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U 73343

Cat. No. M7440
U 73343 Structure
Size Price Availability Quantity
5mg USD 190  USD190 In stock
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Quality Control & Documentation
Biological Activity

U 73343 is a analog of U 73122, it can be used as a negative control. U 73343 inhibits Panx1 currents in HEK cells. U 73343 also inhibits vasopressin- and GTPγS-induced Ca2+ influx in hepatocytes.

Chemical Information
Molecular Weight 466.66
Formula C29H42N2O3
CAS Number 142878-12-4
Form Solid
Solubility (25°C) DMSO 4.67 mg/mL (with gentle warming)
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] Boireau, et al. Neurosci Lett. Thalidomide reduces MPTP-induced decrease in striatal dopamine levels in mice.

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