PDM2

CAS No. 688348-25-6

PDM2( —— )

Catalog No. M18999 CAS No. 688348-25-6

PDM 2 is a potent and selective aryl hydrocarbon receptor (AhR) antagonist.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
10MG 38 In Stock
25MG 71 In Stock
50MG 114 In Stock
100MG 206 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    PDM2
  • Note
    Research use only, not for human use.
  • Brief Description
    PDM 2 is a potent and selective aryl hydrocarbon receptor (AhR) antagonist.
  • Description
    PDM 2 is a potent and selective aryl hydrocarbon receptor (AhR) antagonist.
  • In Vitro
    PDM2 (Compound 4b) exhibits a Ki of 1.2±0.4 nM for AhR and no affinity for estrogen receptor (ER), confirming that replacement of hydroxyl with chloride abolished binding on ER and increased dramatically the affinity for AhR.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    FAAH
  • Recptor
    AhR
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    688348-25-6
  • Formula Weight
    283.58
  • Molecular Formula
    C14H9Cl3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : 50 mg/mL 176.32 mM
  • SMILES
    Clc1ccc(cc1)\C=C\c1cc(Cl)cc(Cl)c1
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.de Medina, P. ,Casper, R.,Savouret, J.F., et al. Journal of Medicinal Chemistry 48, 287-291 (2005).
molnova catalog
related products
  • N-(3-Methoxybenzyl)P...

    N-(3-Methoxybenzyl)Palmitamide is a promising FAAH inhibitor, treatment of pain, inflammation and CNS degenerative disorders.

  • CB2R/FAAH?modulator-...

    CB2R/FAAH?modulator-1, a cannabinoid type 2 receptor (CB2R) agonist, is also a fatty acid amide hydrolase (FAAH) inhibitor (IC50=4 μM) that reduces the production of pro-inflammatory and anti-inflammatory cytokines and is commonly used in inflammation studies.

  • AM 374

    AM 374 (HDSF), a fatty acid amide hydrolase (FAAH) inhibitor, demonstrates the capacity to inhibit amidase activity, boasting an IC50 value of 13 nM.