Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C21H23ClN4O2 |
| Molecular Weight | 398.886 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC1=CC(=CC=C1)N2CCN(CCCN3C(=O)NC4=C(C=CC=C4)C3=O)CC2
InChI
InChIKey=FXZJKVODWNYPKK-UHFFFAOYSA-N
InChI=1S/C21H23ClN4O2/c22-16-5-3-6-17(15-16)25-13-11-24(12-14-25)9-4-10-26-20(27)18-7-1-2-8-19(18)23-21(26)28/h1-3,5-8,15H,4,9-14H2,(H,23,28)
| Molecular Formula | C21H23ClN4O2 |
| Molecular Weight | 398.886 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/5885076
Sources: https://www.ncbi.nlm.nih.gov/pubmed/5885076
Cloperidone is a quinazolinedione derivative with sedative and antihypertensive properties. Cloperidone was discovered in 1965 by Miles Laboratories. The activity of the compound was demonstrated by behavioral observations in dogs and cats, by rotarod and activity cage experiments in mice and in other models.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:42:36 GMT 2025
by
admin
on
Mon Mar 31 18:42:36 GMT 2025
|
| Record UNII |
8FP5Y6U39R
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C29756
Created by
admin on Mon Mar 31 18:42:36 GMT 2025 , Edited by admin on Mon Mar 31 18:42:36 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
4052-13-5
Created by
admin on Mon Mar 31 18:42:36 GMT 2025 , Edited by admin on Mon Mar 31 18:42:36 GMT 2025
|
PRIMARY | |||
|
10675
Created by
admin on Mon Mar 31 18:42:36 GMT 2025 , Edited by admin on Mon Mar 31 18:42:36 GMT 2025
|
PRIMARY | |||
|
C79578
Created by
admin on Mon Mar 31 18:42:36 GMT 2025 , Edited by admin on Mon Mar 31 18:42:36 GMT 2025
|
PRIMARY | |||
|
CHEMBL2110792
Created by
admin on Mon Mar 31 18:42:36 GMT 2025 , Edited by admin on Mon Mar 31 18:42:36 GMT 2025
|
PRIMARY | |||
|
SUB06738MIG
Created by
admin on Mon Mar 31 18:42:36 GMT 2025 , Edited by admin on Mon Mar 31 18:42:36 GMT 2025
|
PRIMARY | |||
|
100000083997
Created by
admin on Mon Mar 31 18:42:36 GMT 2025 , Edited by admin on Mon Mar 31 18:42:36 GMT 2025
|
PRIMARY | |||
|
DTXSID30193530
Created by
admin on Mon Mar 31 18:42:36 GMT 2025 , Edited by admin on Mon Mar 31 18:42:36 GMT 2025
|
PRIMARY | |||
|
8FP5Y6U39R
Created by
admin on Mon Mar 31 18:42:36 GMT 2025 , Edited by admin on Mon Mar 31 18:42:36 GMT 2025
|
PRIMARY | |||
|
2262
Created by
admin on Mon Mar 31 18:42:36 GMT 2025 , Edited by admin on Mon Mar 31 18:42:36 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
METABOLITE ACTIVE -> PARENT |
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |