UNC0642

UNC0642是有效选择性赖氨酸甲基转移酶G9a 和GLP 抑制剂, 抑制G9a 的IC50值小于2.5 nM。

CAS号

1481677-78-4

分子式

C29H44F2N6O2

主要靶点

Histone Methyltransferase

仅限科研使用

Cat No : CM04586

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Synonyms

UNC-0642|UNC 0642



产品信息

UNC0642 is an effective and specific G9a/GLP inhibitor (IC50< 2.5 nM).

CAS号 1481677-78-4
分子式 C29H44F2N6O2
主要靶点 Histone Methyltransferase
主要通路 表观遗传
分子量 546.69
纯度 98.75%, 此纯度可做参考,具体纯度与批次有关系,可咨询客服
储存条件 Powder: -20°C for 3 years | In solvent: -80°C for 1 year
别名 UNC-0642|UNC 0642

靶点活性

G9a:<2.5 nM|GLP:<2.5 nM

体内活性

UNC0642 (5 mg/kg, i.p.) results in a plasma Cmax of 947 ng/mL and an AUC of 1265 h·ng/ml.

体外活性

UNC0642 (Ki: 3.7±1 nM) is competitive with the peptide substrate and non-competitive with the cofactor SAM. UNC0642 is more than 300-fold selective for G9a and GLP over a broad range of kinases, transporters, GPCRs, and ion channels. UNC0642 exhibits high potency at low cell toxicity, reducing the H3K9me2 mark, and good separation of functional potency in a number of cell lines.

溶解度

DMSO:295 mg/mL,Sonification/heating is recommended.

细胞实验

MDA-MB-231, PC3, and U2OS cells are treated with UNC0642 for 48 h. Cell viability assays are performed by incubating cells with 0.1 mg/mL of resazurin for 3 – 4 h. Resazurin reduction is monitored with 544 nm excitation, measuring fluorescence at 590 nm.

动物实验

Mouse: Standard PK studies are performed using male Swiss albino mice. Plasma and brain concentrations are measured at 0.08, 0.25, 0.5, 1, 2, 4, 8, and 24 h following UNC0642 (5 mg/kg, i.p.). The compound concentration at each time point in plasma or brain is the average value from 3 test animals[1].

参考文献

1.Liu F, et al. Discovery of an in vivo chemical probe of the lysine methyltransferases G9a and GLP. J Med Chem. 2013 Nov 14;56(21):8931-42. doi: 10.1021/jm401480r. Epub 2013 Oct 31.

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