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Unbound Medicine.
(Apo Acetaminophen)
5 results
  • Imidazole-rich copper peptides as catalysts in xenobiotic degradation. [Journal Article]
    PLoS One. 2020; 15(11):e0238147.Begum SZ, Nizam NSM, … Abdul Rahman MB
  • Laccases, oxidative copper-enzymes found in fungi and bacteria were used as the basis in the design of nona- and tetrapeptides. Laccases are known to be excellent catalysts for the degradation of phenolic xenobiotic waste. However, since solvent extraction of laccases is environmentally-unfriendly and yields obtained are low, they are less preferred compared to synthetic catalysts. The histidine …
  • The aromatic peroxygenase from Marasmius rutola--a new enzyme for biosensor applications. [Journal Article]
    Anal Bioanal Chem. 2012 Jan; 402(1):405-12.Yarman A, Gröbe G, … Scheller FW
  • The aromatic peroxygenase (APO; EC 1.11.2.1) from the agraric basidomycete Marasmius rotula (MroAPO) immobilized at the chitosan-capped gold-nanoparticle-modified glassy carbon electrode displayed a pair of redox peaks with a midpoint potential of -278.5 mV vs. AgCl/AgCl (1 M KCl) for the Fe(2+)/Fe(3+) redox couple of the heme-thiolate-containing protein. MroAPO oxidizes aromatic substrates such …
  • Role of copper,zinc-superoxide dismutase in catalyzing nitrotyrosine formation in murine liver. [Journal Article]
    Free Radic Biol Med. 2008 Sep 01; 45(5):611-8.Zhu JH, Zhang X, … Lei XG
  • The only known function of Cu,Zn-superoxide dismutase (SOD1) is to catalyze the dismutation of superoxide anion into hydrogen peroxide. Our objective was to determine if SOD1 catalyzes murine liver protein nitration induced by acetaminophen (APAP) and lipopolysaccharide (LPS). Liver and plasma samples were collected from young adult SOD1 knockout mice (SOD1-/-) and wild-type (WT) mice at 5 or 6 h…
  • Paracetamol hepatotoxicity in metallothionein-null mice. [Journal Article]
    Toxicology. 1998 Feb 06; 125(2-3):131-40.Rofe AM, Barry EF, … Coyle P
  • The role of metallothionein (MT) in protecting the liver against paracetamol (PCT) toxicity was investigated in vivo and in vitro in mice lacking expression of MT-1 and MT-2 genes (MT -/-). In the fed, glycogen replete state, hepatotoxicity (PCT 300 mg/kg i.p.) at 6 h was significantly greater in MT -/- than MT +/+ mice. Plasma lactate dehydrogenase (LD) and alanine aminotransferase (ALT) were 5-…
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