Alcools

Trichloroethanol is an alkanoic acid that is used as a solvent and a laboratory reagent. It is also a potential bioactive compound. Trichloroethanol has been shown to have neurotoxic effects in rats, causing histological changes in the trigeminal nerve, which may be due to its inhibition of mitochondrial energy metabolism. Trichloroethanol has been shown to inhibit the activity of matrix metalloproteinase-9 (MMP-9) in human serum and the α1 subunit of Toll-like receptor (TLR) 4 in human monocytes. This compound has also been shown to be toxic to rat liver microsomes at high concentrations.

(-)-Corey lactone diol is a synthetic compound that is soluble in organic solvents. It is used for the synthesis of carbocyclic nucleosides, which are analogs of pyrimidine nucleosides. (-)-Corey lactone diol has been shown to inhibit cholesterol synthesis and the synthesis of alkene. (-)-Corey lactone diol also shows anti-inflammatory properties, which may be due to its inhibition of prostaglandin synthesis.

Quinoline-4-carboxylic acid is a natural compound that is derived from the amino acid tryptophan. It has been shown to have antiinflammatory activity and to be an inhibitor of prostaglandin synthesis. Quinoline-4-carboxylic acid inhibits the growth of carcinoma cells in culture by inducing apoptosis, which is mediated by inhibition of protein synthesis. Quinoline-4-carboxylic acid also has pharmacokinetic properties, including a low volume of distribution, low clearance rate and high bioavailability.

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2-Dimethylaminoethanol (+)-bitartrate salt is a potent, reversible inhibitor of protein synthesis that binds reversibly to the 50S ribosomal subunit. It is used in regulatory toxicology and clinical pathology as a positive control for the study of chronic toxicity and long-term effects. 2-Dimethylaminoethanol (+)-bitartrate salt has shown no treatment effect on ovary weight or estrous cycle length in female Sprague-Dawley rats after chronic exposure and long-term exposure at doses up to 1,000 mg/kg/day. This drug has also shown no effect on rat fertility or reproductive performance, indicating it does not cause reproductive toxicity.

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6,7-Dihydro-5H-quinolin-8-one is a quinoline derivative that can be used to treat cancer. It is an inhibitor of topoisomerase II, which is an enzyme that catalyzes the formation of single stranded breaks in DNA and then reseals them. The inhibition of topoisomerase II leads to the accumulation of single strand breaks, which causes cell death. 6,7-Dihydro-5H-quinolin-8-one has been shown to have inhibitory activity against cancer cells in laboratory tests and also inhibits the growth of breast cancer cells in mice. This compound also has a number of other biological effects including being a ligand for some receptors and amine oxidases as well as having antihistamine properties.

Product FB158451, cis, trans-2-Buten-1,4-diol, is a versatile chemical compound with the CAS number 110-64-5. It is used a key building block in various chemical synthesis processes, making it an essential component for researchers and industrial applications. Its versatile nature allows it to be employed in the production of polymers, resins, and specialty chemicals, making it a valuable asset for a wide range of applications.

Calcipotriol is a synthetic vitamin D3 analog that has been shown to be effective in the treatment of bone cancer. It has a film-forming property and is used in pharmaceutical preparations as well as for wastewater treatment. Calcipotriol monohydrate is made by reacting calcipotriol with hydrochloric acid, which produces an ester bond between the hydroxyl group and the carboxylic acid group. The reaction also produces water, methanol, and methyl ethyl ether. Studies have shown that calcipotriol monohydrate has a chemical stability of over 30 days at room temperature, indicating it can be stored for long periods without degradation.

2,2,4-Trimethyl-1,2-dihydroquinoline is a chemical compound with the formula C8H10N2. It is a white solid that is insoluble in water but soluble in nonpolar solvents such as benzene, toluene and hexane. 2,2,4-Trimethyl-1,2-dihydroquinoline has been shown to induce liver lesions in rats at doses of 1.25 g/kg/day. It also reacts with hydrogen fluoride to form calcium stearate. This compound is also used as a precursor for the synthesis of diazonium salts and has been shown to be carcinogenic in animal studies.

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2-(5-Bromo-2-pyridylazo)-5-(diethylamino)phenol is a chemical that is used for the detection of hydrochloric acid in water vapor. It reacts with zirconium oxide, which generates a red fluorescing complex. The reaction can be detected by using a fluorescence spectrometer with a test sample. 2-(5-Bromo-2-pyridylazo)-5-(diethylamino)phenol is also used to detect the presence of nitrogen atoms and sodium citrate in samples by reacting with them. This chemical reacts with an acid complex to form stable complexes. The analytical method is based on measuring the redox potential of this reaction. The flow system of this technique allows for dehydration of dehydroascorbic acid (DHA).

3,3-Dimethyl-1,2-butanediol is a dioxolane with a constant boiling point of 110°C. This compound is synthesized from the reaction between acetone and formaldehyde, which produces a dioxolane ring. The reaction products can be profiled using gas chromatography to determine the ratio of each product. 3,3-Dimethyl-1,2-butanediol has been shown to have enantiomeric purity of greater than 99%. It has also been used as a chiral building block for the synthesis of carbohydrates with stereospecificity. 3,3-Dimethyl-1,2-butanediol's enzyme catalysis is used in the production of polyesters and polyurethanes.

Phenyl ethyl alcohol is a chemical compound that is used as an antiseptic. It is also known for its ability to reduce the surface tension of water, which makes it useful for cleaning and degreasing. Phenyl ethyl alcohol has been shown to be up-regulated in genes that are responsible for transcriptional regulation, as well as in genes that encode proteins involved in cellular metabolism. This compound has been used as a model system to study hydrogen bonds and biological samples. The structural biology of phenyl ethyl alcohol has been studied using detergent compositions and fatty acid models.

2-[2-[2-(2-Azidoethoxy)ethoxy]ethoxy]ethanol is a PEG polymer categorised as monofunctional (OH-PEG-X). Used as a linker, 2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethanol is used to attached PEG to proteins, peptides, oligonucleotides, nanoparticles and small molecules via pegylation, a bioconjugation technique.

3,4-Diethoxybenzylalcohol is a metabolite produced by the fungus Ustilago maydis. It has been shown to have pleiotropic effects on the metabolism of the organism. 3,4-Diethoxybenzylalcohol is involved in lignin biosynthesis and bond cleavage reactions. In addition to functioning as an intermediate in the pentose phosphate pathway, it is involved in the nature of the basidiomycete cell wall and also plays a role in carbon source utilization.

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