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Details

Stereochemistry ACHIRAL
Molecular Formula C12H15N3O2S
Molecular Weight 265.331
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ALBENDAZOLE

SMILES

CCCSC1=CC=C2N=C(NC(=O)OC)NC2=C1

InChI

InChIKey=HXHWSAZORRCQMX-UHFFFAOYSA-N
InChI=1S/C12H15N3O2S/c1-3-6-18-8-4-5-9-10(7-8)14-11(13-9)15-12(16)17-2/h4-5,7H,3,6H2,1-2H3,(H2,13,14,15,16)

HIDE SMILES / InChI
Molecular Formula C12H15N3O2S
Molecular Weight 265.331
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:05:18 UTC 2023
Edited
by admin
on Fri Dec 15 15:05:18 UTC 2023
Record UNII
F4216019LN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ALBENDAZOLE
EP   GREEN BOOK   HSDB   INN   JAN   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD   WHO-IP  
USAN   INN  
Official Name English
albendazole [INN]
Common Name English
ALBENDAZOLE [USP-RS]
Common Name English
ALBENDAZOLE [USAN]
Common Name English
ALBENZA
Brand Name English
SK&F 62979
Code English
METHYL 5-(PROPYLTHIO)BENZIMIDAZOL-2-YLCARBAMATE
Systematic Name English
ALBENDAZOLE [MI]
Common Name English
ZENTEL
Brand Name English
METHYL N-(5-(PROPYLTHIO)-1H-BENZIMIDAZOL-2-YL)CARBAMATE
Systematic Name English
ALBENDAZOLE [WHO-IP]
Common Name English
ALBENDAZOLE [EP MONOGRAPH]
Common Name English
ALBENDAZOLE [USP MONOGRAPH]
Common Name English
ALBENDAZOLE [VANDF]
Common Name English
SK&F-62979
Code English
Methyl 5-(propylthio)-2-benzimidazolecarbamate
Common Name English
ALBENDAZOLE [JAN]
Common Name English
CARBAMIC ACID, (5-(PROPYLTHIO)-1H-BENZIMIDAZOL-2-YL)-, METHYL ESTER
Common Name English
ALBENDAZOLE [HSDB]
Common Name English
ALBENDAZOLE [GREEN BOOK]
Common Name English
ESKAZOLE
Brand Name English
ALBENDAZOLE [MART.]
Common Name English
Albendazole [WHO-DD]
Common Name English
ALBENDAZOLE [ORANGE BOOK]
Common Name English
ALBENDAZOLUM [WHO-IP]
Common Name English
ANDAZOL
Brand Name English
NSC-220008
Code English
Classification Tree Code System Code
FDA ORPHAN DRUG 94295
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
WHO-ESSENTIAL MEDICINES LIST 6.1.1
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
CFR 21 CFR 520.38A
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
WHO-ATC P02CA03
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
CFR 21 CFR 520.38
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
NCI_THESAURUS C250
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
WHO-VATC QP52AC11
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
CFR 21 CFR 520.38B
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
CFR 21 CFR 556.34
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
FDA ORPHAN DRUG 94195
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
LIVERTOX NBK548360
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
NDF-RT N0000175481
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
WHO-ESSENTIAL MEDICINES LIST 6.1.2
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
Code System Code Type Description
DAILYMED
F4216019LN
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
CHEBI
16664
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
FDA UNII
F4216019LN
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
MERCK INDEX
m1473
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY Merck Index
RS_ITEM_NUM
1012553
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
NSC
220008
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
HSDB
7444
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
PUBCHEM
2082
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
RXCUI
430
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY RxNorm
DRUG BANK
DB00518
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
SMS_ID
100000087712
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
CAS
54965-21-8
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
WIKIPEDIA
ALBENDAZOLE
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
WHO INTERNATIONAL PHARMACOPEIA
ALBENDAZOLE
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY Description: A white or almost white powder. Solubility: Practically insoluble in water; soluble in glacial acetic acid R; slightly soluble in acetone R, very slightly soluble in ethanol (~750 g/l) TS. Category: Anthelminthic. Storage: Albendazole should be kept in a well-closed container, protected from light. Additional information: Melting temperature, about 210?C, with decomposition. Requirement: Albendazole contains not less than 98.0% and not more than 101.0% of C12H15N3O2S, calculated with reference to the dried substance.
MESH
D015766
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
NDF-RT
N0000191624
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY Cytochrome P450 1A Inducers [MoA]
NCI_THESAURUS
C47384
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
INN
3967
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
EVMPD
SUB05295MIG
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
ChEMBL
CHEMBL1483
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
ALANWOOD
albendazole
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
DRUG CENTRAL
103
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
EPA CompTox
DTXSID0022563
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
LACTMED
Albendazole
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
ECHA (EC/EINECS)
259-414-7
Created by admin on Fri Dec 15 15:05:18 UTC 2023 , Edited by admin on Fri Dec 15 15:05:18 UTC 2023
PRIMARY
Related Record Type Details
PLASMA PROTEIN FRACTION (HUMAN)
BINDER->LIGAND
CYTOCHROME P450 3A4
METABOLIC ENZYME -> SUBSTRATE
FETAL HEPATIC FLAVIN-CONTAINING MONOOXYGENASE 3 (HUMAN)
METABOLIC ENZYME -> SUBSTRATE
Structure of ALBENDAZOLE OXIDE
BINDER->LIGAND
BINDING
Related Record Type Details
Structure of ALBENDAZOLE-2-AMINO SULFONE
METABOLITE INACTIVE -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
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Structure of ALBENDAZOLE OXIDE
METABOLITE -> PARENT
Related Record Type Details
Structure of METHYL (5-CHLORO-2-BENZIMIDAZOLYL)CARBAMATE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
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Structure of METHYL N-(4,6-DICHLORO-1H-BENZIMIDAZOL-2-YL)CARBAMATE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of ALBENDAZOLE-2-AMINO SULFONE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of OXIBENDAZOLE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of ALBENDAZOLE SULFONE
IMPURITY -> PARENT
sum of impurities B and C: maximum 0.4 percent
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of ALBENDAZOLE AMINE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of METHYL N-(5-((2-METHYL-4-OXOPENTAN-2-YL)SULFANYL)-1H-BENZIMIDAZOL-2-YL)CARBAMATE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of 5-(S-METHYL) ALBENDAZOLE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of ALBENDAZOLE OXIDE
IMPURITY -> PARENT
sum of impurities B and C: maximum 0.4 percent
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of METHYL N-(5-(BUTYLSULFANYL)-1H-BENZIMIDAZOL-2-YL)CARBAMATE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of METHYL N-(5-((PROPAN-2-YL)SULFANYL)-1H-BENZIMIDAZOL-2-YL)CARBAMATE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of CARBENDAZIM
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
Structure of ALBENDAZOLE
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC
NIH
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