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48 results for “Monoterpene”
Fig. 1 in Leaf isoprene and monoterpene emission distribution across hyperdominant tree genera in the Amazon basin
Fig. 1. Images of the coupled leaf portable photosynthesis (Li6400XT) and volatile emission autosampler (Less-P) system developed in this study for the combined analysis of net photosynthesis and volatile isoprenoid emissions at remote field site locations in the Amazon forest.
Fig. 4 in Leaf isoprene and monoterpene emission distribution across hyperdominant tree genera in the Amazon basin
Fig. 4. Maximum leaf isoprenoid emissions from the light response curve data showing (a) maximum isoprenoid emissions for species where emissions were detected and (b) a histogram representing the distribution of maximum leaf isoprenoid emissions.
Absorption and Bioavailability of Major Monoterpenes in Mastiha Oil; a Kinetic Study in Humans.
ClinicalTrials.gov study NCT04290312. IPD Sharing: NO. Countries: 1. Publications: 8.
Functional investigation of monoterpenes for improved understanding of the relationship between hosts and bark beetle
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Data from: Diversification of the monoterpene synthase gene family (TPSb) in Protium, a highly diverse genus of tropical trees
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Supporting Data for Relative Humidity Effect on the Formation of Highly Oxidized Molecules and New Particles during Monoterpene Oxidation
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Supporting data for: Observations of gas-phase products from the nitrate radical-initiated oxidation of four monoterpenes
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Data from: PbbHLH4 regulates floral monoterpene biosynthesis in Phalaenopsis orchids
Floral scent is an important factor in attracting pollinators and repelling florivores. In Phalaenopsis bellina (Orchidaceae), the major floral scent components are monoterpenoids. Previously, we have identified that expression of GERANYL DIPHOSPHATE SYNTHASE (PbGDPS) is highly correlated with monoterpene biosynthesis in Phalaenosis orchids. Here, we showed that both cis- and trans-regulation were present on the GDPS promoters, with trans-regulation playing a key role. To investigate the regulation of floral scent biosynthesis, we compared the transcriptomic data of two Phalaenopsis orchids with contrasting scent phenotypes. Eight transcription factors (TFs) with sequential elevation expressions through floral development stages in P. bellina were identified, and their transcript levels were higher in the scent orchid than the scentless one. Five of these TFs transactivated several structural genes involved in monoterpene biosynthesis pathway to various extent, including PbbHLH4, PbbHLH6, PbbZIP4, PbERF1, and PbNAC1. Ectopic transient expression of these TFs in scentless orchids revealed that terpenoid biosynthesis was all stimulated. PbbHLH4 most profoundly induced the monoterpene phenotype with a 950-fold increase of monoterpenoid production in the scentless orchid. In conclusion, the orchid floral monoterpenes biosynthesis was regulated sequentially and elaborately, and with PbbHLH4 playing a crucial role for monoterpene phenotype.
Data from: Membrane-assisted extraction of monoterpenes: from in-silico solvent screening towards biotechnological process application
This work focuses on the process development of membrane-assisted solvent extraction of hydrophobic compounds such as monoterpenes. Beginning with the choice of suitable solvents, quantum chemical calculations with the simulation tool COSMO-RS were carried out to predict the partition coefficient (logP) of (S)-(+)-carvone and terpinen-4-ol in various solvent-water systems and validated afterwards with experimental data. COSMO-RS results show good prediction accuracy for nonpolar solvents like n-hexane, ethyl acetate and n-heptane even in the presence of salts and glycerol in aqueous medium. Based on the high logP value, n-heptane was chosen for the extraction of (S)-(+)-carvone in a lab-scale hollow-fiber membrane contactor. Two operation modes are investigated where experimental and theoretical mass transfer values, based on their related partition coefficients were compared. In addition, the process is evaluated in terms of extraction efficiency and overall product recovery, and its biotechnological application potential discussed. Our work demonstrates that the combination of in-silico prediction by COSMO-RS with membrane-assisted extraction is a promising approach for the recovery of hydrophobic compounds from aqueous solutions.
Electric-Field Catalysis on Carbon Nanotubes in Electromicrofluidic Reactors: Monoterpene Cyclizations: Original Data
<p>Original data underlying the publication. Data are assembled according to the supporting information.</p>
Fig. 1 in Monoterpene indole alkaloids from Vinca minor L. (Apocynaceae): Identification of new structural scaffold for treatment of Alzheimer's disease
Fig. 1. Chemical structures of isolated alkaloids from aerial parts of Vinca minor.
Fig. 3 in Acylphloroglucinol-monoterpene meroterpenoids from Eucalyptus tereticornis and their inhibitory activity against ATP citrate lyase
Fig. 3. Key NOESY correlations of 1 and 2.
Fig. 2. Key 1H–1H in Acylphloroglucinol-monoterpene meroterpenoids from Eucalyptus tereticornis and their inhibitory activity against ATP citrate lyase
Fig. 2. Key 1H–1H COSY and HMBC correlations of 1–5.
Fig. 2. 1H–1H in Monoterpene indole alkaloids with diverse skeletons from the stems of Rauvolfia vomitoria and their acetylcholinesterase inhibitory activities
Fig. 2. 1H–1H COSY, key HMBC correlations of 1, 4, and 9.
Fig. 6 in Monoterpene indole alkaloids with diverse skeletons from the stems of Rauvolfia vomitoria and their acetylcholinesterase inhibitory activities
Fig. 6. ORTEP drawing of compound 4.
Fig. 5 in Monoterpene indole alkaloids with diverse skeletons from the stems of Rauvolfia vomitoria and their acetylcholinesterase inhibitory activities
Fig. 5. Comparison of the experimental and calculated ECD spectra of 3.
Fig. 8. Plausible biogenetic pathway for rauvomitorine A in Monoterpene indole alkaloids with diverse skeletons from the stems of Rauvolfia vomitoria and their acetylcholinesterase inhibitory activities
Fig. 8. Plausible biogenetic pathway for rauvomitorine A (1).
Fig. 4 in Monoterpene indole alkaloids with diverse skeletons from the stems of Rauvolfia vomitoria and their acetylcholinesterase inhibitory activities
Fig. 4. Comparison of the experimental ECD spectra of 1 and 18 in MeOH.
Fig. 3 in Monoterpene indole alkaloids with diverse skeletons from the stems of Rauvolfia vomitoria and their acetylcholinesterase inhibitory activities
Fig. 3. Key NOESY correlations of 1, 4, and 9.
Fig. 1 in Monoterpene indole alkaloids with diverse skeletons from the stems of Rauvolfia vomitoria and their acetylcholinesterase inhibitory activities
Fig. 1. Chemical structures of MIAs 1−20.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.