3b-Hydroxy-6b-angeloyloxy-7(11)-eremophilen-12,8b-olide

Metabolite details

Identifier

VHVVIDFLXPOQAK-POHAHGRESA-N

InChI Key

VHVVIDFLXPOQAK-POHAHGRESA-N

IUPAC name

(6-hydroxy-3,4a,5-trimethyl-2-oxo-4,5,6,7,8,8a,9,9a-octahydrobenzo[][1]benzouran-4-yl) (Z)-2-methylbut-2-enoate

Preferred name

3b-Hydroxy-6b-angeloyloxy-7(11)-eremophilen-12,8b-olide

INN name

—

Synonym

—

ChEBI

CHEBI:175442

Reactome pathways

• No Reactome pathways listed for this metabolite.

Observed in studies

• Metabolic Dynamics of In Vitro CD8+ T Cell Activation.
• Mechanical force promotes dimethylarginine dimethylaminohydrolase 1-mediated hydrolysis of the metabolite asymmetric dimethylarginine to enhance bone formation
• Transcriptome and Metabolome Analyses Reveal Differences in Terpenoid and Flavonoid Biosynthesis in Cryptomeria fortunei Needles Across Different Seasons
• Mechanism of interventional effect and targets of Zhuyu Pill in regulating and suppressing colitis and cholestasis

Observed in differential profiles

• G3_Experimental_Sample_0h_vs_G11_Experimental_Sample_96h
• G3_Experimental_Sample_0h_vs_G11_Experimental_Sample_96h
• Control_vs_Exercise
• Summer_vs_Winter
• Control_vs_ZYP_High_Dose