NLRP3-IN-2
目录号: PL07853 纯度: ≥98%
CAS No. :16673-34-0
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中文名称
NLRP3-IN-2
中文别名
4-[2-(2-甲氧基-5-氯苯甲酰胺基)乙基]苯磺酰胺;4-[2-(5-氯-2-甲氧基苯甲酰胺)乙基]苯磺酰胺;4-[2-(5-氯-2-甲氧基-苯甲酰氨基)乙基]苯磺酰胺;N-{2-[4-(氨磺酰基)苯基]乙基}-5-氯-2-甲氧基苯甲酰胺;4-[2-(5-氯-2-甲氧基苯甲酰氨基)乙基]苯磺酰胺;格列本脲杂质Ⅰ;格列本脲杂质A(EP) 标准品;格列苯脲杂质A;格列苯脲杂质I;优降糖相关物质A USP标准品;格列本脲(优降糖),杂质A;格列本脲中间体;格列本脲相关物质A;格列本脲USP RC A;格列本脲(优降糖)杂质A;5-氯-2-甲氧基-N-[2-对氨磺酰苯基)乙基]苯甲酰氨
英文名称
NLRP3-IN-2
英文别名
5-Chloro-2-methoxy-N-(4-sulfamoylphenethyl)benzamide;N-(2-(4-sulfamoyl)phenyl)ethyl-5-chloro-2-methoxybenzamide;4-[2-(5-Chloro-2-Methoxy Benzamido)Ethyl]- Phenyl Sulphonamide;5-Chloro-2-methoxy-N-[2-(4-sulfamoylphenyl)ethyl]benzamide;4-((5-Chloro-2-methoxybenzamido)ethyl)benzenesulfonamide;4-[2-(5-Chloro-2-methoxy benzamido) ethyl] benzene sulfonamide;4-(2-methoxy-5-chlorobenzamidoethyl)benzenesulfonamide;4-(2-(5-Chloro-2-methoxybenzamido)ethyl)benzenesulfamide;5-chloro-2-methoxy-n-(2-(4-sulfamoyl-phenyl)ethyl;N-(2-(4-(Aminosulfonyl)phenyl)ethyl)-5-chloro-2-methoxybenzamide;4-(5-CHLORO-2-METHOXYBENZAMIDOETHYL)BENZENESULFONAMIDE;4-[2-(5-CHLORO-2-METHOXY-BENZAMIDE)ETHYL]-BENZENESULPHONAMIDE;4-(2-(5-CHLORO-2-METHOXYBENZAMIDO)ETHYL)PHENYLSULFONAMIDE;4-[2-(5-CHLORO-2-METHOXYBENZAMIDO)ETHYL]PHENYLSULPHONAMIDE;4-[2-(2-METHOXY-5-CHLOROBENZAMIDO)ETHYL]BENZENESULFONAMIDE;5-Chloro-2-methoxy-N-(4-sulfamoylphenethyl)-benzamide;4-[2-(5-Chloro-2-methoxybenzamido)ethyl]phenylsulfonamide;N-[2-[4-(Aminosulfonyl)phenyl]ethyl]-5-chloro-2-methoxybenzamide;Einecs 240-722-5;Glyburide USP RC A;Glyburide Related CoMpound A;NLRP3 Inflammasome InhibitorⅠ;NLRP3 Inflammasome Inhibitor I;GlibenclaMide (Glyburide) IMpurity A;5-Chloro-N-(p-sulfaMoylphenethyl)-o-anisaMide;5-Chloro-2- methoxy-N-[2-(4-sulphamoylphenyl;NLRP3-IN-2;5-Chloro-2-Methoxy-N-(4-sulfaMoylphenethyl)benzaMide
Cas No.
16673-34-0
分子式
C16H17N2O4Scl
分子量
368.84
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
NLRP3-IN-2 是合成格列本脲的中间底物,可抑制心肌细胞中 NLRP3 炎症小体的形成,在小鼠心肌缺血/再灌注后限制梗死面积,且不影响代谢。
生物活性
NLRP3-IN-2, an intermediate substrate in the synthesis of glyburide, inhibits the formation of the NLRP3 inflammasome in cardiomyocytes and limits the infarct size following myocardial ischemia/reperfusion in the mouse, without affecting glucose metabolism.
性状
Solid
体内研究(In Vivo)
NLRP3-IN-2 is well tolerated with no effects on the glucose levels in vivo.
NLRP3-IN-2 (100 mg/kg) treatment in a model of AMI due to ischemia+reperfusion significantly inhibits the activity of inflammasome (caspase-1) in the heart by 90% (P<0.01) and reduced infarct size, measured at pathology (by >40%, P<0.01) and with troponin I levels (by >70%, P<0.01) .
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
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Carlo Marchetti, et al. A novel pharmacologic inhibitor of the NLRP3 inflammasome limits myocardial injury after ischemia-reperfusion in the mouse. J Cardiovasc Pharmacol. 2014 Apr;63(4):316-322.
溶解度数据
In Vitro: DMSO : 125 mg/mL (338.90 mM; Need ultrasonic)配制储备液
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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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