Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C15H21NO4.ClH |
| Molecular Weight | 315.792 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC(C)(C)NCC(O)COC1=C2C(=O)OCC2=CC=C1
InChI
InChIKey=KTIQCDLYPPAYBF-UHFFFAOYSA-N
InChI=1S/C15H21NO4.ClH/c1-15(2,3)16-7-11(17)9-19-12-6-4-5-10-8-20-14(18)13(10)12;/h4-6,11,16-17H,7-9H2,1-3H3;1H
| Molecular Formula | C15H21NO4 |
| Molecular Weight | 279.3315 |
| 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 |
Alfurolol is a beta-adrenergic blocker. It is non-selective blocking drug with both intrinsic sympathomimetic activity and weak membrane stabilizing activity. There is also evidence that, unlike other beta-blocking drugs, only extremely small amounts of alfurolol cross the blood-brain barrier: because of this property, it has very little effect on the CNS. Alfurolol consistently produced a reduction in exercise heart rate at all times during the seven-hour period of observation, and the reductions were significantly different from the corresponding values after placebo treatment. Alfurolol is active both on heart rate and systolic pressure.
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2094118 Sources: https://www.ncbi.nlm.nih.gov/pubmed/40801 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/40801
Single dose - 8 or 16 mg
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:15:53 GMT 2025
by
admin
on
Mon Mar 31 21:15:53 GMT 2025
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| Record UNII |
03IBM9K96Q
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| Record Status |
Validated (UNII)
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admin on Mon Mar 31 21:15:53 GMT 2025 , Edited by admin on Mon Mar 31 21:15:53 GMT 2025
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
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ACTIVE MOIETY |