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GF 109203X hydrochloride

Cat. No. M7644
GF 109203X hydrochloride Structure
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Biological Activity

Inhibitor of protein kinase C; potent inhibitor of GSK-3.

Chemical Information
Molecular Weight 448.94
Formula C25H24N4O2 · HCl
CAS Number 176504-36-2
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] Bruna Amanda Girardi, et al. Spermidine-induced improvement of reconsolidation of memory involves calcium-dependent protein kinase in rats

[2] Gustavo P Guerra, et al. Spermidine-induced improvement of memory involves a cross-talk between protein kinases C and A

[3] Sofia Cristvo-Ferreira, et al. Adenosine A2A receptors enhance GABA transport into nerve terminals by restraining PKC inhibition of GAT-1

[4] Massimiliano Cristofanilli, et al. Calcium channel and glutamate receptor activities regulate actin organization in salamander retinal neurons

[5] Y Lin, et al. Effect of raloxifene and its interaction with human PTH on bone formation

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