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Ansornitinib

目录号 : GC70992

Ansornitinib是一种口服活性双激酶抑制剂,可抑制血小板衍生生长因子受体(PDGFR)和血管内皮生长因子受体(VEGFR2)。

Ansornitinib Chemical Structure

Cas No.:1448874-96-1

规格 价格 库存 购买数量
1 mg
¥1,575.00
现货
5 mg
¥3,465.00
现货
10 mg
¥5,544.00
现货

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Sample solution is provided at 25 µL, 10mM.

产品文档

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产品描述

Ansornitinib is an orally active dual kinase inhibitor that inhibits platelet-derived growth factor receptor (PDGFR) and vascular endothelial growth factor receptor (VEGFR2). Ansornitinib can be used as an antifibrotic agent in lung, liver, kidney, and gastrointestinal fibrotic diseases.

Ansornitinib (compound I) (0.1 nM-10 μM, 2 h) can significantly inhibit the phosphorylation of PDGFRβ in human hepatic stellate cells and KDR phosphorylation in human umbilical vein endothelial cells (HUVEC)[1].
Ansornitinib (compound I) (0.1-13 μM, 48 h) can induce a decrease in the expression of many different inflammation-related markers, such as macrophage colony-stimulating factor (M-CSF), soluble interleukin 8, and fibrosis-related markers, such as N-calmodulin, α-SMA, etc., in a dose-dependent manner[1].

Ansornitinib (compound I) (25 mg/kg, p.o., twice a day, 4 weeks) can reduce fibrosis in TGFβ positive female mice[1].
Ansornitinib (compound I) (5-45 mg/kg, p.o., twice a day, 4 days) can reduce inflammatory bowel disease (IBD) in TNBS-induced IBD/acute colitis male CD-1 mice[1].

References:
[1]. Shakil ASLAM, et al. Reducing fibrosis and treating related diseases, disorders, and conditions. WO2022006278

Chemical Properties

Cas No. 1448874-96-1 SDF
分子式 C30H32N6O4 分子量 540.61
溶解度 DMSO : 40 mg/mL (73.99 mM; ultrasonic and warming and heat to 80°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO) 储存条件 -20°C
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 1.8498 mL 9.2488 mL 18.4976 mL
5 mM 0.37 mL 1.8498 mL 3.6995 mL
10 mM 0.185 mL 0.9249 mL 1.8498 mL
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