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Details

Stereochemistry ABSOLUTE
Molecular Formula C22H29NO2.ClH
Molecular Weight 375.932
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEVOPROPOXYPHENE HYDROCHLORIDE

SMILES

Cl.CCC(=O)O[C@](CC1=CC=CC=C1)([C@@H](C)CN(C)C)C2=CC=CC=C2

InChI

InChIKey=QMQBBUPJKANITL-VNJAQMQMSA-N
InChI=1S/C22H29NO2.ClH/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;1H/t18-,22+;/m0./s1

HIDE SMILES / InChI
LEVOPROPOXYPHENE is an antitussive drug, one of enantiomer of propoxyphene. Pdropoxyphene is an analgesic in the opioid category, patented in 1955 and manufactured by Eli Lilly and Company. Pdropoxyphene is intended to treat mild pain and also has antitussive (cough suppressant) and local anaesthetic effects.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
NOVRAD

Approved Use

Unknown

Launch Date

1962
Doses

Doses

DosePopulationAdverse events​
100 mg 6 times / day multiple, oral
Highest studied dose
Dose: 100 mg, 6 times / day
Route: oral
Route: multiple
Dose: 100 mg, 6 times / day
Sources:
unhealthy, adult
n = 50
Health Status: unhealthy
Condition: nonproductive cough
Age Group: adult
Sex: M+F
Population Size: 50
Sources:
Disc. AE: Nausea...
AEs leading to
discontinuation/dose reduction:
Nausea
Sources:
AEs

AEs

AESignificanceDosePopulation
Nausea Disc. AE
100 mg 6 times / day multiple, oral
Highest studied dose
Dose: 100 mg, 6 times / day
Route: oral
Route: multiple
Dose: 100 mg, 6 times / day
Sources:
unhealthy, adult
n = 50
Health Status: unhealthy
Condition: nonproductive cough
Age Group: adult
Sex: M+F
Population Size: 50
Sources:
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG



OverviewOther

Other InhibitorOther SubstrateOther Inducer


Drug as perpetrator​

Drug as perpetrator​

TargetModalityActivityMetaboliteClinical evidence
no [Activation >10 uM]
no [Activation >10 uM]
no [Activation >10 uM]
yes [Activation 5.01187 uM]
yes [Activation 7.94328 uM]
PubMed

PubMed

TitleDatePubMed
Patents

Patents

Sample Use Guides

The disposition of propoxyphene and its major biotransformation product norpropoxyphene was studied in normal subjects following a single 130 mg oral dose.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Name Type Language
LEVOPROPOXYPHENE HYDROCHLORIDE
MI  
Common Name English
LEVOPROPOXYPHENE HYDROCHLORIDE [MI]
Common Name English
PROPOXYPHENE HYDROCHLORIDE, (-)-
Common Name English
(.ALPHA.R)-.ALPHA.-((1S)-2-(DIMETHYLAMINO)-1-METHYLETHYL)-.ALPHA.-PHENYLBENZENEETHANOL 1-PROPANOATE HYDROCHLORIDE
Systematic Name English
L-PROPOXYPHENE HYDROCHLORIDE
Common Name English
.ALPHA.-L-PROPOXYPHENE HYDROCHLORIDE
Common Name English
BENZENEETHANOL, .ALPHA.-(2-(DIMETHYLAMINO)-1-METHYLETHYL)-.ALPHA.-PHENYL-, PROPANOATE (ESTER), HYDROCHLORIDE, (R-(R*,S*))-
Systematic Name English
Code System Code Type Description
CHEBI
51178
Created by admin on Sat Dec 16 08:38:24 GMT 2023 , Edited by admin on Sat Dec 16 08:38:24 GMT 2023
PRIMARY
EPA CompTox
DTXSID60936134
Created by admin on Sat Dec 16 08:38:24 GMT 2023 , Edited by admin on Sat Dec 16 08:38:24 GMT 2023
PRIMARY
MERCK INDEX
m6793
Created by admin on Sat Dec 16 08:38:24 GMT 2023 , Edited by admin on Sat Dec 16 08:38:24 GMT 2023
PRIMARY Merck Index
PUBCHEM
20055407
Created by admin on Sat Dec 16 08:38:24 GMT 2023 , Edited by admin on Sat Dec 16 08:38:24 GMT 2023
PRIMARY
ECHA (EC/EINECS)
216-484-3
Created by admin on Sat Dec 16 08:38:24 GMT 2023 , Edited by admin on Sat Dec 16 08:38:24 GMT 2023
PRIMARY
FDA UNII
WYL4776F4M
Created by admin on Sat Dec 16 08:38:24 GMT 2023 , Edited by admin on Sat Dec 16 08:38:24 GMT 2023
PRIMARY
CAS
1596-70-9
Created by admin on Sat Dec 16 08:38:24 GMT 2023 , Edited by admin on Sat Dec 16 08:38:24 GMT 2023
PRIMARY