3-TYP

Research use only, not for human use.

3-TYP is a selective SIRT3 inhibitor.

3-TYP is an inhibitor of SIRT3.(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 O2 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.(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.

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3-TYP

Others

Other Targets

SIRT1| SIRT2| SIRT3

Cancer

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120241-79-4

146.15

C7H6N4

>98% (HPLC)

DMSO : 100 mg/mL. 684.23 mM; Ethanol : 16.67 mg/mL 114.06 mM

C1(C2=CN=NN2)=CC=CN=C1

3-(1H-1,2,3-triazol-4-yl) pyridine

(-20℃)

With Ice Pack

≥ 2 years