A resveratrol-based aryl hydrocarbon receptor antagonist
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PDM 2

Item No. 10006342

Technical Information
Formal Name
1,3-dichloro-5-[(1E)-2-(4-chlorophenyl)ethenyl]-benzene
CAS Number
688348-25-6
Molecular Formula
C14H9Cl3
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMF: 30 mg/mlDMSO: 30 mg/mlEthanol: 2 mg/ml
λmax
214, 302, 313 nm
SMILES
Clc1ccc(cc1)\C=C/c1cc(Cl)cc(Cl)c1
InChi Code
InChI=1S/C14H9Cl3/c15-12-5-3-10(4-6-12)1-2-11-7-13(16)9-14(17)8-11/h1-9H/b2-1+
InChi Key
JMYNPQVCVQVODQ-OWOJBTEDSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    The aryl hydrocarbon receptor (AhR) is a ligand-dependent intracellular transcription factor whose ligands include some of the most infamous xenobiotics, including dioxin, benzo[a]pyrene, and numerous polyaromatics from soot and coal tar.1 PDM 2 is an analog of resveratrol acting as a potent and selective aryl hydrocarbon receptor (AhR) antagonist, with a Ki of 1.2 nM.2 PDM 2 is inactive as a ligand for the estrogen receptor even at 100 µM. As AhR knockout mice are insensitive to the carcinogenic effects of classical AhR ligands, PDM 2 is a potential therapeutic for the treatment for dioxin and other aryl hydrocarbon poisonings.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Denison, M.S., and Nagy, S.R. Activation of the aryl hydrocarbon receptor by structurally diverse exogenous and endogenous chemicals. Annu. Rev. Pharmacol. Toxicol. 43, 309-334 (2003).

    2. de Medina, P., Casper, R., Savouret, J.-F., et alSynthesis and biological properties of new stilbene derivatives of resveratrol as new selective aryl hydrocarbon modulators. J. Med. Chem. 48(1), 287-291 (2005).