Heterocyclic Compounds, 1-Ring
"Heterocyclic Compounds, 1-Ring" 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 that contain a ring structure made up of carbon and one or more additional elements such as nitrogen and oxygen.
Descriptor ID |
D006573
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MeSH Number(s) |
D03.383
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Concept/Terms |
Heterocyclic Compounds, 1-Ring- Heterocyclic Compounds, 1-Ring
- 1-Ring Heterocyclic Compounds
- Heterocyclic Compounds, 1 Ring
- Heterocyclic Cpds, 1-Ring
- 1-Ring Heterocyclic Cpds
- Heterocyclic Cpds, 1 Ring
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Below are MeSH descriptors whose meaning is more general than "Heterocyclic Compounds, 1-Ring".
Below are MeSH descriptors whose meaning is more specific than "Heterocyclic Compounds, 1-Ring".
This graph shows the total number of publications written about "Heterocyclic Compounds, 1-Ring" by people in this website by year, and whether "Heterocyclic Compounds, 1-Ring" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2002 | 1 | 0 | 1 |
2014 | 1 | 0 | 1 |
2017 | 1 | 0 | 1 |
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Below are the most recent publications written about "Heterocyclic Compounds, 1-Ring" by people in Profiles.
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ImmunoPET, [64Cu]Cu-DOTA-Anti-CD33 PET-CT, Imaging of an AML Xenograft Model. Clin Cancer Res. 2019 12 15; 25(24):7463-7474.
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Primary radiation dosimetry of a novel PET radiopharmaceutical 68Ga-NODAGA-glycine in comparison with 99mTc-DTPA in renal studies. Hell J Nucl Med. 2017 Sep-Dec; 20(3):241-246.
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Synthesis and in vivo evaluation of gallium-68-labeled glycine and hippurate conjugates for positron emission tomography renography. J Labelled Comp Radiopharm. 2015 Jan; 58(1):14-9.
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Chemical synthesis of Escherichia coli ST(h) analogues by regioselective disulfide bond formation: biological evaluation of an (111)In-DOTA-Phe(19)-ST(h) analogue for specific targeting of human colon cancers. Bioconjug Chem. 2002 Mar-Apr; 13(2):224-31.