AMIDOX

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C7H8N2O3
Molecular Weight	168.15
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	1
Charge	0

SHOW SMILES / InChI

Structure of AMIDOX

Structure Search

SMILES

N\C(=N/O)C1=CC=C(O)C(O)=C1

InChI

InChIKey=JOAASNKBYBFGDN-UHFFFAOYSA-N

InChI=1S/C7H8N2O3/c8-7(9-12)4-1-2-5(10)6(11)3-4/h1-3,10-12H,(H2,8,9)

HIDE SMILES / InChI

Molecular Formula	C7H8N2O3
Molecular Weight	168.15
Charge	0
Count

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

Approval Year

PubMed

PubMed

Title	Date	PubMed
Selective inhibition of l kappaB alpha phosphorylation and HIV-1 LTR-directed gene expression by novel antioxidant compounds.	1997-08-04	9268159

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:54:05 GMT 2025` Edited by `admin` on `Mon Mar 31 18:54:05 GMT 2025`
Record UNII	505NO62X9Z
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

NSC-343341

Preferred Name

English

AMIDOX

Common Name

English

VF-236

Code

English

N,3,4-TRIHYDROXYBENZAMIDINE

Systematic Name

English

Code System Code Type Description

CAS

95933-72-5

Created by admin on Mon Mar 31 18:54:05 GMT 2025 , Edited by admin on Mon Mar 31 18:54:05 GMT 2025

PRIMARY

FDA UNII

505NO62X9Z

Created by admin on Mon Mar 31 18:54:05 GMT 2025 , Edited by admin on Mon Mar 31 18:54:05 GMT 2025

PRIMARY

EPA CompTox

DTXSID501034538

Created by admin on Mon Mar 31 18:54:05 GMT 2025 , Edited by admin on Mon Mar 31 18:54:05 GMT 2025

PRIMARY

NSC

343341

Created by admin on Mon Mar 31 18:54:05 GMT 2025 , Edited by admin on Mon Mar 31 18:54:05 GMT 2025

PRIMARY

PUBCHEM

124068

Created by admin on Mon Mar 31 18:54:05 GMT 2025 , Edited by admin on Mon Mar 31 18:54:05 GMT 2025

PRIMARY