Pyrroles
"Pyrroles" 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.
Azoles of one NITROGEN and two double bonds that have aromatic chemical properties.
Descriptor ID |
D011758
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MeSH Number(s) |
D03.383.129.578
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Pyrroles".
Below are MeSH descriptors whose meaning is more specific than "Pyrroles".
This graph shows the total number of publications written about "Pyrroles" by people in this website by year, and whether "Pyrroles" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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1993 | 0 | 1 | 1 | 2000 | 0 | 1 | 1 | 2001 | 0 | 1 | 1 | 2003 | 1 | 0 | 1 | 2004 | 0 | 1 | 1 | 2007 | 3 | 0 | 3 | 2008 | 2 | 1 | 3 | 2009 | 1 | 0 | 1 | 2010 | 3 | 1 | 4 | 2011 | 4 | 0 | 4 | 2012 | 1 | 0 | 1 | 2013 | 3 | 0 | 3 | 2014 | 2 | 0 | 2 | 2015 | 1 | 1 | 2 |
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Below are the most recent publications written about "Pyrroles" by people in Profiles.
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Crafter C, Vincent JP, Tang E, Dudley P, James NH, Klinowska T, Davies BR. Combining AZD8931, a novel EGFR/HER2/HER3 signalling inhibitor, with AZD5363 limits AKT inhibitor induced feedback and enhances antitumour efficacy in HER2-amplified breast cancer models. Int J Oncol. 2015 Aug; 47(2):446-54.
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Gherbi K, May LT, Baker JG, Briddon SJ, Hill SJ. Negative cooperativity across ß1-adrenoceptor homodimers provides insights into the nature of the secondary low-affinity CGP 12177 ß1-adrenoceptor binding conformation. FASEB J. 2015 Jul; 29(7):2859-71.
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Gherbi K, Briddon SJ, Hill SJ. Detection of the secondary, low-affinity ß1 -adrenoceptor site in living cells using the fluorescent CGP 12177 derivative BODIPY-TMR-CGP. Br J Pharmacol. 2014 Dec; 171(23):5431-45.
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Park S, Yang G, Madduri N, Abidian MR, Majd S. Hydrogel-mediated direct patterning of conducting polymer films with multiple surface chemistries. Adv Mater. 2014 May; 26(18):2782-7.
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Ou Z, Meng D, Yuan M, Huang W, Fang Y, Kadish KM. Deprotonation reactions and electrochemistry of substituted open-chain pentapyrroles and sapphyrins in basic nonaqueous media. J Phys Chem B. 2013 Oct 31; 117(43):13646-57.
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Yuan M, Ou Z, Fang Y, Huang S, Xue Z, Lu G, Kadish KM. Synthesis, characterization, protonation reactions, and electrochemistry of substituted open-chain pentapyrroles and sapphyrins in nonaqueous media. Inorg Chem. 2013 Jun 03; 52(11):6664-73.
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Hong CM, Statsyuk AV. The development of a one pot, regiocontrolled, three-component reaction for the synthesis of thieno[2,3-c]pyrroles. Org Biomol Chem. 2013 May 14; 11(18):2932-5.
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Gorski A, Gawinkowski S, Herbich J, Krauss O, Brutschy B, Thummel RP, Waluk J. 1H-pyrrolo[3,2-h]quinoline: a benchmark molecule for reliable calculations of vibrational frequencies, IR intensities, and Raman activities. J Phys Chem A. 2012 Dec 06; 116(48):11973-86.
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Lee JT, Chae DH, Ou Z, Kadish KM, Yao Z, Sessler JL. Unconventional Kondo effect in redox active single organic macrocyclic transistors. J Am Chem Soc. 2011 Dec 07; 133(48):19547-52.
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Pejo E, Cotten JF, Kelly EW, Le Ge R, Cuny GD, Laha JK, Liu J, Lin XJ, Raines DE. In vivo and in vitro pharmacological studies of methoxycarbonyl-carboetomidate. Anesth Analg. 2012 Aug; 115(2):297-304.
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