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Item number: TGM-T6073-1mg

Description: OG-L002 is an effective and selective LSD1 inhibitor (IC50: 20 nM), showing 69- and 36-fold selectivity over MAO-A and MAO-B, respectively. Target: HSV, Monoamine Oxidase, Histone Demethylase. Smiles: N[C@H]1C[C@@H]1c1ccc(cc1)-c1cccc(O)c1. References: MBio. 2013, 4(1), e00558-12.

Application:	LSD1 inhibitor
CAS	1357302-64-7
MW:	225.29 D

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OG-L002

Item number: Cay17471-1

Lysine-specific demethylase 1 (LSD1) is a protein lysine demethylase that specifically demethylates histone H3 lysine 4 (H3K4) and H3K9, resulting in transcriptional repression. Host LSD1 is also recruited by certain viruses to limit H3K9 methylation, which can repress viral genes necessary for infection....

Keywords:	4'-[(1R,2S)-2-aminocyclopropyl]-[1,1'-biphenyl]-3-ol
Application:	LSD1 inhibitor
CAS	1357302-64-7
MW:	225.3 D

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