Isomerism
"Isomerism" 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.
The phenomenon whereby certain chemical compounds have structures that are different although the compounds possess the same elemental composition. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed)
Descriptor ID |
D007536
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MeSH Number(s) |
G02.111.570.685 G02.607.500
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Isomerism".
Below are MeSH descriptors whose meaning is more specific than "Isomerism".
This graph shows the total number of publications written about "Isomerism" by people in this website by year, and whether "Isomerism" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1992 | 0 | 1 | 1 | 2002 | 0 | 1 | 1 | 2005 | 0 | 1 | 1 | 2007 | 0 | 3 | 3 | 2008 | 0 | 1 | 1 | 2011 | 0 | 1 | 1 | 2012 | 0 | 1 | 1 | 2015 | 0 | 1 | 1 |
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Below are the most recent publications written about "Isomerism" by people in Profiles.
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Ku AF, Cuny GD. Synthetic studies of 7-oxygenated aporphine alkaloids: preparation of (-)-oliveroline, (-)-nornuciferidine, and derivatives. Org Lett. 2015 Mar 06; 17(5):1134-7.
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Bittner ER, Madalan A, Czader A, Roman G. Quantum origins of molecular recognition and olfaction in Drosophila. J Chem Phys. 2012 Dec 14; 137(22):22A551.
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Eiserbeck C, Nelson RK, Grice K, Curiale J, Reddy CM, Raiteri P. Separation of 18a(H)-, 18ß(H)-oleanane and lupane by comprehensive two-dimensional gas chromatography. J Chromatogr A. 2011 Aug 12; 1218(32):5549-53.
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Sintic PJ, E W, Ou Z, Shao J, McDonald JA, Cai ZL, Kadish KM, Crossley MJ, Reimers JR. Control of the site and potential of reduction and oxidation processes in pi-expanded quinoxalinoporphyrins. Phys Chem Chem Phys. 2008 Jan 14; 10(2):268-80.
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Sintic PJ, E W, Ou Z, Shao J, McDonald JA, Cai ZL, Kadish KM, Crossley MJ, Reimers JR. Control of the site and potential of reduction and oxidation processes in pi-expanded quinoxalinoporphyrins. Phys Chem Chem Phys. 2008 Jan 28; 10(4):515-27.
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Pichumani K, Zou X, Chandra T, Brown KL. Determination of the anomeric configuration in carbohydrates by longitudinal cross-correlated relaxation studies: application to mono- and disaccharides. Magn Reson Chem. 2007 Sep; 45(9):734-8.
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DeBoef B, Counts WR, Gilbertson SR. Rhodium-catalyzed synthesis of eight-membered rings. J Org Chem. 2007 Feb 02; 72(3):799-804.
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Schultz DA, Friedman AM, White MA, Fox RO. The crystal structure of the cis-proline to glycine variant (P114G) of ribonuclease A. Protein Sci. 2005 Nov; 14(11):2862-70.
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Dash C, Vathipadiekal V, George SP, Rao M. Slow-tight binding inhibition of xylanase by an aspartic protease inhibitor: kinetic parameters and conformational changes that determine the affinity and selectivity of the bifunctional nature of the inhibitor. J Biol Chem. 2002 May 17; 277(20):17978-86.
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Brozinick JT, Etgen GJ, Yaspelkis BB, Ivy JL. Contraction-activated glucose uptake is normal in insulin-resistant muscle of the obese Zucker rat. J Appl Physiol (1985). 1992 Jul; 73(1):382-7.
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