Inhibition of alpha-chymotrypsin by D-tryptophan amide covalently bound to macromolecular carriers: specific, steric, and electrostatic effects. 1979

S Blumberg, and E Katchalski-Katzir

UI MeSH Term Description Entries
D007700 Kinetics The rate dynamics in chemical or physical systems.
D009994 Osmolar Concentration The concentration of osmotically active particles in solution expressed in terms of osmoles of solute per liter of solution. Osmolality is expressed in terms of osmoles of solute per kilogram of solvent. Ionic Strength,Osmolality,Osmolarity,Concentration, Osmolar,Concentrations, Osmolar,Ionic Strengths,Osmolalities,Osmolar Concentrations,Osmolarities,Strength, Ionic,Strengths, Ionic
D010455 Peptides Members of the class of compounds composed of AMINO ACIDS joined together by peptide bonds between adjacent amino acids into linear, branched or cyclical structures. OLIGOPEPTIDES are composed of approximately 2-12 amino acids. Polypeptides are composed of approximately 13 or more amino acids. PROTEINS are considered to be larger versions of peptides that can form into complex structures such as ENZYMES and RECEPTORS. Peptide,Polypeptide,Polypeptides
D002918 Chymotrypsin A serine endopeptidase secreted by the pancreas as its zymogen, CHYMOTRYPSINOGEN and carried in the pancreatic juice to the duodenum where it is activated by TRYPSIN. It selectively cleaves aromatic amino acids on the carboxyl side. Alpha-Chymotrypsin Choay,Alphacutanée,Avazyme
D013329 Structure-Activity Relationship The relationship between the chemical structure of a compound and its biological or pharmacological activity. Compounds are often classed together because they have structural characteristics in common including shape, size, stereochemical arrangement, and distribution of functional groups. Relationship, Structure-Activity,Relationships, Structure-Activity,Structure Activity Relationship,Structure-Activity Relationships
D014364 Tryptophan An essential amino acid that is necessary for normal growth in infants and for NITROGEN balance in adults. It is a precursor of INDOLE ALKALOIDS in plants. It is a precursor of SEROTONIN (hence its use as an antidepressant and sleep aid). It can be a precursor to NIACIN, albeit inefficiently, in mammals. Ardeydorm,Ardeytropin,L-Tryptophan,L-Tryptophan-ratiopharm,Levotryptophan,Lyphan,Naturruhe,Optimax,PMS-Tryptophan,Trofan,Tryptacin,Tryptan,Tryptophan Metabolism Alterations,ratio-Tryptophan,L Tryptophan,L Tryptophan ratiopharm,PMS Tryptophan,ratio Tryptophan

Related Publications

S Blumberg, and E Katchalski-Katzir
January 1971, Biokhimiia (Moscow, Russia),
S Blumberg, and E Katchalski-Katzir
January 1988, Acta biochimica et biophysica Hungarica,
S Blumberg, and E Katchalski-Katzir
February 1969, Biochemistry,
S Blumberg, and E Katchalski-Katzir
January 1970, Doklady Akademii nauk SSSR,
S Blumberg, and E Katchalski-Katzir
February 1991, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis,
S Blumberg, and E Katchalski-Katzir
December 1985, Chemical & pharmaceutical bulletin,
S Blumberg, and E Katchalski-Katzir
January 1970, Biokhimiia (Moscow, Russia),
S Blumberg, and E Katchalski-Katzir
August 1974, The Journal of pharmacy and pharmacology,
Copied contents to your clipboard!