 Quinones
"Quinones" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Hydrocarbon rings which contain two ketone moieties in any position. They can be substituted in any position except at the ketone groups.
| Descriptor ID |
D011809
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| MeSH Number(s) |
D02.806
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Quinones".
Below are MeSH descriptors whose meaning is more specific than "Quinones".
This graph shows the total number of publications written about "Quinones" by people in this website by year, and whether "Quinones" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1993 | 0 | 1 | 1 | | 1999 | 0 | 1 | 1 | | 2005 | 1 | 0 | 1 | | 2007 | 1 | 0 | 1 | | 2009 | 0 | 1 | 1 | | 2013 | 0 | 2 | 2 | | 2014 | 1 | 0 | 1 | | 2015 | 3 | 0 | 3 |
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Below are the most recent publications written about "Quinones" by people in Profiles.
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Ross D, Siegel D. The diverse functionality of NQO1 and its roles in redox control. Redox Biol. 2021 05; 41:101950.
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Li J, Yao S, Wang K, Lu Z, Su X, Li L, Yuan C, Feng J, Yan S, Kong B, Song K. Hypocrellin B-loaded, folate-conjugated polymeric micelle for intraperitoneal targeting of ovarian cancer in?vitro and in?vivo. Cancer Sci. 2018 Jun; 109(6):1958-1969.
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Chattaraj R, Mohan P, Livingston CM, Besmer JD, Kumar K, Goodwin AP. Mutually-Reactive, Fluorogenic Hydrocyanine/Quinone Reporter Pairs for In-Solution Biosensing via Nanodroplet Association. ACS Appl Mater Interfaces. 2016 Jan 13; 8(1):802-8.
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Elajaili H, Rinard GA, Yu Z, Mitchell DG, Quine RW, Eaton SS, Eaton GR. Rapid-scan coherence signals in X-band EPR spectra of semiquinones with small hyperfine splittings. J Magn Reson. 2015 Oct; 259:20-3.
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Li Z, Sun L, Lu Z, Su X, Yang Q, Qu X, Li L, Song K, Kong B. Enhanced effect of photodynamic therapy in ovarian cancer using a nanoparticle drug delivery system. Int J Oncol. 2015 Sep; 47(3):1070-6.
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Slikboer S, Grandy L, Blair SL, Nizkorodov SA, Smith RW, Al-Abadleh HA. Formation of Light Absorbing Soluble Secondary Organics and Insoluble Polymeric Particles from the Dark Reaction of Catechol and Guaiacol with Fe(III). Environ Sci Technol. 2015 Jul 07; 49(13):7793-801.
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Blunt CE, Torcuk C, Liu Y, Lewis W, Siegel D, Ross D, Moody CJ. Synthesis and Intracellular Redox Cycling of Natural Quinones and Their Analogues and Identification of Indoleamine-2,3-dioxygenase (IDO) as Potential Target for Anticancer Activity. Angew Chem Int Ed Engl. 2015 Jul 20; 54(30):8740-5.
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Venkatesh R, Ramaiah MJ, Gaikwad HK, Janardhan S, Bantu R, Nagarapu L, Sastry GN, Ganesh AR, Bhadra M. Luotonin-A based quinazolinones cause apoptosis and senescence via HDAC inhibition and activation of tumor suppressor proteins in HeLa cells. Eur J Med Chem. 2015 Apr 13; 94:87-101.
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Elajaili HB, Biller JR, Eaton SS, Eaton GR. Frequency dependence of electron spin-lattice relaxation for semiquinones in alcohol solutions. J Magn Reson. 2014 Oct; 247:81-87.
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Xiong R, Siegel D, Ross D. Quinone-induced protein handling changes: implications for major protein handling systems in quinone-mediated toxicity. Toxicol Appl Pharmacol. 2014 Oct 15; 280(2):285-95.
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