[(5-hydroxy-2-methyl-2H-chromen-2-yl)methoxy]sulfonic acid

Metabolite details

Identifier

UYXDMSXIMGQHKE-UHFFFAOYSA-N

InChI Key

UYXDMSXIMGQHKE-UHFFFAOYSA-N

IUPAC name

(5-hydroxy-2-methylchromen-2-yl)methyl hydrogen sulate

Preferred name

[(5-hydroxy-2-methyl-2H-chromen-2-yl)methoxy]sulfonic acid

INN name

—

Synonym

—

ChEBI

CHEBI:184192

Reactome pathways

• No Reactome pathways listed for this metabolite.

Observed in studies

• Bioaccumulation of therapeutic drugs by human gut bacteria: cross-feeding metabolite analysis (FIA-MS) (E.rectale;S.salivarius assays)
• Multi-Omics Analysis Reveals Disturbance of Nanosecond Pulsed Electric Field in the Serum Metabolic Spectrum and Gut Microbiota
• Mechanical force promotes dimethylarginine dimethylaminohydrolase 1-mediated hydrolysis of the metabolite asymmetric dimethylarginine to enhance bone formation
• Interaction between Cervical Microbiota and Host Gene Regulation in Caesarean Section Scar Diverticulum
• Transcriptomic dynamics control rapid transition of core crop functions in 'lactating' pigeon

Observed in differential profiles

• G4_Eubacterium_rectale_DMSO_30_vs_G3_Eubacterium_rectale_Duloxetine_47
• Control_vs_nsPEF_7_day
• Control_vs_Exercise
• Control_vs_CSD
• Male_19_days_vs_Male_1_day