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ATX inhibitor 13
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。
CAS NO:2485779-34-6
包装与价格:
包装价格(元)
5 mg电议
50 mg电议
100 mg电议

产品介绍
ATX inhibitor 13 (compound 10c) 是一种口服有效的ATX抑制剂,其IC50为 3.4 nM。ATX inhibitor 13 抑制 RAW264.7 细胞的增殖和迁移,诱导细胞凋亡和 G2 期阻滞。ATX inhibitor 13 抑制肿瘤细胞集落形成。

产品描述

ATX inhibitor 13 (10c) is an orally active and potent ATX inhibitor, with an IC 50 of 3.4 nM. ATX inhibitor 13 inhibits proliferation and migration, and induces apoptosis and G2 phase arrest in RAW264.7 cells. ATX inhibitor 13 suppresses tumor cell colony formation [1].

体外活性

ATX inhibitor 13 (compound 10c) (0-20 μM, 72 h) shows cytotoxicity and anti-proliferative activity against MCF-7, MDA-MB-231, A549, NCI-H1581, H2228, Hep3B, and RAW264.7 cells [1]. ATX inhibitor 13 (0-1 μM, 0-72 h) inhibits migration of RAW264.7 cells in a dose-dependent manner, significantly down-regulates both the colony count and colony single area with the concentration elevation [1]. ATX inhibitor 13 (0-1 μM, 72 h) dose dependently suppresses colony formation of RAW264.7 cells [1]. ATX inhibitor 13 (0-1 μM, 48 h) induces weak apoptosis in a dose-dependent manner in RAW264.7 cells [1]. ATX inhibitor 13 (0-1 μM, 48 h) brings G2 phase arrest of RAW264.7 cells [1]. Cell Proliferation Assay Cell Line: MCF-7, MDA-MB-231, A549, NCI-H1581, H2228, Hep3B, RAW264.7 [1] Concentration: 0-20 μM Incubation Time: 72 h Result: Showed cytotoxicity and antiproliferative activity against MCF-7, MDA-MB-231, A549, NCI-H1581, H2228, Hep3B, and RAW264.7 cell lines, with IC 50 values of 3.87 ± 0.37, 3.29 ± 0.37, 6.59 ± 0.26, 4.76 ± 0.57, 4.27 ± 0.21, 0.58 ± 0.11, and 0.63 ± 0.26 μM. Apoptosis Analysis Cell Line: RAW264.7 cells [1] Concentration: 0 μM, 0.1 μM, 0.25 μM, 0.5 μM and 1 μM Incubation Time: 48 h Result: Induced apoptosis in a dose-dependent manner, with the apoptotic rates of 6.48% (0.1 μM), 7.73% (0.25 μM), 8.60% (0.5 μM) and 9.17% (1 μM). Cell Cycle Analysis Cell Line: RAW264.7 cells [1] Concentration: 0 μM, 0.1 μM, 0.25 μM, 0.5 μM and 1 μM Incubation Time: 24 h Result: Led to significant G2 phase arrest in RAW264.7 cells in a dose-dependent manner, the percentage of cells in the G2 phase slightly increased from 10.90% to 90.16% (0-1 μM).

体内活性

ATX inhibitor 13 (compound 10c) (C57BL/6J mice, 0-1000 mg/kg, Orally, once) has an acceptable safety profile [1]. Animal Model: C57BL/6J mice (5 groups,4 mice per group) [1] Dosage: 5000, 3200, 2500 and 1000 mg/kg Administration: Orally, once Result: Had an acceptable safety profile, showed no obvious safety concerns.

Cas No.

2485779-34-6

分子式

C31H35Cl2N5O3

分子量

596.55

储存和溶解度

(< 1 mg/ml refers to the product slightly soluble or insoluble )
Powder: -20°C for 3 years
In solvent: -80°C for 2 years