About: naphthalenesulfonate

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

class of chemical compounds

Attributes	Values
rdf:type	Item
description	class of chemical compounds (en) класс химических соединений (ru) клас хімічних сполук (uk)
rdfs:label	naphthalenesulfonate (en) Naphthalenesulfonate (vi) нафталинсульфонаты (ru) سلفونات النفثالين (ar) 萘磺酸盐 (zh)
skos:prefLabel	naphthalenesulfonate (en) Naphthalenesulfonate (vi) нафталинсульфонаты (ru) سلفونات النفثالين (ar) 萘磺酸盐 (zh)
name	naphthalenesulfonate (en) Naphthalenesulfonate (vi) нафталинсульфонаты (ru) سلفونات النفثالين (ar) 萘磺酸盐 (zh)
Freebase ID	wds:Q6964879-85F141FF-8C73-423A-9559-4DB3BE54CC58
Freebase ID	/m/0dxtc_
subclass of	wds:Q6964879-2b4f14e0-4f7e-2508-6752-ce104b68f862 wds:Q6964879-c02ebec5-44e3-070e-0e54-256d0af1edc9
subclass of	naphthalene arylsulfonates
skos:altLabel	naphthalenesulfonates (en)
UMLS CUI	wds:Q6964879-48F4DC87-FA07-42B8-B288-299A223BEC22
MeSH descriptor ID	wds:Q6964879-9A89455A-A800-497A-BEE7-693F992F2CA9
Microsoft Academic ID	wds:Q6964879-F3F2FAB1-42D3-459B-A78D-EC17D54BEAA9
MeSH tree code	wds:Q6964879-31b1a99a-4e5e-7a6e-4a39-e5016c021cef wds:Q6964879-4251d3a3-4227-1828-f286-acfe081dbd9b wds:Q6964879-5917cbe5-4099-487d-cdfe-a4e18e51d611
topic's main category	wds:Q6964879-08B0D4E4-C908-4E4F-9F1A-CD4E52058016
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/D009282
Microsoft Academic ID	https://makg.org/entity/2780336409
MeSH tree code	http://id.nlm.nih.gov/mesh/D02.455.426.559.847.638.555 http://id.nlm.nih.gov/mesh/D02.886.645.600.080.050.650 http://id.nlm.nih.gov/mesh/D04.615.638.555
UMLS CUI	C0027379
MeSH descriptor ID	D009282
Microsoft Academic ID	2780336409
MeSH tree code	D02.455.426.559.847.638.555 D02.886.645.600.080.050.650 D04.615.638.555
topic's main category	Category:Naphthalenesulfonates
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q6964879 Naphthalenesulfonate https://zh.wikipedia.org/wiki/%E8%90%98%E7%A3%BA%E9%85%B8%E7%9B%90 https://ru.wikipedia.org/wiki/%D0%9D%D0%B0%D1%84%D1%82%D0%B0%D0%BB%D0%B8%D0%BD%D1%81%D1%83%D0%BB%D1%8C%D1%84%D0%BE%D0%BD%D0%B0%D1%82%D1%8B https://ar.wikipedia.org/wiki/%D8%B3%D9%84%D9%81%D9%88%D9%86%D8%A7%D8%AA_%D8%A7%D9%84%D9%86%D9%81%D8%AB%D8%A7%D9%84%D9%8A%D9%86 https://vi.wikipedia.org/wiki/Naphthalenesulfonate
is subclass of of	anilino naphthalenesulfonates
is subclass of of	wds:Q76626708-aa1bb021-495e-8bd0-8c5b-2f2b8da4be5a
is main subject of	Fluorescent probes in model membranes. II. Monolayer studies of 2,2'-(vinylenedi-p-phenylene)bisbenzoxazole, d-3-aminodesoxyequilenin and N-octadecylnaphthyl-2-amino-6-sulfonic acid with host-lipid tetradecanoic acid Synthesis and properties of fluorescent nucleotide substrates for DNA-dependent RNA polymerases Polarization microscopy and microspectrophotometry of Sirius Red, Picrosirius and Chlorantine Fast Red aggregates and of their complexes with collagen URATE AND NON-URATE CHROMOGENS IN HUMAN SERUM The action of general anesthetics. I. Use of 1-anilino-naphthalene-8-sulfonate as a fluorescent probe of the lipid phase of the membrane Specific chemical labeling of DNA fragments Studies on the interaction between Escherichia coli pyruvate oxidase and a detergent activator by utilization of the fluorescence probe bis(8-p-toluidino-1-naphthalene)sulfonate Synthesis and characterization of N-(2,4-diphosphobenzyl)-1-amino-5-naphthalenesulfonic acid, a new fluorescent analogue of diphosphoglyceric acid Interaction of spin-labeled and N-(iodoacetylaminoethyl)-5-naphthylamine-1-sulfonic acid SH1-blocked heavy meromyosin and myosin with actin and adenosine triphosphate 5-Di-n-butylaminonaphthalene-1-sulphonyl chloride — a new reagent for fluorescence labelling of amines, amino acids and peptides Neutral and cationic sulfonamido derivatives of the fluorescent probe 2-p-toluidinylnaphthalene-6-sulfonate. Properties and mechanistic implications Neoprontosil binding to carbonic anhydrase. Resonance Raman and other studies on the ionization behavior of the sulfonamide Use of the nitrazine yellow swab test in the diagnosis of ruptured membranes Effect of P2' substituents on kinetic constants for hydrolysis by cysteine proteinases The question of coproporphyrin chromogens The methodology of intestinal flora analysis with fluorescent-marked antibodies (marking with 1-dimethylamino-naphthalenesulfonic acid) Spectrophotometric determination of photoreceptor cGMP-gated channel Mg2--fluxes using dichlorophosphonazo III An interesting peroxidase staining.--utilization of blended substrate of mixed 2, 7-FDA and Laurent's acid-- (author's transl) Interlaboratory study of acid orange 12 dye binding for measuring protein in meat URINARY EXCRETION OF OESTRONE AND OESTRADIOL AND OF ZIMMERMANN CHROMOGENS IN THE SOW DURING OESTRUS Fluorescent photochemical surface labeling of intact human erythrocytes The interaction of collagen with the hydrophobic fluorescent probe 2-p-toluidinylnaphthalene-6-sulfonate Induction of hepatoma in mice by direct deep Black-Extra (DDB-EX) and occurrence of serum AFP Stacking interactions in fluorescent nucleotide analogs containing 1-aminonaphthalene-5-sulfonate at the phosphoryl terminus Structural studies on des-pentapeptide (B26-30)-insulin. IV. A preliminary investigation on the hydrophobic region by employing a fluorescence probe, 1-p-toluidinylnaphthalene-8-sulphonate Lipoprotein analysis by means of the fluorescence probe 8-anilino-1-naphthalene sulphonic acid (author's transl) Quantitative aspects of the Naphthol Yellow S staining for proteins studied in a model system of polyacrylamide films and in isolated rat liver cells and nuclei PORTER-SILBER CHROMOGEN INTERFERENCE IN THE MEASUREMENT OF BODY FLUID STEROID RESPONSES TO TOTAL FASTING. TECHN DOCUM REP NO. SAM-TDR-64-58 Quantitative cytochemistry of nuclear and cytoplasmic proteins using the Naphthol Yellow S and dinitrofluorobenzene staining methods COMPARATIVE STUDY OF SOME PROCEDURES PROPOSED TO CORRECT THE INTERFERENCE OF NON-SPECIFIC CHROMOGENS IN THE DETERMINATION OF URINARY 17-KETOSTEROIDS WITH METHYLDINITROBENZENE STUDY ON THE USE OF FORMALDEHYDE FOR THE REMOVAL OF PIGMENTS AND NON-SPECIFIC CHROMOGENS IN THE DETERMINATION OF URINARY 17-KETOSTEROIDS. INTERFERENCE OF UREA The interaction of an amphipathic fluorescence probe, 2-p-toluidinonaphthalene-6-sulphonate, with isolated chloroplasts Chromotrop-aniline blue stain for improved demonstration of fresh heart muscle fiber damage Testing for nitrate reduction by bacteria: the use of Cleve's acid (8-aminonaphthalene-2-sulphonic acid) to determine nitrite formation Quantification of nuclear non-histone proteins by Feulgen-Naphthol Yellow S cytophotometry Fluorescent probes for measuring the binding constants and distances between the metal ions bound to Escherichia coli glutamine synthetase Urinary excretion of Zimmermann chromogens, pregnanediol and 17-hydroxycorticosteroids during pregnancy (Observations in a normal woman and a patient with Addison's disease) Romanowsky-Type Staining: Effect of Adding Acid Dyes, Particularly Chromotrope 2R Azofloxin--toluidine blue staining CHEMICAL-BIOLOGICAL STUDY ON ISAMINE BLUE AND ITS ANTIBLASTIC FUNCTION: COMPONENTS AND ANTIMITOTIC ACTION OF VARIOUS FRACTIONS IN EHRLICH CARCINOMA Correspondence: Chromotrope 2R THE AZOSULFAMIDE TEST AS A LIVER FUNCTION TEST Nanosecond relaxation in membranes observed by fluorescence lifetime-resolved emission spectra Comparative characteristics of hydrophobic nature of certain proteins by their interaction with 2-p-toluidinonaphthalene-6-sulfonates Staining with naphthol yellow S. 1. Evaluation of the Keq of the protein-dye binding reaction ZIMMERMANN CHROMOGENS IN THE TISSUE OF THE SKIN Staining with naphthol yellow S. 2. Study of the reversibility of the protein-dye binding reaction

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