| Identification | Back Directory | [Name]
OG-L002 | [CAS]
1357302-64-7 | [Synonyms]
CS-830
OG-L002
OG-L002 USP/EP/BP
OGL002;OG L002;OGL-002
4'-((1R,2S)-2-Aminocyclopropyl)biphenyl-3-ol
4'-((1R,2S)-2-Aminocyclopropyl)-[1,1'-biphenyl]-3-ol
[1,1'-Biphenyl]-3-ol, 4'-[(1R,2S)-2-aminocyclopropyl]-
[1,1'-Biphenyl]-3-ol, 4'-[(1R,2S)-2-aminocyclopropyl]-4'-((1R,2S)-2-Aminocyclopropyl)biphenyl-3-o
OG-L002 4'-((1S,2R)-2-aminocyclopropyl)-[1,1'-biphenyl]-3-ol 3-[4-[(1R,2S)-2-aminocyclopropyl]phenyl]phenol
OG-L002 [1,1'-Biphenyl]-3-ol, 4'-[(1R,2S)-2-aminocyclopropyl]- | [Molecular Formula]
C15H15NO | [MDL Number]
MFCD27997969 | [MOL File]
1357302-64-7.mol | [Molecular Weight]
225.29 |
| Chemical Properties | Back Directory | [Boiling point ]
416.7±45.0 °C(Predicted) | [density ]
1.193±0.06 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [solubility ]
insoluble in H2O; ≥22.5 mg/mL in DMSO; ≥6.82 mg/mL in EtOH | [form ]
solid | [pka]
9.78±0.10(Predicted) | [color ]
White to yellow |
| Hazard Information | Back Directory | [Description]
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. 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. OG-L002 is a potent inhibitor of LSD1 (IC50 = 0.02 μM) that less effectively inhibits the monoamine oxidases A (MAO-A) and MAO-B (IC50s = 1.38 and 0.72 μM). It blocks the expression of immediate early (IE) genes of herpes simplex virus (HSV) in HeLa cells but not that of cellular control genes. OG-L002 also reduces the expression of human cytomegalovirus IE genes and adenovirus E1A gene in mammalian cells. It is effective in vivo, repressing HSV primary infection in mice and blocking HSV reactivation from latency in a mouse ganglion explant model. | [Uses]
OG-L002 is a novel, potent, and selective LSD1/KDM1A inhibitor that epigenetically blocks the herpes simplex lytic replication and reactivation from latency. | [Enzyme inhibitor]
This histone H3K9 demethylase inhibitor (FW = 669.82 g/mol; CAS
1357302-64-7; Solubility: 45 mg/mL DMSO; <1 mg/mL H2O) potently and
specifically inhibits the histone demethylase LSD1 (IC50 = 20 nM),
resulting in increased repressive chromatin assembly and suppression of
gene expression during the lytic phase of herpes simplex virus and
varicella-zoster virus infection. This LSD1 inhibitor also blocks initial gene
expression of the human cytomegalovirus and adenovirus type 5, attesting
to the critical role of LSD1 in regulating DNA virus infection. Because this
small-molecule inhibitor was originally designed to inhibit monoamine
oxidases, it is noteworthy that its affinity for LSD1 is 36x and 69x higher
than MAO-B and MAO-A, respectively. | [target]
LSD1 | [storage]
Store at -20°C |
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