Alcools

<p>3-Bromo-4-fluorophenol is a synthetic, water soluble, and stable compound with a variety of applications. It yields white crystals that are soluble in water, acetone, ethanol, ether, benzene, chloroform, and carbon tetrachloride. 3-Bromo-4-fluorophenol has been shown to have a number of structural modifications that may be advantageous for therapeutic purposes. The most prominent modification is the methylation of the phenolic hydroxyl group (functionalisation). This modification prevents the drug from reacting with nucleophilic sites on proteins and other biological molecules. 3-Bromo-4-fluorophenol interacts with methyltransferase enzymes in cancer cells to inhibit their activity. These methyltransferase enzymes are involved in cellular proliferation and proliferation signalling pathways that may lead to cancer cell death.</p>

Please enquire for more information about (1S, 2R)-1-Phenyl-2-(1-pyrrolidinyl)-1-propanol including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>2,4-Dimethoxyphenylmethylcarbinol is a benzene derivative that can be synthesized from 2,4-dimethoxybenzaldehyde and formaldehyde. This compound is an efficient reductant for hydrazine and has been used as a screening agent for new drugs. It is also a pharmacological active substance with anti-inflammatory properties. 2,4-Dimethoxyphenylmethylcarbinol has shown activity against carrageenan-induced rat paw edema, as well as the vessel and ultrasonic effects of irradiation.</p>

Methyl gamma-linolenate is a fatty acid that is derived from linoleic acid. It has shown to have anti-inflammatory effects and inhibit the growth of prostate cancer cells in vitro. Methyl gamma-linolenate also inhibits caspase-9, an enzyme that plays a key role in the apoptosis pathway. Methyl gamma-linolenate has been shown to regulate the production of amp-activated protein kinase (AMPK), which is a cellular regulator that controls glucose and lipid metabolism, insulin signaling, and inflammation. This activity may be due to its ability to bind to the regulatory domain of AMPK.

<p>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).</p>

<p>Please enquire for more information about tert-Butyl 7-bromo-3,4-dihydroisoquinoline-2(1H)-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (3,5-Diiodo-Tyr1,D-Ala2,N-Me-Phe4,glycinol5)-Enkephalin acetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Androstanolone acetate is a synthetic androgen that has been shown to stimulate the production of testosterone in the testes. Androstanolone acetate has been shown to be effective in treating symptoms of male hypogonadism, as well as erectile dysfunction. The drug also has an antigenic effect, which stimulates the production of antibodies against it. Androstanolone acetate binds to cell specific antigens and stimulates cell proliferation. It has been used in cancer prevention studies, where it was found that it could suppress estrogen-induced endometrial cancer in animals. In addition, Androstanolone acetate is capable of stimulating light emission when incubated with cells and can be detected using chromatographic methods.</p>

<p>3-Methyl-2-nitro-3H-imidazol-4-yl)methanol is a fluorescent probe that can be used to detect hypoxic tumor cells. It has been shown to selectively react with the methylethyl group in Trichomonas vaginalis. 3-Methyl-2-nitro-3H-imidazol-4-yl)methanol is bioreductive and can be activated by nitro groups in proteins, which are found in the active site of enzymes such as bacterial dna gyrase. This probe has been shown to bind to the sn38 position of bacterial DNA, but not mammalian DNA.</p>

<p>5-Bromo-2-fluorophenol is an organic solvent that is used in hydrotalcite to extract biphenyl. 5-Bromo-2-fluorophenol has been shown to have a high affinity for the cavity of hydrotalcite, which is a desorption technique. It can also be used to extract supramolecular systems and biomolecules, such as proteins and nucleic acids. The nature of 5-bromo-2-fluorophenol is an aromatic compound with a density of 1.40 g/mL at 20°C and a boiling point of 221°C. 5-Bromo-2-fluorophenol can be eluted using isopropyl alcohol or ethyl acetate, and the transfer rate depends on the nature of the solvent used in elution.</p>

<p>6-Bromoisoquinoline is a tetradentate ligand that can be used as a molecular model to study the binding of metal ions and organic molecules. 6-Bromoisoquinoline has been shown to bind covalently and noncovalently with phosphate groups on the surface of Caco-2 cells and to induce surface-enhanced Raman spectroscopy. This ligand has a high nucleophilicity and reacts readily with chloride, which is an acidic functional group. The reaction products are hydrochloric acid, trifluoroacetic acid, or both. 6-Bromoisoquinoline can also act as an allosteric modulator in some enzymes, such as phosphofructokinase in glycolysis.</p>

<p>Please enquire for more information about 4-Chlorophenyl-2-pyridinylmethanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

4-Aminophenethyl alcohol is a monosubstituted, basic compound that is used in the laboratory as a cell culture medium supplement to promote growth of fibroblasts. This compound has been shown to stimulate human intestinal cells and human peripheral blood mononuclear cells. 4-Aminophenethyl alcohol acts as a hydroxyl group donor, which may be due to its ability to form hydrogen ions when reacted with sodium hydroxide solution. The reaction of this compound with diazonium salt produces an intermediate, which can be hydrolyzed by the addition of sodium hydroxide solution. The resultant chloride ion reacts with the aminophenethyldihydroxylamine (APDA) moiety to produce APDCl. This product has been shown to increase the population growth rate of fibroblasts in culture by causing DNA synthesis and protein synthesis. Linear regression analysis revealed that there was no statistically significant difference between the control and experimental groups for either DNA

<p>(R)-(+)-3-Chloro-1-phenyl-1-propanol is a substrate for the lactamase of bacteria. The immobilized lipase catalyzes the hydrolysis reaction in which the lactam ring is broken, yielding a propiophenone intermediate. This intermediate can be converted to (S)-(+)-3-chloro-1-phenylpropanol by treatment with an alcohol oxidase or by hydrolysis with hydrogen peroxide. The product has been shown to have antidepressant activity and may modulate the dry weight of bacteria. In vivo studies show that this compound has a high concentration in rats and mice, but it is not active in humans.</p>

<p>Please enquire for more information about ([ring-D5]Phe3)-Octreotide acetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>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.</p>

<p>Please enquire for more information about 5-Amino-2-tert-butoxycarbonyl-1,2,3,4-tetrahydroisoquinoline including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(S)-3,3'-Dibromo-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthalene-2,2'-diol is a synthetic compound that has been prepared by a Diels-Alder reaction. It is used as an asymmetric synthesis catalyst for the production of optically active compounds. The ligands are catalysts for the reaction and can be easily replaced with different ligands to produce different products. This compound has been researched for its potential use in the production of pharmaceuticals and other chemicals.</p>

<p>2,9-Bis(2-phenylethyl)anthraquinone (BPAQ) is a synthetic compound that is used as an fluorescent probe to study biological processes. BPAQ binds to peptides and inhibits their binding to the surface of cells. This property has been used in diagnostic tests for stenosis, infantum, and other conditions. BPAQ has also been shown to inhibit HIV-1 replication in human cells by binding to the HIV-1 envelope protein gp120 and blocking its interaction with CD4 receptors on host cells. The discovery of the antiviral activity of BPAQ was based on its ability to inhibit leishmania growth in animals.</p>

<p>4-Fluoromethyl-alpha-methylbenzyl alcohol is a nonclassical molecule that has been synthesized. This molecule has been modeled computationally and the results indicate that it exhibits a planar geometry with a diastereomeric ratio of 1:1. The theoretical calculations show that the reaction of 4-fluoromethyl-alpha-methylbenzyl alcohol with water is exothermic, which would result in the formation of an intermediate hydroxide ion. Kinetic studies have shown that this molecule can undergo transfer reactions and dehydrogenation reactions, both of which are possible mechanisms for its reactivity.</p>