6b-Hydroxy-8a-methoxy-7(11)-eremophilen-12,8-olide

Metabolite details

Identifier

UTOHVMLCPJSXEB-UHFFFAOYSA-N

InChI Key

UTOHVMLCPJSXEB-UHFFFAOYSA-N

IUPAC name

4-hydroxy-9a-methoxy-3,4a,5-trimethyl-5,6,7,8,8a,9-hexahydro-4H-benzo[][1]benzouran-2-one

Preferred name

6b-Hydroxy-8a-methoxy-7(11)-eremophilen-12,8-olide

INN name

—

Synonym

—

ChEBI

CHEBI:174673

Reactome pathways

• No Reactome pathways listed for this metabolite.

Observed in studies

• Metabolic Dynamics of In Vitro CD8+ T Cell Activation.
• 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
• Metabolism Disorder Promotes Isoproterenol-induced Myocardial Injury in Mice with High Temperature and High Humidity and High-Fat Diet
• Effects of Radiofrequency Field from 5G Communications on fecal microbiome and metabolome profiles in mice

Observed in differential profiles

• G3_Experimental_Sample_0h_vs_G11_Experimental_Sample_96h
• G3_Experimental_Sample_0h_vs_G11_Experimental_Sample_96h
• Control_vs_nsPEF_7_day
• Control_vs_Exercise
• Control_vs_Isoproterenol
• Sham_vs_Radiofrequency