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Details

Stereochemistry ACHIRAL
Molecular Formula C10H9NO6S2
Molecular Weight 303.312
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 7-AMINO-1,3-NAPHTHALENEDISULFONIC ACID

SMILES

NC1=CC2=C(C=C1)C=C(C=C2S(O)(=O)=O)S(O)(=O)=O

InChI

InChIKey=CMOLPZZVECHXKN-UHFFFAOYSA-N
InChI=1S/C10H9NO6S2/c11-7-2-1-6-3-8(18(12,13)14)5-10(9(6)4-7)19(15,16)17/h1-5H,11H2,(H,12,13,14)(H,15,16,17)

HIDE SMILES / InChI

Molecular Formula C10H9NO6S2
Molecular Weight 303.312
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Aromatic sulfonic acids as viral inhibitors. Structure-activity study using rhino, adeno 3, herpes simplex, and influenza viruses.
1971 Jul
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
A novel water-soluble fluorescent probe for the determination of methylamine.
2001 Oct
Fluorophore-assisted carbohydrate electrophoresis: a sensitive and accurate method for the direct analysis of dolichol pyrophosphate-linked oligosaccharides in cell cultures and tissues.
2005 Apr
Ultraviolet photodissociation at 355 nm of fluorescently labeled oligosaccharides.
2008 Jul 1
Induced intersystem crossing at the fluorescence quenching of laser dye 7-amino-1,3-naphthalenedisulfonic acid by paramagnetic metal ions.
2010 Jan
Antiangiogenic activity of 2-deoxy-D-glucose.
2010 Oct 27
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:09:37 GMT 2023
Edited
by admin
on Sat Dec 16 02:09:37 GMT 2023
Record UNII
7C482FX29K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
7-AMINO-1,3-NAPHTHALENEDISULFONIC ACID
Systematic Name English
AMIDO-G-ACID [MI]
Common Name English
AMINO-G-ACID
Common Name English
6,8-DISULFO-2-AMINONAPHTHALENE
Systematic Name English
2-NAPHTHYLAMINE-6,8-DISULFONIC ACID
Common Name English
NSC-4013
Code English
6,8-DISULFO-2-NAPHTHYLAMINE
Systematic Name English
AMIDO-G-ACID
MI  
Common Name English
2-AMINO-6,8-DISULFONAPHTHALENE
Systematic Name English
.BETA.-NAPHTHYLAMINE-6,8-DISULFONIC ACID
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID4058944
Created by admin on Sat Dec 16 02:09:37 GMT 2023 , Edited by admin on Sat Dec 16 02:09:37 GMT 2023
PRIMARY
MERCK INDEX
m1665
Created by admin on Sat Dec 16 02:09:37 GMT 2023 , Edited by admin on Sat Dec 16 02:09:37 GMT 2023
PRIMARY Merck Index
CAS
86-65-7
Created by admin on Sat Dec 16 02:09:37 GMT 2023 , Edited by admin on Sat Dec 16 02:09:37 GMT 2023
PRIMARY
NSC
4013
Created by admin on Sat Dec 16 02:09:37 GMT 2023 , Edited by admin on Sat Dec 16 02:09:37 GMT 2023
PRIMARY
MESH
C033153
Created by admin on Sat Dec 16 02:09:37 GMT 2023 , Edited by admin on Sat Dec 16 02:09:37 GMT 2023
PRIMARY
ECHA (EC/EINECS)
201-689-2
Created by admin on Sat Dec 16 02:09:37 GMT 2023 , Edited by admin on Sat Dec 16 02:09:37 GMT 2023
PRIMARY
PUBCHEM
6851
Created by admin on Sat Dec 16 02:09:37 GMT 2023 , Edited by admin on Sat Dec 16 02:09:37 GMT 2023
PRIMARY
FDA UNII
7C482FX29K
Created by admin on Sat Dec 16 02:09:37 GMT 2023 , Edited by admin on Sat Dec 16 02:09:37 GMT 2023
PRIMARY
Related Record Type Details
SOLVATE->ANHYDROUS
SALT/SOLVATE -> PARENT