中文名 | Pardoprunox hydrochloride |
英文名 | 7-(4-methylpiperazin-1-yl)-3H-1,3-benzoxazol-2-one hydrochloride |
别名 | 盐酸帕多芦诺 帕多芦诺盐酸盐 7-(4-甲基哌嗪-1-基)苯并[D]恶唑-2(3H)-酮盐酸盐 |
英文别名 | SLV308 SLV 308 pardoprunox.HCl pardoprunox.HCl.H2O SLV-308 HYDROCHLORIDE SLV-308 hydrochloride DU-126891 hydrochloride DU-126891 HYDROCHLORIDE Pardoprunox.HCl(SLV-308) Pardoprunox hydrochloride Pardoprunox (hydrochloride) 7-(4-methylpiperazin-1-yl)-3H-1,3-benzoxazol-2-one hydrochloride 2(3H)-BENZOXAZOLONE, 7-(4-METHYL-1-PIPERAZINYL)-, MONOHYDROCHLORIDE |
CAS | 269718-83-4 |
化学式 | C12H16ClN3O2 |
分子量 | 269.72734 |
溶解度 | DMSO: 150毫克/毫升 (556.11毫米; 需要超声波) H2O : <0.1毫克/毫升 (不溶) |
存储条件 | under inert gas (nitrogen or Argon) at 2-8°C |
体外研究 | Pardoprunox (SLV-308) hydrochloride acts as a potent but partial D2 receptor agonist (pEC 50 = 8.0 and pA 2 =8.4) with an efficacy of 50% on forskolin stimulated cAMP accumulation. At human recombinant dopamine D3 receptors, Pardoprunox hydrochloride acts as a partial agonist in the induction of [(35)S]GTPgammaS binding (intrinsic activity of 67%; pEC 50 =9.2) and antagonized the dopamine induction of [(35)S]GTPgammaS binding (pA 2 =9.0). Pardoprunox hydrochloride acts as a full 5-HT1A receptor agonist on forskolin induced cAMP accumulation at cloned human 5-HT1A receptors but with low potency (pEC 50 =6.3). |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 3.707 ml | 18.537 ml | 37.074 ml |
5 mM | 0.741 ml | 3.707 ml | 7.415 ml |
10 mM | 0.371 ml | 1.854 ml | 3.707 ml |
5 mM | 0.074 ml | 0.371 ml | 0.741 ml |
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