Norfenefrine
![]() | |
![]() | |
| Clinical data | |
|---|---|
| AHFS/Drugs.com | International Drug Names |
| ATC code | C01CA05 (WHO) |
| Legal status | |
| Legal status |
|
| Identifiers | |
| |
| Synonyms |
Norfenephrine Norphenephrine Norphenylephrine meta-Norsynephrine meta-Octopamine 3-Octopamine |
| CAS Number |
536-21-0 15308-34-6 (hydrochloride) |
| PubChem (CID) | 4538 |
| ChemSpider |
4379 |
| UNII |
D2P3M6SRN5 |
| KEGG |
D08286 |
| ChEMBL |
CHEMBL358040 |
| ECHA InfoCard | 100.007.844 |
| Chemical and physical data | |
| Formula | C8H11NO2 |
| Molar mass | 153.178 g/mol |
| 3D model (Jmol) | Interactive image |
| |
| |
| | |
Norfenefrine (INN) or meta-octopamine (3-octopamine), also known as 3,β-dihydroxyphenethylamine, is an adrenergic agent used as a sympathomimetic drug which is marketed in Europe, Japan, and Mexico.[1][2] Along with its structural isomer p-octopamine and the tyramines, norfenefrine is a naturally occurring, endogenous trace amine and plays a role as a minor neurotransmitter in the brain.[3]
Some brand names for it include Coritat, Energona, Hypolind, and Novadral.
See also
- m-Tyramine
- Phenylephrine
- Metaraminol
- Norphenylephrine is the precursor used to make Ciclafrine.
References
- ↑ Macdonald F (1997). Dictionary of Pharmacological Agents. CRC Press. p. 104. ISBN 978-0-412-46630-4. Retrieved 24 April 2012.
- ↑ Index Nominum 2000: International Drug Directory. Taylor & Francis. 2000. p. 750. ISBN 978-3-88763-075-1. Retrieved 24 April 2012.
- ↑ Danielson TJ, Boulton AA, Robertson HA (December 1977). "m-Octopamine, p-octopamine and phenylethanolamine in rat brain: a sensitive, specific assay and the effects of some drugs". Journal of Neurochemistry. 29 (6): 1131–5. doi:10.1111/j.1471-4159.1977.tb06519.x. PMID 340613.
This article is issued from Wikipedia - version of the 10/12/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.

-Norfenefrine_molecule_ball.png)