CHEBI:66156 - salvin B

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ChEBI Name salvin B
ChEBI ID CHEBI:66156
Definition A pentacyclic triterpenoid that is urs-12-en-28-oic acid substituted by hydroxy groups at positions 3, 6 and 24 (the 3α,6α stereoisomer). Isolated from Salvia santolinifolia, it exhibits inhibitory activity against cholinesterase.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C30H48O5
Net Charge 0
Average Mass 488.69910
Monoisotopic Mass 488.35017
InChI InChI=1S/C30H48O5/c1-25(2)11-13-30(24(34)35)14-12-28(5)18(19(30)15-25)7-8-21-26(3)10-9-22(33)27(4,17-31)23(26)20(32)16-29(21,28)6/h7,19-23,31-33H,8-17H2,1-6H3,(H,34,35)/t19-,20-,21+,22+,23+,26+,27-,28+,29+,30-/m0/s1
InChIKey XRRLUGUSXUFEDF-ZFZJRSJFSA-N
SMILES [H][C@@]12CC(C)(C)CC[C@@]1(CC[C@]1(C)C2=CC[C@]2([H])[C@@]3(C)CC[C@@H](O)[C@](C)(CO)[C@]3([H])[C@@H](O)C[C@@]12C)C(O)=O
Metabolite of Species Details
Salvia santolinifolia (NCBI:txid392689) Found in whole plant (BTO:0001461). See: PubMed
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.
EC 3.1.1.8 (cholinesterase) inhibitor
An EC 3.1.1.* (carboxylic ester hydrolase) inhibitor that interferes with the action of cholinesterase (EC 3.1.1.8).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing salvin B (CHEBI:66156) has parent hydride ursane (CHEBI:35711)
salvin B (CHEBI:66156) has role EC 3.1.1.8 (cholinesterase) inhibitor (CHEBI:37733)
salvin B (CHEBI:66156) has role metabolite (CHEBI:25212)
salvin B (CHEBI:66156) is a hydroxy monocarboxylic acid (CHEBI:35868)
salvin B (CHEBI:66156) is a pentacyclic triterpenoid (CHEBI:25872)
salvin B (CHEBI:66156) is a triol (CHEBI:27136)
IUPAC Name
(3α,6α)-3,6,24-trihydroxyolean-12-en-28-oic acid
Citation Waiting for Citations Type Source
16596990 PubMed citation Europe PMC
Last Modified
24 April 2013