13-hydroxy-α-tocopherol

Metabolite details

Identifier

URYLCCKXLNXSRS-XIRVVSDESA-N

InChI Key

URYLCCKXLNXSRS-XIRVVSDESA-N

IUPAC name

(2R)-2-[(4R,8S)-13-hydroxy-4,8,12-trimethyltridecyl]-2,5,7,8-tetramethyl-3,4-dihydro-2H-1-benzopyran-6-ol

Preferred name

13-hydroxy-α-tocopherol

INN name

—

Synonym

13-OH-alpha-tocopherol

ChEBI

CHEBI:84962

Reactome pathways

• No Reactome pathways listed for this metabolite.

Observed in studies

• Multi-Omics Analysis Reveals Disturbance of Nanosecond Pulsed Electric Field in the Serum Metabolic Spectrum and Gut Microbiota
• Jasmonate-mediated stomatal closure under elevated CO2 revealed by time-resolved metabolomics
• Mechanical force promotes dimethylarginine dimethylaminohydrolase 1-mediated hydrolysis of the metabolite asymmetric dimethylarginine to enhance bone formation
• Alterations in the gut microbiota and metabolomics of seafarers after a six-month sea voyage

Observed in differential profiles

• Control_vs_nsPEF_7_day
• 400ppm_0min_vs_800ppm_60min
• Control_vs_Exercise
• Control_0d_vs_Treatment_180d