Biochemistry, Pharmacology, Cytochrome P450, Glutathione and Drug metabolism are his primary areas of study. Biochemistry and Molecular biology are frequently intertwined in his study. The study incorporates disciplines such as Microsome and Antioxidant in addition to Pharmacology.
His study in Cytochrome P450 is interdisciplinary in nature, drawing from both Stereochemistry, Homology and Active site. His Glutathione research is multidisciplinary, incorporating elements of Protein adducts, In vitro, Toxicity and Chemical industry. The Drug metabolism study combines topics in areas such as Microsomal epoxide hydrolase, Epoxide hydrolase and Cytochrome P450, family 1, member A1.
His primary scientific interests are in Biochemistry, Glutathione, Cytochrome P450, Stereochemistry and Enzyme. His study in Pharmacology extends to Biochemistry with its themes. His work deals with themes such as Metabolite, In vitro, Lipid peroxidation and Toxicity, which intersect with Glutathione.
His Cytochrome P450 research includes themes of Molecular biology and Hydroxylation. He interconnects Homology modeling, Reactive intermediate, Regioselectivity and Active site in the investigation of issues within Stereochemistry. His work on Monooxygenase, NAD+ kinase, Cytosol and Biotransformation as part of general Enzyme research is often related to Mycobacterium tuberculosis, thus linking different fields of science.
His primary scientific interests are in Biochemistry, Cytochrome P450, Enzyme, Glutathione and Pharmacology. In his work, Regioselectivity is strongly intertwined with Mefenamic acid, which is a subfield of Biochemistry. Jan N. M. Commandeur has included themes like Biosynthesis, Hydroxylation, Heme, Molecular biology and Stereochemistry in his Cytochrome P450 study.
His Enzyme study integrates concerns from other disciplines, such as Drug resistance and Cytotoxicity. His Glutathione study combines topics from a wide range of disciplines, such as In vitro, Oxidative phosphorylation, Cytosol, High-performance liquid chromatography and Trichloroethylene. The Pharmacology study which covers Microsome that intersects with CYP3A4.
His primary areas of investigation include Cytochrome P450, Biochemistry, Enzyme, Glutathione and Pharmacology. His research integrates issues of Reactive intermediate, Stereochemistry and Hydroxylation in his study of Cytochrome P450. His work is connected to Drug metabolism and Metabolite, as a part of Biochemistry.
His research in Drug metabolism intersects with topics in Toxicity and Tissue culture. Jan N. M. Commandeur regularly links together related areas like Microsome in his Glutathione studies. As part of one scientific family, he deals mainly with the area of Pharmacology, narrowing it down to issues related to the Metabolism, and often Acetaminophen, Sulfotransferase, Sulfation and Glucuronosyltransferase.
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Biomarkers of free radical damage: Applications in experimental animals and in humans
L.L. de Zwart;J.H.N. Meerman;J.N.M. Commandeur;N.P.E. Vermeulen.
Free Radical Biology and Medicine (1999)
Enzyme-Catalyzed Activation of Anticancer Prodrugs
Martijn Rooseboom;Jan N. M. Commandeur;Nico P. E. Vermeulen.
Pharmacological Reviews (2004)
Enzymes and transport systems involved in the formation and disposition of glutathione S-conjugates. Role in bioactivation and detoxication mechanisms of xenobiotics.
J.N.M. Commandeur;G.J. Stijntjes;N.P.E. Vermeulen.
Pharmacological Reviews (1995)
Genetic polymorphisms of human N-acetyltransferase, cytochrome P450, glutathione-S-transferase, and epoxide hydrolase enzymes: relevance to xenobiotic metabolism and toxicity.
Lars W. Wormhoudt;Jan N. M. Commandeur;Nico P. E. Vermeulen.
Critical Reviews in Toxicology (1999)
A 3D in vitro model of differentiated HepG2 cell spheroids with improved liver-like properties for repeated dose high-throughput toxicity studies
Sreenivasa C. Ramaiahgari;Michiel W. den Braver;Bram Herpers;Valeska Terpstra.
Archives of Toxicology (2014)
Effects of curcumin on cytochrome P450 and glutathione S-transferase activities in rat liver.
S. Oetari;M. Sudibyo;Jan N.M. Commandeur;R. Samhoedi.
Biochemical Pharmacology (1996)
Inhibition of human recombinant cytochrome P450s by curcumin and curcumin decomposition products.
Regina Appiah-Opong;Jan N M Commandeur;Barbara van Vugt-Lussenburg;Nico P E Vermeulen.
Toxicology (2007)
Synthesis of novel Se-substituted selenocysteine derivatives as potential kidney selective prodrugs of biologically active selenol compounds: evaluation of kinetics of beta-elimination reactions in rat renal cytosol.
Ioanna Andreadou;Wiro M. P. B. Menge;Jan N. M. Commandeur;Eduard A. Worthington.
Journal of Medicinal Chemistry (1996)
Metabolism and kinetics of trichloroethylene in relation to toxicity and carcinogenicity : relevance of the mercapturic acid pathway
A.R. Goeptar;J.N.M. Commandeur;B. van Ommen;P.J. van Bladeren.
Chemical Research in Toxicology (1995)
Identification of critical residues in novel drug metabolizing mutants of cytochrome P450 BM3 using random mutagenesis.
Barbara M A van Vugt-Lussenburg;Eva Stjernschantz;Jeroen Lastdrager;Chris Oostenbrink.
Journal of Medicinal Chemistry (2007)
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