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Literature summary for 2.4.1.1 extracted from

  • Wen, X.; Zhang, P.; Liu, J.; Zhang, L.; Wu, X.; Ni, P.; Sun, H.
    Pentacyclic triterpenes. Part 2: Synthesis and biological evaluation of maslinic acid derivatives as glycogen phosphorylase inhibitors (2006), Bioorg. Med. Chem. Lett., 16, 722-726.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
2-ethoxy-2-oxoethyl (2beta,3alpha,5xi,8alpha,9xi,10alpha,14beta,17alpha,18alpha)-2,3-dihydroxyolean-12-en-28-oate 50% inhibition at 0.019 mM Oryctolagus cuniculus
2-O-acetyl-3-oxomaslinic acid benzyl ester 50% inhibition at 0.029 mM Oryctolagus cuniculus
benzyl (2beta,5xi,8alpha,9xi,10alpha,14beta,17alpha,18alpha)-2-hydroxy-3-oxoolean-12-en-28-oate 50% inhibition at 0.029 mM Oryctolagus cuniculus
benzyl (5xi,8alpha,9xi,10alpha,14beta,17alpha,18alpha)-2-hydroxy-3-oxooleana-1,12-dien-28-oate 50% inhibition at 0.030 mM Oryctolagus cuniculus
maslinic acid 50% inhibition at 0.028 mM Oryctolagus cuniculus
maslinic acid 5-bromopentyl ester 50% inhibition at 0.007 mM Oryctolagus cuniculus
maslinic acid-(2-piperidin-1-yl)ethyl ester 50% inhibition at 0.031 mM Oryctolagus cuniculus
additional information preference for hydrophobic group at C-28 of maslinic acid for enzyme inhibition Oryctolagus cuniculus

Organism

Organism UniProt Comment Textmining
Oryctolagus cuniculus
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-
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Source Tissue

Source Tissue Comment Organism Textmining
muscle
-
Oryctolagus cuniculus
-