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YU142670

商品编号: S1106
图示 货号 库存 价格(¥) 数量

备注:

国外库存,货期2-4周,具体详情请联系销售人员。

质量文档

详细介绍

l  基本信息

产品名称

YU142670

一般描述

YU142670 is a selective inhibitor against OCRL1/INPP5F (IC50 = 0.71 μM;

别称

3-(4-pyridinyl)-1,2,4-Triazolo[3,4-b][1,3,4]thiadiazole, 3-(Pyridin-4-yl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole

纯 度

≥98.0%(HPLC)

CAS NO.

133847-06-0

分子式

C8H5N5S

分子量

203.22

适用范围

生物试剂,适用于细胞培养等

l  理化信息

外 观

白色至浅棕色固体

溶解性(25℃)

DMSO

Slightly soluble

l  生物学信息

生物活性/药理作用

YU142670 is a selective inhibitor against OCRL1/INPP5F (IC50 = 0.71 μM; substrate = PI(4,5)P2) and OCRL2/INPP5B (IC50 = 0.53 and 1.78 μM; substrate = PI3 and INPP5B/PI(4,5)P2, respectively) by targeting OCRL catalytic domain without affecting INPP5A, INPP5E, PTEN, SHP1, shrimp alkaline phosphatase, sphingomyelinase, or SYNJ1. YU142670 causes an increased PI(4,5)P2/PI4P ratio in human skin fibroblasts (by 50%; 50 μM for 1h) and induces upregulated actin nucleation and ruffle activity at the plasma membrane without obvious cytotoxicity. Consistent with the negative regulatory role of PtdIns(4,5)P2 against the calcium channel mucolipin-1 (MCOLN1) that controls autophagosome-lysosome fusion, ehnahced autophagosome accumulation is observed in human kidney proximal tubule cells (PTCs) upon YU142670 (25 μM for 3 hr) or OCRL shRNA treatment.

l  存储

存储温度

-20

l  注意事项及免责声明

本产品仅用于实验研究,不得作为药物使用,不得用于家用或其它用途。

l  参考文献

1.    http://www.drugbank.ca

2.    https://ncit.nci.nih.gov

3.  https://www.ncbi.nlm.nih.gov