"Schiff Bases" 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.
Condensation products of aromatic amines and aldehydes forming azomethines substituted on the N atom, containing the general formula R-N:CHR. (From Grant & Hackh's Chemical Dictionary, 5th ed)
- Schiff Bases
- Bases, Schiff
- Schiff Base
- Base, Schiff
Below are MeSH descriptors whose meaning is more general than "Schiff Bases".
Below are MeSH descriptors whose meaning is more specific than "Schiff Bases".
This graph shows the total number of publications written about "Schiff Bases" by people in Harvard Catalyst Profiles by year, and whether "Schiff Bases" was a major or minor topic of these publication.
To see the data from this visualization as text, click here.
|Year||Major Topic||Minor Topic||Total|
Below are the most recent publications written about "Schiff Bases" by people in Profiles.
Mechanistic Insight through Irreversible Inhibition: DNA Polymerase ? Uses a Common Active Site for Polymerase and Lyase Activities. J Am Chem Soc. 2018 07 25; 140(29):9034-9037.
Improving cytocompatibility of CdTe quantum dots by Schiff-base-coordinated lanthanides surface doping. J Nanobiotechnology. 2018 Apr 19; 16(1):43.
PLP and GABA trigger GabR-mediated transcription regulation in Bacillus subtilis via external aldimine formation. Proc Natl Acad Sci U S A. 2017 04 11; 114(15):3891-3896.
Origin of Water-Induced Fluorescence Turn-On from a Schiff Base Compound: AIE or H-Bonding Promoted ESIPT? J Phys Chem B. 2016 Feb 04; 120(4):766-72.
Increasing the efficiency of precise genome editing with CRISPR-Cas9 by inhibition of nonhomologous end joining. Nat Biotechnol. 2015 May; 33(5):538-42.
Chelating ability and biological activity of hesperetin Schiff base. J Inorg Biochem. 2015 Feb; 143:34-47.
A single molecular probe for multi-analyte (Cr³?, Al³? and Fe³?) detection in aqueous medium and its biological application. Chem Commun (Camb). 2014 Oct 21; 50(82):12258-61.
Palladium(II) complexes with N-heteroaromatic bidentate hydrazone ligands: the effect of the chelate ring size and lipophilicity on in vitro cytotoxic activity. Chem Biol Drug Des. 2014 Sep; 84(3):333-41.
Thermal stability of rhodopsin and progression of retinitis pigmentosa: comparison of S186W and D190N rhodopsin mutants. J Biol Chem. 2013 Jun 14; 288(24):17698-712.
Microplate assay for screening the antibacterial activity of Schiff bases derived from substituted benzopyran-4-one. Spectrochim Acta A Mol Biomol Spectrosc. 2012 Sep; 95:517-25.