Metabolite details
Reactome pathways
- R-HSA-1430728 - Metabolism
- R-HSA-159418 - Recycling of bile acids and salts
- R-HSA-1614558 - Degradation of cysteine and homocysteine
- R-HSA-1614635 - Sulfur amino acid metabolism
- R-HSA-192105 - Synthesis of bile acids and bile salts
- R-HSA-193368 - Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol
- R-HSA-194068 - Bile acid and bile salt metabolism
- R-HSA-352230 - Amino acid transport across the plasma membrane
- R-HSA-382551 - Transport of small molecules
- R-HSA-425407 - SLC-mediated transmembrane transport
- R-HSA-556833 - Metabolism of lipids
- R-HSA-71291 - Metabolism of amino acids and derivatives
- R-HSA-8957322 - Metabolism of steroids
- R-HSA-8963693 - Aspartate and asparagine metabolism
- 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
- Absence of tmRNA increases the persistence to cefotaxime by upregulating the metabolites GlcNAc in Aeromonas veronii
- Distribution of RESV and its metabolite peaks in mouse tissues after oral and skin administration
- Resveratrol metabolism in HepG2 (human hepatocytes), HaCaT (human keratinocytes), and C2C12 (mouse myoblasts)
- 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
- Metabolomic Profile of Diet-Induced Obesity Mice in Response to Human and Small Humanin-like Peptide 2 Treatment
- Four layer multi-omics reveals molecular responses to aneuploidy in <i>Leishmania</i>
- Unknown Metabolite Annotation in Mouse Aging using Ion Mobility Collision Cross-Section Atlas (AllCCS)
- Bioaccumulation of therapeutic drugs by human gut bacteria: cross-feeding metabolite analysis (FIA-MS) (E.rectale;S.salivarius assays)
- Integrative Modeling of Quantitative Plasma Lipoprotein, Metabolic, and Amino Acid Data Reveals a Multiorgan Pathological Signature of SARS-CoV-2 Infection
- Physiological extremes of the human blood metabolome: A metabolomics analysis of highly glycolytic, oxidative, and anabolic athletes
- Human age-declined saliva metabolic markers determined by LC-MS
- Metabolic Dynamics of In Vitro CD8+ T Cell Activation.
- Metabolomic profiling reveals the effects of early-life lactoferrin intervention on protein synthesis, energy production and antioxidative capacity in the liver of suckling piglets
- Bioplatforms Australia: Antibiotic Resistant Sepsis Pathogens Framework Initiative (Klebsiella pneumoniae assays)
- Bioplatforms Australia: Antibiotic Resistant Sepsis Pathogens Framework Initiative (Streptococcus pyogenes 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
- Host autophagy mediates organ wasting and nutrient mobilization for tumor growth.
- Red-Fleshed Apple Anthocyanin Extracts Attenuate Male Reproductive System Dysfunction Caused by Busulfan in Mice (Mouse blood plasma; UPLC-MS/MS assays)
- Metabolic characterization of the natural progression of chronic hepatitis B (Biogenic amine and Acyl-carnitine assays).
- SARS-CoV-2-reprogrammed metabolism and autophagy reduction uncover host-targeting antivirals
- Microbial Diversity and Non-volatile Metabolites Profile of Low-Temperature Sausage Stored at Room Temperature
- Metabolites from surface seawater collected in Narragansett Bay
- Changes and correlations of intestinal flora and liver metabolite profiles in mice with gallstones
- 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)
- Jasmonate-mediated stomatal closure under elevated CO2 revealed by time-resolved metabolomics
- Chronic sleep loss sensitizes Drosophila melanogaster to nitrogen stress
- Metabolite profile data of grapevine plants with brown wood streaking and grapevine leaf stripe (esca complex disease) symptoms
- Metabolic plasticity confers increased resilience to climate variability in temperate compared to tropical lizards
- Distinct succinate modifying products are clinically diagnostic and prognostic biomarkers for fumarate hydratase deficient renal cell carcinoma
- Gut microbiome drives individual memory variation in bumblebees
- The Manchurian Walnut Genome: Insights into Juglone and Lipid Biosynthesis.
- Mechanical force promotes dimethylarginine dimethylaminohydrolase 1-mediated hydrolysis of the metabolite asymmetric dimethylarginine to enhance bone formation
- 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
- Metabolism Disorder Promotes Isoproterenol-induced Myocardial Injury in Mice with High Temperature and High Humidity and High-Fat Diet
- 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
- Transcriptional Shift and Metabolic Adaptations during Leishmania Quiescence Using Stationary Phase and Drug Pressure as Models
- Effects of Radiofrequency Field from 5G Communications on fecal microbiome and metabolome profiles in mice
- Auricularia auricula polysaccharides reduce obesity in mice through gut commensal Papillibacter cinnamivorans
- 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)
- Interaction between Cervical Microbiota and Host Gene Regulation in Caesarean Section Scar Diverticulum
- Mechanism of interventional effect and targets of Zhuyu Pill in regulating and suppressing colitis and cholestasis
- 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
- Transcriptomic dynamics control rapid transition of core crop functions in 'lactating' pigeon
- Effects of Centella asiatica extract on antioxidant status and liver metabolome of rotenone-treated rats using GC-MS
- Stage-specific roles of microbial dysbiosis and metabolic disorders in rheumatoid arthritis
- PKM2 methylation by CARM1 activates aerobic glycolysis to promote tumorigenesis.
- 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)
- Integrated Proteomic and Metabolomic Analyses Show Differential Effects of Glucose Availability in Marine <i>Synechococcus</i> and <i>Prochlorococcus</i>.
- Diverse metabolic reactions activated during 58-hr fasting are revealed by non-targeted metabolomic analysis of human blood.
- Metabolic disorder and intestinal microflora dysbiosis in chronic inflammatory demyelinating polyradiculoneuropathy
- Transcriptomic and lipidomic profiling of subcutaneous and visceral adipose tissues in 15 vertebrates
- Flow cytometry has a significant impact on the cellular metabolome (General LC-MS assay)
- Flow cytometry has a significant impact on the cellular metabolome (Lipidomic LC-MS assay)
- 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
- A Pilot Characterization of the Human Chronobiome
- Extracellular-acidosis restricts one-carbon metabolism and preserves T cell stemness
- Metabolic changes associated with tick-microbe interactions
- Genetic mapping and molecular mechanism behind color variation in the Asian vine snake
- Bacterial Pathogens Hijack the Innate Immune Response by Activation of the Reverse Transsulfuration Pathway.
- Disturbed Microbiota-Metabolites-Immune Interaction Network is Associated with Olfactory Dysfunction in Patients with Chronic Rhinosinusitis
- 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)
- Metabolic effects of an aspartate aminotransferase-inhibitor on two T-cell lines
- Integrated multi-omics analysis of adverse cardiac remodeling and metabolic inflexibility upon ErbB2 and ERRα deficiency.
- Unexpected similarities between the Schizosaccharomyces and human blood metabolomes, and novel human metabolites (Blood fraction)
- Searching for Drug Synergy Against Cancer Through Polyamine Metabolism Impairment: Insight Into the Metabolic Effect of Indomethacin on Lung Cancer Cells.
- Unexpected similarities between the Schizosaccharomyces and human blood metabolomes, and novel human metabolites (Blood plasma and RBC fractions)
Observed in differential profiles
- Control_vs_HIAE
- Control_vs_HIAE
- Control_vs_HIAE
- Control_vs_HIAE
- Control_vs_HIAE
- rps2_wildtype_vs_rps2_A226Y
- Wild_Type_vs_tmRNA_Knockout
- Control_Oral_Blood_vs_RESV_Oral_Blood
- Control_Oral_Blood_vs_RESV_Oral_Blood
- HepG2_0uM_vs_HepG2_200uM
- HepG2_0uM_vs_HepG2_200uM
- HepG2_0uM_vs_HepG2_200uM
- HepG2_0uM_vs_HepG2_200uM
- HepG2_0uM_vs_HepG2_200uM
- HepG2_0uM_vs_HepG2_200uM
- Wild_type_vs_hfq
- Control_16.6_months_vs_Treatment_16.6_months
- Water_vs_HNG
- Water_vs_HNG
- Water_vs_HNG
- Water_vs_HNG
- Nepalese_BPK173_vs_Nepalese_BPK178
- 36_week_vs_104_week
- G4_Eubacterium_rectale_DMSO_30_vs_G3_Eubacterium_rectale_Duloxetine_47
- Healthy_vs_Patient_SARS-CoV-2_Positive
- Control_Baseline_vs_Control_Post-Exercise
- Old_vs_Young
- G3_Experimental_Sample_0h_vs_G11_Experimental_Sample_96h
- G3_Experimental_Sample_0h_vs_G11_Experimental_Sample_96h
- G3_Experimental_Sample_0h_vs_G11_Experimental_Sample_96h
- Control_Day_8_vs_Lactoferrin_Day_8
- G1_Klebsiella_pneumoniae_AJ218_RPMI_vs_G2_Klebsiella_pneumoniae_AJ218_Pooled_sera
- G1_RPMI_modified_Blood_M1T1_5448_vs_G2_Pooled_sera_Blood_M1T1_5448
- Control_vs_nsPEF_7_day
- WT_vs_WT_Aco
- Alcohol_Treatment_vs_Control
- Male_vs_Female
- G1_Frt_Ctrl_Day_6_vs_G3_Rasv12_Scrib_Day_6
- Control_vs_Busulfan_5_mg_kg_RAAE
- Control_vs_Immune_Tolerant
- Control_vs_Immune_Tolerant
- Control_vs_Immune_Tolerant
- Calu3_Mock_DMEM_vs_Calu3_10uM_NIC
- Control_vs_Day_12
- 16_May_2012_vs_8_June_2012
- 16_May_2012_vs_8_June_2012
- Control_vs_Lithogenic_Diet
- Sham_vs_UIR
- Sham_vs_UIR
- 400ppm_0min_vs_800ppm_60min
- Iso31_Control_vs_Fumin_Homozygous_Sleep_Mutants
- Control_vs_Asymptomatic
- T_septentrionalis_cold_vs_T_septentrionalis_warm
- Normal_control_no_tumor_vs_FH_deficient_RCC
- Hindgut_Control_vs_Lactobacillus_apis
- Hindgut_Control_vs_Lactobacillus_apis
- Embryo_S1_vs_Embryo_S4
- Control_vs_Exercise
- G1_PBS_vs_G2_DSS
- Untreated_vs_Antibiotic_Treated
- Untreated_vs_Antibiotic_Treated
- Control_vs_Isoproterenol
- Sham_vs_Heart_Failure_Sedentary
- Sham_vs_Heart_Failure_Sedentary
- G1_Control_vs_G2_Arginine_Addition
- AMAD_Log_vs_AMAE_Sta
- Sham_vs_Radiofrequency
- Basal_vs_High_Fat
- Wild_type_vs_Knock_out
- Wild_Type_vs_Gene_Knockout
- Normal_vs_Neural_Tube_Defect
- Normal_vs_Neural_Tube_Defect
- Control_vs_CSD
- Control_vs_ZYP_High_Dose
- Dc-N_vs_Dc-HS
- Dcs_N_vs_Dcs_HS
- Male_19_days_vs_Male_1_day
- Control_vs_Treatment
- Healthy_vs_RAS4
- Healthy_vs_RAS4
- Control_0d_vs_Treatment_180d
- MCF-7_WT_vs_MCF-7_PKM2_KO
- Normal_Diet_vs_High-fat_Diet
- Normal_Diet_vs_High-fat_Diet
- Normal_Diet_vs_High-fat_Diet
- SS120_Control_vs_SS120_5mM
- SS120_Control_vs_SS120_5mM
- SS120_Control_vs_SS120_5mM
- SS120_Control_vs_SS120_5mM
- Blood_10h_vs_Blood_58h
- CIDP_patient_vs_healthy_control
- G1_Sheep_ASA_SAT_vs_G2_Sheep_GOM_VAT
- G1_Sheep_ASA_SAT_vs_G2_Sheep_GOM_VAT
- Ctrl_vs_Ab
- G1_Ctrl_vs_G2_Ab
- Control_0h_vs_GABA_0h
- Control_vs_Fermented_Mulberry_Leaves
- Plasma_0h_vs_Plasma_48h
- Control_vs_Lactic_Acid
- Uninfected_1h_vs_Anaplasma_phagocytophilum_1h
- Yellow_Skin_vs_Green_Skin
- G1_Infected_Treated_vs_G2_Infected_Untreated
- Normal_vs_Abnormal
- SAR-R_vs_SAR-S
- JURKAT_Control_vs_JURKAT_Treatment
- WT_vs_ErbB2_KI
- A549_0uM_vs_A549_1uM
- Human_Blood_vs_Human_Plasma
- Human_Blood_vs_Human_Plasma
- Human_Blood_vs_Human_Plasma
- Blood_vs_Plasma
- Blood_vs_Plasma