"Pyrans" 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.
No definition found.
| Descriptor ID |
D011714
|
| MeSH Number(s) |
D03.383.663
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Pyrans".
Below are MeSH descriptors whose meaning is more specific than "Pyrans".
This graph shows the total number of publications written about "Pyrans" by people in this website by year, and whether "Pyrans" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 0 | 1 | 1 |
| 2006 | 1 | 0 | 1 |
| 2008 | 2 | 0 | 2 |
| 2010 | 1 | 0 | 1 |
| 2013 | 0 | 1 | 1 |
| 2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Pyrans" by people in Profiles.
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Low-dose salinomycin inhibits breast cancer metastasis by repolarizing tumor hijacked macrophages toward the M1 phenotype. Eur J Pharm Sci. 2021 Feb 01; 157:105629.
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Hbo1 is a cyclin E/CDK2 substrate that enriches breast cancer stem-like cells. Cancer Res. 2013 Sep 01; 73(17):5556-68.
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Rationally simplified bistramide analog reversibly targets actin polymerization and inhibits cancer progression in vitro and in vivo. J Am Chem Soc. 2010 Jun 02; 132(21):7288-90.
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The dual mode of action of bistramide A entails severing of filamentous actin and covalent protein modification. Proc Natl Acad Sci U S A. 2008 Mar 18; 105(11):4088-92.
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Synthesis and evaluation of 18F- and 11C-labeled phenyl-galactopyranosides as potential probes for in vivo visualization of LacZ gene expression using positron emission tomography. Bioconjug Chem. 2008 Feb; 19(2):441-9.
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Structure of bistramide A-actin complex at a 1.35 angstroms resolution. J Am Chem Soc. 2006 Mar 29; 128(12):3882-3.
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Prevention and control of influenza. Recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR Recomm Rep. 2002 Apr 12; 51(RR-3):1-31.
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Selective inhibition of thromboxane A2 biosynthesis in blood platelets. Nature. 1977 Jun 16; 267(5612):627-8.
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A potent inhibitor of thromboxane A2 biosynthesis in aggregating human blood platelets. Pharmacol Res Commun. 1977 Feb; 9(2):109-16.