CHEBI:51174 - levopropoxyphene

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ChEBI Name levopropoxyphene
ChEBI ID CHEBI:51174
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C22H29NO2
Net Charge 0
Average Mass 339.472
Monoisotopic Mass 339.21983
InChI InChI=1S/C22H29NO2/c1-5-21(24)25-22(18(2)17-23(3)4,20-14-10-7-11-15-20)16-19-12-8-6-9-13-19/h6-15,18H,5,16-17H2,1-4H3/t18-,22+/m0/s1
InChIKey XLMALTXPSGQGBX-PGRDOPGGSA-N
SMILES C1=CC=C(C=C1)[C@@](CC2=CC=CC=C2)([C@H](CN(C)C)C)OC(CC)=O
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 levopropoxyphene (CHEBI:51174) has role antitussive (CHEBI:51177)
levopropoxyphene (CHEBI:51174) is a 1-benzyl-3-(dimethylamino)-2-methyl-1-phenylpropyl propanoate (CHEBI:77401)
levopropoxyphene (CHEBI:51174) is enantiomer of dextropropoxyphene (CHEBI:51173)
Incoming levopropoxyphene hydrochloride (CHEBI:51178) has part levopropoxyphene (CHEBI:51174)
levopropoxyphene napsylate (CHEBI:51176) has part levopropoxyphene (CHEBI:51174)
propoxyphene (CHEBI:8497) has part levopropoxyphene (CHEBI:51174)
dextropropoxyphene (CHEBI:51173) is enantiomer of levopropoxyphene (CHEBI:51174)
IUPAC Name
(1R,2S)-1-benzyl-3-(dimethylamino)-2-methyl-1-phenylpropyl propanoate
INNs Sources
levopropoxifeno WHO MedNet
lévopropoxyphène WHO MedNet
levopropoxyphene WHO MedNet
levopropoxyphenum WHO MedNet
Synonyms Sources
(-)-4-(Dimethylamino)-3-methyl-1,2-diphenyl-2-(propionyloxy)butane ChemIDplus
(-)-Propoxyphene ChemIDplus
(R)-alpha-(2-(Dimethylamino)-1-methylethyl)-alpha-phenylbenzeneethanol propanoate ChemIDplus
l-Propoxyphene ChemIDplus
Levopropossifene ChemIDplus
Manual Xref Database
1573 DrugCentral
View more database links
Registry Numbers Types Sources
2338-37-6 CAS Registry Number ChemIDplus
3219811 Beilstein Registry Number Beilstein
Last Modified
22 February 2017