Spectroscopic and electrochemical properties of chloro-N-methylprotoporphyrin IX dimethyl ester iron(II), a species related to the intermediate in the formation of N-alkylprotoporphyrins from the cytochrome P-450 prosthetic group
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Biochemistry
Reference30 articles.
1. N-Methylprotoporphyrin IX: chemical synthesis and identification as the green pigment produced by 3,5-diethoxycarbonyl-1,4-dihydrocollidine treatment.
2. Behavior of hepatic microsomal cytochromes after treatment of mice with drugs known to disturb porphyrin metabolism in liver
3. Effect of 1,4-dihydro-3,5-dicarbethoxycollidine on hepatic microsomal haem, cytochrome b5 and cytochrome P450 in rabbits and mice
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1. Crystal and molecular structure of unsymmetrical N-methyl-substituted μ-oxo diiron(III) tetraphenylporphyrin;Inorganica Chimica Acta;1990-05
2. Some aspects of organometallic chemistry in metalloporphyrin chemistry: synthesis, chemical reactivity, and electrochemical behavior of porphyrins with metal-carbon bonds;Chemical Reviews;1988-11
3. 2,2-Dialkyl-1,2-dihydroquinolines: cytochrome P 450 catalyzed N-alkylporphyrin formation, ferrochelatase inhibition, and induction of 5-aminolevulinic acid synthase activity;Chemical Research in Toxicology;1988-07
4. Studies of the chemical oxidation of iron(II) complexes of N-methylporphyrins to form the corresponding iron(III) complexes;Inorganic Chemistry;1985-07
5. Effect of N-substituents and axial ligands on reduction potentials of N-substituted metalloporphyrins;Inorganic Chemistry;1985-05
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