NAPHTHIONIC ACID

Details

Stereochemistry	ACHIRAL
Molecular Formula	C10H9NO3S
Molecular Weight	223.248
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

NC1=C2C=CC=CC2=C(C=C1)S(O)(=O)=O

InChI

InChIKey=NRZRRZAVMCAKEP-UHFFFAOYSA-N

InChI=1S/C10H9NO3S/c11-9-5-6-10(15(12,13)14)8-4-2-1-3-7(8)9/h1-6H,11H2,(H,12,13,14)

HIDE SMILES / InChI

Molecular Formula	C10H9NO3S
Molecular Weight	223.248
Charge	0
Count

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

Approval Year

PubMed

Title	Date	PubMed
Preparation of a library of EDTA amide x-aminenaphthalene-y-sulfonic acid derivatives on solid phase and their fluorescence behavior toward transition metals.	2009-10-14	19821606
Lack of genotoxic effect of food dyes amaranth, sunset yellow and tartrazine and their metabolites in the gut micronucleus assay in mice.	2009-02	19095036
Detection of conformational changes in immunoglobulin G using isothermal titration calorimetry with low-molecular-weight probes.	2008-09-15	18577365
Two novel mixed-ligand complexes containing organosulfonate ligands.	2008-07	18599971
Regiospecific O-methylation of naphthoic acids catalyzed by NcsB1, an O-methyltransferase involved in the biosynthesis of the enediyne antitumor antibiotic neocarzinostatin.	2008-05-23	18387946
5-Aminonaphthalene-1-sulfonic acid and its manganese, nickel and cobalt salts.	2007-12	18057608
Diaquabis(ethylenediamine)cadmium(II) bis(4-aminonaphthalene-1-sulfonate) dihydrate.	2006-09	16954629
Recognition-induced supramolecular porous nanosphere formation from cyclodextrin conjugated by cholic acid.	2006-03-28	16548612
Synthetic organic food colouring agents and their degraded products: effects on human and rat cholinesterases.	2004	15462257
Synthesis of naphthalenesulfonic acid small molecules as selective inhibitors of the DNA polymerase and ribonuclease H activities of HIV-1 reverse transcriptase.	1994-08-05	7520080
Structure-activity relationship studies with symmetric naphthalenesulfonic acid derivatives. Synthesis and influence of spacer and naphthalenesulfonic acid moiety on anti-HIV-1 activity.	1993-07-09	8336338
Inhibition of HIV replication by naphthalenemonosulfonic acid derivatives and a bis naphthalenedisulfonic acid compound.	1990	2122146

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:21:51 GMT 2025` Edited by `admin` on `Mon Mar 31 21:21:51 GMT 2025`
Record UNII	8ZIK65C5CD
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

1-NAPHTHYLAMINE-4-SULFONIC ACID

Preferred Name

English

NAPHTHIONIC ACID

Systematic Name

English

1-AMINO-4-NAPHTHALENESULFONIC ACID

Systematic Name

English

.ALPHA.-NAPHTHYLAMINE-4-SULFONIC ACID

Common Name

English

1,4-NAPHTHIONIC ACID

Common Name

English

4-AMINO-1-NAPHTHALENESULFONIC ACID

Systematic Name

English

4-AMINO-1-NAPHTHALENESULPHONIC ACID

Systematic Name

English

1-NAPHTHYLAMINE-4-SULFONIC ACID [MI]

Common Name

English

1-AMINO-4-SULFONAPHTHALENE

Systematic Name

English

NSC-4155

Code

English

PIRIA'S ACID

Common Name

English

Code System Code Type Description

FDA UNII

8ZIK65C5CD