3-Hydroxyl kyneurenine
                        Formula: C10H12N2O4 (224.0797)
                        
                        Chinese Name:  3-羟基-DL-犬尿素, DL-3-羟基犬尿素, 3-羟基犬尿氨酸
                        BioDeep ID: BioDeep_00000001751 
                        ( View LC/MS Profile)
                        SMILES:  C1=CC(=C(C(=C1)O)N)C(=O)CC(C(=O)O)N
                    
Found 12 Sample Hits
| m/z | Adducts | Species | Organ | Scanning | Sample | |
|---|---|---|---|---|---|---|
| 224.1001 | [M-H2O+NH4]+PPM:12.8 | 
                                    Marker Pen | NA | DESI (None) | 
                                        3ul_0.8Mpa_RAW_20241016-PAPER PNMK - MEMI_testResolution: 30μm, 315x42
                                             By writing the four English letters “PNMK” on white paper with a marker pen, and then scanning with a DESI ion source to obtain the scanning result. The signal of the chemical substances on the marker pen used appears on the channel with an m/z value of   | 
                                    
                                        
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| 207.0788 | [M+H-H2O]+PPM:11.5 | 
                                    Plant | Root | MALDI (DHB) | 
                                        MPIMM_035_QE_P_PO_6pm - MPIMM_035_QE_P_PO_6pmResolution: 30μm, 165x170
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| 224.105 | [M-H2O+NH4]+PPM:9.1 | 
                                    Plant | Root | MALDI (DHB) | 
                                        MPIMM_035_QE_P_PO_6pm - MPIMM_035_QE_P_PO_6pmResolution: 30μm, 165x170
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| 225.0898 | [M+H]+PPM:12.5 | 
                                    Plant | Root | MALDI (DHB) | 
                                        MPIMM_035_QE_P_PO_6pm - MPIMM_035_QE_P_PO_6pmResolution: 30μm, 165x170
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| 224.106 | [M-H2O+NH4]+PPM:13.5 | 
                                    Homo sapiens | Liver | MALDI (DHB) | 
                                        20171107_FIT4_DHBpos_p70_s50 - Rappez et al (2021) SpaceM reveals metabolic states of single cellsResolution: 50μm, 70x70
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| 207.0769 | [M+H-H2O]+PPM:2.3 | 
                                    Homo sapiens | esophagus | DESI () | 
                                        LNTO22_1_4 - MTBLS385Resolution: 17μm, 82x80
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| 224.1034 | [M-H2O+NH4]+PPM:1.9 | 
                                    Homo sapiens | esophagus | DESI () | 
                                        LNTO22_1_4 - MTBLS385Resolution: 17μm, 82x80
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| 242.118 | [M+NH4]+PPM:18.5 | 
                                    Homo sapiens | esophagus | DESI () | 
                                        LNTO22_1_4 - MTBLS385Resolution: 17μm, 82x80
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| 207.0787 | [M+H-H2O]+PPM:11 | 
                                    Mus musculus | Liver | MALDI (CHCA) | 
                                        Salmonella_final_pos_recal - MTBLS2671Resolution: 17μm, 691x430
                                             A more complete and holistic view on host–microbe interactions is needed to understand the physiological and cellular barriers that affect the efficacy of drug treatments and allow the discovery and development of new therapeutics. Here, we developed a multimodal imaging approach combining histopathology with mass spectrometry imaging (MSI) and same section imaging mass cytometry (IMC) to study the effects of Salmonella Typhimurium infection in the liver of a mouse model using the S. Typhimurium strains SL3261 and SL1344. This approach enables correlation of tissue morphology and specific cell phenotypes with molecular images of tissue metabolism. IMC revealed a marked increase in immune cell markers and localization in immune aggregates in infected tissues. A correlative computational method (network analysis) was deployed to find metabolic features associated with infection and revealed metabolic clusters of acetyl carnitines, as well as phosphatidylcholine and phosphatidylethanolamine plasmalogen species, which could be associated with pro-inflammatory immune cell types. By developing an IMC marker for the detection of Salmonella LPS, we were further able to identify and characterize those cell types which contained S. Typhimurium.
[dataset] Nicole Strittmatter. Holistic Characterization of a Salmonella Typhimurium Infection Model Using Integrated Molecular Imaging, metabolights_dataset, V1; 2022. https://www.ebi.ac.uk/metabolights/MTBLS2671.  | 
                                    
                                        
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| 225.089 | [M+H]+PPM:9 | 
                                    Mus musculus | Liver | MALDI (CHCA) | 
                                        Salmonella_final_pos_recal - MTBLS2671Resolution: 17μm, 691x430
                                             A more complete and holistic view on host–microbe interactions is needed to understand the physiological and cellular barriers that affect the efficacy of drug treatments and allow the discovery and development of new therapeutics. Here, we developed a multimodal imaging approach combining histopathology with mass spectrometry imaging (MSI) and same section imaging mass cytometry (IMC) to study the effects of Salmonella Typhimurium infection in the liver of a mouse model using the S. Typhimurium strains SL3261 and SL1344. This approach enables correlation of tissue morphology and specific cell phenotypes with molecular images of tissue metabolism. IMC revealed a marked increase in immune cell markers and localization in immune aggregates in infected tissues. A correlative computational method (network analysis) was deployed to find metabolic features associated with infection and revealed metabolic clusters of acetyl carnitines, as well as phosphatidylcholine and phosphatidylethanolamine plasmalogen species, which could be associated with pro-inflammatory immune cell types. By developing an IMC marker for the detection of Salmonella LPS, we were further able to identify and characterize those cell types which contained S. Typhimurium.
[dataset] Nicole Strittmatter. Holistic Characterization of a Salmonella Typhimurium Infection Model Using Integrated Molecular Imaging, metabolights_dataset, V1; 2022. https://www.ebi.ac.uk/metabolights/MTBLS2671.  | 
                                    
                                        
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| 224.1039 | [M-H2O+NH4]+PPM:4.2 | 
                                    Homo sapiens | esophagus | DESI () | 
                                        TO31T - MTBLS385Resolution: 75μm, 56x54
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| 224.1043 | [M-H2O+NH4]+PPM:6 | 
                                    Homo sapiens | esophagus | DESI () | 
                                        TO29T - MTBLS385Resolution: 75μm, 56x48
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Hydroxykynurenine is a free radical generator and a bioprecursor quinolinic acid which is a endogenous excitotoxin (PMID 16697652). It is a product of enzyme kynurenine 3-monooxygenase in the tryptophan catabolism pathway (Reactome http://www.reactome.org). [HMDB] Hydroxykynurenine is a free radical generator and a bioprecursor quinolinic acid which is a endogenous excitotoxin (PMID 16697652). It is a product of enzyme kynurenine 3-monooxygenase in the tryptophan catabolism pathway (Reactome http://www.reactome.org). Acquisition and generation of the data is financially supported in part by CREST/JST. [Raw Data] CBA12_3-OH-kynurenine_pos_20eV_1-4_01_802.txt [Raw Data] CBA12_3-OH-kynurenine_pos_10eV_1-4_01_801.txt [Raw Data] CBA12_3-OH-kynurenine_pos_50eV_1-4_01_805.txt [Raw Data] CBA12_3-OH-kynurenine_pos_40eV_1-4_01_804.txt [Raw Data] CBA12_3-OH-kynurenine_pos_30eV_1-4_01_803.txt C26170 - Protective Agent > C275 - Antioxidant KEIO_ID H050; [MS3] KO009001 KEIO_ID H050; [MS2] KO009000 KEIO_ID H050
