Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C18H29NO4 |
| Molecular Weight | 323.4272 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)NCC(O)COC1=CC=C(OCCOCC2CC2)C=C1
InChI
InChIKey=JNDJPKHYZWRRIS-UHFFFAOYSA-N
InChI=1S/C18H29NO4/c1-14(2)19-11-16(20)13-23-18-7-5-17(6-8-18)22-10-9-21-12-15-3-4-15/h5-8,14-16,19-20H,3-4,9-13H2,1-2H3
| Molecular Formula | C18H29NO4 |
| Molecular Weight | 323.4272 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Cicloprolol is a beta-adrenoceptor antagonist patented by French pharmaceutical company Synthelabo S. A. for treatment of heart disorders. Cicloprolol has a weak beta-agonistic effect at normal levels of adrenergic discharge and acts as an antagonist at high levels of discharge. In clinical trials, Cicloprolol did not affect resting heart rate and blood pressure, but it reduced significantly peak exercise heart rate and peak rate-pressure product. The effect was especially significant in patients with sinus rhythm. The drug did not induce bradycardia or arrhyth- mias. Resting and exercise ejection rate were not affected. Cicloprolol improved the quality of life and the work capacity of 40% of patients with congestive failure due to ischemic etiology. Side effects were few and similar to placebo and cicloprolol.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/1347258
100 mg/day for 2 weeks
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:21:59 GMT 2025
by
admin
on
Mon Mar 31 18:21:59 GMT 2025
|
| Record UNII |
1K2ACH4U3R
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C29576
Created by
admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
637
Created by
admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
|
PRIMARY | |||
|
C79559
Created by
admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
|
PRIMARY | |||
|
CHEMBL2110772
Created by
admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
|
PRIMARY | |||
|
5250
Created by
admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
|
PRIMARY | |||
|
63659-12-1
Created by
admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
|
PRIMARY | |||
|
100000081285
Created by
admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
|
PRIMARY | |||
|
SUB06248MIG
Created by
admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
|
PRIMARY | |||
|
C053708
Created by
admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
|
PRIMARY | |||
|
1K2ACH4U3R
Created by
admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
|
PRIMARY | |||
|
146294
Created by
admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
|
PRIMARY | |||
|
Cicloprolol
Created by
admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ENANTIOMER -> RACEMATE | |||
|
|
ENANTIOMER -> RACEMATE | |||
|
|
SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |