Debrisoquine
 ![]()  | |
| Names | |
|---|---|
|  IUPAC name
 1,2,3,4-tetrahydroisoquinoline-2-carboximidamide  | |
| Identifiers | |
|  1131-64-2  | |
| 3D model (Jmol) | Interactive image | 
| ChEBI |  CHEBI:34665  | 
| ChEMBL |  ChEMBL169901  | 
| ChemSpider |  2860  | 
| DrugBank |  DB04840  | 
| ECHA InfoCard | 100.013.155 | 
| KEGG |  C13650  | 
| MeSH | Debrisoquine | 
| PubChem | 2966 | 
| UNII |  X31CDK040E  | 
 
  | |
 
  | |
| Properties | |
| C10H13N3 | |
| Molar mass | 175.23032 | 
| Pharmacology | |
| C02CC04 (WHO) | |
|   Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).  | |
|   | |
| Infobox references | |
Debrisoquine is a derivative of guanidine. It is an antihypertensive drug similar to guanethidine. Debrisoquine is frequently used for phenotyping the CYP2D6 enzyme, a drug metabolizing enzyme.[2]
See also
The guanidine part of the molecule also appears in guanoxan and guanadrel.
- The 7-bromo analog of Debrisoquine is called Guanisoquin.
 
References
- ↑ Debrisoquine – Compound Summary, PubChem.
 - ↑ Fuhr, U.; Jetter, A.; Kirchheiner, J. (2007). "Appropriate Phenotyping Procedures for Drug Metabolizing Enzymes and Transporters in Humans and Their Simultaneous Use in the "Cocktail" Approach". Clinical Pharmacology & Therapeutics. 81 (2): 270–283. doi:10.1038/sj.clpt.6100050.
 
This article is issued from Wikipedia - version of the 2/28/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.
