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Oxotremorine M

Cat. No. M7976
Oxotremorine M Structure
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Biological Activity

Nonselective muscarinic acetylcholine receptor agonist.

Chemical Information
Molecular Weight 322.19
Formula C11H19IN2O
CAS Number 63939-65-1
Solubility (25°C) Water: 24 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] Ruud Zwart, et al. Oxotremorine-M potentiates NMDA receptors by muscarinic receptor dependent and independent mechanisms

[2] Ruud Zwart, et al. A novel muscarinic receptor-independent mechanism of KCNQ2/3 potassium channel blockade by Oxotremorine-M

[3] B Lockhart, et al. Differential inhibition of [3H]-oxotremorine-M and [3H]-quinuclinidyl benzilate binding to muscarinic receptors in rat brain membranes with acetylcholinesterase inhibitors

[4] A C Boschero, et al. Oxotremorine-m potentiation of glucose-induced insulin release from rat islets involves M3 muscarinic receptors

[5] R Reitstetter, et al. Oxotremorine-M activates single nicotinic acetylcholine receptor channels in cultured Xenopus myocytes

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