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

Details

Stereochemistry ACHIRAL
Molecular Formula C15H12FN3O5S
Molecular Weight 365.336
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LUXABENDAZOLE

SMILES

COC(=O)NC1=NC2=CC=C(OS(=O)(=O)C3=CC=C(F)C=C3)C=C2N1

InChI

InChIKey=ZVIDWFUBDDXAJA-UHFFFAOYSA-N
InChI=1S/C15H12FN3O5S/c1-23-15(20)19-14-17-12-7-4-10(8-13(12)18-14)24-25(21,22)11-5-2-9(16)3-6-11/h2-8H,1H3,(H2,17,18,19,20)

HIDE SMILES / InChI

Molecular Formula C15H12FN3O5S
Molecular Weight 365.336
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Luxabendazole is a benzimidazole carbamate antihelmintic agent. In animal studies, it was effective against adult and immature stages of the major gastrointestinal nematodes, trematodes and cestodes.

Approval Year

PubMed

PubMed

TitleDatePubMed
Activity of luxabendazole against liver flukes, gastrointestinal roundworms, and lungworms in naturally infected sheep.
1988
Pharmacokinetics of luxabendazole after oral and intravenous administration to sheep.
1997 Nov
Pharmacokinetics of intravenous luxabendazole in rabbits: influence of the enterohepatic circulation.
1998 Jul
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 17:51:06 GMT 2023
Edited
by admin
on Sat Dec 16 17:51:06 GMT 2023
Record UNII
34S1S00GV3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LUXABENDAZOLE
INN  
INN  
Official Name English
luxabendazole [INN]
Common Name English
HOE-216V
Code English
METHYL 5-HYDROXY-2-BENZIMIDAZOLECARBAMATE, P-FLUOROBENZENESULFONATE (ESTER)
Common Name English
HOE 216V
Code English
Classification Tree Code System Code
NCI_THESAURUS C250
Created by admin on Sat Dec 16 17:51:06 GMT 2023 , Edited by admin on Sat Dec 16 17:51:06 GMT 2023
Code System Code Type Description
CAS
90509-02-7
Created by admin on Sat Dec 16 17:51:06 GMT 2023 , Edited by admin on Sat Dec 16 17:51:06 GMT 2023
PRIMARY
SMS_ID
100000082294
Created by admin on Sat Dec 16 17:51:06 GMT 2023 , Edited by admin on Sat Dec 16 17:51:06 GMT 2023
PRIMARY
EPA CompTox
DTXSID00238189
Created by admin on Sat Dec 16 17:51:06 GMT 2023 , Edited by admin on Sat Dec 16 17:51:06 GMT 2023
PRIMARY
EVMPD
SUB08624MIG
Created by admin on Sat Dec 16 17:51:06 GMT 2023 , Edited by admin on Sat Dec 16 17:51:06 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104764
Created by admin on Sat Dec 16 17:51:06 GMT 2023 , Edited by admin on Sat Dec 16 17:51:06 GMT 2023
PRIMARY
PUBCHEM
72019
Created by admin on Sat Dec 16 17:51:06 GMT 2023 , Edited by admin on Sat Dec 16 17:51:06 GMT 2023
PRIMARY
INN
5628
Created by admin on Sat Dec 16 17:51:06 GMT 2023 , Edited by admin on Sat Dec 16 17:51:06 GMT 2023
PRIMARY
NCI_THESAURUS
C66043
Created by admin on Sat Dec 16 17:51:06 GMT 2023 , Edited by admin on Sat Dec 16 17:51:06 GMT 2023
PRIMARY
MESH
C058092
Created by admin on Sat Dec 16 17:51:06 GMT 2023 , Edited by admin on Sat Dec 16 17:51:06 GMT 2023
PRIMARY
FDA UNII
34S1S00GV3
Created by admin on Sat Dec 16 17:51:06 GMT 2023 , Edited by admin on Sat Dec 16 17:51:06 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY