| 产品详情 |
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| Product Name | AT 56 |
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| Description | MW: 397.52. Purity ≥98% by HPLC. Background: AT-56 is a selective, competitive, and highly bioavailable inhibitor of L-PGDS (lipocalin-type prostaglandin D synthase) (Ki = 75 uM). It inhibits the production of PGD2 by L-PGDS purified from human CSF and recombinant mouse cells with an IC?? value of 95 uM. At concentrations as high as 100 uM in vitro or 30 mg/kg in vivo, AT-56 does not affect the production of PGE2, PGF2alpha, or H-PGDS-catalyzed PGD2. |
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| Size | 5 mg, 25 mg |
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| Concentration | n/a |
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| Applications | n/a |
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| Other Names | [4-(5H-Dibenzo[a,d]cyclohepten-5-ylidene)-1-[4-(2H-tetrazol-5-yl)butyl]-piperidine] |
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| Gene, Accession, CAS # | CAS: 162640-98-4 |
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| Catalog # | MBS842995 |
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| Order / More Info | AT 56 from MYBIOSOURCE INC. |
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| Product Specific References | n/a |
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| 产品资料 |
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