返回ChemicalBook首页>CAS数据库列表>14907-98-3

14907-98-3

中文名称 鸦胆子苦醇
英文名称 brusatol
CAS 14907-98-3
分子式 C26H32O11
分子量 520.53
MOL 文件 14907-98-3.mol
更新日期 2024/04/19 16:13:44
14907-98-3 结构式 14907-98-3 结构式

基本信息

中文别名
鸦胆苦醇
鸦胆子苦醇对照品
BRUSATOL 鸦胆子苦醇
英文别名
100935
Brusato1
Brustaol
Yatansin
NSC 172924
(+)-Brusatol
Brusatol >=95% (HPLC)
Picras-3-en-21-oic acid, 13,20-epoxy-3,11,12-trihydroxy-15-[(3-methyl-1-oxo-2-buten-1-yl)oxy]-
13,20-Epoxy-3,11β,12α-trihydroxy-15β-[(3-methyl-1-oxo-2-butenyl)oxy]-2,16-dioxopicras-3-en-21-oic acid methyl ester
13,20-Epoxy-3,11β,12α-trihydroxy-15β-[(3-methyl-1-oxo-2-butenyl)oxy]-2,16-dioxopicrasa-3-ene-21-oic acid methyl ester
所属类别
生物化工:提取物

物理化学性质

外观性状白色结晶性粉末,可溶于甲醇、乙醇、DMSO等有机溶剂,来源于鸦胆子Brucea javanica。
沸点724.3±60.0 °C(Predicted)
密度1.46±0.1 g/cm3 (20 ºC 760 Torr)
储存条件-20°C
溶解度DMF: 1 mg/ml; DMSO: 1 mg/ml; DMSO:PBS (pH 7.2) (1:1): 0.5 mg/ml
酸度系数(pKa)8.81±0.70(Predicted)
形态粉末
颜色白色至米色
旋光性 (optical activity)[α]/D +35 to +44°, c = 0.5 in acetone
LogP0.393 (est)

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H315-H319-H335

应用领域

用途1
一种来源于植物的天然类西林类药物,通过抑制细胞蛋白的从头合成,在肿瘤培养中表现出广泛的细胞毒性。
鸦胆子苦醇价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/01/16S7956鸦胆子苦醇
Brusatol
14907-98-32mg949.85元
2024/01/16S7956Brusatol14907-98-310mM (1mL in DMSO)1613.43元
2024/01/16S7956鸦胆子苦醇
Brusatol
14907-98-35mg1663.54元

常见问题列表

生物活性
Brusatol (NSC 172924),可分离自B. javanica果实,是一种NRF2抑制剂。
靶点
TargetValue
Nrf2
()
体外研究

A potential therapeutic application of an Nrf2 inhibitor such as Brusatol (NSC 172924) is the downregulation of Nrf2 pathway components in cells harboring constitutively high levels of the transcription factor. Brusatol (NSC 172924) provokes the depletion of Nrf2 via a mechanism that is not dependent on Keap1 and the proteasomal and autophagic protein degradation systems. Brusatol (NSC 172924) provokes a rapid and transient depletion of Nrf2 protein, through a posttranscriptional mechanism, in mouse Hepa-1c1c7 hepatoma cells. Brusatol (NSC 172924) also inhibits Nrf2 in freshly isolated primary human hepatocytes. To explore the possible synergistic cytotoxicity of Brusatol (NSC 172924) in combination with CDDP, the study investigates the effects of Brusatol and CDDP cotreatment on CT-26 cell viability using an MTT assay. CT-26 cells are treated with various concentrations of Brusatol (0.05, 0.15, 0.45, 1.35, 4.05 and 12.15 μg/mL) and CDDP (0.05, 0.15, 0.45, 1.35, 4.05 and 12.15 μg/mL) for 48 h, either alone or in combination. Following treatment with Brusatol (NSC 172924) and CDDP for 48 h, the viability of CT-26 cells is reduced in a dose-dependent manner, with IC 50 values of 0.27±0.01 and 1.44±0.22 μg/mL, respectively. When Brusatol (NSC 172924) is combined with CDDP at a constant concentration ratio of 1:1, cell growth inhibition is markedly enhanced compared with single-agent treatment; the IC 50 value of Brusatol (NSC 172924) and CDDP cotreatment is 0.19±0.02 μg/mL.

体内研究

To explore the anticancer effect of Brusatol in vivo, A549 xenografts grown in nude mice are used as a model. Nude mice are injected with A549 cells to induce tumor growth, followed by a single i.p. injection of 2 mg/kg Brusatol. Tumors are isolated 24 h or 48 h postinjection. Nrf2 protein levels are significantly decreased at 24 h or 48 h postinjection, indicating that Brusatol (NSC 172924) is able to reach the tumor tissue and inhibit the Nrf2 pathway. To measure tumor growth, two different experiments are performed. In the first experiment, once the tumor size reaches an average of 230 mm 3 , DMSO, Brusatol (NSC 172924) (2 mg/kg), Cisplatin (2 mg/kg), or Cisplatin (2 mg/kg) and Brusatol (2 mg/kg) combined treatment is i.p. injected every other day for a total of five times. Cisplatin or Brusatol (NSC 172924) alone does not inhibit tumor growth significantly, whereas in the combination group, tumor size is significantly reduced.

"14907-98-3" 相关产品信息
99132-97-5 95258-13-2 95258-12-1 25514-29-8 95258-15-4 95258-14-3 25514-31-2 21499-66-1 505-52-2 2104-19-0 37443-42-8 85064-61-5