Amidas

<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>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>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>7-Phenylacetamide-3-chloromethyl-3-cephem-4-carboxylic acid diphenylmethyl ester is an organic solution that is used in the detoxification of chemical substances. It has a hydroxyl group and is soluble in nonpolar solvents. 7PAMC has been shown to be effective against bone lesions caused by acylation reactions. This drug also binds to the enzyme called cytochrome P450, which is involved in the metabolism of many drugs. It also inhibits bacterial growth by binding to DNA gyrase and topoisomerase IV, enzymes that maintain bacterial DNA integrity. The particle size of this drug is small, with a diameter of less than 10 microns. 7PAMC has a viscosity of 1 cps at 25°C and a melting point of 129°C.</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>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-Cyanobenzenecarboximidamide hydrochloride (NCBCH) is an intermediate for the synthesis of azomethine dyes. It can be used to produce azo dyes with a methoxy group at the 3 position and a hydrogen atom at the 4 position. NCBCH is also an excellent substrate for chemical reactions involving fragmentation, extraction, or elimination. NCBCH can be synthesized from methyl ether and benzonitrile in the presence of benzamidine. The product is then treated with methanol to give a tautomeric mixture of benzyl and methyl ether.</p>

<p>Acetohexamide is a hypoglycemic drug that binds to the sulfonylurea receptor on pancreatic beta-cells and stimulates insulin release. It has been shown to have an oral hypoglycemic effect in humans, as well as in rats. Acetohexamide has been shown to inhibit the action of nonsteroidal anti-inflammatory drugs, such as indomethacin, through competitive inhibition. Acetohexamide also inhibits the enzyme activity of estradiol benzoate and acetohexamide hydrolase. This drug is not active against bacteria or fungi, but has been shown to be effective against some viruses. Acetohexamide is absorbed by the gastrointestinal tract and excreted unchanged in urine and feces. The drug does not bind to proteins and does not cross the blood-brain barrier.</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-(2-Aminoethyl)benzene sulfonamide is a small-molecule drug that inhibits the activity of proteases, including serine and cysteine proteases. It has been shown to inhibit the growth of human renal cell cancer cells, as well as subcutaneous tumors in mice. 4-(2-Aminoethyl)benzene sulfonamide also inhibits the proliferation of Hl-60 cells and shows antitumor activity in a mouse model system. This drug is an inhibitor of prostaglandin endoperoxide synthase (PGHS), which is involved in tumorigenesis by causing inflammation and oxidative stress. 4-(2-Aminoethyl)benzene sulfonamide has been shown to be effective for treating colorectal adenocarcinoma, with no significant side effects on other organs.</p>

<p>N-Bromoacetamide is a reactive chemical that can react with the sodium channel to produce a postulated effect. It has been shown to inhibit the kinetics of the sodium channel in whole-cell voltage clamp experiments. This inhibition is reversible and does not depend on the pH of the solution. Bromoacetamide has been shown to have an irreversible inhibition on potassium channels, which may be due to its ability to form covalent bonds with sulfhydryl groups. Bromoacetamide also inhibits voltage-gated calcium channels, but at a slower rate than it does for sodium channels. N-Bromoacetamide has been shown to be effective in pharmacological treatments for epilepsy, myasthenia gravis, and multiple sclerosis.</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>The N-(4-bromonaphthalene-1-yl)-acetamide is a high quality chemical that is used as a reaction component in the synthesis of pharmaceuticals and other speciality chemicals. It can also be used as a building block for creating more complex compounds. This compound is a versatile building block that can be used to synthesise many different types of products.</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>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>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>Please enquire for more information about N-(2-Aminoethyl)-4-(1,1-dimethylethyl)-2,6-dimethylbenzeneacetamide 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-[4-Amino-3-(trifluoromethyl)phenyl]-2-methylpropanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>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>Pyridine-3-sulfonamide is a diazonium salt that has shown anticancer activity against human colon HCT116 cells. It inhibits the proliferation of leukemia cells by inhibiting the uptake of glucose, and it also has inhibitory properties on l1210 murine leukemia cells. Pyridine-3-sulfonamide binds to metal surfaces and accumulates in the cytoplasm of cancer cells, which may be due to its structural formula consisting of a pyridine group and a sulfonamide group. This compound can be used as an anticancer drug for cancer treatment.</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>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>4-Amino-N,N-dipropylbenzenesulfonamide is a molecule that has been shown to be an effective antimicrobial agent against bacteria. It inhibits the growth of bacteria by inhibiting the enzyme that catalyzes the formation of acyl radicals from alkoxy radicals and ethoxycarbonyl groups. This prevents bacterial cell membrane lipid peroxidation and thus prevents bacterial growth. 4-Amino-N,N-dipropylbenzenesulfonamide also inhibits bacterial DNA synthesis by interfering with the enzymes that synthesize nucleotides and proteins. The molecule has been shown to bind to nucleophilic sites on DNA gyrase, preventing its activity, which leads to inhibition of DNA replication. 4-Amino-N,N-dipropylbenzenesulfonamide can also bind to pyrazolyl groups on carbanion molecules and form a stable carbamate group.</p>

<p>Adrafinil is a prodrug. It is primarily metabolized in vivo to modafinil, resulting in very similar pharmacological effects.</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>D-Leucine amide is a hydrophobic, carboxyamide amino acid that is found in the fungus Ochrobactrum anthropi. D-Leucine amide has been shown to catalyze the formation of tripeptides, such as d-alanine and d-tryptophan, from their monomers. The presence of this compound enhances the expression of genes encoding proteins involved in the synthesis of these amino acids. This compound also has been shown to enhance gene analysis by increasing the stability of DNA and RNA molecules.</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>Deshydroxy bicalutamide is a ligand that has been synthesized to bind to the androgen receptor. It is an antagonist of the androgen receptor. Deshydroxy bicalutamide has been shown to inhibit cancer cell growth in prostate cancer cell lines, which is due to its ability to bind and block the ligand-binding domain of the androgen receptor. Molecular modelling has shown that deshydroxy bicalutamide binds in the hydroxyl group region of the binding site, which blocks it from binding with other ligands such as testosterone. This may lead to decreased levels of testosterone in males, leading to decreased levels of androgens in prostate cancer cells.</p>

<p>N-Desmethyl loperamide is a prodrug of loperamide, which is a peripherally acting μ-opioid receptor agonist. It has been shown to be effective in reducing the uptake of radiation in wild-type mice. This drug also inhibits p-glycoprotein (p-gp), and has been shown to reduce the uptake of pyridinium ions and amide substrates. N-Desmethyl loperamide has been shown to have anticancer properties, including resistance to radiation, inhibition of tumor growth and metastasis, and induction of apoptosis, which may be due to its ability to inhibit cellular proliferation and induce cell death. The mechanism by which this drug functions is not yet clear but it may involve inhibition of the expression or function of p-gp or other efflux pumps in cells that are sensitive to these drugs.</p>

<p>5-Diazoimidazole-4-carboxamide is an inhibitor of energy metabolism. It was found that dacarbazine, a drug used to treat cancer, and 5-diazoimidazole-4-carboxamide form a reversible complex. The formation of this complex leads to the irreversible inhibition of cellular respiration and cell lysis. This drug has been shown to be effective against malignant melanoma cells in animals and can be used as a photoinitiator for polymerization. 5-Diazoimidazole-4-carboxamide has also been shown to have an inhibitory effect on blood pressure in animals.</p>

<p>4-(4-Aminophenoxy)(2-pyridyl)]-N-methylcarboxamide is a chemical compound that inhibits the growth of cancer cells by binding to the active site of b-raf and blocking its activity. It has been shown in a pharmacokinetics study that 4-(4-aminophenoxy)(2-pyridyl)]-N-methylcarboxamide is absorbed rapidly through the oral administration, excreted in urine, and eliminated rapidly from the body. The optimal reaction for this drug was found to be at pH 7.0 with an ionic strength of 0.1 M (sodium chloride). This drug also has significant inhibitory activities against human cervical carcinoma and breast cancer cell lines (MDA-MB-231).</p>

<p>Benzenesulphonamide is a biologically active compound that has been shown to bind to an integrin receptor, which mediates the attachment of leukocytes to the endothelium. It also binds to a basic protein found in human immunoglobulin. Benzenesulphonamide has been shown to have cytotoxic effects on synchronous fluorescence cells and can be used for the treatment of bowel disease. This drug has also been shown to be toxic in vitro and in vivo, with a moderate acute oral toxicity and low chronic oral toxicity. Benzenesulphonamide has been shown to act as a surfactant by binding with sodium dodecyl sulfate (SDS), which is commonly used in detergents, disinfectants, shampoos, soaps, and other household products. The biological properties of benzenesulphonamide are not well-known due to its low solubility in water.</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>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-Cyano-N-cyclohexyl-N-methylacetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Lacosamide is an antiepileptic drug that has been shown to be bioequivalent to the reference product, Gabapentin. Lacosamide binds to voltage-gated sodium channels and is thought to have a similar clinical profile as Gabapentin. It is used in the treatment of partial seizures (with or without secondary generalization) and adjunctive therapy for generalized seizures in adults and children aged 2 years or older. Lacosamide can interact with other drugs, such as gabapentin, by increasing their serum concentrations. This interaction may lead to adverse effects such as dizziness and confusion. Lacosamide plasma concentrations are measured using LC-MS/MS methods after a two-way crossover study in healthy human volunteers. This study also showed that lacosamide is excreted unchanged in urine samples at a rate of about 50% over 24 hours, indicating that it does not undergo extensive metabolism in humans.</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>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>

<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-(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 N-(tert-Butoxycarbonyl)glycine N'-methoxy-N'-methylamide 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>Please enquire for more information about Tridecafluoro-N-(2-Hydroxyethyl)-N-Methylhexanesulphonamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>Acetyl-L-alanine methyl amide is a pharmaceutical drug that is structurally similar to L-lysine. It has been synthesized as a model system for the study of receptor binding and intracellular signaling. Acetyl-L-alanine methyl amide has shown to be reactive and can form intramolecular hydrogen bonds with other molecules in the cell. This drug also reacts with microglia cells, which are responsible for clearing out dead cells and debris in the brain. Acetyl-L-alanine methyl amide is a proton donor, which may cause steric interactions with lysine residues on proteins due to their proximity within the cell. This drug also has an intermolecular hydrogen bond between its two molecules that could lead to an α subunit conformational change within the protein.</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>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>