Chloropyramine HCl

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Chemical Structure| 6170-42-9 同义名 : 盐酸氯吡胺 ;Chloropyramine hydrochloride; Halopyramine hydrochloride; Alergosan, Allergan S hydrochloride, Chloropyramine hydrochloride, Chloropyramine HCl, Chloropyribenzamine hydrochloride, Halopyramine hydrochloride, Nilfan, Sinopen, Suprastin
CAS号 : 6170-42-9
货号 : A897986
分子式 : C16H21Cl2N3
纯度 : 99%+
分子量 : 326.26
MDL号 : MFCD00079009
存储条件:

Pure form Sealed in dry,2-8°C

In solvent -20°C:3-6个月-80°C:12个月

溶解度 : -
动物实验配方:
生物活性
描述 BT474 cells demonstrate a high sensitivity to Chloropyramine hydrochloride (compound 1), with a 1 µM concentration leading to a 40% reduction in cell viability after 48 hours. At the same 1 µM concentration, the viability of MCF7-pcDNA3 cells remains significantly higher compared to MCF7-VEGFR-3 cells (P<0.01), and at a 10 µM concentration, the viability difference doubles (P<0.001). Additionally, a concentration-dependent decrease in cell proliferation is observed in BT474 cells treated with Chloropyramine hydrochloride. A continued 48-hour treatment at higher doses leads to apoptosis in breast cancer cells overexpressing VEGFR-3, with a 10 µM dose inducing apoptosis in over 60% of these cells. In comparative treatments, MCF7-pcDNA3 and MCF7-VEGFR-3 cells treated with 10 µM Chloropyramine hydrochloride for 48 hours show a fourfold increase in apoptotic cell death in the VEGFR-3 overexpressed line (18% vs. 76% respectively)[1].
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

3.07mL

0.61mL

0.31mL

15.33mL

3.07mL

1.53mL

30.65mL

6.13mL

3.07mL

参考文献

[1]Kurenova EV, et al. Small molecule chloropyramine hydrochloride (C4) targets the binding site of focal adhesion kinase and vascular endothelial growth factor receptor 3 and suppresses breast cancer growth in vivo. J Med Chem. 2009 Aug 13;52(15):4716-24.