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PF-05105679 

Cat. No. M28327
PF-05105679  Structure
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Biological Activity

PF-05105679 is an orally active and selective TRPM8 antagonist with an IC50 of 103 nM. PF-05105679 has the potential for cold-related pain.

Chemical Information
Molecular Weight 428.45
Formula C26H21FN2O3
CAS Number 1398583-31-7
Form Solid
Solubility (25°C) DMSO 125 mg/mL (ultrasonic)
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] James R Gosset, et al. Eur J Pharm Sci. A cross-species translational pharmacokinetic-pharmacodynamic evaluation of core body temperature reduction by the TRPM8 blocker PF-05105679

[2] Mark D Andrews, et al. ACS Med Chem Lett. Discovery of a Selective TRPM8 Antagonist with Clinical Efficacy in Cold-Related Pain

[3] Wendy J Winchester, et al. J Pharmacol Exp Ther. Inhibition of TRPM8 channels reduces pain in the cold pressor test in humans

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Keywords: PF-05105679  supplier, TRP Channel, inhibitors, activators


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