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161
datasets available to search
ShareScore release 0.9.0
Dataset results
161 results for “Acorus calamus”
Acorus calamus L. (BR0000012303021)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Acorus calamus L. (BR0000011301875)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Acorus calamus L. (BR0000011300823)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Acorus calamus L. (BR0000011300359)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Acorus calamus L. (BR0000011300755)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Acorus calamus L. (BR0000021325069)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Acorus calamus L. (BR0000021325076)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Acorus calamus L. (BR0000011301547)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Acorus calamus L. (BR0000005396290)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Acorus calamus L. (BR0000012331185)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Acorus calamus L. (BR0000011300298)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Fig. 3 in Identification and characterization of three nearly identical linalool/ nerolidol synthase from Acorus calamus
Fig. 3. GC-MS of the products generated in vitro from Acorus calamus rhizomes cell-free extracts (protein crude extracts). (A) A. calamus rhizome protein crude extracts enzyme assay using GPP as substrate. (B) A. calamus rhizome protein crude extracts enzyme assay using FPP. (C) A. calamus rhizome protein crude extracts enzyme assay using NPP.
Fig. 2 in Identification and characterization of three nearly identical linalool/ nerolidol synthase from Acorus calamus
Fig. 2. GC-MS of the products generated in vitro from Acorus calamus leaves cell-free extracts (protein crude extracts). (A) A. calamus leaves protein crude extracts enzyme assay using GPP as substrate. (B) A. calamus leaves protein crude extracts enzyme assay using FPP. (C) A. calamus leaves protein crude extracts enzyme assay using NPP.
Fig. 6 in Identification and characterization of three nearly identical linalool/ nerolidol synthase from Acorus calamus
Fig. 6. Expression patterns of AcTPS genes in different tissues of Acorus calamus. Quantification of AcTPSs transcript levels by real-time RT-PCR analysis normalized to actin transcripts. All analyses were performed using three biological replicates.
Fig. 5 in Identification and characterization of three nearly identical linalool/ nerolidol synthase from Acorus calamus
Fig. 5. Analyses of products formed by AcTPS enzymes from geranyl diphosphate (GPP) and farnesyl diphosphate (FPP). GC-MS analysis of products formed by recombinant AcTPS3, AcTPS4, and AcTPS5 from GPP (A–C), from FPP (E–F), respectively. (D, H) GC-MS chromatograms of the products formed by extracts of Escherichia coli expressing the pEXP5 vector without an insert (control) in the presence of GPP (D) and FPP (H), respectively.
Fig. 1 in Identification and characterization of three nearly identical linalool/ nerolidol synthase from Acorus calamus
Fig. 1. The most abundant terpenes and phenylpropanoids in Acorus calamus leaves and rhizomes. (A) The level of terpenes founds only in A. calamus leaves. (B) The level of terpenes founds only in A. calamus rhizomes. (C) The level of most abundant terpenes founds in A. calamus leaves and rhizomes. (D) The level of phenylpropanoids founds only in A. calamus leaves and rhizomes. All analyses were performed using ten biological replicates. Columns marked with different letters differ significantly at P <0.05 (Tukey–Kramer HSD means comparison test). All analyses were performed using five biological replicates.
Fig. 2 in The asarone-derived phenylpropanoids from the rhizome of Acorus calamus var. angustatus Besser
Fig. 2. (A) Chiral HPLC profiles of compound 8a and 8b [Column: UniChiral OD-5H; Column size: 5 μm, 4.6 × 250 mm; Mobile phase: 90% n-hexane/10% ethanol (v/v); Flow rate: 1.0 mL/min; Wave length: UV 310 nm; Temperature: 25 ̊C.]; (B) calculated and experimental ECD spectra of 8a and 8b; (C) ΔδH(S−R) values (ppm, in pyridine-d5) obtained for the MTPA esters 8a.
Fig. 3. 1H in The asarone-derived phenylpropanoids from the rhizome of Acorus calamus var. angustatus Besser
Fig. 3. 1H NMR Spectrum of Z-to-E conversion of compound 2b after 10 days storage in CDCl3 solution at ambient temperature under daylight conditions.
Fig. 4 in The asarone-derived phenylpropanoids from the rhizome of Acorus calamus var. angustatus Besser
Fig. 4. Effects of compounds 1–9 and stiripentol (STP) in human neuroblastoma cell SH-SY5Y. (A) Effects of compounds 1–9 and STP on cell viability in SH-SY5Y were measured by a CCK-8 assay. (B) Effects of 1–9 and STP on Lactate dehydrogenase (LDH) release in H2O2-injured SH-SY5Y. The results are expressed as mean ± SEM (n = 8). *p <0.05 and **p <0.01, compared with H2O2 group; #p <0.05, compared with the control.
Fig. 1 in The asarone-derived phenylpropanoids from the rhizome of Acorus calamus var. angustatus Besser
Fig. 1. Chemical structures of compounds 1–20 (Green: undescribed compounds; Pink: previously described compounds with further structural analysis; '*': compounds were isolated from Acorus calamus var. angustatus Besser for the first time).
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