80284-15-7Relevant articles and documents
Self-assembly of the oxy-tyrosinase core and the fundamental components of phenolic hydroxylation
Citek, Cooper,Lyons, Christopher T.,Wasinger, Erik C.,Stack, T. Daniel P.
experimental part, p. 317 - 322 (2012/06/30)
The enzyme tyrosinase contains two CuI centres, trigonally coordinated by imidazole nitrogens of six conserved histidine residues. The enzyme activates O2 to form a μ-η2: η2-peroxo-dicopper(II) core, which hydroxylates tyrosine to a catechol in the first committed step of melanin biosynthesis. Here, we report a family of synthetic peroxo complexes, with spectroscopic and chemical features consistent with those of oxygenated tyrosinase, formed through the self-assembly of monodentate imidazole ligands, CuI and O2 at-125 °C. An extensively studied complex reproduces the enzymatic electrophilic oxidation of exogenous phenolic substrates to catechols in good stoichiometric yields. The self-assembly and subsequent reactivity support the intrinsic stability of the Cu2O2 core with imidazole ligation, in the absence of a polypeptide framework, and the innate capacity to effect hydroxylation of phenolic substrates. These observations suggest that a foundational role of the protein matrix is to facilitate expression of properties native to the core by bearing the entropic costs of assembly and precluding undesired oxidative degradation pathways.
The ortho-Acetoxylation of Phenols by Copper(II) Acetate
Takizawa, Yasuomi,Tateishi, Akira,Sugiyama, Junichi,Yoshida, Hiroyuki,Yoshihara, Nobutoshi
, p. 104 - 105 (2007/10/02)
Oxidation of p-methoxyphenols and 6-chromanols by copper(II) acetate in acetic acid gave the corresponding o-acetoxyphenols and 5-acetoxy-6-chromanols, which were easily hydrolysed in MeOH-H2O containing HCl to give catechol-type phenols.
Evaluation of the cytotoxic potential of catechols and quinones structurally related to butylated hydroxyanisole
Lam,Garg,Swanson,Pezzuto
, p. 393 - 395 (2007/10/02)
The cytotoxicity of 2- and 3-butylated hydroxyanisole (BHA) and 18 related aromatic compounds has been determined employing cultured P388 and KB cells. The phenolic compounds, 3-BHA and 2-BHA, had moderately low cytotoxic activity. Their corresponding catechols had ED50 values that were much lower than those of the parent compounds. This substantial increase in the cytotoxic activity is attributed to the presence of the catechol group, which is known to undergo one-electron oxidation readily to give the corresponding semiquinone radical. Other related catechols had similar cytotoxic activity. In general, derivatization of the catechol functionality resulted in a decrease of the cytotoxic potential of the compounds. Monoacetylation or monomethylation of the catechols gave products that were less potent cytotoxic agents than the parent compounds. Further loss of activity was observed when both hydroxy groups of the catechol function were blocked. Substitution of a methoxy group in place of a hydrogen atom in these compounds resulted in a significant increase of cytotoxicity, whereas the replacement of a methoxy group with a methyl group reduced the cytotoxicity. The catechols and quinones derived from 2-BHA were more active when compared with those derived from 3-BHA. The t-butyl group adjacent to the catechol or quinone moiety in the 3-BHA derivatives appeared to exert a significant steric effect toward the cytotoxic potential of these compounds. These results suggest the potential use of o-quinones and catechols as cytotoxic and antitumor agents.
