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ChEBI

3-O-trans-p-coumaroyl actinidic acid

Term ID
CHEBI:65661
Synonyms
  • (2alpha,3beta)-2,23-dihydroxy-3-{[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}ursa-12,20(30)-dien-28-oic acid
  • 3beta-(trans-p-coumaroyl)oxy-2alpha,23-dihydroxyurs-12(13),20(30)-dien-28-oic acid
Definition
A pentacyclic triterpenoid that is the cinnamate ester obtained by the formal condensation of the carboxy group of trans-4-coumaric acid with the hydroxy group at position 3 of actinidic acid (the 2alpha,3beta stereoisomer). It is isolated from the roots of Actinidia arguta and exhibits inhibitory activity towards pancreatic lipase.
References
Ontology
ChEBI  ( EBI )
Relationships
is a type of
has_functional_parent
has_role
Phenotype
Phenotype resulting from 3-O-trans-p-coumaroyl actinidic acid
Phenotype where environments contain 3-O-trans-p-coumaroyl actinidic acid
Phenotype modified by environments containing 3-O-trans-p-coumaroyl actinidic acid
Human Disease / Model Data
Citations