CHEBI:71253 - asenapine

ChEBI IDCHEBI:71253
ChEBI Nameasenapine
Stars
DefinitionA racemate consisting of equal amounts of (R,R)- and (S,S)-asenapine. Used as its maleate salt for the acute treatment of schizophrenia and acute treatment of manic or mixed episodes associated with bipolar I disorder with or without psychotic features.
Last Modified22 February 2017
SubmitterSteve
Wikipedia
Roles Classification
Biological Roles:
dopaminergic antagonist  A drug that binds to but does not activate dopamine receptors, thereby blocking the actions of dopamine or exogenous agonists.
alpha-adrenergic antagonist  An agent that binds to but does not activate α-adrenergic receptors thereby blocking the actions of endogenous or exogenous α-adrenergic agonists. α-Adrenergic antagonists are used in the treatment of hypertension, vasospasm, peripheral vascular disease, shock, and pheochromocytoma.
beta-adrenergic antagonist  An agent that binds to but does not activate β-adrenergic receptors thereby blocking the actions of endogenous or exogenous β-adrenergic agonists. β-Adrenergic antagonists are used for treatment of hypertension, cardiac arrhythmias, angina pectoris, glaucoma, migraine headaches and anxiety.
serotonergic antagonist  Drugs that bind to but do not activate serotonin receptors, thereby blocking the actions of serotonin or serotonergic agonists.
Applications:
dopaminergic antagonist  A drug that binds to but does not activate dopamine receptors, thereby blocking the actions of dopamine or exogenous agonists.
psychotropic drug  A loosely defined grouping of drugs that have effects on psychological function.
alpha-adrenergic antagonist  An agent that binds to but does not activate α-adrenergic receptors thereby blocking the actions of endogenous or exogenous α-adrenergic agonists. α-Adrenergic antagonists are used in the treatment of hypertension, vasospasm, peripheral vascular disease, shock, and pheochromocytoma.
second generation antipsychotic  Antipsychotic drugs which can have different modes of action but which tend to be less likely than first generation antipsychotics to cause extrapyramidal motor control disabilities such as body rigidity or Parkinson's disease-type movements.
beta-adrenergic antagonist  An agent that binds to but does not activate β-adrenergic receptors thereby blocking the actions of endogenous or exogenous β-adrenergic agonists. β-Adrenergic antagonists are used for treatment of hypertension, cardiac arrhythmias, angina pectoris, glaucoma, migraine headaches and anxiety.
serotonergic antagonist  Drugs that bind to but do not activate serotonin receptors, thereby blocking the actions of serotonin or serotonergic agonists.
ChEBI Ontology
Outgoing Relation(s)
asenapine (CHEBI:71253) has part (R,R)-asenapine (CHEBI:71256)
asenapine (CHEBI:71253) has part (S,S)-asenapine (CHEBI:71257)
asenapine (CHEBI:71253) has role dopaminergic antagonist (CHEBI:48561)
asenapine (CHEBI:71253) has role psychotropic drug (CHEBI:35471)
asenapine (CHEBI:71253) has role second generation antipsychotic (CHEBI:65191)
asenapine (CHEBI:71253) has role serotonergic antagonist (CHEBI:48279)
asenapine (CHEBI:71253) has role α-adrenergic antagonist (CHEBI:37890)
asenapine (CHEBI:71253) has role β-adrenergic antagonist (CHEBI:35530)
asenapine (CHEBI:71253) is a racemate (CHEBI:60911)
asenapine (CHEBI:71253) is conjugate base of asenapine(1+) (CHEBI:71249)
Incoming Relation(s)
asenapine(1+) (CHEBI:71249) is conjugate acid of asenapine (CHEBI:71253)
IUPAC Name 
rac-(3aR,12bR)-5-chloro-2-methyl-2,3,3a,12b-tetrahydro-1H-dibenzo[2,3:6,7]oxepino[4,5-c]pyrrole
INNs  Source
asenapinaWHO MedNet
asénapineWHO MedNet
asenapinumWHO MedNet
asenapineWHO MedNet
Synonyms  Source
trans-5-Chloro-2,3,3a,12b-tetrahydro-2-methyl-1H-dibenz(2,3:6,7)oxepino(4,5-c)pyrroleChemIDplus
(3aRS,12bRS)-5-chloro-2-methyl-2,3,3a,12b-tetrahydro-1H-dibenzo[2,3:6,7]oxepino[4,5-c]pyrroleChEBI
(±)-asenapineChEBI
Manual XrefsDatabases
WO2012040845Patent
WO2012038975Patent
WO2012123325Patent
US2006229352Patent
US2005119248Patent
AsenapineWikipedia
US2006084692Patent
Registry NumbersSources
Reaxys:3654823Reaxys
CAS:65576-45-6ChemIDplus
Citations