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Details

Stereochemistry RACEMIC
Molecular Formula C20H23NO
Molecular Weight 293.4027
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of QUIFENADINE

SMILES

OC(C1CN2CCC1CC2)(C3=CC=CC=C3)C4=CC=CC=C4

InChI

InChIKey=PZMAHNDJABQWGS-UHFFFAOYSA-N
InChI=1S/C20H23NO/c22-20(17-7-3-1-4-8-17,18-9-5-2-6-10-18)19-15-21-13-11-16(19)12-14-21/h1-10,16,19,22H,11-15H2

HIDE SMILES / InChI

Molecular Formula C20H23NO
Molecular Weight 293.4027
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Quifenadine is an antihistaminic agent. Quifenadine both blocks histamine H1-receptors in the peripheral tissues, and activates enzyme diaminoxidase (histaminase), due to this decreasing the histamine concentration in tissues. It is indicated in cases of pollinosis, acute and chronic urticaria, seasonal rhinitis (hay fever), allergic rhinitis, allergic conjunctivitis, angioneurotic Quinqe’s edema, dermatosis (eczema, neurodermatitis, pruritus etc.), allergic reactions caused by food or medicines. Quifanidine exhibits antiarrhythmic activity in children with frequent premature beats, without significant QT prolongation, or sinus node depression.

Approval Year

Sample Use Guides

For adults: single dose is 25-50 mg 2-4 times a day. Maximum daily dose is 200 mg. For children older than 12 years - 25 mg 2-3 times a day. The duration of the course of treatment is 10-20 days. If it is necessary, the course of treatment may be repeated.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:19:08 GMT 2023
Edited
by admin
on Fri Dec 15 16:19:08 GMT 2023
Record UNII
W9A18RJ49B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
QUIFENADINE
INN   WHO-DD  
INN  
Official Name English
quifenadine [INN]
Common Name English
.ALPHA.,.ALPHA.-DIPHENYL-3-QUINUCLIDINEMETHANOL
Systematic Name English
Quifenadine [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29578
Created by admin on Fri Dec 15 16:19:08 GMT 2023 , Edited by admin on Fri Dec 15 16:19:08 GMT 2023
WHO-VATC QR06AX31
Created by admin on Fri Dec 15 16:19:08 GMT 2023 , Edited by admin on Fri Dec 15 16:19:08 GMT 2023
WHO-ATC R06AX31
Created by admin on Fri Dec 15 16:19:08 GMT 2023 , Edited by admin on Fri Dec 15 16:19:08 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C81147
Created by admin on Fri Dec 15 16:19:08 GMT 2023 , Edited by admin on Fri Dec 15 16:19:08 GMT 2023
PRIMARY
EVMPD
SUB10193MIG
Created by admin on Fri Dec 15 16:19:08 GMT 2023 , Edited by admin on Fri Dec 15 16:19:08 GMT 2023
PRIMARY
DRUG BANK
DB13713
Created by admin on Fri Dec 15 16:19:08 GMT 2023 , Edited by admin on Fri Dec 15 16:19:08 GMT 2023
PRIMARY
CAS
10447-39-9
Created by admin on Fri Dec 15 16:19:08 GMT 2023 , Edited by admin on Fri Dec 15 16:19:08 GMT 2023
PRIMARY
DRUG CENTRAL
4748
Created by admin on Fri Dec 15 16:19:08 GMT 2023 , Edited by admin on Fri Dec 15 16:19:08 GMT 2023
PRIMARY
SMS_ID
100000081083
Created by admin on Fri Dec 15 16:19:08 GMT 2023 , Edited by admin on Fri Dec 15 16:19:08 GMT 2023
PRIMARY
ChEMBL
CHEMBL1187694
Created by admin on Fri Dec 15 16:19:08 GMT 2023 , Edited by admin on Fri Dec 15 16:19:08 GMT 2023
PRIMARY
PUBCHEM
65600
Created by admin on Fri Dec 15 16:19:08 GMT 2023 , Edited by admin on Fri Dec 15 16:19:08 GMT 2023
PRIMARY
INN
4714
Created by admin on Fri Dec 15 16:19:08 GMT 2023 , Edited by admin on Fri Dec 15 16:19:08 GMT 2023
PRIMARY
EPA CompTox
DTXSID6046187
Created by admin on Fri Dec 15 16:19:08 GMT 2023 , Edited by admin on Fri Dec 15 16:19:08 GMT 2023
PRIMARY
MESH
C014742
Created by admin on Fri Dec 15 16:19:08 GMT 2023 , Edited by admin on Fri Dec 15 16:19:08 GMT 2023
PRIMARY
FDA UNII
W9A18RJ49B
Created by admin on Fri Dec 15 16:19:08 GMT 2023 , Edited by admin on Fri Dec 15 16:19:08 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY