STF 083010

STF 083010

中文名称STF 083010
中文同义词IRE1抑制剂(STF-083010);N-[(2-羟基-1-萘基)亚甲基]-2-噻吩磺酰胺;STF-083010游离态;英文名称:STF 083010;N-((2-羟基萘-1-基)亚甲基)噻吩-2-磺酰胺
英文名称STF 083010
英文同义词STF 083010;(E)-N-((2-hydroxynaphthalen-1-yl)methylene)thiophene-2-sulfonamide;N-[(2-Hydroxy-1-naphthalenyl)methylene]-2-thiophenesulfonamide;STF-083010;STF083010;STF 083010;CS-2595;CS-2901;2-Thiophenesulfonamide, N-[(2-hydroxy-1-naphthalenyl)methylene]-;N-((2-Hydroxynaphthalen-1-yl)methylene)thiophene-2-sulfonamide
CAS号307543-71-1
分子式C15H11NO3S2
分子量317.38
EINECS号
相关类别小分子抑制剂,天然产物;细胞生物学试剂;Inhibitors
Mol文件307543-71-1.mol
结构式STF 083010 结构式

STF 083010 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。

STF 083010 用途与合成方法

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。

Ire1

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.

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.

安全信息

危险品标志Xn
危险类别码22
WGK Germany3

MSDS信息

更新日期产品编号产品名称CAS号包装价格
2024/01/25HY-15845STF-0830101 mg250元
2024/01/25HY-15845STF 083010
STF-083010
307543-71-15mg550元

STF 083010 上下游产品信息

"STF 083010"相关产品信息
FATOSTATINA 2-Methoxy-4-[(5,6,7,8-tetrahydro-benzo[4,5]thieno[2,3-d]pyrimidin-4-yl)-hydrazonomethyl]-phenol CS-2426 丙氯拉嗪 NULL STF-118804
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