BIOMAT Database Logo BIOMAT Database Logo

Histidine-containing cyclic dipeptides as catalysis in the hydrolysis of carbonic acid p-nitrophenyl esters. 1977

Y Imanishi, and M Tanihara, and T Sugihara, and T Higashimura

UI MeSH Term Description Entries
D007093 Imidazoles Compounds containing 1,3-diazole, a five membered aromatic ring containing two nitrogen atoms separated by one of the carbons. Chemically reduced ones include IMIDAZOLINES and IMIDAZOLIDINES. Distinguish from 1,2-diazole (PYRAZOLES).
D009596 Nitrophenols PHENOLS carrying nitro group substituents. Nitrophenol
D010456 Peptides, Cyclic Peptides whose amino acid residues are linked together forming a circular chain. Some of them are ANTI-INFECTIVE AGENTS; some are biosynthesized non-ribosomally (PEPTIDE BIOSYNTHESIS, NON-RIBOSOMAL). Circular Peptide,Cyclic Peptide,Cyclic Peptides,Cyclopeptide,Orbitide,Circular Peptides,Cyclopeptides,Orbitides,Peptide, Circular,Peptide, Cyclic,Peptides, Circular
D002264 Carboxylic Acids Organic compounds containing the carboxy group (-COOH). This group of compounds includes amino acids and fatty acids. Carboxylic acids can be saturated, unsaturated, or aromatic. Carboxylic Acid,Acid, Carboxylic,Acids, Carboxylic
D002384 Catalysis The facilitation of a chemical reaction by material (catalyst) that is not consumed by the reaction. Catalyses
D004151 Dipeptides Peptides composed of two amino acid units. Dipeptide
D004952 Esters Compounds derived from organic or inorganic acids in which at least one hydroxyl group is replaced by an –O-alkyl or another organic group. They can be represented by the structure formula RCOOR’ and are usually formed by the reaction between an acid and an alcohol with elimination of water. Ester
D006639 Histidine An essential amino acid that is required for the production of HISTAMINE. Histidine, L-isomer,L-Histidine,Histidine, L isomer,L-isomer Histidine
D006868 Hydrolysis The process of cleaving a chemical compound by the addition of a molecule of water.

Related Publications

Y Imanishi, and M Tanihara, and T Sugihara, and T Higashimura
Thrombin-catalyzed hydrolysis of p-nitrophenyl esters.
January 1962, Archives of biochemistry and biophysics,
Y Imanishi, and M Tanihara, and T Sugihara, and T Higashimura
Catalysis by human leukocyte elastase: III. Steady-state kinetics for the hydrolysis of p-nitrophenyl esters.
February 1985, Archives of biochemistry and biophysics,
Y Imanishi, and M Tanihara, and T Sugihara, and T Higashimura
[THE REACTIVITY OF CYCLIC DIPEPTIDES OF HISTIDINE IN RELATION TO ENZYME CATALYSIS].
January 1964, Hoppe-Seyler's Zeitschrift fur physiologische Chemie,
Y Imanishi, and M Tanihara, and T Sugihara, and T Higashimura
Specificity of -chymotrypsin. The -chymotrypsin-catalyzed hydrolysis of N-acylamino acid p-nitrophenyl esters.
July 1973, Biochemistry,
Y Imanishi, and M Tanihara, and T Sugihara, and T Higashimura
Effect of cyclic dipeptides containing histidine on pentobarbital narcosis.
May 1981, Journal of pharmacobio-dynamics,
Y Imanishi, and M Tanihara, and T Sugihara, and T Higashimura
Structure-activity relationship in the chymotrypsin hydrolysis of p-nitrophenyl esters.
January 1972, The Journal of organic chemistry,
Y Imanishi, and M Tanihara, and T Sugihara, and T Higashimura
The catalysis of the non-chymotryptic hydrolysis of p-nitrophenyl acetate.
August 1957, The Journal of biological chemistry,
Y Imanishi, and M Tanihara, and T Sugihara, and T Higashimura
Antioxidative activities of histidine containing caffeic acid-dipeptides.
July 2010, Bioorganic & medicinal chemistry letters,
Y Imanishi, and M Tanihara, and T Sugihara, and T Higashimura
The influence of temperature on the alpha-chymotrypsin-catalyzed hydrolysis of N-acylamino acid p-nitrophenyl esters.
January 1974, Biochimie,
Y Imanishi, and M Tanihara, and T Sugihara, and T Higashimura
On the mechanism of hydrolysis of N-acylamino acid nitrophenyl esters.
June 1966, Biochemical and biophysical research communications,
Copied contents to your clipboard!