产品信息
抗原名称
O-GlcNAcase
商品描述
Thiamet G是一种有效的，选择性O-GlcNAcase抑制剂，Ki为21 nM，选择性比人溶酶体氨基己糖苷酶高37,000倍。
分子量
248.3
纯度
＞98%
可溶性
DMSO ：50 mg/mL (201.36 mM)
Water ：50 mg/mL (201.36 mM)
Water ：50 mg/mL (201.36 mM)
外观
white to beige powder
In vitro(体外研究)
In NGF-differentiated PC-12 cells, inhibition of O-GlcNAcase by Thiamet G increases the cellular levels of O-GlcNAc with EC50 of approximately 30 nM. Thiamet G (100 mM) reduces tau phosphorylation by approximately 2.1-fold, 2.7-fold, 1.2-fold and 1.3-fold for Ser396, Thr231, Ser422 and Ser262, respectively. Thiamet G (12.5 nM and 25 nM) significantly enhances p38 phosphorylation by increasing O-GlcNAcylation in mesangial cells. In O-GlcNAc transferase or O-GlcNAcase gain of function cells, thiamet-G restores the assembly of the spindle and partially rescues histone phosphorylation.
In vivo(体内研究)
In rats, thiamet G (50 mg/kg) administrated by i.v. crosses the blood brain barrier and then results in increase in brain O-GlcNAc levels in a dose- and time-dependent manner, and reduction of tau phosphorylation in rat brain. Thiamet G is also orally bioavailable. O-GlcNAc accumulation induced by thiamet G stimulates chondrogenic differentiation in C57/bl mice by increasing the gene expression of differentiation markers, as well as the activity of MMP-2 and -9.
背景
别名
Thiamet-G
分子式
C9H16N2O4S
CAS号
1009816-48-1
制备和贮存
保存方式
Store at -20℃ for one year（Powder）；Store at 2-4℃ for two weeks；Store at -20℃ for six months after dissolution.
参考图片
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