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Ro 6842262,LPA1拮抗剂

    
≥99%

Ro 6842262

源叶(MedMol)
V37279 一键复制产品信息
1396006-71-5
C₂₈H₂₆N₄O₄
482.53
1-[4'-[4-甲基-5-[[[((R)-1-苯基乙氧基]羰基氨基] -1H-1,2,3-三唑-1-基] [1,1'-联苯]-4-基]环丙烷甲酸;1-[4'-[4-Methyl-5-[[[(1R)-1-phenylethoxy]carbonylamino]-1H-1,2,3-triazol-1-yl][1,1'-biphenyl]-4-yl]cyclopropanecarboxylic acid;LPA1 receptor antagonist 1
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
V37279-1mg
≥99%

¥1290.00

货期:3-5天 - - - -
V37279-5mg
≥99%

¥3290.00

货期:3-5天 - - - -
V37279-10mg
≥99%

¥4730.00

货期:3-5天 - - - -
V37279-25mg
≥99%

¥7260.00

货期:3-5天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: LPA1 receptor antagonist 1 是具有高度选择性的,溶血磷脂酸 (LPA1) 受体的一个拮抗剂,其 IC50 值为 25 nM
靶点: IC50: 25 nM (LPA1).
体内研究: Oral dosing of LPA1 receptor antagonist 1 in mice causes a dose-dependent reduction in serum histamine levels induced following intravenous LPA stimulation. When mice are orally dosed with LPA1 antagonist 1 (100 mg/kg, aqueous suspension) prior to intravenous LPA injection, the LPA-induced histamine level is significantly blocked A clear PK/PD relationship is demonstrated by the correlation between the levels of LPA1 receptor antagonist 1 and LPA-induced histamine concentrations in plasma. Although AM095 almost completely blocks histamine release (100 mg/kg), analysis of plasma samples revealed more than 65-fold higher concentrations of AM095 than LPA1 receptor antagonist 1 (100 mg/kg). The ability of LPA1 receptor antagonist 1 to block histamine release at much lower plasma concentration suggests that further improvement of pharmacokinetic properties of this chemical class could lower the effective dose.
保存条件: -20°C
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.072 ml 10.362 ml 20.724 ml
5 mM 0.414 ml 2.072 ml 4.145 ml
10 mM 0.207 ml 1.036 ml 2.072 ml
50 mM 0.041 ml 0.207 ml 0.414 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

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