Imines
"Imines" 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.
Organic compounds containing a carbon-nitrogen double bond where a NITROGEN atom can be attached to HYDROGEN or an alkyl or aryl group.
Descriptor ID |
D007097
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MeSH Number(s) |
D02.491
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Imines".
Below are MeSH descriptors whose meaning is more specific than "Imines".
This graph shows the total number of publications written about "Imines" by people in this website by year, and whether "Imines" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2005 | 1 | 1 | 2 | 2006 | 1 | 0 | 1 | 2016 | 0 | 1 | 1 | 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Imines" by people in Profiles.
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Arnold CG, Dylla L, Monte AA, Heard K, Heard S, D'Alessandro A, Reynolds K, Dart R, Rumack B, Sonn B. Metabolomic Evaluation of N-Acetyl-p-Benzoquinone Imine Protein Adduct Formation with Therapeutic Acetaminophen Administration: Sex-based Physiologic Differences. J Med Toxicol. 2022 10; 18(4):297-310.
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Yip L, Heard K. Potential adjunct treatment for high-risk acetaminophen overdose. Clin Toxicol (Phila). 2016 Jun; 54(5):459.
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Towner RA, Gillespie DL, Schwager A, Saunders DG, Smith N, Njoku CE, Krysiak RS, Larabee C, Iqbal H, Floyd RA, Bourne DW, Abdullah O, Hsu EW, Jensen RL. Regression of glioma tumor growth in F98 and U87 rat glioma models by the Nitrone OKN-007. Neuro Oncol. 2013 Mar; 15(3):330-40.
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Latham MP, Pardi A. Measurement of imino 1H-1H residual dipolar couplings in RNA. J Biomol NMR. 2009 Feb; 43(2):121-9.
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Lee JH, Jucker F, Pardi A. Imino proton exchange rates imply an induced-fit binding mechanism for the VEGF165-targeting aptamer, Macugen. FEBS Lett. 2008 Jun 11; 582(13):1835-9.
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Ying J, Grishaev A, Latham MP, Pardi A, Bax A. Magnetic field induced residual dipolar couplings of imino groups in nucleic acids from measurements at a single magnetic field. J Biomol NMR. 2007 Oct; 39(2):91-6.
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Arnold MA, Day KA, Dur?n SG, Gin DY. Total synthesis of (+)-batzelladine A and (-)-batzelladine D via [4 + 2]-annulation of vinyl carbodiimides with N-alkyl imines. J Am Chem Soc. 2006 Oct 11; 128(40):13255-60.
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Zhang Y, Sammakia T. Double diastereoselective acetate aldol reactions with chiral N-acetyl thiazolidinethione reagents. J Org Chem. 2006 Aug 04; 71(16):6262-5.
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Que LG, Liu L, Yan Y, Whitehead GS, Gavett SH, Schwartz DA, Stamler JS. Protection from experimental asthma by an endogenous bronchodilator. Science. 2005 Jun 10; 308(5728):1618-21.
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Arnold MA, Dur?n SG, Gin DY. Diastereoselective [4+2] annulation of vinyl carbodiimides with N-alkyl imines. Asymmetric synthetic access to the batzelladine alkaloids. J Am Chem Soc. 2005 May 18; 127(19):6924-5.
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