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Details

Stereochemistry ACHIRAL
Molecular Formula C13H17N3O2.ClH
Molecular Weight 283.754
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PARBENDAZOLE HYDROCHLORIDE

SMILES

Cl.CCCCC1=CC2=C(NC(NC(=O)OC)=N2)C=C1

InChI

InChIKey=KQIVUXJJSRFRFM-UHFFFAOYSA-N
InChI=1S/C13H17N3O2.ClH/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);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 C13H17N3O2
Molecular Weight 247.293
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description

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

Unknown
149124
Targets

Targets

Primary TargetPharmacologyConditionPotency
Inhibitor
8504
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 21:58:32 GMT 2025
Edited
by admin
on Mon Mar 31 21:58:32 GMT 2025
Record UNII
YV5RTO20GO
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CARBAMIC ACID, (5-BUTYL-1H-BENZIMIDAZOL-2-YL)-, METHYL ESTER, MONOHYDROCHLORIDE
Preferred Name English
PARBENDAZOLE HYDROCHLORIDE
Common Name English
PARBENDAZOLE MONOHYDROCHLORIDE
Common Name English
Code System Code Type Description
CAS
83601-81-4
Created by admin on Mon Mar 31 21:58:32 GMT 2025 , Edited by admin on Mon Mar 31 21:58:32 GMT 2025
PRIMARY
PUBCHEM
76210635
Created by admin on Mon Mar 31 21:58:32 GMT 2025 , Edited by admin on Mon Mar 31 21:58:32 GMT 2025
PRIMARY
EPA CompTox
DTXSID80109166
Created by admin on Mon Mar 31 21:58:32 GMT 2025 , Edited by admin on Mon Mar 31 21:58:32 GMT 2025
PRIMARY
FDA UNII
YV5RTO20GO
Created by admin on Mon Mar 31 21:58:32 GMT 2025 , Edited by admin on Mon Mar 31 21:58:32 GMT 2025
PRIMARY
Related Record Type Details
Structure of PARBENDAZOLE
PARENT -> SALT/SOLVATE
Related Record Type Details
Structure of PARBENDAZOLE
ACTIVE MOIETY
NIH
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