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Catechols (7)


Articles on Catechols

  1. In situ electrogeneration of o-benzoquinone and high yield reaction with benzenethiols in a microflow system.

    Chem Commun (London) 48(22):2806-8 (2012) PMID 22301533

    We have successfully demonstrated that a microflow reactor is extremely useful in controlling reactions involving an unstable o-benzoquinone. The key features of the method are an effective o-benzoquinone generation and its rapid use for the following reaction without decomposition in a microflow sy...
  2. A chemical proteomic probe for detecting dehydrogenases: catechol rhodanine.

    Methods Mol Biol (2012) PMID 22065218

    We describe such a fluorescent probe, based on a catechol rhodanine acetic acid (CRAA) ligand that binds to dehydrogenases. The CRAA ligand is fluorescent and binds to dehydrogenases at pH > 7, and hence can be used effectively to stain dehydrogenases in native gels to identify what subset of protei...
  3. Salicylic acid mediates the reduced growth of lignin down-regulated plants.

    Proc Natl Acad Sci U S A 108(51):20814-9 (2011) PMID 22123972 PMCID PMC3251142

    Our data place SA as a central component in growth signaling pathways that either sense flux into the monolignol pathway or respond to secondary cell-wall integrity, and indicate that it is possible to engineer plants with highly reduced cell-wall recalcitrance without negatively impacting growth....
  4. A seven-transmembrane receptor that mediates avoidance response to dihydrocaffeic acid, a water-soluble repellent in Caenorhabditis elegans.

    J Neurosci 31(46):16603-10 (2011) PMID 22090488

    We identified a candidate dihydrocaffeic acid receptor (DCAR), DCAR-1. DCAR-1 is a novel seven-transmembrane protein that is expressed in the ASH avoidance sensory neurons of C. elegans. dcar-1 mutant animals are defective in avoidance response to DHCA, and cell-specific expression of dcar-1 in the...
  5. 6-gingerol, an active ingredient of ginger, protects acetaminophen-induced hepatotoxicity in mice.

    Zhong Xi Yi Jie He Xue Bao 9(11):1264-9 (2011) PMID 22088594

    To investigate the hepatoprotective efficacy of 6-gingerol against acetaminophen-induced hepatotoxicity in mice. Mice were injected with a single dose of acetaminophen (900 mg/kg) to induce hepatotoxicity, while 6-gingerol (30 mg/kg) or the standard drug silymarin (25...
  6. Pharmacokinetics of phenolic compounds of Danshen extract in rat blood and brain by microdialysis sampling.

    J Ethnopharmacol 136(1):129-36 (2011) PMID 21527333

    To evaluate the pharmacokinetics of phenolic compounds after oral administration of Danshen extract in rat brain. Blood and brain microdialysis probes were inserted into jugular vein and cerebral cortex of rat under anesthesia and perfused with ringer's solution at th...
  7. [Investigation on simultaneous determination of dihydroxybenzene isomers in water samples using multi-walled carbon nanotube modified screen...

    Environ Sci Technol 32(2):488-93 (2011) PMID 21528572

    These results indicate MWCNT/SPE can be applied to rapid in-situ determination of dihydroxybenzenes-polluted water samples....
  8. Inhibitors of catechol-O-methyltransferase sensitize mice to pain.

    Br J Pharmacol 161(7):1553-65 (2010) PMID 20726980 PMCID PMC3010567

    We have assessed the effects of acute and repeated administrations of COMT inhibitors on mechanical, thermal and carrageenan-induced nociception in male mice. We used single and repeated administration of a peripherally restricted, short-acting (nitecapone) and also a centrally actin...
  9. Selective catechol-triggered supramolecular gel disassembly.

    Audio, Transactions of the IRE Professio... 46(42):7996-8 (2010) PMID 20865202

    Supramolecular gels formed by an isonicotinic acid derivative in toluene are selectively disassembled in the presence of catechol. The results represent a unique example of molecular recognition associated to gel rupture which is of interest, for example, in controlled drug release applications.
  10. Substrate binding mechanism of a type I extradiol dioxygenase.

    J Biol Chem 285(45):34643-52 (2010) PMID 20810655 PMCID PMC2966080

    I extradiol dioxygenase, and the enzyme substrate (3-methylcatechol) complex revealed the substrate binding process of extradiol dioxygenase. AkbC is composed of an N-domain and an active C-domain, which contains iron coordinated by a 2-His-1-carboxylate facial triad motif. The C-domain includes a ...