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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
Structure of AFUROLOL HYDROCHLORIDE

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

HIDE SMILES / InChI

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

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 ( + / - )

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

Targets

Primary TargetPharmacologyConditionPotency

Sample Use Guides

In Vivo Use Guide
Single dose - 8 or 16 mg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:55:50 GMT 2023
Edited
by admin
on Sat Dec 16 02:55:50 GMT 2023
Record UNII
03IBM9K96Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AFUROLOL HYDROCHLORIDE
Common Name English
1(3H)-ISOBENZOFURANONE, 7-(3-((1,1-DIMETHYLETHYL)AMINO)-2-HYDROXYPROPOXY)-, HYDROCHLORIDE (1:1)
Systematic Name English
Code System Code Type Description
CAS
55104-39-7
Created by admin on Sat Dec 16 02:55:50 GMT 2023 , Edited by admin on Sat Dec 16 02:55:50 GMT 2023
PRIMARY
PUBCHEM
193930
Created by admin on Sat Dec 16 02:55:50 GMT 2023 , Edited by admin on Sat Dec 16 02:55:50 GMT 2023
PRIMARY
EPA CompTox
DTXSID60970477
Created by admin on Sat Dec 16 02:55:50 GMT 2023 , Edited by admin on Sat Dec 16 02:55:50 GMT 2023
PRIMARY
FDA UNII
03IBM9K96Q
Created by admin on Sat Dec 16 02:55:50 GMT 2023 , Edited by admin on Sat Dec 16 02:55:50 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY