Metabolite details
Reactome pathways
- No Reactome pathways listed for this metabolite.
Observed in studies
- 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)
- Plant hosts modify belowground microbial community response to extreme drought
- Metabolomics analysis identifies metabolites associated with systemic acquired resistance in Arabidopsis
- Four layer multi-omics reveals molecular responses to aneuploidy in <i>Leishmania</i>
- 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.
- The impact of slyA on cell metabolism of Salmonella Typhimurium: a joint study of transcriptomics and
- Large-Scale Plasma Analysis Revealed New Mechanisms and Molecules Associated with the Host Response to SARS-CoV-2.
- Fruit setting rewires central metabolism via gibberellin cascades
- Chemotaxis shapes the microscale organization of the ocean’s microbiome
- 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
- 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.
- Metabolomic profiling reveals the effects of early-life lactoferrin intervention on protein synthesis, energy production and antioxidative capacity in the liver of suckling piglets
- Proteomic analysis validates previous findings on wounding-responsive plant hormone signaling and primary metabolism contributing to the biosynthesis of secondary metabolites based on metabolomic analysis in harvested broccoli (Brassica oleracea L. var. italica)
- Towards engineering ectomycorrhization into switchgrass bioenergy crops via a lectin receptor‐like kinase
- Host autophagy mediates organ wasting and nutrient mobilization for tumor growth.
- Dissecting Metabolism of Leaf Nodules in <i>Ardisia crenata</i> and <i>Psychotria punctata</i>.
- A Phosphate starvation response gene (psr1-like) is present in Micromonas pusilla and other marine algae and coordinates the metabolic response to phosphate deficiency
- Tissue- and Pathway-Specific Metabolomic Profiles of the Steroid Receptor Coactivator (SRC) family
- Jasmonate-mediated stomatal closure under elevated CO2 revealed by time-resolved metabolomics
- eRah: A computational tool integrating spectral deconvolution and alignment with quantification and identification of metabolites in GCMS- based metabolomics
- Chronic sleep loss sensitizes Drosophila melanogaster to nitrogen stress
- Metabolomics Analysis of the Effect of GAT-2 Deficiency on Th1 Cells in Mice
- Metabolite profile data of grapevine plants with brown wood streaking and grapevine leaf stripe (esca complex disease) symptoms
- Evaluation of algorithms for multiple alignment of GCxGC-MS data
- Metabolic profilings of rat INS-1 β-cells under changing levels of essential amino acids
- Altered fecal metabolomics and potential biomarkers of psoriatic arthritis differing from rheumatoid arthritis
- Auricularia auricula polysaccharides reduce obesity in mice through gut commensal Papillibacter cinnamivorans
- Bioinspired Rhamnolipid Protects Wheat Against Zymoseptoria tritici Through Mainly Direct Antifungal Activity and Without Major Impact on Leaf Physiology
- Intergenerational Association of Gut Microbiota and Metabolism between Perinatal Folic Acid Metabolism and Neural Tube Defects (Brain tissue metabolomics)
- Effects of Centella asiatica extract on antioxidant status and liver metabolome of rotenone-treated rats using GC-MS
- PKM2 methylation by CARM1 activates aerobic glycolysis to promote tumorigenesis.
- 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.
- 4-Octyl itaconate as a metabolite derivative inhibits inflammation via alkylation of STING
- Metabolic Changes of Maternal Uterine Fluid, Uterus, and Plasma during the Peri-implantation Period of Early Pregnancy in Mice.
- Flow cytometry has a significant impact on the cellular metabolome (GC-MS assay)
- A Pilot Characterization of the Human Chronobiome
- 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
- Metabolic changes associated with tick-microbe interactions
- Metabolic profiling with UPLC-MS orbitrap of diatoms Coscinodiscus granii infected with parasitic oomycete Lagenisma coscinodisci
- 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)
- Unexpected similarities between the Schizosaccharomyces and human blood metabolomes, and novel human metabolites (Blood plasma and RBC fractions)
- Metabolic alterations in pea leaves during arbuscular mycorrhiza development.
Observed in differential profiles
- 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
- T0_vs_T3
- Local_Leaf_Control_vs_Local_Leaf_Avr
- Nepalese_BPK173_vs_Nepalese_BPK178
- NM-control_vs_NM-Pb
- slyA_vs_wild_type
- non_COVID_19_healthy_vs_non_critical_COVID_19
- G1_Wild_Type_Day_-2_Pollination_0_vs_G3_Wild_Type_Day_2_Pollination_1
- Alexandrium_vs_Amphidinium
- 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
- 280_mOsm_vs_480_mOsm
- Control_Day_8_vs_Lactoferrin_Day_8
- Control_Head_vs_Floret
- Wild_Type_vs_Transgenic
- G1_Frt_Ctrl_Day_6_vs_G3_Rasv12_Scrib_Day_6
- Ardisia_crenata_Stage_I_lamina_vs_nodule
- Intracellular_vs_Extracellular
- SRC1_Knockout_Fed_Liver_vs_SRC1_Wildtype_Fed_Liver
- 400ppm_0min_vs_800ppm_60min
- Healthy_vs_HIAE
- Iso31_Control_vs_Fumin_Homozygous_Sleep_Mutants
- GAT-2_Knockout_vs_Wild_Type
- Control_vs_Asymptomatic
- CC406_t2_vs_Stm6Glc4_t2
- G1_Control_vs_G2_Arginine_Addition
- G1_Control_vs_G2_Arginine_Addition
- Healthy_Control_vs_Psoriatic_Arthritis
- Healthy_Control_vs_Psoriatic_Arthritis
- Basal_vs_High_Fat
- Mock_Non_Inoculated_0d_vs_Rhamnol_Non_Inoculated_0d
- Normal_vs_Neural_Tube_Defect
- Control_vs_Treatment
- MCF-7_WT_vs_MCF-7_PKM2_KO
- SS120_Control_vs_SS120_5mM
- SS120_Control_vs_SS120_5mM
- 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
- Control_vs_DMXAA16h
- Pregnant_Blood_Plasma_Day_1_vs_Pregnant_Blood_Plasma_Day_4
- Ctrl_vs_Ab
- Plasma_0h_vs_Plasma_48h
- wild_type_vs_patA_deletion
- Uninfected_1h_vs_Anaplasma_phagocytophilum_1h
- Healthy_vs_Infected
- JURKAT_Control_vs_JURKAT_Treatment
- WT_vs_ErbB2_KI
- Human_Blood_vs_Human_Plasma
- Human_Blood_vs_Human_Plasma
- Blood_vs_Plasma
- 21d_Control_vs_21d_AM