8-AMINO-1,3,6-NAPHTHALENETRISULFONIC ACID

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

Structure Search

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

Title	Date	PubMed
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
On-line capillary electrophoresis with mass spectrometry detection for the analysis of carbohydrates after derivatization with 8-aminonaphthalene-1,3,6-trisulfonic acid.	2001 Nov 16	11762766
Capillary electrophoresis/electrospray ion trap mass spectrometry for the analysis of negatively charged derivatized and underivatized glycans.	2002	11803540
Microscale analysis of mucin-type O-glycans by a coordinated fluorophore-assisted carbohydrate electrophoresis and mass spectrometry approach.	2003 Feb	12601728
Search for serum protein-binding disaccharides and disaccharide-binding serum proteins by affinity capillary electrophoresis.	2004 Mar	15004849
Effects of human lactoferrin on the cytoplasmic membrane of Candida albicans cells related with its candidacidal activity.	2004 Oct 1	15364102
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	15804603
Application of fluorophore-assisted carbohydrate electrophoresis to analysis of disaccharides and oligosaccharides derived from glycosaminoglycans.	2005 Aug 15	16004957
Hydrolysis characteristics of a beta-1,3-D-glucan elicitor from yeast.	2005 Dec	15877544
Selective cytochrome c displacement by phosphate and Ca(2+) in brain mitochondria.	2006	17334837
Kinetic analysis using low-molecular mass xyloglucan oligosaccharides defines the catalytic mechanism of a Populus xyloglucan endotransglycosylase.	2006 Apr 1	16356166
Recovery of free oligosaccharides from derivatives labeled by reductive amination.	2006 Jul 1	16701074
Active-site mapping of a Populus xyloglucan endo-transglycosylase with a library of xylogluco-oligosaccharides.	2008 Aug 8	18511421
Analysis of interactions between carbohydrates and proteins using fluorescent labeling and SDS-PAGE.	2008 Mar-Apr	18533480
Methods to monitor liposome fusion, permeability, and interaction with cells.	2010	20013400
Gramicidin-based fluorescence assay; for determining small molecules potential for modifying lipid bilayer properties.	2010 Oct 13	20972414

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

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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