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Desipramine hydrochloride

Cat. No. M6664
Desipramine hydrochloride Structure
Size Price Availability Quantity
100mg USD 60  USD60 In stock
500mg USD 96  USD96 In stock
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Quality Control & Documentation
Biological Activity

Desipramine hydrochloride is an inhibitor of norepinephrine transporter (NET), 5-HT transporter (SERT) and dopamine transporter (DAT) with Kis of 4, 61 and 78,720 nM, respectively.

Chemical Information
Molecular Weight 302.84
Formula C18H22N2.HCl
CAS Number 58-28-6
Solubility (25°C) DMSO ≥ 90 mg/mL
Storage 2-8°C, dry, sealed
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] Coe, et al. J Med Chem. Varenicline: an α4β2 nicotinic receptor partial agonist for smoking cessation.

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