Diacetazotol

目录号: PL08216 纯度: ≥90.0%
Diacetazotol 抑制二恶英诱导的乙氧基烯丙醇-O-脱乙基酶 (EROD) 活性,IC50 为 75±4 nM。Diacetazotol 是专利文献 US20070032458 中的化合物 3。
CAS No. :83-63-6
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中文名称
Diacetazotol
中文别名
二乙酰氨基偶氮甲苯;N,N,-二乙酰邻氨基偶氮甲苯;N,N-Diacetyl-o-aminoazotoluene N,N,-二乙酰邻氨基偶氮甲苯;N,N-二乙酰-o-氨基偶氮甲苯;N,N-二乙酰基-o-氨基氮杂甲苯;双醋佐托
英文名称
Diacetazotol
英文别名
Acetamide,N-acetyl-N-[2-methyl-4-[2-(2-methylphenyl)diazenyl]phenyl]-;N,N-Diacetyl-o-aminoazotoluene;Diacetotoluide;N-acetyl-N-[2-methyl-4-[(2-methylphenyl)diazenyl]phenyl]acetamide;4'-Diacetamino-2.3'-dimethyl-azobenzol;4'-Diacetylamino-2.3'-dimethyl-azobenzol;5-o-Toluolazo-2-diacetylamino-toluol;Dermagan;Dermagen;Diacetazotol;Diacetylaminoazotoluen;Diamazo;Dimazon;Epidermol;N-(2-Methyl-4-o-tolylazo-phenyl)-diacetamid;N-(2-methyl-4-o-tolylazo-phenyl)-diacetamide;Pellidol;Pellidole;Periphermin;Acetamide,N-acetyl-N-[2-methyl-4-[(2-methylphenyl)azo]phenyl]- (9CI);o-Diacetotoluidide,4''-(o-tolylazo)- (7CI,8CI);4''-(o-Tolylazo)-o-diacetotoluidide;Diacetylaminoazotoluene;Epithelone;Granulin;Granulin (ointment);NSC 6509;NSC 7221;4-o-Tolylazo-o-diacetotoluide;4''-(ortho-Tolylazo)-ortho-diacetoluidide;N,N-Diacetyl-o-tolylazo-o-toluidine;4'-(o-Tolylazo)-o-diacetotoluidide;N-(4-o-Tolylazo-o-tolyl)diacetamide;Acetamide, N-acetyl-N-[2-methyl-4-[(2-methylphenyl)azo]phenyl]-;o-Diacetotoluidid
Cas No.
83-63-6
分子式
C18H19N3O2
分子量
309.36
包装储存
Powder -20°C 3 years;4°C 2 years
详情描述
Diacetazotol 抑制二恶英诱导的乙氧基烯丙醇-O-脱乙基酶 (EROD) 活性,IC50 为 75±4 nM。Diacetazotol 是专利文献 US20070032458 中的化合物 3。
产品详情
Diacetazotol 抑制二恶英诱导的乙氧基烯丙醇-O-脱乙基酶 (EROD) 活性,IC50 为 75±4 nM。Diacetazotol 是专利文献 US20070032458 中的化合物 3。
生物活性
Diacetazotol inhibits dioxin-induced ethoxyresorufin-O-deethylase (EROD) activity with IC 50 of 75±4 nM. Diacetazotol extracts from patent US20070032458, compound 3.
性状
Solid
IC50 & Target[1][2]
IC50: 75±4 nM (Dioxin-induced EROD activity)
体外研究(In Vitro)
Diacetazotol has activity for inhibiting dioxin toxicity. 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]. Pann Suh, et al. Compound having activity for inhibiting dioxin toxicity, pharmaceutical composition comprising the compound and method for treating disease resulting from dioxin toxicity using the compound .US 20070032458 A1.
溶解度数据
In Vitro: DMSO : 100 mg/mL (323.25 mM; Need ultrasonic)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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