CAIX Inhibitor S4
目录号: PL01838 纯度: ≥98%
CAS No. :1330061-67-0
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中文名称
CAIX Inhibitor S4
中文别名
S4
英文名称
CAIX Inhibitor S4
英文别名
S4;4-(3′-(3″,5″-Dimethylphenyl)ureido)phenyl sulfamate;4-[(3,5-Dimethylphenyl)ureido]phenyl sulfamate;4-[[[(3,5-Dimethylphenyl)amino]carbonyl]amino]phenyl sulfamic acid ester;BDBM50387131;S4, >=98% (HPLC);4-(3-(3,5-Dimethylphenyl)ureido)phenyl sulfamate;4-[[[(3,5-Dimethylphenyl)amino]carbonyl]amino]phenyl sulfamate;CAIX Inhibitor S4
Cas No.
1330061-67-0
分子式
C15H17N3O4S
分子量
335.38
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
CAIX Inhibitor S4 是一种有效和选择性的碳酸酐酶 IX/XII (CA IX/XII) 的抑制剂,Ki 值分别为 7 nM 和 2 nM。CAIX Inhibitor S4 还抑制 CA II 和 CA I (Ki=546 nM, 5600 nM)。CAIX Inhibitor S4 可以抑制原位 MDA-MB-231 小鼠模型中肺转移的数量,而不影响原发肿瘤的生长。
生物活性
CAIX Inhibitor S4 is a potent and selective inhibitor of carbonic anhydrase IX/XII (CA IX/XII), with a K i of 7 nM and 2 nM, respectively. CAIX Inhibitor S4 also inhibits CA II and CA I (K i =546 and 5600 nM, respectively). CAIX Inhibitor S4 can inhibit the number of lung metastasis in orthotopic MDA-MB-231 mouse model without affecting primary tumor growth.
性状
Solid
IC50 & Target[1][2]
Ki: 2 nM (CA XII), 7 nM (CA IX), 546 nM (CA II), 5600 nM (CA I)
体外研究(In Vitro)
CAIX Inhibitor S4 (1-100 μM; 24 h) inhibits the proliferation of MDA-MB-231, HCT116 and HT29 cells in a dose-dependent manner.
CAIX Inhibitor S4 (3.3-33 μM; 24 h) inhibits the eGFP-MDA-MB-231 cell migration in anoxia in a concentration- dependent manner.
CAIX Inhibitor S4 (33 μM; 15-60 min) delays the cell spreading of MDA-MB-231 cells in anoxia but essentially not in normoxia. has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究(In Vivo)
CAIX Inhibitor S4 (10 mg/kg; i.p. for 14 days) inhibits metastatic tumor burden in MDA-MB-231 model while having no effect on primary tumor growth or mouse condition. 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]. Gieling RG, et, al. Antimetastatic effect of sulfamate carbonic anhydrase IX inhibitors in breast carcinoma xenografts. J Med Chem. 2012 Jun 14;55(11):5591-600.
溶解度数据
In Vitro: DMSO : 250 mg/mL (745.42 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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