LEDAZEROL

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C11H12N2O2
Molecular Weight	204.2252
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of LEDAZEROL

Structure Search

SMILES

OCC1=C(O)C(CC2=CN=CN2)=CC=C1

InChI

InChIKey=PGVXBSSEVQUMQM-UHFFFAOYSA-N

InChI=1S/C11H12N2O2/c14-6-9-3-1-2-8(11(9)15)4-10-5-12-7-13-10/h1-3,5,7,14-15H,4,6H2,(H,12,13)

HIDE SMILES / InChI

Molecular Formula	C11H12N2O2
Molecular Weight	204.2252
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Description
Sources: https://adisinsight.springer.com/drugs/800006647

LEDAZEROL is a derivative of mivazerol. It was under development as an antianginal agent.

Originator

Approval Year

Patents

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:19:50 GMT 2025` Edited by `admin` on `Mon Mar 31 18:19:50 GMT 2025`
Record UNII	P13OO3FPZB
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

LEDAZEROL

Official Name

English

ledazerol [INN]

Preferred Name

English

2-HYDROXY-3-(IMIDAZOL-4-YLMETHYL)BENZYL ALCOHOL

Systematic Name

English

Classification Tree Code System Code

NCI_THESAURUS

C29707

Created by admin on Mon Mar 31 18:19:50 GMT 2025 , Edited by admin on Mon Mar 31 18:19:50 GMT 2025

Code System Code Type Description

SMS_ID

100000082564

Created by admin on Mon Mar 31 18:19:50 GMT 2025 , Edited by admin on Mon Mar 31 18:19:50 GMT 2025

PRIMARY

NCI_THESAURUS

C81348

Created by admin on Mon Mar 31 18:19:50 GMT 2025 , Edited by admin on Mon Mar 31 18:19:50 GMT 2025

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INN

6619

Created by admin on Mon Mar 31 18:19:50 GMT 2025 , Edited by admin on Mon Mar 31 18:19:50 GMT 2025

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ChEMBL

CHEMBL2104355

Created by admin on Mon Mar 31 18:19:50 GMT 2025 , Edited by admin on Mon Mar 31 18:19:50 GMT 2025

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EVMPD

SUB08420MIG

Created by admin on Mon Mar 31 18:19:50 GMT 2025 , Edited by admin on Mon Mar 31 18:19:50 GMT 2025

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CAS

116795-97-2

Created by admin on Mon Mar 31 18:19:50 GMT 2025 , Edited by admin on Mon Mar 31 18:19:50 GMT 2025

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FDA UNII

P13OO3FPZB

Created by admin on Mon Mar 31 18:19:50 GMT 2025 , Edited by admin on Mon Mar 31 18:19:50 GMT 2025

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EPA CompTox

DTXSID50151516

Created by admin on Mon Mar 31 18:19:50 GMT 2025 , Edited by admin on Mon Mar 31 18:19:50 GMT 2025

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PUBCHEM

65932

Created by admin on Mon Mar 31 18:19:50 GMT 2025 , Edited by admin on Mon Mar 31 18:19:50 GMT 2025

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Related Record Type Details


					P13OO3FPZB

LEDAZEROL

ACTIVE MOIETY