CHEBI:65456 - asprellic acid C

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ChEBI Name asprellic acid C
ChEBI ID CHEBI:65456
Definition A pentacyclic triterpenoid that is the diester obtained by the global condensation of the hydroxy groups of (3β)-3,27-dihydroxyolean-12-en-28-oic acid with trans-4-coumaric acid and cis-4-coumaric acid respectively. It is isolated from the dried leaves of Ilex asprella and exhibits significant toxicity against KB (epidermoid carcinoma of the nasopharynx) and RPMI-7951 (melanoma) cell lines.
Stars This entity has been manually annotated by the ChEBI Team.
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Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
Related Structures
asprellic acid C is a Structural Derivative of
(3beta)-3,27-dihydroxyolean-12-en-28-oic acid
Mass : 472.69970
Formula : C30H48O4
71171
trans-4-coumaric acid
Mass : 164.15802
Formula : C9H8O3
32374
cis-4-coumaric acid
Mass : 164.15802
Formula : C9H8O3
17450
triterpene
Definition : A C30 terpene.
terpene
Definition : A hydrocarbon of biological origin having carbon skeleton formally derived from isoprene [CH22C(CH3)CH2CH2].
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