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sinapaldehyde  (MedChemExpress)


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    Structured Review

    MedChemExpress sinapaldehyde
    The changes of monolignol metabolites of (A) the debarked stems on Populus trichocarpa and (B) the stems on Eucalyptus grandis after one month of ASAP treatment. (C) Lignin deposition on roots and the changes of monolignol metabolites on stems and leaves of Solanum lycopersicum (tomato) after 24 hours of ASAP treatment. Ten monolignol metabolites were quantified using LC-SRM-MS analysis. Metabolites in the main fluxes of H-lignin, G-lignin and S-lignin biosynthesis are represented. The detected compounds were highlighted, pink for significant up-regulation, dark grey for no significant change, light grey for no detection. C-Aci, caffeic acid; G-Aci, ferulic acid; 5H-Aci, 5-hydroxyferulic acid; S-Aci, sinapic acid; G-Ald, coniferaldehyde; 5H-Ald, 5-hydroxyconiferaldehyde; S-Ald, <t>sinapaldehyde;</t> H-Alc, 4-coumaryl alcohol; G-Alc, coniferyl alcohol; S-Alc, sinapyl alcohol. Lignin staining using 5% phloroglucinol in ethanol for tomato roots. The lignified tissues were showed as the pink-red coloration. Three individual plants were performed as biological replicates for each treatment.
    Sinapaldehyde, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 93/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/sinapaldehyde/product/MedChemExpress
    Average 93 stars, based on 2 article reviews
    sinapaldehyde - by Bioz Stars, 2026-02
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    Images

    1) Product Images from "A Sap Peptide Conserved across Flowering Plants Positively Regulates Lignin Biosynthesis, Biomass and Immunity"

    Article Title: A Sap Peptide Conserved across Flowering Plants Positively Regulates Lignin Biosynthesis, Biomass and Immunity

    Journal: bioRxiv

    doi: 10.1101/2024.05.20.594799

    The changes of monolignol metabolites of (A) the debarked stems on Populus trichocarpa and (B) the stems on Eucalyptus grandis after one month of ASAP treatment. (C) Lignin deposition on roots and the changes of monolignol metabolites on stems and leaves of Solanum lycopersicum (tomato) after 24 hours of ASAP treatment. Ten monolignol metabolites were quantified using LC-SRM-MS analysis. Metabolites in the main fluxes of H-lignin, G-lignin and S-lignin biosynthesis are represented. The detected compounds were highlighted, pink for significant up-regulation, dark grey for no significant change, light grey for no detection. C-Aci, caffeic acid; G-Aci, ferulic acid; 5H-Aci, 5-hydroxyferulic acid; S-Aci, sinapic acid; G-Ald, coniferaldehyde; 5H-Ald, 5-hydroxyconiferaldehyde; S-Ald, sinapaldehyde; H-Alc, 4-coumaryl alcohol; G-Alc, coniferyl alcohol; S-Alc, sinapyl alcohol. Lignin staining using 5% phloroglucinol in ethanol for tomato roots. The lignified tissues were showed as the pink-red coloration. Three individual plants were performed as biological replicates for each treatment.
    Figure Legend Snippet: The changes of monolignol metabolites of (A) the debarked stems on Populus trichocarpa and (B) the stems on Eucalyptus grandis after one month of ASAP treatment. (C) Lignin deposition on roots and the changes of monolignol metabolites on stems and leaves of Solanum lycopersicum (tomato) after 24 hours of ASAP treatment. Ten monolignol metabolites were quantified using LC-SRM-MS analysis. Metabolites in the main fluxes of H-lignin, G-lignin and S-lignin biosynthesis are represented. The detected compounds were highlighted, pink for significant up-regulation, dark grey for no significant change, light grey for no detection. C-Aci, caffeic acid; G-Aci, ferulic acid; 5H-Aci, 5-hydroxyferulic acid; S-Aci, sinapic acid; G-Ald, coniferaldehyde; 5H-Ald, 5-hydroxyconiferaldehyde; S-Ald, sinapaldehyde; H-Alc, 4-coumaryl alcohol; G-Alc, coniferyl alcohol; S-Alc, sinapyl alcohol. Lignin staining using 5% phloroglucinol in ethanol for tomato roots. The lignified tissues were showed as the pink-red coloration. Three individual plants were performed as biological replicates for each treatment.

    Techniques Used: Staining

    The changes of monolignol metabolites on (A) the debarked stems of Populus trichocarpa and (B) the stems of Eucalyptus grandis with different concentrations (0.1 μM, 0.5 μM and 1 μM) of ASAP treatment after one month, and (C) the leaves and (D) the stems of Solanum lycopersicum (tomato) with 1 μM ASAP treatment after 24 hours. Ten monolignol metabolites were quantified using LC-SRM-MS analysis. Metabolites in the main fluxes of H-lignin, G-lignin and S-lignin biosynthesis are represented. The detected compounds were highlighted, pink for significant up-regulation, dark grey for no significant change, light grey for no detection. C-Aci, caffeic acid; G-Aci, ferulic acid; 5H-Aci, 5-hydroxyferulic acid; S-Aci, sinapic acid; G-Ald, coniferaldehyde; 5H-Ald, 5-hydroxyconiferaldehyde; S-Ald, sinapaldehyde; H-Alc, 4-coumaryl alcohol; G-Alc, coniferyl alcohol; S-Alc, sinapyl alcohol. One and two asterisks represent Student’s t -test p < 0.05 and 0.01, respectively. Three individual plants were performed as biological replicates for each treatment.
    Figure Legend Snippet: The changes of monolignol metabolites on (A) the debarked stems of Populus trichocarpa and (B) the stems of Eucalyptus grandis with different concentrations (0.1 μM, 0.5 μM and 1 μM) of ASAP treatment after one month, and (C) the leaves and (D) the stems of Solanum lycopersicum (tomato) with 1 μM ASAP treatment after 24 hours. Ten monolignol metabolites were quantified using LC-SRM-MS analysis. Metabolites in the main fluxes of H-lignin, G-lignin and S-lignin biosynthesis are represented. The detected compounds were highlighted, pink for significant up-regulation, dark grey for no significant change, light grey for no detection. C-Aci, caffeic acid; G-Aci, ferulic acid; 5H-Aci, 5-hydroxyferulic acid; S-Aci, sinapic acid; G-Ald, coniferaldehyde; 5H-Ald, 5-hydroxyconiferaldehyde; S-Ald, sinapaldehyde; H-Alc, 4-coumaryl alcohol; G-Alc, coniferyl alcohol; S-Alc, sinapyl alcohol. One and two asterisks represent Student’s t -test p < 0.05 and 0.01, respectively. Three individual plants were performed as biological replicates for each treatment.

    Techniques Used:



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    Image Search Results


    The changes of monolignol metabolites of (A) the debarked stems on Populus trichocarpa and (B) the stems on Eucalyptus grandis after one month of ASAP treatment. (C) Lignin deposition on roots and the changes of monolignol metabolites on stems and leaves of Solanum lycopersicum (tomato) after 24 hours of ASAP treatment. Ten monolignol metabolites were quantified using LC-SRM-MS analysis. Metabolites in the main fluxes of H-lignin, G-lignin and S-lignin biosynthesis are represented. The detected compounds were highlighted, pink for significant up-regulation, dark grey for no significant change, light grey for no detection. C-Aci, caffeic acid; G-Aci, ferulic acid; 5H-Aci, 5-hydroxyferulic acid; S-Aci, sinapic acid; G-Ald, coniferaldehyde; 5H-Ald, 5-hydroxyconiferaldehyde; S-Ald, sinapaldehyde; H-Alc, 4-coumaryl alcohol; G-Alc, coniferyl alcohol; S-Alc, sinapyl alcohol. Lignin staining using 5% phloroglucinol in ethanol for tomato roots. The lignified tissues were showed as the pink-red coloration. Three individual plants were performed as biological replicates for each treatment.

    Journal: bioRxiv

    Article Title: A Sap Peptide Conserved across Flowering Plants Positively Regulates Lignin Biosynthesis, Biomass and Immunity

    doi: 10.1101/2024.05.20.594799

    Figure Lengend Snippet: The changes of monolignol metabolites of (A) the debarked stems on Populus trichocarpa and (B) the stems on Eucalyptus grandis after one month of ASAP treatment. (C) Lignin deposition on roots and the changes of monolignol metabolites on stems and leaves of Solanum lycopersicum (tomato) after 24 hours of ASAP treatment. Ten monolignol metabolites were quantified using LC-SRM-MS analysis. Metabolites in the main fluxes of H-lignin, G-lignin and S-lignin biosynthesis are represented. The detected compounds were highlighted, pink for significant up-regulation, dark grey for no significant change, light grey for no detection. C-Aci, caffeic acid; G-Aci, ferulic acid; 5H-Aci, 5-hydroxyferulic acid; S-Aci, sinapic acid; G-Ald, coniferaldehyde; 5H-Ald, 5-hydroxyconiferaldehyde; S-Ald, sinapaldehyde; H-Alc, 4-coumaryl alcohol; G-Alc, coniferyl alcohol; S-Alc, sinapyl alcohol. Lignin staining using 5% phloroglucinol in ethanol for tomato roots. The lignified tissues were showed as the pink-red coloration. Three individual plants were performed as biological replicates for each treatment.

    Article Snippet: Nine standards were purchased, including caffeic acid (98%, AK Scientific), ferulic acid (99%, Acros Organics), 4-coumaryl alcohol (98%, Toronto Research Chemicals), coniferaldehyde (99.94%, MedChemExpress), coniferyl alcohol (97.5%, Supelco Merck), 5-hydroxyferulic acid (95%, Sigma-Aldrich Merck), sinapic acid (98%, AK Scientific), sinapaldehyde (99.96%, MedChemExpress) and sinapyl alcohol (95%, Biosynth).

    Techniques: Staining

    The changes of monolignol metabolites on (A) the debarked stems of Populus trichocarpa and (B) the stems of Eucalyptus grandis with different concentrations (0.1 μM, 0.5 μM and 1 μM) of ASAP treatment after one month, and (C) the leaves and (D) the stems of Solanum lycopersicum (tomato) with 1 μM ASAP treatment after 24 hours. Ten monolignol metabolites were quantified using LC-SRM-MS analysis. Metabolites in the main fluxes of H-lignin, G-lignin and S-lignin biosynthesis are represented. The detected compounds were highlighted, pink for significant up-regulation, dark grey for no significant change, light grey for no detection. C-Aci, caffeic acid; G-Aci, ferulic acid; 5H-Aci, 5-hydroxyferulic acid; S-Aci, sinapic acid; G-Ald, coniferaldehyde; 5H-Ald, 5-hydroxyconiferaldehyde; S-Ald, sinapaldehyde; H-Alc, 4-coumaryl alcohol; G-Alc, coniferyl alcohol; S-Alc, sinapyl alcohol. One and two asterisks represent Student’s t -test p < 0.05 and 0.01, respectively. Three individual plants were performed as biological replicates for each treatment.

    Journal: bioRxiv

    Article Title: A Sap Peptide Conserved across Flowering Plants Positively Regulates Lignin Biosynthesis, Biomass and Immunity

    doi: 10.1101/2024.05.20.594799

    Figure Lengend Snippet: The changes of monolignol metabolites on (A) the debarked stems of Populus trichocarpa and (B) the stems of Eucalyptus grandis with different concentrations (0.1 μM, 0.5 μM and 1 μM) of ASAP treatment after one month, and (C) the leaves and (D) the stems of Solanum lycopersicum (tomato) with 1 μM ASAP treatment after 24 hours. Ten monolignol metabolites were quantified using LC-SRM-MS analysis. Metabolites in the main fluxes of H-lignin, G-lignin and S-lignin biosynthesis are represented. The detected compounds were highlighted, pink for significant up-regulation, dark grey for no significant change, light grey for no detection. C-Aci, caffeic acid; G-Aci, ferulic acid; 5H-Aci, 5-hydroxyferulic acid; S-Aci, sinapic acid; G-Ald, coniferaldehyde; 5H-Ald, 5-hydroxyconiferaldehyde; S-Ald, sinapaldehyde; H-Alc, 4-coumaryl alcohol; G-Alc, coniferyl alcohol; S-Alc, sinapyl alcohol. One and two asterisks represent Student’s t -test p < 0.05 and 0.01, respectively. Three individual plants were performed as biological replicates for each treatment.

    Article Snippet: Nine standards were purchased, including caffeic acid (98%, AK Scientific), ferulic acid (99%, Acros Organics), 4-coumaryl alcohol (98%, Toronto Research Chemicals), coniferaldehyde (99.94%, MedChemExpress), coniferyl alcohol (97.5%, Supelco Merck), 5-hydroxyferulic acid (95%, Sigma-Aldrich Merck), sinapic acid (98%, AK Scientific), sinapaldehyde (99.96%, MedChemExpress) and sinapyl alcohol (95%, Biosynth).

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