Álcoois

3-Aminobutan-1-ol is an amine that is synthesized industrially by the reduction of soybean trypsin with borohydride. This chemical has been used as a substrate in asymmetric synthesis and can be detected by high detection sensitivity. 3-Aminobutan-1-ol binds to the carbonyl group of amino acid residues and causes a reaction with chloride ions for detection. The product of this reaction is an enantiomer, which can be separated from other reaction products by purified chiral stationary phases. 3-Aminobutan-1-ol is also involved in the biosynthesis of proteins and enzymes. It reacts with hydrochloric acid to form a salt, which can then be used as an enzyme inhibitor.

Arotinolol hydrochloride is a beta-blocker that, in contrast to propranolol, has a higher selectivity for the β1 receptor. It is used to treat hypertension and angina pectoris. Arotinolol hydrochloride lowers blood pressure by inhibiting the activity of α-adrenergic receptors, which are found in the heart and vascular smooth muscle. This inhibition reduces the release of norepinephrine and causes vasodilation. Arotinolol hydrochloride also has a positive effect on cardiac function as it decreases myocardial oxygen demand and increases coronary flow. Arotinolol hydrochloride has been shown to lower systolic pressure in anesthetized dogs with an intravenous dose of sodium citrate. The drug also lowers diastolic pressure in conscious dogs at doses of 0.5 mg/kg (0.2 mg/lb) or greater when given intravenously or subcutaneously.

5-Methylpyrimidin-2-ol is a photophysical, hydroxy group, and hydroxyl group. It has been shown to have an inhibitory effect on DNA methylation by glycosidic bond with the sugar moiety of the nucleotide. 5-Methylpyrimidin-2-ol reacts with the base moiety of the nucleotide to form an analog that inhibits RNA synthesis and is competitive against pyrimidine nucleosides. 5-Methylpyrimidin-2-ol also has a hydrogen bonding property that can react with other molecules such as proteins or sugars to form hydrogen bonds. This reaction rate is increased by fluorescence resonance energy transfer (FRET).

2,6-dimethoxy-4-methylphenol is a synthetic chemical with potential use as an insecticide. It is a cholinesterase inhibitor that inhibits the action of acetylcholinesterase, an enzyme that breaks down acetylcholine, which is a neurotransmitter important for cognitive function and muscle control. 2,6-dimethoxy-4-methylphenol has been shown to be toxic to insects in a sensitivity test and has also shown some toxicity to rats when administered orally at high doses. This chemical has been shown to inhibit the production of fatty acids in plants and can be used as a potential insecticide for human food crops.

Rac-falcarinol is an organic compound that has the chemical formula CH(OH)CH(COOH)(CH). It is a colorless solid and is soluble in alcohol, acetone, and ether. Rac-falcarinol has been used as a versatile building block to make complex compounds with high purity. It has also been used as a reaction component for research chemicals. The compound can be used for making fine chemicals or speciality chemicals.

4-tert-Butyl-2,6-dinitrophenol is a yellowish solid that is soluble in organic solvents. It is used as an intermediate for the synthesis of dyes, pesticides and pharmaceuticals. 4-tert-Butyl-2,6-dinitrophenol has been shown to cause respiratory tract irritation and narcosis in animals. The toxic effects of 4-tert-Butyl-2,6-dinitrophenol are due to its high electrophilicity and nitro group (NO) which causes oxidative stress. The logistic regression analysis showed that the population growth of ciliates was negatively affected by the presence of halogens in the water.

2,2,2-tribromoethanol or TBE derives from ethanol, where the hydrogen atoms from one carbon are substituted by bromine. 2,2,2-tribromoethanol is frequently used as initiator for synthesising functionalised polymers with end hydroxyl groups. In addition, 2,2,2-tribromoethanol is also often used in a labroatory setting to anaethetise mice.

7-Octyn-1-ol is a synthetic compound that is used for the synthesis of deuterated compounds. It has been shown to have neurotrophic effects and the ability to modulate carbon chains. In addition, 7-octyn-1-ol may be used as an intermediate in the synthesis of nicotine. 7-Octyn-1-ol is also an isomeric form of octyne, which is a natural product found in malonate and fatty acids.

3-(4-Methoxyphenoxy)-1,2-propanediol is a chiral molecule that can be found in various products. It has been used in the synthesis of a variety of drugs and other organic compounds. 3-(4-Methoxyphenoxy)-1,2-propanediol is an intermediate for the synthesis of natural products such as benzofuran and benzothiophene. This compound is also used as a reagent in the asymmetric dihydroxylation of epoxides. The rate at which this reaction proceeds depends on the kinetic parameters, such as the concentration of reactant and transition state analogues, and on the reaction conditions, such as temperature and pH. The product of this reaction is an epoxide hydrolase inhibitor with a reactive anion that can be used to synthesize pharmaceuticals.

6-Amino-2,4-dichlorophenol is an organic solution that has been shown to inhibit the uptake of quinoline derivatives by lung fibroblasts. It also inhibits cellular targets such as flavin, blood pressure and v79 cells. 6-Amino-2,4-dichlorophenol has potent antibacterial activity and a reactive nucleophilic group that can form covalent bonds with proteins in the cell membrane. 6-Amino-2,4-dichlorophenol is a reactive agent that binds to DNA and RNA in the bacterial cell's cytoplasmic membrane and inhibits protein synthesis.

2-Methoxyresorcinol is a metabolite that is formed by the oxidation of resorcinol. It has two methoxy groups, which are functional groups that are usually found in organic compounds. 2-Methoxyresorcinol has been shown to inhibit the growth of tumour cells in vitro and in vivo. It also inhibits cell growth by decreasing protein synthesis and cell division. This compound is an analytical method for measuring hematocrit levels and can be used as a natural compound for the treatment of chronic kidney disease.

2,6-Dinitrobenzene-1,4-dimethanol is a developer that has been shown to have a sensitivity of 0.5 mg/ml and a molecular weight of 235.3 g/mol. It is also an amplified developer that has been shown to reduce the weight of polymers by up to 20%. This molecule can be used for the production of polymers with functional moieties and monomers with chemically reactive groups. 2,6-Dinitrobenzene-1,4-dimethanol is soluble in organic solvents and can be used as a monomer in polymerization reactions.

2-Ethyl-2-adamantanol is a polymerization inhibitor that can be used to prevent the formation of polymers. 2-Ethyl-2-adamantanol inhibits the reaction by reacting with chloride, preventing the formation of a covalent bond. This inhibition is reversible and does not affect other reactions. The use of 2-ethyl-2-adamantanol as an inhibitor has been shown to increase the reaction yield when using bromoethane as a feedstock. It also increases the selectivity for ethyl groups in this process, making it an excellent choice for synthesizing lanthanides.

9'-cis-Neoxanthin is a carotenoid that belongs to the class of xanthophylls. It is found in high concentrations in the seeds of peas, spinach, and corn. 9'-cis-Neoxanthin has been shown to inhibit prostate cancer cells by targeting their transcriptional regulation. 9'-cis-Neoxanthin is a precursor for violaxanthin, which is a powerful antioxidant that can scavenge free radicals. This molecule also binds to DNA polymerase and inhibits its activity. The structural analysis of 9'-cis-Neoxanthin has revealed that it contains two chromophores: one with an oxygenated end (the neoxanthin side chain) and one with an unsaturated end (the other side chain).

6-Bromo-4-chloroquinoline is a chemical compound with the molecular formula C8H6BrClN. It belongs to the class of heterocyclic compounds and has been used in the synthesis of other compounds, such as pharmaceuticals. 6-Bromo-4-chloroquinoline has been shown to be an effective anticancer drug, with measurable levels in the blood after oral administration. This drug interacts with hydrogen bonding interactions with thp-1 cells, which are erythrocytes derived from human peripheral blood lymphocytes. 6-Bromo-4-chloroquinoline also interacts with sodium sulfide, which is found in human liver and kidney cells. The pharmacokinetic properties of 6-bromo-4-chloroquine have been studied in rats and mice.

1-Chloro-3-[4-(2-methoxyethyl)phenoxy]-2-propanol is a potent antihypertensive agent that is synthesized by the chemoenzymatic process. It differs from other antihypertensive drugs in that it incorporates an oxirane group, which makes it more hydrophobic than other drugs. 1-Chloro-3-[4-(2-methoxyethyl)phenoxy]-2-propanol is a crystalline solid with a melting point of 128°C and a density of 1.0 g/mL. The chemical name for this drug is 4-[(1E)-1-(chloromethoxy)propyl]phenol, which has potent antihypertensive activity and high enantioselectivity.

Inhibitor of tyrosinase; skin whitener

3-(Dimethylamino)phenol is a chemical that is used as an additive in cosmetics. It has been shown to inhibit the production of epidermal growth factor and to have a growth-inhibiting effect on cells. 3-(Dimethylamino)phenol is found in many different types of products, including sunscreens, hair dyes, shampoos, and skin lotions. It has also been used as a preservative in food products, although it can be toxic at high doses. 3- (Dimethylamino)phenol has been shown to inhibit the production of fatty acids by inhibiting the activity of the enzyme lipoxygenase.