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Merck
CN

P0373

Sigma-Aldrich

PSB 1115 potassium salt hydrate

≥95% (HPLC)

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别名:
1-Propyl-8-(4-sulfophenyl)xanthine potassium salt hydrate
经验公式(希尔记法):
C14H13KN4O5S · xH2O
分子量:
388.44 (anhydrous basis)
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77

质量水平

检测方案

≥95% (HPLC)

形式

powder

储存条件

desiccated

颜色

white to beige

溶解性

DMSO: 1 mg/mL, clear (warmed)

储存温度

2-8°C

SMILES字符串

CCCN1C(=O)Nc2nc([nH]c2C1=O)-c3ccc(cc3)S(=O)(=O)O[K]

InChI

1S/C14H14N4O5S.K/c1-2-7-18-13(19)10-12(17-14(18)20)16-11(15-10)8-3-5-9(6-4-8)24(21,22)23;/h3-6H,2,7H2,1H3,(H,15,16)(H,17,20)(H,21,22,23);/q;+1/p-1

InChI key

CJOWSBOERSTJAR-UHFFFAOYSA-M

生化/生理作用

PSB 1115 is a highly selective, water-soluble, human A2B adenosine receptor antagonist.

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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Osama M Abo-Salem et al.
The Journal of pharmacology and experimental therapeutics, 308(1), 358-366 (2003-10-18)
Caffeine, an adenosine A1, A2A, and A2B receptor antagonist, is frequently used as an adjuvant analgesic in combination with nonsteroidal anti-inflammatory drugs or opioids. In this study, we have examined the effects of novel specific adenosine receptor antagonists in an
Luo Yan et al.
Journal of medicinal chemistry, 47(4), 1031-1043 (2004-02-06)
Many currently known antagonists for P2 purinergic receptors are anionic molecules bearing one or several phenylsulfonate groups. Among the P1 (adenosine) receptor antagonists, the xanthine phenylsulfonates are a potent class of compounds. Due to their high acidity, phenylsulfonates are negatively

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