Quinotolast sodium (Synonyms: FR71021)
目录号: PL06107 纯度: ≥98%
CAS No. :101193-62-8
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中文名称
Quinotolast sodium
中文别名
喹托司特钠
英文名称
Quinotolast sodium
英文别名
4H-Quinolizine-3-carboxamide,4-oxo-1-phenoxy-N-2H-tetrazol-5-yl-, sodium salt (1:1);FR71021;4H-Quinolizine-3-carboxamide,4-oxo-1-phenoxy-N-1H-tetrazol-5-yl-, monosodium salt (9CI);FR-71021;Quinotolast sodium;CID 138395027
Cas No.
101193-62-8
分子式
C17H11N6NaO3
分子量
370.30
包装储存
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
产品详情
Quinotolast sodium (浓度范围为 1-100 μg/mL) 抑制组胺,LTC4 和 PGD2 释放,这种作用具有浓度依赖性。
生物活性
Quinotolast sodium in the concentration range of 1-100 μg/mL inhibits histamine, LTC 4 and PGD 2 release in a concentration-dependent manner.
性状
Solid
IC50 & Target[1][2]
Histamine LTC4
体外研究(In Vitro)
Quinotolast inhibits the release of histamine and the generation of leukotriene (LT) C4 and prostaglandin (PG) D2 from dispersed human lung cells. Quinotolast (100 μg/mL) significantly inhibits PGD2 and LTC4 release. Quinotolast inhibits PGD2 release by 100% and LTC4 release by 54%. The inhibitory effect of Quinotolast on histamine release from dispersed lung cells is largely independent of the preincubation period, no tachyphylaxis being observed. Quinotolast shows a significant inhibition of inflammatory mediators from human dispersed lung cells. Quinotolast also shows strong inhibitory effects on histamine and peptide leukotrienes release from guinea pig lung fragments or mouse cultured mast cells. Quinotolast concentration-dependently inhibits pLTs release from cultured mast cells. The IC50 value
体内研究(In Vivo)
Quinotolast potently inhibits such type I allergic reactions as passive cutaneous anaphylaxis (PCA) and anaphylactic bronchoconstriction in rats by both intravenous and oral dosing. When Quinotolast is given i.v. to rats, Quinotolast, dose-dependently inhibits PCA. The doses of Quinotolast required to inhibit the reaction by 50% (ED 50 ) is 0.0063 mg/kg. Given p.o., Quinotolast inhibits the reaction. ED 50 value for Quinotolast is 0.0081 mg/kg. Although almost complete inhibition is observed with Quinotolast at a dose of 0.32 mg/kg, its effect is slightly attenuated at a dose of 1 mg/kg. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
参考文献
[1]. Okayama Y, et al. Inhibition of histamine and eicosanoid release from dispersed human lung cells in vitro byquinotolast. Jpn J Pharmacol. 1995 Dec;69(4):375-80.
[2]. Kobayashi K, et al. Effects of quinotolast, a new orally active antiallergic drug, on experimental allergic models. Jpn J Pharmacol. 1993 Sep;63(1):73-81.
溶解度数据
In Vitro: DMSO : 115 mg/mL (309.71 mM; ultrasonic and warming and heat to 60°C)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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