Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C15H15N3O |
| Molecular Weight | 253.2991 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN1C=C2NC(=O)CN=C(C2=C1C)C3=CC=CC=C3
InChI
InChIKey=CNWSHOJSFGGNLC-UHFFFAOYSA-N
InChI=1S/C15H15N3O/c1-10-14-12(9-18(10)2)17-13(19)8-16-15(14)11-6-4-3-5-7-11/h3-7,9H,8H2,1-2H3,(H,17,19)
Premazepam is a pyrrolodiazepine derivative patented by Gruppi Lepetit S.p.A. as a muscle relaxant. Premazepam is a partial agonist of benzodiazepine receptors and was shown in 1984 to possess both anxiolytic and sedative properties in humans. Premazepam had a different EEG profile from diazepam, producing slower and less fast wave activity. In the single dose study, its effects were similar to diazepam for sedative action and most of the psychological tests, with a tendency towards greater psychomotor impairment. In the repeated dose study, however, premazepam caused less sedation and also tended to produce less psychomotor impairment.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6148956
5 and 10 mg twice-daily
Route of Administration:
Oral
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Official Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C1012
Created by
admin on Wed Apr 02 09:53:22 GMT 2025 , Edited by admin on Wed Apr 02 09:53:22 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
57435-86-6
Created by
admin on Wed Apr 02 09:53:22 GMT 2025 , Edited by admin on Wed Apr 02 09:53:22 GMT 2025
|
PRIMARY | |||
|
Premazepam
Created by
admin on Wed Apr 02 09:53:22 GMT 2025 , Edited by admin on Wed Apr 02 09:53:22 GMT 2025
|
PRIMARY | |||
|
72104
Created by
admin on Wed Apr 02 09:53:22 GMT 2025 , Edited by admin on Wed Apr 02 09:53:22 GMT 2025
|
PRIMARY | |||
|
OI7443PDLB
Created by
admin on Wed Apr 02 09:53:22 GMT 2025 , Edited by admin on Wed Apr 02 09:53:22 GMT 2025
|
PRIMARY | |||
|
C66465
Created by
admin on Wed Apr 02 09:53:22 GMT 2025 , Edited by admin on Wed Apr 02 09:53:22 GMT 2025
|
PRIMARY | |||
|
SUB10026MIG
Created by
admin on Wed Apr 02 09:53:22 GMT 2025 , Edited by admin on Wed Apr 02 09:53:22 GMT 2025
|
PRIMARY | |||
|
DTXSID60206026
Created by
admin on Wed Apr 02 09:53:22 GMT 2025 , Edited by admin on Wed Apr 02 09:53:22 GMT 2025
|
PRIMARY | |||
|
5039
Created by
admin on Wed Apr 02 09:53:22 GMT 2025 , Edited by admin on Wed Apr 02 09:53:22 GMT 2025
|
PRIMARY | |||
|
100000081408
Created by
admin on Wed Apr 02 09:53:22 GMT 2025 , Edited by admin on Wed Apr 02 09:53:22 GMT 2025
|
PRIMARY | |||
|
C041286
Created by
admin on Wed Apr 02 09:53:22 GMT 2025 , Edited by admin on Wed Apr 02 09:53:22 GMT 2025
|
PRIMARY | |||
|
CHEMBL2104741
Created by
admin on Wed Apr 02 09:53:22 GMT 2025 , Edited by admin on Wed Apr 02 09:53:22 GMT 2025
|
PRIMARY | |||
|
290940
Created by
admin on Wed Apr 02 09:53:22 GMT 2025 , Edited by admin on Wed Apr 02 09:53:22 GMT 2025
|
PRIMARY |
ACTIVE MOIETY