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A6770
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。
A6770图片
CAS NO:1331754-16-5
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品介绍
A6770 是一种口服有效的1-磷酸鞘氨醇 (S1P) 裂解酶 (S1PL) 抑制剂。A6770 可以被磷酸化,磷酸化形式直接抑制 S1P 裂解。A6770 是 THI 的潜在关键代谢产物,可诱导 [3H]dhS1P 增加。
生物活性

A6770 is an orally active, potentsphingosine 1-phosphate (S1P) lyase (S1PL)inhibitor. A6770 is phosphorylated and the phosphorylated form directly inhibits S1P lyased.A6770, a potential key metabolite of THI, induces a [3H]dhS1P increase[1][2].

体外研究
(In Vitro)

A6770 causes concentration-dependent increases in [3H] dhS1P with the EC50ranging from 30 to 200 μM under the normal condition[1].
A6770 leads to S1PL inhibition rather than SPHK activation or SPP inhibition[2].

体内研究
(In Vivo)

A6770 (1, 10, 100mg/kg; po; single dose) induces reductions in peripheral lymphocyte number in rats[2]

分子量

140.14

Formula

C6H8N2O2

CAS 号

1331754-16-5

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.