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Chenomx Inc nmr suite version 10 0 software
Nmr Suite Version 10 0 Software, supplied by Chenomx Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/nmr+software/chenomx+nmr+suite/pm42116468-116-7-12
Average 86 stars, based on 1 article reviews
nmr suite version 10 0 software - by Bioz Stars, 2026-09
86/100 stars

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Labeling:

Article Title: Effects of Clinacanthus nutans leaf extract on lipopolysaccharide -induced neuroinflammation in rats: A behavioral and 1 H NMR-based metabolomics study
Article Snippet: .. Identified metabolites were labeled and assigned based on similarity search using the Chenomx NMR software database and accessible metabolomic databases, such as HMDB (http://www.hmdb.ca), METLIN (http://metlin.scripps.edu), and KEGG (http://www.kegg.jp). ..

Nuclear Magnetic Resonance:

Article Title: Effects of Clinacanthus nutans leaf extract on lipopolysaccharide -induced neuroinflammation in rats: A behavioral and 1 H NMR-based metabolomics study
Article Snippet: .. Identified metabolites were labeled and assigned based on similarity search using the Chenomx NMR software database and accessible metabolomic databases, such as HMDB (http://www.hmdb.ca), METLIN (http://metlin.scripps.edu), and KEGG (http://www.kegg.jp). ..

Article Title: Quantification of whisky congeners by 1 H NMR spectroscopy
Article Snippet: .. The main issue that complicates quantitative analysis of whisky compounds – an overlap of NMR signals – was addressed by using Chenomx NMR software, which provided reliable deconvolution of resolved, but overlapping signals. ..

Article Title: Gut Microbiota-Derived Propionate Regulates the Expression of Reg3 Mucosal Lectins and Ameliorates Experimental Colitis in Mice
Article Snippet: Analysis of short-chain fatty acids SCFA levels from caecal contents and faeces were determined by 1 H-NMR spectroscopy using a UNITY INOVA 600 NMR spectrometer [Varian] as previously described. .. 32 Spectra were analysed using the Chenomx NMR software. ..

Article Title: Metabolomic profiling reveals muscle metabolic changes following iliac arteriovenous fistula creation in mice.
Article Snippet: For peaks with overlap, Chenomx Suite 8.6 NMR software (Chenomx, Edmonton, AB, Canada) was used to determine concentrations. .. Previously published work (5, 24, 27, 28), Chenomx Suite 8.6 NMR software, the biological magnetic resonance bank (29), and a set of 2-D spectra were used to assign and verify metabolite identity (see Supplemental Figs. S4, S5, S6, and S7). ..

Software:

Article Title: Effects of Clinacanthus nutans leaf extract on lipopolysaccharide -induced neuroinflammation in rats: A behavioral and 1 H NMR-based metabolomics study
Article Snippet: .. Identified metabolites were labeled and assigned based on similarity search using the Chenomx NMR software database and accessible metabolomic databases, such as HMDB (http://www.hmdb.ca), METLIN (http://metlin.scripps.edu), and KEGG (http://www.kegg.jp). ..

Article Title: Quantification of whisky congeners by 1 H NMR spectroscopy
Article Snippet: .. The main issue that complicates quantitative analysis of whisky compounds – an overlap of NMR signals – was addressed by using Chenomx NMR software, which provided reliable deconvolution of resolved, but overlapping signals. ..

Article Title: Gut Microbiota-Derived Propionate Regulates the Expression of Reg3 Mucosal Lectins and Ameliorates Experimental Colitis in Mice
Article Snippet: Analysis of short-chain fatty acids SCFA levels from caecal contents and faeces were determined by 1 H-NMR spectroscopy using a UNITY INOVA 600 NMR spectrometer [Varian] as previously described. .. 32 Spectra were analysed using the Chenomx NMR software. ..

Article Title: Metabolomic profiling reveals muscle metabolic changes following iliac arteriovenous fistula creation in mice.
Article Snippet: For peaks with overlap, Chenomx Suite 8.6 NMR software (Chenomx, Edmonton, AB, Canada) was used to determine concentrations. .. Previously published work (5, 24, 27, 28), Chenomx Suite 8.6 NMR software, the biological magnetic resonance bank (29), and a set of 2-D spectra were used to assign and verify metabolite identity (see Supplemental Figs. S4, S5, S6, and S7). ..

Metabolomic:

Article Title: Effects of Clinacanthus nutans leaf extract on lipopolysaccharide -induced neuroinflammation in rats: A behavioral and 1 H NMR-based metabolomics study
Article Snippet: .. Identified metabolites were labeled and assigned based on similarity search using the Chenomx NMR software database and accessible metabolomic databases, such as HMDB (http://www.hmdb.ca), METLIN (http://metlin.scripps.edu), and KEGG (http://www.kegg.jp). ..

other:

Article Title: Metabolomics Analyses from Tissues in Parkinson’s disease
Article Snippet: 1 1 The identification of metabolites in a 1D 1H NMR spectrum is performed with software programs such as Chenomx.

Article Title: NMR Metabolomics Show Evidence for Mitochondrial Oxidative Stress in a Mouse Model of Polycystic Ovary Syndrome
Article Snippet: NMR signals arising from small metabolites (<1000 Da) were identified and quantified relative to formate (1 mM) as the internal reference by Chenomx software version 6 ( http://www.chenomx.com ).

Article Title: Metabolomics of the Protective Effect of Ampelopsis grossedentata and Its Major Active Compound Dihydromyricetin on the Liver of High-Fat Diet Hamster
Article Snippet: Fourier transformation, phase adjustment, and baseline correction of the 1 H NMR free induction decay (FID) signal was done with Chenomx NMR suit (version 8.1, Chenomx, Edmonton, Canada).

Article Title: Metabolic Reprogramming by 3-Iodothyronamine (T1AM): A New Perspective to Reverse Obesity through Co-Regulation of Sirtuin 4 and 6 Expression
Article Snippet: NMR signals arising from small water-soluble metabolites (<1000 Da) were identified and quantified relative to formate (1 mM) as the internal reference by Chenomx software version 6 ( http://www.chenomx.com ).



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Glucose metabolism is the main pathway for aryl hydrocarbon receptor (AhR) activation to down-regulate the neutrophil elastase (NE) activity. (a) The diagram of glucose metabolism. (b-e) The neutrophils were treated with FICZ (100 nM), DIM (10 μM) or CH223191 (10 μM) at the present or absence of lipopolysaccharide (LPS, 10 μg/mL) or phorbol-12-myristate-13-acetate (PMA, 50 nM). The levels of Magt1, Magt 2, Magt 4, Magt5 and glutamine-fructose-6-phosphate transaminase (GFPT) were detected. (f-j) The neutrophils were treated with FICZ (100 nM) at the present or absence of LPS (10 μg/mL), and the intracellular metabolites were detected using a high-resolution <t>nuclear</t> <t>magnetic</t> resonance <t>(NMR).</t> The results were analyzed by PCA (f) , PLS (g) , OPLS (h) , KEGG enrichment analysis (i) and cluster analysis (j) . (k, l) The neutrophils were treated with FICZ (100 nM), DIM (10 μM) or CH223191 (10 μM) at the present or absence of LPS (10 μg/mL) or PMA (50 nM). The relative glucose uptake (k) and intracellular pH values (l) were determined. (m, n) The neutrophils were treated with FICZ (100 nM) or DIM (10 μM) alone or in combination with L-sodium lactate (20 mM), ATP (100 μM) or GlcNAc (20 mM) at the present or absence of LPS (10 μg/mL) or PMA (50 nM), and the release of dsDNA (m) and NE activity (n) was determined. The data were presented as the means ± S.E.M. of three or five independent experiments. ## p < 0.01 vs. Control group; * p < 0.05, ** p < 0.01 vs. LPS group; $$ p < 0.01 vs. LPS + FICZ group; ++ p < 0.01 vs. LPS + DIM group.
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Image Search Results


Glucose metabolism is the main pathway for aryl hydrocarbon receptor (AhR) activation to down-regulate the neutrophil elastase (NE) activity. (a) The diagram of glucose metabolism. (b-e) The neutrophils were treated with FICZ (100 nM), DIM (10 μM) or CH223191 (10 μM) at the present or absence of lipopolysaccharide (LPS, 10 μg/mL) or phorbol-12-myristate-13-acetate (PMA, 50 nM). The levels of Magt1, Magt 2, Magt 4, Magt5 and glutamine-fructose-6-phosphate transaminase (GFPT) were detected. (f-j) The neutrophils were treated with FICZ (100 nM) at the present or absence of LPS (10 μg/mL), and the intracellular metabolites were detected using a high-resolution nuclear magnetic resonance (NMR). The results were analyzed by PCA (f) , PLS (g) , OPLS (h) , KEGG enrichment analysis (i) and cluster analysis (j) . (k, l) The neutrophils were treated with FICZ (100 nM), DIM (10 μM) or CH223191 (10 μM) at the present or absence of LPS (10 μg/mL) or PMA (50 nM). The relative glucose uptake (k) and intracellular pH values (l) were determined. (m, n) The neutrophils were treated with FICZ (100 nM) or DIM (10 μM) alone or in combination with L-sodium lactate (20 mM), ATP (100 μM) or GlcNAc (20 mM) at the present or absence of LPS (10 μg/mL) or PMA (50 nM), and the release of dsDNA (m) and NE activity (n) was determined. The data were presented as the means ± S.E.M. of three or five independent experiments. ## p < 0.01 vs. Control group; * p < 0.05, ** p < 0.01 vs. LPS group; $$ p < 0.01 vs. LPS + FICZ group; ++ p < 0.01 vs. LPS + DIM group.

Journal: Journal of Advanced Research

Article Title: Aryl hydrocarbon receptor impairs HK2-controlled flux of the hexosamine biosynthesis pathway to suppress NETosis in an N -glycosylation-dependent manner

doi: 10.1016/j.jare.2025.06.078

Figure Lengend Snippet: Glucose metabolism is the main pathway for aryl hydrocarbon receptor (AhR) activation to down-regulate the neutrophil elastase (NE) activity. (a) The diagram of glucose metabolism. (b-e) The neutrophils were treated with FICZ (100 nM), DIM (10 μM) or CH223191 (10 μM) at the present or absence of lipopolysaccharide (LPS, 10 μg/mL) or phorbol-12-myristate-13-acetate (PMA, 50 nM). The levels of Magt1, Magt 2, Magt 4, Magt5 and glutamine-fructose-6-phosphate transaminase (GFPT) were detected. (f-j) The neutrophils were treated with FICZ (100 nM) at the present or absence of LPS (10 μg/mL), and the intracellular metabolites were detected using a high-resolution nuclear magnetic resonance (NMR). The results were analyzed by PCA (f) , PLS (g) , OPLS (h) , KEGG enrichment analysis (i) and cluster analysis (j) . (k, l) The neutrophils were treated with FICZ (100 nM), DIM (10 μM) or CH223191 (10 μM) at the present or absence of LPS (10 μg/mL) or PMA (50 nM). The relative glucose uptake (k) and intracellular pH values (l) were determined. (m, n) The neutrophils were treated with FICZ (100 nM) or DIM (10 μM) alone or in combination with L-sodium lactate (20 mM), ATP (100 μM) or GlcNAc (20 mM) at the present or absence of LPS (10 μg/mL) or PMA (50 nM), and the release of dsDNA (m) and NE activity (n) was determined. The data were presented as the means ± S.E.M. of three or five independent experiments. ## p < 0.01 vs. Control group; * p < 0.05, ** p < 0.01 vs. LPS group; $$ p < 0.01 vs. LPS + FICZ group; ++ p < 0.01 vs. LPS + DIM group.

Article Snippet: The collected nuclear magnetic resonance (NMR) spectra were analysed using Chenomx NMR Suite software, and statistical analysis with data visualisation was performed using the MetaboAnalyst platform.

Techniques: Activation Assay, Activity Assay, Nuclear Magnetic Resonance, Control