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Details

Stereochemistry ACHIRAL
Molecular Formula C20H33NO3
Molecular Weight 335.4809
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OXELADIN

SMILES

CCN(CC)CCOCCOC(=O)C(CC)(CC)C1=CC=CC=C1

InChI

InChIKey=IQADUMSPOQKAAO-UHFFFAOYSA-N
InChI=1S/C20H33NO3/c1-5-20(6-2,18-12-10-9-11-13-18)19(22)24-17-16-23-15-14-21(7-3)8-4/h9-13H,5-8,14-17H2,1-4H3

HIDE SMILES / InChI

Description
Curator's Comment: Description was created based on several sources, including http://www.fda.gov.ph/consumers-corner/registered-drugs-2/337707-DR-X1387

Oxeladin citrate is a cough suppressant, is a highly potent and effective drug used to treat all types of cough of various etiologies. Withdrawn from the Canadian, US, and UK markets in 1976 due to carcinogenicity. Oxeladine is a component of antitussive drug, Altussan, approved in Philippines.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
Altussan

Approved Use

For the relief of all types of cough w/ acute and chronic inflammation due to upper and lower respiratory tract infections
PubMed

PubMed

TitleDatePubMed
Patents

Patents

Sample Use Guides

Cap Adult 1 cap. Syr Adult 1 tbsp (15 mL). Childn 1 tsp (5 mL). Infant ¼-½ tsp (1.25-2.5 mL). All doses to be taken 3 hrly.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Name Type Language
OXELADIN
INN   MI   WHO-DD  
INN  
Official Name English
oxeladin [INN]
Common Name English
Oxeladin [WHO-DD]
Common Name English
OXELADIN [MI]
Common Name English
2-(2-DIETHYLAMINOETHOXY)-ETHYL 2-ETHYL-2-PHENYLBUTYRATE
Systematic Name English
Classification Tree Code System Code
WHO-VATC QR05DB09
Created by admin on Fri Dec 15 15:12:58 UTC 2023 , Edited by admin on Fri Dec 15 15:12:58 UTC 2023
WHO-ATC R05DB09
Created by admin on Fri Dec 15 15:12:58 UTC 2023 , Edited by admin on Fri Dec 15 15:12:58 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C170272
Created by admin on Fri Dec 15 15:12:58 UTC 2023 , Edited by admin on Fri Dec 15 15:12:58 UTC 2023
PRIMARY
ChEMBL
CHEMBL1500276
Created by admin on Fri Dec 15 15:12:58 UTC 2023 , Edited by admin on Fri Dec 15 15:12:58 UTC 2023
PRIMARY
PUBCHEM
4619
Created by admin on Fri Dec 15 15:12:58 UTC 2023 , Edited by admin on Fri Dec 15 15:12:58 UTC 2023
PRIMARY
MESH
C005461
Created by admin on Fri Dec 15 15:12:58 UTC 2023 , Edited by admin on Fri Dec 15 15:12:58 UTC 2023
PRIMARY
WIKIPEDIA
Oxeladin
Created by admin on Fri Dec 15 15:12:58 UTC 2023 , Edited by admin on Fri Dec 15 15:12:58 UTC 2023
PRIMARY
FDA UNII
SNC1080T5Y
Created by admin on Fri Dec 15 15:12:58 UTC 2023 , Edited by admin on Fri Dec 15 15:12:58 UTC 2023
PRIMARY
CAS
468-61-1
Created by admin on Fri Dec 15 15:12:58 UTC 2023 , Edited by admin on Fri Dec 15 15:12:58 UTC 2023
PRIMARY
MERCK INDEX
m8299
Created by admin on Fri Dec 15 15:12:58 UTC 2023 , Edited by admin on Fri Dec 15 15:12:58 UTC 2023
PRIMARY Merck Index
DRUG CENTRAL
2018
Created by admin on Fri Dec 15 15:12:58 UTC 2023 , Edited by admin on Fri Dec 15 15:12:58 UTC 2023
PRIMARY
DRUG BANK
DB04822
Created by admin on Fri Dec 15 15:12:58 UTC 2023 , Edited by admin on Fri Dec 15 15:12:58 UTC 2023
PRIMARY
ECHA (EC/EINECS)
207-412-1
Created by admin on Fri Dec 15 15:12:58 UTC 2023 , Edited by admin on Fri Dec 15 15:12:58 UTC 2023
PRIMARY
EVMPD
SUB09513MIG
Created by admin on Fri Dec 15 15:12:58 UTC 2023 , Edited by admin on Fri Dec 15 15:12:58 UTC 2023
PRIMARY
INN
677
Created by admin on Fri Dec 15 15:12:58 UTC 2023 , Edited by admin on Fri Dec 15 15:12:58 UTC 2023
PRIMARY
SMS_ID
100000083056
Created by admin on Fri Dec 15 15:12:58 UTC 2023 , Edited by admin on Fri Dec 15 15:12:58 UTC 2023
PRIMARY
RXCUI
32626
Created by admin on Fri Dec 15 15:12:58 UTC 2023 , Edited by admin on Fri Dec 15 15:12:58 UTC 2023
PRIMARY RxNorm
EPA CompTox
DTXSID0048343
Created by admin on Fri Dec 15 15:12:58 UTC 2023 , Edited by admin on Fri Dec 15 15:12:58 UTC 2023
PRIMARY