"Stereoisomerism" 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 compounds whose molecules have the same number and kind of atoms and the same atomic arrangement, but differ in their spatial relationships. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed)
| Descriptor ID |
D013237
|
| MeSH Number(s) |
G02.607.445.682
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Stereoisomerism".
Below are MeSH descriptors whose meaning is more specific than "Stereoisomerism".
This graph shows the total number of publications written about "Stereoisomerism" by people in this website by year, and whether "Stereoisomerism" 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 |
|---|
| 1994 | 0 | 1 | 1 |
| 1996 | 0 | 1 | 1 |
| 1998 | 0 | 4 | 4 |
| 1999 | 0 | 1 | 1 |
| 2000 | 0 | 4 | 4 |
| 2001 | 0 | 2 | 2 |
| 2002 | 0 | 6 | 6 |
| 2003 | 0 | 10 | 10 |
| 2004 | 0 | 7 | 7 |
| 2005 | 0 | 10 | 10 |
| 2006 | 0 | 14 | 14 |
| 2007 | 0 | 15 | 15 |
| 2008 | 0 | 9 | 9 |
| 2009 | 0 | 7 | 7 |
| 2010 | 0 | 8 | 8 |
| 2011 | 0 | 11 | 11 |
| 2012 | 0 | 4 | 4 |
| 2013 | 0 | 5 | 5 |
| 2014 | 0 | 6 | 6 |
| 2015 | 0 | 9 | 9 |
| 2016 | 0 | 1 | 1 |
| 2017 | 0 | 1 | 1 |
| 2018 | 0 | 1 | 1 |
| 2019 | 0 | 2 | 2 |
| 2020 | 0 | 2 | 2 |
| 2021 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "Stereoisomerism" by people in Profiles.
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Domzalski A, Margent L, Vigo V, Dewan F, Pilarsetty NVK, Xu Y, Kawamura A. Unambiguous Stereochemical Assignment of Cyclo(Phe-Pro), Cyclo(Leu-Pro), and Cyclo(Val-Pro) by Electronic Circular Dichroic Spectroscopy. Molecules. 2021 Oct 02; 26(19).
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Harris KJ, Subbiah S, Tabatabai M, Archibong AE, Singh KP, Anderson TA, Adunyah SE, Ramesh A. Pressurized liquid extraction followed by liquid chromatography coupled to a fluorescence detector and atmospheric pressure chemical ionization mass spectrometry for the determination of benzo(a)pyrene metabolites in liver tissue of an animal model of colon cancer. J Chromatogr A. 2020 Jul 05; 1622:461126.
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Lin Q, Tan X, Wang W, Zeng W, Gui L, Su M, Liu C, Jia W, Xu L, Lan K. Species Differences of Bile Acid Redox Metabolism: Tertiary Oxidation of Deoxycholate is Conserved in Preclinical Animals. Drug Metab Dispos. 2020 06; 48(6):499-507.
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Onyameh EK, Bricker BA, Ofori E, Ablordeppey SY. Enantioseparation of 5-chloro-2-{2-[3,4-dihydroisoquinoline-2(1H)-yl]ethyl}-2-methyl-2,3-dihydro-1H-inden-1-one (SYA 40247), a high-affinity 5-HT7 receptor ligand, by HPLC-PDA using amylose tris-(3, 5- dimethylphenylcarbamate) as a chiral stationary phase. Biomed Chromatogr. 2019 Sep; 33(9):e4565.
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Hodgdon EA, Hallett RH, Wallin KF, Stratton CA, Chen YH. Racemic Pheromone Blends Disrupt Mate Location in the Invasive Swede Midge, Contarinia nasturtii. J Chem Ecol. 2019 Jul; 45(7):549-558.
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Wei W, Khangarot RK, Stahl L, Veresmortean C, Pradhan P, Yang L, Zajc B. Generating Stereodiversity: Diastereoselective Fluorination and Highly Diastereoselective Epimerization of a-Amino Acid Building Blocks. Org Lett. 2018 06 15; 20(12):3574-3578.
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Ho TC, Shimada N, Tius MA, Nikas SP, Zhang W, Makriyannis A. C1'-Azacycloalkyl Hexahydrocannabinols. J Org Chem. 2017 08 04; 82(15):7839-7849.
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Liu J, Zheng S, Akerstrom VL, Yuan C, Ma Y, Zhong Q, Zhang C, Zhang Q, Guo S, Ma P, Skripnikova EV, Bratton MR, Pannuti A, Miele L, Wiese TE, Wang G. Fulvestrant-3 Boronic Acid (ZB716): An Orally Bioavailable Selective Estrogen Receptor Downregulator (SERD). J Med Chem. 2016 09 08; 59(17):8134-40.
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Fan Y, Feng Q, Lai K, Huang W, Zhang C, Li QX. Toxic effects of indoxacarb enantiomers on the embryonic development and induction of apoptosis in zebrafish larvae (Danio rerio). Environ Toxicol. 2017 Jan; 32(1):7-16.
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Altiti AS, Bachan S, Alrowhani W, Mootoo DR. An organocatalytic strategy for the stereoselective synthesis of C-galactosides with fluorine at the pseudoanomeric carbon. Org Biomol Chem. 2015 Nov 07; 13(41):10328-35.