"Esters" 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.
Compounds derived from organic or inorganic acids in which at least one hydroxyl group is replaced by an –O-alkyl or other organic group. They can be represented by the structure formula RCOOR’ and are usually formed by the reaction between an acid and an alcohol with elimination of water.
| Descriptor ID |
D004952
|
| MeSH Number(s) |
D02.241.400
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Esters".
Below are MeSH descriptors whose meaning is more specific than "Esters".
This graph shows the total number of publications written about "Esters" by people in this website by year, and whether "Esters" 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 |
|---|
| 1999 | 0 | 1 | 1 |
| 2001 | 0 | 1 | 1 |
| 2005 | 0 | 3 | 3 |
| 2007 | 0 | 1 | 1 |
| 2008 | 0 | 2 | 2 |
| 2009 | 0 | 1 | 1 |
| 2010 | 1 | 1 | 2 |
| 2011 | 0 | 3 | 3 |
| 2012 | 0 | 2 | 2 |
| 2013 | 0 | 2 | 2 |
| 2015 | 0 | 1 | 1 |
| 2018 | 1 | 0 | 1 |
| 2019 | 0 | 1 | 1 |
| 2021 | 0 | 1 | 1 |
| 2022 | 0 | 1 | 1 |
| 2023 | 0 | 1 | 1 |
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Below are the most recent publications written about "Esters" by people in Profiles.
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Wu L, Zhang M, Liu WH, Chen YF, Yin XW, Han Z, Ren FC, Pu XD, Liu XH, Shi JB, Shen CP. The intramolecular SN2 reaction tautomeric ent-Kauranoids isolated from the aerial parts of Isodon amethystoides. Fitoterapia. 2024 Mar; 173:105788.
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Dahiya R, Dahiya S, Chennupati SV, Davis V, Sahadeo V, Patel JK. Towards the Synthesis of a Heterocyclic Analogue of Natural Cyclooligopeptide with Improved Bio-properties. Curr Org Synth. 2022 03 03; 19(2):267-278.
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Xu X, Kang C, Sun R, Zuo YY. Biophysical properties of tear film lipid layer II. Polymorphism of FAHFA. Biophys J. 2022 02 01; 121(3):451-458.
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Gharaie Fathabad S, Arumanayagam AS, Tabatabai B, Chen H, Lu J, Sitther V. Augmenting Fremyella diplosiphon Cellular Lipid Content and Unsaturated Fatty Acid Methyl Esters Via Sterol Desaturase Gene Overexpression. Appl Biochem Biotechnol. 2019 Dec; 189(4):1127-1140.
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Bernal CA, Castellanos L, Arag?n DM, Mart?nez-Matamoros D, Jim?nez C, Baena Y, Ramos FA. Peruvioses A to F, sucrose esters from the exudate of Physalis peruviana fruit as a-amylase inhibitors. Carbohydr Res. 2018 May 22; 461:4-10.
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Graves RA, Ledet GA, Glotser EY, Mitchner DM, Bostanian LA, Mandal TK. Formulation and evaluation of biodegradable nanoparticles for the oral delivery of fenretinide. Eur J Pharm Sci. 2015 Aug 30; 76:1-9.
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Deng QH, Rettenmeier C, Wadepohl H, Gade LH. Copper-boxmi complexes as highly enantioselective catalysts for electrophilic trifluoromethylthiolations. Chemistry. 2014 Jan 03; 20(1):93-7.
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Barron GA, Valentine R, Moseley H, Brancaleon L, Hill C, Woods JA. Porphyrin profile in four human cell lines after supplementation with 5-aminolaevulinic acid and its methyl ester. Photodiagnosis Photodyn Ther. 2013 Dec; 10(4):654-63.
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Betts BS, Obregon I, Tsin AT. Cultured M?ller cells from mammals can synthesize and accumulate retinyl esters. Exp Eye Res. 2012 Aug; 101:56-9.
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Shimada N, Stewart C, Bow WF, Jolit A, Wong K, Zhou Z, Tius MA. Neutral Nazarov-type cyclization catalyzed by palladium(0). Angew Chem Int Ed Engl. 2012 Jun 04; 51(23):5727-9.