PD 144418 oxalate

CAS No. 1794760-28-3

PD 144418 oxalate( —— )

Catalog No. M35099 CAS No. 1794760-28-3

PD 144418 oxalate is a highly potent and selective sigma 1 (σ1) receptor ligand with a Ki value of 0.08 nM for σ1 and 1377 nM for σ2, exhibiting negligible affinity for other receptors, ion channels, and enzymes, and demonstrating potential antipsychotic activity.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 128 In Stock
10MG 186 In Stock
25MG 321 In Stock
50MG 458 In Stock
100MG 669 In Stock
200MG 918 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    PD 144418 oxalate
  • Note
    Research use only, not for human use.
  • Brief Description
    PD 144418 oxalate is a highly potent and selective sigma 1 (σ1) receptor ligand with a Ki value of 0.08 nM for σ1 and 1377 nM for σ2, exhibiting negligible affinity for other receptors, ion channels, and enzymes, and demonstrating potential antipsychotic activity.
  • Description
    PD 144418 oxalate is a highly affinity, potent and selective sigma 1 (σ1) receptor ligand (Ki values of 0.08 nM and 1377 nM for σ1 and σ2 respectively). PD 144418 oxalate devoids of any significant affinity for other receptors, ion channels and enzymes.PD 144418 oxalate shows potential antipsychotic activity.
  • In Vitro
    In vitro, PD 144418 reverses the N-methyl-D-aspartate (NMDA)-induced increase in cyclic GMP (cGMP) in rat cerebellar slices without affecting the basal levels, suggesting that σ1 sites may be important in the regulation of glutamine-induced actions. PD 144418 potentiates the decrease in 5-hydroxytryptophan caused by Haloperidol in the mesolimbic region, but by itself has no effect in 5-HT and dopamine (DA) synthesis.
  • In Vivo
    PD 144418 (10 mg/kg; intraperitoneal injection; male CD-1 mice) treatment antagonizes Mescaline-induced scratching at doses that did not alter spontaneous motor activity, with PD 144418 showing ED50 values of 7.0 mg/kg i.p..Animal Model:Male CD-1 mice induced with Mescaline Dosage:10 mg/kg Administration:Intraperitoneal injection; once Result:Antagonized mescaline-induced scratching at doses that did not alter spontaneous motor activity.
  • Synonyms
    ——
  • Pathway
    Autophagy
  • Target
    Sigma receptor
  • Recptor
    Sigma receptor
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1794760-28-3
  • Formula Weight
    372.42
  • Molecular Formula
    C20H24N2O5
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    O=C(O)C(=O)O.N=1OC(=CC1C=2C=CC(=CC2)C)C3=CCCN(C3)CCC
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Akunne HC, et al. The pharmacology of the novel and selective sigma ligand, PD 144418. Neuropharmacology. 1997 Jan;36(1):51-62.?
molnova catalog
related products
  • EST64454

    EST64454 is a highly soluble σ1 receptor antagonist (Ki : 22 nM),has the potential for?Pain Management.

  • Glycerol phenylbutyr...

    Glycerol phenylbutyrate (GPB) is a new generation ammonia scavenger drug and it also is a sigma-2 (σ2) receptor ligand (pKi: 8.02).Glycerol phenylbutyrate may have therapeutic potential in additional conditions such as chronic hepatic encephalopathy or other inherited metabolic disorders. Glycerol phenylbutyrate also has the potential for the treatment of hyperammonemia.

  • Sigma-1 receptor ant...

    Sigma-1 receptor antagonist 1 is an effective and selective antagonist of sigma-1 receptor.