Avenestergenin A1

Metabolite details

Identifier

DESUBBPDSFNHTF-UHFFFAOYSA-N

InChI Key

DESUBBPDSFNHTF-UHFFFAOYSA-N

IUPAC name

[2-ormyl-5,10-dihydroxy-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-14-oxo-3,4,5,6,6a,7,8,8a,10,11,12,13,14a,14b-tetradecahydro-1H-picen-3-yl] 2-(methylamino)benzoate

Preferred name

Avenestergenin A1

INN name

—

Synonym

3,16,23-Trihydroxy-12,29-dioxooleanan-21-yl 2-(methylamino)benzoate

ChEBI

CHEBI:184208

Reactome pathways

• No Reactome pathways listed for this metabolite.

Observed in studies

• Mechanical force promotes dimethylarginine dimethylaminohydrolase 1-mediated hydrolysis of the metabolite asymmetric dimethylarginine to enhance bone formation
• Transcriptomic dynamics control rapid transition of core crop functions in 'lactating' pigeon
• PatA mediates biofilm formation and drugs resistance through regulating the synthesis of glycolipids and lipids in mycobacterium PatA mediates a novel mycolic acid synthesis pathway and regulates biofilm formation in mycobacterium

Observed in differential profiles

• Control_vs_Exercise
• Male_19_days_vs_Male_1_day
• wild_type_vs_patA_deletion