M/Z: 232.1085


Hit 2 annotations:  Nalidixic Acid_[M-H2O+NH4]+; Melatonin_[M]+


在BioDeep NovoCell知识数据库中,参考离子总共被划分为4个级别。
  • Confirmed: 这个参考离子已经通过手动审计得到确认和验证。
  • Reliable: 这个参考离子可能在特定的解剖组织环境中高度保守。
  • Unreliable: 这个参考离子具有较高的排名价值,但缺乏可重复性。
  • Unavailable: 由于排名价值低且缺乏可重复性,这个参考离子不应用于注释。

Found 5 Reference Ions Near m/z 232.1085
NovoCell ID m/z Mass Window Metabolite Ranking Anatomy Context
MSI_000032067 Unreliable 232.1025 232.1024 ~ 232.1026
MzDiff: 1.1 ppm
Cryptolepine (BioDeep_00000007194)
Formula: C16H12N2 (232.1)
2.22 (100%) Posidonia oceanica
[PO:0005020] vascular bundle
MSI_000034903 Unavailable 232.1024 232.1024 ~ 232.1024
MzDiff: none
Cryptolepine (BioDeep_00000007194)
Formula: C16H12N2 (232.1)
-0.29 (100%) Posidonia oceanica
[PO:0006036] root epidermis
MSI_000035594 Unavailable 232.1024 232.1024 ~ 232.1024
MzDiff: none
Cryptolepine (BioDeep_00000007194)
Formula: C16H12N2 (232.1)
-0.17 (100%) Posidonia oceanica
[PO:0006203] pericycle
MSI_000038483 Unreliable 232.1026 232.1026 ~ 232.1026
MzDiff: none
Cryptolepine (BioDeep_00000007194)
Formula: C16H12N2 (232.1)
1.93 (100%) Posidonia oceanica
[PO:0005059] root endodermis
MSI_000057518 Unreliable 232.1085 232.1085 ~ 232.1085
MzDiff: none
Nalidixic Acid (BioDeep_00000001809)
Formula: C12H12N2O3 (232.0848)
0.89 (100%) Homo sapiens
[UBERON:0007779] transudate

Found 3 Sample Hits
Metabolite Species Sample
Nalidixic Acid

Formula: C12H12N2O3 (232.0848)
Adducts: [M-H2O+NH4]+ (Ppm: 1.9)
Homo sapiens (esophagus)
LNTO22_1_4
Resolution: 17μm, 82x80

Description

Nalidixic Acid

Formula: C12H12N2O3 (232.0848)
Adducts: [M-H2O+NH4]+ (Ppm: 18.7)
Mus musculus (Liver)
Salmonella_final_pos_recal
Resolution: 17μm, 691x430

Description

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.

Melatonin

Formula: C13H16N2O2 (232.1212)
Adducts: [M]+ (Ppm: 14.1)
Mus musculus (Liver)
Salmonella_final_pos_recal
Resolution: 17μm, 691x430

Description

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.