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

Details

Stereochemistry RACEMIC
Molecular Formula C22H23NS.ClH
Molecular Weight 369.951
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of TROPATEPINE HYDROCHLORIDE

SMILES

Cl.CN1[C@H]2CC[C@@H]1C\C(C2)=C3\C4=CC=CC=C4CSC5=C3C=CC=C5

InChI

InChIKey=LVASURLUIYTDHW-ZCTOARNVSA-N
InChI=1S/C22H23NS.ClH/c1-23-17-10-11-18(23)13-16(12-17)22-19-7-3-2-6-15(19)14-24-21-9-5-4-8-20(21)22;/h2-9,17-18H,10-14H2,1H3;1H/b22-16-;/t17-,18+;/m0./s1

HIDE SMILES / InChI

Molecular Formula C22H23NS
Molecular Weight 333.49
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 1
Optical Activity UNSPECIFIED

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

Tropatepine is an anticholinergic drug. Intramuscular injections of tropatepine are used to counteract the extrapyramidal effects of neuroleptic drugs and for the treatment of Parkinson's disease. The drug is marketed in Europe under tradename Lepticur.

Approval Year

PubMed

PubMed

TitleDatePubMed
Effect of tropatepine, an anticholinergic drug, on regional cerebral blood flow in patients with Parkinson's disease.
1989 Jul
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:15:29 GMT 2023
Edited
by admin
on Fri Dec 15 19:15:29 GMT 2023
Record UNII
17N1U39U3Z
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TROPATEPINE HYDROCHLORIDE
MART.   WHO-DD  
Common Name English
TROPATEPINE HYDROCHLORIDE [MART.]
Common Name English
SD-1248-17
Code English
Tropatepine hydrochloride [WHO-DD]
Common Name English
TROPATEPINE HCL
Common Name English
3-(DIBENZO(B,E)THIEPIN-11(6H)-YLIDENE)TROPANE HYDROCHLORIDE
Systematic Name English
Code System Code Type Description
RXCUI
236190
Created by admin on Fri Dec 15 19:15:29 GMT 2023 , Edited by admin on Fri Dec 15 19:15:29 GMT 2023
PRIMARY RxNorm
EPA CompTox
DTXSID90950242
Created by admin on Fri Dec 15 19:15:29 GMT 2023 , Edited by admin on Fri Dec 15 19:15:29 GMT 2023
PRIMARY
ECHA (EC/EINECS)
248-535-0
Created by admin on Fri Dec 15 19:15:29 GMT 2023 , Edited by admin on Fri Dec 15 19:15:29 GMT 2023
PRIMARY
SMS_ID
100000084898
Created by admin on Fri Dec 15 19:15:29 GMT 2023 , Edited by admin on Fri Dec 15 19:15:29 GMT 2023
PRIMARY
EVMPD
SUB04998MIG
Created by admin on Fri Dec 15 19:15:29 GMT 2023 , Edited by admin on Fri Dec 15 19:15:29 GMT 2023
PRIMARY
CAS
27574-25-0
Created by admin on Fri Dec 15 19:15:29 GMT 2023 , Edited by admin on Fri Dec 15 19:15:29 GMT 2023
PRIMARY
FDA UNII
17N1U39U3Z
Created by admin on Fri Dec 15 19:15:29 GMT 2023 , Edited by admin on Fri Dec 15 19:15:29 GMT 2023
PRIMARY
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ACTIVE MOIETY