| 产品详情 |
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| Product Name | Pimelic Diphenylamide 106 |
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| Description | Purity >98%. Pimelic diphenylamide 106 is a slow, tight-binding inhibitor of class I histone deacetylases (HDACs). Unlike the HDAC inhibitor suberoylanilide hydroamic acid, which has a fast-on/fast-off HDAC binding rate, pimelic diphenylamide 106 progressively binds HDACs and remains bound after wash-out. As a result, the IC50 of pimelic diphenylamide 106 decreases over time. With prolonged preincubation (1-3 hours), pimelic diphenylamide inhibits the class I HDACs (IC50 = 150, 760, 370, and 5,000 nM for HDAC1, 2, 3, and 8, respectively) but not the class II HDACs (IC50 > 180 µM for HDAC4, 5, and 7). Pimelic diphenylamide 106 and related benzamide HDAC inhibitors may have therapeutic value in Friedrich's ataxia1, and Huntington's disease, in part due to their low animal toxicity. |
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| Size | n/a |
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| Concentration | n/a |
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| Applications | n/a |
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| Other Names | N1-(2-aminophenyl)-N7-(4-methylphenyl)-heptanediamide, Histone Deacetylase Inhibitor VII, TC-H 106 |
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| Gene, Accession, CAS # | CAS: 937039-45-7 |
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| Catalog # | LS-H9417 |
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| Order / More Info | Pimelic Diphenylamide 106 from LIFESPAN BIOSCIENCES INC. |
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| Product Specific References | n/a |
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