![](../../files/images/goods/119-84-6.png)
Hydrocoumarin
CAS No. 119-84-6
Hydrocoumarin ( Hydrocoumarin | Chroman-2-one )
产品货号. M17874 CAS No. 119-84-6
香料,用于食品,也用作香豆素的替代品;用于化妆品。
纯度: >98% (HPLC)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
规格 | 价格/人民币 | 库存 | 数量 |
25MG | ¥441 | 有现货 |
![]() ![]() |
100MG | 获取报价 | 有现货 |
![]() ![]() |
200MG | 获取报价 | 有现货 |
![]() ![]() |
500MG | 获取报价 | 有现货 |
![]() ![]() |
1G | 获取报价 | 有现货 |
![]() ![]() |
生物学信息
-
产品名称Hydrocoumarin
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述香料,用于食品,也用作香豆素的替代品;用于化妆品。
-
产品描述Spice, used in food, also used as a substitute for coumarin; used in cosmetics.
-
体外实验Dihydrocoumarin induces a concentration-dependent inhibition of SIRT1 (IC50 of 208 μM) in an in vitro enzymatic assay. A decrease in SIRT1 deacetylase activity is observed even at micromolar doses (85±5.8 and 73±13.7% activity at 1.6 μM and 8 μM, respectively). The microtubule SIRT2 deacetylase is also inhibited with a similar dose dependency (IC50 of 295 μM).Dihydrocoumarin (1-5 mM) increases cytotoxicity in the TK6 cell line in a dose-dependent manner following a 24-h exposure. Dihydrocoumarin (1-5 mM) increases apoptosis in a dose-dependent manner in the TK6 cell line at the 6-h time point. A 5-mM dose of Dihydrocoumarin increases apoptosis at the 6-h time point in the TK6 cell line.Dihydrocoumarin (1-5 mM) increases p53 lysine 373 and 382 acetylation in a dose-dependent manner in the TK6 cell line following a 24-h exposure period.
-
体内实验——
-
同义词Hydrocoumarin | Chroman-2-one
-
通路Others
-
靶点Other Targets
-
受体Others
-
研究领域Others-Field
-
适应症——
化学信息
-
CAS Number119-84-6
-
分子量148.16
-
分子式C9H8O2
-
纯度>98% (HPLC)
-
溶解度In Vitro:?DMSO : 100 mg/mL (674.95 mM)
-
SMILESC1CC(=O)OC2=CC=CC=C21
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
产品手册
![](/themes/theme/en/images/ct.png)
![](/themes/theme/en/images/new12.jpg)
![](/themes/theme/en/images/gift.jpg)
![](/themes/theme/en/images/ct2.png)
关联产品
-
TC-N 1752
TC-N 1752 是一种有效和具有口服活性的 Nav1.7 抑制剂,抑制 hNav1.7,hNav1.3,hNav1.4,hNaV1.5 和 rNav1.8 的 IC50 值分别为 0.17 μM,0.3 μM,0.4 μM,1.1 μM 和 2.2 μM。TC-N 1752 还抑制河豚毒素敏感的钠通道。TC-N 1752 在福尔马林疼痛模型中显示出镇痛效果。
-
NSC19005
NSC19005 在结构上与倍他司汀相关。 NSC19005 是倍他司汀的二聚体。
-
Daphnetin 7-methyl e...
Daphnetin 7-methyl ether has anti-inflammatory activity.