BIOMAT Database Logo BIOMAT Database Logo

Sensitized photooxidation of histidine and its derivatives. Products and mechanism of the reaction. 1969

M Tomita, and M Irie, and T Ukita

UI MeSH Term Description Entries
D007259 Infrared Rays That portion of the electromagnetic spectrum usually sensed as heat. Infrared wavelengths are longer than those of visible light, extending into the microwave frequencies. They are used therapeutically as heat, and also to warm food in restaurants. Heat Waves,Heat Wave,Infrared Ray,Ray, Infrared,Rays, Infrared,Wave, Heat,Waves, Heat
D008027 Light That portion of the electromagnetic spectrum in the visible, ultraviolet, and infrared range. Light, Visible,Photoradiation,Radiation, Visible,Visible Radiation,Photoradiations,Radiations, Visible,Visible Light,Visible Radiations
D008365 Manometry Measurement of the pressure or tension of liquids or gases with a manometer. Tonometry,Manometries
D008745 Methylation Addition of methyl groups. In histo-chemistry methylation is used to esterify carboxyl groups and remove sulfate groups by treating tissue sections with hot methanol in the presence of hydrochloric acid. (From Stedman, 25th ed) Methylations
D008751 Methylene Blue A compound consisting of dark green crystals or crystalline powder, having a bronze-like luster. Solutions in water or alcohol have a deep blue color. Methylene blue is used as a bacteriologic stain and as an indicator. It inhibits GUANYLATE CYCLASE, and has been used to treat cyanide poisoning and to lower levels of METHEMOGLOBIN. Methylthionine Chloride,Swiss Blue,Basic Blue 9,Chromosmon,Methylene Blue N,Methylthioninium Chloride,Urolene Blue,Blue 9, Basic,Blue N, Methylene,Blue, Methylene,Blue, Swiss,Blue, Urolene
D009682 Magnetic Resonance Spectroscopy Spectroscopic method of measuring the magnetic moment of elementary particles such as atomic nuclei, protons or electrons. It is employed in clinical applications such as NMR Tomography (MAGNETIC RESONANCE IMAGING). In Vivo NMR Spectroscopy,MR Spectroscopy,Magnetic Resonance,NMR Spectroscopy,NMR Spectroscopy, In Vivo,Nuclear Magnetic Resonance,Spectroscopy, Magnetic Resonance,Spectroscopy, NMR,Spectroscopy, Nuclear Magnetic Resonance,Magnetic Resonance Spectroscopies,Magnetic Resonance, Nuclear,NMR Spectroscopies,Resonance Spectroscopy, Magnetic,Resonance, Magnetic,Resonance, Nuclear Magnetic,Spectroscopies, NMR,Spectroscopy, MR
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
D010101 Oxygen Consumption The rate at which oxygen is used by a tissue; microliters of oxygen STPD used per milligram of tissue per hour; the rate at which oxygen enters the blood from alveolar gas, equal in the steady state to the consumption of oxygen by tissue metabolism throughout the body. (Stedman, 25th ed, p346) Consumption, Oxygen,Consumptions, Oxygen,Oxygen Consumptions
D010545 Peroxides A group of compounds that contain a bivalent O-O group, i.e., the oxygen atoms are univalent. They can either be inorganic or organic in nature. Such compounds release atomic (nascent) oxygen readily. Thus they are strong oxidizing agents and fire hazards when in contact with combustible materials, especially under high-temperature conditions. The chief industrial uses of peroxides are as oxidizing agents, bleaching agents, and initiators of polymerization. (From Hawley's Condensed Chemical Dictionary, 11th ed) Peroxide
D011830 Radiation Effects The effects of ionizing and nonionizing radiation upon living organisms, organs and tissues, and their constituents, and upon physiologic processes. It includes the effect of irradiation on food, drugs, and chemicals. Effects, Radiation,Effect, Radiation,Radiation Effect

Related Publications

M Tomita, and M Irie, and T Ukita
Flavin-sensitized photooxidation of histidine.
March 1975, Photochemistry and photobiology,
M Tomita, and M Irie, and T Ukita
Riboflavin-sensitized photooxidation of isohumulones and derivatives.
April 2004, Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology,
M Tomita, and M Irie, and T Ukita
THE DYE-SENSITIZED PHOTOOXIDATION OF PURINE AND PYRIMIDINE DERIVATIVES.
April 1964, Archives of biochemistry and biophysics,
M Tomita, and M Irie, and T Ukita
[Photooxidation of tyrosine sensitized by chlorophyll derivatives].
January 1967, Biofizika,
M Tomita, and M Irie, and T Ukita
[Enzymatic deiodination of thyroxin and its derivatives. II. Products formed and mechanism of the reaction].
January 1961, Bulletin de la Societe de chimie biologique,
M Tomita, and M Irie, and T Ukita
Kinetics and mechanism of the vitamin B2-sensitized photooxidation of isoproterenol.
May 2004, Photochemistry and photobiology,
M Tomita, and M Irie, and T Ukita
Kinetics of photooxidation of papaverine hydrochloride and its major photooxidation products.
June 2006, Journal of pharmaceutical and biomedical analysis,
M Tomita, and M Irie, and T Ukita
Formation of phytosterol photooxidation products: A chemical reaction mechanism for light-induced oxidation.
December 2020, Food chemistry,
M Tomita, and M Irie, and T Ukita
Mechanism of photooxidation of folic acid sensitized by unconjugated pterins.
December 2010, Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology,
M Tomita, and M Irie, and T Ukita
Essential histidine residues in coenzyme B12-dependent diol dehydrase: dye-sensitized photooxidation and ethoxycarbonylation.
February 1990, Archives of biochemistry and biophysics,
Copied contents to your clipboard!