Details
Stereochemistry | RACEMIC |
Molecular Formula | C16H26N2O4.ClH |
Molecular Weight | 346.85 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CNC(=O)COC1=C(OCC(O)CNC(C)(C)C)C=CC=C1
InChI
InChIKey=CRYTUFSEASFGMP-UHFFFAOYSA-N
InChI=1S/C16H26N2O4.ClH/c1-16(2,3)18-9-12(19)10-21-13-7-5-6-8-14(13)22-11-15(20)17-4;/h5-8,12,18-19H,9-11H2,1-4H3,(H,17,20);1H
Molecular Formula | C16H26N2O4 |
Molecular Weight | 310.3886 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
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 |
Cetamolol is a beta adrenergic antagonist with intrinsic sympathomimetic activity, patented by Imperial Chemical Industries Ltd for cardiovascular disease treatment. The average plasma half-life of cetamolol is 6.4 hours in humans and peak serum levels are reached 1 to 2 hours after drug intake; oral doses as low as 10 mg produced significant reductions in exercise-induced tachycardia 24 hours after drug administration. Cetamolol is approximately three times as potent as atenolol in blocking exercise-induced tachycardia.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2905711
15 mg/day
Route of Administration:
Oral
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:07:24 GMT 2023
by
admin
on
Fri Dec 15 15:07:24 GMT 2023
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Record UNII |
5UNK5C6QM5
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C29576
Created by
admin on Fri Dec 15 15:07:24 GMT 2023 , Edited by admin on Fri Dec 15 15:07:24 GMT 2023
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m1066
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PRIMARY | Merck Index | ||
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CHEMBL156885
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DTXSID30998805
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5UNK5C6QM5
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C81652
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278-729-0
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53697
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77590-95-5
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admin on Fri Dec 15 15:07:24 GMT 2023 , Edited by admin on Fri Dec 15 15:07:24 GMT 2023
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Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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PARENT -> SALT/SOLVATE | |||
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ENANTIOMER -> RACEMATE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |