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dibenzazepine
Sign in to saveAlso known as iminostilbene, 5H-Dibenz[b,f]azepin, o,o'-iminostilbene, 2,2'-iminostilbene, 2,3,6,7-dibenzazepine, 5H-dibenz[b,f]azepine, dibenz(b,f)azepine, 5H-dibenzazepine
Dibenzazepine (iminostilbene) is a chemical compound with two benzene rings fused to an azepine ring. Many pharmaceuticals, such as carbamazepine, oxcarbazepine, and depramine, are based on a dibenzazepine structure.
Chemical data
- Formula
- C14H11N
- Molecular weight
- 193.24 g/mol
- IUPAC name
- 11H-benzo[b][1]benzazepine
- SMILES
- C1=CC=C2C(=C1)C=CC3=CC=CC=C3N2
- InChIKey
- LCGTWRLJTMHIQZ-UHFFFAOYSA-N
- XLogP
- 4
- Polar surface area
- 12 Ų
- H-bond donors
- 1
- H-bond acceptors
- 1
- Formal charge
- 0
via PubChem
Research
44,031 papers- Dibenzazepine combats acute liver injury in rats via amendments of Notch signaling and activation of autophagy.Naunyn-Schmiedeberg's archives of pharmacology · 2021
- Effects of dibenzazepine compounds on Na(v)1.2 channels and neuronal network activity: A systematic comparison.European journal of pharmacology · 2025
- Dibenzazepine-linked isoxazoles: New and potent class of α-glucosidase inhibitors.Bioorganic & medicinal chemistry letters · 2021
- Dibenzazepine promotes cochlear supporting cell proliferation and hair cell regeneration in neonatal mice.Cell proliferation · 2020
- Dibenzazepine, a γ-Secretase Enzyme Inhibitor, Protects Against Doxorubicin-Induced Cardiotoxicity by Suppressing NF-κB, iNOS, and Hes1/Hey1 Expression.Inflammation · 2025
via PubMed
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Encyclopedic overview
3 sectionsContents
- See also
- References
- External links
Dibenzazepine (iminostilbene) is a chemical compound with two benzene rings fused to an azepine ring. Many pharmaceuticals, such as carbamazepine, oxcarbazepine, and depramine, are based on a dibenzazepine structure.
== See also == Benzazepine Dibenzothiazepine Dibenzothiepin Dibenzoxepin Iminodibenzyl
Excerpted from Wikipedia’s “dibenzazepine” article, available under the CC BY-SA 4.0 licence.