CHEBI:65465 - bassiatin

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ChEBI Name bassiatin
Definition A member of the class of morpholines that is morpholine-2,5-dione substituted by a benzyl, isopropyl and a methyl group at positions 3, 6 and 4 respectively. It is isolated from the culture broth of the fungus Beauveria bassiana and acts as a platelet aggregation inhibitor.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C15H19NO3
Net Charge 0
Average Mass 261.31630
Monoisotopic Mass 261.13649
InChI InChI=1S/C15H19NO3/c1-10(2)13-14(17)16(3)12(15(18)19-13)9-11-7-5-4-6-8-11/h4-8,10,12-13H,9H2,1-3H3/t12-,13+/m0/s1
SMILES CC(C)[C@H]1OC(=O)[C@H](Cc2ccccc2)N(C)C1=O
Metabolite of Species Details
Beauveria bassiana (NCBI:txid176275) of strain K 717 See: PubMed
Roles Classification
Biological Role(s): antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Application(s): platelet aggregation inhibitor
A drug or agent which antagonizes or impairs any mechanism leading to blood platelet aggregation, whether during the phases of activation and shape change or following the dense-granule release reaction and stimulation of the prostaglandin-thromboxane system.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing bassiatin (CHEBI:65465) has role antimicrobial agent (CHEBI:33281)
bassiatin (CHEBI:65465) has role metabolite (CHEBI:25212)
bassiatin (CHEBI:65465) has role platelet aggregation inhibitor (CHEBI:50427)
bassiatin (CHEBI:65465) is a diketone (CHEBI:46640)
bassiatin (CHEBI:65465) is a morpholines (CHEBI:38785)
Synonyms Sources
(3S,6R)-3-benzyl-6-isopropyl-4-methyl-2,5-morpholinedione ChEBI
(3S,6R)-4-methyl-6-(1-methylethyl)-3-(phenylmethyl)-2,5-morpholinedione ChEBI
(3S,6R)-4-methyl-6-(1-methylethyl)-3-phenylmethyl-1,4-perhydrooxazine-2,5-dione ChEBI
Lateritin ChemIDplus
Registry Numbers Types Sources
65454-13-9 CAS Registry Number ChemIDplus
7466012 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
8557595 PubMed citation Europe PMC
Last Modified
19 November 2012