| CAS NO: | 138-52-3 |
| 包装 | 价格(元) |
| 10 mM * 1 mL in DMSO | 电议 |
| 500mg | 电议 |
| 1 g | 电议 |
| 5 g | 电议 |
| 10 g | 电议 |
| 50 g | 电议 |
| 生物活性 | Salicin is a naturalCOXinhibitor. | ||||||||||||||||
| IC50& Target[1] |
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| 体外研究 (In Vitro) | Significant down regulation of PGE2, the enzymatic product of COX2, to 76% in lysate and 70% in supernatant is observed with Salicin 10 μM treatment in COLO cells when compare to the COLO control. This is accompanied with a minimal COX1 inhibition to 91% of the CCD control on the genetic level. Treatment with Salicin 1 μM decreases colon cancer cell proliferation rates from 144% to 113% at 24 hours and 187% to 130% at 48 hours, with 10 μM decreasing proliferation rates to 108% at 24 hours and 119% at 48 hours[1]. The concentrations of TNF-α, IL-1β and IL-6 of LPS-induced cells pretreated with 0.07, 0.14 and 0.28 μM Salicin are significant reduced compare with LPS group[2]. | ||||||||||||||||
| 体内研究 (In Vivo) | Salicin (D(-)-Salicin) (35, 70, 140 μM) markedly inhibits the LPS-induced pathological changes. MPO activity in LPS-induced lung tissue is significantly increased compare with control group. However, Salicin (35, 70, 140 μM) markedly inhibits this change. Pretreatment with Salicin inhibits LPS-induced activation of JNK, ERK, p38/MAPK and p65 in a dose-dependent manner[2]. | ||||||||||||||||
| 分子量 | 286.28 | ||||||||||||||||
| 性状 | Solid | ||||||||||||||||
| Formula | C13H18O7 | ||||||||||||||||
| CAS 号 | 138-52-3 | ||||||||||||||||
| 中文名称 | 水杨苷 | ||||||||||||||||
| 结构分类 |
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| 来源 |
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| 运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
| 储存方式 |
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| 溶解性数据 | In Vitro: DMSO : 150 mg/mL(523.96 mM;Need ultrasonic and warming) H2O : 12.5 mg/mL(43.66 mM;ultrasonic and warming and heat to 60℃) 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 |
