ML355
目录号: PL06747 纯度: ≥98%
CAS No. :1532593-30-8
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PL06747-2mg 2mg ¥1360.00 请登录
PL06747-5mg 5mg ¥1978.18 请登录
PL06747-10mg 10mg ¥3214.55 请登录
PL06747-50mg 50mg ¥11250.91 请登录
PL06747-100mg 100mg ¥17309.09 请登录
PL06747-200mg 200mg 询价 询价
PL06747-500mg 500mg 询价 询价
PL06747-10mM*1mLinDMSO 10mM*1mLinDMSO ¥1921.31 请登录
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中文名称
ML355
英文名称
ML355
英文别名
ML355;ML-355;ML355 free base;JKU4XCC48Y;N-(1,3-benzothiazol-2-yl)-4-[(2-hydroxy-3-methoxyphenyl)methylamino]benzenesulfonamide;N-2-benzothiazolyl-4-[[(2-hydroxy-3-methoxyphenyl)methyl]amino]-benzenesulfonamide;GTPL8752;BCP28954;BDBM50447175;ML 355;s6557;AK547442;B8014;Q27087172;N-(2-Benzothiazolyl)-4-(2-hydroxy-3-methox
Cas No.
1532593-30-8
分子式
C21H19N3O4S2
分子量
441.52
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
ML355 是一高效、选择性 12-LOX 抑制剂,IC50值为 0.34 μM,对其他脂氧化酶和环氧化酶有很好的选择性,具有较好的药物动力学特征。
生物活性
ML355 is a potent and selective inhibitor of 12-Lipoxygenase (12-LOX) with an IC 50 of 0.34 μM, shows excellent selectivity over related lipoxygenases and cyclooxygenases, and possesses favorable ADME properties.
性状
Solid
IC50 & Target[1][2]
12-LOX 0.34 μM (IC50)
体外研究(In Vitro)
ML355 inhibits PAR-4 induced aggregation and calcium mobilization in human platelets and reduce 12-HETE in β-cells. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
ML355 (1.88-30 mg/kg; i.g.; 2 times per day for two days) strongly inhibits the thrombus formation in mice at higher dose compared to WT controls. has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model:
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Luci DK, et al. Synthesis and structure-activity relationship studies of 4-((2-hydroxy-3-methoxybenzyl)amino)benzenesulfonamide derivatives as potent and selective inhibitors of 12-lipoxygenase. J Med Chem. 2014 Jan 23;57(2):495-506.
[2]. Zhang XJ, et al. An ALOX12-12-HETE-GPR31 signaling axis is a key mediator of hepatic ischemia-reperfusion injury. Nat Med. 2018 Jan;24(1):73-83.
溶解度数据
In Vitro: DMSO : ≥ 42 mg/mL (95.13 mM)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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