"Purine Nucleosides" 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.
Purines with a RIBOSE attached that can be phosphorylated to PURINE NUCLEOTIDES.
Descriptor ID |
D011684
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MeSH Number(s) |
D03.633.100.759.590 D13.570.583
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Purine Nucleosides".
Below are MeSH descriptors whose meaning is more specific than "Purine Nucleosides".
This graph shows the total number of publications written about "Purine Nucleosides" by people in this website by year, and whether "Purine Nucleosides" 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 |
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1998 | 1 | 0 | 1 |
2006 | 2 | 0 | 2 |
2009 | 2 | 0 | 2 |
2010 | 2 | 0 | 2 |
2011 | 1 | 0 | 1 |
2012 | 0 | 2 | 2 |
2013 | 1 | 0 | 1 |
2014 | 1 | 0 | 1 |
2016 | 1 | 0 | 1 |
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Below are the most recent publications written about "Purine Nucleosides" by people in Profiles.
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Basava V, Yang L, Pradhan P, Lakshman MK. A novel bis(pinacolato)diboron-mediated N-O bond deoxygenative route to C6 benzotriazolyl purine nucleoside derivatives. Org Biomol Chem. 2016 Aug 07; 14(29):7069-83.
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Chai X, Youn UJ, Sun D, Dai J, Williams P, Kondratyuk TP, Borris RP, Davies J, Villanueva IG, Pezzuto JM, Chang LC. Herbicidin congeners, undecose nucleosides from an organic extract of Streptomyces sp. L-9-10. J Nat Prod. 2014 Feb 28; 77(2):227-33.
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Chamala RR, Parrish D, Pradhan P, Lakshman MK. Purinyl N1-directed aromatic C-H oxidation in 6-arylpurines and 6-arylpurine nucleosides. J Org Chem. 2013 Aug 02; 78(15):7423-35.
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Gu J, Leszczynski J, Schaefer HF. Interactions of electrons with bare and hydrated biomolecules: from nucleic acid bases to DNA segments. Chem Rev. 2012 Nov 14; 112(11):5603-40.
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Gurram V, Pottabathini N, Garlapati R, Chaudhary AB, Patro B, Lakshman MK. C-C cross-coupling reactions of O6-alkyl-2-haloinosine derivatives and a one-pot cross-coupling/O6-deprotection procedure. Chem Asian J. 2012 Aug; 7(8):1853-61.
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Lakshman MK, Deb AC, Chamala RR, Pradhan P, Pratap R. Direct arylation of 6-phenylpurine and 6-arylpurine nucleosides by ruthenium-catalyzed C-H bond activation. Angew Chem Int Ed Engl. 2011 Nov 25; 50(48):11400-4.
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Kokatla HP, Lakshman MK. One-pot etherification of purine nucleosides and pyrimidines. Org Lett. 2010 Oct 15; 12(20):4478-81.
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Lakshman MK, Singh MK, Parrish D, Balachandran R, Day BW. Azide-tetrazole equilibrium of C-6 azidopurine nucleosides and their ligation reactions with alkynes. J Org Chem. 2010 Apr 16; 75(8):2461-73.
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Lakshman MK, Frank J. A simple method for C-6 modification of guanine nucleosides. Org Biomol Chem. 2009 Jul 21; 7(14):2933-40.
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Bae S, Chaturvedi S, Lakshman MK. O6-(benzotriazol-1-yl)inosine derivatives for C6 modification of purine nucleosides. Curr Protoc Nucleic Acid Chem. 2009 Mar; Chapter 1:Unit 1.22.