| 词条 | 2-Phenylindole |
| 释义 |
| ImageFile = 2-Phenylindole.svg | ImageSize = 250px | IUPACName = 2-Phenyl-1H-indole | OtherNames = | Section1 = {{Chembox Identifiers | CASNo = | PubChem = 13698 | ChemSpiderID = 13105 | SMILES = c1ccc(cc1)c2cc3ccccc3[nH]2 | InChI = 1/C14H11N/c1-2-6-11(7-3-1)14-10-12-8-4-5-9-13(12)15-14/h1-10,15H | InChIKey = KLLLJCACIRKBDT-UHFFFAOYAH | StdInChI = 1S/C14H11N/c1-2-6-11(7-3-1)14-10-12-8-4-5-9-13(12)15-14/h1-10,15H | StdInChIKey = KLLLJCACIRKBDT-UHFFFAOYSA-N | Section2 = {{Chembox Properties | C=14|H=11|N=1 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = | Section3 = {{Chembox Hazards | MainHazards = | FlashPt = | Autoignition = }}2-Phenylindole is an organic compound. It is the parent structure of a group of nonsteroidal selective estrogen receptor modulators (SERMs) that includes zindoxifene, bazedoxifene, and pipendoxifene, as well as the nonsteroidal estrogen D-15414 (the major metabolite of zindoxifene).[1][2][3] References1. ^{{cite book|author1=Michael Oettel|author2=Ekkehard Schillinger|title=Estrogens and Antiestrogens I: Physiology and Mechanisms of Action of Estrogens and Antiestrogens|url=https://books.google.com/books?id=0BfrCAAAQBAJ&pg=PA68|date=6 December 2012|publisher=Springer Science & Business Media|isbn=978-3-642-58616-3|pages=68–69}} {{DEFAULTSORT:Phenylindole, 2-}}{{heterocyclic-stub}}2. ^{{cite book|title=International position paper on women's health and menopause : a comprehensive approach|url=https://books.google.com/books?id=NCzYsz6Uv0IC&pg=PA111|publisher=DIANE Publishing|isbn=978-1-4289-0521-4|pages=111–}} 3. ^{{cite book|author=Gordon W. Gribble|title=Heterocyclic Scaffolds II:: Reactions and Applications of Indoles|url=https://books.google.com/books?id=srxzzUskq4wC&pg=PA14|date=9 October 2010|publisher=Springer Science & Business Media|isbn=978-3-642-15732-5|pages=14–}} 1 : Indoles |
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