 Polyenes
"Polyenes" 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.
Hydrocarbons with more than one double bond. They are a reduced form of POLYYNES.
| Descriptor ID |
D011090
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| MeSH Number(s) |
D02.455.326.271.665
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Polyenes".
Below are MeSH descriptors whose meaning is more specific than "Polyenes".
This graph shows the total number of publications written about "Polyenes" by people in this website by year, and whether "Polyenes" 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 |
|---|
| 1997 | 1 | 0 | 1 | | 2007 | 1 | 0 | 1 | | 2009 | 1 | 0 | 1 | | 2010 | 2 | 0 | 2 | | 2018 | 1 | 0 | 1 | | 2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Polyenes" by people in Profiles.
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Park JD, Moon K, Miller C, Rose J, Xu F, Ebmeier CC, Jacobsen JR, Mao D, Old WM, DeShazer D, Seyedsayamdost MR. Thailandenes, Cryptic Polyene Natural Products Isolated from Burkholderia thailandensis Using Phenotype-Guided Transposon Mutagenesis. ACS Chem Biol. 2020 05 15; 15(5):1195-1203.
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Zhang X, Firkowska-Boden I, Arras MML, Kastantin MJ, Helbing C, ?zogul A, Gnecco E, Schwartz DK, Jandt KD. Nanoconfinement and Sansetsukon-like Nanocrawling Govern Fibrinogen Dynamics and Self-Assembly on Nanostructured Polymeric Surfaces. Langmuir. 2018 11 27; 34(47):14309-14316.
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Craig NC, Chen Y, Fuson HA, Tian H, van Besien H, Conrad AR, Tubergen MJ, Rudolph HD, Demaison J. Microwave spectra of the deuterium isotopologues of cis-hexatriene and a semiexperimental equilibrium structure. J Phys Chem A. 2013 Oct 03; 117(39):9391-400.
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Zhang Y, Arpin CC, Cullen AJ, Mitton-Fry MJ, Sammakia T. Total synthesis of dermostatin A. J Org Chem. 2011 Oct 07; 76(19):7641-53.
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Bolard J, Ch?ron M, Cleary JD, Kramer RE. The contribution of Raman scattering to the fluorescence of the polyene antibiotic amphotericin B. J Fluoresc. 2011 Mar; 21(2):831-4.
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Volcke C, Gandhiraman RP, Gubala V, Raj J, Cummins T, Fonder G, Nooney RI, Mekhalif Z, Herzog G, Daniels S, Arrigan DW, Cafolla AA, Williams DE. Reactive amine surfaces for biosensor applications, prepared by plasma-enhanced chemical vapour modification of polyolefin materials. Biosens Bioelectron. 2010 Apr 15; 25(8):1875-80.
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Volkis V, Mei H, Shoemaker RK, Michl J. LiCB(11)(CH(3))(12)-catalyzed radical polymerization of isobutylene: highly branched polyisobutylene and an isobutylene-ethyl acrylate copolymer. J Am Chem Soc. 2009 Mar 11; 131(9):3132-3.
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Bolard J, Cleary JD, Kramer RE. Evidence that impurities contribute to the fluorescence of the polyene antibiotic amphotericin B. J Antimicrob Chemother. 2009 May; 63(5):921-7.
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Cleary JD, Chapman SW, Swiatlo E, Kramer R. High purity amphotericin B. J Antimicrob Chemother. 2007 Dec; 60(6):1331-40.
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Mitton-Fry MJ, Cullen AJ, Sammakia T. The total synthesis of the oxopolyene macrolide RK-397. Angew Chem Int Ed Engl. 2007; 46(7):1066-70.
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