CHEBI:28986 - anabasine

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ChEBI Name anabasine
ChEBI ID CHEBI:28986
Definition A pyridine alkaloid that is pyridine substituted by a piperidin-2-yl group at position 3.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:2695, CHEBI:22540
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Formula C10H14N2
Net Charge 0
Average Mass 162.23164
Monoisotopic Mass 162.11570
InChI InChI=1S/C10H14N2/c1-2-7-12-10(5-1)9-4-3-6-11-8-9/h3-4,6,8,10,12H,1-2,5,7H2
InChIKey MTXSIJUGVMTTMU-UHFFFAOYSA-N
SMILES C1CCC(NC1)c1cccnc1
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.
teratogenic agent
A role played by a chemical compound in biological systems with adverse consequences in embryo developments, leading to birth defects, embryo death or altered development, growth retardation and functional defect.
nicotinic acetylcholine receptor agonist
An agonist that selectively binds to and activates a nicotinic acetylcholine receptor.
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): nicotinic acetylcholine receptor agonist
An agonist that selectively binds to and activates a nicotinic acetylcholine receptor.
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ChEBI Ontology
Outgoing anabasine (CHEBI:28986) has role nicotinic acetylcholine receptor agonist (CHEBI:47958)
anabasine (CHEBI:28986) has role plant metabolite (CHEBI:76924)
anabasine (CHEBI:28986) has role teratogenic agent (CHEBI:50905)
anabasine (CHEBI:28986) is a piperidine alkaloid (CHEBI:26147)
anabasine (CHEBI:28986) is a pyridine alkaloid (CHEBI:26416)
Incoming tetrahydroanabasine(1+) (CHEBI:197286) has functional parent anabasine (CHEBI:28986)
(S)-anabasine (CHEBI:74) is a anabasine (CHEBI:28986)
IUPAC Name
3-(piperidin-2-yl)pyridine
Synonyms Sources
(±)-anabasine ChemIDplus
Anabasine KEGG COMPOUND
Manual Xrefs Databases
Anabasine Wikipedia
C06180 KEGG COMPOUND
LSM-4371 LINCS
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Registry Numbers Types Sources
13078-04-1 CAS Registry Number KEGG COMPOUND
13078-04-1 CAS Registry Number ChemIDplus
82639 Reaxys Registry Number Reaxys
82639 Beilstein Registry Number Beilstein
Citations Waiting for Citations Types Sources
25122040 PubMed citation Europe PMC
7226846 PubMed citation Europe PMC
Last Modified
25 February 2016