Find research datasets worth reusing

opennotspecifiedJan 2021View details →

Fig. 10. Experiment 3 in Headspace GC-MS analysis of differences in intra- and interspecific Terpene profiles of Picea pungens Engelm. and P. abies (L.) Karst

Fig. 10. Experiment 3, PCA of B1–B11 and N1–N11 run over two days (standardized TIC responses). Circles show 95% confidence limits.

opennotspecifiedJan 2021View details →

Fig. 5. Experiment 1 in Headspace GC-MS analysis of differences in intra- and interspecific Terpene profiles of Picea pungens Engelm. and P. abies (L.) Karst

Fig. 5. Experiment 1, PCA of B1, N1, and C1 over time (standardized TIC responses). Samples were collected and analyzed roughly every week over an 8-month time period (September 2018 through April 2019). Circles show 95% confidence limits.

opennotspecifiedJan 2021View details →

Fig. 8. Experiment 2 in Headspace GC-MS analysis of differences in intra- and interspecific Terpene profiles of Picea pungens Engelm. and P. abies (L.) Karst

Fig. 8. Experiment 2, PCA of B1–B11, N1–N11, and C1 run over two days (standardized TIC responses). Circles show 95% confidence limits.

opennotspecifiedJan 2020View details →

Fig. 3. a in Sequencing and variation of terpene synthase gene (TPS2) as the major gene in biosynthesis of thymol in different Thymus species

Fig. 3. a. Maximum likelihood tree of Thymus species based on 16 sequences of the TPS of cDNA. Numbers above branches are support values from bootstrap resembling. Accession numbers of TPS2 sequences obtained from the NCBI GenBank are shown in parentheses (Accession numbers starting with MH were obtained through this study). For the studied species, the main monoterpenes in the essential oil are included T: Thymol; C: Carvacrol; PC: p-Cymene; AT: α-Terpineol; L: Linalool. b. Dendrogram of nine studied Thymus species using Ward clustering method based on Tohidi et al. (2017).

opennotspecifiedJan 2020View details →

Fig. 2 in Sequencing and variation of terpene synthase gene (TPS2) as the major gene in biosynthesis of thymol in different Thymus species

Fig. 2. Amino acid alignment of Ttps2 sequences of nine studied Thymus species. The four motifs, conserved in all species terpene synthases, are indicated in red (top). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opennotspecifiedJan 2020View details →

Fig. 1 in Sequencing and variation of terpene synthase gene (TPS2) as the major gene in biosynthesis of thymol in different Thymus species

Fig. 1. Predicted biosynthetic pathway of terpene synthases in Thymus genus leading to the formation of α-terpineol and γ-terpinene, the precursor of thymol and carvacrol Adapted from Lima et al. (2013).

ClinicalTrials.gov32/100

Potential Benefits of Dietary Advices Alone or Associated to Nutraceutical Food Supplements Argan Oil, VSL#3 Probiotic Blend, 5203-L Fruit Extract Terpene

ClinicalTrials.gov study NCT01069445. IPD Sharing: Not stated. Countries: 1. Publications: 6.

restrictedIPD-UNDECIDEDFeb 2026View details →

dryad28/100

Data from: Cannabis labelling is associated with genetic variation in terpene synthase genes

<p>Genetic data consisting of >100,000 single nucleotide polymorphisms (SNPs) collected using genotype-by-sequencing, from 137 drug-type Cannabis samples from the Netherlands. This genetic data along with terpene and cannabinoid content data collected with GC-FID, was used to analyze Cannabis labelling and to perfom a genome-wide association study.</p>

opencc-zeroJul 2021View details →

opencc-by-4.0Jan 2023View details →

Solvent spotlight: Terpenes limonene and p-cymene

<p>Information about the use and properties of bio-based solvents limonene and p-cymene.</p>

opennotspecifiedApr 2022View details →

Fig. 2 in Chemical diversity of k¯anuka: Inter- and intraspecific variation of foliage terpenes and flavanones of Kunzea (Myrtaceae) in Aotearoa/New Zealand

Fig. 2. Sites of Kunzea collections used in this study.

Fig. 8 in Terpene Shikimate conjugated meroterpenoids from the endophytic fungus Guignardia mangiferae

Fig. 8. ΔδH(S-R) value of MTPA esters of 6 in CDCl3.

Fig. 5 in Terpene Shikimate conjugated meroterpenoids from the endophytic fungus Guignardia mangiferae

Fig. 5. Experimental Mo2(OCOCH3)4-induced ECD spectrum of 4 in DMSO.

Fig. 4 in Terpene Shikimate conjugated meroterpenoids from the endophytic fungus Guignardia mangiferae

Fig. 4. Experimental ECD spectra of mangnardones A D (1–4) in MeOH.

Fig. 1 in Terpene Shikimate conjugated meroterpenoids from the endophytic fungus Guignardia mangiferae

Fig. 1. Chemical structures of compounds 1–18.

Fig. 7 in Terpene Shikimate conjugated meroterpenoids from the endophytic fungus Guignardia mangiferae

Fig. 7. Experimental ECD spectra of mangnardones F–H (6–9) in MeOH.

Fig. 3 in Terpene Shikimate conjugated meroterpenoids from the endophytic fungus Guignardia mangiferae

Fig. 3. Key NOESY correlations of compounds 1, 3, 6, and 9.

Fig. 2. Key 1H–1H in Terpene Shikimate conjugated meroterpenoids from the endophytic fungus Guignardia mangiferae

Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1, 3, 6, and 9.

Fig. 9. X in Terpene Shikimate conjugated meroterpenoids from the endophytic fungus Guignardia mangiferae

Fig. 9. X-ray ORTEP drawing of 9.