Calixarenes

"Calixarenes" 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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

Phenolic metacyclophanes derived from condensation of PHENOLS and ALDEHYDES. The name derives from the vase-like molecular structures. A bracketed [n] indicates the number of aromatic rings.

Descriptor ID

D047250

MeSH Number(s)

D04.345.025

Concept/Terms

Calixarenes

Below are MeSH descriptors whose meaning is more general than "Calixarenes".

Chemicals and Drugs [D]
Polycyclic Compounds [D04]
Macrocyclic Compounds [D04.345]
Calixarenes [D04.345.025]

Below are MeSH descriptors whose meaning is related to "Calixarenes".

Below are MeSH descriptors whose meaning is more specific than "Calixarenes".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Calixarenes" by people in Harvard Catalyst Profiles by year, and whether "Calixarenes" was a major or minor topic of these publication.

Bar chart showing 3 publications over 1 distinct years, with a maximum of 3 publications in 2005

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
2005	3	0	3

Below are the most recent publications written about "Calixarenes" by people in Profiles.

Halogen bonding for molecular recognition: new developments in materials and biological sciences. Chem Commun (Camb). 2020 May 07; 56(37):4970-4981.

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Molecular Containers Bind Drugs of Abuse in Vitro and Reverse the Hyperlocomotive Effect of Methamphetamine in Rats. Chembiochem. 2017 08 17; 18(16):1583-1588.

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Supramolecular Guest-Host Interactions for the Preparation of Biomedical Materials. Bioconjug Chem. 2015 Dec 16; 26(12):2279-89.

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Polymorphism control of an active pharmaceutical ingredient beneath calixarene-based Langmuir monolayers. Chem Commun (Camb). 2014 Apr 18; 50(30):3938-40.

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Guest covalent capture by a host: a biomimetic strategy for the selective functionalization of a cavity. Chemistry. 2013 Jan 07; 19(2):642-53.

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On the role of flexibility in protein-ligand interactions: the example of p53 tetramerization domain. Chem Asian J. 2011 Jun 06; 6(6):1463-9.

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Water-soluble calix[4]resorcinarenes as chiral NMR solvating agents for bicyclic aromatic compounds. Chirality. 2009 Nov; 21(10):911-21.

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Nanoporous crystals of calixarene/porphyrin supramolecular complex functionalized by diffusion and coordination of metal ions. J Am Chem Soc. 2009 Feb 25; 131(7):2487-9.

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Stability and structural recovery of the tetramerization domain of p53-R337H mutant induced by a designed templating ligand. Proc Natl Acad Sci U S A. 2008 Oct 28; 105(43):16426-31.

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Noncovalent synthesis in aqueous solution and spectroscopic characterization of multi-porphyrin complexes. Chemistry. 2006 Mar 20; 12(10):2722-9.

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J Am Chem Soc
Chemistry
Chem Commun (Camb)
Proc Natl Acad Sci U S A
Org Lett
Oncogene
J Org Chem
Chirality
Chem Asian J
Bioconjug Chem