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Details

Stereochemistry ACHIRAL
Molecular Formula C10H9NO9S3
Molecular Weight 383.375
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 8-AMINO-1,3,6-NAPHTHALENETRISULFONIC ACID

SMILES

NC1=C2C(=CC(=C1)S(O)(=O)=O)C=C(C=C2S(O)(=O)=O)S(O)(=O)=O

InChI

InChIKey=UBDHSURDYAETAL-UHFFFAOYSA-N
InChI=1S/C10H9NO9S3/c11-8-3-6(21(12,13)14)1-5-2-7(22(15,16)17)4-9(10(5)8)23(18,19)20/h1-4H,11H2,(H,12,13,14)(H,15,16,17)(H,18,19,20)

HIDE SMILES / InChI

Molecular Formula C10H9NO9S3
Molecular Weight 383.375
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
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
Fluorescent staining of glycoproteins on polyvinylidene difluoride membrane with 8-aminonaphthalene-1,3,6-trisulfonate.
2001 Jun
Tryptophan-rich antimicrobial peptides: comparative properties and membrane interactions.
2002
Capillary electrophoresis/electrospray ion trap mass spectrometry for the analysis of negatively charged derivatized and underivatized glycans.
2002
Diffusional water permeability (PDW) of adult and neonatal rabbit renal brush border membrane vesicles.
2002 Jun 1
Microscale analysis of mucin-type O-glycans by a coordinated fluorophore-assisted carbohydrate electrophoresis and mass spectrometry approach.
2003 Feb
Effects of human lactoferrin on the cytoplasmic membrane of Candida albicans cells related with its candidacidal activity.
2004 Oct 1
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
Hydrolysis characteristics of a beta-1,3-D-glucan elicitor from yeast.
2005 Dec
Influence of culture conditions on the N-glycosylation of a monoclonal antibody specific for recombinant hepatitis B surface antigen.
2005 Feb
Interactions of carbohydrates and proteins by fluorophore-assisted carbohydrate electrophoresis.
2006 Jun
[Expression and characterization of human sTNFR II-IgG Fc fusion protein in Pichia pastoris].
2007 Jun
Simultaneous chiral resolution of monosaccharides as 8-aminonaphthalene-1,3,6-trisulfonate derivatives by ligand-exchange CE using borate as a central ion of the chiral selector.
2007 Nov
Optimization of fluorophore-assisted carbohydrate electrophoresis.
2008 Jul-Aug
Analysis of interactions between carbohydrates and proteins using fluorescent labeling and SDS-PAGE.
2008 Mar-Apr
Fluorophore-assisted carbohydrate electrophoresis for the determination of molecular mass of heparins and low-molecular-weight (LMW) heparins.
2008 Nov
Formation of soluble amyloid oligomers and amyloid fibrils by the multifunctional protein vitronectin.
2008 Oct 21
Methods to monitor liposome fusion, permeability, and interaction with cells.
2010
HAMLET interacts with lipid membranes and perturbs their structure and integrity.
2010 Feb 23
Determination of molecular mass values of chondroitin sulfates by fluorophore-assisted carbohydrate electrophoresis (FACE).
2010 Mar 11
Gramicidin-based fluorescence assay; for determining small molecules potential for modifying lipid bilayer properties.
2010 Oct 13
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:39:49 GMT 2023
Edited
by admin
on Sat Dec 16 09:39:49 GMT 2023
Record UNII
D33V8NB7KB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
8-AMINO-1,3,6-NAPHTHALENETRISULFONIC ACID
Systematic Name English
3,6,8-TRISULFO-1-NAPHTHYLAMINE
Systematic Name English
NSC-227195
Code English
KOCH'S ACID
Common Name English
1-AMINONAPHTHALENE-3,6,8-TRISULFONIC ACID
Systematic Name English
1-NAPHTHYLAMINE-3,6,8-TRISULFONIC ACID
Common Name English
1,3,6-NAPHTHALENETRISULFONIC ACID, 8-AMINO-
Systematic Name English
KOCH ACID
Common Name English
T ACID
Common Name English
AMINO-H ACID
Common Name English
Code System Code Type Description
FDA UNII
D33V8NB7KB
Created by admin on Sat Dec 16 09:39:49 GMT 2023 , Edited by admin on Sat Dec 16 09:39:49 GMT 2023
PRIMARY
EPA CompTox
DTXSID5059454
Created by admin on Sat Dec 16 09:39:49 GMT 2023 , Edited by admin on Sat Dec 16 09:39:49 GMT 2023
PRIMARY
ECHA (EC/EINECS)
204-188-7
Created by admin on Sat Dec 16 09:39:49 GMT 2023 , Edited by admin on Sat Dec 16 09:39:49 GMT 2023
PRIMARY
NSC
227195
Created by admin on Sat Dec 16 09:39:49 GMT 2023 , Edited by admin on Sat Dec 16 09:39:49 GMT 2023
PRIMARY
CAS
117-42-0
Created by admin on Sat Dec 16 09:39:49 GMT 2023 , Edited by admin on Sat Dec 16 09:39:49 GMT 2023
PRIMARY
PUBCHEM
64951
Created by admin on Sat Dec 16 09:39:49 GMT 2023 , Edited by admin on Sat Dec 16 09:39:49 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT