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Literature summary for 3.5.3.1 extracted from

  • Busnel, O.; Carreaux, F.; Carboni, B.; Pethe, S.; Goff, S.V.; Mansuy, D.; Boucher, J.L.
    Synthesis and evaluation of new omega-borono-alpha-amino acids as rat liver arginase inhibitors (2005), Bioorg. Med. Chem., 13, 2373-2379.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
S-(2-boronoethyl)-L-cysteine i.e. BEC, 50% inhibition at 0.005 mM, pH 7.4, or at 0.020 mM, pH 9.0 Rattus norvegicus
S-(2-boronomethyl)-L-cysteine i.e. BMC, 50% inhibition at 3.8 mM, pH 7.4, or at 7.5 mM, pH 9.0 Rattus norvegicus
S-(2-boronomethyl)-L-homocysteine i.e. BMHC, 50% inhibition at 0.35 mM, pH 7.4, or above 1 mM, pH 9.0 Rattus norvegicus

Organism

Organism UniProt Comment Textmining
Rattus norvegicus P07824
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-

Source Tissue

Source Tissue Comment Organism Textmining