Cer(d18:1/20:4(6E,8Z,11Z,14Z)+=O(5))
                        Formula: C38H65NO4 (599.4913)
                        
                        Chinese Name:  
                        BioDeep ID: BioDeep_00000215012 
                        ( View LC/MS Profile)
                        SMILES:  [H][C@@](CO)(NC(=O)CCCC(=O)\C=C\C=C/C\C=C/C\C=C/CCCCC)[C@H](O)\C=C\CCCCCCCCCCCCC
                    
Found 17 Sample Hits
| m/z | Adducts | Species | Organ | Scanning | Sample | |
|---|---|---|---|---|---|---|
| 600.5061 | [M+H]+PPM:12.5 | 
                                    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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| 600.5068 | [M+H]+PPM:13.6 | 
                                    Rattus norvegicus | Epididymis | MALDI (DHB) | 
                                        epik_dhb_head_ito03_17 - MTBLS58Resolution: 17μm, 208x108
                                             1 male adult wild-type rat was obtained from Inserm U1085 - Irset Research Institute (University of Rennes1, France). Animals were age 60 days and were reared under ad-lib conditions. Care and handling of all animals complied with EU directive 2010/63/EU on the protection of animals used for scientific purposes. The whole epididymis was excised from each animal immediately post-mortem, loosely wrapped rapidly in an aluminum foil and a 2.5% (w/v) carboxymethylcellulose (CMC) solution was poured to embed the epididymis to preserve their morphology. To remove air bubbles, the filled aluminum molds was gently freezed by depositing it on isopentane or dry ice, then on the nitrogen vapors and finally by progressively dipping the CMC/sample coated with aluminum foil into liquid nitrogen (or only flush with liquid nitrogen). Frozen tissues were stored at -80 °C until use to avoid degradation.  | 
                                    
                                        
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| 600.5068 | [M+H]+PPM:13.6 | 
                                    Rattus norvegicus | Epididymis | MALDI (DHB) | 
                                        epik_dhb_head_ito03_18 - MTBLS58Resolution: 17μm, 208x104
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| 600.5068 | [M+H]+PPM:13.6 | 
                                    Rattus norvegicus | Epididymis | MALDI (DHB) | 
                                        epik_dhb_head_ito08_43 - MTBLS58Resolution: 17μm, 298x106
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| 600.5068 | [M+H]+PPM:13.6 | 
                                    Rattus norvegicus | Epididymis | MALDI (DHB) | 
                                        epik_dhb_head_ito08_44 - MTBLS58Resolution: 17μm, 299x111
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| 600.5068 | [M+H]+PPM:13.6 | 
                                    Rattus norvegicus | Epididymis | MALDI (DHB) | 
                                        epik_dhb_head_ito08_46 - MTBLS58Resolution: 17μm, 298x106
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| 600.5067 | [M+H]+PPM:13.5 | 
                                    Rattus norvegicus | Epididymis | MALDI (DHB) | 
                                        epik_dhb_head_ito08_47 - MTBLS58Resolution: 17μm, 301x111
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| 600.5068 | [M+H]+PPM:13.6 | 
                                    Rattus norvegicus | Epididymis | MALDI (DHB) | 
                                        epik_dhb_head_ito08_48 - MTBLS58Resolution: 17μm, 294x107
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| 600.5068 | [M+H]+PPM:13.6 | 
                                    Rattus norvegicus | Epididymis | MALDI (DHB) | 
                                        epik_dhb_head_ito01_04 - MTBLS58Resolution: 17μm, 178x91
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| 600.5068 | [M+H]+PPM:13.6 | 
                                    Rattus norvegicus | Epididymis | MALDI (DHB) | 
                                        epik_dhb_head_ito01_03 - MTBLS58Resolution: 17μm, 159x110
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| 600.5069 | [M+H]+PPM:13.8 | 
                                    Rattus norvegicus | normal | MALDI (DHB) | 
                                        epik_dhb_head_ito01_05 - MTBLS58Resolution: 17μm, 183x105
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| 600.5068 | [M+H]+PPM:13.6 | 
                                    Rattus norvegicus | Epididymis | MALDI (DHB) | 
                                        epik_dhb_head_ito01_06 - MTBLS58Resolution: 17μm, 183x103
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| 600.5068 | [M+H]+PPM:13.6 | 
                                    Rattus norvegicus | Epididymis | MALDI (DHB) | 
                                        epik_dhb_head_ito03_14 - MTBLS58Resolution: 17μm, 205x103
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| 600.5068 | [M+H]+PPM:13.6 | 
                                    Mus musculus | Left upper arm | MALDI (CHCA) | 
                                        357_l_total ion count - Limb defect imaging - Monash UniversityResolution: 50μm, 97x131
                                             Diseased  | 
                                    
                                        
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| 599.5033 | [M-H2O+NH4]+PPM:18.8 | 
                                    Macropus giganteus | Brain | MALDI (BPYN) | 
                                        170321_kangaroobrain-dan3-pos_maxof50.0_med1 - 170321_kangaroobrain-dan3-pos_maxof50.0_med1Resolution: 50μm, 81x50
                                             Sample information
Organism: Macropus giganteus (kangaroo)
Organism part: Brain
Condition: Wildtype
Sample growth conditions: Wild  | 
                                    
                                        
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| 600.504 | [M+H]+PPM:9 | 
                                    Macropus giganteus | Brain | MALDI (BPYN) | 
                                        170321_kangaroobrain-dan3-pos_maxof50.0_med1 - 170321_kangaroobrain-dan3-pos_maxof50.0_med1Resolution: 50μm, 81x50
                                             Sample information
Organism: Macropus giganteus (kangaroo)
Organism part: Brain
Condition: Wildtype
Sample growth conditions: Wild  | 
                                    
                                        
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| 600.4986 | [M+H]+PPM: | 
                                    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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Cer(d18:1/20:4(6E,8Z,11Z,14Z)+=O(5)) is an oxidized ceramide (Cer). As all ceramides, oxidized ceramides are members of the class of compounds known as sphingolipids (SPs), or glycosylceramides. SPs are lipids containing a backbone of sphingoid bases (e.g. sphingosine or sphinganine) that are often covalently bound to a fatty acid derivative through N-acylation. SPs are found in cell membranes, particularly in peripheral nerve cells and the cells found in the central nervous system (including the brain and spinal cord). Sphingolipids are extremely versatile molecules that have functions controlling fundamental cellular processes such as cell division, differentiation, and cell death. Impairments associated with sphingolipid metabolism are associated with many common human diseases such as diabetes, various cancers, microbial infections, diseases of the cardiovascular and respiratory systems, Alzheimer’s disease and other neurological syndromes. The biosynthesis and catabolism of sphingolipids involves a large number of intermediate metabolites where many different enzymes are involved. Simple sphingolipids, which include the sphingoid bases and ceramides, make up the early products of the sphingolipid synthetic pathways, while complex sphingolipids may be formed by the addition of head groups to the ceramide template (Wikipedia). In humans, ceramides are phosphorylated to ceramide phosphates (CerPs) through the action of a specific ceramide kinase (CerK). Ceramide phosphates are important metabolites of ceramides as they act as a mediators of the inflammatory response. Ceramides are also one of the hydrolysis byproducts of sphingomyelins (SMs) through the action of the enzyme sphingomyelin phosphodiesterase, which has been identified in the subcellular fractions of human epidermis (PMID: 25935) and many other tissues. Ceramides can also be synthesized from serine and palmitate in a de novo pathway and are regarded as important cellular signals for inducing apoptosis (PMID: 14998372). Ceramides are key in the biosynthesis of glycosphingolipids and gangliosides. In terms of its appearance and structure, Cer(d18:1/22:1(13Z)) is a colorless solid that consists of an unsaturated 18-carbon sphingoid base with an attached unsaturated 13Z-docosenoyl fatty acid side chain. In most mammalian SPs, the 18-carbon sphingoid bases are predominant (PMID: 9759481).
