Metabolite details
Reactome pathways
- R-HSA-109582 - Hemostasis
- R-HSA-111885 - Opioid Signalling
- R-HSA-112040 - G-protein mediated events
- R-HSA-112314 - Neurotransmitter receptors and postsynaptic signal transmission
- R-HSA-112315 - Transmission across Chemical Synapses
- R-HSA-112316 - Neuronal System
- R-HSA-114608 - Platelet degranulation
- R-HSA-1266738 - Developmental Biology
- R-HSA-1430728 - Metabolism
- R-HSA-1445148 - Translocation of SLC2A4 (GLUT4) to the plasma membrane
- R-HSA-157118 - Signaling by NOTCH
- R-HSA-162582 - Signal Transduction
- R-HSA-162587 - HIV Life Cycle
- R-HSA-162599 - Late Phase of HIV Life Cycle
- R-HSA-162906 - HIV Infection
- R-HSA-162909 - Host Interactions of HIV factors
- R-HSA-163685 - Integration of energy metabolism
- R-HSA-1643685 - Disease
- R-HSA-165054 - Rev-mediated nuclear export of HIV RNA
- R-HSA-170670 - Adenylate cyclase inhibitory pathway
- R-HSA-177243 - Interactions of Rev with host cellular proteins
- R-HSA-180746 - Nuclear import of Rev protein
- R-HSA-1852241 - Organelle biogenesis and maintenance
- R-HSA-1912399 - Pre-NOTCH Processing in the Endoplasmic Reticulum
- R-HSA-1912422 - Pre-NOTCH Expression and Processing
- R-HSA-193648 - NRAGE signals death through JNK
- R-HSA-193704 - p75 NTR receptor-mediated signalling
- R-HSA-194138 - Signaling by VEGF
- R-HSA-199991 - Membrane Trafficking
- R-HSA-204998 - Cell death signalling via NRAGE, NRIF and NADE
- R-HSA-2682334 - EPH-Ephrin signaling
- R-HSA-372790 - Signaling by GPCR
- R-HSA-373755 - Semaphorin interactions
- R-HSA-381676 - Glucagon-like Peptide-1 (GLP1) regulates insulin secretion
- R-HSA-388396 - GPCR downstream signalling
- R-HSA-392170 - ADP signalling through P2Y purinoceptor 12
- R-HSA-392499 - Metabolism of proteins
- R-HSA-392518 - Signal amplification
- R-HSA-392851 - Prostacyclin signalling through prostacyclin receptor
- R-HSA-3928662 - EPHB-mediated forward signaling
- R-HSA-3928664 - Ephrin signaling
- R-HSA-399955 - SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion
- R-HSA-399997 - Acetylcholine regulates insulin secretion
- R-HSA-400451 - Free fatty acids regulate insulin secretion
- R-HSA-400685 - Sema4D in semaphorin signaling
- R-HSA-416476 - G alpha (q) signalling events
- R-HSA-416482 - G alpha (12/13) signalling events
- R-HSA-416550 - Sema4D mediated inhibition of cell attachment and migration
- R-HSA-416572 - Sema4D induced cell migration and growth-cone collapse
- R-HSA-418346 - Platelet homeostasis
- R-HSA-418592 - ADP signalling through P2Y purinoceptor 1
- R-HSA-418594 - G alpha (i) signalling events
- R-HSA-418597 - G alpha (z) signalling events
- R-HSA-422356 - Regulation of insulin secretion
- R-HSA-422475 - Axon guidance
- R-HSA-428930 - Thromboxane signalling through TP receptor
- R-HSA-434316 - Fatty Acids bound to GPR40 (FFAR1) regulate insulin secretion
- R-HSA-4420097 - VEGFA-VEGFR2 Pathway
- R-HSA-456926 - Thrombin signalling through proteinase activated receptors (PARs)
- R-HSA-5173105 - O-linked glycosylation
- R-HSA-5617833 - Cilium Assembly
- R-HSA-5620920 - Cargo trafficking to the periciliary membrane
- R-HSA-5624138 - Trafficking of myristoylated proteins to the cilium
- R-HSA-5653656 - Vesicle-mediated transport
- R-HSA-5663205 - Infectious disease
- R-HSA-597592 - Post-translational protein modification
- R-HSA-72086 - mRNA Capping
- R-HSA-73887 - Death Receptor Signaling
- R-HSA-76002 - Platelet activation, signaling and aggregation
- R-HSA-76005 - Response to elevated platelet cytosolic Ca2+
- R-HSA-8854214 - TBC/RABGAPs
- R-HSA-8939211 - ESR-mediated signaling
- R-HSA-8953854 - Metabolism of RNA
- R-HSA-9006931 - Signaling by Nuclear Receptors
- R-HSA-9006934 - Signaling by Receptor Tyrosine Kinases
- R-HSA-9007101 - Rab regulation of trafficking
- R-HSA-9009391 - Extra-nuclear estrogen signaling
- R-HSA-9675108 - Nervous system development
- R-HSA-977443 - GABA receptor activation
- R-HSA-977444 - GABA B receptor activation
- R-HSA-9824446 - Viral Infection Pathways
- R-HSA-991365 - Activation of GABAB receptors
Observed in studies
- Absence of tmRNA Increases the Persistence to Cefotaxime and the Intercellular Accumulation of Metabolite GlcNAc in <i>Aeromonas veronii</i>.
- 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)
- Cell-based and multi-omics profiling reveal dynamic metabolic repurposing of mitochondria to drive developmental progression of Trypanosoma brucei
- Hfq Regulates Efflux Pump Expression and Purine Metabolic Pathway to Increase the Trimethoprim Resistance in Aeromonas veronii
- Mitochondrial respiration controls neoangiogenesis during wound healing and tumour growth
- 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
- 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
- Multiomics of tomato glandular trichomes reveals distinct features of central carbon metabolism supporting high productivity of specialized metabolites
- Metabolomics dataset of PPAR-pan treated rat liver (acyl-carnitine and aqueous metabolite assays)
- F1Fo-ATP synthase subunit determines lethal pathogenic fungi infection
- Metabolomics and lipidomics reveal perturbation of sphingolipid metabolism by a novel anti-trypanosomal 3-(oxazolo[4,5-b]pyridine-2-yl)anilide
- Long-term low-dose ionizing radiation induced chromosome-aberration-specific metabolic phenotype changes in radiation workers
- 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
- TFAM loss induces nuclear actin assembly upon mDia2 malonylation to promote liver cancer metastasis.
- Comparative Metabolomic Profiling of Compatible and Incompatible Interactions Between Potato and Phytophthora infestans
- Phosphoproteomic and Metabolomic Profiling Uncovers the Roles of CcPmk1 in the Pathogenicity of <i>Cytospora chrysosperma</i>
- Limited nutrient availability in the tumor microenvironment renders pancreatic tumors sensitive to allosteric IDH1 inhibitors
- 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
- Diverse metabolic reactions activated during 58-hr fasting are revealed by non-targeted metabolomic analysis of human blood.
- Transcriptomics and metabolomics analysis reveal the anti-oxidation and immune boosting effects of mulberry leaves in growing mutton sheep
- Extracellular-acidosis restricts one-carbon metabolism and preserves T cell stemness
- Metabolomic Analysis of Fission Yeast at the Onset of Nitrogen Starvation
- 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
- 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)
Observed in differential profiles
- Wild_Type_vs_tmRNA_Deletion
- 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
- Non_Induced_0_Day_vs_Induced_8_Day
- Non_Induced_0_Day_vs_Induced_8_Day
- Wild_type_vs_hfq
- Control_vs_COX10_Knockout
- G3_Experimental_Sample_0h_vs_G11_Experimental_Sample_96h
- 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
- Calu3_Mock_DMEM_vs_Calu3_10uM_NIC
- Control_vs_Day_12
- Solanum_habrochaites_leaf_vs_glandular_trichome
- Control_vs_High
- WT_vs_16R
- Control_vs_OXPA_Treatment
- Control_vs_OXPA_Treatment
- LLIR_vs_Control
- G1_Control_vs_G2_Arginine_Addition
- Wild_Type_vs_Gene_Knockdown
- Glu_BW25113_vs_Pyr_BW25113
- Control_Cytoplasm_vs_TFAM_Knockdown_Cytoplasm
- Ziyun_No.1_0h_vs_Ziyun_No.1_96h
- CcPmk1_vs_Wild_type
- Wild_Type_vs_Gene_Knockout
- Dc-N_vs_Dc-HS
- Dcs_N_vs_Dcs_HS
- Blood_10h_vs_Blood_58h
- Control_vs_Fermented_Mulberry_Leaves
- Control_vs_Lactic_Acid
- 0_min_vs_60_min
- Control_vs_TGF-beta_Treatment
- Arginine_Replenished_Ctrl_vs_Arginine_Starved_48h
- Human_Blood_vs_Human_Plasma
- Human_Blood_vs_Human_Plasma
- Human_Blood_vs_Human_Plasma
- Blood_vs_Plasma
- Blood_vs_Plasma