G256
G256 is a cytochrome P450 substrate with antiarrhythmic properties. In recombinant monooxygenase systems, G256 undergoes N-hydroxylation of the terminal aminoguanidine nitrogen, as well as ring hydroxylation catalyzed by cytochrome P4502C3. G256 generates N-hydroxyaminoguanidine metabolites via N-hydroxylation in liver microsomal fractions. G256 produces phenol metabolites through ring hydroxylation in both liver microsomal fractions and recombinant cytochrome P450 systems. G256 can be used for research on arrhythmias.
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- CAS No.: 134867-97-3
- Formule: C14H14ClN5
- Masse moléculaire:287.75
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Stockage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Activité biologique
G256 (compound 1) undergoes P450-dependent N-hydroxylation catalyzed by rabbit liver microsomes to form NOH-G256, with a Km value of 62.9 μM[1].
G256 undergoes N-hydroxylation catalyzed by rat liver microsomes to form NOH-G256[1].
G256 undergoes N-hydroxylation to form NOH-G256 under the catalysis of recombinant systems rich in rabbit liver P450 or purified recombinant P4502C3 systems[1].
G256 undergoes aromatic hydroxylation catalyzed by rabbit and rat liver microsomes as well as the recombinant rabbit liver P450 monooxygenase system to form phenolic metabolites[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 134867-97-3
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Masse moléculaire 287.75
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Formule C14H14ClN5
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SMILES
N=C(N)N/N=C(C1=CC=CC=C1)\C2=C(N)C=CC(Cl)=C2
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureté et documentation
Références
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)