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Literature summary for 3.4.21.26 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
Search for more literature for 3.4.21.26

Inhibitors

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

Organism

Organism UniProt Comment Textmining
Elizabethkingia meningoseptica
-
 commercial preparation
-