Bamifylline
 | |
 | |
| Names | |
|---|---|
| IUPAC name
8-benzyl-7-[2-[ethyl(2-hydroxyethyl)amino]ethyl]-1,3-dimethylpurine-2,6-dione | |
| Identifiers | |
2016-63-9  | |
| 3D model (Jmol) | Interactive image |
| ChEMBL | ChEMBL2110760 |
| ChemSpider | 15401  |
| ECHA InfoCard | 100.116.522 |
| PubChem | 16229 |
| UNII | ZTY15D026H |
| |
| |
| Properties | |
| C20H27N5O3 | |
| Molar mass | 385.46008 |
| Pharmacology | |
| R03DA08 (WHO) | |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| verify (what is ?) | |
| Infobox references | |
Bamifylline is a drug of the xanthine chemical class which acts as a selective adenosine A1 receptor antagonist.[1][2]
See also
References
- ↑ Tomai F, Crea F, Gaspardone A, Versaci F, De Paulis R, Polisca P, Chiariello L, Gioffrè PA (June 1996). "Effects of A1 adenosine receptor blockade by bamiphylline on ischaemic preconditioning during coronary angioplasty". European Heart Journal. 17 (6): 846–53. doi:10.1093/oxfordjournals.eurheartj.a014965. PMID 8781823.
- ↑ Kofman, J.; Grosclaude, M.; Ouechni, M. M.; Perrin-Fayolle, M. (1982). "Comparative effects of bamifylline and theophylline on allergenic bronchospasm induced by the provocative inhalation test : Double-blind cross-over study". Le Poumon et le coeur. 38 (3): 197–202. PMID 6752929.
This article is issued from Wikipedia - version of the 6/7/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.