Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C13H19Cl2NO2 |
| Molecular Weight | 292.201 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(C)NCC(O)COC1=C(Cl)C=CC(Cl)=C1
InChI
InChIKey=XYCMOTOFHFTUIU-UHFFFAOYSA-N
InChI=1S/C13H19Cl2NO2/c1-13(2,3)16-7-10(17)8-18-12-6-9(14)4-5-11(12)15/h4-6,10,16-17H,7-8H2,1-3H3
| Molecular Formula | C13H19Cl2NO2 |
| Molecular Weight | 292.201 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Cloranolol is a specific beta-adrenergic antagonist. It is used as an antiarrhythmic agent. Its antiarrhythmic effectiveness stronger than propranol and equal or surpass the effectivity of pindolol. It has a negligible cardiodepressant activity as compared to other beta-adrenergic antagonists. Cloranolol has mainly cardiorespiratory side effects judging from the beta-blocker characteristics
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/1685755
Single dose - 10 mg
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 09:57:08 GMT 2025
by
admin
on
Wed Apr 02 09:57:08 GMT 2025
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| Record UNII |
Q3U058H86V
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| Record Status |
Validated (UNII)
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Preferred Name | English | ||
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WHO-ATC |
C07AA27
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NCI_THESAURUS |
C29576
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WHO-VATC |
QC07AA27
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100000084023
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CHEMBL156791
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39563-28-5
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SUB06752MIG
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Cloranolol
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m1083
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DB13508
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4646
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Q3U058H86V
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65814
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C025725
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C81658
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710
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| Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT | |||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |