Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C19H23NO3.ClH |
Molecular Weight | 349.852 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.COC1=CC=CC(=C1)C(=O)CCN[C@@H](C)[C@H](O)C2=CC=CC=C2
InChI
InChIKey=JMUPNNYLJGSMPK-JPJJPTBZSA-N
InChI=1S/C19H23NO3.ClH/c1-14(19(22)15-7-4-3-5-8-15)20-12-11-18(21)16-9-6-10-17(13-16)23-2;/h3-10,13-14,19-20,22H,11-12H2,1-2H3;1H/t14-,19-;/m0./s1
Originator
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
[The management of angina pectoris using Ildamen, a new coronary- and cardiac-active substance, in a double-blind study]. | 1967 Sep 10 |
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[Stimulation of adrenergic beta-receptors in the heart of normal and reserpinized guinea pigs by oxyfedrine]. | 1969 Sep |
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Pulmonary and systemic circulatory effects and -adrenergic selectivity of hexoprenaline, salbutamol, oxyfedrine, and isoproterenol. | 1971 Jul |
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Effects of oxyfedrine on regional myocardial blood flow in patients with coronary artery disease. | 1991 Dec |
Patents
Sample Use Guides
Oral
Myocardial infarction, Angina pectoris
Adult: 8-24 mg tid.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/14521236
Oxyfedrine was tested in vitro against 471 strains of bacteria from two Gram positive and fourteen Gram negative genera. The minimum inhibitory concentration (MIC) of oxyfedrine was determined by agar dilution method, which ranged from 50-200 ug/ml in most of the strains, while some strains were inhibited at even lower concentrations.
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29707
Created by
admin on Fri Dec 15 16:27:53 GMT 2023 , Edited by admin on Fri Dec 15 16:27:53 GMT 2023
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NCI_THESAURUS |
C48149
Created by
admin on Fri Dec 15 16:27:53 GMT 2023 , Edited by admin on Fri Dec 15 16:27:53 GMT 2023
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Code System | Code | Type | Description | ||
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C77154
Created by
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PRIMARY | |||
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DTXSID0048632
Created by
admin on Fri Dec 15 16:27:53 GMT 2023 , Edited by admin on Fri Dec 15 16:27:53 GMT 2023
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PRIMARY | |||
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63CF9XK7DA
Created by
admin on Fri Dec 15 16:27:53 GMT 2023 , Edited by admin on Fri Dec 15 16:27:53 GMT 2023
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PRIMARY | |||
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CHEMBL1651913
Created by
admin on Fri Dec 15 16:27:53 GMT 2023 , Edited by admin on Fri Dec 15 16:27:53 GMT 2023
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PRIMARY | |||
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100000085492
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admin on Fri Dec 15 16:27:53 GMT 2023 , Edited by admin on Fri Dec 15 16:27:53 GMT 2023
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PRIMARY | |||
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5489012
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admin on Fri Dec 15 16:27:53 GMT 2023 , Edited by admin on Fri Dec 15 16:27:53 GMT 2023
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PRIMARY | |||
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236758
Created by
admin on Fri Dec 15 16:27:53 GMT 2023 , Edited by admin on Fri Dec 15 16:27:53 GMT 2023
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240-696-5
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admin on Fri Dec 15 16:27:53 GMT 2023 , Edited by admin on Fri Dec 15 16:27:53 GMT 2023
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PRIMARY | |||
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16648-69-4
Created by
admin on Fri Dec 15 16:27:53 GMT 2023 , Edited by admin on Fri Dec 15 16:27:53 GMT 2023
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NON-SPECIFIC STEREOCHEMISTRY | |||
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SUB03586MIG
Created by
admin on Fri Dec 15 16:27:53 GMT 2023 , Edited by admin on Fri Dec 15 16:27:53 GMT 2023
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PRIMARY | |||
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16777-42-7
Created by
admin on Fri Dec 15 16:27:53 GMT 2023 , Edited by admin on Fri Dec 15 16:27:53 GMT 2023
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PRIMARY | |||
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m8331
Created by
admin on Fri Dec 15 16:27:53 GMT 2023 , Edited by admin on Fri Dec 15 16:27:53 GMT 2023
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PRIMARY | Merck Index |
ACTIVE MOIETY
SUBSTANCE RECORD