Disease relevance of Aminodecane

• The joint toxicity of nonylamine and decylamine and of atrazine and decylamine was evaluated in assays with the green alga Selenastrum capricornutum based on an isobologram method [1].

High impact information on Aminodecane

• In the beef brain cortex n-octylamine showed marked preference for MAO-B, whereas n-decylamine was selective toward-MAO-A [2].
• Deamination of n-octylamine and n-decylamine has been studied in various tissues using a new bioluminescence technique [2].
• Human thyroxine binding globulin (TBG) was purified to near homogeneity by chromatography on thyroxine-substituted Sepharose 4B, DEAE-Sephadex A-50, Sephadex G-150 and n-decylamine-substituted Sepharose 4B [3].
• The electric capacitance of isolated rat mast cells and its change under the influence of either n-decylamine or toluidine blue was investigated [4].
• N-decylamine released histamine without accompanying degranulation; and it caused a marked swelling of mast cells and a striking decrease of capacitance, although electric capacitance is usually proportional to the size of the cell [4].

Biological context of Aminodecane

• Among various amine derivatives, only n-decylamine was found to induce lipolysis in the endogenous lipid droplets [5].

Anatomical context of Aminodecane

• Lipolytic activities of p-aminophenol and n-decylamine in endogenous lipid droplets from rat adipocytes [5].

Analytical, diagnostic and therapeutic context of Aminodecane

• The analyte was eluted from the extraction column and chromatographed by reversed-phase HPLC using decylamine as a competing-ion reagent [6].

References