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Kifunensine

Cat. No. M27790
Kifunensine Structure
Synonym:

FR-900494

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1mg USD 185  USD185 In stock
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Quality Control & Documentation
Biological Activity

Kifunensine, a potent and selective inhibitor of class I α-mannosidases isolated from Actinomycete, prevents α-mannosidases I from trimming mannose residues on glycoproteins. Kifunensine inhibits ERAD.

Product Citations
Chemical Information
Molecular Weight 232.19
Formula C8H12N2O6
CAS Number 109944-15-2
Form Solid
Solubility (25°C) DMSO 10 mg/mL (ultrasonic)
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] Khadeja-Tul Kubra, et al. Curr Res Toxicol. Luminespib counteracts the Kifunensine-induced lung endothelial barrier dysfunction

[2] Kantharakorn Macharoen, et al. Int J Mol Sci. Effects of Kifunensine on Production and N-Glycosylation Modification of Butyrylcholinesterase in a Transgenic Rice Cell Culture Bioreactor

[3] Mohammad Shohel Akhter, et al. Microvasc Res. Kifunensine compromises lung endothelial barrier function

[4] A D Elbein, et al. J Biol Chem. Kifunensine, a potent inhibitor of the glycoprotein processing mannosidase I

[5] A D Elbein, et al. Arch Biochem Biophys. Kifunensine inhibits glycoprotein processing and the function of the modified LDL receptor in endothelial cells

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