Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C21H19NO |
| Molecular Weight | 301.3817 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC([C@@H]1C[C@H]1C2=CC=NC=C2)(C3=CC=CC=C3)C4=CC=CC=C4
InChI
InChIKey=KPUSUIKQQCFQCX-VQTJNVASSA-N
InChI=1S/C21H19NO/c23-21(17-7-3-1-4-8-17,18-9-5-2-6-10-18)20-15-19(20)16-11-13-22-14-12-16/h1-14,19-20,23H,15H2/t19-,20+/m0/s1
| Molecular Formula | C21H19NO |
| Molecular Weight | 301.3817 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Cyprolidol is a pyridylcyclopropane derivative, developed by Neisler Laboratories. In animal models, cyprolidol produced an antidepressant effect qualitatively similar to those produced by imipramine. The compound blocked the tyramine-induced rise in blood pressure only in anesthetized dogs but potentiated it in conscious dogs. In man, cyprolidol was less effective than imipramine.
Originator
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:56:59 GMT 2023
by
admin
on
Fri Dec 15 18:56:59 GMT 2023
|
| Record UNII |
321552050N
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
CHEMBL2110906
Created by
admin on Fri Dec 15 18:56:59 GMT 2023 , Edited by admin on Fri Dec 15 18:56:59 GMT 2023
|
PRIMARY | |||
|
321552050N
Created by
admin on Fri Dec 15 18:56:59 GMT 2023 , Edited by admin on Fri Dec 15 18:56:59 GMT 2023
|
PRIMARY | |||
|
199758
Created by
admin on Fri Dec 15 18:56:59 GMT 2023 , Edited by admin on Fri Dec 15 18:56:59 GMT 2023
|
PRIMARY | |||
|
C166627
Created by
admin on Fri Dec 15 18:56:59 GMT 2023 , Edited by admin on Fri Dec 15 18:56:59 GMT 2023
|
PRIMARY | |||
|
DTXSID801014478
Created by
admin on Fri Dec 15 18:56:59 GMT 2023 , Edited by admin on Fri Dec 15 18:56:59 GMT 2023
|
PRIMARY | |||
|
4904-00-1
Created by
admin on Fri Dec 15 18:56:59 GMT 2023 , Edited by admin on Fri Dec 15 18:56:59 GMT 2023
|
PRIMARY | |||
|
100000083969
Created by
admin on Fri Dec 15 18:56:59 GMT 2023 , Edited by admin on Fri Dec 15 18:56:59 GMT 2023
|
PRIMARY | |||
|
2093
Created by
admin on Fri Dec 15 18:56:59 GMT 2023 , Edited by admin on Fri Dec 15 18:56:59 GMT 2023
|
PRIMARY | |||
|
SUB06876MIG
Created by
admin on Fri Dec 15 18:56:59 GMT 2023 , Edited by admin on Fri Dec 15 18:56:59 GMT 2023
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |
