规格 | 价格 | 会员价 | 库存 | 数量 | |||
---|---|---|---|---|---|---|---|
{[ item.pr_size ]} |
{[ getRatePrice(item.pr_rmb, 1,1) ]} {[ getRatePrice(item.pr_rmb_sale, 1,1) ]} {[ suihuo_tips(item.pr_am, item.pr_size) ]} |
{[ getRatePrice(item.pr_rmb, 1,1) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,1) ]} {[ suihuo_tips(item.pr_am, item.pr_size) ]} |
{[ getRatePrice(item.pr_rmb, 1,1) ]}{[ suihuo_tips(item.pr_am, item.pr_size) ]} | {[ getRatePrice(item.pr_rmb_sale, 1,1) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate) ]} | 现货 | 咨询 | - + |
快速发货 顺丰冷链运输,1-2 天到达
品质保证
技术支持
免费溶解
描述 | BMS-P5 is a specific and orally active inhibitor of peptidylarginine deiminase 4 (PAD4). BMS-P5 free base inhibits MM-induced NET formation and slows the progression of MM in a syngeneic mouse model [1]. |
体内研究 | Administration of BMS-P5 (50 mg/kg, oral gavage) significantly prolongs the survival of mice with MM [1]. BMS-P5 (50 mg/kg, oral gavage) may reduce the presence of pro-tumorigenic proteins in the tumor microenvironment, thereby delaying tumor progression [1]. |
体外研究 | BMS-P5 inhibits the citrullination of histone H3 induced by calcium ionophore [1]. BMS-P5 also inhibits the formation of NETs induced by primary MM cells isolated from the bone marrow of patients with MM [1]. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.12mL 0.42mL 0.21mL |
10.58mL 2.12mL 1.06mL |
21.16mL 4.23mL 2.12mL |
CAS号 | 1550371-22-6 |
分子式 | C27H32N6O2 |
分子量 | 472.582 |
别名 | BMS-P5 |
运输 | 蓝冰 |
存储条件 |
液体 -20°C:3-6个月-80°C:12个月 粉末 Inert atmosphere,Store in freezer, under -20°C |
溶解度 |
DMSO: 250 mg/mL(529.01 mM),配合低频超声助溶,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 |