黄柏苷

黄柏苷

中文名称黄柏苷
中文同义词二氢黄柏苷;黄柏甙;(二氢)黄柏甙;黄柏苷
英文名称phellamurin
英文同义词phellamurin;(2R)-7-(β-D-Glucopyranosyloxy)-2,3-dihydro-3β,5-dihydroxy-2α-(4-hydroxyphenyl)-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one;(dihydro) Phellodendron;4H-1-Benzopyran-4-one,7-(b-D-glucopyranosyloxy)-2,3-dihydro-3,5-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-,(2R,3R)-;4H-1-Benzopyran-4-one, 7-(β-D-glucopyranosyloxy)-2,3-dihydro-3,5-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-, (2R,3R)-;(2R,3R)-3,5-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one;Cluster of differentiation 243,intestinal,anti-tumor,inhibit,MDR1,Pgp,CD243,glycoside,p-AKT,p-mTOR,p-PI3K,Multidrug resistance protein 1,P-glycoprotein,P-gp,ABCB1,Apoptosis,Flavonone,Phellamurin,Inhibitor
CAS号52589-11-4
分子式C26H30O11
分子量518.52
EINECS号
相关类别标准品;植物提取物;标准品 -对照药材;黄酮
Mol文件52589-11-4.mol
结构式黄柏苷 结构式

黄柏苷 性质

沸点861.5±65.0 °C(Predicted)
密度1.504±0.06 g/cm3(Predicted)
溶解度溶于氯仿、二氯甲烷、乙酸乙酯、DMSO、丙酮等。
形态粉末
酸度系数(pKa)7.15±0.60(Predicted)

黄柏苷 用途与合成方法

Phellamurin 是一种来自 Phellodendron amurense 叶的植物黄酮糖苷,可抑制肠道 P-糖蛋白 (P-glycoprotein)。Phellamurin 还抑制凤蝶的产卵。Phellamurin 诱导细胞凋亡 (apoptosis),并具有抗肿瘤活性。

Phellamurin (0-10 μg/mL; 48 hours; U2OS and Saos-2 cells) treatment leads to a repression of cell viability in U2OS and Saos-2 cells in a dose-dependent manner.
Phellamurin (0-10 μg/mL; 48 hours; U2OS and Saos-2 cells) treatment concentration-dependently promots the apoptosis of U2OS and Saos-2 cells.
Phellamurin (0-10 μg/mL; 48 hours; U2OS and Saos-2 cells) treatment declines the ratios of p-PI3K/PI3K, p-AKT/AKT, and p-mTOR/mTOR in U2OS and Saos-2 cells.

Cell Viability Assay

Cell Line: U2OS and Saos-2 cells
Concentration: 0 μg/mL, 2.5 μg/mL, 5 μg/mL, and 10 μg/mL
Incubation Time: 48 hours
Result: Suppressed the viability of U2OS and Saos-2 cells in a concentration-dependent manner.

Apoptosis Analysis

Cell Line: U2OS and Saos-2 cells
Concentration: 0 μg/mL, 2.5 μg/mL, 5 μg/mL, and 10 μg/mL
Incubation Time: 48 hours
Result: Induced apoptosis of U2OS and Saos-2 cells in a concentration-dependent manner.

Western Blot Analysis

Cell Line: U2OS and Saos-2 cells
Concentration: 0 μg/mL and 10 μg/mL
Incubation Time: 48 hours
Result: Repressed the PI3K/AKT/mTOR pathway in U2OS and Saos-2 cells.

Phellamurin (50 mg/kg/day; intraperitoneal injection; daily; for 21 days; female BALB/c nude mice) treatment represses osteosarcoma tumor growth in vivo. The ratios of p-PI3K/PI3K, p-AKT/AKT, and p-mTOR/mTOR are decreased in xenograft in Phellamurin-treated mice.

Animal Model: Athymic female BALB/c nude mice (6 weeks old ) injected with U2OS cells
Dosage: 50 mg/kg/day
Administration: Intraperitoneal injection; daily; for 21 days
Result: Repressed osteosarcoma tumor growth in vivo.

安全信息

MSDS信息

黄柏苷 上下游产品信息

"黄柏苷"相关产品信息
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