苯奈达林

苯奈达林
临床资料
给药途径	Oral
ATC码	未分配;
法律规范状态
法律规范	Unscheduled;
识别信息
	IUPAC命名法 N,N,N-Trimethyl-N-(3-phenylindol-1-yl)ethane-1,2-diamine; ;
CAS号	60662-16-0
PubChem CID	42510;
ChemSpider	38769 ;
UNII	3AVG9P140R;
ChEMBL	ChEMBL2104611 ;
CompTox Dashboard（英语：CompTox Chemicals Dashboard） (EPA)	DTXSID20209472 ;
化学信息
化学式	C19H23N3
摩尔质量	293.41 g·mol−1
3D模型（JSmol（英语：JSmol））	交互式图像;
	SMILES c1cccc2c1c(cn2N(CCN(C)C)C)c3ccccc3;
	InChI InChI=1S/C19H23N3/c1-20(2)13-14-21(3)22-15-18(16-9-5-4-6-10-16)17-11-7-8-12-19(17)22/h4-12,15H,13-14H2,1-3H3 ; Key:SXYFFMXPDDGOEK-UHFFFAOYSA-N ;

苯奈达林（英语：Binedaline或binodaline）是一种含氮有机化合物，分子式C₁₉H₂₃N₃，通常以盐酸盐的形式存在^[1]，能用作抗抑郁药^[2]，从未上市销售^[3]。

参考文献

^ Milne GW. 3043: Binedaline hydrochloride. Milne GW (编). Drugs: Synonyms and Properties. Routledge. 2017. ISBN 9781351755092.
^ Faltus F, Geerling FC. A controlled double-blind study comparing binedaline and imipramine in the treatment of endogenous depression. Neuropsychobiology. 1984, 12 (1): 34–38. PMID 6239991. doi:10.1159/000118107.
^ Triggle DJ. Dictionary of Pharmacological Agents. Boca Raton: Chapman & Hall/CRC. 1996. ISBN 0-412-46630-9.
^ Schatz F, Jahn U, Wagner-Jauregg T, Zirngibl L, Thiele K. 1-amino-3-phenylindoles with antidepressant activity. Binodaline hydrochloride and related substances. Arzneimittel-Forschung. 1980, 30 (6): 919–923. PMID 7191264. doi:10.1002/chin.198038207.
^ DE 2512702,Fischer K, Jahn U, Schatz F, Stammbach C, Thiele K, Wagner-Jauregg T. Zirngibl L,“New Hydrazines and Methods of Manufacturing Them”,发行于23 September 1982,指定于Siegfried AG
^ US 4204998,Schatz F, Stammbach C, Thiele K, Theodor W. Wagner-Jauregg, Zirngibl L, Fischer J, Jahn U,“N-Amino indole derivatives having pharmacological activity”,发行于27 May 1980,指定于Siegfried AG