"Glycosides" 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.
Any compound that contains a constituent sugar, in which the hydroxyl group attached to the first carbon is substituted by an alcoholic, phenolic, or other group. They are named specifically for the sugar contained, such as glucoside (glucose), pentoside (pentose), fructoside (fructose), etc. Upon hydrolysis, a sugar and nonsugar component (aglycone) are formed. (From Dorland, 28th ed; From Miall's Dictionary of Chemistry, 5th ed)
| Descriptor ID |
D006027
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| MeSH Number(s) |
D09.408
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Glycosides".
Below are MeSH descriptors whose meaning is more specific than "Glycosides".
This graph shows the total number of publications written about "Glycosides" by people in this website by year, and whether "Glycosides" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 2 | 0 | 2 |
| 2004 | 2 | 1 | 3 |
| 2005 | 0 | 1 | 1 |
| 2008 | 1 | 0 | 1 |
| 2009 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Glycosides" by people in Profiles.
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Li T, Li T, Zhang Y, Schmidt RR, Peng P. Preparation of Tea Aroma Precursor Glycosides: An Efficient and Sustainable Approach via Chemical Glycosidation. J Agric Food Chem. 2022 Feb 23; 70(7):2320-2327.
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Kumar A, Kumar V, Dere RT, Schmidt RR. Glycoside bond formation via acid-base catalysis. Org Lett. 2011 Jul 15; 13(14):3612-5.
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Reddy BG, Silk JD, Salio M, Balamurugan R, Shepherd D, Ritter G, Cerundolo V, Schmidt RR. Nonglycosidic agonists of invariant NKT cells for use as vaccine adjuvants. ChemMedChem. 2009 Feb; 4(2):171-5.
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Reddy BG, Schmidt RR. 2-Nitroglycals: versatile intermediates for efficient and highly stereoselective base-catalyzed glycoside bond formations. Nat Protoc. 2008; 3(1):114-21.
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Biskup MB, Müller JU, Weingart R, Schmidt RR. New methods for the generation of carbohydrate arrays on glass slides and their evaluation. Chembiochem. 2005 Jun; 6(6):1007-15.
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Zhu X, Stolz F, Schmidt RR. Synthesis of thioglycoside-based UDP-sugar analogues. J Org Chem. 2004 Oct 15; 69(21):7367-70.
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Barroca N, Schmidt RR. 2-nitro thioglycoside donors: versatile precursors of beta-D-glycosides of aminosugars. Org Lett. 2004 May 13; 6(10):1551-4.
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Zhu X, Schmidt RR. Glycosylthiomethyl chloride: a new species for S-neoglycoconjugate synthesis. Synthesis of 1-N-glycosylthiomethyl-1,2,3-triazoles. J Org Chem. 2004 Feb 20; 69(4):1081-5.
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Schwörer R, Schmidt RR. Efficient sialyltransferase inhibitors based on glycosides of N-acetylglucosamine. J Am Chem Soc. 2002 Feb 27; 124(8):1632-7.
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Abdel-Rahman AA, El Ashry el SH, Schmidt RR. Efficient intramolecular beta-mannoside formation using m-xylylene and isophthaloyl derivatives as rigid spacers. Carbohydr Res. 2002 Feb 11; 337(3):195-206.