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| Product Name | JNJ-1661010 |
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| Description | Purity >98% by NMR, TLC. JNJ-1661010 is a potent and selective FAAH inhibitor. Initially forms a covalent adduct with FAAH but is slowly released, IC50 = 12 nM. 100-fold selectivity for FAAH-1 over FAAH-2. Cell permeable and active in vivo. JNJ-1661010 displays analgesic activity in various animal models. |
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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 | 4-(3-Phenyl-[1,2,4]thizdiazol-5-yl)-piperazine-1-carboxylic acid phenylamide |
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| Gene, Accession, CAS # | CAS: 681136-29-8 |
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| Catalog # | LS-H14723 |
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| Order / More Info | JNJ-1661010 from LIFESPAN BIOSCIENCES INC. |
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| Product Specific References | n/a |
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