Works matching DE "MONOTERPENOIDS"
Results: 243
Emission patterns of volatile organic compounds from Norway spruce logs following bark beetle (Ips typographus L.) infestation.
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- Tree Physiology, 2025, v. 45, n. 1, p. 1, doi. 10.1093/treephys/tpae152
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Host plants selection of Centranthera grandiflora Benth. and nontargeted metabolomics analysis of its parasitic and non-parasitic samples.
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- PLoS ONE, 2025, v. 20, n. 2, p. 1, doi. 10.1371/journal.pone.0310786
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Transcriptome analysis reveals regulatory mechanism of methyl jasmonate-induced monoterpenoid biosynthesis in Mentha arvensis L.
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- Frontiers in Plant Science, 2025, p. 1, doi. 10.3389/fpls.2024.1517851
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β-Thujaplicin modulates estrogen receptor signaling and inhibits proliferation of human breast cancer cells.
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- Bioscience, Biotechnology & Biochemistry, 2015, v. 79, n. 6, p. 1011, doi. 10.1080/09168451.2015.1008978
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Geissoschizine synthase controls flux in the formation of monoterpenoid indole alkaloids in a Catharanthus roseus mutant.
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- Planta: An International Journal of Plant Biology, 2018, v. 247, n. 3, p. 625, doi. 10.1007/s00425-017-2812-7
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A tabersonine 3-reductase Catharanthus roseus mutant accumulates vindoline pathway intermediates.
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- Planta: An International Journal of Plant Biology, 2018, v. 247, n. 1, p. 155, doi. 10.1007/s00425-017-2775-8
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A novel cinnamyl alcohol dehydrogenase (CAD)-like reductase contributes to the structural diversity of monoterpenoid indole alkaloids in Rauvolfia.
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- Planta: An International Journal of Plant Biology, 2016, v. 243, n. 3, p. 813, doi. 10.1007/s00425-015-2446-6
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Two New Monoterpenoids from the Fresh Leaves of Syringa oblata.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 6, p. 1023, doi. 10.1007/s10600-016-1852-8
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Synthesis and Analgesic Activity of 4,7-Dimethyl-3,4,4a,5,8,8a-Hexahydro-2 H-Chromen-4,8-Diols Containing Thiophene Substituents.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 5, p. 813, doi. 10.1007/s10600-016-1785-2
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A New Monoterpenoid Indole Alkaloid from Tabernaemontana corymbosa.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 269, doi. 10.1007/s10600-016-1611-x
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Synthesis of Derivatives of the Monoterpenoid Pulegone.
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- Chemistry of Natural Compounds, 2015, v. 51, n. 3, p. 488, doi. 10.1007/s10600-015-1321-9
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Analysis of Monoterpenoid Indole Alkaloids Using Electrospray Ionization Tandem Mass Spectrometry.
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- Chemistry of Natural Compounds, 2015, v. 51, n. 1, p. 116, doi. 10.1007/s10600-015-1215-x
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Sulfur-Containing Derivatives of Mono- and Bicyclic Natural Monoterpenoids.
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- Chemistry of Natural Compounds, 2014, v. 50, n. 1, p. 22, doi. 10.1007/s10600-014-0862-7
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Biotransformation of menthol by Chlorella vulgaris and study of the pathways involved.
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- Chemistry of Natural Compounds, 2014, v. 49, n. 6, p. 1160, doi. 10.1007/s10600-014-0849-4
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Aroma volatile compounds in Mussaenda pubescens.
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- Chemistry of Natural Compounds, 2013, v. 49, n. 2, p. 358, doi. 10.1007/s10600-013-0606-0
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Synthesis of new monoterpene sulfonylimidazoles.
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- Chemistry of Natural Compounds, 2012, v. 48, n. 1, p. 38, doi. 10.1007/s10600-012-0153-0
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Monoterpenoid biosynthesis by engineered microbes.
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- Journal of Industrial Microbiology & Biotechnology, 2021, v. 48, n. 9/10, p. 1, doi. 10.1093/jimb/kuab065
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Recent progress in chemistry and bioactivity of monoterpenoid indole alkaloids from the genus gelsemium: a comprehensive review.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2023, v. 38, n. 1, p. 1, doi. 10.1080/14756366.2022.2155639
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New Efficient Approach to the Preparation of (+)-Camphor and (–)-Fenchone Anils under Homogeneous Catalysis Conditions.
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- Doklady Chemistry, 2023, v. 512, n. 1, p. 260, doi. 10.1134/S0012500823600700
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Chiral N-(Octahydro-2H-chromen-4-yl)-2-(dialkylamino)acetamides: Synthesis and Analgesic Activity.
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- Doklady Chemistry, 2023, v. 512, n. 1, p. 242, doi. 10.1134/S0012500823600694
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Continuous ex situ recovery of volatile monoterpenoids produced by genetically engineered Escherichia coli.
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- Canadian Journal of Chemical Engineering, 2022, v. 100, n. 9, p. 2204, doi. 10.1002/cjce.24486
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Multi-omics analysis the differences of VOCs terpenoid synthesis pathway in maintaining obligate mutualism between Ficus hirta Vahl and its pollinators.
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- Frontiers in Plant Science, 2022, v. 13, p. 1, doi. 10.3389/fpls.2022.1006291
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Monoterpenoid aryl hydrocarbon receptor allosteric antagonists protect against ultraviolet skin damage in female mice.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-38478-6
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Plasticity engineering of plant monoterpene synthases and application for microbial production of monoterpenoids.
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- Biotechnology for Biofuels, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s13068-021-01998-8
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Analytical Method for Quantifying Monoterpenoids (p-Cymene and Myrcene) in Nanoemulsions Using High-Performance Liquid Chromatography.
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- Journal of AOAC International, 2024, v. 107, n. 3, p. 506, doi. 10.1093/jaoacint/qsae012
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Monoterpene indole alkaloids from Gelsemium elegans.
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- Natural Product Research, 2025, v. 39, n. 2, p. 233, doi. 10.1080/14786419.2023.2261070
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A new anti-inflammatory thujane monoterpenoid glycoside ester from Pittosporum heterophyllum Franch.
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- Natural Product Research, 2025, v. 39, n. 2, p. 400, doi. 10.1080/14786419.2023.2258541
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New monoterpenoid indole alkaloids from the stems of Tabernaemontana bovina Lour (Apocynaceae).
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- Natural Product Research, 2024, v. 38, n. 14, p. 2447, doi. 10.1080/14786419.2023.2180503
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Synthesis and antifungal activity of monoterpenoids of the carane series.
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- Pharmaceutical Chemistry Journal, 2012, v. 45, n. 11, p. 664, doi. 10.1007/s11094-012-0699-y
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Structure of [Pd(HL)Cl] and [Pd(HL)Cl]•0.5CHCl compounds with chiral bis-α-sulfanyl oxime, a derivative of natural monoterpenoid (+)-3-carene (Hl).
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- Journal of Structural Chemistry, 2015, v. 56, n. 5, p. 919, doi. 10.1134/S0022476615050145
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Chemical compositions of essential oils from two Artemisia species used in Mongolian traditional medicine.
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- Mongolian Journal of Chemistry, 2017, v. 18, n. 44, p. 48, doi. 10.5564/mjc.v18i44.881
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Natural Compounds with Antifungal Properties against Candida albicans and Identification of Hinokitiol as a Promising Antifungal Drug.
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- Antibiotics (2079-6382), 2023, v. 12, n. 11, p. 1603, doi. 10.3390/antibiotics12111603
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Synthesis and Antimicrobial Activity of Sulfenimines Based on Pinane Hydroxythiols.
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- Antibiotics (2079-6382), 2022, v. 11, n. 11, p. 1548, doi. 10.3390/antibiotics11111548
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Conjugates of Bispidine and Monoterpenoids as Ligands of Metal Complex Catalysts for the Henry Reaction.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 11, p. 1969, doi. 10.1134/S1070428020110123
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Stereoselective synthesis of amino ketones of the pinane series.
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- Russian Journal of Organic Chemistry, 2015, v. 51, n. 7, p. 1030, doi. 10.1134/S1070428015070246
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Synthesis and Properties of New Conjugates of Isatin and Bicyclic Monoterpenes.
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- Russian Journal of General Chemistry, 2024, v. 94, n. 1, p. 81, doi. 10.1134/S1070363224010080
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Synergistic Toxicity Interactions between Plant Essential Oil Components against the Common Bed Bug (Cimex lectularius L.).
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- Insects (2075-4450), 2020, v. 11, n. 2, p. 133, doi. 10.3390/insects11020133
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essential oil proile Melissa.
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- Aromatherapy Today, 2012, v. 55, p. 2
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A tissue-specific profile of miRNAs and their targets related to paeoniaflorin and monoterpenoids biosynthesis in Paeonia lactiflora Pall. by transcriptome, small RNAs and degradome sequencing.
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- PLoS ONE, 2023, v. 17, n. 1, p. 1, doi. 10.1371/journal.pone.0279992
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- Article
Acute Toxicity, Synergistic and Antagonistic Effects of 12 Monoterpenoids Against the Poratrioza sinica Yang et Li (Hemiptera: Psyllidae).
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- Pakistan Journal of Zoology, 2024, v. 56, n. 1, p. 225, doi. 10.17582/journal.pjz/20211022051038
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A comparative study of monoterpenoids and phenylpropanoids from essential oils against stored grain insects: acute toxins or feeding deterrents.
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- Journal of Pest Science, 2017, v. 90, n. 2, p. 531, doi. 10.1007/s10340-016-0800-5
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Monoterpenes Released from Fruit, Plant, and Vegetable Systems.
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- Sensors (14248220), 2014, v. 14, n. 10, p. 18286, doi. 10.3390/s141018286
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The Tunisian Artemisia Essential Oil for Reducing Contamination of Stored Cereals by Tribolium castaneum.
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- Food Technology & Biotechnology, 2018, v. 56, n. 2, p. 247, doi. 10.17113/ftb.56.02.18.5414
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Harvest time on the content and chemical composition of essential oil from leaves of guava.
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- Ciência Rural, 2016, v. 46, n. 10, p. 1771, doi. 10.1590/0103-8478cr20150947
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- Article
1,8-Cineole blocks voltage-gated L-type calcium channels in tracheal smooth muscle.
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- Pflügers Archiv: European Journal of Physiology, 2018, v. 470, n. 12, p. 1803, doi. 10.1007/s00424-018-2201-5
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Biotransformation of (-)-verbenone by some fungi.
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- Journal of Chemical Research, 2011, v. 35, n. 3, p. 133, doi. 10.3184/174751911X12964930076764
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- Article
Calcium and oxidative stress mediate perillaldehyde-induced apoptosis in Candida albicans.
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- Applied Microbiology & Biotechnology, 2017, v. 101, n. 8, p. 3335, doi. 10.1007/s00253-017-8146-3
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Prokaryotic squalene-hopene cyclases can be converted to citronellal cyclases by single amino acid exchange.
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- Applied Microbiology & Biotechnology, 2013, v. 97, n. 4, p. 1571, doi. 10.1007/s00253-012-4008-1
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Flavour-active wine yeasts.
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- Applied Microbiology & Biotechnology, 2012, v. 96, n. 3, p. 601, doi. 10.1007/s00253-012-4370-z
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- Article
Biologically active terpenoid constituents from shoot cultures of Carpesium divaricatum.
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- Biotechnologia, 2018, v. 99, n. 3, p. 264
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