CHEBI:66555 - laurinterol

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ChEBI Name laurinterol
ChEBI ID CHEBI:66555
Definition A sesquiterpenoid isolated from Laurencia intermedia and Aplysia kurodai and has been found to exhibit antibacterial activity,
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C15H19BrO
Net Charge 0
Average Mass 295.21500
Monoisotopic Mass 294.062
InChI InChI=1S/C15H19BrO/c1-9-6-13(17)11(7-12(9)16)14(2)5-4-10-8-15(10,14)3/h6-7,10,17H,4-5,8H2,1-3H3/t10-,14+,15+/m1/s1
InChIKey UGGAHNIITODSKB-ONERCXAPSA-N
SMILES [H][C@]12CC[C@@](C)(c3cc(Br)c(C)cc3O)[C@@]1(C)C2
Metabolite of Species Details
Laurencia intermedia (99900:NCBI) See: DOI
Aplysia kurodai (NCBI:txid6501) 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.
apoptosis inducer
Any substance that induces the process of apoptosis (programmed cell death) in multi-celled organisms.
antibacterial agent
A substance that kills or slows the growth of bacteria.
EC 3.6.3.9 (Na(+)/K(+)-transporting ATPase) inhibitor
An EC 3.6.3.* (acid anhydride hydrolase catalysing transmembrane movement of substances) inhibitor that interferes with the action of Na+/K+-transporting ATPase (EC 3.6.3.9).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing laurinterol (CHEBI:66555) has role antibacterial agent (CHEBI:33282)
laurinterol (CHEBI:66555) has role apoptosis inducer (CHEBI:68495)
laurinterol (CHEBI:66555) has role EC 3.6.3.9 (Na+/K+-transporting ATPase) inhibitor (CHEBI:63510)
laurinterol (CHEBI:66555) has role metabolite (CHEBI:25212)
laurinterol (CHEBI:66555) is a organobromine compound (CHEBI:37141)
laurinterol (CHEBI:66555) is a phenols (CHEBI:33853)
laurinterol (CHEBI:66555) is a sesquiterpenoid (CHEBI:26658)
Incoming debromolaurinterol (CHEBI:66556) has functional parent laurinterol (CHEBI:66555)
Database Links Databases
C17136 KEGG COMPOUND
JP8245359 Patent
WO2009048195 Patent
View more database links
Registry Numbers Types Sources
10539-87-4 CAS Registry Number ChemIDplus
1880118 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
11302194 PubMed citation Europe PMC
15549668 PubMed citation Europe PMC
18598167 PubMed citation Europe PMC
Last Modified
03 March 2014