Ketones

<p>1,2,3,4,5,6-Hexahydro-1,5-methano-pyrido-[1,2-a][1,5]diazocin-8-one is a cholinergic drug that is used as a research tool in vitro. It has been shown to increase the concentration of acetylcholine in the synapse. It is also known as cytisine and varenicline. 1,2,3,4,5,6-Hexahydro-1,5-methano-pyrido-[1,2-a][1,5]diazocin-8-one binds to nicotinic receptors and stimulates them. This increased activity of nicotinic receptors leads to the release of acetylcholine (ACh), which is an important neurotransmitter in the brain. 1,2,3,4 5 6 hexahydro - 1 5</p>

<p>4-Pregnen-17a,20b-diol-3-one is a synthetic androgen with anabolic and androgenic activity. It has been shown in animal studies to increase maximal responses of the reproductive tract to gonadotropin stimulation. 4-Pregnen-17a,20b-diol-3-one binds to the activin receptor on the cell membrane, which leads to increased expression of a gene encoding for 3β-hydroxysteroid dehydrogenase (3βHSD), an enzyme involved in testosterone synthesis. This drug also increases the sensitivity of ovarian follicles to gonadotropins and decreases basal plasma levels of LH and FSH. 4-Pregnen-17a,20b-diol-3-one has not been found to be toxicologically significant at doses up to 10 mg/kg body weight per day.</p>

<p>1-Pentyl-1H-indole-2,3-dione is a synthetic cannabinoid that is used as a recreational drug. It has been shown to be thermally labile and can decompose at high temperatures. 1-Pentyl-1H-indole-2,3-dione is an acidic compound with a melting point of 79°C. The compound is also oxidant and therefore can react with other compounds to create new substances. This reaction can be accelerated by light or heat, which may result in the formation of hazardous products such as naphthalene.</p>

<p>5-Chloro-2-pentanone is a reactive, unsaturated ketone. It is a colorless liquid with a pungent odor. 5-Chloro-2-pentanone can be used in the synthesis of other organic compounds, such as covid-19 pandemic. The reaction of carbonyl groups with hydrogen chloride and chlorine atom to form hydrochloric acid and chlorocarbons is an example of a reaction that 5-chloro-2-pentanone can take part in. When 5-chloro-2-pentanone reacts with hydrogen chloride (HCl) and chlorine atom (Cl), the reaction products are hydrochloric acid (HCl) and chlorocarbons. This process is called nucleophilic attack and proceeds as follows: 5CH=C(CH)COH + HCl + Cl → CH=C(CH)COCl + H+ + Cl 5CH=C</p>

<p>Please enquire for more information about 6-(2,3,4-Trimethoxyphenyl)-1,5,6,7-tetrahydro-4H-indazol-4-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Clobetasol propionate is an organic acid with a chemical structure that is stable in pharmaceutical preparations. It is used to treat inflammatory skin disorders such as psoriasis and atopic dermatitis. Clobetasol propionate is an impurity of clobetasol, which has been shown to be chemically stable in preparations. The clobetasol propionate compound has been found to be more potent than other topical corticosteroids for the treatment of plaque psoriasis and atopic dermatitis.</p>

<p>Please enquire for more information about 1-(Piperidine-4-carbonyl)piperidin-4-one hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>21-Chloro-9-fluoro-11beta,17-dihydroxy-16alpha-methylpregna-1,4-diene-3,20-dione 17-propionate is an ester of ketoconazole and the propionic acid. It is used as a pharmaceutical formulation and has been shown to be stable in an HPLC method. This compound also has an optical isomer that was validated by a stability test. This product has been shown to have antiinflammatory properties and may be used as a topical treatment for skin disorders such as clobetasol propionate.</p>

<p>3-(4-Chloro-phenyl)-7-hydroxy-chromen-4-one is an intermediate that is used in the research of Alzheimer's disease. It coordinates transition metals, such as copper (Cu), zinc (Zn), and nickel (Ni) to form a pharmacophore. This pharmacophore binds with flavones, which are compounds found in plants that have hypotensive and antihypertensive properties. 3-(4-Chloro-phenyl)-7-hydroxy-chromen-4-one has been shown to be an effective inhibitor of angiotensin II type 1 receptors and has a crystalline structure. 3-(4--Chloro---&gt;</p>

<p>2-Amino-1-(4-fluorophenyl)-1-propanone (Fluoroamphetamine) is a chemical that binds to the serotonin transporter, which is responsible for the reuptake of serotonin into the presynaptic neuron. Fluoroamphetamine has been shown to lower empathy and increase feelings of reward in animals. This drug has no significant effect on dopamine and noradrenaline levels but does cause an increase in metabolic acidosis. Fluoroamphetamine is most often used by analytical laboratories as a synthetic intermediate, but it can also be used as a strategy to develop specific antidotes against serotonin blockers. Fluoroamphetamine's health effects are similar to those of amphetamine with regards to cardiovascular risks and addictive potential.</p>

<p>Please enquire for more information about cis-5-Benzyltetrahydropyrrolo[3,4-c]pyrrole-1,3(2H,3ah)-dione 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 (4-Phenylpiperazin-1-yl)piperidin-4-yl-methanone dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Cyclobutanone is a chemical compound that is used as a model system for studying the oxidation of organic compounds. Cyclobutanone can be synthesized by the reaction of trifluoroacetic acid with cyclohexanone, which in turn can be produced from the hydrogenation of acetone or by dehydration of propionaldehyde. This chemical has been shown to inhibit the growth of infectious bacteria such as Mycobacterium tuberculosis and Streptococcus pneumoniae. It is also effective against other bacterial strains, such as Escherichia coli, Salmonella typhi, and Pseudomonas aeruginosa. Cyclobutanone inhibits the metabolism of glucose in cells by blocking the enzyme hexokinase and preventing glycolysis from occurring, leading to an accumulation of lactic acid in blood and urine. This effect on glucose metabolism may contribute to some autoimmune diseases, such as type 1 diabetes mellitus and celiac disease. The structure of cycl</p>

<p>Please enquire for more information about 1-(1-Benzyl-1H-indol-3-yl)ethanone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(3,5-Dimethoxy-4-hydroxyphenyl)acetone is a phenolic compound that is used as a calibration standard in the analysis of tannins. It has been shown to have a catalytic effect on the oxidation of oleic acid and linoleic acid in the presence of peroxides. The addition of (3,5-dimethoxy-4-hydroxyphenyl)acetone to an oil or fat emulsion at room temperature leads to an increase in the viscosity of the emulsion. This compound can be found in many plants, such as tea and coffee beans, cocoa beans, and red wine grapes.</p>

<p>Please enquire for more information about 5alpha-Pregnan-20beta-Ol-3-one 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 (R,S)-1,3,4,5-Tetrahydro-5-phenyl-2H-1,4-benzodiazepin-2-one hydrochloride 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 1-Acetyl-3-(acetyloxy)-7-chloro-5-(2-chlorophenyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one 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 (6a,11b,16a)-21-(Acetyloxy)-9-bromo-6-fluoro-11-hydroxy-16-methyl-pregna-1,4-diene-3,20-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(2S,3S)-5-[2-(Dimethylamino)ethyl]-3-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-1,5-benzothiazepin-4-one hydrochloride is a racemic mixture of two enantiomers. It is a prodrug that is hydrolyzed to its active form, diltiazem. The drug has been shown to be effective in the treatment of hypertension and angina pectoris. (2S,3S)-5-[2-(Dimethylamino)ethyl]-3-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-1,5-benzothiazepin-4-one hydrochloride has been shown to inhibit the activity of the enzyme phosphodiesterase which breaks down cyclic AMP. This inhibition results in an increase in levels of</p>

<p>11alpha-Methylandrostan-17beta-ol-3-one is a pharmacological agent that belongs to the group of androgens. It is an oral preparation and has been used in the treatment of infectious diseases, autoimmune diseases, and metabolic disorders. It has also been used as a matrix effect control in biological samples. The biological effects of 11alpha-Methylandrostan-17beta-ol-3-one are mediated by its direct action on cells or through conversion to testosterone or dihydrotestosterone (DHT). These effects include increasing protein synthesis, promoting bone formation, lowering cholesterol levels, stimulating the production of red blood cells, and decreasing fat deposition. The main side effects are acne vulgaris, male pattern baldness, prostate enlargement, increased risk for prostate cancer, and increased risk for developing breast cancer.</p>

<p>6,7-Dimethoxy-1,4-dihydro-3H-isochromen-3-one is a hydrazide with the chemical formula C8H8N2O3. It belongs to the family of natural products and has the molecular weight of 172.15. 6,7-Dimethoxy-1,4-dihydro-3H-isochromen-3-one is an isoquinolone derivative that contains two methyl groups on carbons 6 and 7. The compound is a symmetric molecule that can be found as a hydroxy or methoxy derivative. It reacts with 3,4 dimethoxyphenylacetic acid to form yohimbane in the presence of an oxidizing agent such as electrochemical oxidation or maldi tof. 6,7 Dimethoxy 1,4 dihydro 3H isochromen 3 one was obtained from endohedral metalloful</p>

<p>Cyclopropyl 2-fluorobenzyl ketone is an inhibitor that blocks the production of cyclic nucleotides and thereby inhibits the activity of the enzyme phosphodiesterase. It has been shown to inhibit platelets and inhibit the metabolic rate in rats. The drug also has a cytotoxic effect on rat liver cells, which may be due to its ability to bind hydrogen bonds. Cyclopropyl 2-fluorobenzyl ketone has been found to have a strong inhibitory effect on ticagrelor, statins, and anti-platelet agents. This drug has also shown a potential for adverse drug interactions with other biological products such as erythropoietin, insulin, or heparin.</p>

<p>2-Amino-2-(2-chlorophenyl)cyclohexan-1-one is an anesthetic drug that belongs to the group of ketamine. It is a chiral compound and has been shown to have central nervous system depressant effects, which are more pronounced than those of ketamine. This drug also affects the cardiovascular system and can cause respiratory depression. 2-Amino-2-(2-chlorophenyl)cyclohexan-1-one has been shown to be metabolized in humans by cytochrome P450 (CYP3A4). It may potentiate the effect of drugs that induce CYP3A4 activity such as erythromycin, rifampin, and phenobarbital.<br> 2-Amino-2-(2-chlorophenyl)cyclohexan-1-one is not active against MRSA or methicillin resistant pseudomonas aeruginosa (MR</p>

<p>Please enquire for more information about (17b)-17-(Benzoyloxy)-4-oxaandrost-5-en-3-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-tert-Butylpentane-2,4-dione is a chemical compound that can be synthesized in two steps from benzene, nitromethane and perchloric acid. It is used as a precursor to produce polymers with different properties. In the first step of the synthesis, 3-tert-butylpentane-2,4-dione condenses with nitromethane to form an oligomer. The resulting product is then oxidized to form a perchlorate ester which yields polymers with different properties depending on the type of monomer used.</p>

<p>3-(Dimethylaminomethyl)-5-methyl-2-hexanone is a chemical compound that can be used as an intermediate in the synthesis of tetrabenazine. It is a colorless liquid that can be synthesized from 2,4-diiodobenzene and dimethylamine. The optimal reaction time for this chemical is at reflux conditions. 3-(Dimethylaminomethyl)-5-methyl-2-hexanone has a molecular weight of 164.27 g/mol and an elemental composition of C: 68.09%, H: 18.07%, N: 7.91%. The target product for this chemical is 2,5-dimethyloctane, which has a molecular weight of 116.14 g/mol and an elemental composition of C: 73.06%, H: 9.11%, N: 5.79%. This chemical reacts with triethylbenzylammonium to form 3-(dim</p>

<p>Please enquire for more information about 1-(2-Aminopyrimidin-5-yl)ethanone 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 2-(Fluoromethyl)-3-(2-methylphenyl)-6-nitro-3H-quinazolin-4-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5alpha-Androstan-3-one is a metabolic intermediate of testosterone. It is found in the urine of humans and other mammals, but at concentrations that are 10 to 100 times lower than those of testosterone. It is also found in some plants and fungi. 5alpha-Androstan-3-one can be synthesized from cholesterol, or it can be formed by the hydroxylation of testosterone in response to the action of cytochrome P450 enzymes. The synthesis of 5alpha-androstan-3-one from cholesterol requires a significant amount of energy, so it is not likely to be a major route for its production. In contrast, the conversion of testosterone to 5alpha-androstan-3-one is an important pathway for maintaining physiological levels of this metabolite. The activity of 5alpha-androstan-3-one has been shown to depend on its concentration in tissues and cells. At low concentrations (less than 10 nM) 5alpha -</p>

<p>9-Fluoro-11b,21-dihydroxy-16a-methylpregna-1,4-diene-3,20-dione is a potent antiandrogen that is used to treat alopecia areata and other skin disorders. 9-Fluoro-11b,21-dihydroxy-16a-methylpregna-1,4-diene-3,20-dione has been shown to have an inhibitory effect on the growth of skin tumors in mice. This drug also has a protective effect against chemical stability. It binds to fatty acids and epidermal growth factor (EGF), which may be related to its ability to regulate transcriptional processes and inflammatory skin diseases.</p>

<p>Please enquire for more information about 2-n-Butyl-1,3-diaza-spiro[4,4]non-1-en-4-one HCl 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 Fluorescein-6-carbonyl-Ile-Glu(OMe)-Thr-DL-Asp(OMe)-fluoromethylketone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>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.</p>

<p>1,3-Indanedione is a precursor of indane diones that is used in the synthesis of fluorescent molecules. In the presence of light, 1,3-indanedione produces light emission and can be used as a chemiluminescent probe. In the presence of trifluoroacetic acid and copper complex, 1,3-indanedione undergoes intramolecular hydrogen transfer to form an intermediate which reacts with malonic acid to form an alkyl radical. The alkyl radical then reacts with hydrochloric acid to produce an ionic polymerization product. The biological sample is reactive with fatty acids and can be used for the detection of prostate cancer cells.</p>

<p>3-(2-(3,4-Dimethoxybenzoyl)-4,5-dimethoxyphenyl)pentan-2-one is an alkylene that is produced by the reaction of hydrazine with 2,3,4-trimethoxybenzoic acid. This molecule has been shown to have anxiolytic properties in animal studies and hydrolyzes to form ethylene glycol. 3-(2-(3,4-Dimethoxybenzoyl)-4,5-dimethoxyphenyl)pentan-2-one also has a hydrolysis product of tofisopam. Tofisopam is an organic acid that has been used as an antidepressant for the treatment of anxiety disorders.</p>

<p>4-Bromo-1-indanone is a molecule that has been shown to have neuroprotective properties in vitro. It has also been shown to inhibit the amines, which may be due to its ability to act as an aromatic hydrocarbon. This molecule has not been approved for use as a drug substance or drug product and its safety and efficacy are unknown.</p>

<p>Maleimide is a chemical compound with the molecular formula CH2=C(O)NHC(=O)CH2-CO2H. It is a reactive monomer that polymerizes in the presence of an initiator to form polymers. Maleimides are also used as cross-linking agents, and have been shown to be thermostable and stable at high temperatures. This particular maleimide is a colorless solid that has been shown to copolymerize with methyl methacrylate and other monomers to form thermally stable, hydrophobic polymers.</p>

<p>Z-Phe-Phe-diazomethylketone is a cathepsin inhibitor that has been shown to inhibit the proteolytic activity of various enzymes, including serine proteases and thrombotic thrombocytopenic. This compound inhibits the growth of Leishmania parasites in cell culture and has been shown to have a high affinity for carboxy terminal and proximal tubules. Z-Phe-Phe-diazomethylketone has a neutral pH, with an optimum at 7.0, which may be due to its ability to bind to proteins or other components of cells without affecting their functions.</p>

<p>Please enquire for more information about Ac-Cys(dodecyl)-chloromethylketone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Z-Leu-Tyr-chloromethylketone is a peptide that binds to the reticulum and prevents the release of calcium ions. It is a chloromethyl ketone, which inhibits the L-type calcium channels in cells. Z-Leu-Tyr-chloromethylketone has been shown to block the influx of calcium ions into cytosolic compartments. This process leads to inhibition of protein synthesis and cell death by apoptosis.</p>

<p>1,3-Difluoroacetone is a chemical compound that is used for biological studies. It has been shown to have protease activity in biological samples. 1,3-Difluoroacetone has been studied for its potential as an anti-cancer drug and has also been shown to have toxic effects on prostate cancer cells. It has also been found to induce pluripotent stem cells from human fibroblasts and hl-60 cells (a leukemia cell line). The mechanism of action of 1,3-difluoroacetone is not well understood but it seems to be irreversible inhibition of mitochondrial membrane potential.</p>

<p>Please enquire for more information about 7alpha-Methyl-3,3-dimethoxy-5(10)-estrene-17-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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

<p>1-(4-Chlorothiophen-2-yl)ethanone is an oxychloride that belongs to the family of thiourea derivatives. It is synthesized by reacting phosphorus oxychloride with 2,3-dichloroacetophenone in a solvent such as dioxane or acetonitrile. The final product is purified by means of vacuum distillation and recrystallization from diethyl ether, hexane, and chlorinated hydrocarbons.</p>

<p>Z-Ala-Pro-Phe-chloromethylketone is a cytosolic protein that performs its function by denaturing proteins and is localized in the cytosol. It has been shown to be active against a number of bacteria, including Bacillus licheniformis and Listeria monocytogenes, as well as some fungi. Z-Ala-Pro-Phe-chloromethylketone targets the membrane potential in mitochondria and chloromethyl ketone is a strategy for inhibiting membrane potential in mitochondria. The x-ray diffraction data show that this protein forms a molecule with an alpha helix structure. It binds to the mitochondrial inner membrane by ligation and inhibits mitochondrial membrane potential.</p>

<p>Please enquire for more information about (2S)-2-Amino-4-methyl-1-[(2R)-2-methyloxiranyl]-1-pentanone trifluoroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Fluoro-3-methoxyphenylacetone is a high quality reagent that can be used as an intermediate in the synthesis of complex compounds. This compound is also useful for creating fine chemicals and speciality chemicals, for research purposes. 4-Fluoro-3-methoxyphenylacetone has been shown to be a versatile building block in organic synthesis, with many possible applications. It can react with other compounds to create new compounds or react with itself to form new molecules. CAS No. 320338-98-5</p>

<p>Please enquire for more information about 4-{[4-(4-Methyloxyphenyl)-piperazin-1-yl]-phenyl}-2,4-dihydro-[1,2,4]-triazol-3-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>