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Roquinimex

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Chemical Structure| 84088-42-6 同义名 : 罗喹美克 ;Linomide;ABR212616;Linomide. US brand name: Linomide.;Roquinimex, FCF-89;PNU 212616;LS 2616;FCF89
CAS号 : 84088-42-6
货号 : A809531
分子式 : C18H16N2O3
纯度 : 99%+
分子量 : 308.331
MDL号 : MFCD00866331
存储条件:

粉末 Inert atmosphere,Room Temperature

液体 -20°C:3-6个月-80°C:12个月

溶解度 :

DMSO: 85 mg/mL(275.68 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方:
生物活性
描述 Roquinimex (Linomide; PNU212616; ABR212616) is a quinoline derivative immunostimulant that enhances NK cell activity and macrophage cytotoxicity, inhibits angiogenesis, and reduces TNF alpha secretion. Its IC50 value for TNF alpha is noteworthy. Prophylactic administration of roquinimex to DSS-treated mice significantly diminishes clinical signs of colitis, MDS, and CH-reduction. Additionally, in roquinimex-treated animals, MPO activity is notably reduced by over 50% compared to DSS control mice. Therapeutic administration of roquinimex in DSS-treated mice also significantly hampers MDS, CH-reduction, and MPO activity [2]. Linomide, a synthetic immunomodulator, at effective concentrations in vivo , reduces the number of MBP-reactive TNF-alpha and increases MBP-reactive IL-10 and TGF-beta mRNA expressing mononuclear cells (MNC) from MS patients' blood when analyzed in vitro. Compared to dexamethasone, Linomide upregulates levels of blood MNC expressing mRNA of TGF-beta after culture in the presence of MBP [3].
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

3.24mL

0.65mL

0.32mL

16.22mL

3.24mL

1.62mL

32.43mL

6.49mL

3.24mL

参考文献

[1]Liu Q, et al. Roquinimex inhibits dextran sodium sulfate-induced murine colitis. Inflamm Res. 2003 Feb;52(2):64-8.

[2]Tian WZ, et al. Linomide (roquinimex) affects the balance between pro- and anti-inflammatory cytokines in vitro in multiple sclerosis. Acta Neurol Scand. 1998 Aug;98(2):94-101.