U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C17H20ClNO.ClH
Molecular Weight 326.261
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHLOPHEDIANOL HYDROCHLORIDE

SMILES

Cl.CN(C)CCC(O)(C1=CC=CC=C1)C2=C(Cl)C=CC=C2

InChI

InChIKey=XYGSFNHCFFAJPO-UHFFFAOYSA-N
InChI=1S/C17H20ClNO.ClH/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;1H

HIDE SMILES / InChI

Molecular Formula C17H20ClNO
Molecular Weight 289.8
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including http://www.hmdb.ca/metabolites/HMDB15585 | https://www.ncbi.nlm.nih.gov/pubmed/24671376

Chlophedianol (Clofedanol) is a centrally-acting cough suppressant, although the mechanism of action is not known. It is available in Canada under the trade name Ulone. It is not available in the United States. Chlophedianol (Clofedanol) suppresses the cough reflex by a direct effect on the cough center in the medulla of the brain. It also has local anesthetic and antihistamine properties, and may have anticholinergic effects at high doses.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
ULONE

Approved Use

Indicated for the symptomatic relief of nonproductive cough. Chlophedianol is used to provide relief of acute cough due to minor throat and bronchial irritation occurring with colds or inhaled irritants.
Doses

Doses

DosePopulationAdverse events​
20 mg 3 times / day steady, oral
Recommended
Dose: 20 mg, 3 times / day
Route: oral
Route: steady
Dose: 20 mg, 3 times / day
Sources:
healthy, adult
n = 12
Health Status: healthy
Condition: cough
Age Group: adult
Sex: unknown
Population Size: 12
Sources:
Disc. AE: Allergic rash...
AEs leading to
discontinuation/dose reduction:
Allergic rash (1 patient)
Sources:
AEs

AEs

AESignificanceDosePopulation
Allergic rash 1 patient
Disc. AE
20 mg 3 times / day steady, oral
Recommended
Dose: 20 mg, 3 times / day
Route: oral
Route: steady
Dose: 20 mg, 3 times / day
Sources:
healthy, adult
n = 12
Health Status: healthy
Condition: cough
Age Group: adult
Sex: unknown
Population Size: 12
Sources:
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG

OverviewOther

Other InhibitorOther SubstrateOther Inducer


Drug as victim

Drug as victim

TargetModalityActivityMetaboliteClinical evidence
yes
yes
PubMed

PubMed

TitleDatePubMed
Chlophedianol Hydrochloride: A New Antitussive Agent.
1960 Dec 17
Clinical evaluation of chlophedianol a new nonnarcotic antitussive.
1962 Sep
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Usual adult and adolescent dose is 25 mg every six to eight hours as needed.
Route of Administration: Oral
In Vitro Use Guide
The inhibition of specific binding of [3H]dextromethorphan (4 nM) to guinea pig brain homogenate was determined. Chlophedianol, a phenylalkylamine, had an IC value of 1300 nM.
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:25:56 GMT 2023
Edited
by admin
on Fri Dec 15 16:25:56 GMT 2023
Record UNII
69QQ58998Y
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHLOPHEDIANOL HYDROCHLORIDE
MI   ORANGE BOOK   USAN  
USAN  
Official Name English
CLOFEDANOL HYDROCHLORIDE [MART.]
Common Name English
COLDRIN
Brand Name English
CLOFEDANOL HYDROCHLORIDE [JAN]
Common Name English
ULONE
Brand Name English
CHLOPHEDIANOL HCL
Common Name English
CHLOPHEDIANOL HYDROCHLORIDE [MI]
Common Name English
BENZENEMETHANOL, 2-CHLORO-.ALPHA.-(2-(DIMETHYLAMINO)ETHYL)-.ALPHA.-PHENYL-, HYDROCHLORIDE
Systematic Name English
Clofedanol hydrochloride [WHO-DD]
Common Name English
SK-74
Common Name English
SL-501
Code English
CLOFEDANOL HYDROCHLORIDE
MART.   WHO-DD  
Common Name English
PECTOLITAN
Brand Name English
2-Chloro-α-[2-(dimethylamino)ethyl]benzhydrol hydrochloride
Systematic Name English
SL 501
Code English
CHLOPHEDIANOL HYDROCHLORIDE [USAN]
Common Name English
ULO
Brand Name English
CHLOPHEDIANOL HYDROCHLORIDE [ORANGE BOOK]
Common Name English
BAYER-186
Code English
Classification Tree Code System Code
CFR 21 CFR 341.14
Created by admin on Fri Dec 15 16:25:56 GMT 2023 , Edited by admin on Fri Dec 15 16:25:56 GMT 2023
CFR 21 CFR 341.74
Created by admin on Fri Dec 15 16:25:56 GMT 2023 , Edited by admin on Fri Dec 15 16:25:56 GMT 2023
NCI_THESAURUS C66880
Created by admin on Fri Dec 15 16:25:56 GMT 2023 , Edited by admin on Fri Dec 15 16:25:56 GMT 2023
Code System Code Type Description
FDA UNII
69QQ58998Y
Created by admin on Fri Dec 15 16:25:56 GMT 2023 , Edited by admin on Fri Dec 15 16:25:56 GMT 2023
PRIMARY
RXCUI
1014329
Created by admin on Fri Dec 15 16:25:56 GMT 2023 , Edited by admin on Fri Dec 15 16:25:56 GMT 2023
PRIMARY RxNorm
EVMPD
SUB01354MIG
Created by admin on Fri Dec 15 16:25:56 GMT 2023 , Edited by admin on Fri Dec 15 16:25:56 GMT 2023
PRIMARY
SMS_ID
100000085212
Created by admin on Fri Dec 15 16:25:56 GMT 2023 , Edited by admin on Fri Dec 15 16:25:56 GMT 2023
PRIMARY
ECHA (EC/EINECS)
208-124-9
Created by admin on Fri Dec 15 16:25:56 GMT 2023 , Edited by admin on Fri Dec 15 16:25:56 GMT 2023
PRIMARY
DAILYMED
69QQ58998Y
Created by admin on Fri Dec 15 16:25:56 GMT 2023 , Edited by admin on Fri Dec 15 16:25:56 GMT 2023
PRIMARY
CAS
511-13-7
Created by admin on Fri Dec 15 16:25:56 GMT 2023 , Edited by admin on Fri Dec 15 16:25:56 GMT 2023
PRIMARY
NCI_THESAURUS
C65312
Created by admin on Fri Dec 15 16:25:56 GMT 2023 , Edited by admin on Fri Dec 15 16:25:56 GMT 2023
PRIMARY
MERCK INDEX
m3336
Created by admin on Fri Dec 15 16:25:56 GMT 2023 , Edited by admin on Fri Dec 15 16:25:56 GMT 2023
PRIMARY Merck Index
MESH
C010432
Created by admin on Fri Dec 15 16:25:56 GMT 2023 , Edited by admin on Fri Dec 15 16:25:56 GMT 2023
PRIMARY
ChEMBL
CHEMBL1201313
Created by admin on Fri Dec 15 16:25:56 GMT 2023 , Edited by admin on Fri Dec 15 16:25:56 GMT 2023
PRIMARY
DRUG BANK
DBSALT001414
Created by admin on Fri Dec 15 16:25:56 GMT 2023 , Edited by admin on Fri Dec 15 16:25:56 GMT 2023
PRIMARY
EPA CompTox
DTXSID30965375
Created by admin on Fri Dec 15 16:25:56 GMT 2023 , Edited by admin on Fri Dec 15 16:25:56 GMT 2023
PRIMARY
PUBCHEM
83813
Created by admin on Fri Dec 15 16:25:56 GMT 2023 , Edited by admin on Fri Dec 15 16:25:56 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY