 Amines
"Amines" 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.
A group of compounds derived from ammonia by substituting organic radicals for the hydrogens. (From Grant & Hackh's Chemical Dictionary, 5th ed)
| Descriptor ID |
D000588
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| MeSH Number(s) |
D02.092
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Amines".
Below are MeSH descriptors whose meaning is more specific than "Amines".
This graph shows the total number of publications written about "Amines" by people in this website by year, and whether "Amines" 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 |
|---|
| 2000 | 0 | 1 | 1 | | 2001 | 1 | 1 | 2 | | 2002 | 0 | 1 | 1 | | 2003 | 2 | 0 | 2 | | 2006 | 1 | 1 | 2 | | 2007 | 1 | 0 | 1 | | 2009 | 1 | 2 | 3 | | 2010 | 2 | 1 | 3 | | 2011 | 2 | 2 | 4 | | 2012 | 2 | 0 | 2 | | 2013 | 5 | 1 | 6 | | 2015 | 0 | 1 | 1 | | 2019 | 1 | 0 | 1 | | 2020 | 0 | 2 | 2 |
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Below are the most recent publications written about "Amines" by people in Profiles.
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Bram AI, Gouzman I, Bolker A, Eliaz N, Verker R. The Effect of POSS Type on the Shape Memory Properties of Epoxy-Based Nanocomposites. Molecules. 2020 Sep 14; 25(18).
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Sheshachala S, Grösche M, Scherr T, Hu Y, Sun P, Bartschat A, Mikut R, Niemeyer CM. Segregation of Dispersed Silica Nanoparticles in Microfluidic Water-in-Oil Droplets: A Kinetic Study. Chemphyschem. 2020 05 18; 21(10):1070-1078.
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Kim K, Singstock NR, Childress KK, Sinha J, Salazar AM, Whitfield SN, Holder AM, Stansbury JW, Musgrave CB. Rational Design of Efficient Amine Reductant Initiators for Amine-Peroxide Redox Polymerization. J Am Chem Soc. 2019 04 17; 141(15):6279-6291.
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Nelson N, Schwartz DK. Unbiased Clustering of Molecular Dynamics for Spatially Resolved Analysis of Chemically Heterogeneous Surfaces. Langmuir. 2015 Jun 09; 31(22):6099-106.
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Thorson MK, Van Wagoner RM, Harper MK, Ireland CM, Majtan T, Kraus JP, Barrios AM. Marine natural products as inhibitors of cystathionine beta-synthase activity. Bioorg Med Chem Lett. 2015 Mar 01; 25(5):1064-6.
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Kapil V, Green JL, Le Lait MC, Wood DM, Dargan PI. Misuse of the ?-aminobutyric acid analogues baclofen, gabapentin and pregabalin in the UK. Br J Clin Pharmacol. 2014 Jul; 78(1):190-1.
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Kaye AD, Beuno FR, Katalenich B, Stell C, Liu H, Rosinia FA, Luk E, Ehrhardt K, Fox CJ. The effects of gastroretentive gabapentin (Gralise®) on spinal stenosis patients with radicular pain. Pain Physician. 2014 Mar-Apr; 17(2):169-78.
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Carbain B, Coxon CR, Lebraud H, Elliott KJ, Matheson CJ, Meschini E, Roberts AR, Turner DM, Wong C, Cano C, Griffin RJ, Hardcastle IR, Golding BT. Trifluoroacetic acid in 2,2,2-trifluoroethanol facilitates S(N)Ar reactions of heterocycles with arylamines. Chemistry. 2014 Feb 17; 20(8):2311-7.
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Almeida J, Schobesberger S, Kürten A, Ortega IK, Kupiainen-Määttä O, Praplan AP, Adamov A, Amorim A, Bianchi F, Breitenlechner M, David A, Dommen J, Donahue NM, Downard A, Dunne E, Duplissy J, Ehrhart S, Flagan RC, Franchin A, Guida R, Hakala J, Hansel A, Heinritzi M, Henschel H, Jokinen T, Junninen H, Kajos M, Kangasluoma J, Keskinen H, Kupc A, Kurtén T, Kvashin AN, Laaksonen A, Lehtipalo K, Leiminger M, Leppä J, Loukonen V, Makhmutov V, Mathot S, McGrath MJ, Nieminen T, Olenius T, Onnela A, Petäjä T, Riccobono F, Riipinen I, Rissanen M, Rondo L, Ruuskanen T, Santos FD, Sarnela N, Schallhart S, Schnitzhofer R, Seinfeld JH, Simon M, Sipilä M, Stozhkov Y, Stratmann F, Tomé A, Tröstl J, Tsagkogeorgas G, Vaattovaara P, Viisanen Y, Virtanen A, Vrtala A, Wagner PE, Weingartner E, Wex H, Williamson C, Wimmer D, Ye P, Yli-Juuti T, Carslaw KS, Kulmala M, Curtius J, Baltensperger U, Worsnop DR, Vehkamäki H, Kirkby J. Molecular understanding of sulphuric acid-amine particle nucleation in the atmosphere. Nature. 2013 Oct 17; 502(7471):359-63.
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Nordwald EM, Kaar JL. Stabilization of enzymes in ionic liquids via modification of enzyme charge. Biotechnol Bioeng. 2013 Sep; 110(9):2352-60.
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