIQZ-UHFFFAOYSA-N
SMILES
N1C2=C(C=CC=C2)C=CC2=C1C=CC=C2
Roles Classification
Biological Role
(s):
marine xenobiotic metabolite
Any metabolite produced by metabolism of a xenobiotic compound in marine macro- and microorganisms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
5
H
-dibenzo[
b
,
f
]azepine (
CHEBI:47802
)
has role
marine xenobiotic metabolite (
CHEBI:83399
)
5
H
-dibenzo[
b
,
f
]azepine (
CHEBI:47802
)
is a
dibenzoazepine (
CHEBI:47804
)
5
H
-dibenzo[
b
,
f
]azepine (
CHEBI:47802
)
is a
mancude organic heterotricyclic parent (
CHEBI:36416
)
Incoming
5
H
-dibenzo[
b
,
f
]azepin-2-ol (
CHEBI:80599
)
has parent hydride
5
H
-dibenzo[
b
,
f
]azepine (
CHEBI:47802
)
imipramine (
CHEBI:47499
)
has parent hydride
5
H
-dibenzo[
b
,
f
]azepine (
CHEBI:47802
)
IUPAC Name
5
H
-dibenzo[
b
,
f
]azepine
Synonyms
Sources
2,2'-iminostilbene
ChemIDplus
2,3,6,7-dibenzazepine
NIST Chemistry WebBook
5
H
-Dibenz[
b
,
f
]azepin
NIST Chemistry WebBook
5
H
-dibenz[
b
,
f
]azepine
NIST Chemistry WebBook
5
H
-dibenzazepine
ChEBI
dibenz(
b
,
f
)azepine
NIST Chemistry WebBook
dibenzazepine
ChEBI
iminostilbene
ChemIDplus
o
,
o
'-iminostilbene
NIST Chemistry WebBook
Manual Xrefs
Databases
8857
ChemSpider
Dibenzazepine
Wikipedia
ONB
PDBeChem
View more database links
Registry Numbers
Types
Sources
1343358
Reaxys Registry Number
Reaxys
256-96-2
CAS Registry Number
NIST Chemistry WebBook
256-96-2
CAS Registry Number
ChemIDplus
Citations
Types
Sources
11767950
PubMed citation
Europe PMC
12052500
PubMed citation
Europe PMC
12061877
PubMed citation
Europe PMC
15837018
PubMed citation
Europe PMC
16203183
PubMed citation
Europe PMC
17236778
PubMed citation
Europe PMC
18779941
PubMed citation
Europe PMC
19486265
PubMed citation
Europe PMC
19774656
PubMed citation
Europe PMC
20922935
PubMed citation
Europe PMC
21087114
PubMed citation
Europe PMC
21441615
PubMed citation
Europe PMC
22322005
PubMed citation
Europe PMC
22751668
PubMed citation
Europe PMC
2322636
PubMed citation
Europe PMC
24358274
PubMed citation
Europe PMC
27175105
PubMed citation
Europe PMC
27389944
PubMed citation
Europe PMC
27807790
PubMed citation
Europe PMC
30660838
PubMed citation
Europe PMC
30754023
PubMed citation
Europe PMC
30823329
PubMed citation
Europe PMC
31718245
PubMed citation
Europe PMC
33381027
PubMed citation
Europe PMC
33842007
PubMed citation
Europe PMC
3680120
PubMed citation
Europe PMC
4146691
PubMed citation
Europe PMC
5982986
PubMed citation
Europe PMC
7587936
PubMed citation
Europe PMC
8385460
PubMed citation
Europe PMC
870507
PubMed citation
Europe PMC
Last Modified
21 May 2021
General Comments
2014-10-29
Metabolite of Carbamazepine
2014-10-29
Stravs M, Schymanski E, Singer H, Department of Environmental Chemistry, Eawag