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Details

Stereochemistry RACEMIC
Molecular Formula C13H20N2O2
Molecular Weight 236.3101
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DROPROPIZINE

SMILES

OCC(O)CN1CCN(CC1)C2=CC=CC=C2

InChI

InChIKey=PTVWPYVOOKLBCG-UHFFFAOYSA-N
InChI=1S/C13H20N2O2/c16-11-13(17)10-14-6-8-15(9-7-14)12-4-2-1-3-5-12/h1-5,13,16-17H,6-11H2

HIDE SMILES / InChI

Molecular Formula C13H20N2O2
Molecular Weight 236.3101
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Description
Curator's Comment: Description was created based on several sources, including https://www.epharmapedia.com/medicine/profile/193457/Troferit.html?lang=en&tab=druginfo https://www.ncbi.nlm.nih.gov/pubmed/7649341

Dropropizine is a cough suppressant. It has peripheral action in non-productive cough. Dropropizine is commercialized in Latin American and African countries.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
TROFERIT

Approved Use

Dropropizine is primarily indicated in conditions like Non-productive cough.
PubMed

PubMed

TitleDatePubMed
Antitussive activity of the fruit extract of Emblica officinalis Gaertn. (Euphorbiaceae).
2003
Toxicological detection of the new designer drug 1-(4-methoxyphenyl)piperazine and its metabolites in urine and differentiation from an intake of structurally related medicaments using gas chromatography-mass spectrometry.
2003 Dec 25
Antitussive effect of diltiazem in experimental conditions.
2004
Studies on the human metabolism and the toxicologic detection of the cough suppressant dropropizine in urine using gas chromatography-mass spectrometry.
2004 Aug
The influence of animal species on the relationship between ATP-sensitive potassium ion channels and defense reflexes of the airways.
2009
Sensitive spectrophotometric method for quantitation of guaifenesin and dropropizine in their dosage forms.
2010
Effects of four antitussives on airway neurogenic inflammation in a guinea pig model of chronic cough induced by cigarette smoke exposure.
2013 Dec
Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: can also be used rectally http://www.ndrugs.com/?s=troferit
30 mg 6 or 8 hourly
Route of Administration: Oral
In Vitro Use Guide
When the Chinese hamster V79 cells were treated with the highest concentration of Dropropizine (8000 ug/ml), cytostatic effects lasting 24 h were observed
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:11:04 UTC 2023
Edited
by admin
on Sat Dec 16 17:11:04 UTC 2023
Record UNII
U0K8WHL37U
Record Status Validated (UNII)
Record Version
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Name Type Language
DROPROPIZINE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
DIPROPIZINE
Common Name English
RIBEX
Brand Name English
DROPROPIZINE [MI]
Common Name English
1,2-PROPANEDIOL, 3-(4-PHENYL-1-PIPERAZINYL)-
Systematic Name English
CATABEX
Brand Name English
dropropizine [INN]
Common Name English
LARYLIN
Brand Name English
DROPROPIZINE [MART.]
Common Name English
KATRIL
Brand Name English
(±)-DROPROPIZINE
Common Name English
U.C.B.-1967
Code English
NSC-757820
Code English
DOPROPIZIN
Common Name English
UCB 1967
Code English
UCB-1967
Code English
DITUSTAT
Brand Name English
Dropropizine [WHO-DD]
Common Name English
3-(4-PHENYL-1-PIPERAZINYL)-1,2-PROPANEDIOL
Systematic Name English
TUSSILEX
Brand Name English
Classification Tree Code System Code
NCI_THESAURUS C29698
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
WHO-VATC QR05DB19
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
WHO-ATC R05DB19
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
Code System Code Type Description
WIKIPEDIA
DROPROPIZINE
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
PRIMARY
MERCK INDEX
m4770
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
PRIMARY Merck Index
INN
2332
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
PRIMARY
EVMPD
SUB06412MIG
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
PRIMARY
DRUG CENTRAL
967
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
PRIMARY
NSC
757820
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
PRIMARY
RXCUI
23419
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
PRIMARY RxNorm
PUBCHEM
3169
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
PRIMARY
NCI_THESAURUS
C73179
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
PRIMARY
SMS_ID
100000092095
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
PRIMARY
ECHA (EC/EINECS)
241-683-7
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
PRIMARY
EPA CompTox
DTXSID0045624
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
PRIMARY
FDA UNII
U0K8WHL37U
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
PRIMARY
CAS
117067-01-3
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
SUPERSEDED
MESH
C035916
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
PRIMARY
DRUG BANK
DB13785
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
PRIMARY
CAS
17692-31-8
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
PRIMARY
ChEMBL
CHEMBL151445
Created by admin on Sat Dec 16 17:11:04 UTC 2023 , Edited by admin on Sat Dec 16 17:11:04 UTC 2023
PRIMARY
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ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
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ACTIVE MOIETY