"Catechols" 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.
A group of 1,2-benzenediols that contain the general formula R-C6H5O2.
| Descriptor ID |
D002396
|
| MeSH Number(s) |
D02.455.426.559.389.657.166
|
| Concept/Terms |
Catechols- Catechols
- Pyrocatechols
- o-Dihydroxybenzenes
- o Dihydroxybenzenes
- ortho-Dihydroxybenzenes
- ortho Dihydroxybenzenes
|
Below are MeSH descriptors whose meaning is more general than "Catechols".
Below are MeSH descriptors whose meaning is more specific than "Catechols".
This graph shows the total number of publications written about "Catechols" by people in this website by year, and whether "Catechols" was a major or minor topic of these publications.
To see the data from this visualization as text,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2009 | 0 | 1 | 1 |
| 2010 | 0 | 1 | 1 |
| 2011 | 0 | 1 | 1 |
| 2012 | 0 | 1 | 1 |
| 2015 | 1 | 0 | 1 |
| 2017 | 0 | 1 | 1 |
| 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Catechols" by people in Profiles.
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Antibiotic repurposing: bis-catechol- and mixed ligand (bis-catechol-mono-hydroxamate)-teicoplanin conjugates are active against multidrug resistant Acinetobacter baumannii. J Antibiot (Tokyo). 2020 03; 73(3):152-157.
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Methodology for Monobactam Diversification: Syntheses and Studies of 4-Thiomethyl Substituted ?-Lactams with Activity against Gram-Negative Bacteria, Including Carbapenemase Producing Acinetobacter baumannii. J Med Chem. 2017 11 09; 60(21):8933-8944.
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A novel component from citrus, ginger, and mushroom family exhibits antitumor activity on human meningioma cells through suppressing the Wnt/?-catenin signaling pathway. Tumour Biol. 2015 Sep; 36(9):7027-34.
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Iron transport-mediated drug delivery: practical syntheses and in vitro antibacterial studies of tris-catecholate siderophore-aminopenicillin conjugates reveals selectively potent antipseudomonal activity. J Am Chem Soc. 2012 Jun 20; 134(24):9898-901.
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Syntheses and studies of amamistatin B analogs reveals that anticancer activity is relatively independent of stereochemistry, ester or amide linkage and select replacement of one of the metal chelating groups. Bioorg Med Chem Lett. 2011 May 01; 21(9):2611-5.
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Combined anticancer effects of sphingosine kinase inhibitors and sorafenib. Invest New Drugs. 2011 Dec; 29(6):1132-42.
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Rutin metabolites: novel inhibitors of nonoxidative advanced glycation end products. Free Radic Biol Med. 2010 Mar 01; 48(5):656-63.
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Biochemistry of catecholamines. Annu Rev Biochem. 1971; 40:465-500.