Enzymatic, Polymer-Supported Formation of an Analog of the Trypsin Inhibitor A90720A: A Screening Strategy for Macrocyclic Peptidase Inhibitors
- 1 December 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 119 (51) , 12697-12698
- https://doi.org/10.1021/ja971216c
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- The preparation and properties of two new chromogenic substrates of trypsinPublished by Elsevier ,2004
- Combinatorial chemistry searching for a winning combinationCurrent Opinion in Chemical Biology, 1997
- Ortho-Substituted Benzofused Macrocyclic Lactams as Zinc Metalloprotease InhibitorsJournal of Medicinal Chemistry, 1997
- A90720A, a serine protease inhibitor isolated from a terrestrial blue-green alga Microchaete loktakensisTetrahedron, 1996
- Reagents for Combinatorial Organic Synthesis: Development of a New o-Nitrobenzyl Photolabile Linker for Solid Phase SynthesisThe Journal of Organic Chemistry, 1995
- Portion-mixing peptide libraries of quenched fluorogenic substrates for complete subsite mapping of endoprotease specificity.Proceedings of the National Academy of Sciences, 1994
- Basic Principles of Protease‐Catalyzed Peptide Bond FormationAngewandte Chemie International Edition in English, 1985