U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C13H17N3O2
Molecular Weight 247.293
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PARBENDAZOLE

SMILES

CCCCC1=CC2=C(C=C1)N=C(NC(=O)OC)N2

InChI

InChIKey=YRWLZFXJFBZBEY-UHFFFAOYSA-N
InChI=1S/C13H17N3O2/c1-3-4-5-9-6-7-10-11(8-9)15-12(14-10)16-13(17)18-2/h6-8H,3-5H2,1-2H3,(H2,14,15,16,17)

HIDE SMILES / InChI

Molecular Formula C13H17N3O2
Molecular Weight 247.293
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Parbendazole is a potent inhibitor of microtubule assembly that was studied as an anthelmintic agent. Information about the current use of this drug is not available.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
PubMed

PubMed

TitleDatePubMed
Parbendazole.
2010
Epidemiological aspects of the first outbreak of Baylisascaris procyonis larva migrans in rabbits in Japan.
2003-04
In vitro susceptibilities of the AIDS-associated microsporidian Encephalitozoon intestinalis to albendazole, its sulfoxide metabolite, and 12 additional benzimidazole derivatives.
1997-12
Activity of benzimidazoles against cryptosporidiosis in neonatal BALB/c mice.
1995-10
In vitro susceptibility of the opportunistic fungus Cryptococcus neoformans to anthelmintic benzimidazoles.
1994-02
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:55:13 GMT 2025
Edited
by admin
on Mon Mar 31 17:55:13 GMT 2025
Record UNII
N4X8WVX2UG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-256420
Preferred Name English
PARBENDAZOLE
INN   MI   USAN   USP-RS  
INN   USAN  
Official Name English
SK&F-29044
Code English
SK&F 29044
Code English
PARBENDAZOLE [USP-RS]
Common Name English
TCMDC-131798
Code English
PARBENDAZOLE [USAN]
Common Name English
CARBAMIC ACID, (5-BUTYL-1H-BENZIMIDAZOL-2-YL)-, METHYL ESTER
Common Name English
PARBENDAZOLE [MI]
Common Name English
parbendazole [INN]
Common Name English
Methyl 5-butyl-2-benzimidazolecarbamate
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C250
Created by admin on Mon Mar 31 17:55:13 GMT 2025 , Edited by admin on Mon Mar 31 17:55:13 GMT 2025
WHO-VATC QP52AC03
Created by admin on Mon Mar 31 17:55:13 GMT 2025 , Edited by admin on Mon Mar 31 17:55:13 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID0045410
Created by admin on Mon Mar 31 17:55:13 GMT 2025 , Edited by admin on Mon Mar 31 17:55:13 GMT 2025
PRIMARY
ECHA (EC/EINECS)
238-133-3
Created by admin on Mon Mar 31 17:55:13 GMT 2025 , Edited by admin on Mon Mar 31 17:55:13 GMT 2025
PRIMARY
EVMPD
SUB09620MIG
Created by admin on Mon Mar 31 17:55:13 GMT 2025 , Edited by admin on Mon Mar 31 17:55:13 GMT 2025
PRIMARY
CAS
14255-87-9
Created by admin on Mon Mar 31 17:55:13 GMT 2025 , Edited by admin on Mon Mar 31 17:55:13 GMT 2025
PRIMARY
MESH
C100292
Created by admin on Mon Mar 31 17:55:13 GMT 2025 , Edited by admin on Mon Mar 31 17:55:13 GMT 2025
PRIMARY
FDA UNII
N4X8WVX2UG
Created by admin on Mon Mar 31 17:55:13 GMT 2025 , Edited by admin on Mon Mar 31 17:55:13 GMT 2025
PRIMARY
SMS_ID
100000082794
Created by admin on Mon Mar 31 17:55:13 GMT 2025 , Edited by admin on Mon Mar 31 17:55:13 GMT 2025
PRIMARY
NCI_THESAURUS
C96752
Created by admin on Mon Mar 31 17:55:13 GMT 2025 , Edited by admin on Mon Mar 31 17:55:13 GMT 2025
PRIMARY
INN
2503
Created by admin on Mon Mar 31 17:55:13 GMT 2025 , Edited by admin on Mon Mar 31 17:55:13 GMT 2025
PRIMARY
RS_ITEM_NUM
1498706
Created by admin on Mon Mar 31 17:55:13 GMT 2025 , Edited by admin on Mon Mar 31 17:55:13 GMT 2025
PRIMARY
PUBCHEM
26596
Created by admin on Mon Mar 31 17:55:13 GMT 2025 , Edited by admin on Mon Mar 31 17:55:13 GMT 2025
PRIMARY
ChEMBL
CHEMBL528271
Created by admin on Mon Mar 31 17:55:13 GMT 2025 , Edited by admin on Mon Mar 31 17:55:13 GMT 2025
PRIMARY
MERCK INDEX
m8409
Created by admin on Mon Mar 31 17:55:13 GMT 2025 , Edited by admin on Mon Mar 31 17:55:13 GMT 2025
PRIMARY Merck Index
NSC
256420
Created by admin on Mon Mar 31 17:55:13 GMT 2025 , Edited by admin on Mon Mar 31 17:55:13 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY