| 词条 | Dibenzoxepin |
| 释义 |
| ImageFile = Dibenz(b,e)oxepin.svg | ImageSize = 200px | ImageAlt = | IUPACName = Benzo[c][1]benzoxepine | OtherNames = Dibenz[b,e]oxepin; Dibenzo[b,e]oxepine | Section1 = {{Chembox Identifiers | CASNo = | ChEMBL = | ChemSpiderID = 11273007 | PubChem = 20373272 | StdInChI = 1S/C14H10O/c1-2-7-13-10-15-14-8-4-3-6-12(14)9-11(13)5-1/h1-10H | StdInChIKey = APMCUORPNXHBQK-UHFFFAOYSA-N | SMILES = C1=CC=C2C(=C1)C=C3C=CC=CC3=CO2 | Section2 = {{Chembox Properties | C=14 | H=10 | O=1 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = | Section3 = {{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }}Dibenzoxepin, or dibenz[b,e]oxepin, is a tricyclic compound. It is the parent structure of certain drugs such as the tricyclic antidepressant doxepin and the analgesic fluradoline.[1][2][3] The former is the only tricyclic antidepressant that is a dibenzoxepin.[3] See also
References1. ^{{cite book|title=Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 17: Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles|url=https://books.google.com/books?id=jOaIAwAAQBAJ&pg=PA1919|date=14 May 2014|publisher=Thieme|isbn=978-3-13-178081-2|pages=1919–1922}} {{Tricyclics}}{{organic-compound-stub}}2. ^{{cite book|author=Patricia K. Anthony|title=Pharmacology Secrets|url=https://books.google.com/books?id=_QQsj3PAUrEC&pg=PA39|year=2002|publisher=Elsevier Health Sciences|isbn=1-56053-470-2|pages=39–}} 3. ^1 {{cite book|author=Manuchair Ebadi|title=Desk Reference of Clinical Pharmacology, Second Edition|url=https://books.google.com/books?id=ihxyHbnj3qYC&pg=PA329|date=31 October 2007|publisher=CRC Press|isbn=978-1-4200-4744-8|pages=329–}} 1 : Dibenzoxepins |
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