lysine-tyrosylquinone and butylphen

lysine-tyrosylquinone has been researched along with butylphen* in 1 studies

Other Studies

1 other study(ies) available for lysine-tyrosylquinone and butylphen

Article	Year
Copper-promoted overall transformation of 4-tert-butylphenol to its para-hydroxyquinonic derivative, 2-hydroxy-5-tert-butyl-1,4-benzoquinone. Biomimetic studies on the generation of topaquinone in copper amine oxidases. Bioorganic & medicinal chemistry letters, 2000, May-01, Volume: 10, Issue:9 Topaquinone (TPQ) is a cofactor present at the active site of copper amine oxidases, derived from a Tyr residue inserted in the polypeptide chain through a copper-dependent but otherwise largely unknown mechanism. A simple model system was developed that permits to obtain the overall transformation of 4-tert-butylphenol, chosen as a model for Tyr, into a TPQ-like, para-hydroxyquinonic structure in the presence of Cu(II)-imidazole mononuclear complexes. Topics: Amine Oxidase (Copper-Containing); Benzoquinones; Copper; Dihydroxyphenylalanine; Hydrogen-Ion Concentration; Hydroxylation; Lysine; Oxidation-Reduction; Phenols; Quinones	2000

Article

Year

Copper-promoted overall transformation of 4-tert-butylphenol to its para-hydroxyquinonic derivative, 2-hydroxy-5-tert-butyl-1,4-benzoquinone. Biomimetic studies on the generation of topaquinone in copper amine oxidases.

Bioorganic & medicinal chemistry letters, 2000, May-01, Volume: 10, Issue:9

Topaquinone (TPQ) is a cofactor present at the active site of copper amine oxidases, derived from a Tyr residue inserted in the polypeptide chain through a copper-dependent but otherwise largely unknown mechanism. A simple model system was developed that permits to obtain the overall transformation of 4-tert-butylphenol, chosen as a model for Tyr, into a TPQ-like, para-hydroxyquinonic structure in the presence of Cu(II)-imidazole mononuclear complexes.

Topics: Amine Oxidase (Copper-Containing); Benzoquinones; Copper; Dihydroxyphenylalanine; Hydrogen-Ion Concentration; Hydroxylation; Lysine; Oxidation-Reduction; Phenols; Quinones

2000