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Literature summary for 5.3.99.2 extracted from

  • Li, W.; Mase, M.; Inui, T.; Shimoda, M.; Isomura, K.; Oda, H.; Yamada, K.; Urade, Y.
    Pharmacokinetics of recombinant human lipocalin-type prostaglandin D synthase/beta-trace in canine (2008), Neurosci. Res., 61, 289-293.
    View publication on PubMed

Application

Application Comment Organism
medicine study on the pharmacokinetics of recombinant human lipocalin-type prostaglandin-D synthase in canines. After an intravenous bolus injection, the serum concentration decreases biexponentially with a half-life of the terminal line phase of 0.77 h. L-PGDS is distributed mainly in the blood. Only 10.3% of the administered enzyme is excreted to the urine, suggesting that L-PGDS is actively degraded within the body Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
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lipocalin-type prostaglandin D synthase. Isoform is identical to beta-trace, a major protein in human cerebrospinal fluid, and acts as both a PGD2-producing enzyme and as an extracellular transporter for lipophilic ligands
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Source Tissue

Source Tissue Comment Organism Textmining