CHEBI:2866 - ascaridole

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ChEBI Name ascaridole
ChEBI ID CHEBI:2866
Definition A p-menthane monoterpenoid that is p-menth-2-ene with a peroxy group across position 1 to 4.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C10H16O2
Net Charge 0
Average Mass 168.23284
Monoisotopic Mass 168.115
InChI InChI=1S/C10H16O2/c1-8(2)10-6-4-9(3,5-7-10)11-12-10/h4,6,8H,5,7H2,1-3H3
InChIKey MGYMHQJELJYRQS-UHFFFAOYSA-N
SMILES CC(C)C12CCC(C)(OO1)C=C2
Roles Classification
Biological Role(s): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
antileishmanial agent
An antiprotozoal drug used to treat or prevent infections caused by protozoan parasites that belong to the genus Leishmania.
Application(s): antileishmanial agent
An antiprotozoal drug used to treat or prevent infections caused by protozoan parasites that belong to the genus Leishmania.
antinematodal drug
A substance used in the treatment or control of nematode infestations.
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ChEBI Ontology
Outgoing ascaridole (CHEBI:2866) has role antileishmanial agent (CHEBI:70868)
ascaridole (CHEBI:2866) has role antinematodal drug (CHEBI:35444)
ascaridole (CHEBI:2866) has role plant metabolite (CHEBI:76924)
ascaridole (CHEBI:2866) is a p-menthane monoterpenoid (CHEBI:25186)
ascaridole (CHEBI:2866) is a organic heterobicyclic compound (CHEBI:27171)
ascaridole (CHEBI:2866) is a organic peroxide (CHEBI:25702)
IUPAC Name
4-methyl-1-(propan-2-yl)-2,3-dioxabicyclo[2.2.2]oct-5-ene
Synonyms Sources
1,4-epidioxy-p-menth-2-ene ChemIDplus
1,4-peroxido-p-menthene-2 ChemIDplus
1,4-peroxy-p-menth-2-ene NIST Chemistry WebBook
1-isopropyl-4-methyl-2,3-dioxabicyclo[2.2.2]oct-5-ene NIST Chemistry WebBook
1-methyl-4-(1-methylethyl)-2,3-dioxabicyclo[2.2.2]oct-5-ene NIST Chemistry WebBook
Ascaridole KEGG COMPOUND
Database Links Databases
Ascaridole Wikipedia
C00003027 KNApSAcK
C09836 KEGG COMPOUND
HMDB0035766 HMDB
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Registry Numbers Types Sources
121382 Beilstein Registry Number Beilstein
121382 Reaxys Registry Number Reaxys
512-85-6 CAS Registry Number KEGG COMPOUND
512-85-6 CAS Registry Number NIST Chemistry WebBook
512-85-6 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
24184772 PubMed citation Europe PMC
24645715 PubMed citation Europe PMC
Last Modified
09 February 2015