CHEBI:135207 - clofedanol

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ChEBI Name clofedanol
ChEBI ID CHEBI:135207
Definition A diarylmethane that is 2-chlorophenyl(phenyl)methane substituted on the methane carbon by a 2-(dimethylamino)ethyl group. Used in the treatment of dry cough, it suppresses the cough reflex by a direct effect on the cough centre in the medulla of the brain.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C17H20ClNO
Net Charge 0
Average Mass 289.800
Monoisotopic Mass 289.12334
InChI InChI=1S/C17H20ClNO/c1-19(2)13-12-17(20,14-8-4-3-5-9-14)15-10-6-7-11-16(15)18/h3-11,20H,12-13H2,1-2H3
InChIKey WRCHFMBCVFFYEQ-UHFFFAOYSA-N
SMILES C(CCN(C)C)(O)(C1=C(Cl)C=CC=C1)C2=CC=CC=C2
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Application(s): antitussive
An agent that suppresses cough. Antitussives have a central or a peripheral action on the cough reflex, or a combination of both. Compare with expectorants, which are considered to increase the volume of secretions in the respiratory tract, so facilitating their removal by ciliary action and coughing, and mucolytics, which decrease the viscosity of mucus, facilitating its removal by ciliary action and expectoration.
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ChEBI Ontology
Outgoing clofedanol (CHEBI:135207) has role antitussive (CHEBI:51177)
clofedanol (CHEBI:135207) is a diarylmethane (CHEBI:51614)
clofedanol (CHEBI:135207) is a tertiary amino compound (CHEBI:50996)
clofedanol (CHEBI:135207) is conjugate base of clofedanol(1+) (CHEBI:187895)
Incoming clofedanol(1+) (CHEBI:187895) is conjugate acid of clofedanol (CHEBI:135207)
IUPAC Name
1-(2-chlorophenyl)-3-(dimethylamino)-1-phenylpropan-1-ol
INNs Sources
clofédanol WHO MedNet
clofedanol WHO MedNet
clofedanol ChemIDplus
clofedanolum ChEBI
Synonym Source
chlophedianol DrugCentral
Manual Xrefs Databases
585 DrugCentral
Clofedanol Wikipedia
CN101844989 Patent
D07721 KEGG DRUG
DB04837 DrugBank
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Registry Numbers Types Sources
2813922 Reaxys Registry Number Reaxys
2813922 Beilstein Registry Number ChemIDplus
791-35-5 CAS Registry Number DrugCentral
791-35-5 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
14478530 PubMed citation Europe PMC
29438107 PubMed citation Europe PMC
Last Modified
14 June 2018