CHEBI:7035 - muscimol

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ChEBI Name muscimol
ChEBI ID CHEBI:7035
Definition A member of the class of isoxazoles that is 1,2-oxazol-3(2H)-one substituted by an aminomethyl group at position 5. It has been isolated from mushrooms of the genus Amanita.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C4H6N2O2
Net Charge 0
Average Mass 114.10260
Monoisotopic Mass 114.043
InChI InChI=1S/C4H6N2O2/c5-2-3-1-4(7)6-8-3/h1H,2,5H2,(H,6,7)
InChIKey ZJQHPWUVQPJPQT-UHFFFAOYSA-N
SMILES NCc1cc(=O)[nH]o1
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): fungal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
GABA agonist
A drug that binds to and activates gamma-aminobutyric acid receptors.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via alkaloid )
Application(s): GABA agonist
A drug that binds to and activates gamma-aminobutyric acid receptors.
psychotropic drug
A loosely defined grouping of drugs that have effects on psychological function.
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ChEBI Ontology
Outgoing muscimol (CHEBI:7035) has role fungal metabolite (CHEBI:76946)
muscimol (CHEBI:7035) has role GABA agonist (CHEBI:51373)
muscimol (CHEBI:7035) has role psychotropic drug (CHEBI:35471)
muscimol (CHEBI:7035) is a alkaloid (CHEBI:22315)
muscimol (CHEBI:7035) is a isoxazoles (CHEBI:55373)
muscimol (CHEBI:7035) is a primary amino compound (CHEBI:50994)
IUPAC Name
5-(aminomethyl)-1,2-oxazol-3(2H)-one
Synonyms Sources
5-(aminomethyl)-3(2H)-isoxazolone ChemIDplus
Muscimol KEGG COMPOUND
Manual Xrefs Databases
C00001423 KNApSAcK
C08311 KEGG COMPOUND
Muscimol Wikipedia
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Registry Numbers Types Sources
2763-96-4 CAS Registry Number ChemIDplus
774694 Beilstein Registry Number Beilstein
774694 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
18599311 PubMed citation Europe PMC
21427702 PubMed citation Europe PMC
21751026 PubMed citation Europe PMC
2181052 PubMed citation Europe PMC
22049436 PubMed citation Europe PMC
24259680 PubMed citation Europe PMC
24316475 PubMed citation Europe PMC
24473816 PubMed citation Europe PMC
Last Modified
28 July 2014