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Du sökte efter: N-(4-Biphenylyl)-1-naphthylamine

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Organisk referensstandard, 2-Naftylamin 10 µg/ml i acetonitril

Artikel nummer : (EHERL10206355AL)

Leverantör: EHRENSTORFER

Beskrivning: Organic Standard, 2-Naftylamin 10 µg/ml i acetonitril, Förpackningstyp: Glass bottle

UOM: 1 * 10 mL

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8-Amino-2-naphthalenesulphonic acid 95%

Leverantör: Thermo Fisher Scientific

Beskrivning: 8-Amino-2-naphthalenesulphonic acid 95%

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8-Anilino-1-naphthalenesulphonic acid 95%

Leverantör: Thermo Fisher Scientific

Beskrivning: 8-Anilino-1-naphthalenesulphonic acid 95%

Säkerhetsdatablad Certifikat

8-Anilino-1-naphthalenesulphonic acid ≥95%

Leverantör: Spectrum Chemical

Beskrivning: 8-Anilino-1-naphthalenesulfonic Acid is also known as ANS contains an amine group and a sulfonic acid. 8-Anilino-1-naphthalenesulfonic acid is a fluorescent dye with high affinity towards hydrophobic surfaces of proteins. It is useful for determining the affinity of hydrophobic ligands to their corresponding binding proteins and is used as a probe to monitor protein-folding.

8-Anilino-1-naphthalenesulphonic acid, dark powder

Leverantör: MP Biomedicals

Beskrivning: 8-Anilino-1-naphthalene Sulphonic Acid is a hydrophobic polarity sensitive fluorescent dye useful as a site probe to detect conformational changes in cell and micelle membranes and molecules such as proteins.

3'-Carbamoyl-[1,1'-biphenyl]-3-ylcyclohexylcarbamate ≥98%

Artikel nummer : (ENZOBMLEI3270025)

Leverantör: ENZO LIFE SCIENCES

Beskrivning: URB-597 is a potent and selective inhibitor of the enzyme fatty acid amide hydrolase (FAAH), which is involved in the hydrolysis of endogenous cannabinoids such as anandamide. Inhibition of FAAH may serve to enhance the analgesic effects of endogenous cannabinoids. URB-597 has been shown to inhibit FAAH in rat cortical neuron membranes and in intact neurons with IC50 values of 4.6nM and 0.5nM, respectively. The compound has also been shown to have anxiolytic effects in rats (ID50=0.15mg/kg). Because URB-597 acts on FAAH and does not interfere with the binding of anandamide to the CB1 and CB2 receptors, it is a novel tool for drug development.

UOM: 1 * 25 mg

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