8-hydroxyquinoline (8-HQ) is a bicyclic compound derived from quinoline (1-azanaphthalene) and consist of two rings system: carbocyclic ring and pyridine ring with hydroxyl group substituted at position-8. 8-HQ is one of the most popular and versatile organic compound is an organic crystalline material. 8-HQ has typical phenolic properties, e.g. it gives violet colour with ferric chloride, couple with diazonium cations, and participate in Reimer-Tiemann and Bucherer reactions; its acetate ester usually undergoes the Fries rearrangement with aluminium chloride to give acetyl derivative [1]. As a result of the proximity of the hydroxyl group to the heterocyclic nitrogen, 8-HQ forms insoluble chelate complexes with a great variety of metal ions, including Cu2+, Bi2+, Mn2+, Mg2+, Fe3+, Al3+, Zn2+and Ni3+ [3]. The hydrogen of the hydroxyl group in 8-HQ is displaced and the metal is linked to both the oxygen and nitrogen.
The Effect of Different Concentrations of the Enzyme Catechol Oxidase on the Rate of Benzoquinone Production When Mixed with Pure Catechol
As you can see in the attached diagram, the Beetle has two glands which produce a chemical that, when mixed with Hydrogen peroxide, explodes as a boiling hot gas. The H2O2 is stored in little sacks. The mixture runs into a chamber at the back of the abdomen so it explodes outward.
Most people in the Africa population (about 20%) are born with a glucose-6-phosphate dehydrogenase deficiency (G6PD deficiency) (Campbell and Tishkoff, 2008). Primaquine is dangerous in patient with G6PD deficiency and it is known to cause haemolysis in people with inborn G6PD deficiency (Bradford, 2002). Therefore, the use of primaquine with artemether results in severity of adverse effects such as anaemia, haemolysis and GIT disturbances. However, this is a dose independent physiological effect, not all doses of primaquine results in such adverse effects.
Hydrindantin reacts with Ninhydrin and ammonia in a condensation reaction to form a purple pigment.
Quinolines are remarkable scaffold found in several biological and pharmaceutical agents.1 Many tetrahydroquinoline moieties are known to be an interesting therapeutic agents.2 For example, the tetrahydroquinoline-based natural product (Fig.1) isolated from Galipea officinalis have been reported as potent antimalarial
Polyhydroxyalkanoate(s) (PHA) are a group of natural biopolymers which are synthesised by a wide variety of microbial genera. They are biodegradable and biocompatible thermoplastics consisting of a repeated chain of various hydroxyalkanoate(s) (HA) monomers. PHA are intracellular carbon/energy storage compounds produced under stress conditions caused by nutrient limitation. Under restricted microbial growth conditions, excessive carbon sources are converted to PHA, which exist as discrete inclusion bodies (granules). The granules are typically 0.2 to 0.9 μm in diameter and are localised in a mobile amorphous state within the cell cytoplasm. As these granules are highly refractive they are clearly visualised under a phase contrast microscope
Gold M et al. Open-label treatment of moderate or marked melasma with a 4% hydroquinone skin care system plus 0.05% tretinoin cream. J Clin Aesthet Dermatol. 2013 Nov;6(11):32-8.
Pamaquine (Figure 2.5b) is an 8-aminoquinoline, synthesized based on the structure of methylene blue (Figure 2.5a). It is the first antimalarial drug that has activity against liver stage parasites, and can prevent the relapse of P. vivax malaria. Although pamaquine can delay the first attachment of malaria, it is an incomplete protection. So at that time, pamaquine was usually combined with quinine to treat malaria. However, pamaquine was reported with severe toxicological concerns, relating with glucose 6-phosphate dehydrogenase (G6PD) deficiency, and it is not as efficient as primaquine. Because of these problems, pamaquine is no longer used.
Two famous methodologies, the chemical or electrochemical oxidation of phenylenediamines yields the analogous poly(phenylenediamines) and their potential application for the removal of lead ions from water [1, 3, 11].
A highly chemo-selective and efficient method for the oxidation of sulfides to the corresponding sulfoxide in the absence of any solvent and thiols to their corresponding disulfides in ethanol with aqueous hydrogen peroxide as oxidant and the synthesis of 2,3-dihydroquinazolin-4(1H)-one derivatives in water at room temperature using heterogeneous ZnO (acac)2 catalyst grafted on mesoporous silica MCM-41 has been developed. The simplicity in operation, general applicability, Short reaction times, easy purification, high yields, mild conditions, and recyclability make this procedure more
Methotrexate is a phase-specific substance the main action of which is directed to the S-phase of cell mitosis. It acts generally most effectively on actively increasing tissues, such as malignant cells, bone marrow, foetal cells, oral and intestinal mucosa as well as urinary bladder cells. As the production of malignant cells is higher than that of most normal cells, methotrexate can slow down the production of malignant cells without causing, however, irreversible damage to normal tissue.
Docosahexaenoic acid (DHA) is an omega-3 fatty acid that is a primary structural component of the human brain, cerebral cortex, skin, sperm, testicles and retina. It can be synthesized from alpha-linolenic acid or obtained directly from maternal milk or fish oil.
As mention earlier, lignin composes of phenolic groups in structure. An electrochemistry of lignin based on electroactive quinone-hydroquinone couples which can be generated by demethylation of aromatic methoxy groups (Scheme 2-1). Quinone-hydroquinone couples are an example of organic redox systems occurring phenolic-type compounds in nature (e.g., humic acids, flavonoids, tannic acid, and dopamine).
The anodic oxidation of a catechol generates a reactive o-benzoquinone that can be used to trigger a number of interesting reactions [1-5] and play an important role in the redox electron transport chains of living systems [6-8] for example, vitamine K is known to play an important role in blood coagulation mechanism and also in photosynthesis, vitamine E is important factor in electron transport and oxidative phosphorylation. More complex quinonoic
Three new hydrazone ligands, H2L1, H2L2 and H4L3, were prepared by condensation of 4,6-bis(1-hydrazonoethyl)benzene-1,3-diol with furan-2-carboxaldehyde, thiophene-2-carboxaldehyde and 1H-pyrrole-2-carboxaldehyde, respectively. The ligands reacted with copper(II), nickel(II), cobalt(II), zinc(II), cadmium(II) and dioxouranium(VI) ions, to yield binuclear complexes formulated as [(L)M2(OAc)2(H2O)n(EtOH)m]•xH2O•yEtOH where L = L1 or L2; M = Cu, Ni, Co, Zn or Cd; n = nil, 1 or 4; m, x and y = nil or 1, [(H2L2)Cd2(OAc)4(H2O)2]•EtOH, [(L)(UO2)2(OAc)2(H2O)2Y2]•nH2O where L = L1 or L2; Y = nil or H2O; n = 2.5 or 7, [(L3)M2(H2O)6]•nH2O where M = Cu or Zn; n = 1 or 6, [(L3)(UO2)2(H2O)4]•2.5H2O and dimeric complexes; [(L1)2Ni2]•3H2O and [(H2L3)2M2]•nH2O where M = Ni or Co; n = 1.5 or 3. The ligands and their metal complexes were characterized by elemental analyses, IR, 1H and 13C NMR, electronic, ESR and mass spectra, conductivity, magnetic susceptibility measurements and powder XRD as well as thermal analyses. The coordinating sites are phenolic oxygens, azomethine nitrogens and the hetero O/N/S atoms. Octahedral, tetrahedral and