Bamifilin je lek iz ksantinske hemijske klase koji deluje kao selektivan antagonist adenozinskog A1 receptora.[4]
| Bamifilin
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| IUPAC ime
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|---|
| 8-benzil-7-[2-[etil(2-hidroksietil)amino]etil]-1,3-dimetilpurin-2,6-dion |
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| Identifikacija
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| CAS registarski broj
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2016-63-9  Y
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| PubChem[1][2]
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16229
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| ChemSpider[3]
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15401 Y
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| UNII
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ZTY15D026H Y
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| Jmol-3D slike
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Slika 1
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|---|
O=C2N(c1nc(n(c1C(=O)N2C)CCN(CC)CCO)Cc3ccccc3)C |
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|---|
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 Y
Kod: VVUYEFBRTFASAH-UHFFFAOYSA-N Y
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
Kod: VVUYEFBRTFASAH-UHFFFAOYAJ |
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| Svojstva
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| Molekulska formula
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C20H27N5O3
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| Molarna masa
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385,46008
|
|
 Y (šta je ovo?)
(verifikuj)
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
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| Infobox references
|
- ↑ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit
- ↑ Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
- ↑ Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit
- ↑ 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. PMID 8781823.
