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MG-262 

Cat. No. M28862
MG-262  Structure
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Biological Activity

MG-262 is a reversible proteasome inhibitor with diverse biological activities.

Chemical Information
Molecular Weight 491.43
Formula C25H42BN3O6
CAS Number 179324-22-2
Form Solid
Storage Powder -20°C
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] Hui Cao, et al. Front Pharmacol. Unbiased transcriptome mapping and modeling identify candidate genes and compounds of osteoarthritis

[2] Chen Qian, et al. Front Genet. A Novel Extracellular Matrix Gene-Based Prognostic Model to Predict Overall Survive in Patients With Glioblastoma

[3] Masaaki Kageyama, et al. PLoS One. Chemical proteasome inhibition as a novel animal model of inner retinal degeneration in rats

[4] Ivana Zavrski, et al. Biochem Biophys Res Commun. Proteasome inhibitors abrogate osteoclast differentiation and osteoclast function

[5] Alexei Terman, et al. Ann N Y Acad Sci. Proteasome inhibition enhances lipofuscin formation

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  Catalog
Abmole Inhibitor Catalog




Keywords: MG-262  supplier, Proteasome, inhibitors, activators


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