OG-L002
目录号: PL07502 纯度: ≥99%
CAS No. :1357302-64-7
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中文名称
OG-L002
中文别名
4'-((1R,2S)-2-氨基环丙基)联苯-3-醇;OG-L002 抑制剂
英文名称
OG-L002
英文别名
OG-L002;[1,​1'-​Biphenyl]​-​3-​ol, 4'-​[(1R,​2S)​-​2-​aminocyclopropyl]​-
Cas No.
1357302-64-7
分子式
C15H15NO
分子量
225.29
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
OG-L002 是一种有效且高度选择性的 LSD1 抑制剂,IC50 为 0.02 μM。OG-L002 是一种有效的单胺氧化酶 (MAO) 抑制剂,对 MAO-A 和 MAO-B 的 IC50 分别为 1.38 μM 和 0.72 μM。OG-L002 有效抑制 HSV IE 基因的表达。
生物活性
OG-L002 is a potent and highly selective LSD1 inhibitor with an IC 50 of 0.02 μM. OG-L002 is a potent monoamine oxidases (MAO) inhibitor with IC 50 s of 1.38 μM and 0.72 μM for MAO-A and MAO-B, respectively. OG-L002 potently inhibits the expression of HSV IE genes.
性状
Solid
IC50 & Target[1][2]
IC50: 0.02 μM (LSD1), 1.38 μM (MAO-A), 0.72 μM (MAO-B), HSV IE
体外研究(In Vitro)
OG-L002 inhibits viral IE gene expression in both cells with a significantly reduced IC50 (IC50: ~10 μM in HeLa cells; IC50: ~3 μM in HFF cells) relative to the control MAOI TCP (IC50: ~1 mM). has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
OG-L002 (i.p.; 6-40 mg/kg; daily; for 7 days) reduces the levels of detectable viral genomes in the ganglia in a dose-dependent manner at both 3 and 5 days postinfection. has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model:
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]. Liang Y, et al. A novel selective LSD1/KDM1A inhibitor epigenetically blocks herpes simplex virus lytic replication and reactivation from latency. mBio. 2013 Feb 5;4(1):e00558-12.
溶解度数据
In Vitro: DMSO : 250 mg/mL (1109.68 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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