Pyrrolidine, 1-(m-methoxycinnamoyl)-

Metabolite details

Identifier

LAPTWLCIZWFMJK-BQYQJAHWSA-N

InChI Key

LAPTWLCIZWFMJK-BQYQJAHWSA-N

IUPAC name

(E)-3-(3-methoxyphenyl)-1-pyrrolidin-1-ylprop-2-en-1-one

Preferred name

Pyrrolidine, 1-(m-methoxycinnamoyl)-

INN name

—

Synonym

—

ChEBI

CHEBI:157735

Reactome pathways

• No Reactome pathways listed for this metabolite.

Observed in studies

• 3D Imaging and metabolomic profiling reveal higher neuroactive kavalactone contents in lateral roots and crown root peels of Piper methysticum (kava)
• Multi-Omics Analysis Reveals Disturbance of Nanosecond Pulsed Electric Field in the Serum Metabolic Spectrum and Gut Microbiota
• Diallyl disulfide (DADS) ameliorates intestinal Candida albicans infection by modulating the gut microbiota and metabolites and providing intestinal protection in mice
• Transcriptomic and lipidomic profiling of subcutaneous and visceral adipose tissues in 15 vertebrates

Observed in differential profiles

• Crown_root_peel_vs_Crown_root_with_no_peel
• Control_vs_nsPEF_7_day
• G1_PBS_vs_G2_DSS
• G1_Sheep_ASA_SAT_vs_G2_Sheep_GOM_VAT