Debrisoquine
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| 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 |
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| 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). | |
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| 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.
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