LY2955303
目录号: PL10817 纯度: ≥99%
CAS No. :1433497-19-8
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中文名称
LY2955303
英文名称
LY2955303
英文别名
4-[5-[3,5-bis(1,1-Dimethylethyl)phenyl]-1-[4-[(4-methyl-1-piperazinyl)carbonyl]phenyl]-1H-pyrazol-3-yl]-benzoic acid;LY 2955303;LY2955303;EGR6ZG7M0Z;4-(5-(3,5-di-tert-butylphenyl)-1-(4-(4-methylpiperazine-1-carbonyl)phenyl)-1H-pyrazol-3-yl)benzoic acid;4-[5-(3,5-ditert-butylphenyl)-1-[4-(4-methylpiperazine-1-carbonyl)phenyl]pyrazol-3-yl]benzoic acid;BCP20655;BDBM50178962;C72700;4-(5-(3,5-Di-tert-butylphenyl)-1-(4-((4-methylpiperazin-1-yl)carbonyl) phenyl)-1H-pyrazol-3-yl)benzoic acid;4-[5-(3,5-Di-tert-buty
Cas No.
1433497-19-8
分子式
C36H42N4O3
分子量
578.74
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
LY2955303 是一种有效且有选择性的视黄酸受体 γ (RARγ) 的拮抗剂,其 Ki 值为 1.09 nM。
生物活性
LY2955303 is a potent and selective retinoic acid receptor gamma (RARγ) antagonist with a K i of 1.09 nM.
性状
Solid
IC50 & Target[1][2]
Ki: 1.09 nM (RARγ)
体外研究(In Vitro)
LY2955303 is tested and observed that the binding Kis for RARα, RARβ and RARγ are >1700, >2980 and 1.09 nM, respectively. The functional Ki for RARγ is 7.1±4.9 nM. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
A single oral dose of LY2955303 demonstrates a dose responsive effect whereby the rat reduces differential weight bearing (ED 50 =0.72 mg/kg). has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Hughes NE, et al. Identification of potent and selective retinoic acid receptor gamma (RARγ) antagonists for the treatment of osteoarthritis pain using structure based drug design. Bioorg Med Chem Lett. 2016 Jul 15;26(14):3274-3277.
溶解度数据
In Vitro: DMSO : 30 mg/mL (51.84 mM; Need ultrasonic and warming)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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