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299-75-2

中文名称 曲奥舒凡
英文名称 treosulfan
CAS 299-75-2
分子式 C6H14O8S2
分子量 278.301
MOL 文件 299-75-2.mol
更新日期 2023/03/20 15:41:25
299-75-2 结构式 299-75-2 结构式

基本信息

中文别名
曲奥舒凡
英文别名
CB-2562
Cb 40067
NSC 39069
Leo 40067
treosulfan
TREOSULPHAN
THREOSULFAN
Dihydroxymyleran
Dihydroxybusulfan
L-Dihydroxy-Busulfan
所属类别
生物化工:激动剂抑制剂

物理化学性质

熔点76-78 °C
沸点359.3°C (rough estimate)
密度1.305 (estimate)
折射率1.5630 (estimate)
储存条件-20°C储存
溶解度丙酮(微溶)、DMSO(微溶)、甲醇(微溶)、水(微溶)
酸度系数(pKa)12.36±0.20(Predicted)
形态固体
颜色灰白色至浅米色
CAS 数据库299-75-2
(IARC)致癌物分类1 (Vol. 26, Sup 7, 100A) 2012
EPA化学物质信息Treosulfan (299-75-2)

安全数据

危险性符号(GHS)
GHS08
警示词危险
危险性描述H340-H350-H361f
危险品运输编号2811
危险等级6.1(b)
包装类别III
毒性LDLo intravenous in dog: 222mg/kg
曲奥舒凡价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/04/30HY-16503曲奥舒凡
Treosulfan
299-75-25mg700元
2024/04/30HY-16503曲奥舒凡
Treosulfan
299-75-210mM * 1mLin DMSO770元
2024/04/30HY-16503曲奥舒凡
Treosulfan
299-75-210mg1100元

常见问题列表

生物活性
Treosulfan (NSC 39069, Treosulphan) 是一种用于常规和大剂量化疗方案的烷基化 alkylating 药剂。Treosulfan 对胰腺癌细胞系具有强大的细胞毒性。
靶点

DNA Alkylator

体外研究

Treosulfan is an alkylating agent. Treosulfan inhibits several cancer cell lines, such as Panc-1, Miapaca-2 and Capan-2 cells, with IC 50 s of 3.6 μg/mL, 1.8 μg/mL and 2.1 μg/mL respectively, and shows nearly 100% cytotoxicity on these cell lines at 100 μg/mL. Treosulfan (0.1-100 μg/mL) in combination with LY 188011 exhibits enhanced activity against cancer cells. However, Treosulfan (1, 2.5, 5 μg/ml) combined with 5-FU (0.1, 0.25, 0.5 μg/ml) has antagonistic effect on Panc-1 cells at intermediate and high concentrations, and on Miapaca-2 cells at all doses. Treosulfan (800 µg/mL) dramatically reduces erythrocyte forward scatter, increases the percentage of annexin-V-binding cells, [Ca 2+ ] i , and ROS. Removal of extracellular Ca 2+ abrogates the effect of Treosulfan on annexin-V-binding.

体内研究

Treosulfan (1.5 g/kg/day) induces a rapid myeloablation, depletes the splenic B and T cells in mice. Treosulfan (1.5 g/kg/day) causes olny interleukin-2 production in spleen cells for a short time and without obvious significant effect on synthesis of tumor necrosis factor-α and/or IFN-γ in mice.

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