BIOMAT Database Logo BIOMAT Database Logo

A cytochrome P-450-piperonyl butoxide spectrum similar to that produced by ethyl isocyanide. 1971

R M Philpot, and E Hodgson

UI MeSH Term Description Entries
D007306 Insecticides Pesticides designed to control insects that are harmful to man. The insects may be directly harmful, as those acting as disease vectors, or indirectly harmful, as destroyers of crops, food products, or textile fabrics. Insecticide
D007700 Kinetics The rate dynamics in chemical or physical systems.
D008297 Male Males
D008862 Microsomes, Liver Closed vesicles of fragmented endoplasmic reticulum created when liver cells or tissue are disrupted by homogenization. They may be smooth or rough. Liver Microsomes,Liver Microsome,Microsome, Liver
D009249 NADP Nicotinamide adenine dinucleotide phosphate. A coenzyme composed of ribosylnicotinamide 5'-phosphate (NMN) coupled by pyrophosphate linkage to the 5'-phosphate adenosine 2',5'-bisphosphate. It serves as an electron carrier in a number of reactions, being alternately oxidized (NADP+) and reduced (NADPH). (Dorland, 27th ed) Coenzyme II,Nicotinamide-Adenine Dinucleotide Phosphate,Triphosphopyridine Nucleotide,NADPH,Dinucleotide Phosphate, Nicotinamide-Adenine,Nicotinamide Adenine Dinucleotide Phosphate,Nucleotide, Triphosphopyridine,Phosphate, Nicotinamide-Adenine Dinucleotide
D010084 Oxidation-Reduction A chemical reaction in which an electron is transferred from one molecule to another. The electron-donating molecule is the reducing agent or reductant; the electron-accepting molecule is the oxidizing agent or oxidant. Reducing and oxidizing agents function as conjugate reductant-oxidant pairs or redox pairs (Lehninger, Principles of Biochemistry, 1982, p471). Redox,Oxidation Reduction
D010860 Pigments, Biological Any normal or abnormal coloring matter in PLANTS; ANIMALS or micro-organisms. Biological Pigments
D003486 Cyanides Inorganic salts of HYDROGEN CYANIDE containing the -CN radical. The concept also includes isocyanides. It is distinguished from NITRILES, which denotes organic compounds containing the -CN radical. Cyanide,Isocyanide,Isocyanides
D003580 Cytochromes Hemeproteins whose characteristic mode of action involves transfer of reducing equivalents which are associated with a reversible change in oxidation state of the prosthetic group. Formally, this redox change involves a single-electron, reversible equilibrium between the Fe(II) and Fe(III) states of the central iron atom (From Enzyme Nomenclature, 1992, p539). The various cytochrome subclasses are organized by the type of HEME and by the wavelength range of their reduced alpha-absorption bands. Cytochrome
D004149 Dioxoles

Related Publications

R M Philpot, and E Hodgson
Ethyl isocyanide complexes of bacterial cytochrome P-450.
July 1971, Archives of biochemistry and biophysics,
R M Philpot, and E Hodgson
Piperonyl butoxide metabolism by cytochrome P-450: factors affecting the formation and disappearance of the metabolite-cytochrome P-450 complex.
November 1972, Xenobiotica; the fate of foreign compounds in biological systems,
R M Philpot, and E Hodgson
Spectral interactions of piperonyl butoxide and isocyanides with purified hepatic cytochrome P-450 from uninduced mice.
January 1985, General pharmacology,
R M Philpot, and E Hodgson
The effect of piperonyl butoxide on hepatic cytochrome P-450-dependent monooxygenase activities in rainbow trout (Salmo gairdneri).
June 1988, Toxicology and applied pharmacology,
R M Philpot, and E Hodgson
The affinity of cytochrome P-450 for ethyl isocyanide: an explanation of double soret spectra.
February 1978, Chemico-biological interactions,
R M Philpot, and E Hodgson
Formation rates of the two ethyl isocyanide compounds of liver cytochrome P-450 at low temperatures.
October 1971, The Journal of biological chemistry,
R M Philpot, and E Hodgson
Hepatic glutathione and hepatotoxicity: effects of cytochrome P-450 complexing compounds SKF 525-A, L-alpha acetylmethadol (LAAM), norLAAM, and piperonyl butoxide.
May 1982, Biochemical pharmacology,
R M Philpot, and E Hodgson
Studies of microsomal cytochrome P-450 with isocyanide spin label.
March 1972, Biochimica et biophysica acta,
R M Philpot, and E Hodgson
Metabolism of dihydroergotamine by a cytochrome P-450 similar to that involved in the metabolism of macrolide antibiotics.
November 1989, Xenobiotica; the fate of foreign compounds in biological systems,
R M Philpot, and E Hodgson
Effect of ionic strength on the ethyl isocyanide difference spectrum of reduced P-450 in liver microsomes.
February 1968, Journal of biochemistry,
Copied contents to your clipboard!