Álcoois

Please enquire for more information about 2-(2,4-Difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)-3-(4H-1,2,4-triazol-4-yl)propan-2-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page

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

4-Fluoro-3-nitrobenzyl alcohol (4FNA) is a potent, orally bioavailable, and selective inhibitor of the tyrosine kinase AXL. 4FNA binds to the ATP binding site on AXL and blocks phosphorylation of its tyrosine kinase domain. This binding leads to a conformational change in the AXL protein that prevents it from interacting with downstream signaling molecules, inhibiting T cell activation.

2,4-Dibromobenzyl alcohol is a selective inhibitor of sglt2, which is an enzyme that inactivates the incretin hormones glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP). It has been shown to have a strong inhibitory effect on the activity of sglt2 in vitro. This inhibition leads to increased levels of GLP-1 and GIP, which may help improve glycemic control. 2,4-Dibromobenzyl alcohol has been shown to reduce blood glucose levels in diabetic mice to the same degree as tofogliflozin, which is marketed for diabetes treatment.

Please enquire for more information about Z-D-Alaninol including the price, delivery time and more detailed product information at the technical inquiry form on this page

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.

Glycerol tristearate is a triglyceride, which is derived from the esterification of glycerol with stearic acid, a saturated fatty acid. This compound is typically sourced from natural fats and oils through a process involving the hydrogenation of vegetable oils, which facilitates its pure and controlled production.The mode of action of glycerol tristearate involves its function as an effective emulsifier. It stabilizes mixtures of water and oil by reducing interfacial tension, thus enabling the formation of stable emulsions. Its solid form at room temperature also contributes to its ability to enhance texture and stability in various formulations.Glycerol tristearate is widely used in diverse applications including the food industry, where it acts as a texturizer and stabilizer in products like margarine, chocolate, and confectionery. Additionally, it plays a significant role in the cosmetics and personal care sectors, where it improves the texture and stability of creams and lotions. Its properties make it a valuable ingredient for controlling crystallization and improving consistency across multiple industry settings.

Please enquire for more information about 9,11b-Epoxidetriamcinolone including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Bromobenzene-1,2-diol is a reactive substance that has been shown to have receptor binding and reaction intermediates. It has been shown to inhibit the formation of reactive oxygen species in rat liver microsomes. The formation rate of 4-bromobenzene-1,2-diol is increased by carbon source such as bromobenzene. This substance has also been shown to be an inhibitor of the reaction mechanism. 4-Bromobenzene-1,2-diol is used as a reactant in organic synthesis reactions and can be found in dry weight measurements.

Please enquire for more information about 1-Oleoyl-3-palmitoyl-rac-glycero-2-phosphoethanolamine including the price, delivery time and more detailed product information at the technical inquiry form on this page

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

Schisanhenol is a natural drug that belongs to the class of fructus. It has been shown to have cytosolic calcium-lowering effects in vitro. Schisanhenol has been shown to inhibit polymerase chain reaction (PCR) and reverse transcriptase activity, which may be due to its ability to inhibit oxidative injury, such as free radicals. This drug also inhibits sulfa drugs and integrin receptors, which may be due to its antioxidant properties. Schisanhenol has been shown to inhibit the growth of cancer cells in vitro and has been used as an adjuvant treatment for adriamycin.

(S)-(-)-3-Chloro-1-phenyl-1-propanol is an efficient method for the synthesis of chiral propiophenone. It is synthesized by reacting a mixture of borane and tetrahydrofuran with (S)-(-)-3-chloro-1-phenylpropanol. This reaction produces the desired compound in good yield and high diastereoselectivity. The synthesis of this compound has been shown to be useful for the production of antidepressant drugs, such as κ-opioid receptor ligands, which are used to treat depression, anxiety, and chronic pain.

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.

Rac-1-anthracen-2-yl-ethanol is an apolar, injecting alcohol. It has two isomers. Rac-1-anthracen-2-yl-ethanol has a selectivity profile that is different from other compounds in its class, and it outperforms amine solvents in the separation of similar compounds. This compound's selectivity profile is due to interactions with the solvent and stationary phase that are unique to this compound. Rac-1-anthracen-2-yl-ethanol also has a low nature and low toxicity profile.

2-Aminoresorcinol is a synthetic chemical compound that inhibits the reaction of amines with chlorine atoms. It is used as an intermediate in the production of resorcinol and 2-aminophenol. The reaction mechanism involves the formation of a chloramine (chlorine atom attached to an amine) which, in turn, reacts with malonic acid to produce an intermediate that undergoes intramolecular hydrogen transfer. This reaction results in the formation of a chloroform molecule. A second step involves hydroxylation by hydrochloric acid, which leads to the formation of chloral hydrate. In this way, 2-aminoresorcinol can be used for the synthesis of both resorcinol and 2-aminophenol. 2-Aminoresorcinol is also known for its inhibitory effects on certain reactions involving amines and sulfur compounds such as thiourea and carbonyl compounds such as malonic acid.

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.

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.

5-Glutinen-3-ol is an antiinflammatory compound that belongs to the group of bioactive phenolic compounds. It has significant cytotoxicity and can be used in cancer therapy. 5-Glutinen-3-ol has been shown to inhibit the proliferation of cervical cancer cells by inducing apoptosis through a mechanism involving the activation of gamma-aminobutyric acid (GABA) receptors. This compound also inhibits oxidative stress induced by reactive oxygen species and protects cells from DNA damage, which may protect against cancer. 5-Glutinen-3-ol also has antioxidant properties, which can help prevent or alleviate metabolic disorders such as diabetes mellitus and atherosclerosis.

Please enquire for more information about 2,6-Difluoro-4-methoxyphenol including the price, delivery time and more detailed product information at the technical inquiry form on this page

Codlemone is a pheromone that is secreted by the female codling moth (Cydia pomonella) to attract males for mating. This compound has been shown to have pesticidal activity against various insect species, including codling moths, fruit flies, and aphids. Codlemone is an odorant that binds to olfactory receptors in insects and mammals. It has been shown to bind to the OR1 receptor in mammalian cells and may be involved in physiological functions such as reproduction, stress response, and sexual behavior. The biosynthesis of codlemone starts with the conversion of fatty acid into fatty acid esters by means of transfer reactions with alcohols or alkyl halides. These esters are then converted into dienols by the action of aldehyde oxidase. The dienols are then converted into the final product by means of a palladium-catalyzed coupling reaction with acetaldehyde.

Triglycerol monolaurate (GLA) is a fatty acid that can be synthesized by reacting glycerol with lauric acid. It has been shown to have antimicrobial properties, inhibiting the growth of fungi such as flavus and staphylococcus. GLA also inhibits the production of lipase and protease, enzymes that are required for the digestion of dietary fats. GLA has been used in infant formulas to inhibit the growth of bacteria, such as p. aeruginosa, which may cause infantile diarrhea. Triglycerol monolaurate is also used as dietary supplement to treat eczema due to its inhibitory effect on inflammatory cytokines such as tumor necrosis factor-α (TNF-α).

Pregnenolone is a steroid hormone that is synthesized from cholesterol and secreted into the blood. It can be converted to other steroids such as progesterone, testosterone, and estradiol. Pregnenolone sulfate (PS) is a metabolite of pregnenolone that is produced by the enzyme steroid sulfatase. PS is an endogenous steroid hormone that has been shown to have potentiating effects on memory. This drug also inhibits the activity of sulfatase enzymes, which are responsible for breaking down steroids in the body.

7-Fluoro-2-methylquinoline is a multistep synthetic compound that belongs to the family of quinoxalines. It has been shown to have potent antibacterial activity against a wide range of bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and Mycobacterium tuberculosis. 7-Fluoro-2-methylquinoline was developed as an analog of the natural product quinoxaline. The key step in its synthesis is the reaction between an aldehyde and hydroxyalkylating reagent in the presence of iron catalyst. This process results in the formation of functional groups such as hydroxyls, alkoxy, or halogens.

Please enquire for more information about (4S)-3,4-Dihydro-2-(3-methoxypropyl)-2H-thieno[3,2-e]-1,2-thiazin-4-ol 1,1-dioxide including the price, delivery time and more detailed product information at the technical inquiry form on this page