Raphin1
目录号 : GC38189Raphin1 is an orally bioavailable, selective inhibitor of R15B (PPP1R15B, a regulatory subunit of protein phosphatase 1). Raphin1 binds strongly to the R15B-PP1c holophosphatase with Kd of 33 nM.
Cas No.:2022961-17-5
Sample solution is provided at 25 µL, 10mM.
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Raphin1 is an orally bioavailable, selective inhibitor of R15B (PPP1R15B, a regulatory subunit of protein phosphatase 1). Raphin1 binds strongly to the R15B-PP1c holophosphatase with Kd of 33 nM.
[1] Agnieszka Krzyzosiak, et al. Cell. 2018 Aug 23;174(5):1216-1228.e19.
Cas No. | 2022961-17-5 | SDF | |
Canonical SMILES | N=C(N/N=C/C1=CC=CC(Cl)=C1Cl)N | ||
分子式 | C8H8Cl2N4 | 分子量 | 231.08 |
溶解度 | DMSO: 125 mg/mL (540.94 mM) | 储存条件 | Store at -20°C |
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1 mg | 5 mg | 10 mg | |
1 mM | 4.3275 mL | 21.6375 mL | 43.2751 mL |
5 mM | 0.8655 mL | 4.3275 mL | 8.655 mL |
10 mM | 0.4328 mL | 2.1638 mL | 4.3275 mL |
第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量) | ||||||||||
给药剂量 | mg/kg | 动物平均体重 | g | 每只动物给药体积 | ul | 动物数量 | 只 | |||
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% DMSO % % Tween 80 % saline | ||||||||||
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工作液浓度: mg/ml;
DMSO母液配制方法: mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL,
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1. 首先保证母液是澄清的;
2.
一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
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PP1 Phosphatase Complexes: Undruggable No Longer
Cell 2018 Aug 23;174(5):1049-1051.PMID:30142342DOI:10.1016/j.cell.2018.08.007.
The identification of inhibitors targeting regulatory subunits of serine/threonine PP1 phosphatases reported by Krzyzosiak et al. is a significant step in expanding the pharmacological regulation of phosphorylation beyond kinases. The selective inhibitor of the R15B phosphatase regulatory subunit, termed Raphin1, protects cells from stress and delays neurodegeneration in a mouse model of Huntington's disease.
Target-Based Discovery of an Inhibitor of the Regulatory Phosphatase PPP1R15B
Cell 2018 Aug 23;174(5):1216-1228.e19.PMID:30057111DOI:10.1016/j.cell.2018.06.030.
Protein phosphorylation is a prevalent and ubiquitous mechanism of regulation. Kinases are popular drug targets, but identifying selective phosphatase inhibitors has been challenging. Here, we used surface plasmon resonance to design a method to enable target-based discovery of selective serine/threonine phosphatase inhibitors. The method targeted a regulatory subunit of protein phosphatase 1, PPP1R15B (R15B), a negative regulator of proteostasis. This yielded Raphin1, a selective inhibitor of R15B. In cells, Raphin1 caused a rapid and transient accumulation of its phosphorylated substrate, resulting in a transient attenuation of protein synthesis. In vitro, Raphin1 inhibits the recombinant R15B-PP1c holoenzyme, but not the closely related R15A-PP1c, by interfering with substrate recruitment. Raphin1 was orally bioavailable, crossed the blood-brain barrier, and demonstrated efficacy in a mouse model of Huntington's disease. This identifies R15B as a druggable target and provides a platform for target-based discovery of inhibitors of serine/threonine phosphatases.