EBERCONAZOLE

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

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C18H14Cl2N2
Molecular Weight	329.223
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of EBERCONAZOLE

Structure Search

SMILES

ClC1=CC(Cl)=C2C(N3C=CN=C3)C4=CC=CC=C4CCC2=C1

InChI

InChIKey=MPTJIDOGFUQSQH-UHFFFAOYSA-N

InChI=1S/C18H14Cl2N2/c19-14-9-13-6-5-12-3-1-2-4-15(12)18(17(13)16(20)10-14)22-8-7-21-11-22/h1-4,7-11,18H,5-6H2

HIDE SMILES / InChI

Molecular Formula	C18H14Cl2N2
Molecular Weight	329.223
Charge	0
Count

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

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 15:29:11 UTC 2023` Edited by `admin` on `Fri Dec 15 15:29:11 UTC 2023`
Record UNII	V7O1U41C9B
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

EBERCONAZOLE

Official Name

English

Eberconazole [WHO-DD]

Common Name

English

eberconazole [INN]

Common Name

English

(±)-1-(2,4-DICHLORO-10,11-DIHYDRO-5H-DIBENZO(A,D)CYCLOHEPTEN-5-YL)IMIDAZOLE

Systematic Name

English

Classification Tree Code System Code

WHO-VATC

QD01AC17

Created by admin on Fri Dec 15 15:29:11 UTC 2023 , Edited by admin on Fri Dec 15 15:29:11 UTC 2023

WHO-ATC

D01AC17

Created by admin on Fri Dec 15 15:29:11 UTC 2023 , Edited by admin on Fri Dec 15 15:29:11 UTC 2023

NCI_THESAURUS

C514

Created by admin on Fri Dec 15 15:29:11 UTC 2023 , Edited by admin on Fri Dec 15 15:29:11 UTC 2023

Code System Code Type Description

INN

6680

Created by admin on Fri Dec 15 15:29:11 UTC 2023 , Edited by admin on Fri Dec 15 15:29:11 UTC 2023

PRIMARY

SMS_ID

100000080501

Created by admin on Fri Dec 15 15:29:11 UTC 2023 , Edited by admin on Fri Dec 15 15:29:11 UTC 2023

PRIMARY

MESH

C118963

Created by admin on Fri Dec 15 15:29:11 UTC 2023 , Edited by admin on Fri Dec 15 15:29:11 UTC 2023

PRIMARY

FDA UNII

V7O1U41C9B

Created by admin on Fri Dec 15 15:29:11 UTC 2023 , Edited by admin on Fri Dec 15 15:29:11 UTC 2023

PRIMARY

NCI_THESAURUS

C72961

Created by admin on Fri Dec 15 15:29:11 UTC 2023 , Edited by admin on Fri Dec 15 15:29:11 UTC 2023

PRIMARY

WIKIPEDIA

Eberconazole

Created by admin on Fri Dec 15 15:29:11 UTC 2023 , Edited by admin on Fri Dec 15 15:29:11 UTC 2023

PRIMARY

DRUG CENTRAL

978

Created by admin on Fri Dec 15 15:29:11 UTC 2023 , Edited by admin on Fri Dec 15 15:29:11 UTC 2023

PRIMARY

PUBCHEM

72051

Created by admin on Fri Dec 15 15:29:11 UTC 2023 , Edited by admin on Fri Dec 15 15:29:11 UTC 2023

PRIMARY

ChEMBL

CHEMBL558722

Created by admin on Fri Dec 15 15:29:11 UTC 2023 , Edited by admin on Fri Dec 15 15:29:11 UTC 2023

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CAS

128326-82-9

Created by admin on Fri Dec 15 15:29:11 UTC 2023 , Edited by admin on Fri Dec 15 15:29:11 UTC 2023

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EPA CompTox

DTXSID90926104

Created by admin on Fri Dec 15 15:29:11 UTC 2023 , Edited by admin on Fri Dec 15 15:29:11 UTC 2023

PRIMARY

EVMPD

SUB06436MIG

Created by admin on Fri Dec 15 15:29:11 UTC 2023 , Edited by admin on Fri Dec 15 15:29:11 UTC 2023

PRIMARY

DRUG BANK

DB13656

Created by admin on Fri Dec 15 15:29:11 UTC 2023 , Edited by admin on Fri Dec 15 15:29:11 UTC 2023

PRIMARY

CHEBI

82862

Created by admin on Fri Dec 15 15:29:11 UTC 2023 , Edited by admin on Fri Dec 15 15:29:11 UTC 2023

PRIMARY

Related Record Type Details


					Z30RAY509F

TARGET -> INHIBITOR


					66T020757Q

EBERCONAZOLE, (S)-

ENANTIOMER -> RACEMATE


					LSL8E59V2V

EBERCONAZOLE NITRATE

SALT/SOLVATE -> PARENT

Amount:


					9NQ62W0N3G

EBERCONAZOLE, (R)-

ENANTIOMER -> RACEMATE

Related Record Type Details


					V7O1U41C9B

ACTIVE MOIETY