187269-40-5
基本信息
Bimosiamose
[1,1'-Biphenyl]-3-acetic acid, 3',3'''-(1,6-hexanediyl)bis[6'-(α-D-mannopyranosyloxy)-
物理化学性质
熔点 | 115-117° |
沸点 | 1051.0±65.0 °C(Predicted) |
密度 | 1.417±0.06 g/cm3(Predicted) |
储存条件 | -20°C储存 |
溶解度 | DMSO:100.0(Max Conc. mg/mL);115.89(Max Conc. mM) 0.1 M NaOH:25.0(Max Conc. mg/mL);28.97(Max Conc. mM) |
酸度系数(pKa) | 3.95±0.10(Predicted) |
形态 | 结晶固体 |
颜色 | White to off-white |
安全数据
危险性符号(GHS) | GHS07 |
警示词 | 警告 |
危险性描述 | H302-H315-H319-H335 |
防范说明 | P261-P280-P301+P312-P302+P352-P305+P351+P338 |
常见问题列表
IC50: 88 μM (E-selectin), 20 μM (P-selectin), 86 μM (L-selectin)
Bimosiamose (TBC-1269) operates by inhibiting neutrophil recruitment to the site of inflammation through blocking the initial rolling phase of recruitment. Bimosiamose (TBC-1269) inhibits cell recruitment and does not possess any cytotoxic effect on neutrophils.
Bimosiamose (TBC-1269; 25 mg/kg; intravenous injection; Sprague-Dawley rats) treatment shows a significant increase in survival. Best overall survival, 70%, is observed when TBC-1269 is administered 15 minutes before reperfusion, and also shows a marked decrease in liver enzyme levels at 6 hours after reperfusion. Neutrophil migration is also significantly ameliorated (81%). The histologic damage scores is also improved.
Animal Model: | Sprague-Dawley rats (200-225g) with ischemia and reperfusion (I/R) |
Dosage: | 25 mg/kg |
Administration: | Intravenous injection |
Result: | Showed a significant increase in survival compared with controls. |