1 h nmr analysis Search Results


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Chem Impex International n n dimethyl formamide dmf
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Daebong LS 1 h nmr spectra
Principal component analysis (PCA) generated with 1 H <t>NMR</t> <t>spectra</t> of peel and pulp extracts collected from five different fruits, demonstrating clear metabolic differentiations between the fruits and between their pulps and peels.
1 H Nmr Spectra, supplied by Daebong LS, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Silatronix Inc 1 h nmr analysis
Principal component analysis (PCA) generated with 1 H <t>NMR</t> <t>spectra</t> of peel and pulp extracts collected from five different fruits, demonstrating clear metabolic differentiations between the fruits and between their pulps and peels.
1 H Nmr Analysis, supplied by Silatronix Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Sequent Scientific 1 h nmr
Principal component analysis (PCA) generated with 1 H <t>NMR</t> <t>spectra</t> of peel and pulp extracts collected from five different fruits, demonstrating clear metabolic differentiations between the fruits and between their pulps and peels.
1 H Nmr, supplied by Sequent Scientific, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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PureCircle Ltd 500-mhz 1 h nmr spectrum of commercial reba
Principal component analysis (PCA) generated with 1 H <t>NMR</t> <t>spectra</t> of peel and pulp extracts collected from five different fruits, demonstrating clear metabolic differentiations between the fruits and between their pulps and peels.
500 Mhz 1 H Nmr Spectrum Of Commercial Reba, supplied by PureCircle Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cambridge Isotope Laboratories 1 h nmr and noesy spectra
Principal component analysis (PCA) generated with 1 H <t>NMR</t> <t>spectra</t> of peel and pulp extracts collected from five different fruits, demonstrating clear metabolic differentiations between the fruits and between their pulps and peels.
1 H Nmr And Noesy Spectra, supplied by Cambridge Isotope Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Gallus BioPharmaceuticals 1 h, 15 n best-trosy nmr spectra
Principal component analysis (PCA) generated with 1 H <t>NMR</t> <t>spectra</t> of peel and pulp extracts collected from five different fruits, demonstrating clear metabolic differentiations between the fruits and between their pulps and peels.
1 H, 15 N Best Trosy Nmr Spectra, supplied by Gallus BioPharmaceuticals, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Pfeuffer GmbH 1 h nmr spectrosocpy
Principal component analysis (PCA) generated with 1 H <t>NMR</t> <t>spectra</t> of peel and pulp extracts collected from five different fruits, demonstrating clear metabolic differentiations between the fruits and between their pulps and peels.
1 H Nmr Spectrosocpy, supplied by Pfeuffer GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Johns Hopkins HealthCare h and c-13 nmr analysis
Principal component analysis (PCA) generated with 1 H <t>NMR</t> <t>spectra</t> of peel and pulp extracts collected from five different fruits, demonstrating clear metabolic differentiations between the fruits and between their pulps and peels.
H And C 13 Nmr Analysis, supplied by Johns Hopkins HealthCare, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cambridge Isotope Laboratories 1 h nmr 500 mhz
Principal component analysis (PCA) generated with 1 H <t>NMR</t> <t>spectra</t> of peel and pulp extracts collected from five different fruits, demonstrating clear metabolic differentiations between the fruits and between their pulps and peels.
1 H Nmr 500 Mhz, supplied by Cambridge Isotope Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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TA Instruments portable 1 h nmr unit
Principal component analysis (PCA) generated with 1 H <t>NMR</t> <t>spectra</t> of peel and pulp extracts collected from five different fruits, demonstrating clear metabolic differentiations between the fruits and between their pulps and peels.
Portable 1 H Nmr Unit, supplied by TA Instruments, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Principal component analysis (PCA) generated with 1 H NMR spectra of peel and pulp extracts collected from five different fruits, demonstrating clear metabolic differentiations between the fruits and between their pulps and peels.

Journal: Current Research in Food Science

Article Title: A strategy for healthy eating habits of daily fruits revisited: A metabolomics study

doi: 10.1016/j.crfs.2023.100440

Figure Lengend Snippet: Principal component analysis (PCA) generated with 1 H NMR spectra of peel and pulp extracts collected from five different fruits, demonstrating clear metabolic differentiations between the fruits and between their pulps and peels.

Article Snippet: 1 H NMR spectra of the secondary metabolites highlighted in peel of Daebong persimmon (A), sweet persimmon (B), grape (C), apple (D), and peach (E).

Techniques: Generated

OPLS-DA score (A, C, E, G, and I) and loading (B, D, F, H, and J) plot generated with 1 H NMR spectra of pulps and peels of Daebong persimmon (A and B), sweet persimmon (C and D), peach (E and F), apple (G and H), and grape (I and J) for comprehensive identification of metabolites that were different between pulps and peels. Ala, alanine; Arg, arginine; Asp, aspartic acid; C, catechin; CGA, chlorogenic acid; nCGA, neochlorogenic acid; EC, epicatechin; EGC, Epigallocatechin; FA, formic acid; Fru, fructose; GA, gallic acid; GABA, gamma-amynobutyric acid; Glc, glucose; Gln, glutamine; K, kaempferol; MA, malic acid; Phz, phloridzin; Pro, proline; Q, quercetin; QD, quercetin derivatives; QG, quercetin glucoside; p -Cou, p -coumaric acid; Rtn, rutin; Suc, sucrose; Thr, threonine; Trg, trigonelline. The upper sections in OPLS-DA loading plots represent relatively higher amounts of metabolites in the peels of each fruits, compared to their pulps (B, D, F, H, and J), whereas the lower sections indicate relatively lower amounts of metabolites in the peels.

Journal: Current Research in Food Science

Article Title: A strategy for healthy eating habits of daily fruits revisited: A metabolomics study

doi: 10.1016/j.crfs.2023.100440

Figure Lengend Snippet: OPLS-DA score (A, C, E, G, and I) and loading (B, D, F, H, and J) plot generated with 1 H NMR spectra of pulps and peels of Daebong persimmon (A and B), sweet persimmon (C and D), peach (E and F), apple (G and H), and grape (I and J) for comprehensive identification of metabolites that were different between pulps and peels. Ala, alanine; Arg, arginine; Asp, aspartic acid; C, catechin; CGA, chlorogenic acid; nCGA, neochlorogenic acid; EC, epicatechin; EGC, Epigallocatechin; FA, formic acid; Fru, fructose; GA, gallic acid; GABA, gamma-amynobutyric acid; Glc, glucose; Gln, glutamine; K, kaempferol; MA, malic acid; Phz, phloridzin; Pro, proline; Q, quercetin; QD, quercetin derivatives; QG, quercetin glucoside; p -Cou, p -coumaric acid; Rtn, rutin; Suc, sucrose; Thr, threonine; Trg, trigonelline. The upper sections in OPLS-DA loading plots represent relatively higher amounts of metabolites in the peels of each fruits, compared to their pulps (B, D, F, H, and J), whereas the lower sections indicate relatively lower amounts of metabolites in the peels.

Article Snippet: 1 H NMR spectra of the secondary metabolites highlighted in peel of Daebong persimmon (A), sweet persimmon (B), grape (C), apple (D), and peach (E).

Techniques: Generated

Representative 1 H NMR spectra of pulps (A) and peels (B) collected from Daebong persimmon. Leu, leucine; Thr, threonine; Ala, alanine; Arg, arginine; GABA, gamma-aminobutyric acid; Gln, glutamine; Glu, glutamic acid; MA, malic acid; SA, succinic acid; Asp, aspartic acid; EtOH, ethanol; Glc, glucose; Suc, sucrose; Fru, fructose; FUA, fumaric acid; GA, gallic acid; Phe, phenylalanine; Trp, tryptophan; GC, gallocatechin; K, kaempferol; Q, quercetin; QD, quercetin derivatives; FA, formic acid.

Journal: Current Research in Food Science

Article Title: A strategy for healthy eating habits of daily fruits revisited: A metabolomics study

doi: 10.1016/j.crfs.2023.100440

Figure Lengend Snippet: Representative 1 H NMR spectra of pulps (A) and peels (B) collected from Daebong persimmon. Leu, leucine; Thr, threonine; Ala, alanine; Arg, arginine; GABA, gamma-aminobutyric acid; Gln, glutamine; Glu, glutamic acid; MA, malic acid; SA, succinic acid; Asp, aspartic acid; EtOH, ethanol; Glc, glucose; Suc, sucrose; Fru, fructose; FUA, fumaric acid; GA, gallic acid; Phe, phenylalanine; Trp, tryptophan; GC, gallocatechin; K, kaempferol; Q, quercetin; QD, quercetin derivatives; FA, formic acid.

Article Snippet: 1 H NMR spectra of the secondary metabolites highlighted in peel of Daebong persimmon (A), sweet persimmon (B), grape (C), apple (D), and peach (E).

Techniques:

OPLS-DA score (A and C) and loading (B and D) plot generated with 1 H NMR spectra of Daebong persimmon pulps and peels for comprehensive identifications of metabolites that were different between before and after postharvest ripening.

Journal: Current Research in Food Science

Article Title: A strategy for healthy eating habits of daily fruits revisited: A metabolomics study

doi: 10.1016/j.crfs.2023.100440

Figure Lengend Snippet: OPLS-DA score (A and C) and loading (B and D) plot generated with 1 H NMR spectra of Daebong persimmon pulps and peels for comprehensive identifications of metabolites that were different between before and after postharvest ripening.

Article Snippet: 1 H NMR spectra of the secondary metabolites highlighted in peel of Daebong persimmon (A), sweet persimmon (B), grape (C), apple (D), and peach (E).

Techniques: Generated

1 H NMR spectra of the secondary metabolites highlighted in peel of Daebong persimmon (A), sweet persimmon (B), grape (C), apple (D), and peach (E). These spectra were plotted after their normalization methanol, and the amounts of secondary metabolites were thus comparable among the fruits. K, kaempferol; Q, Quercetin; QD, quercetin derivatives; QG, quercetin glucoside; CGA, chlorogenic acid; nCGA, neochlorogenic acid; C, catechin; GC, gallocatechin; EC, epicatechin; EGC, epigallocatechin.

Journal: Current Research in Food Science

Article Title: A strategy for healthy eating habits of daily fruits revisited: A metabolomics study

doi: 10.1016/j.crfs.2023.100440

Figure Lengend Snippet: 1 H NMR spectra of the secondary metabolites highlighted in peel of Daebong persimmon (A), sweet persimmon (B), grape (C), apple (D), and peach (E). These spectra were plotted after their normalization methanol, and the amounts of secondary metabolites were thus comparable among the fruits. K, kaempferol; Q, Quercetin; QD, quercetin derivatives; QG, quercetin glucoside; CGA, chlorogenic acid; nCGA, neochlorogenic acid; C, catechin; GC, gallocatechin; EC, epicatechin; EGC, epigallocatechin.

Article Snippet: 1 H NMR spectra of the secondary metabolites highlighted in peel of Daebong persimmon (A), sweet persimmon (B), grape (C), apple (D), and peach (E).

Techniques:

Total phenolics contents (TPC), total flavonoid contents (TFC), scavenging activities against DPPH and ABTS free radicals, and α-amylase inhibitory activity (α-AI) in the pulps and peels from five fruits (A–C) and from Daebong persimmon after postharvest ripening (D). The panel C denotes α-amylase inhibitory activity dependent on concentrations of the Daebong persimmon pulps and Daebong persimmon, sweet persimmon, and grape peels. The panels E, F, G, H, and I demonstrate the differences in the secondary metabolite levels between pulps and peels of Daebong persimmon, sweet persimmon, apple, grape, and peach, respectively, which were calculated by the integral area of 1 H NMR peaks corresponding to the metabolites and expressed as ratio of metabolites to methanol. The panel J shows the changes in the secondary metabolite levels in the pulp, peel, and endocarp of Daebong persimmon before and after postharvest ripening. The panel K shows correlations of secondary metabolites with antioxidant and α-amylase inhibitory activities. Direction and strength of the correlations in the panel B are visualized with an oval shape and a color gradient. †Quercetin, quercetin derivatives and kaempferol were significantly correlated with ABTS and DPPH free radical-scavenging activity in correlation analysis within a single fruit, for example, using only the dataset from the Daebong persimmon pulp and peel ( P < 0.05). GC, gallocatechin; EC, epicatechin; EGC, epigallocatechin; CGA, chlorogenic acid; nCGA, neochlorogenic acid; Phz, phloridzin; QG, quercetin glucoside; p -Cou, p -coumaric acid. *, P < 0.05; **, P < 0.01; ***, P < 0.001. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Journal: Current Research in Food Science

Article Title: A strategy for healthy eating habits of daily fruits revisited: A metabolomics study

doi: 10.1016/j.crfs.2023.100440

Figure Lengend Snippet: Total phenolics contents (TPC), total flavonoid contents (TFC), scavenging activities against DPPH and ABTS free radicals, and α-amylase inhibitory activity (α-AI) in the pulps and peels from five fruits (A–C) and from Daebong persimmon after postharvest ripening (D). The panel C denotes α-amylase inhibitory activity dependent on concentrations of the Daebong persimmon pulps and Daebong persimmon, sweet persimmon, and grape peels. The panels E, F, G, H, and I demonstrate the differences in the secondary metabolite levels between pulps and peels of Daebong persimmon, sweet persimmon, apple, grape, and peach, respectively, which were calculated by the integral area of 1 H NMR peaks corresponding to the metabolites and expressed as ratio of metabolites to methanol. The panel J shows the changes in the secondary metabolite levels in the pulp, peel, and endocarp of Daebong persimmon before and after postharvest ripening. The panel K shows correlations of secondary metabolites with antioxidant and α-amylase inhibitory activities. Direction and strength of the correlations in the panel B are visualized with an oval shape and a color gradient. †Quercetin, quercetin derivatives and kaempferol were significantly correlated with ABTS and DPPH free radical-scavenging activity in correlation analysis within a single fruit, for example, using only the dataset from the Daebong persimmon pulp and peel ( P < 0.05). GC, gallocatechin; EC, epicatechin; EGC, epigallocatechin; CGA, chlorogenic acid; nCGA, neochlorogenic acid; Phz, phloridzin; QG, quercetin glucoside; p -Cou, p -coumaric acid. *, P < 0.05; **, P < 0.01; ***, P < 0.001. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Article Snippet: 1 H NMR spectra of the secondary metabolites highlighted in peel of Daebong persimmon (A), sweet persimmon (B), grape (C), apple (D), and peach (E).

Techniques: Activity Assay