六氢姜黄素

六氢姜黄素

中文名称六氢姜黄素
中文同义词六氢姜黄素;六氢姜黄素?, BR;COX-2抑制剂(HEXAHYDROCURCUMIN);六氢姜黄素 标准品
英文名称HEXAHYDROCURCUMIN
英文同义词HEXAHYDROCURCUMIN;5-Hydroxy-1-(4-hydroxy-3-Methoxycyclohexyl)-7-(4-hydroxy-3-Methoxyphenyl)heptan-3-one;(RS)-5-Hydroxy-1,7-bis(4-hydroxy-3-methoxyphenyl)-3-heptanone;1,7-Bis(3-methoxy-4-hydroxyphenyl)-5-hydroxy-3-heptanone;1,7-Bis(4-hydroxy-3-methoxyphenyl)-5-hydroxyheptan-3-one;5-Hydroxy-1,7-bis(4-hydroxy-3-methoxyphenyl)-3-heptanone;Hexahydrocurcumin, BR;3-Heptanone, 5-hydroxy-1,7-bis(4-hydroxy-3-methoxyphenyl)-
CAS号36062-05-2
分子式C21H26O6
分子量374.43
EINECS号
相关类别标准品;植物提取物;细胞生物学试剂;对照品;中药对照品;标准品 -对照药材;其它酚类;标准品-对照品;标准品,对照品;对照品
Mol文件36062-05-2.mol
结构式六氢姜黄素 结构式

六氢姜黄素 性质

熔点80-82℃
沸点622.6±55.0 °C(Predicted)
密度1.226
闪点218℃
储存条件2-8°C
溶解度可溶于氯仿(少量)、乙酸乙酯(少量)、DCM、DMSO
酸度系数(pKa)10.02±0.20(Predicted)
颜色淡黄色低
BRN2486876

六氢姜黄素 用途与合成方法

Hexahydrocurcumin 是姜黄素的主要代谢产物之一,是一种选择性的口服活性 COX-2 抑制剂,对 COX-1 无活性。Hexahydrocurcumin 具有抗氧化,抗癌和抗炎的作用。

COX-2

Hexahydrocurcumin (0-25 μM; 24-48 hours; HT-29 cells) treatment significantly decreased the viability of HT-29 colon cancer cells in a time- and concentration-dependent. The respective IC 50 values for 24 and 48 h of Hexahydrocurcumin exposureare 77.05 and 56.95, respectively.
Hexahydrocurcumin (0-25 μM; 24-48 hours; HT-29 cells) combined with 5-fluorouracil (5-FU; 5 µM) markedly reduces the COX-2 expression. The level of COX-1 is not altered.
Hexahydrocurcumin (0-25 μM; 24-48 hours; HT-29 cells) combined with 5-fluorouracil (5-FU; 5 µM) markedly reduces the COX-2 protein. The level of COX-1 protein is not altered.
Hexahydrocurcumin (7-14 μM; 24 hours) attenuates lipopolysaccharide (LPS)-elicited increase of prostaglandin E 2 (PGE 2 ) in murine macrophages (RAW 264.7) in a concentration-dependent manner.

Cell Viability Assay

Cell Line: HT-29 cells
Concentration: 0 µM, 5 µM, 10 µM, 25 µM
Incubation Time: 24 hours or 48 hours
Result: Significantly decreased the viability of HT-29 colon cancer cells.

RT-PCR

Cell Line: HT-29 cells
Concentration: 25 µM
Incubation Time: 24 hours
Result: Combined with 5-fluorouracil (5-FU; 5 µM) markedly reduced the COX-2 expression.

Western Blot Analysis

Cell Line: HT-29 cells
Concentration: 25 µM
Incubation Time: 24 hours
Result: Combined with 5-fluorouracil (5-FU; 5 µM) markedly reduced the COX-2 protein.

Hexahydrocurcumin (50 mg/kg; oral administration; daily; for 16 weeks; male Wistar rats) treatment significantly reduces the numbers of aberrant crypt foci (ACF) in colon cancer rats. Hexahydrocurcumin also markedly decreases COX-2 protein expression. The levels of COX-1 protein is not different from normal rats.

Animal Model: Male Wistar rats (100-120 g) injected with dimethylhydrazine (DMH)
Dosage: 50 mg/kg
Administration: Oral administration; daily; for 16 weeks
Result: Significantly reduced the numbers of ACF in colon cancer rats. Also markedly decreased COX-2 protein expression.

安全信息

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-N0929Hexahydrocurcumin1 mg1309元
2024/01/25HY-N0929六氢姜黄素
Hexahydrocurcumin
36062-05-25mg3600元

六氢姜黄素 上下游产品信息

"六氢姜黄素"相关产品信息
五氯化磷 CHEBULAEFRUCTUSIMMATURUS 去甲氧基姜黄素 双去甲氧基姜黄素 5-羟基-7-(4-羟基-3,5-二甲氧基苯基)-1-(4-羟基-3-甲氧基苯基)-3-庚酮 八氢姜黄素 四甲基姜黄素 二氢姜黄素 姜黄素 二甲基姜黄素 四氢姜黄素 四氢姜黄素 六氢哒嗪
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