2,2' - ((((((亚甲基双(2-氯-4,1-亚苯基))二(氮烷二基))二(羰基))双(氮烷二
中文名称 | 2,2' - ((((((亚甲基双(2-氯-4,1-亚苯基))二(氮烷二基))二(羰基))双(氮烷二 |
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中文同义词 | 2,2' - ((((((亚甲基双(2-氯-4,1-亚苯基))二(氮烷二基))二(羰基))双(氮烷二;2,2'-((((((亚甲基双(2-氯-4,1-亚苯基))二(氮烷二基))二(羰基))双(氮烷二基))二(4,1-亚苯基))二( 氧基))双(2-甲基丙酸);化合物LR-90;2,2' - ((((((亚甲基双(2-氯-4,1-亚苯基))二(氮烷二基))二(羰基))双(氮烷二 |
英文名称 | 2,2'-(4,4'-(4,4'-Methylenebis(2-chloro-4,1-phenylene))bis(azanediyl)bis(oxoMethylene)bis(azanediyl)bis(4,1-phenylene))bis(oxy)bis(2-Methylpropanoic acid) |
英文同义词 | 2,2'-(4,4'-(4,4'-Methylenebis(2-chloro-4,1-phenylene))bis(azanediyl)bis(oxoMethylene)bis(azanediyl)bis(4,1-phenylene))bis(oxy)bis(2-Methylpropanoic acid);2,2'-{Methylenebis[(2-chloro-4,1-phenylene)carbamoylimino-4,1-phenyleneoxy]}bis(2-methylpropanoic acid);2,2-[Methylenebis[(2-chloro-4,1-phenylene)iminocarbonylimino-4,1-phenyleneoxy]]bis[2-methylpropanoic acid];2,2'-((((((methylenebis(2-chloro-4,1-phenylene))bis(azanediyl))bis(carbonyl))bis(azanediyl))bis(4,1-phenylene))bis(oxy))bis(2-methylpropanoic acid);LR-90;Propanoic acid, 2,2'-[methylenebis[(2-chloro-4,1-phenylene)iminocarbonylimino-4,1-phenyleneoxy]]bis[2-methyl-;inhibit,Inhibitor,LR-90,LR90,LR 90;2,2'-(4,4'-(4,4'-Methylenebis(2-chloro-4,1-phenylene))bis(azanediyl)bis(oxoMethylene)bis(azanediyl)bis(4,1-phenylene))bis(oxy)bis(2-Methylpropanoic acid) |
CAS号 | 245075-84-7 |
分子式 | C35H34Cl2N4O8 |
分子量 | 709.57 |
EINECS号 | |
相关类别 | 生物活性分子-API |
Mol文件 | 245075-84-7.mol |
结构式 | ![]() |
2,2' - ((((((亚甲基双(2-氯-4,1-亚苯基))二(氮烷二基))二(羰基))双(氮烷二 性质
沸点 | 726.0±60.0 °C(Predicted) |
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密度 | 1.448±0.06 g/cm3(Predicted) |
储存条件 | Store at -20°C |
溶解度 | DMSO:≥ 100 mg/mL (140.93 mM);水:< 0.1 mg/mL(不溶) |
形态 | 固体 |
酸度系数(pKa) | 3.01±0.10(Predicted) |
颜色 | 白色至米白色 |
AGE
LR-90 (0, 25, 50, 100, and 200 μM) inhibits RAGE, MCP-1, COX-2, IP-10 and NOX2 mRNA expression in THP-1 cells in a dose-dependent manner, after pretreatment 1 h befor S100b stimulatation for 4 hours.
LR-90 (0, 25, 50, 100, and 200 μM) dose-dependently and significantly blocks THP-1 cells adherence to endothelial cells after pretreatment 1 h befor S100b stimulatation for 24 hours.
LR-90 (0, 25, 50, 100, and 200 μM, for 24 hours) shows no effect on the cell viability of THP-1 cells.
Cell Viability Assay
Cell Line: | THP-1 cells |
Concentration: | 0, 25, 50, 100, and 200 μM |
Incubation Time: | 24 hours |
Result: | Showed no cytotoxicity to THP-1 cells. |
RT-PCR
Cell Line: | THP-1 cells |
Concentration: | 0, 25, 50, 100, and 200 μM |
Incubation Time: | One hour before S100b addition for 4 hours |
Result: | Dose-dependently inhibited mRNA expression of RAGE, MCP-1, COX-2, IP-10, and NOX2 stimulated with S100b. |
LR-90 (50 mg/L, p.o. for 27 weeks) significantly reduces plasma lipids, modestly affects hyperglycaemia in ZDF rats.
LR-90 (50 mg/L) decreases renal AGE, AGER and lipid peroxidation.
Animal Model: | Male ZDF rats (13 to 40 weeks) |
Dosage: | 50 mg/L |
Administration: | P.O. for 27 weeks |
Result: | Significantly reduced plasma triacylglycerol and cholesterol by ∼55% and ∼30%, respectively. Modestly affected hyperglycaemia and blood pressure. Lowered the body weight. |
安全信息
更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
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2024/04/30 | HY-76383 | 2,2' - ((((((亚甲基双(2-氯-4,1-亚苯基))二(氮烷二基))二(羰基))双(氮烷二 LR-90 | 245075-84-7 | 5mg | 1800元 |
2024/04/30 | HY-76383 | 2,2' - ((((((亚甲基双(2-氯-4,1-亚苯基))二(氮烷二基))二(羰基))双(氮烷二 LR-90 | 245075-84-7 | 10mM * 1mLin DMSO | 2810元 |