Bamifylline

Bamifylline
Names
	IUPAC name 8-benzyl-7-[2-[ethyl(2-hydroxyethyl)amino]ethyl]-1,3-dimethylpurine-2,6-dione
Identifiers
CAS Number	2016-63-9 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL2110760 ;
ChemSpider	15401 ;
ECHA InfoCard	Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value).
PubChem CID	16229;
UNII	ZTY15D026H ;
	InChI InChI=1S/C20H27N5O3/c1-4-24(12-13-26)10-11-25-16(14-15-8-6-5-7-9-15)21-18-17(25)19(27)23(3)20(28)22(18)2/h5-9,26H,4,10-14H2,1-3H3 Key: VVUYEFBRTFASAH-UHFFFAOYSA-N ; InChI=1/C20H27N5O3/c1-4-24(12-13-26)10-11-25-16(14-15-8-6-5-7-9-15)21-18-17(25)19(27)23(3)20(28)22(18)2/h5-9,26H,4,10-14H2,1-3H3 Key: VVUYEFBRTFASAH-UHFFFAOYAJ;
	SMILES O=C2N(c1nc(n(c1C(=O)N2C)CCN(CC)CCO)Cc3ccccc3)C;
Properties
Chemical formula	C20H27N5O3
Molar mass	385.46008
	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

Bamifylline is a drug of the xanthine chemical class which acts as a selective adenosine A₁ receptor antagonist.^[1]^[2]

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.
↑ PMID 6752929 (PMID 6752929)
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