Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C18H25NO.ClH |
| Molecular Weight | 307.858 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC2(CCN1CCCCC1)C(=O)CCC3=C2C=CC=C3
InChI
InChIKey=DWXUSWVHSCQVTM-UHFFFAOYSA-N
InChI=1S/C18H25NO.ClH/c1-18(11-14-19-12-5-2-6-13-19)16-8-4-3-7-15(16)9-10-17(18)20;/h3-4,7-8H,2,5-6,9-14H2,1H3;1H
| 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 |
| Molecular Formula | C18H25NO |
| Molecular Weight | 271.3972 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Nepinalone is a new alchilaminate derivative of β-tetralone, which possess a non-opioid antitussive activity. Nepinalone racemus exerted a significant antitussive activity and both L- and D-isomers confirmed to possess a significant dose-correlated antitussive effect with better trend of activity for D-isomer, but not statistically significant. It was predicted to act via sigma receptors. Occasionally, episodes of gastric intolerance have been reported and rapidly receded when treatment was stopped. The use of doses higher than those recommended could cause drowsiness.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:05:50 GMT 2025
by
admin
on
Mon Mar 31 21:05:50 GMT 2025
|
| Record UNII |
68J256455O
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
100000093025
Created by
admin on Mon Mar 31 21:05:50 GMT 2025 , Edited by admin on Mon Mar 31 21:05:50 GMT 2025
|
PRIMARY | |||
|
21742207
Created by
admin on Mon Mar 31 21:05:50 GMT 2025 , Edited by admin on Mon Mar 31 21:05:50 GMT 2025
|
PRIMARY | |||
|
22443-55-6
Created by
admin on Mon Mar 31 21:05:50 GMT 2025 , Edited by admin on Mon Mar 31 21:05:50 GMT 2025
|
PRIMARY | |||
|
SUB28841
Created by
admin on Mon Mar 31 21:05:50 GMT 2025 , Edited by admin on Mon Mar 31 21:05:50 GMT 2025
|
PRIMARY | |||
|
68J256455O
Created by
admin on Mon Mar 31 21:05:50 GMT 2025 , Edited by admin on Mon Mar 31 21:05:50 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
PARENT -> SALT/SOLVATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
ACTIVE MOIETY |