 Monoterpenes
"Monoterpenes" 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.
Compounds with a core of 10 carbons generally formed via the mevalonate pathway from the combination of 3,3-dimethylallyl pyrophosphate and isopentenyl pyrophosphate. They are cyclized and oxidized in a variety of ways. Due to the low molecular weight many of them exist in the form of essential oils (OILS, VOLATILE).
| Descriptor ID |
D039821
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| MeSH Number(s) |
D02.455.849.575
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Monoterpenes".
Below are MeSH descriptors whose meaning is more specific than "Monoterpenes".
This graph shows the total number of publications written about "Monoterpenes" by people in this website by year, and whether "Monoterpenes" 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 |
|---|
| 1999 | 1 | 0 | 1 | | 2002 | 1 | 0 | 1 | | 2003 | 1 | 0 | 1 | | 2005 | 1 | 1 | 2 | | 2008 | 2 | 0 | 2 | | 2009 | 0 | 1 | 1 | | 2011 | 0 | 1 | 1 | | 2016 | 1 | 0 | 1 | | 2019 | 1 | 1 | 2 |
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Below are the most recent publications written about "Monoterpenes" by people in Profiles.
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Ye Q, Wang M, Hofbauer V, Stolzenburg D, Chen D, Schervish M, Vogel A, Mauldin RL, Baalbaki R, Brilke S, Dada L, Dias A, Duplissy J, El Haddad I, Finkenzeller H, Fischer L, He X, Kim C, Kürten A, Lamkaddam H, Lee CP, Lehtipalo K, Leiminger M, Manninen HE, Marten R, Mentler B, Partoll E, Petäjä T, Rissanen M, Schobesberger S, Schuchmann S, Simon M, Tham YJ, Vazquez-Pufleau M, Wagner AC, Wang Y, Wu Y, Xiao M, Baltensperger U, Curtius J, Flagan R, Kirkby J, Kulmala M, Volkamer R, Winkler PM, Worsnop D, Donahue NM. Molecular Composition and Volatility of Nucleated Particles from a-Pinene Oxidation between -50 °C and +25 °C. Environ Sci Technol. 2019 Nov 05; 53(21):12357-12365.
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Brandt K, Dötterl S, Fuchs R, Navarro DMDAF, Machado ICS, Dobler D, Reiser O, Ayasse M, Milet-Pinheiro P. Subtle Chemical Variations with Strong Ecological Significance: Stereoselective Responses of Male Orchid Bees to Stereoisomers of Carvone Epoxide. J Chem Ecol. 2019 Jun; 45(5-6):464-473.
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Trowbridge AM, Bowers MD, Monson RK. Conifer Monoterpene Chemistry during an Outbreak Enhances Consumption and Immune Response of an Eruptive Folivore. J Chem Ecol. 2016 Dec; 42(12):1281-1292.
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Shrestha M, Zhang Y, Upshur MA, Liu P, Blair SL, Wang HF, Nizkorodov SA, Thomson RJ, Martin ST, Geiger FM. On surface order and disorder of a-pinene-derived secondary organic material. J Phys Chem A. 2015 May 14; 119(19):4609-17.
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Epstein SA, Blair SL, Nizkorodov SA. Direct photolysis of a-pinene ozonolysis secondary organic aerosol: effect on particle mass and peroxide content. Environ Sci Technol. 2014 Oct 07; 48(19):11251-8.
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Prado R, Francis SO, Mason MN, Wing G, Gamble RG, Dellavalle R. Nonmelanoma skin cancer chemoprevention. Dermatol Surg. 2011 Nov; 37(11):1566-78.
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Ziemann PJ. Atmospheric chemistry: Thwarting the seeds of clouds. Nature. 2009 Sep 17; 461(7262):353-4.
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Sakulyanontvittaya T, Guenther A, Helmig D, Milford J, Wiedinmyer C. Secondary organic aerosol from sesquiterpene and monoterpene emissions in the United States. Environ Sci Technol. 2008 Dec 01; 42(23):8784-90.
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Sakulyanontvittaya T, Duhl T, Wiedinmyer C, Helmig D, Matsunaga S, Potosnak M, Milford J, Guenther A. Monoterpene and sesquiterpene emission estimates for the United States. Environ Sci Technol. 2008 Mar 01; 42(5):1623-9.
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Medina AL, Lucero ME, Holguin FO, Estell RE, Posakony JJ, Simon J, O'Connell MA. Composition and Antimicrobial Activity of Anemopsis californica leaf oil. J Agric Food Chem. 2005 Nov 02; 53(22):8694-8.
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