Results 71 to 80 of about 959 (115)

Potential Azo-8-hydroxyquinoline derivatives as multi-target lead candidates for Alzheimer's disease: An in-depth in silico study of monoamine oxidase and cholinesterase inhibitors. [PDF]

PLoS One
Guerguer FZ, Rossafi B, Abchir O, Raouf YS, Albalushi DB, Samadi A, Chtita S.   +6 more
europepmc   +1 more source

[Oxyquinolines once more. A danish viewpoint].

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 1971
openaire   +1 more source

Extraction of wood vinegar from bagasse and its application as bio-reducer to produce stable silver nanoparticles with enhanced antibacterial activity. [PDF]

Heliyon
Rabbi MA, Akter R, Khatun MH, Ahmed F, Kadri HJ, Maitra B, Uddin Rasel MZ, Al-Amin M, Kabir SR, Habib MR.   +9 more
europepmc   +1 more source

Targeting amino acid metabolic pathways: a novel therapeutic strategy for hyperuricemia-associated complications. [PDF]

Amino Acids
Zhang X, Wang W, Yang L, Sun Y, Sun H, Zhao X, Sun H, Yan G, Wang X.   +8 more
europepmc   +1 more source

[Biological activity of tissues treated with ortho-oxyquinoline].

Vestnik dermatologii i venerologii, 1975
Iu F, Nikiforov, I M, Akim
openaire   +1 more source

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Oxidative polycondensation of 8-oxyquinoline alcoholate

Polymer, 1989
Abstract Oxidative polycondensation of 8-oxyquinoline alcoholate by molecular oxygen has been accomplished at 323–371 K. Product compositions, structures and molecular weights were determined by elemental and chemical analyses, by gel permeation chromatography, and infra-red and ultra-violet spectroscopy.
A.V. Ragimov, B.A. Mamedov, Sh.I. Mustafaeva   +2 more
openaire   +1 more source

Final Report on the Safety Assessment of Oxyquinoline and Oxyquinoline Sulfate

Journal of the American College of Toxicology, 1992
Oxyquinoline is a heterocyclic phenol which is used as a fungicide and bactericide in cosmetic formulations at concentrations at, or less than 1.0%. Oxyquinoline is metabolized and excreted in the urine as glucuronides. The acute oral LD50 toxicity in rats was 1.2 g/kg. In subchronic studies, no deaths occurred in male and female rats at 5 doses up to
openaire   +1 more source

The determination of uranium with o‐oxyquinoline

Recueil des Travaux Chimiques des Pays-Bas, 1946
AbstractHecht and Reich‐Rohrwig's method for the determination of uranium by means of o‐oxyquinoline was subjected to a critical investigation. It was found that washing the precipitate with hot water, as prescribed in the original procedure, leads to heavy losses, which can be prevented by washing with a hot 0.04% oxine solution.
A. Claassen, J. Visser
openaire   +1 more source

Permanent Mounts Of Chromosomes After 8-Oxyquinoline and Squashing

Stain Technology, 1952
Fresh young root tips or free-hand cross sections thereof were placed in 0.002 M 8-oxyquinoline (aq.) at 10-14oC. for 3 hours. After rinsing in water 1-2 minutes, they were soaked in N HC1 at 55oC. for 25 minutes, rinsed again and squashed under a cover glass on a dry slide.
A K, SHARMA, D, BHATTACHARJEE
openaire   +2 more sources