CHEBI:67292 - desfuranoazadiradione

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ChEBI Name desfuranoazadiradione
ChEBI ID CHEBI:67292
Definition A limonoid that is azadiradione in which the furanyl group at position 17 is replaced by a hydrogen. It has been isolated from Azadirachta indica.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C24H32O4
Net Charge 0
Average Mass 384.50850
Monoisotopic Mass 384.23006
InChI InChI=1S/C24H32O4/c1-14(25)28-20-12-17-21(2,3)19(27)8-10-23(17,5)16-7-9-22(4)13-15(26)11-18(22)24(16,20)6/h8,10-11,16-17,20H,7,9,12-13H2,1-6H3/t16-,17+,20-,22+,23-,24-/m1/s1
InChIKey RACYWTTYSJTPOV-TUJRATNISA-N
SMILES CC(=O)O[C@@H]1C[C@H]2C(C)(C)C(=O)C=C[C@]2(C)[C@H]2CC[C@@]3(C)CC(=O)C=C3[C@]12C
Metabolite of Species Details
Azadirachta indica (NCBI:txid124943) Found in seed (BTO:0001226). Defatted MeOH extract of seeds 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.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing desfuranoazadiradione (CHEBI:67292) has functional parent azadiradione (CHEBI:67280)
desfuranoazadiradione (CHEBI:67292) has role metabolite (CHEBI:25212)
desfuranoazadiradione (CHEBI:67292) has role plant metabolite (CHEBI:76924)
desfuranoazadiradione (CHEBI:67292) is a acetate ester (CHEBI:47622)
desfuranoazadiradione (CHEBI:67292) is a cyclic terpene ketone (CHEBI:36130)
desfuranoazadiradione (CHEBI:67292) is a limonoid (CHEBI:39434)
desfuranoazadiradione (CHEBI:67292) is a tetracyclic triterpenoid (CHEBI:26893)
IUPAC Name
(5α,7α,13α)-4,4,8-trimethyl-3,16-dioxoandrosta-1,14-dien-7-yl acetate
Registry Number Type Source
5833387 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
21381696 PubMed citation Europe PMC
Last Modified
18 November 2013