Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C18H27NO2 |
| Molecular Weight | 289.4125 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@H](NCCC(=O)C1CCCCC1)[C@H](O)C2=CC=CC=C2
InChI
InChIKey=UEELVIXXTBPOCF-KSSFIOAISA-N
InChI=1S/C18H27NO2/c1-14(18(21)16-10-6-3-7-11-16)19-13-12-17(20)15-8-4-2-5-9-15/h3,6-7,10-11,14-15,18-19,21H,2,4-5,8-9,12-13H2,1H3/t14-,18-/m0/s1
| Molecular Formula | C18H27NO2 |
| Molecular Weight | 289.4125 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Alifedrine, a beta-adrenergic partial agonist, significantly improved performance of the failing heart. Alifedrine resulted in a significant dose-dependent increase in cardiac output. There were significant reductions in peripheral resistance, but little observed change in arterial pressure. With intravenous alifedrine, there were significant increases in stroke volume with little change in heart rate. With the 40 mg oral dose, there was a small increase in heart rate There were no clinically or statistically significant changes in arterial (non-invasive), pulmonary artery, pulmonary capillary or right atrial pressures with any dose of alifedrine. No significant arrhythmias were noted clinically with the doses studied.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:17:40 GMT 2025
by
admin
on
Mon Mar 31 18:17:40 GMT 2025
|
| Record UNII |
K2PM66M0VQ
|
| Record Status |
Validated (UNII)
|
| Record Version |
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-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
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Official Name | English | ||
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Preferred Name | English | ||
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Common Name | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C48149
Created by
admin on Mon Mar 31 18:17:40 GMT 2025 , Edited by admin on Mon Mar 31 18:17:40 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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Alifedrine
Created by
admin on Mon Mar 31 18:17:40 GMT 2025 , Edited by admin on Mon Mar 31 18:17:40 GMT 2025
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PRIMARY | |||
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C039523
Created by
admin on Mon Mar 31 18:17:40 GMT 2025 , Edited by admin on Mon Mar 31 18:17:40 GMT 2025
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PRIMARY | |||
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51719
Created by
admin on Mon Mar 31 18:17:40 GMT 2025 , Edited by admin on Mon Mar 31 18:17:40 GMT 2025
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PRIMARY | |||
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100000087412
Created by
admin on Mon Mar 31 18:17:40 GMT 2025 , Edited by admin on Mon Mar 31 18:17:40 GMT 2025
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PRIMARY | |||
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K2PM66M0VQ
Created by
admin on Mon Mar 31 18:17:40 GMT 2025 , Edited by admin on Mon Mar 31 18:17:40 GMT 2025
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PRIMARY | |||
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DTXSID00229274
Created by
admin on Mon Mar 31 18:17:40 GMT 2025 , Edited by admin on Mon Mar 31 18:17:40 GMT 2025
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PRIMARY | |||
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C77931
Created by
admin on Mon Mar 31 18:17:40 GMT 2025 , Edited by admin on Mon Mar 31 18:17:40 GMT 2025
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PRIMARY | |||
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CHEMBL2104023
Created by
admin on Mon Mar 31 18:17:40 GMT 2025 , Edited by admin on Mon Mar 31 18:17:40 GMT 2025
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PRIMARY | |||
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5301
Created by
admin on Mon Mar 31 18:17:40 GMT 2025 , Edited by admin on Mon Mar 31 18:17:40 GMT 2025
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PRIMARY | |||
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78756-61-3
Created by
admin on Mon Mar 31 18:17:40 GMT 2025 , Edited by admin on Mon Mar 31 18:17:40 GMT 2025
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PRIMARY | |||
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SUB05325MIG
Created by
admin on Mon Mar 31 18:17:40 GMT 2025 , Edited by admin on Mon Mar 31 18:17:40 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |