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307543-71-1

中文名称 STF 083010
英文名称 STF 083010
CAS 307543-71-1
分子式 C15H11NO3S2
分子量 317.38
MOL 文件 307543-71-1.mol
更新日期 2024/06/05 14:37:12
307543-71-1 结构式 307543-71-1 结构式

基本信息

中文别名
IRE1抑制剂(STF-083010)
N-[(2-羟基-1-萘基)亚甲基]-2-噻吩磺酰胺
英文别名
CS-2901
CS-2595
STF 083010
STF-083010
STF083010
STF 083010
N-[(2-Hydroxy-1-naphthalenyl)methylene]-2-thiophenesulfonamide
2-Thiophenesulfonamide, N-[(2-hydroxy-1-naphthalenyl)methylene]-
(E)-N-((2-hydroxynaphthalen-1-yl)methylene)thiophene-2-sulfonamide
所属类别
生物化工:激动剂抑制剂

物理化学性质

熔点199-201°C
沸点548.4±56.0 °C(Predicted)
密度1.40±0.1 g/cm3(Predicted)
储存条件-20°C
溶解度DMSO:可溶,5mg/mL(澄清溶液)
酸度系数(pKa)7.31±0.50(Predicted)
形态粉末
颜色淡黄色至黄绿色
稳定性自购买之日起 1 年内保持稳定。 DMSO 中的溶液可在 -20° 下保存长达 3 个月。

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H302
危险品标志Xn
危险类别码22
WGK Germany3

常见问题列表

生物活性
STF-083010 是一种 IRE1α 特异性抑制剂。在内质网应激后,STF-083010 抑制 Ire1 内切核酸酶活性,而不影响其激酶活性。
靶点

Ire1

体外研究

STF-083010 shows cytostatic and cytotoxic activity in a dose- and time-dependent manner. Treatment with STF-083010 shows significant antimyeloma activity in model human multiple myeloma (MM) xenografts. RPMI 8226 human MM cells grown as tumor xenografts are treated in NSG mice. Intraperitoneal injection of STF-083010 alone (day 1, day 8) significantly inhibits the growth of these tumors. STF-083010 is an IRE1α-specific inhibitor. Four pancreatic cancer cell lines (Panc0403, Panc1005, BxPc3, MiaPaCa2) are treated with different combination of Bortezomib (10 or 50 nM) and STF (10 or 50 μM). The normalized isobologram analysis demonstrates synergistic activity between 10 μM STF and either 10 or 50 nM bortezomib in all four cell lines. Moreover, a higher concentration of STF (50 μM) attains synergy after addition of bortezomib either at a concentration of 10 nM when tested against BxPc3 cells, at a concentration of 50 nM against Panc1005 cells, and at either 10 or 50 nM against Panc0403 cells. STF-083010 (50 μM) suppresses the growth of p53-deficient human cancer cells.

体内研究

Treatment with STF-083010 reduces the viability of HCT116 p53 -/- cells by approximately 20% compared with that of HCT116 p53 -/- cells. Administration of STF-083010 to tumors induced by HCT116 p53 -/- cells significantly reduces tumor volume and weight by 75% and 73% at the endpoint, respectively.

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