(+)-3-Carene

(+)-3-carene is a lipid of Prenol Lipids (PR) class.

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There are no associated biomedical information in the current reference collection.

Current reference collection contains 304 references associated with (+)-3-Carene 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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All references with (+)-3-Carene

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Authors Title Published Journal PubMed Link
Falk A et al. Human exposure to 3-carene by inhalation: toxicokinetics, effects on pulmonary function and occurrence of irritative and CNS symptoms. 1991 Toxicol. Appl. Pharmacol. pmid:1891768
Ma Y et al. Mechanisms for the formation of organic acids in the gas-phase ozonolysis of 3-carene. 2009 Phys Chem Chem Phys pmid:19458820
Wang JL et al. Evaluation of monoterpenes for the control of Tribolium castaneum (Herbst) and Sitophilus zeamaise Motschulsky. 2009 Nat. Prod. Res. pmid:19662572
Zécri FJ et al. Pyrazole derived from (+)-3-carene; a novel potent, selective scaffold for sphingosine-1-phosphate (S1P(1)) receptor agonists. 2010 Bioorg. Med. Chem. Lett. pmid:19954976
Nair LG et al. A facile and efficient synthesis of 3,3-dimethyl isopropylidene proline from (+)-3-carene. 2010 J. Org. Chem. pmid:20108962
Lu M et al. Complex interactions among host pines and fungi vectored by an invasive bark beetle. 2010 New Phytol. pmid:20546136
Zhao T et al. The influence of Ceratocystis polonica inoculation and methyl jasmonate application on terpene chemistry of Norway spruce, Picea abies. 2010 Phytochemistry pmid:20557909
Lu TJ and Lin CK Asymmetric synthesis of α-methyl-α-amino acids via diastereoselective alkylation of (1S)-(+)-3-carene derived tricyclic iminolactone. 2011 J. Org. Chem. pmid:21306163
Hall DE et al. An integrated genomic, proteomic and biochemical analysis of (+)-3-carene biosynthesis in Sitka spruce (Picea sitchensis) genotypes that are resistant or susceptible to white pine weevil. 2011 Plant J. pmid:21323772
Gholivand MB et al. Determination of the chemical composition and in vitro antioxidant activities of essential oil and methanol extracts of Echinophora platyloba DC. 2011 Nat. Prod. Res. pmid:21644173
Lehnert N et al. Bioconversion of car-3-ene by a dioxygenase of Pleurotus sapidus. 2012 J. Biotechnol. pmid:21723336
Medini H et al. Chemical composition and antioxidant activity of the essential oil of Juniperus phoenicea L. berries. 2011 Nat. Prod. Res. pmid:21838538
Aazza S et al. Antioxidant and antiacetylcholinesterase activities of some commercial essential oils and their major compounds. 2011 Molecules pmid:21900869
Olounladé PA et al. In vitro anthelmintic activity of the essential oils of Zanthoxylum zanthoxyloides and Newbouldia laevis against Strongyloides ratti. 2012 Parasitol. Res. pmid:21960378
Kurttio P et al. Mutagenic compounds in wood-chip drying fumes. 1990 Mutat. Res. pmid:2202897
Danielsson M et al. Chemical and transcriptional responses of Norway spruce genotypes with different susceptibility to Heterobasidion spp. infection. 2011 BMC Plant Biol. pmid:22067529
Lu M et al. Do novel genotypes drive the success of an invasive bark beetle-fungus complex? Implications for potential reinvasion. 2011 Ecology pmid:22164824
Dvorakova M et al. Biotransformation of (1S)-2-carene and (1S)-3-carene by Picea abies suspension culture. 2011 Molecules pmid:22183881
Saverini M et al. Genotoxicity of citrus wastewater in prokaryotic and eukaryotic cells and efficiency of heterogeneous photocatalysis by TiO(2). 2012 J. Photochem. Photobiol. B, Biol. pmid:22257631
Cano-Ramírez C et al. Electrophysiological and behavioral responses of the bark beetle Dendroctonus rhizophagus to volatiles from host pines and conspecifics. 2012 J. Chem. Ecol. pmid:22544334