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4-Nitroimidazole

Cat. No. M9777
4-Nitroimidazole Structure
Synonym:

4-nitro-1H-imidazole

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5g USD 25  USD25 In stock
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Quality Control & Documentation
Biological Activity

4-Nitroimidazole is an intermediate during the synthesis of 1-methyl-2,4,5-trinitro imidazole. 4-Nitroimidazole was used in a study to investigate the catalytic efficiency of heterocyclic compounds in the peroxyoxalate chemiluminescence reaction using bis(2,4,6-trichlorophenyl)oxalate as reagent.

Chemical Information
Molecular Weight 113.07
Formula C3H3N3O2
CAS Number 3034-38-6
Storage 18-25°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] James E Erman, et al. Biochim Biophys Acta. Binding of imidazole, 1-methylimidazole and 4-nitroimidazole to yeast cytochrome c peroxidase (CcP) and the distal histidine mutant, CcP(H52L)

[2] Claire Ceballos, et al. Bioconjug Chem. Cationic nucleoside lipids derived from universal bases: A rational approach for siRNA transfection

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Keywords: 4-Nitroimidazole, 4-nitro-1H-imidazole supplier, inhibitors, activators


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