CHEBI:66593 - lucialdehyde B

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ChEBI Name lucialdehyde B
ChEBI ID CHEBI:66593
Definition A tetracyclic triterpenoid that is lanosta-8,24-dien-26-al substituted by oxo groups at positions 3 and 7. Isolated from Ganoderma lucidum and Ganoderma pfeifferi, it exhibits antiviral and cytotoxic activities.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C30H44O3
Net Charge 0
Average Mass 452.670
Monoisotopic Mass 452.32905
InChI InChI=1S/C30H44O3/c1-19(18-31)9-8-10-20(2)21-11-16-30(7)26-22(12-15-29(21,30)6)28(5)14-13-25(33)27(3,4)24(28)17-23(26)32/h9,18,20-21,24H,8,10-17H2,1-7H3/b19-9+/t20-,21-,24+,28-,29-,30+/m1/s1
InChIKey KZOBOICRKKYGAQ-GOUGDUPLSA-N
SMILES CC1(C)C(=O)CC[C@@]2(C3=C(C(C[C@@]12[H])=O)[C@@]4(CC[C@@]([C@@]4(C)CC3)([C@@H](CC/C=C(/C=O)\C)C)[H])C)C
Metabolite of Species Details
Ganoderma pfeifferi (NCBI:txid34464) See: PubMed
Ganoderma lucidum (NCBI:txid5315) See: PubMed
Roles Classification
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
anti-HSV agent
An antiviral agent that destroys or inhibits the replication of the herpes simplex virus (also known as the human herpes virus).
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing lucialdehyde B (CHEBI:66593) has parent hydride lanostane (CHEBI:20265)
lucialdehyde B (CHEBI:66593) has role anti-HSV agent (CHEBI:64952)
lucialdehyde B (CHEBI:66593) has role antineoplastic agent (CHEBI:35610)
lucialdehyde B (CHEBI:66593) has role metabolite (CHEBI:25212)
lucialdehyde B (CHEBI:66593) is a 3-oxo-5α-steroid (CHEBI:13601)
lucialdehyde B (CHEBI:66593) is a 7-oxo steroid (CHEBI:47789)
lucialdehyde B (CHEBI:66593) is a cyclic terpene ketone (CHEBI:36130)
lucialdehyde B (CHEBI:66593) is a steroid aldehyde (CHEBI:131565)
lucialdehyde B (CHEBI:66593) is a tetracyclic triterpenoid (CHEBI:26893)
IUPAC Name
(24E)-3,7-dioxolanosta-8,24-dien-26-al
Registry Number Type Source
9238781 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
12045343 PubMed citation Europe PMC
16378363 PubMed citation Europe PMC
Last Modified
06 November 2019