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Details

Stereochemistry RACEMIC
Molecular Formula C19H23NO6
Molecular Weight 361.389
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BUTOCROLOL

SMILES

CC1=CC(=O)C2=C(O1)C(OCC(O)CNC(C)(C)C)=C3OC=CC3=C2O

InChI

InChIKey=RRTGJSZJWLUVRE-UHFFFAOYSA-N
InChI=1S/C19H23NO6/c1-10-7-13(22)14-15(23)12-5-6-24-16(12)18(17(14)26-10)25-9-11(21)8-20-19(2,3)4/h5-7,11,20-21,23H,8-9H2,1-4H3

HIDE SMILES / InChI

Molecular Formula C19H23NO6
Molecular Weight 361.389
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Butocrolol amino alcohol derivative with β-adrenolytic, antiarrhythmic, and local anesthetic properties having sympatholytic and antiarrhythmic effects comparable to those of propranolol, but with lower local anesthetic effects.

Approval Year

Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:17:44 GMT 2025
Edited
by admin
on Mon Mar 31 18:17:44 GMT 2025
Record UNII
F63SY70KV0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(±)-BUTOCROLOL
Preferred Name English
BUTOCROLOL
INN  
INN  
Official Name English
butocrolol [INN]
Common Name English
5H-FURO(3,2-G)(1)BENZOPYRAN-5-ONE, 9-(3-((1,1-DIMETHYLETHYL)AMINO)-2-HYDROXYPROPOXY)-4-HYDROXY-7-METHYL-
Systematic Name English
BUTOCROLOL, (±)-
Common Name English
9-(3-(TERT-BUTYLAMINO)-2-HYDROXYPROPOXYL)-4-HYDROXY-7-METHYL-5H-FURO(3,2-G)(1)BENZOPYRAN-5-ONE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29576
Created by admin on Mon Mar 31 18:17:44 GMT 2025 , Edited by admin on Mon Mar 31 18:17:44 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID40866465
Created by admin on Mon Mar 31 18:17:44 GMT 2025 , Edited by admin on Mon Mar 31 18:17:44 GMT 2025
PRIMARY
NCI_THESAURUS
C77939
Created by admin on Mon Mar 31 18:17:44 GMT 2025 , Edited by admin on Mon Mar 31 18:17:44 GMT 2025
PRIMARY
CAS
55165-22-5
Created by admin on Mon Mar 31 18:17:44 GMT 2025 , Edited by admin on Mon Mar 31 18:17:44 GMT 2025
PRIMARY
INN
4350
Created by admin on Mon Mar 31 18:17:44 GMT 2025 , Edited by admin on Mon Mar 31 18:17:44 GMT 2025
PRIMARY
PUBCHEM
189906
Created by admin on Mon Mar 31 18:17:44 GMT 2025 , Edited by admin on Mon Mar 31 18:17:44 GMT 2025
PRIMARY
SMS_ID
100000088653
Created by admin on Mon Mar 31 18:17:44 GMT 2025 , Edited by admin on Mon Mar 31 18:17:44 GMT 2025
PRIMARY
ChEMBL
CHEMBL1742434
Created by admin on Mon Mar 31 18:17:44 GMT 2025 , Edited by admin on Mon Mar 31 18:17:44 GMT 2025
PRIMARY
EVMPD
SUB06027MIG
Created by admin on Mon Mar 31 18:17:44 GMT 2025 , Edited by admin on Mon Mar 31 18:17:44 GMT 2025
PRIMARY
FDA UNII
F63SY70KV0
Created by admin on Mon Mar 31 18:17:44 GMT 2025 , Edited by admin on Mon Mar 31 18:17:44 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY