CNO (Clozapine N-oxide)

CNO (Clozapine N-oxide) is a metabolite of Clozapine (GLXC-06516) and an agonist of human muscarinic designer receptors (Designer Receptors Exclusively Activated by Designer Drugs, DREADDs). Clozapine is a potent dopamine (DA) antagonist and a selective muscarinic M4 receptor agonist.Solutions are unstable and should be fresh-prepared.

CNO (Clozapine N-oxide) Chemical Structure

CNO (Clozapine N-oxide) Chemical Structure

CAS: 34233-69-7

Selleck's CNO (Clozapine N-oxide) has been cited by 5 publications

Purity & Quality Control

Batch: Purity: 99.9%
99.9

Products often used together with CNO (Clozapine N-oxide)

JHU37152


Clozapine N-oxide exhibits lower in vivo DREADD potency, while JHU37152 exhibits high in vivo DREADD potency.

Bonaventura J, et al. Nat Commun. 2019 Oct 11;10(1):4627.

JHU37160


JHU37160 exhibits higher blood-brain barrier penetrance and DREADD selectivity in vivo than Clozapine N-oxide.

Savage JV, et al. Behav Brain Res. 2023 Aug 24;452:114553.

Deschloroclozapine


Clozapine N-oxide and Deschloroclozapine activate the DREADD to suppress neuronal activity in rhesus monkeys.

Eldridge MA, et al. Curr Res Neurobiol. 2023 Mar 22;4:100085.

DREADD agonist 21


Clozapine N-oxide and DREADD agonist 21 repeated administration contributes to an unusual organization of the gut microbiota in adult mice.

Guo W, et al. Brain Res Bull. 2021 Aug;173:66-73.

Choose Selective AChR Inhibitors

Biological Activity

Description CNO (Clozapine N-oxide) is a metabolite of Clozapine (GLXC-06516) and an agonist of human muscarinic designer receptors (Designer Receptors Exclusively Activated by Designer Drugs, DREADDs). Clozapine is a potent dopamine (DA) antagonist and a selective muscarinic M4 receptor agonist.Solutions are unstable and should be fresh-prepared.
Targets
DREADD [1] Dopamine receptor [2] muscarinic M4 receptor [1]
In vitro
In vitro

CNO is a synthetic small molecule actuator for muscarinic acetylcholine DREADDs.

In Vivo
In vivo

Clozapine N-oxide (CNO), an agonist of human muscarinic designer receptor (DREADDs), is converted to clozapine and exerts clozapine-like behavioral effects in both mice and rats further emphasizes the need for appropriate control groups in studies employing DREADDs.[4]

Animal Research Animal Models standard laboratory rats and mice
Dosages 1.0, 3.2, 10.0 mg/kg for rats; 1.25, 2.5, 5.0, 10.0, 20.0 mg/kg for mice
Administration i.p.
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT00372242 Completed Mild and Moderate Malnourished Children International Centre for Diarrhoeal Disease Research Bangladesh December 2000 Not Applicable

Chemical lnformation & Solubility

Molecular Weight 342.82 Formula

C18H19ClN4O

CAS No. 34233-69-7 SDF --
Smiles C[N+]1([O-])CCN(CC1)C2=NC3=C(NC4=CC=CC=C24)C=CC(=C3)Cl
Storage (From the date of receipt) 3 years -20°C powder Solutions are unstable. Prepare fresh or purchase small, pre-packaged sizes. Repackage upon receipt.

In vitro
Batch:

DMSO : 68 mg/mL ( (198.35 mM); Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : 68 mg/mL

Ethanol : 8 mg/mL


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In vivo
Batch:

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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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Tech Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

Handling Instructions

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