Amidi

<p>N,N-Dimethyl decanamide is a fatty acid ester that is used as an amide with sodium carbonate and tebuconazole to form a particle. The particle has a diameter of about 0.5 microns and is thermally stable. N,N-Dimethyl decanamide can be used for the removal of organic substances from water by absorption onto the particle surface. It has been shown to be more efficient than other amides in removing these substances from water.</p>

Please enquire for more information about N-(5-bromo-pyridin-2-yl)-2,2-dimethyl-propionamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>L-Tryptophanamide hydrochloride is a fluorescent compound that belongs to the amides. It has been shown to have invertase activity and be hydrated in both isooctane and water. L-Tryptophanamide hydrochloride also has an anxiolytic effect on mice, which may be due to its ability to inhibit the production of serotonin at synapses by blocking the enzyme tryptophan hydroxylase. The drug is used for the treatment of anxiety disorders, including generalized anxiety disorder (GAD) and posttraumatic stress disorder (PTSD). This drug has a molecular profile that can be detected by fluorescence spectrometry, with an enhancement factor of 1.5-2.5.</p>

<p>Please enquire for more information about 3-Amino-2-hydroxy-N,N-dimethylbenzamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>Thionicotinamide is a drug that belongs to the group of ethionamide. It is a synthetic compound with synergistic activity against tuberculosis bacteria. Thionicotinamide inhibits bacterial growth by binding to mycolic acid, which is a component of the cell wall. Thionicotinamide also has conformational properties, which inhibit the enzyme activities. This drug also interacts with other drugs, such as ethionamide, and may have an effect on the metabolism of these drugs in humans. Thionicotinamide binds to lipids and reduces the activity of enzymes that are involved in lipid synthesis. The nitrogen atoms of thionicotinamide bind to four oxygen atoms from two molecules of glycol ethers in a 1:1 ratio. This binding leads to the formation of hydrogen bonds between these molecules, resulting in an increase in kinetic energy for these reactions and improved structural analysis for this molecule.</p>

Fluoxetine is a potent inhibitor of the enzyme cytochrome P450 (CYP) 2C19. The inhibition of CYP2C19 by fluoxetine may lead to an increase in the plasma concentration of other drugs that are metabolized by this enzyme, such as glipizide and hydroxycyclohexyl. Fluoxetine inhibits human uric acid secretion and increases plasma concentrations of uric acid. This drug also inhibits human erythrocyte dihydropyrimidine dehydrogenase, leading to increased blood levels of pyrimidines, especially cytotoxic ones like 6-fluoro-3-indoxyl-beta-D-galactopyranoside. Fluoxetine has been shown to have a protective effect against acetaminophen toxicity in rats because it enhances the conversion of acetaminophen to its less toxic metabolite N-acetylcysteine.

<p>Please enquire for more information about 4-(2-Chloro-4-nitrophenyl)piperazine-1-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Hydroxy-N-1H-1,2,4-triazol-3-ylbenzamide is a synthetic product that is a white crystalline solid. It has a melting point of 105°C and an average particle diameter of 3.5 nm. This compound is used as a precursor to produce the peroxide 2,2'-dihydroxybenzophenone, which can be used in the synthesis of other organic compounds. It can also be used in the production of amides and quaternary ammonium salts. 2-Hydroxy-N-1H-1,2,4-triazol-3-ylbenzamide is structurally similar to hydrotalcite and hydroxyl group which are both natural products found in nature.</p>

<p>Please enquire for more information about N-tert-Butoxycarbonyl-L-isoleucineamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

N-Methoxy-N-methylacetamide is a nucleophilic amide that can be synthesized by the reaction of acetamide with methylmagnesium chloride. It has been used to synthesize an enantiopure derivative of 2-aminopropanol, which is used in the synthesis of potent antitumor agents. N-Methoxy-N-methylacetamide has shown potent anticancer activity in mice and rats. This molecule exhibits a carbonyl group that can act as an enolate, which is a reactive intermediate within chemical reactions. The nucleophilic attack on this carbonyl group leads to intramolecular hydrogen transfer, producing a more stable product.

5-(2-Aminopropyl)-2-methoxybenzenesulphonamide is a trimethyl derivative of the aminopropyl group. It is used as a reagent to introduce hydroxymethyl groups into organic compounds. 5-(2-Aminopropyl)-2-methoxybenzenesulphonamide reacts with hydrochloric acid and an organic solvent in the preparation process. In the Friedel-Crafts reaction, 5-(2-Aminopropyl)-2-methoxybenzenesulphonamide reacts with d-alanine to form an optical isomer, which can be converted to its racemic form by ammonolysis. This compound is also used as a prostatic agent and an amide in the synthesis of benzene and phenoxymethyl alcohols.

<p>Please enquire for more information about N-(3-Bromo-4-hydroxyphenethyl)-N-(2-bromo-5-hydroxy-4-methoxybenzyl)formamide 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 N,N-bis(2-Chloroethyl) benzenesulfonamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

D-Glutamic acid alpha-amide is a carbohydrate that has been shown to have antibiotic properties. It can be produced by chemoenzymatic synthesis and is used as an animal feed additive. D-Glutamic acid alpha-amide is a conjugate of D-glutamic acid with either glycine or beta-alanine. The residue of this compound on red blood cells is measured in order to assess the amount of D-glutamic acid alpha-amide that has been ingested. This compound has also been shown to have antigenic properties, which can elicit immune responses when injected into animals. The meningococcal vaccine that contains D-glutamic acid alpha-amide was found to be effective at stimulating an immune response in mice against meningitis caused by gram negative species, such as Neisseria meningitidis.

N'-Hydroxycyclopropanecarboximidamide (N-HCPC) is an alkoxycarbonyl-containing heterocycle that is structurally related to the benzodiazepine class of drugs. It has been shown to have depressant activity in animal models and may be useful as a treatment for epilepsy, but it also has psychoactive properties. N-HCPC can cause epileptic seizures in humans, although this effect appears to be dose dependent. It may also have potential use as a treatment for Alzheimer's disease and depression due to its ability to bind to the benzodiazepine receptor. The drug binds with high affinity to muscle tissue, which may explain its effects on muscle control and movement.

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<p>N,N'-Dimethylethanebis(thioamide) is a ligand that binds to the metal rhenium. It has been shown to be an efficient catalyst for the oxidation of nitrates and organic compounds. N,N'-Dimethylethanebis(thioamide) is also used as a fertility agent in oral doses because it can increase the production of sperm in males and ovulation in females. The vibrational spectra of this compound show strong intermolecular hydrogen bonds with halogens and nitrogen atoms. This ligand has been shown to have high affinity for metal ions such as rhenium due to its chelate ring structure.</p>

<p>L-Serine amide hydrochloride is a synthetic, anti-HIV drug that is used as an antiviral agent. It inhibits the viral life cycle by inhibiting the activity of acyclic nucleoside phosphonates, which are vital to viral DNA synthesis. L-Serine amide hydrochloride binds to the cyclopentane ring of guanosine and prevents its interaction with the enzyme ribonucleotide reductase. This binding prevents the conversion of guanosine into GTP, thereby preventing HIV from using this molecule in their life cycle. L-Serine amide hydrochloride is not active against cellular proteins or prostaglandins.</p>

<p>Please enquire for more information about 2-Chloro-N-(3-cyano-4,5-dimethylthien-2-yl)acetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>