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| Product | Description | |
|---|---|---|
| OG-L002 | OG-L002 potently inhibits HSV IE gene expression in both HeLa and HFF cells with IC50s of ~10 μM and ~3 μM, respectively. OG-L002 is a potent and highly selective inhibitor of LSD1 (IC50 = 0.02 μM), and is a potent inhibitor of monoamine oxidases (MAO) with IC50s of 1.38 and 0.72 μM for MAO-A and MAO-B, respectively. Synonyms: 4'-[(1R,2S)-2-Aminocyclopropyl]-[1,1'-biphenyl]-3-ol; 4'-((1R,2S)-2-Aminocyclopropyl)biphenyl-3-ol; [1,1'-Biphenyl]-3-ol, 4'-[(1R,2S)-2-aminocyclopropyl]-; 4'-[(1R,2S)-2-Aminocyclopropyl]-3-biphenylol. Grades: >98%. CAS No. 1357302-64-7. Molecular formula: C15H15NO. Mole weight: 225.29. |  |
| OG-L002 hydrochloride | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| OG-L002 hydrochloride | OG-L002 hydrochloride is a selective inhibitor of lysine specific demethylase 1 (LSD1/KDM1A/H3K9 demethylase). OG-L002 effectively inhibits herpes simplex virus (HSV) IE gene expression, genome replication, and reactivation from latency. Synonyms: OG-L002 HCl; OG L002 HCl; OGL002 HCl; OG-L002 Hydrochloride; OG L002 Hydrochloride; OGL002 Hydrochloride; 4-[(1R,2S)-2-Aminocyclopropyl]-[1,1-biphenyl]-3-ol Hydrochloride. Grades: 99%. CAS No. 1357298-75-9. Molecular formula: C15H15NO.HCl. Mole weight: 261.75. | |
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