| 產(chǎn)品詳情 |
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| Product Name | OG-L002 |
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| Description | A potent inhibitor of LSD1 (IC50 = 0.02 μM) that less effectively inhibits MAO-A and MAO-B (IC50s = 1.38 and 0.72 μM); blocks the expression of IE genes of HSV and hCMV in mammalian cells; represses HSV primary infection in mice and blocks HSV reactivation from latency in a mouse ganglion explant model |
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| Size | 25 mg |
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| Concentration | n/a |
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| Applications | n/a |
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| Other Names | 1332859-11-6 1357300-15-2 1357298-75-9 1357299-45-6 biochemical inhibitor inhibit cancer demethylase epigenetics histone modification gene regulation intracellular signaling antiviral infectious disease lysine-specific demethylase 1 LSD1 protein OGL002 anti-viral LSD |
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| Gene, Accession, CAS # | CAS: 1357302-64-7 |
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| Catalog # | 17471-25 |
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| Price | |
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| Order / More Info | OG-L002 from CAYMAN CHEMICAL COMPANY |
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| Product Specific References | n/a |
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| 產(chǎn)品資料 |
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