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去甲苯福林

维基百科,自由的百科全书
去甲苯福林
Ball-and-stick model of (R)-Norfenefrine
临床资料
其他名称间章胺
3-章胺
3,β-二羟基苯乙胺
AHFS/Drugs.com国际药品名称
ATC码
法律规范状态
法律规范
  • 处方药(-only)
药物动力学数据
药物代谢m-hydroxymandelic acid[1][2]
识别信息
  • 3-(2-Amino-1-hydroxyethyl)phenol
CAS号536-21-0  checkY
15308-34-6盐酸盐
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard英语CompTox Chemicals Dashboard (EPA)
ECHA InfoCard100.007.844 编辑维基数据链接
化学信息
化学式C8H11NO2
摩尔质量153.18 g·mol−1
3D模型(JSmol英语JSmol
  • OC(c1cc(O)ccc1)CN
  • InChI=1S/C8H11NO2/c9-5-8(11)6-2-1-3-7(10)4-6/h1-4,8,10-11H,5,9H2 checkY
  • Key:LRCXRAABFLIVAI-UHFFFAOYSA-N checkY

去甲苯福林(英语:Norfenefrine,也称作间章胺meta-octopamine3-章胺3-octopamine3,β-二羟基苯乙胺3,β-dihydroxyphenethylamine)是章胺同分异构体,分子式C8H11NO2,是一种拟交感神经药[3][4]

参考文献

[编辑]
  1. ^ Hengstmann JH, Konen W, Konen C, Eichelbaum M, Dengler HJ. The physiological disposition of p-octopamine in man. Naunyn-Schmiedeberg's Archives of Pharmacology. 1974, 283 (1): 93–106. PMID 4277715. S2CID 35523412. doi:10.1007/bf00500148. 
  2. ^ D'Andrea G, Nordera G, Pizzolato G, Bolner A, Colavito D, Flaibani R, Leon A. Trace amine metabolism in Parkinson's disease: low circulating levels of octopamine in early disease stages. Neuroscience Letters. January 2010, 469 (3): 348–351. PMID 20026245. S2CID 12797090. doi:10.1016/j.neulet.2009.12.025. 
  3. ^ Macdonald F. Dictionary of Pharmacological Agents. CRC Press. 1997: 104 [24 April 2012]. ISBN 978-0-412-46630-4. 
  4. ^ Index Nominum 2000: International Drug Directory. Taylor & Francis. 2000: 750 [24 April 2012]. ISBN 978-3-88763-075-1.