Details
| Stereochemistry | UNKNOWN |
| Molecular Formula | C21H19NO.ClH |
| Molecular Weight | 337.843 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.OC(C1CC1C2=CC=NC=C2)(C3=CC=CC=C3)C4=CC=CC=C4
InChI
InChIKey=ZKNXZJZQQIQXOD-UHFFFAOYSA-N
InChI=1S/C21H19NO.ClH/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;1H
| Molecular Formula | C21H19NO |
| Molecular Weight | 301.3817 |
| Charge | 0 |
| Count |
|
| Stereochemistry | MIXED |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
| 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 |
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 14:58:48 GMT 2023
by
admin
on
Fri Dec 15 14:58:48 GMT 2023
|
| Record UNII |
7UQN2OJ7SM
|
| Record Status |
Validated (UNII)
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| Record Version |
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7UQN2OJ7SM
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2364-72-9
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84973
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66260
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CHEMBL2110906
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C167048
Created by
admin on Fri Dec 15 14:58:48 GMT 2023 , Edited by admin on Fri Dec 15 14:58:48 GMT 2023
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| Related Record | Type | Details | ||
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