Catalog Number: 3531
Chemical Name: 4-(5H-Dibenzo[a,d]cyclohepten-5-ylidene)-1-[4-(2H-tetrazol-5-yl)butyl]-piperidine
Biological Activity
Orally active inhibitor of lipocalin-type prostaglandin D synthase (L-PGDS) (Ki = 75 μM, IC50 = 95 μM). Inhibits the production of PGD2 from PGH2 in vitro, with no effect on PGE2 or PGF2α production.
Technical Data
  • M.Wt:
    397.52
  • Formula:
    C25H27N5
  • Solubility:
    Soluble to 50 mM in DMSO
  • Purity:
    >99%
  • Storage:
    Store at -20°C
  • CAS No:
    162640-98-4
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis. All Tocris products are intended for laboratory research use only.
Background References
  1. Biochemical, functional and pharmacological characterization of AT-56, an orally active and selective inhibitor of lipocalin-type prostaglandin D synthase.
    Irikura et al.
    J.Biol.Chem., 2009;284:7623
Citations:

The citations listed below are publications that use Tocris products. Selected citations for AT 56 include:

1 Citations: Showing 1 - 1

  1. Zic1 controls placode progenitor formation non-cell autonomously by regulating retinoic acid production and transport.
    Authors: Jaurena Et al.
    Elife 2015;6:7476

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