High impact information on n-Hexylamine

• The noncompetitive mode of interaction affected the accessibility of the active site to productive amine substrates since the reductive trapping of n-hexylamine to lysyl oxidase was largely prevented by the presence of TCP [1].
• DeltapH was independent of the amount of thylakoids used or of the concentration of hexylamine [2].
• Optimum conditions were found when using a gradient from 5 mM hexylamine in water (pH 6.3) to 90% methanol/10% 10 mM ammonium acetate (pH 8.5) [3].
• Study of the hydrolysis and ionization constants of Schiff base from pyridoxal 5'-phosphate and n-hexylamine in partially aqueous solvents. An application to phosphorylase b [4].
• Cytosolic fractions were subjected to hexylamine agarose chromatography, Sepharose S-300 filtration and hydroxylapatite chromatography [5].

Anatomical context of n-Hexylamine

• A novel probe using fluorescamine, coupled to hexylamine, detected 22.9% of cells, apparently of the B-cell series, counted by fluorescence microscopy [6].
• Single-channel conductance of the K+ channel from sarcoplasmic reticulum (SR) was reduced by aminoglycoside antibiotics such as neomycin and ribostamycin and also by n-hexylamine from either side of the membrane in a dose- and voltage-dependent manner [7].
• It was suggested that the catecholamine-related compounds and hexylamine can act on relaxing nerve endings to increase neurotransmitter serotonin in the junctional clefts, and mersalyl antagonizes the relaxation in response to these compounds by blocking the serotonin [8].

Associations of n-Hexylamine with other chemical compounds

• The membrane permeability of octylamine is approximately 15-20 times that of hexylamine [9].
• Photophysical study of the Schiff bases of 5'-deoxypyridoxal and n-hexylamine in cationic micelles [10].
• The method described here fulfils the need for a suitable analytical method to determine the concentrations of single and mixed aliphatic amines in the range from hexylamine (C6) to octadecylamine (C18) in flotation test solutions and in commercial flotation collectors [11].
• The cation-polymer and hydrogen bonding interactions of branched poly(ethylenimine) (BPEI) complexed with LiCF(3)SO(3) were modeled by the solutions of hexylamine and dipropylamine containing dissolved LiCF(3)SO(3) [12].

Gene context of n-Hexylamine

• The chromatographic separation was achieved with an aqueous solution containing hexylamine (pH 3)-acetonitrile as the mobile phase, a Spherisorb C18 column and UV detection at 220 nm [13].

Analytical, diagnostic and therapeutic context of n-Hexylamine

• The critical factor of the HPLC method is the use of a basic amine, like n-hexylamine, as a solvent additive to facilitate the elution of HALS additives [14].
• The immobilization procedure consists of grafting an epoxysilane onto microelectronic grade Si/SiO(2) substrates, and coupling oligonucleotides bearing a hexylamine linker onto the epoxy moiety [15].

References