 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 | | 2004 | 0 | 1 | 1 | | 2005 | 1 | 1 | 2 | | 2009 | 0 | 1 | 1 | | 2011 | 1 | 1 | 2 | | 2013 | 0 | 1 | 1 | | 2016 | 1 | 1 | 2 | | 2018 | 1 | 0 | 1 | | 2019 | 1 | 1 | 2 | | 2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Monoterpenes" by people in Profiles.
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Coggon MM, Gkatzelis GI, McDonald BC, Gilman JB, Schwantes RH, Abuhassan N, Aikin KC, Arend MF, Berkoff TA, Brown SS, Campos TL, Dickerson RR, Gronoff G, Hurley JF, Isaacman-VanWertz G, Koss AR, Li M, McKeen SA, Moshary F, Peischl J, Pospisilova V, Ren X, Wilson A, Wu Y, Trainer M, Warneke C. Volatile chemical product emissions enhance ozone and modulate urban chemistry. Proc Natl Acad Sci U S A. 2021 08 10; 118(32).
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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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Zhang H, Yee LD, Lee BH, Curtis MP, Worton DR, Isaacman-VanWertz G, Offenberg JH, Lewandowski M, Kleindienst TE, Beaver MR, Holder AL, Lonneman WA, Docherty KS, Jaoui M, Pye HOT, Hu W, Day DA, Campuzano-Jost P, Jimenez JL, Guo H, Weber RJ, de Gouw J, Koss AR, Edgerton ES, Brune W, Mohr C, Lopez-Hilfiker FD, Lutz A, Kreisberg NM, Spielman SR, Hering SV, Wilson KR, Thornton JA, Goldstein AH. Monoterpenes are the largest source of summertime organic aerosol in the southeastern United States. Proc Natl Acad Sci U S A. 2018 02 27; 115(9):2038-2043.
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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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Kirkby J, Duplissy J, Sengupta K, Frege C, Gordon H, Williamson C, Heinritzi M, Simon M, Yan C, Almeida J, Tröstl J, Nieminen T, Ortega IK, Wagner R, Adamov A, Amorim A, Bernhammer AK, Bianchi F, Breitenlechner M, Brilke S, Chen X, Craven J, Dias A, Ehrhart S, Flagan RC, Franchin A, Fuchs C, Guida R, Hakala J, Hoyle CR, Jokinen T, Junninen H, Kangasluoma J, Kim J, Krapf M, Kürten A, Laaksonen A, Lehtipalo K, Makhmutov V, Mathot S, Molteni U, Onnela A, Peräkylä O, Piel F, Petäjä T, Praplan AP, Pringle K, Rap A, Richards NA, Riipinen I, Rissanen MP, Rondo L, Sarnela N, Schobesberger S, Scott CE, Seinfeld JH, Sipilä M, Steiner G, Stozhkov Y, Stratmann F, Tomé A, Virtanen A, Vogel AL, Wagner AC, Wagner PE, Weingartner E, Wimmer D, Winkler PM, Ye P, Zhang X, Hansel A, Dommen J, Donahue NM, Worsnop DR, Baltensperger U, Kulmala M, Carslaw KS, Curtius J. Ion-induced nucleation of pure biogenic particles. Nature. 2016 05 26; 533(7604):521-6.
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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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Reilly JM, Telezhkin V, Passmore GM, Marsh SJ, Brown DA. Kv7/M-type potassium channels in rat skin keratinocytes. Pflugers Arch. 2013 Sep; 465(9):1371-81.
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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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