ZOFICONAZOLE

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C20H19Cl3N2O2
Molecular Weight	425.736
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of ZOFICONAZOLE

Structure Search

SMILES

ClC1=CC=C(OCCCOC(CN2C=CN=C2)C3=C(Cl)C=C(Cl)C=C3)C=C1

InChI

InChIKey=KHNOGVLYRLJXPL-UHFFFAOYSA-N

InChI=1S/C20H19Cl3N2O2/c21-15-2-5-17(6-3-15)26-10-1-11-27-20(13-25-9-8-24-14-25)18-7-4-16(22)12-19(18)23/h2-9,12,14,20H,1,10-11,13H2

HIDE SMILES / InChI

Molecular Formula	C20H19Cl3N2O2
Molecular Weight	425.736
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Description
Sources: Bycroft Barrie W., Payne David J., Dictionary of Antibiotics and Related Substances: with CD-ROM, Second Edition, p. 1825, retrieved from: https://books.google.ru/books?id=x0hZDwAAQBAJ&pg=PA1825&lpg=PA1825&dq=ZOFICONAZOLE&source=bl&ots=AdUEOR_g6M&sig=ACfU3U2-97u6vpyBJXft-crzhYeCeYz_Fg&hl=ru&sa=X&ved=2ahUKEwjL0oHn2rnjAhV1wsQBHfwZAd84FBDoATABegQICBAB#v=onepage&q=ZOFICONAZOLE&f=false

Zoficonazole was developed as an antibacterial and an antifungal agent. Information about the current use of this compound is not available.

Approval Year

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:10:19 GMT 2025` Edited by `admin` on `Mon Mar 31 18:10:19 GMT 2025`
Record UNII	FZA518V67A
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

(±)-1-(2,4-DICHLORO-.BETA.-(3-(P-CHLOROPHENOXY)PROPOXY)PHENETHYL)IMIDAZOLE

Preferred Name

English

ZOFICONAZOLE

Official Name

English

zoficonazole [INN]

Common Name

English

1-(2,4-DICHLORO-.BETA.-(3-(P-CHLOROPHENOXY)PROPOXY)PHENETHYL)IMIDAZOLE, (±)-

Common Name

English

Classification Tree Code System Code

NCI_THESAURUS

C514

Created by admin on Mon Mar 31 18:10:19 GMT 2025 , Edited by admin on Mon Mar 31 18:10:19 GMT 2025

Code System Code Type Description

ChEMBL

CHEMBL2105577

Created by admin on Mon Mar 31 18:10:19 GMT 2025 , Edited by admin on Mon Mar 31 18:10:19 GMT 2025

PRIMARY

EPA CompTox

DTXSID30867986

Created by admin on Mon Mar 31 18:10:19 GMT 2025 , Edited by admin on Mon Mar 31 18:10:19 GMT 2025

PRIMARY

NCI_THESAURUS

C66701

Created by admin on Mon Mar 31 18:10:19 GMT 2025 , Edited by admin on Mon Mar 31 18:10:19 GMT 2025

PRIMARY

INN

4796

Created by admin on Mon Mar 31 18:10:19 GMT 2025 , Edited by admin on Mon Mar 31 18:10:19 GMT 2025

PRIMARY

EVMPD

SUB00172MIG

Created by admin on Mon Mar 31 18:10:19 GMT 2025 , Edited by admin on Mon Mar 31 18:10:19 GMT 2025

PRIMARY

SMS_ID

100000078792

Created by admin on Mon Mar 31 18:10:19 GMT 2025 , Edited by admin on Mon Mar 31 18:10:19 GMT 2025

PRIMARY

FDA UNII

FZA518V67A

Created by admin on Mon Mar 31 18:10:19 GMT 2025 , Edited by admin on Mon Mar 31 18:10:19 GMT 2025

PRIMARY

CAS

71097-23-9

Created by admin on Mon Mar 31 18:10:19 GMT 2025 , Edited by admin on Mon Mar 31 18:10:19 GMT 2025

PRIMARY

PUBCHEM

3054320

Created by admin on Mon Mar 31 18:10:19 GMT 2025 , Edited by admin on Mon Mar 31 18:10:19 GMT 2025

PRIMARY

Related Record Type Details


					9NK2V6EBRZ

ZOFICONAZOLE, (S)-

ENANTIOMER -> RACEMATE


					11VLX38JLU

ZOFICONAZOLE, (R)-

ENANTIOMER -> RACEMATE

Related Record Type Details


					FZA518V67A

ACTIVE MOIETY