BAY885
目录号: PL01986 纯度: ≥99%
CAS No. :2307249-33-6
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中文名称
BAY885
中文别名
2-氨基-4-(三氟甲氧基)苯基][4-[7-(4-甲基-1-哌嗪基)吡啶[3,2-D]嘧啶-4-基]-1-哌啶基]甲基酮;化合物BAY885;(2-氨基-4-(三氟甲氧基)苯基)(4-(7-(4-甲基哌嗪-1-基)吡啶并[3,2-D]嘧啶-4-基)哌啶-1-基)甲酮
英文名称
BAY885
英文别名
BAY885;GTPL10183;s8896;compound 41 [PMID: 30563338];(2-amino-4-(trifluoromethoxy)phenyl)(4-(7-(4-methylpiperazin-1-yl)pyrido[3,2-d]pyrimidin-4-yl)piperidin-1-yl)methanone;[2-amino-4-(trifluoromethoxy)phenyl]-[4-[7-(4-methylpiperazin-1-yl)pyrido[3,2-d]pyrimidin-4-yl]piperidin-1-yl]methanone;CID 134128280
Cas No.
2307249-33-6
分子式
C25H28F3N7O2
分子量
515.53
包装储存
-20°C, stored under nitrogen In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)
产品详情
BAY885 是一种高效的选择性 ERK5 抑制剂,IC50 为 35 nM,对其他激酶的抑制作用较弱。
生物活性
BAY885 is a highly potent and selective ERK5 inhibitor with an IC 50 of 35 nM. BAY885 shows weak inhibition on others kinases.
性状
Solid
IC50 & Target[1][2]
ERK5 35 nM (IC50)
体外研究(In Vitro)
The ERK5 probe 41 (BAY-885) showed potent ERK5 kinase and transcriptional inhibition in the SN12C-MEF2 reporter cell line (IC50 = 115 nM/IC90 = 691 nM) and had no effects on a reporter control cell line with constitutive luciferase expression (SN12C-CMV-luc, IC50 > 30 μM). 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
-20°C, stored under nitrogen In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)
参考文献
[1]. Nguyen D, et al. Discovery and Characterization of the Potent and Highly Selective (Piperidin-4-yl)pyrido[3,2- d]pyrimidine Based in Vitro Probe BAY-885 for the Kinase ERK5. J Med Chem. 2019 Jan 24;62(2):928-940.
溶解度数据
In Vitro: DMSO : 16.67 mg/mL (32.34 mM; Need ultrasonic)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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