Clozapine N-oxide dihydrochloride

CAS No. 2250025-93-3

Clozapine N-oxide dihydrochloride( —— )

Catalog No. M36444 CAS No. 2250025-93-3

Clozapine N-oxide dihydrochloride, a derivative of Clozapine and an agonist of human muscarinic design receptors (DREADDs), crosses the blood-brain barrier and activates DREADD receptors hM3Dq and hM4Di.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 44 Get Quote
10MG 73 Get Quote
25MG 117 Get Quote
50MG 172 Get Quote
500MG Get Quote Get Quote
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Biological Information

  • Product Name
    Clozapine N-oxide dihydrochloride
  • Note
    Research use only, not for human use.
  • Brief Description
    Clozapine N-oxide dihydrochloride, a derivative of Clozapine and an agonist of human muscarinic design receptors (DREADDs), crosses the blood-brain barrier and activates DREADD receptors hM3Dq and hM4Di.
  • Description
    Clozapine N-oxide dihydrochloride is a major metabolite of Clozapine and a human muscarinic designer receptors (DREADDs) agonist. Clozapine N-oxide dihydrochloride activates the DREADD receptor hM3Dq and hM4Di. Clozapine N-oxide dihydrochloride can cross the blood-brain barrier. Clozapine is a potent dopamine antagonist and also a potent and selective muscarinic M4 receptor (EC50=11 nM) agonist.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    AChE
  • Recptor
    AChE
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2250025-93-3
  • Formula Weight
    452.2
  • Molecular Formula
    C18H22Cl4N4O
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 240 mg/mL (577.28 mM; Ultrasonic ) H2O : 100 mg/mL (240.53 mM; Ultrasonic)
  • SMILES
    C[N+]1([O-])CCN(CC1)C2=NC3=CC(Cl)=CC=C3NC4=C2C=CC=C4.Cl.Cl.Cl
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Wess J, et al. Novel designer receptors to probe GPCR signaling and physiology. Trends Pharmacol Sci. 2013 Jul;34(7):385-92.?
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