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Cirtuvivint
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Cirtuvivint图片
规格:98%
分子量:427.5
包装与价格:
包装价格(元)
5mg询价
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25mg询价

Cirtuvivint (SM08502) 是一种有效的具有口服活性的 CDC 样激酶 (CLK) 抑制剂,可用于实体瘤的研究。
货号:ajcx35756
CAS:2143917-62-6
分子式:C24H25N7O
分子量:427.5
溶解度:DMSO : 12.5 mg/mL (29.24 mM; ultrasonic and warming and heat to 60°C)
纯度:98%
存储:Store at -20°C
库存:现货

Background:

Cirtuvivint (SM08502) is a potent and orally active CDC-like kinase (CLK) inhibitor. Cirtuvivint can be used for solid tumors research[1].

Cirtuvivint (SM08502) inhibits serine and arginine rich splicing factor (SRSF) phosphorylation and disrupted spliceosome activity, which is associated with inhibition of Wnt pathway-related gene and protein expression. Cirtuvivint induces the generation of splicing variants of Wnt pathway genes, suggesting that its mechanism for inhibition of gene expression includes effects on alternative splicing[1].

Orally administered Cirtuvivint (SM08502) significantly inhibits growth of gastrointestinal tumors and decreased SRSF phosphorylation and Wnt pathway gene expression in xenograft mouse models[1].

[1]. Betty Y Tam, et al. The CLK inhibitor SM08502 induces anti-tumor activity and reduces Wnt pathway gene expression in gastrointestinal cancer models. Cancer Lett. 2020 Mar 31;473:186-197.

 
 
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