METHOD OF PRODUCING NEW CHROMOGEN ENZYME SUBSTRATE

Method for the quantitative determination of serine proteases which includes contacting the substance for which the determination is desired with a diagnostically active chromogenic substrate with good stability and high specificity to serine proteases having the formula: H-D-A1-A2-A3-NH-R or salts...

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Bibliographische Detailangaben
Hauptverfasser:	AURELL,LEIF E.,SE, CLAESON,KARL G.,SE, GUSTAVSSON,STIG I.,SE, CLAUSSON,GUN A.,SE, AF EKENSTAM,BO THURESSONAF,SE, KARLSSON,BIRGITTA G.,SE
Format:	Patent
Sprache:	eng
Schlagworte:	BEER BIOCHEMISTRY CHEMISTRY COMPOSITIONS OR TEST PAPERS THEREFOR CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES ENZYMOLOGY HUMAN NECESSITIES HYGIENE MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS MEDICAL OR VETERINARY SCIENCE METALLURGY MICROBIOLOGY MUTATION OR GENETIC ENGINEERING ORGANIC CHEMISTRY PEPTIDES PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES PROCESSES OF PREPARING SUCH COMPOSITIONS SPIRITS VINEGAR WINE
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Beschreibung
Zusammenfassung:	Method for the quantitative determination of serine proteases which includes contacting the substance for which the determination is desired with a diagnostically active chromogenic substrate with good stability and high specificity to serine proteases having the formula: H-D-A1-A2-A3-NH-R or salts thereof, wherein A1 is Gly, Ala, Val, Leu, Ile, Pip, Pro, or Aze; A2 is Gly, Ala, Val, Leu, Ile, Pip, Pro, Aze, or Phe; A3 is Arg, Lys, or Orn, and R is a chromophoric group.