P-gp inhibitor 1
CAS No. 2050747-49-2
P-gp inhibitor 1 ( —— )
产品货号. M26354 CAS No. 2050747-49-2
P-gp inhibitor 1 inhibits reversing P-glycoprotein-mediated multidrug resistance with an EC50 of 57.9 nM (K562/A02 cells).
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥1037 | 有现货 |
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10MG | ¥1725 | 有现货 |
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25MG | ¥3467 | 有现货 |
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50MG | ¥5176 | 有现货 |
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100MG | ¥7209 | 有现货 |
|
500MG | ¥14823 | 有现货 |
|
1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称P-gp inhibitor 1
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述P-gp inhibitor 1 inhibits reversing P-glycoprotein-mediated multidrug resistance with an EC50 of 57.9 nM (K562/A02 cells).
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产品描述P-gp inhibitor 1 inhibits reversing P-glycoprotein-mediated multidrug resistance with an EC50 of 57.9 nM (K562/A02 cells).(In Vitro):In K562/A02 MDR cells, P-gp inhibitor 1 (0.1, 1, 5 μM, 1 h) boosts the potency of other MDR-related cytotoxic agents with different structures, increases the accumulation of DOX, blocks Pgp-mediated Rh123 efflux, and suppresses P-gp ATPase activity.
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同义词——
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通路Others
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靶点Other Targets
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受体Histamine Receptor
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研究领域——
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适应症——
化学信息
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CAS Number2050747-49-2
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分子量517.6
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分子式C32H31N5O2
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纯度>98% (HPLC)
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溶解度——
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SMILESCOc1cc2CCN(CCc3ccc(Nc4nc(nc5ccccc45)-c4ccncc4)cc3)Cc2cc1OC
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Miura M, Uno T. Clinical pharmacokinetics of fexofenadine enantiomers. Expert Opin Drug Metab Toxicol. 2010 Jan;6(1):69-74.
产品手册
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