OG-L002 |CAS:1357302-64-7 Probechem Biochemicals

Chemical Structure : OG-L002

CAS No.: 1357302-64-7

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OG-L002 (OG L002)

货号: PC-61746Not For Human Use, Lab Use Only.

OG-L002 is a novel selective LSD1 inhibitor with IC50 of 20 nM.

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10 mg	￥1180	In stock
25 mg	￥1880	In stock
50 mg	￥2980	In stock
100 mg		Get quote

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生物&药学活性

OG-L002 is a potent, selective LSD1 inhibitor with IC50 of 20 nM.
OG-L002 demonstrates significant potency both in inhibition of HSV IE gene expression and in suppression of viral reactivation from latency in a mouse ganglion explant model.
OG-L002 also suppresses the expression of the initial class of hCMV and adenovirus genes in vitro.
OG-L002 reduces the induction of TNF-α mRNA in splenocytes from mice.

物理化学性质&存储条件

分子量	225.3
分子式	C15H15NO
外观性状	Solid
CAS No.
储存条件	固体粉末 -20 °C 12 个月; 4°C 6 个月	配置液 -80 °C 6 个月; -20°C 6 个月
Shipping
Solubility	10 mM in DMSO
Chemical Name/SMILES	4'-[(1R,2S)-2-aminocyclopropyl]-[1,1'-biphenyl]-3-ol

参考文献

1. Seifermann M, et al. DNA Repair (Amst). 2017 Oct;58:13-20.

2. Liang Y, et al. MBio. 2013 Feb 5;4(1):e00558-12.

OG-L002 (OG L002)

生物&药学活性

物理化学性质&存储条件

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OG-L002 (OG L002)

生物&药学活性

物理化学性质&存储条件

参考文献

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