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Synthesis of dinitrophenyltetrapeptides as chromophoric substrates of endoproteinases

Authors :
Kulikov, S.
Sokolova, N.
Rodin, S.
Samartsev, M.
Source :
Chemistry of Natural Compounds; July 1983, Vol. 19 Issue: 4 p469-475, 7p
Publication Year :
1983

Abstract

The synthesis has been performed of ten tetrapeptides of the general formula Dnp-Gly-Gly-X-Arg-OH, where X = Val, Phe, Abu, Asp (OBut), Asp, Met, D-Phe, Ser, Thr, or Trp. The synthesis was carried out with Dnp-Gly-Gly-ONp, activated esters of protected amino acids, and arginine with an unprotected carboxy group. The coefficients of molar extinction of the tetrapeptides at 660 nm are given. It has been shown that the peptides can be used to determine the activities of neutral and alkaline proteinases from various sources, the peptides with X = Phe, Met, and Abu exhibiting the highest sensitivity to enzymatic hydrolysis.

Details

Language :
English
ISSN :
00093130 and 15738388
Volume :
19
Issue :
4
Database :
Supplemental Index
Journal :
Chemistry of Natural Compounds
Publication Type :
Periodical
Accession number :
ejs15982324
Full Text :
https://doi.org/10.1007/BF00575711