Name | 8DFW6D5G55 |
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Synonyms |
8DFW6D5G55
8-epi-Xanthatin 2H-Cyclohepta[b]furan-2-one, 3,3a,4,7,8,8a-hexahydro-7-methyl-3-methylene-6-[(1E)-3-oxo-1-buten-1-yl]-, (3aR,7S,8aR)- (3aR,7S,8aR)-7-Methyl-3-methylene-6-[(1E)-3-oxo-1-buten-1-yl]-3,3a,4,7,8,8a-hexahydro-2H-cyclohepta[b]furan-2-one |
Description | 8-Epixanthatin is a potential colchicine binding site inhibitor isolated from Xanthium chinese Mill. 8-Epixanthatin can inhibit the activation of STAT3, induce apoptosis, and has anti-tumor activity[1]. |
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Related Catalog | |
In Vitro | 8-Epixanthatin(2-20 μM, 12 h) 可以以剂量依赖性方式抑制 DU145 细胞增殖和 DU145 细胞的 p-STAT3 水平,其 IC50 值为 3.2 μM[1]。 8-Epixanthatin可以通过诱导 DU145 癌细胞中 ROS 的产生抑制 STAT3 的激活和细胞增殖[1]。 Cell Proliferation Assay[1] Cell Line: DU145 cell Concentration: 2, 5, 10, and 20 μM Incubation Time: 12 h or 48 h Result: Reduced STAT3 phosphorylation by 90% at a concentration of 20 μM but not p-JAK2-Y1007/1008. Significantly reduced the amount of BCL-2 and BCL-xL, and induces BCL-xL PARP cleavage, the percentage of cells in G0/G1 phase decreased. |
In Vivo | 8-Epixanthatin (i.p., 50 mg/kg, 5 days per week for 25 days) 在 DU145 细胞的小鼠异种移植模型中,可以通过 STAT3 失活抑制肿瘤生长,小鼠肿瘤体积减少了40.1%,肿瘤重量减少了40.0%,肿瘤中 p-STAT3 水平显著降低[1]。 |
References |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 444.3±45.0 °C at 760 mmHg |
Molecular Formula | C15H18O3 |
Molecular Weight | 246.302 |
Flash Point | 199.1±28.8 °C |
Exact Mass | 246.125595 |
LogP | 1.58 |
Vapour Pressure | 0.0±1.1 mmHg at 25°C |
Index of Refraction | 1.528 |
Storage condition | 2-8℃ |