CHEBI:31859 - modafinil

ChEBI IDCHEBI:31859
ChEBI Namemodafinil
Stars
DefinitionA racemate comprising equimolar amounts of armodafinil and (S)-modafinil. A central nervous system stimulant, it is used for the treatment of sleeping disorders such as narcolepsy, obstructive sleep apnoea, and shift-work sleep disorder. The optical enantiomers of modafinil have similar pharmacological actions in animals.
Last Modified22 February 2017
Wikipedia
Roles Classification
Biological Roles:
analgesic  An agent capable of relieving pain without the loss of consciousness or without producing anaesthesia. In addition, analgesic is a role played by a compound which is exhibited by a capability to cause a reduction of pain symptoms.
immunosuppressive agent  An agent that suppresses immune function by one of several mechanisms of action. Classical cytotoxic immunosuppressants act by inhibiting DNA synthesis. Others may act through activation of T-cells or by inhibiting the activation of helper cells. In addition, an immunosuppressive agent is a role played by a compound which is exhibited by a capability to diminish the extent and/or voracity of an immune response.
Applications:
antidepressant  Antidepressants are mood-stimulating drugs used primarily in the treatment of affective disorders and related conditions.
central nervous system stimulant  Any drug that enhances the activity of the central nervous system.
eugeroic  A phsychotropic drug that improves wakefulness and alertness, and reduces tiredness, drowsiness, and the need for sleep. Eugeroics are relatively non-addictive and are used in the treatment of narcolepsy and other sleep disorders.
analgesic  An agent capable of relieving pain without the loss of consciousness or without producing anaesthesia. In addition, analgesic is a role played by a compound which is exhibited by a capability to cause a reduction of pain symptoms.
antineoplastic agent  A substance that inhibits or prevents the proliferation of neoplasms.
antipsychotic agent  Antipsychotic drugs are agents that control agitated psychotic behaviour, alleviate acute psychotic states, reduce psychotic symptoms, and exert a quieting effect.
immunosuppressive agent  An agent that suppresses immune function by one of several mechanisms of action. Classical cytotoxic immunosuppressants act by inhibiting DNA synthesis. Others may act through activation of T-cells or by inhibiting the activation of helper cells. In addition, an immunosuppressive agent is a role played by a compound which is exhibited by a capability to diminish the extent and/or voracity of an immune response.
vasoconstrictor agent  Drug used to cause constriction of the blood vessels.
antiparkinson drug  A drug used in the treatment of Parkinson's disease.
ChEBI Ontology
Outgoing Relation(s)
modafinil (CHEBI:31859) has part (S)-modafinil (CHEBI:77591)
modafinil (CHEBI:31859) has part armodafinil (CHEBI:77590)
modafinil (CHEBI:31859) has role analgesic (CHEBI:35480)
modafinil (CHEBI:31859) has role antidepressant (CHEBI:35469)
modafinil (CHEBI:31859) has role antineoplastic agent (CHEBI:35610)
modafinil (CHEBI:31859) has role antiparkinson drug (CHEBI:48407)
modafinil (CHEBI:31859) has role antipsychotic agent (CHEBI:35476)
modafinil (CHEBI:31859) has role central nervous system stimulant (CHEBI:35337)
modafinil (CHEBI:31859) has role eugeroic (CHEBI:77567)
modafinil (CHEBI:31859) has role immunosuppressive agent (CHEBI:35705)
modafinil (CHEBI:31859) has role vasoconstrictor agent (CHEBI:50514)
modafinil (CHEBI:31859) is a organic molecular entity (CHEBI:50860)
modafinil (CHEBI:31859) is a racemate (CHEBI:60911)
IUPAC Name 
rac-2-[(diphenylmethyl)sulfinyl]acetamide
INNs  Source
modafinilWHO MedNet
modafinilWHO MedNet
modafiniloWHO MedNet
modafinilumWHO MedNet
Synonyms  Source
2-(benzhydrylsulfinyl)acetamideChemIDplus
CEP 1538ChEMBL
CEP-1538ChEBI
CRC-40476ChEMBL
CRL 40476ChemIDplus
CRL-40476ChEBI
Brand Name  Source
ProvigilKEGG DRUG
Manual XrefsDatabases
D01832KEGG DRUG
DB00745DrugBank
DE2809625Patent
HMDB0014883HMDB
ModafinilWikipedia
US4177290Patent
Registry NumbersSources
Reaxys:1978970Reaxys
CAS:68693-11-8ChemIDplus
Citations