Metabolite details
Reactome pathways
- R-HSA-112310 - Neurotransmitter release cycle
- R-HSA-112313 - Neurotransmitter uptake and metabolism In glial cells
- R-HSA-112315 - Transmission across Chemical Synapses
- R-HSA-112316 - Neuronal System
- R-HSA-1430728 - Metabolism
- R-HSA-156580 - Phase II - Conjugation of compounds
- R-HSA-156587 - Amino Acid conjugation
- R-HSA-15869 - Metabolism of nucleotides
- R-HSA-159424 - Conjugation of carboxylic acids
- R-HSA-1643685 - Disease
- R-HSA-177162 - Conjugation of phenylacetate with glutamine
- R-HSA-196807 - Nicotinate metabolism
- R-HSA-196849 - Metabolism of water-soluble vitamins and cofactors
- R-HSA-196854 - Metabolism of vitamins and cofactors
- R-HSA-210455 - Astrocytic Glutamate-Glutamine Uptake And Metabolism
- R-HSA-210500 - Glutamate Neurotransmitter Release Cycle
- R-HSA-211859 - Biological oxidations
- R-HSA-212436 - Generic Transcription Pathway
- R-HSA-352230 - Amino acid transport across the plasma membrane
- R-HSA-3700989 - Transcriptional Regulation by TP53
- R-HSA-3781865 - Diseases of glycosylation
- R-HSA-379716 - Cytosolic tRNA aminoacylation
- R-HSA-379724 - tRNA Aminoacylation
- R-HSA-379726 - Mitochondrial tRNA aminoacylation
- R-HSA-382551 - Transport of small molecules
- R-HSA-392499 - Metabolism of proteins
- R-HSA-4085023 - Defective GFPT1 causes CMSTA1
- R-HSA-425407 - SLC-mediated transmembrane transport
- R-HSA-442660 - SLC-mediated transport of neurotransmitters
- R-HSA-446193 - Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein
- R-HSA-446203 - Asparagine N-linked glycosylation
- R-HSA-446210 - Synthesis of UDP-N-acetyl-glucosamine
- R-HSA-446219 - Synthesis of substrates in N-glycan biosythesis
- R-HSA-499943 - Interconversion of nucleotide di- and triphosphates
- R-HSA-500753 - Pyrimidine biosynthesis
- R-HSA-5609975 - Diseases associated with glycosylation precursor biosynthesis
- R-HSA-5619044 - Defective SLC6A19 causes Hartnup disorder (HND)
- R-HSA-5619102 - SLC transporter disorders
- R-HSA-5619115 - Disorders of transmembrane transporters
- R-HSA-5628897 - TP53 Regulates Metabolic Genes
- R-HSA-5659735 - Defective SLC6A19 causes Hartnup disorder (HND)
- R-HSA-5668914 - Diseases of metabolism
- R-HSA-597592 - Post-translational protein modification
- R-HSA-71291 - Metabolism of amino acids and derivatives
- R-HSA-72766 - Translation
- R-HSA-73817 - Purine ribonucleoside monophosphate biosynthesis
- R-HSA-73857 - RNA Polymerase II Transcription
- R-HSA-74160 - Gene expression (Transcription)
- R-HSA-8956320 - Nucleotide biosynthesis
- R-HSA-8963693 - Aspartate and asparagine metabolism
- R-HSA-8964539 - Glutamate and glutamine metabolism
- R-HSA-9748784 - Drug ADME
- R-HSA-9748787 - Azathioprine ADME
- R-HSA-9958863 - SLC-mediated transport of amino acids
Observed in studies
- Metabolomics reveals impaired maturation of HDL particles in adolescents with hyperinsulinaemic androgen excess
- Biological effect of chronic mistranslation in mammalian cells
- Untargeted metabolomics to understand the basis of phenotypic differences in amphotericin B-resistant Leishmania parasites
- Absence of tmRNA Increases the Persistence to Cefotaxime and the Intercellular Accumulation of Metabolite GlcNAc in <i>Aeromonas veronii</i>.
- Absence of tmRNA increases the persistence to cefotaxime by upregulating the metabolites GlcNAc in Aeromonas veronii
- Cell-based and multi-omics profiling reveal dynamic metabolic repurposing of mitochondria to drive developmental progression of Trypanosoma brucei
- Metabolome analysis via an HPLC-ESI-MS-based experimental and computational pipeline for chronic nephron toxicity profiling
- Hfq Regulates Efflux Pump Expression and Purine Metabolic Pathway to Increase the Trimethoprim Resistance in Aeromonas veronii
- Effect of L-carnitine administration on lipid and metabolite content in sheep infraspinatus muscle after tendon release
- A metabolite roadmap of the wood-forming tissue in Populus tremula (GC-MS assay; Wood ring and extraxylary tissue)
- Pb Stress and Ectomycorrhizas: Strong Protective Proteomic Responses in Poplar Roots Inoculated with <i>Paxillus involutus</i> Isolate and Characterized by Low Root Colonization Intensity.
- Large-Scale Plasma Analysis Revealed New Mechanisms and Molecules Associated with the Host Response to SARS-CoV-2.
- The response of Chlamydomonas reinhardtii to nitrogen deprivation: a systems biology analysis
- Global Metabonomic and Proteomic Analysis of Human Conjunctival Epithelial Cells (IOBA-NHC) in Response to Hyperosmotic Stress
- Metabolic Dynamics of In Vitro CD8+ T Cell Activation.
- Global analysis of plasma lipidomics reveals altered lipid signatures in patients with osteonecrosis of the femoral head
- Bioplatforms Australia: Antibiotic Resistant Sepsis Pathogens Framework Initiative (Streptococcus pneumoniae assays)
- Multi-Omics Analysis Reveals Disturbance of Nanosecond Pulsed Electric Field in the Serum Metabolic Spectrum and Gut Microbiota
- Transcriptional differentiation of Trypanosoma brucei during in vitro acquisition of resistance to acoziborole
- Integrated Analyses of the Gut Microbiota, Intestinal Permeability and Serum Metabolome Phenotype in Rats with Alcohol Withdrawal Syndrome
- Fat Deposition in the Muscle of Female and Male Yak and the Correlation of Yak Meat Quality with Fat
- Metabolic characterization of the natural progression of chronic hepatitis B (Biogenic amine and Acyl-carnitine assays).
- Transcriptomics and metabolomics of engineered Synechococcus elongatus during photomixotrophic growth
- SARS-CoV-2-reprogrammed metabolism and autophagy reduction uncover host-targeting antivirals
- Metabolic Responses of a Model Green Microalga Euglena gracilis to Different Environmental Stresses
- Metabolites from surface seawater collected in Narragansett Bay
- Changes and correlations of intestinal flora and liver metabolite profiles in mice with gallstones
- A Phosphate starvation response gene (psr1-like) is present in Micromonas pusilla and other marine algae and coordinates the metabolic response to phosphate deficiency
- Multiomics of tomato glandular trichomes reveals distinct features of central carbon metabolism supporting high productivity of specialized metabolites
- Distinct metabolic profiling is correlated with bisexual flowers formation resulting from exogenous ethephon induction in melon (<i>Cucumis melo</i> L.)
- Anti-anemia drug FG4592 retards the AKI to CKD transition by improving vascular regeneration and anti-oxidative capability (day 21)
- Anti-anemia drug FG4592 retards the AKI to CKD transition by improving vascular regeneration and anti-oxidative capability (day 10)
- Multiple biochemical indices and metabolomics of Clonorchis sinensis provide a novel interpretation of biomarkers
- Analysis of Growth Phases of Enterotoxigenic Escherichia coli Reveals a Distinct Transition Phase before Entry into Early Stationary Phase with Shifts in Tryptophan, Fucose, and Putrescine Metabolism and Degradation of Neurotransmitter Precursors
- Metabolomics and lipidomics reveal perturbation of sphingolipid metabolism by a novel anti-trypanosomal 3-(oxazolo[4,5-b]pyridine-2-yl)anilide
- Distinct succinate modifying products are clinically diagnostic and prognostic biomarkers for fumarate hydratase deficient renal cell carcinoma
- The Manchurian Walnut Genome: Insights into Juglone and Lipid Biosynthesis.
- Effects of MeJA on Arabidopsis metabolome under endogenous JA deficiency
- Diallyl disulfide (DADS) ameliorates intestinal Candida albicans infection by modulating the gut microbiota and metabolites and providing intestinal protection in mice
- Appropriate taxonomic classification of intestinal microbiome by 16S rRNA gene targeting metagenomic approach
- Exercise-generated β-aminoisobutyric acid (BAIBA) reduces cardiomyocytes metabolic stress and apoptosis caused by mitochondrial dysfunction through the miR-208b/AMPK pathway
- Characterization of white tea metabolome: comparison against green and black tea by a nontargeted metabolomics approach.
- Transcriptional Shift and Metabolic Adaptations during Leishmania Quiescence Using Stationary Phase and Drug Pressure as Models
- Proteomic and metabolic changes in cancer cells after alternation of SHMT2 expressions
- Transcriptome and Metabolome Analyses Reveal Differences in Terpenoid and Flavonoid Biosynthesis in Cryptomeria fortunei Needles Across Different Seasons
- Effects of Radiofrequency Field from 5G Communications on fecal microbiome and metabolome profiles in mice
- Novel Potential Diagnostic Serum Biomarkers of Metabolomics in Osteoarticular Tuberculosis Patients: A Preliminary Study
- Altered fecal metabolomics and potential biomarkers of psoriatic arthritis differing from rheumatoid arthritis
- Homeostasis of the biosynthetic E. coli metabolome
- Mining for metabolic responses to long-term salt stress: a case study on the model legume Lotus japonicus (A)
- Mining for metabolic responses to long-term salt stress: a case study on the model legume Lotus japonicus (B)
- Metabolomic correlation-network modules in Arabidopsis based on a graph-clustering approach
- Cardiac disruption of SDHAF4-mediated mitochondrial complex II assembly promotes dilated cardiomyopathy.
- Limited nutrient availability in the tumor microenvironment renders pancreatic tumors sensitive to allosteric IDH1 inhibitors
- Intergenerational Association of Gut Microbiota and Metabolism between Perinatal Folic Acid Metabolism and Neural Tube Defects (Feces metabolomics)
- Stage-specific roles of microbial dysbiosis and metabolic disorders in rheumatoid arthritis
- Alterations in the gut microbiota and metabolomics of seafarers after a six-month sea voyage
- Bile acid is a significant host factor shaping the gut microbiome of diet induced obese mice (untargeted metabolome profile assay)
- Metabolic disorder and intestinal microflora dysbiosis in chronic inflammatory demyelinating polyradiculoneuropathy
- GABA regulates IL-1β production in macrophages
- Transcriptomics and metabolomics analysis reveal the anti-oxidation and immune boosting effects of mulberry leaves in growing mutton sheep
- PatA mediates biofilm formation and drugs resistance through regulating the synthesis of glycolipids and lipids in mycobacterium PatA mediates a novel mycolic acid synthesis pathway and regulates biofilm formation in mycobacterium
- TGF-β uncouples glycolysis and inflammation in macrophages and controls the survival during sepsis
- Unraveling the metabolic effects of benzophenone-3 on the endosymbiotic dinoflagellate Cladocopium goreaui
- Metabolic consequences of cobalamin scarcity in diatoms as revealed through metabolomics (Thalassiosira pseudonana study)
- Metabolic consequences of cobalamin scarcity in diatoms as revealed through metabolomics (Navicula pelliculosa study)
- Human Gut Microbiota from Autism Spectrum Disorder Promote Behavioral Symptoms in Mice
- 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 positive mode)
- 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)
- Changing environments and genetic variation: inbreeding does not compromise short-term physiological responses
Observed in differential profiles
- Control_vs_HIAE
- Control_vs_HIAE
- Control_vs_HIAE
- rps2_wildtype_vs_rps2_A226Y
- G1_Wild_Type_vs_G2_AmBRAcl1
- Wild_Type_vs_tmRNA_Deletion
- Wild_Type_vs_tmRNA_Knockout
- Wild_Type_vs_tmRNA_Knockout
- Non_Induced_0_Day_vs_Induced_8_Day
- Non_Induced_0_Day_vs_Induced_8_Day
- Control_1_day_vs_High_14_day
- Control_1_day_vs_High_14_day
- Wild_type_vs_hfq
- Wild_type_vs_hfq
- Control_16.6_months_vs_Treatment_16.6_months
- Phloem_vs_Cambium
- NM-control_vs_NM-Pb
- non_COVID_19_healthy_vs_non_critical_COVID_19
- 0h_vs_24h
- G3_Experimental_Sample_0h_vs_G11_Experimental_Sample_96h
- G3_Experimental_Sample_0h_vs_G11_Experimental_Sample_96h
- 280_mOsm_vs_480_mOsm
- Control_vs_AONFH_Stage_III_IV
- G1_Pooled_Sera_Blood_4559_vs_G2_RPMI_Glucose_Blood_4559
- G1_Pooled_Sera_Blood_4559_vs_G2_RPMI_Glucose_Blood_4559
- Control_vs_nsPEF_7_day
- WT_vs_WT_Aco
- Alcohol_Treatment_vs_Control
- Male_vs_Female
- Control_vs_Immune_Tolerant
- Control_vs_Immune_Tolerant
- Control_vs_Immune_Tolerant
- Wild_Type_vs_YQ2-gal
- Calu3_Mock_DMEM_vs_Calu3_10uM_NIC
- Control_vs_Paramycin
- 16_May_2012_vs_8_June_2012
- Control_vs_Lithogenic_Diet
- Intracellular_vs_Extracellular
- Solanum_habrochaites_leaf_vs_glandular_trichome
- Control_vs_Ethephon_Treatment
- Sham_vs_UIR
- Sham_vs_UIR
- Control_14dpi_vs_Infected_14dpi
- Control_14dpi_vs_Infected_14dpi
- E1777_Intracellular_MidLog_vs_E1777_Intracellular_EarlyStationary
- Control_vs_OXPA_Treatment
- Control_vs_OXPA_Treatment
- Normal_control_no_tumor_vs_FH_deficient_RCC
- Embryo_S1_vs_Embryo_S4
- G1_PBS_vs_G2_DSS
- WT_no_treatment_vs_opr3_8h
- Untreated_vs_Antibiotic_Treated
- Untreated_vs_Antibiotic_Treated
- Sham_vs_Heart_Failure_Sedentary
- Sham_vs_Heart_Failure_Sedentary
- White_Tea_0h_vs_White_Tea_36h
- AMAD_Log_vs_AMAE_Sta
- Control_No_Glycine_vs_SHMT2_Upregulated_No_Glycine
- Control_No_Glycine_vs_SHMT2_Upregulated_No_Glycine
- Summer_vs_Winter
- Sham_vs_Radiofrequency
- Healthy_Control_vs_Osteoarticular_Tuberculosis
- Healthy_Control_vs_Psoriatic_Arthritis
- Glu_BW25113_vs_Pyr_BW25113
- Control_vs_150mM
- Control_vs_150mM
- Wild_type_vs_Knock_out
- Col-0_Root_vs_tt4_Root
- Wild_Type_vs_Gene_Knockout
- Normal_vs_Neural_Tube_Defect
- Healthy_vs_RAS4
- Healthy_vs_RAS4
- Control_0d_vs_Treatment_180d
- Normal_Diet_vs_High-fat_Diet
- Normal_Diet_vs_High-fat_Diet
- Normal_Diet_vs_High-fat_Diet
- CIDP_patient_vs_healthy_control
- CIDP_patient_vs_healthy_control
- Control_0h_vs_GABA_0h
- Control_vs_Fermented_Mulberry_Leaves
- wild_type_vs_patA_deletion
- Control_vs_TGF-beta_Treatment
- Control_vs_BP3_Low_Concentration
- Saturating_Limiting_vs_Saturating_Replete
- Navicula_pelliculosa_Saturating_Limiting_vs_Saturating_Replete
- ASD_Fecal_vs_TD_Fecal
- Arginine_Replenished_Ctrl_vs_Arginine_Starved_48h
- SAR-S_vs_SAR-R
- SAR-R_vs_SAR-S
- Inbreeding_Growth_Chamber_0_day_vs_Inbreeding_Growth_Chamber_92_day