ALBENDAZOLE OXIDE

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C12H15N3O3S
Molecular Weight	281.331
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of ALBENDAZOLE OXIDE

Structure Search

SMILES

CCC[S+]([O-])C1=CC=C2NC(NC(=O)OC)=NC2=C1

InChI

InChIKey=VXTGHWHFYNYFFV-UHFFFAOYSA-N

InChI=1S/C12H15N3O3S/c1-3-6-19(17)8-4-5-9-10(7-8)14-11(13-9)15-12(16)18-2/h4-5,7H,3,6H2,1-2H3,(H2,13,14,15,16)

HIDE SMILES / InChI

Molecular Formula	C12H15N3O3S
Molecular Weight	281.331
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 16:12:26 UTC 2023` Edited by `admin` on `Fri Dec 15 16:12:26 UTC 2023`
Record UNII	J39B52TV34
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

ALBENDAZOLE OXIDE

Official Name

English

RS8852

Code

English

RICOBENDAZOLE

Common Name

English

ALBENDAZOLE SULFOXIDE

Common Name

English

RYCOBEN

Brand Name

English

albendazole oxide [INN]

Common Name

English

RYCOBENDAZOLE

Common Name

English

METHYL 5-(PROPYLSULFINYL)-2-BENZIMIDAZOLECARBAMATE

Common Name

English

METHYL N-(5-(PROPYLSULFINYL)-1H-BENZIMIDAZOL-2-YL)CARBAMATE

Systematic Name

English

(±)-ALBENDAZOLE SULFOXIDE

Common Name

English

RS-8852

Code

English

ALBENDAZOLE SULFOXIDE [MI]

Common Name

English

ALBENDAZOLE IMPURITY B [EP IMPURITY]

Common Name

English

METHYL (5-(PROPYLSULFINYL)-1H-BENZO(D)IMIDAZOL-2-YL)CARBAMATE

Systematic Name

English

Classification Tree Code System Code

NCI_THESAURUS

C250

Created by admin on Fri Dec 15 16:12:26 UTC 2023 , Edited by admin on Fri Dec 15 16:12:26 UTC 2023

Code System Code Type Description

SMS_ID

100000087715

Created by admin on Fri Dec 15 16:12:26 UTC 2023 , Edited by admin on Fri Dec 15 16:12:26 UTC 2023

PRIMARY

PUBCHEM

83969

Created by admin on Fri Dec 15 16:12:26 UTC 2023 , Edited by admin on Fri Dec 15 16:12:26 UTC 2023

PRIMARY

EVMPD

SUB05296MIG

Created by admin on Fri Dec 15 16:12:26 UTC 2023 , Edited by admin on Fri Dec 15 16:12:26 UTC 2023

PRIMARY

CHEBI

16959

Created by admin on Fri Dec 15 16:12:26 UTC 2023 , Edited by admin on Fri Dec 15 16:12:26 UTC 2023

PRIMARY

FDA UNII

J39B52TV34

Created by admin on Fri Dec 15 16:12:26 UTC 2023 , Edited by admin on Fri Dec 15 16:12:26 UTC 2023

PRIMARY

MESH

C027186

Created by admin on Fri Dec 15 16:12:26 UTC 2023 , Edited by admin on Fri Dec 15 16:12:26 UTC 2023

PRIMARY

CAS

54029-12-8

Created by admin on Fri Dec 15 16:12:26 UTC 2023 , Edited by admin on Fri Dec 15 16:12:26 UTC 2023

PRIMARY

EPA CompTox

DTXSID4057768

Created by admin on Fri Dec 15 16:12:26 UTC 2023 , Edited by admin on Fri Dec 15 16:12:26 UTC 2023

PRIMARY

NCI_THESAURUS

C72157

Created by admin on Fri Dec 15 16:12:26 UTC 2023 , Edited by admin on Fri Dec 15 16:12:26 UTC 2023

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DRUG CENTRAL

104

Created by admin on Fri Dec 15 16:12:26 UTC 2023 , Edited by admin on Fri Dec 15 16:12:26 UTC 2023

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MERCK INDEX

m1473

Created by admin on Fri Dec 15 16:12:26 UTC 2023 , Edited by admin on Fri Dec 15 16:12:26 UTC 2023

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Merck Index

DRUG BANK

DB13871

Created by admin on Fri Dec 15 16:12:26 UTC 2023 , Edited by admin on Fri Dec 15 16:12:26 UTC 2023

PRIMARY

INN

5979

Created by admin on Fri Dec 15 16:12:26 UTC 2023 , Edited by admin on Fri Dec 15 16:12:26 UTC 2023

PRIMARY

ChEMBL

CHEMBL1665

Created by admin on Fri Dec 15 16:12:26 UTC 2023 , Edited by admin on Fri Dec 15 16:12:26 UTC 2023

PRIMARY

Related Record Type Details


					6D53G0FD0Z

PLASMA PROTEIN FRACTION (HUMAN)

BINDER->LIGAND

Amount:


					F4216019LN

LIGAND->BINDER

Related Record Type Details


					F4216019LN

PARENT -> METABOLITE

Amount:

Related Record Type Details


					F4216019LN

PARENT -> IMPURITY

Comments:

sum of impurities B and C: maximum 0.4 percent

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:

Related Record Type Details


					J39B52TV34

ALBENDAZOLE OXIDE

ACTIVE MOIETY