Amides

<p>N-(3-Aminopropyl)acetamide is a secondary amine that is used as a reagent in the profiling of tissues. It has been shown to inhibit the growth of Thermus thermophilus and other bacteria, including Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa. N-(3-Aminopropyl)acetamide has also been shown to inhibit the growth of cancer cells in cell culture. It was found to be effective against logarithmic growth phase cells and not against stationary phase cells. However, its mechanism of action is unknown.</p>

<p>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.</p>

<p>N-(6-Phenylhexyl)-5-chloro-1-naphthalenesulfonamide is a dibutyryl camp analog that has been shown to inhibit the L-type calcium channel in a dose-dependent manner. It has an effect on both spermatozoa and glioma cells, with its most significant effect being inhibition of the intracellular calcium ion. This drug inhibits the growth rate of these cells, which may be due to its ability to activate adrenergic receptors and cause increased intracellular calcium ion levels. N-(6-Phenylhexyl)-5-chloro-1-naphthalenesulfonamide also slows the cycle of the cell, which may be due to a kinetic effect.</p>

<p>L-proline analogue</p>

<p>Please enquire for more information about 4-Hydrazino-N-methyl benzene methanesulfonamide, hydrochloride (1:1) 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-Methyl-2-[[3-[(1e)-2-(2-pyridinyl)ethenyl]-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-yl]thio]benzamide 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 16-Phenoxy tetranor pgf2alfa cyclopropyl methylamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N,N-Dimethyformamide diethy acetal is a compound with a pyrazole ring and an ethyl formate substituent. It is an amide that can be synthesized by the reaction of dimethylformamide with ethyl formate. This compound has been found to inhibit the production of inflammatory cytokines such as chemokines in bowel disease patients. N,N-Dimethyformamide diethy acetal's amine group can also bind to adenosine receptors with high affinity. The hybridized nitrogen atoms in this molecule are more soluble than other amines and can be used as a supercritical fluid extraction solvent for solubility data.</p>

<p>Please enquire for more information about N-(2-Benzoyl-4-chlorophenyl)-2-chloro-N-methylacetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Amino-5-methoxy-2-methyl-N-methylbenzenesulfonamide is a surfactant that is used in the chemical industry to dissolve diazotized aromatic amines. It is also used in the preparation of coupling agents, such as naphthol, and hydrochloric acid. 4-Amino-5-methoxy-2-methylbenzenesulfonamide can be prepared by the diazotization of aniline followed by coupling with hydrochloric acid and sodium phosphate. The product can then be purified by recrystallization from a salt solution containing sodium acetate.</p>

<p>Please enquire for more information about 4-(Aminomethyl)-N-Methylbenzenesulfonamide 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-Dimethyl 4-boronobenzenesulfonamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>WAY 316606 is a potent, orally administered small molecule that inhibits the Wnt signaling pathway by blocking the action of β-catenin. It has been shown to have potential for treating eye disorders, including age-related macular degeneration. This drug also has potential for treatment of cell and nervous system diseases such as Alzheimer's disease and Huntington's disease. WAY 316606 inhibits the transcriptional activity of the β-catenin/Tcf4 complex by binding to it and preventing its translocation into the nucleus. In addition, WAY 316606 prevents downstream activation of genes regulated by β-catenin signaling, including c-myc and cyclin D1. This drug also blocks growth factor receptor tyrosine kinases and monoclonal antibodies that activate these receptors.</p>

<p>2-Chloro-N-(2-oxotetrahydro-3-thienyl)acetamide is a chemical compound that is used as an intermediate in the synthesis of other organic compounds. The impurities are minimized by using organic solvents such as acetone, pyridine, and tetrahydrofuran. The product can be precipitated by adding sodium carbonate or potassium carbonate to the solution, or it can be crystallized from a mixture of methanol and water. 2-Chloro-N-(2-oxotetrahydro-3-thienyl)acetamide is also soluble in ethers such as erdosteine and acetonitrile, which can be used to remove the last traces of water.</p>

<p>Please enquire for more information about N-(4-Hydroxyphenyl)-N-methylacetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>C8-Ceramide is a glucosylceramide that is involved in the production of C8-ceramides. It has shown to have potent apoptosis activity and inhibit p21, an inhibitor of cell cycle progression. C8-Ceramide also has been shown to be an inhibitor of tumor necrosis factor alpha (TNF-α) induced inflammation and apoptosis in mouse tumor cells. In addition, it can induce apoptosis by inhibiting the epidermal growth factor receptor (EGFR) pathway. This polymerase chain reaction (PCR) product was found to bind to DNA in a model system using calf thymus DNA as well as bacterial DNA gyrase and topoisomerase IV enzymes.</p>

<p>Please enquire for more information about N-(4-(4-Fluorophenyl)-5-(hydroxymethyl)-6-isopropylpyrimidin-2-yl)-Nmethylmethanesulfonamide 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 Dorzolamide hydrochloride related compound A including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-(2-Aminoethyl)-N-methyl-1H-indole-5-methanesulfonamide (AMIS) is an intermediate in the preparation of medicaments. It is a stable process and can be used as an intermediate for other compounds. AMIS is prepared by reacting methanesulfonic acid with methanol and ammonium carbonate, which produces methanesulfonamide, succinic acid and ammonium hydroxide. The reaction liquid is then heated to produce a crystalline solid. The crystals are then recrystallized to yield AMIS as a white solid.</p>

<p>Please enquire for more information about 4-(2,3-Epoxypropoxy)phenylacetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<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.</p>

<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>

<p>(2R)-2-Amino-3-phenylpropionyl amide is a synthetic cannabinoid that has been shown to bind to the CB2 receptor. It has been found to be an effective analgesic in rat models of inflammatory and neuropathic pain. This drug is also a serine protease inhibitor, with activity against ochrobactrum, an antibiotic-resistant bacteria. (2R)-2-Amino-3-phenylpropionyl amide is also used as a substrate for d-alanine synthesis and has been sequenced. It can form hydrogen bonds with water molecules and chloride ions. (2R)-2-Amino-3-phenylpropionyl amide has been synthesized by Clostridium coli K12 cells and is expected to have similar effects on human cells.</p>

<p>2-Chloro-N-1-naphthylacetamide is a synthetic organic compound that belongs to the class of sulfur compounds. It is used in the synthesis of other compounds and has been shown to be a potent inhibitor of hydroxylapatite and sulfate hydrolysis. The reaction mechanism for this compound’s inhibition of sulfate hydrolysis is not known, but it may be due to its ability to act as an electron donor or acceptor. 2-Chloro-N-1-naphthylacetamide also has carcinogenic properties, with some studies suggesting that it can cause liver cancer in rodents.</p>

<p>N-Phenylpropanamide is a chemical inhibitor that has been shown to have a protective effect against the light-induced degradation of drugs in urine samples. The compound also inhibits the hydrolysis of amides by hydrochloric acid and hydrogen bonds with the receptor binding site on human liver cells. N-Phenylpropanamide has been shown to affect cardiac function, as well as growth factor production.</p>

<p>Please enquire for more information about (R)-Dragonfly N-trifluoroacetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-(p-Hydroxyphenethyl)-N-(2-bromo-5-hydroxy-4-methoxybenzyl)formamide is an anticancer drug that belongs to the class of phenethyl derivatives. It is a radiosensitizer that inhibits DNA and RNA synthesis, leading to cancer cell death. The drug has been shown to have a chiral center and two enantiomers, with the (S)-enantiomer being more active than the (R)-enantiomer. N-(p-Hydroxyphenethyl)-N-(2-bromo-5-hydroxy-4-methoxybenzyl)formamide has been shown to be effective in animal models for brain tumors and breast cancer cells. It has also been shown to be effective against leukemia cells, which are resistant to other treatments. N-(p-Hydroxyphenethyl)-N-(2-bromo-5-hydroxy-4</p>

<p>Dopamine (D2) receptor antagonist</p>

<p>(R)-5-(2-Aminopropyl)-2-methoxybenzenesulfonamide is an amide. It is a hydrochloric acid salt that can regulate the reaction system and introduce filtration, which can be used to separate the components of the reaction system. The kinetic and chiral properties of this compound are derived from Friedel-Crafts reactions with phosphites and Friedel-Crafts reactions with d-alanine. (R)-5-(2-Aminopropyl)-2-methoxybenzenesulfonamide can also catalyze ammonolysis and catalysis with phenoxy.</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>

<p>L-Phenylalanine b-naphthylamide is a phenylalanine derivative that can be used as an indicator for the detection of Clostridium, 2-naphthylamine, and other anaerobes. This compound is a chromogenic substrate that reacts with amino groups in amino acids and amides in peptides to form a variety of color products. The condensation of phenylalanine with 2-naphthylamine is catalyzed by enzymes found in clostridia. When L-phenylalanine b-naphthylamide is incubated with tissue from animals or humans, it produces a pink coloration that indicates the presence of clostridia. The aerobic conditions necessary for this reaction are also found in the environment and within the body.</p>

<p>Please enquire for more information about 2-Chloro-N-(2,3-dihydro-1H-inden-2-yl)acetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>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>

<p>Please enquire for more information about 4-Amino-1-Boc-piperidine-4-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Ethyl-2-phenylmalonamide (2-EPMA) is a metabolite of primidone that acts as an inhibitor of glutamate dehydrogenase and may be used in the treatment of epilepsy. It has been shown to be effective in treating seizures caused by carbamazepine, phenobarbital, or phenytoin. 2-EPMA is also used to measure enzyme activities in serum, which can be used as a diagnostic tool for liver diseases. 2-EPMA is typically prepared for use as an enzyme inhibitor by diluting it with high salt or human serum. This compound may have carcinogenic potential and should not be administered with single doses greater than 100 mg/kg body weight. 2-EPMA interacts with many other drugs such as phenobarbital, phenytoin, and carbamazepine.</p>

<p>Please enquire for more information about 2-(Diethylamino)-N-(2,4-dimethylphenyl ) acetamide HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Carisoprodol Related Compound AMeprobamate is a carbamate derivative used as an anxiolytic drug.</p>

<p>Please enquire for more information about 5[(R)-(2-Aminopropyl)]-2-methoxybenzenesulfonamide 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 2-(2,5-Dimethoxyphenyl)ethylformamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Methylbenzenesulfonamide is a chemical compound that has been shown to induce apoptosis in bladder cancer cells. It is an acid conjugate of the drug 2-methylbenzene-1,4-sulfonamide and it can be used for the treatment of bladder cancer. The compound binds to the apoptosis protein and inhibits its function, leading to cell death. The cytotoxic effects of 2-methylbenzenesulfonamide have been shown in short term toxicity studies in rats. In long term animal studies, this compound showed no adverse effects on the liver or kidneys, but did show some indication of reproductive toxicity. 2-Methylbenzenesulfonamide is not mutagenic and does not affect male fertility when given orally at doses up to 2000 mg/kg body weight for 90 days. 2-Methylbenzenesulfonamide binds to receptors on the surface of cancerous cells and induces apoptosis by inhib</p>

<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>Formamide is a colorless, volatile chemical compound that is most commonly used in the laboratory for the preparation of dna duplexes. It can also be used to treat bowel disease and HIV infection. It is not active against viruses or bacteria but has been shown to bind to toll-like receptors on cells. Formamide is an organic substance that exists as a gas at room temperature and pressure. Formaldehyde reacts with water in the presence of sodium carbonate to form formamide, which is soluble in water. Formamide has been used as a reaction solution for surface methodology experiments because it evaporates quickly and leaves no residue on surfaces. Formamide has been shown to inhibit epidermal growth factor (EGF) activity by binding to the EGF receptor protein and preventing its activation. This inhibition leads to decreased cell proliferation, reduced protein synthesis, and inhibition of DNA replication.</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>

<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>Beta-alanine amide HCl is a research chemical that belongs to the class of beta-amino acid derivatives. Beta-alanine amide HCl is an activator of nucleophiles and can be used in analytical chemistry as an indicator for chloride ions. It has been shown to react with asparagine, yielding beta-alanine and ammonia. The reaction system can be analysed by measuring the elimination of a hydrogen chloride ion from the beta-alanine amide HCl molecule and the subsequent increase in pH. The analytical method has also been used to measure concentrations of deamination reactions and redox potentials at high concentrations.</p>

<p>L-2-Aminobutanamide is a compound that is used as an industrial preparation and as a reagent in kinetic studies. It has been shown to be effective in the analytical method for the determination of hydrochloric acid in titration, with a detection limit of 0.1%. L-2-Aminobutanamide can also be used to produce asymmetric synthesis by adding it with sodium hydroxide solution or hydroxide solution and using chromatographic science. This compound has been shown to have antibacterial effects on Brucella, which can be attributed to its ability to inhibit protein synthesis and disrupt cell membrane integrity. L-2-Aminobutanamide is a chiral compound that can exist in two different forms, L -(+)-2-aminobutanamide or D -(-)-2-aminobutanamide.</p>

<p>Please enquire for more information about N-(4-Aminophenyl)butanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Acetylglycinamide is an amide that is structurally similar to the amino acid glycine. It has been shown to have anti-inflammatory properties by inhibiting prostaglandin synthesis in vitro. In vivo, N-acetylglycinamide is metabolized and excreted as the non-polar solvents n-acetylglycine and chloride. This amide is soluble in non-polar solvents such as chloroform, dichloromethane, or ether. N-acetylglycinamide also has a pairwise orientational order with respect to solvent molecules and exhibits a low degree of hydrogen bonding interactions with water molecules.</p>

<p>3-Bromopropionamide is an antibacterial agent that inhibits bacterial growth by blocking the synthesis of proteins. It is a synthetic amide with significant antibacterial activity against S. aureus. 3-Bromopropionamide has been shown to be effective against drug-resistant bacteria, including those that are resistant to metalloid salts or alkylene compounds. This substance also has psychomimetic effects and may be useful for studying the kinetics of protein synthesis in cells. 3-Bromopropionamide can be used as a linker to attach other molecules to proteins, which could allow them to penetrate cell membranes more easily.</p>

<p>Ceramide is a group of sphingolipids that are found in the outermost layer of cells. Ceramides have been shown to be important for maintaining cell structure and function, as well as regulating cellular processes such as apoptosis, insulin resistance, and inflammation. A ceramide profile can be used to identify an individual's risk for developing certain conditions such as cardiovascular disease, chronic kidney disease, or cancer. In addition to its role in cell biology, ceramide has been shown to increase insulin sensitivity in animals by increasing glucose uptake in adipocytes. Ceramides are also produced by the body from other lipids such as cholesterol or fatty acids. They are found in various tissues and organs including the brain, skin, lungs, and gut.</p>