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

Details

Stereochemistry ACHIRAL
Molecular Formula C22H27NO
Molecular Weight 321.4559
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHYBENZTROPINE

SMILES

CCN1[C@H]2CC[C@@H]1C[C@@H](C2)OC(C3=CC=CC=C3)C4=CC=CC=C4

InChI

InChIKey=PHTMLLGDZBZXMW-AERCQKQUSA-N
InChI=1S/C22H27NO/c1-2-23-19-13-14-20(23)16-21(15-19)24-22(17-9-5-3-6-10-17)18-11-7-4-8-12-18/h3-12,19-22H,2,13-16H2,1H3/t19-,20+,21+

HIDE SMILES / InChI

Molecular Formula C22H27NO
Molecular Weight 321.4559
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Ethybenzatropine (Ponalid) is an anticholinergic and antihistaminergic drug. It was used as an antiparkinsonian agent. A significant increase in the duration of action of levodopa-induced improvement in parkinsonian symptoms was observed following the administration of ethybenzatropine. Ethybenzatropine also improved, or tended to improve the duration and seventy of onset and end-of-dose levodopa-induced dyskinesias. Thus when levodopa is administered together with etybenzatropine, its length of action on parkinsonian symptoms is prolonged.

Approval Year

PubMed

PubMed

TitleDatePubMed
Effects of etybenzatropine and diazepam on levodopa-induced diphasic dyskinesias in Parkinson's disease.
1989

Sample Use Guides

Nine patients with Parkinson’s disease: Levodopa was given orally together with a peripheral DOPA-decarboxylase inhibitor at the usual effective morning dosage for each patient. The same dose of levodopa was administered the next day in addition to ethybenzatropine, 5 mg given i.v. Ethybenzatropine was administered between 0 and 15 min after the first dose of levodopa
Route of Administration: Intravenous
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:13:00 GMT 2023
Edited
by admin
on Fri Dec 15 16:13:00 GMT 2023
Record UNII
G1X2X9N95N
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETHYBENZTROPINE
MI   USAN  
USAN  
Official Name English
ETYBENZATROPINE
INN   MART.   WHO-DD  
INN  
Official Name English
Etybenzatropine [WHO-DD]
Common Name English
etybenzatropine [INN]
Common Name English
ETHYBENZTROPINE [MI]
Common Name English
UK-738
Code English
8-AZABICYCLO(3.2.1)OCTANE, 3-(DIPHENYLMETHOXY)-8-ETHYL-, ENDO-
Common Name English
ETYBENZATROPINE [MART.]
Common Name English
PANOLID
Brand Name English
ETHYBENZTROPINE [USAN]
Common Name English
3α-(Diphenylmethoxy)-8-ethyl-1αH,5αH-nortropane
Common Name English
Classification Tree Code System Code
WHO-VATC QN04AC30
Created by admin on Fri Dec 15 16:13:00 GMT 2023 , Edited by admin on Fri Dec 15 16:13:00 GMT 2023
WHO-ATC N04AC30
Created by admin on Fri Dec 15 16:13:00 GMT 2023 , Edited by admin on Fri Dec 15 16:13:00 GMT 2023
NCI_THESAURUS C66880
Created by admin on Fri Dec 15 16:13:00 GMT 2023 , Edited by admin on Fri Dec 15 16:13:00 GMT 2023
Code System Code Type Description
DAILYMED
G1X2X9N95N
Created by admin on Fri Dec 15 16:13:00 GMT 2023 , Edited by admin on Fri Dec 15 16:13:00 GMT 2023
PRIMARY
CAS
524-83-4
Created by admin on Fri Dec 15 16:13:00 GMT 2023 , Edited by admin on Fri Dec 15 16:13:00 GMT 2023
PRIMARY
RXCUI
1358000
Created by admin on Fri Dec 15 16:13:00 GMT 2023 , Edited by admin on Fri Dec 15 16:13:00 GMT 2023
PRIMARY RxNorm
FDA UNII
G1X2X9N95N
Created by admin on Fri Dec 15 16:13:00 GMT 2023 , Edited by admin on Fri Dec 15 16:13:00 GMT 2023
PRIMARY
MERCK INDEX
m5080
Created by admin on Fri Dec 15 16:13:00 GMT 2023 , Edited by admin on Fri Dec 15 16:13:00 GMT 2023
PRIMARY Merck Index
EVMPD
SUB07348MIG
Created by admin on Fri Dec 15 16:13:00 GMT 2023 , Edited by admin on Fri Dec 15 16:13:00 GMT 2023
PRIMARY
NCI_THESAURUS
C65562
Created by admin on Fri Dec 15 16:13:00 GMT 2023 , Edited by admin on Fri Dec 15 16:13:00 GMT 2023
PRIMARY
DRUG BANK
DB13468
Created by admin on Fri Dec 15 16:13:00 GMT 2023 , Edited by admin on Fri Dec 15 16:13:00 GMT 2023
PRIMARY
EPA CompTox
DTXSID50905096
Created by admin on Fri Dec 15 16:13:00 GMT 2023 , Edited by admin on Fri Dec 15 16:13:00 GMT 2023
PRIMARY
INN
1247
Created by admin on Fri Dec 15 16:13:00 GMT 2023 , Edited by admin on Fri Dec 15 16:13:00 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104273
Created by admin on Fri Dec 15 16:13:00 GMT 2023 , Edited by admin on Fri Dec 15 16:13:00 GMT 2023
PRIMARY
DRUG CENTRAL
4423
Created by admin on Fri Dec 15 16:13:00 GMT 2023 , Edited by admin on Fri Dec 15 16:13:00 GMT 2023
PRIMARY
SMS_ID
100000082136
Created by admin on Fri Dec 15 16:13:00 GMT 2023 , Edited by admin on Fri Dec 15 16:13:00 GMT 2023
PRIMARY
WIKIPEDIA
Etybenzatropine
Created by admin on Fri Dec 15 16:13:00 GMT 2023 , Edited by admin on Fri Dec 15 16:13:00 GMT 2023
PRIMARY
MESH
C027641
Created by admin on Fri Dec 15 16:13:00 GMT 2023 , Edited by admin on Fri Dec 15 16:13:00 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY