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Details

Stereochemistry RACEMIC
Molecular Formula C17H25N3O5.ClH
Molecular Weight 387.858
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ZOLEPRODOLOL HYDROCHLORIDE

SMILES

Cl.COC1=NOC(COC2=C(OCC(O)CNC(C)(C)C)C=CC=C2)=N1

InChI

InChIKey=IQEOUWNTUSFDSZ-UHFFFAOYSA-N
InChI=1S/C17H25N3O5.ClH/c1-17(2,3)18-9-12(21)10-23-13-7-5-6-8-14(13)24-11-15-19-16(22-4)20-25-15;/h5-8,12,18,21H,9-11H2,1-4H3;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 C17H25N3O5
Molecular Weight 351.3975
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Description

Zoleprodolol was developed as an adrenoreceptor antagonist. Information about the current use of this compound is not available.

Approval Year

Unknown
149124
Substance Class Chemical
Created
by admin
on Tue Apr 01 16:20:26 GMT 2025
Edited
by admin
on Tue Apr 01 16:20:26 GMT 2025
Record UNII
87016Q25GZ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ZOLEPRODOLOL HYDROCHLORIDE
Common Name English
PROXODOLOL
WHO-DD  
Preferred Name English
Proxodolol [WHO-DD]
Common Name English
5-(2-(3-TERT-BUTYLAMINO-2-HYDROXYPROPOXY)PHENOXYMETHYL)-3-METHYL-1,2,4-OXADIAZOLE HYDROCHLORIDE
Systematic Name English
2-PROPANOL, 1-((1,1-DIMETHYLETHYL)AMINO)-3-(2-((3-METHOXY-1,2,4-OXADIAZOL-5-YL)METHOXY)PHENOXY)-, HYDROCHLORIDE (1:1)
Systematic Name English
Code System Code Type Description
PUBCHEM
133046
Created by admin on Tue Apr 01 16:20:26 GMT 2025 , Edited by admin on Tue Apr 01 16:20:26 GMT 2025
PRIMARY
FDA UNII
87016Q25GZ
Created by admin on Tue Apr 01 16:20:26 GMT 2025 , Edited by admin on Tue Apr 01 16:20:26 GMT 2025
PRIMARY
EPA CompTox
DTXSID20935921
Created by admin on Tue Apr 01 16:20:26 GMT 2025 , Edited by admin on Tue Apr 01 16:20:26 GMT 2025
PRIMARY
CAS
158446-41-4
Created by admin on Tue Apr 01 16:20:26 GMT 2025 , Edited by admin on Tue Apr 01 16:20:26 GMT 2025
PRIMARY
Related Record Type Details
Structure of ZOLEPRODOLOL HYDROCHLORIDE, (S)-
ENANTIOMER -> RACEMATE
Structure of ZOLEPRODOLOL HYDROCHLORIDE, (R)-
ENANTIOMER -> RACEMATE
Structure of ZOLEPRODOLOL
PARENT -> SALT/SOLVATE
Related Record Type Details
Structure of ZOLEPRODOLOL
ACTIVE MOIETY
NIH
NCATS
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