نتایج جستجو برای: quinone

تعداد نتایج: 5334  

Journal: :journal of sciences islamic republic of iran 0

during the development of a new regiospecific synthetic methodology for 1,5 dihydroxy- 9,lo-anthraquinone, it was observed that (anthrufin) preparative tlc of 1,2,3,4,5,6,7,8-octahydro-9,lo-dihyd roxy- 1,5-anthracenedione on silica gel produced a well-defined 1:l complex of the dione and an aerial oxidation product of it, the quinone dimethide 1,2,3,4,5,6,7- hexahydro-9,lo-dihydroxy-1 ,5-anthra...

During the development of a new regiospecific synthetic methodology for 1,5 dihydroxy- 9,lO-anthraquinone, it was observed that (anthrufin) preparative TLC of 1,2,3,4,5,6,7,8-octahydro-9,lO-dihyd roxy- 1,5-anthracenedione on silica gel produced a well-defined 1:l complex of the dione and an aerial oxidation product of it, the quinone dimethide 1,2,3,4,5,6,7- hexahydro-9,lO-dihydroxy-1 ,5-...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2004
Kan He Rasmy E Talaat Thomas F Woolf

Troglitazone (TGZ) was the first glitazone used for the treatment of type II diabetes mellitus. TGZ undergoes an oxidative chroman ring-opening reaction to form a quinone product. Recently, cytochrome P450 (P450) was shown to be able to catalyze the formation of TGZ quinone. TGZ quinone was the major metabolite formed by dexamethasone-induced rat liver microsomes or myeloperoxidase (MPO) incuba...

Journal: :Biochimica et biophysica acta 1993
K Kano T Mori B Uno M Goto T Ikeda

Electrochemical characterization of topa quinone (6-hydroxydopa quinone), the organic cofactor of copper-containing amine oxidases, has been performed with the aid of spectroscopy and ab initio energy minimization technique. Topa quinone exhibits a totally reversible cyclic voltammogram at a mercury electrode, which is ascribed to a two-step one-electron conversion between topa quinone and topa...

Journal: :Chemistry 2001
S Arndt U Emde S Bäurle T Friedrich L Grubert U Koert

The natural product hybrids quinone-mucocin and quinone- squamocin D were synthesized. In these hybrids, the butenolide unit of the annonaceous acetogenins mucocin and squamocin D is exchanged for the quinone moiety of the natural complex I substrate ubiquinone. For both syntheses, a modular, highly convergent approach was applied. Quinone-mucocin was constructed out of a tetrahydropyran (THP) ...

Journal: :International journal of molecular sciences 2016
Shosuke Ito Yuta Yamanaka Makoto Ojika Kazumasa Wakamatsu

ortho-Quinones are produced in vivo through the oxidation of catecholic substrates by enzymes such as tyrosinase or by transition metal ions. Neuromelanin, a dark pigment present in the substantia nigra and locus coeruleus of the brain, is produced from dopamine (DA) and norepinephrine (NE) via an interaction with cysteine, but it also incorporates their alcoholic and acidic metabolites. In thi...

Journal: :Biochemical Society transactions 2009
Sophie A Weiss Lars J C Jeuken

Quinone oxidoreductases are a class of membrane enzymes that catalyse the oxidation or reduction of membrane-bound quinols/quinones. The conversion of quinone/quinol by these enzymes is difficult to study because of the hydrophobic nature of the enzymes and their substrates. We describe some biochemical properties of quinones and quinone oxidoreductases and then look in more detail at two model...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2013
Quanjiang Ji Liang Zhang Marcus B Jones Fei Sun Xin Deng Haihua Liang Hoonsik Cho Pedro Brugarolas Yihe N Gao Scott N Peterson Lefu Lan Taeok Bae Chuan He

Quinone molecules are intracellular electron-transport carriers, as well as critical intra- and extracellular signals. However, transcriptional regulation of quinone signaling and its molecular basis are poorly understood. Here, we identify a thiol-stress-sensing regulator YodB family transcriptional regulator as a central component of quinone stress response of Staphylococcus aureus, which we ...

Journal: :Organic letters 2005
Yaodong Huang Jinsong Zhang Thomas R R Pettus

[reaction: see text] A short synthesis of (+/-)-brazilin is reported. This synthesis uses several interesting and underutilized transformations including a regioselective dirhodium-catalyzed aryl C-H insertion, a regioselective IBX phenol --> o-quinone oxidation, a tautomerization of an o-quinone to a p-quinone methide, and an intramolecular aryl cyclization with a p-quinone methide.

Journal: :Cancer research 1987
G Powis E M Hodnett K S Santone K L See D C Melder

Quinone(di)imines are nitrogen analogues of quinones in which one or both quinone oxygens are replaced by an imino group. A series of quinone(di)imines with antitumor activity has been studied for its in vitro chemical reactivity, metabolism, acute toxicity to primary cultured rat hepatocytes, and growth-inhibitory activity with Chinese hamster ovary (CHO) cells. The quinone(di)imines exhibited...

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