Arecoline

GPTKB entity

Statements (50)
Predicate Object
gptkbp:instanceOf gptkb:chemical_compound
alkaloid
gptkbp:actsOn muscarinic acetylcholine receptor agonist
gptkbp:associatedWith gptkb:oral_submucous_fibrosis
oral cancer risk
gptkbp:boilingPoint 208 °C
gptkbp:CASNumber 300-08-3
gptkbp:chemicalFormula C8H13NO2
gptkbp:class tertiary amine
controlled substance (various countries)
Schedule I drug (Brazil)
Schedule IV drug (Germany)
gptkbp:drugClass parasympathomimetic
gptkbp:excretion kidneys
gptkbp:foundIn areca nut
gptkbp:hasInChIKey NETRQNHSXWFDAY-UHFFFAOYSA-N
gptkbp:hasSignalWord Danger
gptkbp:hasSMILES CN1CCC=CC1C(=O)OC
https://www.w3.org/2000/01/rdf-schema#label Arecoline
gptkbp:isSolubleIn gptkb:beer
gptkb:water
gptkb:chloroform
Ether
gptkbp:IUPACName methyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate
gptkbp:meltingPoint 62 °C
gptkbp:metabolism liver
gptkbp:molecularWeight 155.196 g/mol
gptkbp:producedBy gptkb:Areca_catechu
gptkbp:PubChem_CID 222
28039
gptkbp:relatedTo gptkb:guvacine
arecaidine
areca nut chewing
gptkbp:riskFactor H301 (Toxic if swallowed)
H311 (Toxic in contact with skin)
H331 (Toxic if inhaled)
gptkbp:sideEffect nausea
vomiting
salivation
tremor
sweating
bronchoconstriction
gptkbp:toxicity true
gptkbp:UNII 7M8A1834G3
gptkbp:usedAs stimulant
gptkbp:usedFor investigational drug
anthelmintic (historically)
gptkbp:usedIn research on Alzheimer's disease
gptkbp:bfsParent gptkb:Betel_nut
gptkbp:bfsLayer 6