CAS NO: | 120241-79-4 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | 3-TYP is a selectiveSIRT3inhibitor, with anIC50of 16 nM, more potent overSIRT1(IC50=88 nM),SIRT2(IC50=92 nM). | ||||||||||||||||
IC50& Target[3] |
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体外研究 (In Vitro) | 3-TYP inhibits melatonin-enhanced SIRT3 activity but does not affect SIRT3 protein expression. 3-TYP pretreatment reverses the protective effects of melatonin on cadmium (Cd)-induced mitochondrial-derived O2o–production and autophagic cell death. 3-TYP significantly attenuates melatonin-induced increases in deacetylated-SOD2 expression and SOD2 activity in HepG2 cells exposed to Cd[1]. | ||||||||||||||||
体内研究 (In Vivo) | 3-TYP (50 mg/kg, i.p.) does not significantly influence the LVEF, LVFS, infarct size, serum LDH levels, apoptosis, and oxidative stress compared with those of the Sham group. Moreover, 3-TYP has little effect on gp91phox, Nrf2, NQO 1, Bax, Bcl-2, Caspase-3, and cleaved Caspase-3 expression levels, compared with the Sham group. 3-TYP significantly decreases SIRT3 activity and increases the acetylation of SOD2 compared with that in the control group, without influencing SIRT3 expression. 3-TYP attenuates the cardioprotective effects of melatonin by decreasing the LVEF and LVFS after 24 hour of reperfusion. 3-TYP also increases the infarct size, serum LDH levels, and apoptotic ratio compared with those in the IR+Mel group[2]. | ||||||||||||||||
分子量 | 146.15 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C7H6N4 | ||||||||||||||||
CAS 号 | 120241-79-4 | ||||||||||||||||
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 : 125 mg/mL(855.29 mM;Need ultrasonic) Ethanol : 16.67 mg/mL(114.06 mM;Need ultrasonic) H2O : 1 mg/mL(6.84 mM;ultrasonic and warming and heat to 60℃) 配制储备液
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以下溶剂前显示的百
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