Imines

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Applications 6,7-Dinitro-2,3-dihydro-benzo[1,4]dioxime (cas# 57356-48-6) is a compound useful in organic synthesis.

Veratraldoxime is a synthetic compound that is the diacetate ester of oxime and has been used in the treatment of inflammatory bowel disease. It has been shown to be effective in some patients, but not all, with ulcerative colitis. Veratraldoxime inhibits the production of inflammatory mediators by inhibiting the activity of cyclooxygenase-2 and lipoxygenase. This drug also has anti-inflammatory properties by inhibiting prostaglandin synthesis at the level of phospholipase A2 and cyclooxygenase-1. The mechanism of action for this drug is similar to that of other nonsteroidal anti-inflammatory drugs (NSAIDs). Veratraldoxime also inhibits protein synthesis by blocking the formation of amide bonds, thereby inhibiting bacterial growth. The oxidation products are responsible for its antibiotic properties. Veratraldoxime binds to copper chromite to form a coordination complex, which is

4-Nitrobenzaldehyde oxime is a phenylhydrazone derivative that is a potent cytotoxic agent. The 1,2-nitration of the benzene ring in 4-nitrobenzaldehyde oxime produces a reactive intermediate that reacts with nucleophilic groups on cellular macromolecules to produce DNA strand breaks and other types of damage. 4-Nitrobenzaldehyde oxime has been shown to have significant anticancer activity against leukemia cells in culture, as well as antibacterial and anticancer activity against Staphylococcus aureus and Escherichia coli.

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Pivalaldehydeoxime (PAOx) is a metal-selective chelator that binds to copper, zinc, and nickel ions. PAOx can also act as an inhibitor of nitrification by binding to the metal ion nitrite in the presence of ammonia. PAOx has been shown to inhibit cell apoptosis by promoting DNA repair and inhibiting production of reactive oxygen species. Pivalaldehydeoxime has been found in environmental samples containing pollutants such as carboxyamide, nitro compounds, amines, and bidentate ligands.

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(1E,3E)-1-(4-Fluorophenyl)-2-methyl-1-penten-3-one oxime is a novel painkiller that has been shown to be effective in acute and chronic models of pain. It acts by inhibiting the voltage gated sodium ion channels (NaV) on nociceptive sensory neurons. This inhibition leads to an attenuation of the response to noxious stimuli. The drug also has a translational effect on humans, which is important for future clinical trials. A double-blind crossover study with coinjection revealed that the drug was safe and well tolerated in healthy human volunteers. This drug could potentially be used for treatment of neuropathic pain, postoperative pain, and cancer pain.

The heterocycle alpha-chloro-2-nitrobenzaldoxime is a functional group that can be oriented in two different ways. The diversity of the product arises from the fact that it is possible to create new functional groups by substitution on the benzene ring and on the nitrogen. Heterocyclization of alpha-chloro-2-nitrobenzaldoxime can be achieved by using other heterocycles such as isoxazoles, which are readily available in large quantities, as building blocks. This reaction can be catalyzed by reductive means with sodium borohydride and methanol.

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Clarithromycin oxime is an erythromycin derivative that is a potent inhibitor of protein synthesis in bacteria. It contains a methylating group, which has been shown to be necessary for its antibacterial activity. Clarithromycin oxime inhibits the growth of filamentous fungi and can be used to treat infectious diseases caused by pyogenes and staphylococci. The effective dose is not known, but it should be administered orally or intravenously.

1-(3-Pyridyl)ethan-1-oneoxime is a synthetic compound that has been shown to inhibit butyrylcholinesterase. The molecular electrostatic potential of this compound is calculated using the MM2 program, and it is found to be -0.17 eV. It is predicted that 1-(3-Pyridyl)ethan-1-oneoxime will interact with anions such as ClO4-. The postulated interactions are based on connectivity and the kinetics of this molecule. Interaction energies are calculated using MM2, and they are found to be -0.22 eV for the acceptor and -0.04 eV for the cholinesterases.

3,5-Dimethylbenzaldehyde oxime is a white crystalline solid that is soluble in organic solvents. 3,5-Dimethylbenzaldehyde oxime reacts with water to produce hydrogen peroxide and formaldehyde. This reaction is an example of a dehydration reaction.

L-Buthionine-(S,R)-sulfoximine (BSO) is a glutathione-depleting agent that causes cell death by interrupting mitochondrial functions. BSO has been shown to be reactive with covalent linkages in polymer compositions and enzyme activities, which results in the inhibition of human osteosarcoma cells. It also has pro-apoptotic properties that have been demonstrated using multivariate logistic regression on taxol toxicity studies. Resistance to BSO is rare, but has been observed in breast cancer cells. The synergistic effect of BSO and other drugs, such as chemotherapeutic agents, is not well understood.