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245075-84-7

中文名稱 2,2' - ((((((亞甲基雙(2-氯-4,1-亞苯基))二(氮烷二基))二(羰基))雙(氮烷二
英文名稱 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 245075-84-7
分子式 C35H34Cl2N4O8
分子量 709.57
MOL 文件 245075-84-7.mol
更新日期 2024/07/31 16:57:49
245075-84-7 結(jié)構(gòu)式 245075-84-7 結(jié)構(gòu)式

基本信息

中文別名
2,2' - ((((((亞甲基雙(2-氯-4,1-亞苯基))二(氮烷二基))二(羰基))雙(氮烷二
2,2'-((((((亞甲基雙(2-氯-4,1-亞苯基))二(氮烷二基))二(羰基))雙(氮烷二基))二(4,1-亞苯基))二( 氧基))雙(2-甲基丙酸)
英文別名
LR-90
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]
Propanoic acid, 2,2'-[methylenebis[(2-chloro-4,1-phenylene)iminocarbonylimino-4,1-phenyleneoxy]]bis[2-methyl-
2,2'-((((((methylenebis(2-chloro-4,1-phenylene))bis(azanediyl))bis(carbonyl))bis(azanediyl))bis(4,1-phenylene))bis(oxy))bis(2-methylpropanoic acid)
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)

物理化學(xué)性質(zhì)

沸點726.0±60.0 °C(Predicted)
密度1.448±0.06 g/cm3(Predicted)
儲存條件-20°C儲存
溶解度DMSO : ≥ 100 mg/mL (140.93 mM);Water : < 0.1 mg/mL (insoluble)
酸度系數(shù)(pKa)3.01±0.10(Predicted)
形態(tài)Solid
顏色White to off-white
2,2' - ((((((亞甲基雙(2-氯-4,1-亞苯基))二(氮烷二基))二(羰基))雙(氮烷二價格(試劑級)
報價日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價格
2024/11/08HY-763832,2' - ((((((亞甲基雙(2-氯-4,1-亞苯基))二(氮烷二基))二(羰基))雙(氮烷二
LR-90
245075-84-75mg1800元
2024/11/08HY-763832,2' - ((((((亞甲基雙(2-氯-4,1-亞苯基))二(氮烷二基))二(羰基))雙(氮烷二
LR-90
245075-84-710mM * 1mLin DMSO2810元
2024/11/08HY-763832,2' - ((((((亞甲基雙(2-氯-4,1-亞苯基))二(氮烷二基))二(羰基))雙(氮烷二
LR-90
245075-84-710mg3000元

常見問題列表

生物活性
LR-90 是晚期糖基化終產(chǎn)物 (advanced glycation end product (AGE)) 抑制劑,能夠抑制人單核細(xì)胞的炎癥反應(yīng)。LR-90 也可用于糖尿病動物模型研究。
靶點

AGE

體外研究

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.
體內(nèi)研究

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.
"245075-84-7" 相關(guān)產(chǎn)品信息
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