Metabolite details
Reactome pathways
- No Reactome pathways listed for this metabolite.
Observed in studies
- Biological effect of chronic mistranslation in mammalian cells
- Absence of tmRNA increases the persistence to cefotaxime by upregulating the metabolites GlcNAc in Aeromonas veronii
- Hfq Regulates Efflux Pump Expression and Purine Metabolic Pathway to Increase the Trimethoprim Resistance in Aeromonas veronii
- Hierarchical Carbon Metabolism in Iron-Deficient Bacteria Favors Iron-Scavenging Strategy
- Bioplatforms Australia: Antibiotic Resistant Sepsis Pathogens Framework Initiative (Escherichia coli assays)
- Metabolic Dynamics of In Vitro CD8+ T Cell Activation.
- Bioplatforms Australia: Antibiotic Resistant Sepsis Pathogens Framework Initiative (Klebsiella pneumoniae assays)
- Metabolomic Insights into the Browning of the Peel of Bagging ‘Rui Xue’ Apple Fruit
- Multi-Omics Analysis Reveals Disturbance of Nanosecond Pulsed Electric Field in the Serum Metabolic Spectrum and Gut Microbiota
- Host autophagy mediates organ wasting and nutrient mobilization for tumor growth.
- Transcriptomics and metabolomics of engineered Synechococcus elongatus during photomixotrophic growth
- Changes and correlations of intestinal flora and liver metabolite profiles in mice with gallstones
- Multiomics of tomato glandular trichomes reveals distinct features of central carbon metabolism supporting high productivity of specialized metabolites
- Multiple biochemical indices and metabolomics of Clonorchis sinensis provide a novel interpretation of biomarkers
- F1Fo-ATP synthase subunit determines lethal pathogenic fungi infection
- Metabolomic analysis of the mechanism of action of yerba mate extract on Salmonella Typhimurium
- The Manchurian Walnut Genome: Insights into Juglone and Lipid Biosynthesis.
- Metabolic signatures of Arabidopsis thaliana abiotic stress responses elucidate patterns in stress priming, acclimation, and recovery
- Exercise-generated β-aminoisobutyric acid (BAIBA) reduces cardiomyocytes metabolic stress and apoptosis caused by mitochondrial dysfunction through the miR-208b/AMPK pathway
- Metabolic profilings of rat INS-1 β-cells under changing levels of essential amino acids
- The functional role of OGDH for maintaining mitochondrial respiration and identity of primed human embryonic stem cells
- Homeostasis of the biosynthetic E. coli metabolome
- AMPK activation orchestrated replicative senescence of periodontal ligament stem cells via regulating metabolomics
- Limited nutrient availability in the tumor microenvironment renders pancreatic tumors sensitive to allosteric IDH1 inhibitors
- Integrated Metabolomics and Transcriptomics Analyses Reveal Anthocyanin and Carotenoid Biosynthesis Involved in Color Development in Willow Bark
- Intergenerational Association of Gut Microbiota and Metabolism between Perinatal Folic Acid Metabolism and Neural Tube Defects (Feces metabolomics)
- Intergenerational Association of Gut Microbiota and Metabolism between Perinatal Folic Acid Metabolism and Neural Tube Defects (Brain tissue metabolomics)
- Interaction between Cervical Microbiota and Host Gene Regulation in Caesarean Section Scar Diverticulum
- Multiomic analysis revealed the potential role of rumen microbes in heat stress
- Effect of heat stress on serum enzyme activity, antioxidant capacity and immune parameter metabolomics datasets in Holstein cows at different growth stages
- GABA regulates IL-1β production in macrophages
- Extracellular-acidosis restricts one-carbon metabolism and preserves T cell stemness
- TGF-β uncouples glycolysis and inflammation in macrophages and controls the survival during sepsis
- Arginine starvation kills tumor cells through aspartate exhaustion and mitochondrial dysfunction
- L-leucine increases the sensitivity of drug-resistant Salmonella to sarafloxacin by stimulating central carbon metabolism and increasing intracellular reactive oxygen species level (LC-MS negative mode)
Observed in differential profiles
- rps2_wildtype_vs_rps2_A226Y
- Wild_Type_vs_tmRNA_Knockout
- Wild_type_vs_hfq
- FeInt_T1_vs_FeLim_T3
- RPMI_B36_vs_Pooled_Sera_B36
- RPMI_B36_vs_Pooled_Sera_B36
- G3_Experimental_Sample_0h_vs_G11_Experimental_Sample_96h
- G1_Klebsiella_pneumoniae_AJ218_RPMI_vs_G2_Klebsiella_pneumoniae_AJ218_Pooled_sera
- Non_Bagged_Fruits_vs_Bagged_Fruits_With_Browning
- Control_vs_nsPEF_7_day
- G1_Frt_Ctrl_Day_6_vs_G3_Rasv12_Scrib_Day_6
- Wild_Type_vs_YQ2-gal
- Wild_Type_vs_YQ2-gal
- Control_vs_Lithogenic_Diet
- Solanum_habrochaites_leaf_vs_glandular_trichome
- Control_14dpi_vs_Infected_14dpi
- WT_vs_16R
- No_Tea_0min_vs_Tea_240min
- Embryo_S1_vs_Embryo_S4
- Control_vs_Basal_cold
- Sham_vs_Heart_Failure_Sedentary
- G1_Control_vs_G2_Arginine_Addition
- Wild_Type_vs_Gene_Knockdown
- Glu_BW25113_vs_Pyr_BW25113
- Passage_4_vs_Passage_20
- Wild_Type_vs_Gene_Knockout
- Purple_vs_Green
- Normal_vs_Neural_Tube_Defect
- Normal_vs_Neural_Tube_Defect
- Control_vs_CSD
- Dc-N_vs_Dc-HS
- Dcs_N_vs_Dcs_HS
- Control_0h_vs_GABA_0h
- Control_vs_Lactic_Acid
- Control_vs_TGF-beta_Treatment
- Arginine_Replenished_Ctrl_vs_Arginine_Starved_48h
- SAR-R_vs_SAR-S