Fenchone

Fenchone is a lipid of Prenol Lipids (PR) class.

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Current reference collection contains 404 references associated with Fenchone in LipidPedia. Due to lack of full text of references or no associated biomedical terms are recognized in our current text-mining method, we cannot extract any biomedical terms related to diseases, pathways, locations, functions, genes, lipids, and animal models from the associated reference collection.

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Authors Title Published Journal PubMed Link
Rolim TL et al. Toxicity and antitumor potential of Mesosphaerum sidifolium (Lamiaceae) oil and fenchone, its major component. 2017 BMC Complement Altern Med pmid:28673306
Marumoto S et al. Inhibition of β-Secretase Activity by Monoterpenes, Sesquiterpenes, and C13 Norisoprenoids. 2017 J Oleo Sci pmid:28381772
Simon C et al. Screening of endocrine activity of compounds migrating from plastic baby bottles using a multi-receptor panel of in vitro bioassays. 2016 Toxicol In Vitro pmid:27633901
Over B et al. Natural-product-derived fragments for fragment-based ligand discovery. 2013 Nat Chem pmid:23247173
Nakahashi H et al. Biotransformation of (+)-fenchone by Salmonella typhimurium OY1002/2A6 expressing human CYP2A6 and NADPH-P450 reductase. 2013 J Oleo Sci pmid:23648403
Zheljazkov VD et al. Distillation time modifies essential oil yield, composition, and antioxidant capacity of fennel (Foeniculum vulgare Mill). 2013 J Oleo Sci pmid:24005011
Ceacero-Vega AA et al. Kinetics and mechanisms of the tropospheric reactions of menthol, borneol, fenchol, camphor, and fenchone with hydroxyl radicals (OH) and chlorine atoms (Cl). 2012 J Phys Chem A pmid:22448964
Walch SG et al. Holistic Control of Herbal Teas and Tinctures Based on Sage (Salvia officinalis L.) for Compounds with Beneficial and Adverse Effects using NMR Spectroscopy. 2012 Anal Chem Insights pmid:22493561
Messaoud C et al. Chemical composition and antioxidant activities of essential oils and methanol extracts of three wild Lavandula L. species. 2012 Nat. Prod. Res. pmid:22117129
Băjan M et al. [Chemical composition of essential oil obtained from Romanian fennel fruits]. 2011 Apr-Jun Rev Med Chir Soc Med Nat Iasi pmid:21870762
Biswas R et al. Thujone-Rich Fraction of Thuja occidentalis Demonstrates Major Anti-Cancer Potentials: Evidences from In Vitro Studies on A375 Cells. 2011 Evid Based Complement Alternat Med pmid:21647317
Shahat AA et al. Chemical composition, antimicrobial and antioxidant activities of essential oils from organically cultivated fennel cultivars. 2011 Molecules pmid:21285921
de Boer HJ et al. Steam sauna and mother roasting in Lao PDR: practices and chemical constituents of essential oils of plant species used in postpartum recovery. 2011 BMC Complement Altern Med pmid:22171719
Isa IM et al. Cobalt(II) selective membrane electrode based on palladium(II) dichloro acetylthiophene fenchone azine. 2011 Talanta pmid:22099672
Miguel MG and Antunes MD Is propolis safe as an alternative medicine? 2011 J Pharm Bioallied Sci pmid:22219581
Gazim ZC et al. Seasonal variation, chemical composition, and analgesic and antimicrobial activities of the essential oil from leaves of Tetradenia riparia (Hochst.) Codd in southern Brazil. 2010 Molecules pmid:20714310
Bohbot JD and Dickens JC Insect repellents: modulators of mosquito odorant receptor activity. 2010 PLoS ONE pmid:20725637
Mothana RA et al. Chemical analysis and biological activity of the essential oils of two endemic Soqotri Commiphora species. 2010 Molecules pmid:20335939
Kasashima Y et al. Iodine-catalyzed synthesis of five-membered cyclic ethers from 1,3-diols under solvent-free conditions. 2009 J Oleo Sci pmid:19584568
Tsiri D et al. Chemosystematic value of the essential oil composition of Thuja species cultivated in Poland-antimicrobial activity. 2009 Molecules pmid:19935470
Lachenmeier DW et al. Long-term stability of thujone, fenchone, and pinocamphone in vintage preban absinthe. 2009 J. Agric. Food Chem. pmid:19256492
Sapra B et al. Percutaneous permeation enhancement by terpenes: mechanistic view. 2008 AAPS J pmid:18446512
Kasashima Y et al. An efficient synthesis of five-membered cyclic ethers from 1,3-diols using molecular iodine as a catalyst. 2008 J Oleo Sci pmid:18622127
Alpagut Y et al. Control of asymmetric biaryl conformations with terpenol moieties: syntheses, structures and energetics of new enantiopure C2-symmetric diols. 2008 Beilstein J Org Chem pmid:18941496
Lachenmeier DW et al. Chemical composition of vintage preban absinthe with special reference to thujone, fenchone, pinocamphone, methanol, copper, and antimony concentrations. 2008 J. Agric. Food Chem. pmid:18419128
Shiraiwa T Multimodal chemosensory integration through the maxillary palp in Drosophila. 2008 PLoS ONE pmid:18478104
Miyazawa M and Gyoubu K Metabolism of (-)-fenchone by CYP2A6 and CYP2B6 in human liver microsomes. 2007 Xenobiotica pmid:17484521
Lans C et al. Ethnoveterinary medicines used for ruminants in British Columbia, Canada. 2007 J Ethnobiol Ethnomed pmid:17324258
Ozcan MM et al. Comparative essential oil composition and antifungal effect of bitter fennel (Foeniculum vulgare ssp. piperitum) fruit oils obtained during different vegetation. 2006 J Med Food pmid:17201644
Longhi G et al. Fenchone, camphor, 2-methylenefenchone and 2-methylenecamphor: a vibrational circular dichroism study. 2006 J Phys Chem A pmid:16610813
Miyazawa M and Gyoubu K Metabolism of (+)-fenchone by CYP2A6 and CYP2B6 in human liver microsomes. 2006 Biol. Pharm. Bull. pmid:17142962
Kop-Weiershausen T et al. An exceptional P-H phosphonite: biphenyl-2,2'-bisfenchylchlorophosphite and derived ligands (BIFOPs) in enantioselective copper-catalyzed 1,4-additions. 2005 Beilstein J Org Chem pmid:16542019
Chiang LC et al. Antiviral activities of extracts and selected pure constituents of Ocimum basilicum. 2005 Clin. Exp. Pharmacol. Physiol. pmid:16173941
Lee HS Acaricidal activity of constituents identified in Foeniculum vulgare fruit oil against Dermatophagoides spp. (Acari: Pyroglyphidae). 2004 J. Agric. Food Chem. pmid:15137830
Steuer B and Schulz H Near-infrared analysis of fennel (Foeniculum vulgare Miller) on different spectrometers--basic considerations for a reliable network. 2003 Sep-Oct Phytochem Anal pmid:14516000
Nuessli J et al. Crystal structure of amylose complexes with small ligands. 2003 Int. J. Biol. Macromol. pmid:14607368
de la Moya Cerero S et al. C10-substituted camphors and fenchones by electrophilic treatment of 2-methylenenorbornan-1-ols: enantiospecificity, scope, and limitations. 2003 J. Org. Chem. pmid:12585887
Bulman Page PC et al. Asymmetric electrophilic amination of various carbon nucleophiles with enantiomerically pure chiral N-h oxaziridines derived from camphor and fenchone. 2002 J. Org. Chem. pmid:12398504
Vokou D et al. Activation of soil respiration and shift of the microbial population balance in soil as a response to Lavandula stoechas essential oil. 2002 J. Chem. Ecol. pmid:12035924
Kim DH et al. Repellent activity of constituents identified in Foeniculum vulgare fruit against Aedes aegypti (Diptera: Culicidae). 2002 J. Agric. Food Chem. pmid:12428949
Prasad S and Mitra S Role of protein and substrate dynamics in catalysis by Pseudomonas putida cytochrome P450cam. 2002 Biochemistry pmid:12463748
Kim DH and Ahn YJ Contact and fumigant activities of constituents of Foeniculum vulgare fruit against three coleopteran stored-product insects. 2001 Pest Manag. Sci. pmid:11455661
Goldfuss B et al. Rationalization of enantioselectivities in dialkylzinc additions to benzaldehyde catalyzed by fenchone derivatives. 2000 J. Org. Chem. pmid:10813898
Simándi B et al. Supercritical carbon dioxide extraction and fractionation of fennel oil. 1999 J. Agric. Food Chem. pmid:10564030
Bondavalli F et al. N'-acyl-N,N-(1,3,3-trimethylbicyclo [2.2.1]hept-2-ylidene)benzamidines with hypotensive activity. 1987 Farmaco Sci pmid:3609291
Bondavalli F et al. Esters of N-methyl-N-(2-hydroxyethyl or 3-hydroxypropyl)-1,3,3-trimethylbicyclo [2.2.1]heptan-2-endo-amine with hypotensive activity. 1987 Farmaco Sci pmid:3653384
Croteau R et al. Biosynthesis of monoterpenes: conversion of the acyclic precursors geranyl pyrophosphate and neryl pyrophosphate to the rearranged monoterpenes fenchol and fenchone by a soluble enzyme preparation from fennel (Foeniculum vulgare). 1980 Arch. Biochem. Biophys. pmid:7436420
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