Archiv der Pharmazie · 2003 · 15 citations · 20 references
PharmacyBiochemistryMedicinal ChemistryDrug DesignDrug DiscoveryEnzymologyEnzyme InhibitionHit-to-lead OptimizationLead Compound DesignLead DiscoveryNatural Product Drug DiscoveryProtein ChemistryLead Compound IdentificationLead Discovery From Natural ProductsMarine Secondary MetabolitesSeaweed Secondary MetabolitesSecondary MetabolitesStructure-based Lead DiscoveryStructure-guided Lead DiscoverySuitable Target
This paper deals with the design, syntheses, and inhibition tests of new low molecular weight thrombin inhibitors utilizing cyanopeptides, the secondary metabolites of cyanobacteria with interesting biological activities, as new lead structures. Starting with aeruginosin 98-B (1) as a lead structure, we have developed and synthesised new, selective acting inhibitors of serine proteases (RA-1005 and RA-1009, which are suitable targets for further structure-activity studies.
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The determination of enzyme inhibitor constants
Martin Dixon · Biochemical Journal · 1953 · 4.1K citations · Full text
Aeruginosins, protease inhibitors from the cyanobacterium Microcystis aeruginosa
Keishi Ishida, Yuji Okita, Hisashi Matsuda et al. · Tetrahedron · 1999 · 160 citations