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Xanomeline

Cat. No. M10906
Xanomeline  Structure
Synonym:

LY-246708

Size Price Availability Quantity
5mg USD 55  USD55 In stock
10mg USD 95  USD95 In stock
25mg USD 185  USD185 In stock
50mg USD 300  USD300 In stock
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Quality Control & Documentation
Biological Activity

Xanomeline increases neuronal excitability as a potent selective muscarinic 1 and type 4 (M1/M4) receptor agonist. Xanomeline can be used in the study of neurological disorders such as schizophrenia.

Chemical Information
Molecular Weight 281.42
Formula C14H23N3OS
CAS Number 131986-45-3
Solubility (25°C) DMSO ≥ 20 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Stephen K Brannan, et al. N Engl J Med. Muscarinic Cholinergic Receptor Agonist and Peripheral Antagonist for Schizophrenia

[2] Rujuan Xin, et al. Front Physiol. Xanomeline Protects Cortical Cells From Oxygen-Glucose Deprivation via Inhibiting Oxidative Stress and Apoptosis

[3] Aaron M Bender, et al. ACS Chem Neurosci. Classics in Chemical Neuroscience: Xanomeline

[4] Naheed R Mirza, et al. CNS Drug Rev. Xanomeline and the antipsychotic potential of muscarinic receptor subtype selective agonists

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