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品牌: |
未填 |
所在地: |
廣東 深圳市 |
起訂: |
≥1 件 |
供貨總量: |
1 件 |
有效期至: |
長期有效 |
生物活性靶點(diǎn)體外研究體內(nèi)研究 用途與合成方法 MSDS 六氫姜黃素價格(試劑級) 上下游產(chǎn)品信息
中文名稱 | 六氫姜黃素 |
---|---|
中文同義詞 | 六氫姜黃素;六氫姜黃素?, BR;COX-2抑制劑(HEXAHYDROCURCUMIN);六氫姜黃素 標(biāo)準(zhǔn)品;5-羥基-1,7-雙(4-羥基-3-甲氧基苯基)庚烷-3-酮 |
英文名稱 | HEXAHYDROCURCUMIN |
英文同義詞 | 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號 | 36062-05-2 |
分子式 | C21H26O6 |
分子量 | 374.43 |
EINECS號 | |
相關(guān)類別 | 細(xì)胞生物學(xué)試劑;對照品;中藥對照品;標(biāo)準(zhǔn)品;植物提取物;標(biāo)準(zhǔn)品 -對照藥材;其它酚類;標(biāo)準(zhǔn)品,對照品;對照品;標(biāo)準(zhǔn)品-對照品 |
Mol文件 | 36062-05-2.mol |
結(jié)構(gòu)式 | ![]() |
熔點(diǎn) | 80-82℃ |
---|---|
沸點(diǎn) | 622.6±55.0 °C(Predicted) |
密度 | 1.226 |
閃點(diǎn) | 218℃ |
儲存條件 | 2-8°C |
溶解度 | 可溶于氯仿(少量)、乙酸乙酯(少量)、DCM、DMSO |
酸度系數(shù)(pKa) | 10.02±0.20(Predicted) |
形態(tài) | 固體 |
顏色 | 淡黃色低 |
BRN | 2486876 |
生物活性
Hexahydrocurcumin 是姜黃素的主要代謝產(chǎn)物之一,是一種選擇性的口服活性 COX-2 抑制劑,對 COX-1 無活性。Hexahydrocurcumin 具有抗氧化,抗癌和抗炎的作用。
靶點(diǎn)
COX-2
|
體外研究
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. |
體內(nèi)研究
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. |
WGK Germany | 3 |
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更新日期 | 產(chǎn)品編號 | 產(chǎn)品名稱 | CAS號 | 包裝 | 價格 |
---|---|---|---|---|---|
2024/08/19 | HY-N0929 | Hexahydrocurcumin | 1 mg | 1309元 | |
2024/08/19 | HY-N0929 | 六氫姜黃素 Hexahydrocurcumin | 36062-05-2 | 5mg | 3600元 |
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