Anilino Naphthalenesulfonates

"Anilino Naphthalenesulfonates" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

A class of organic compounds which contain an anilino (phenylamino) group linked to a salt or ester of naphthalenesulfonic acid. They are frequently used as fluorescent dyes and sulfhydryl reagents.

Descriptor ID

D000817

MeSH Number(s)

D02.092.146.125

D02.455.426.559.847.638.555.282

D02.886.645.600.080.050.650.050

D04.615.638.555.282

Concept/Terms

Anilino Naphthalenesulfonates

Below are MeSH descriptors whose meaning is more general than "Anilino Naphthalenesulfonates".

Chemicals and Drugs [D]
Organic Chemicals [D02]
Amines [D02.092]
Aniline Compounds [D02.092.146]
Anilino Naphthalenesulfonates [D02.092.146.125]
Hydrocarbons [D02.455]
Hydrocarbons, Cyclic [D02.455.426]
Hydrocarbons, Aromatic [D02.455.426.559]
Polycyclic Hydrocarbons, Aromatic [D02.455.426.559.847]
Naphthalenes [D02.455.426.559.847.638]
Naphthalenesulfonates [D02.455.426.559.847.638.555]
Anilino Naphthalenesulfonates [D02.455.426.559.847.638.555.282]
Sulfur Compounds [D02.886]
Sulfur Acids [D02.886.645]
Sulfonic Acids [D02.886.645.600]
Arylsulfonic Acids [D02.886.645.600.080]
Arylsulfonates [D02.886.645.600.080.050]
Naphthalenesulfonates [D02.886.645.600.080.050.650]
Anilino Naphthalenesulfonates [D02.886.645.600.080.050.650.050]
Polycyclic Compounds [D04]
Polycyclic Hydrocarbons, Aromatic [D04.615]
Naphthalenes [D04.615.638]
Naphthalenesulfonates [D04.615.638.555]
Anilino Naphthalenesulfonates [D04.615.638.555.282]

Below are MeSH descriptors whose meaning is related to "Anilino Naphthalenesulfonates".

Below are MeSH descriptors whose meaning is more specific than "Anilino Naphthalenesulfonates".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Anilino Naphthalenesulfonates" by people in Harvard Catalyst Profiles by year, and whether "Anilino Naphthalenesulfonates" was a major or minor topic of these publication.

Bar chart showing 10 publications over 7 distinct years, with a maximum of 2 publications in 1998 and 2001 and 2009

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1995	0	1	1
1998	1	1	2
2001	0	2	2
2005	0	1	1
2009	0	2	2
2016	0	1	1
2017	0	1	1

Below are the most recent publications written about "Anilino Naphthalenesulfonates" by people in Profiles.

Thioflavin T fluorescence to analyse amyloid formation kinetics: Measurement frequency as a factor explaining irreproducibility. Anal Biochem. 2017 09 01; 532:83-86.

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Trimethylamine-N-oxide switches from stabilizing nature: A mechanistic outlook through experimental techniques and molecular dynamics simulation. Sci Rep. 2016 Mar 30; 6:23656.

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Biophysical analysis of apolipoprotein E3 variants linked with development of type III hyperlipoproteinemia. PLoS One. 2011; 6(11):e27037.

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Kinetic and thermodynamic characterization of dihydrotestosterone-induced conformational perturbations in androgen receptor ligand-binding domain. Mol Endocrinol. 2009 Aug; 23(8):1231-41.

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Agitation and high ionic strength induce amyloidogenesis of a folded PDZ domain in native conditions. Biophys J. 2009 Mar 18; 96(6):2289-98.

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Multiple Ca(2+)-binding sites in the extracellular domain of the Ca(2+)-sensing receptor corresponding to cooperative Ca(2+) response. Biochemistry. 2009 Jan 20; 48(2):388-98.

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SecB-mediated protein export need not occur via kinetic partitioning. J Mol Biol. 2009 Jan 30; 385(4):1243-56.

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Characterization of the folding and unfolding reactions of single-chain monellin: evidence for multiple intermediates and competing pathways. Biochemistry. 2007 Oct 23; 46(42):11727-43.

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Lead (Pb) exposure and its effect on APP proteolysis and Abeta aggregation. FASEB J. 2005 Dec; 19(14):2083-4.

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Activity, folding, misfolding, and aggregation in vitro of the naturally occurring human tissue factor mutant R200W. Biochemistry. 2005 May 10; 44(18):6755-63.

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