Details
Stereochemistry | RACEMIC |
Molecular Formula | C19H23NO2S |
Molecular Weight | 329.456 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC2=C(SC3=CC=CC=C3C2(O)CCCN(C)C)C=C1
InChI
InChIKey=LAYVFLWAVIGDLK-UHFFFAOYSA-N
InChI=1S/C19H23NO2S/c1-20(2)12-6-11-19(21)15-7-4-5-8-17(15)23-18-10-9-14(22-3)13-16(18)19/h4-5,7-10,13,21H,6,11-12H2,1-3H3
Meprotixol is a thiaxanthene derivative. Meprotixol revealed a potent antitussive activity. It has slight central depressive effect. Meprotixol reduces the spontaneous motor activity of mice, but its potency is negligible in comparison with those of neuroleptics such as chlorpromazine and chlorprothixene. Meprotixol in suitable doses reduces the quantity of barbiturate required to secure anesthesia. Meprotixol showed a potent broncho-spasmolytic effect against 5-hydroxytryptamine spasms in guinea pigs. This compound has a marked inhibitory effect against various forms of edema and exudation in the granuloma pouch, though the inhibition of granuloma formation was only slight. Phenylbutazone seemed to be more effective than meprotixol in the treatment of rheumatic disease.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/5338050
10 mg 3 times a day
Route of Administration:
Oral
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C66917
Created by
admin on Fri Dec 15 16:46:29 GMT 2023 , Edited by admin on Fri Dec 15 16:46:29 GMT 2023
|
||
|
WHO-ATC |
R05DB22
Created by
admin on Fri Dec 15 16:46:29 GMT 2023 , Edited by admin on Fri Dec 15 16:46:29 GMT 2023
|
||
|
WHO-VATC |
QR05DB22
Created by
admin on Fri Dec 15 16:46:29 GMT 2023 , Edited by admin on Fri Dec 15 16:46:29 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
C87660
Created by
admin on Fri Dec 15 16:46:29 GMT 2023 , Edited by admin on Fri Dec 15 16:46:29 GMT 2023
|
PRIMARY | |||
|
SUB08759MIG
Created by
admin on Fri Dec 15 16:46:29 GMT 2023 , Edited by admin on Fri Dec 15 16:46:29 GMT 2023
|
PRIMARY | |||
|
4656
Created by
admin on Fri Dec 15 16:46:29 GMT 2023 , Edited by admin on Fri Dec 15 16:46:29 GMT 2023
|
PRIMARY | |||
|
MEPROTIXOL
Created by
admin on Fri Dec 15 16:46:29 GMT 2023 , Edited by admin on Fri Dec 15 16:46:29 GMT 2023
|
PRIMARY | |||
|
1569
Created by
admin on Fri Dec 15 16:46:29 GMT 2023 , Edited by admin on Fri Dec 15 16:46:29 GMT 2023
|
PRIMARY | |||
|
4295-63-0
Created by
admin on Fri Dec 15 16:46:29 GMT 2023 , Edited by admin on Fri Dec 15 16:46:29 GMT 2023
|
PRIMARY | |||
|
71195
Created by
admin on Fri Dec 15 16:46:29 GMT 2023 , Edited by admin on Fri Dec 15 16:46:29 GMT 2023
|
PRIMARY | |||
|
2JXZ154Z0Q
Created by
admin on Fri Dec 15 16:46:29 GMT 2023 , Edited by admin on Fri Dec 15 16:46:29 GMT 2023
|
PRIMARY | |||
|
CHEMBL2105167
Created by
admin on Fri Dec 15 16:46:29 GMT 2023 , Edited by admin on Fri Dec 15 16:46:29 GMT 2023
|
PRIMARY | |||
|
DTXSID40863358
Created by
admin on Fri Dec 15 16:46:29 GMT 2023 , Edited by admin on Fri Dec 15 16:46:29 GMT 2023
|
PRIMARY | |||
|
DB13822
Created by
admin on Fri Dec 15 16:46:29 GMT 2023 , Edited by admin on Fri Dec 15 16:46:29 GMT 2023
|
PRIMARY | |||
|
100000081481
Created by
admin on Fri Dec 15 16:46:29 GMT 2023 , Edited by admin on Fri Dec 15 16:46:29 GMT 2023
|
PRIMARY |
ACTIVE MOIETY