8-环戊基-1,3-二丙基黄嘌呤

• 未分配

• Uncontrolled

• 8-cyclopentyl-1,3-dipropyl-7H-purine-2,6-dione

• 1329

• 386

• 1289 ^Y

• 9PTP4FOI9E

• CHEBI:73282 ^N

• ChEMBL183 ^Y

• DTXSID50144706

• 交互式图像

• CCCn3c(=O)c2nc(C1CCCC1)[nH]c2n(CCC)c3=O

• InChI=1S/C16H24N4O2/c1-3-9-19-14-12(15(21)20(10-4-2)16(19)22)17-13(18-14)11-7-5-6-8-11/h11H,3-10H2,1-2H3,(H,17,18) ^Y
• Key:FFBDFADSZUINTG-UHFFFAOYSA-N ^Y

参考文献

1. ^ Martinson EA, Johnson RA, Wells JN. Potent adenosine receptor antagonists that are selective for the A1 receptor subtype. Molecular Pharmacology. March 1987, 31 (3): 247–52. PMID 3561384. 
2. ^ Lohse MJ, Klotz KN, Lindenborn-Fotinos J, Reddington M, Schwabe U, Olsson RA. 8-Cyclopentyl-1,3-dipropylxanthine (DPCPX)--a selective high affinity antagonist radioligand for A1 adenosine receptors. Naunyn-Schmiedeberg's Archives of Pharmacology. August 1987, 336 (2): 204–10. PMID 2825043. S2CID 20549217. doi:10.1007/BF00165806. 

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