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Literature summary extracted from

  • Amor, E.C.; Villasenor, I.M.; Yasin, A.; Choudhary, M.I.
    Prolyl endopeptidase inhibitors from Syzygium samarangense (Blume) Merr. & L. M. Perry (2004), Z. Naturforsch. C, 59, 86-92.
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
3.4.21.26 2',4'-dihydroxy-6'-methoxy-3',5'-dimethylchalcone 50% inhibition at 0.15 mM Elizabethkingia meningoseptica
3.4.21.26 2',4'-dihydroxy-6'-methoxy-3',5'-dimethyldihydrochalcone 50% inhibition at 0.098 mM Elizabethkingia meningoseptica
3.4.21.26 2',4'-dihydroxy-6'-methoxy-3'-methylchalcone 50% inhibition at 0.0375 mM Elizabethkingia meningoseptica
3.4.21.26 2',4'-dihydroxy-6'-methoxy-3'-methyldihydrochalcone 50% inhibition at 0.0125 mM Elizabethkingia meningoseptica
3.4.21.26 2'-hydroxy-4',6'-dimethoxy-3'-methylchalcone 50% inhibition above 0.2 mM Elizabethkingia meningoseptica
3.4.21.26 2'-hydroxy-4',6'-dimethoxy-3'-methyldihydrochalcone 50% inhibition at 0.158 mM Elizabethkingia meningoseptica
3.4.21.26 7-hydroxy-5-methoxy-6,8-dimethylflavanone 14% inhibition at 0.5 mM Elizabethkingia meningoseptica
3.4.21.26 alpha-/beta-carotene mixture of alpha- and beta-form, 64.4% inhibition at 0.5 mM Elizabethkingia meningoseptica
3.4.21.26 bacitracin 50% inhibition at 0.130 mM Elizabethkingia meningoseptica
3.4.21.26 betulin 50% inhibition at 0.101 mM Elizabethkingia meningoseptica
3.4.21.26 epi-betulinic acid 50% inhibition at 0.015 mM Elizabethkingia meningoseptica
3.4.21.26 lupeol 50% inhibition at 0.065 mM Elizabethkingia meningoseptica
3.4.21.26 additional information comparison of inhibitory effects of methylchalcones on enzyme, trypsin and thrombin Elizabethkingia meningoseptica

Organism

EC Number Organism UniProt Comment Textmining
3.4.21.26 Elizabethkingia meningoseptica
-
 commercial preparation
-