MONOSODIUM 8-AMINO-1-NAPHTHOL-3,6-DISULFONATE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C10H7NO7S2.Na.H
Molecular Weight	341.293
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of MONOSODIUM 8-AMINO-1-NAPHTHOL-3,6-DISULFONATE

SMILES

[H+].[Na+].NC1=CC(=CC2=C1C(O)=CC(=C2)S([O-])(=O)=O)S([O-])(=O)=O

InChI

InChIKey=QPILZZVXGUNELN-UHFFFAOYSA-M

InChI=1S/C10H9NO7S2.Na/c11-8-3-6(19(13,14)15)1-5-2-7(20(16,17)18)4-9(12)10(5)8;/h1-4,12H,11H2,(H,13,14,15)(H,16,17,18);/q;+1/p-1

HIDE SMILES / InChI

Approval Year

PubMed

Show entries

Title	Date	PubMed
Inhibition of HIV replication by naphthalenemonosulfonic acid derivatives and a bis naphthalenedisulfonic acid compound.	1990	2122146
Potential anti-AIDS naphthalenesulfonic acid derivatives. Synthesis and inhibition of HIV-1 induced cytopathogenesis and HIV-1 and HIV-2 reverse transcriptase activities.	1992 Dec 25	1282569
Structure-activity relationship studies with symmetric naphthalenesulfonic acid derivatives. Synthesis and influence of spacer and naphthalenesulfonic acid moiety on anti-HIV-1 activity.	1993 Jul 9	8336338

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Patents

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Name

Type

Language

MONOSODIUM 8-AMINO-1-NAPHTHOL-3,6-DISULFONATE

Systematic Name

English

MONOSODIUM 4-AMINO-5-HYDROXY-2,7-NAPHTHALENEDISULFONATE

Systematic Name

English

NSC-8632

Code

English

H ACID MONOSODIUM SALT

Common Name

English

2,7-NAPHTHALENEDISULFONIC ACID, 4-AMINO-5-HYDROXY-, SODIUM SALT (1:1)

Systematic Name

English

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Code System

Code

Type

Description

PUBCHEM

23664361

PRIMARY

FDA UNII

BQX9B4J4FO

PRIMARY

NSC

8632

PRIMARY

CAS

5460-09-3

PRIMARY

ECHA (EC/EINECS)

226-736-4

PRIMARY

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SUBSTANCE RECORD


					BQX9B4J4FO

MONOSODIUM 8-AMINO-1-NAPHTHOL-3,6-DISULFONATE