Imines

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Applications Acetone oxime was one of the reagents used as a part of preparation of arylbenzoxazoles as potent and selective estrogen receptor-β ligands. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Malamas, M., et al.: J. Med. Chem., 47, 5021 (2004)

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Cyclopentan-1-one oxime is a nitroalkane that is synthesized by the reaction of phosphorus pentachloride and fatty acids. The structure of cyclopentan-1-one oxime has been determined by FTIR spectroscopy, and it can be characterized as a skeleton with a hydroxyl group and polycarboxylic acid. Cyclopentan-1-one oxime has an active methylene group that can react with water vapor to form hydroxylamine. It also reacts with oxygen to form a particle. Cyclopentan-1-one oxime is used in flow system for the production of microparticles, which are amides that have a variety of uses including pharmaceuticals, food additives, cosmetics, and other applications.

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Chroman-4-One Oxime is an oxime derivative that has shown antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA). It is synthesized by the reaction of dimethylformamide with tosylates, followed by acidic alkylation. The molecule has the following functional groups: an oxime group, a methyl group, and a carbonyl group. Chroman-4-One Oxime binds to the bacterial ribosome and prevents protein synthesis through inhibition of aminoacyl tRNA binding. This leads to cell death due to lack of proteins necessary for cell division.

beta-Resorcylic aldehyde oxime is a compound that can be used as a reagent, speciality chemical, and research chemical. It has the CAS number 5399-68-8, and it is a fine chemical that has been shown to be useful in organic synthesis. beta-Resorcylic aldehyde oxime is soluble in methanol, ethanol, benzene, diethyl ether, and acetone. This compound can be used as a building block for other compounds by reacting with amines or carboxylic acids. It can also be used as an intermediate for other reactions. beta-Resorcylic aldehyde oxime has been shown to have versatile properties that make it an excellent scaffold for creating new compounds.

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Diphenylglyoxime is a redox potential indicator that can be used to measure the activity of hydrogen peroxide. It has been used in gravimetric analysis, patterning, and as a substrate in electrochemical experiments. Diphenylglyoxime reacts with picolinic acid (PCA) to form a redox-active molecule that can be detected using nmr spectroscopy. The reaction mechanism of this process is not well understood, but it is believed that diphenylglyoxime first reacts with PCA to form a phenylhydroxypicolinic acid ester that undergoes an intramolecular cyclization reaction. This results in the formation of diphenylhydroxyquinone-2-carboxylic acid and diphenylglyoxylic acid. The hydroxyl group on the phenolic ring of diphenylglyoxylic acid reacts with the nitrogen atoms on PCA to form a five membered heterocycl

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Testosterone 3-(O-carboxymethyl)oxime is an inactive prodrug of testosterone. It is a potent and selective inhibitor of angiotensin II that causes vasodilation by blocking the conversion of angiotensin I to angiotensin II. Testosterone 3-(O-carboxymethyl)oxime has been shown to be effective in lowering blood pressure in patients with congestive heart failure, although it may cause side effects such as dizziness, headache, and nausea. This drug can also be used to treat prostate cancer because it inhibits the production of testosterone and reduces serum levels of luteinizing hormone. Testosterone 3-(O-carboxymethyl)oxime can also be used for diagnostic purposes as a marker for polycystic ovary syndrome (PCOS).

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Salicylaldoxime is a coordination compound that is used for the treatment of malaria. Salicylaldoxime has a high affinity for the cell nuclei, which leads to its inhibitory properties. It binds to cell factor and inhibits the growth of malarial parasites. The inhibition of x-ray crystal structures by salicylaldoxime has been shown in Langmuir adsorption isotherms and electrochemical impedance spectroscopy. This drug binds to metal ions and forms complexes with them, which can be detected through plasma mass spectrometry. The coordination geometry and reaction solution were also analyzed using structural analysis. Hydrogen bonding interactions are present in salicylaldoxime due to its formation of chelates with metals such as iron, copper, cobalt, nickel, and zinc.

(4-Chloro-phenyl)-oxo-acetaldehydeoxime is a thiosemicarbazone that has been shown to be effective against the H1N1 pandemic. This compound has been shown to bind to the influenza virus and block its ability to infect cells by interfering with the fusion of the viral envelope with the host cell membrane. (4-Chloro-phenyl)-oxo-acetaldehydeoxime interacts with the lipid bilayer of influenza A viruses, enhancing membrane permeability and causing leakage of viral contents. In addition, it inhibits viral replication in infected cells. Covid-19 is an antiviral drug that is used for treatment of pandemics caused by influenza A virus subtype H1N1. Covid-19 was developed by Roche Pharmaceuticals and is approved for marketing in many countries around the world.

4-Nitro-alpha-chlorobenzaldoxime is a novel synthetic compound that is synthesized through the Diels-Alder reaction. The synthesis of this compound is both stereoselective and efficient. 4-Nitro-alpha-chlorobenzaldoxime has been shown to be an effective anti-fungal agent against Candida albicans, Cryptococcus neoformans, and Aspergillus niger. It also inhibits the growth of other fungi such as Trichophyton mentagrophytes, Trichophyton rubrum, and Microsporum canis. This drug is not active against bacteria or other types of fungus. 4-Nitro-alpha-chlorobenzaldoxime inhibits the biosynthesis of diacylglycerol (DAG) by inhibiting the enzyme DAG kinase (DGK). This inhibition blocks signal transduction in cells and prevents cell proliferation.

Please enquire for more information about 2',3',9',10'-Tetrahydrospiro[cyclohexane-1,8'-cyclopenta[c]pyrano[3,2-g]chromen]-4'(1'H)-one oxime including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Cyclopropanecarboxamidoxime hydrochloride (CPCA) is a diazine compound that is used as an anti-tuberculosis drug. It is the most potent of the diazine compounds for the treatment of tuberculosis. CPCA inhibits bacterial growth by binding to DNA-dependent RNA polymerase, thereby preventing transcription and replication. The high frequency of human activity has been shown using a patch-clamp technique on human erythrocytes. This active form is metabolized through a number of metabolic transformations, including hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid. CPCA also specifically binds to markers expressed at high levels in Mycobacterium tuberculosis strains (e.g., ESX-1 secretion system protein) and inhibits cell growth in culture.

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2-Naphthaldehyde oxime is a reactive aldoxime that can be used as an oxidant in organic chemistry. It is able to increase the rate of hydrolysis by acid catalysts, and has been shown to cause biomolecular damage due to its ability to react with functional groups such as amines and alcohols. 2-Naphthaldehyde oxime reacts with silicon, styrene, and polystyrene. The reaction produces carbon dioxide, hydrogen, and water. This product also has the capability of solvating organic compounds through the use of water molecules. Hypervalent oxidation reactions may occur with 2-naphthaldehyde oxime due to its ability to form multiple bonds with oxygen atoms.

4-Phenylcyclohexanone oxime is a reagent that is used in organic synthesis. It is a hydroxamic acid derivative that inhibits the catalytic activity of metalloproteinases, such as matrix metalloproteinase and cathepsin B. 4-Phenylcyclohexanone oxime has been shown to inhibit the production of reactive oxygen species, which are toxic to cells. It can also be used as a radiation sensitizer for radiotherapy. The compound also has pharmacological properties and can be used to synthesize semicarbazones.

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Thiophene-2-carbaldehyde oxime is a reaction product of 2-aminoethanethiol and thiophene-2-carbaldehyde. It has a high antibacterial activity against Pseudomonas aeruginosa, which is the most common cause of hospital-acquired infections. Thiophene-2-carbaldehyde oxime has been shown to react with metal ions to form an insoluble precipitate in aqueous solution, which may be responsible for its antibacterial activity. It also inhibits acetylcholinesterase (AChE) by forming an adduct with the enzyme's active site. The inhibition of AChE results in increased levels of acetylcholine, leading to increased muscle contractions and paralysis.

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The conformational and rotameric properties of 5-fluoro-2,4(1H,3H)-pyrimidinedione 4-oxime (5F-2,4(1H,3H)-PDO) have been investigated by molecular mechanics calculations. The stabilization of the tautomeric isomers was found to be due to the steric hindrance between the hydrogen atom attached to the nitrogen atom and the methyl group in position 2. The interactions between 5F-2,4(1H,3H)-PDO and thymidine were studied at different temperatures. The protonation state of 5F-2,4(1H,3H)-PDO has been determined experimentally by elemental analysis and nuclear magnetic resonance spectroscopy. Structural isomers were also characterized by 1D and 2D NMR spectroscopy.