Amides

<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>

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>Dopamine (D2) receptor antagonist</p>

Please enquire for more information about N-Ethyl-1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluoro-N-(2-hydroxyethyl)Hexane-1-sulfonamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

<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 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>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>N,N-Dimethyl-2-chloroacetamide is a chlorinated organic compound that has a reaction rate of 1.4 × 10^6. It is used as a treatment for acrylonitrile poisoning, and it is also used in the synthesis of thienopyridine and cetirizine. N,N-Dimethyl-2-chloroacetamide reacts with an amine to produce an amide; this reaction takes place in an organic solvent with a dicarboxylate, such as ethyl acetate or butyl acetate. This reaction produces a solution that is colorless to pale yellow. The time required for the reaction to complete depends on the concentration of reactants and the type of solvent used.</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>

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>Please enquire for more information about N-(2-Cyano-4-oxo-4H-1-benzopyran-8-yl)-4-(4-phenylbutoxy)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 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>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>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>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>Please enquire for more information about N-(p-Hydroxyphenethyl)-N-(3-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 (9Z)-N-[(3-Methoxyphenyl)methyl]-9-octadecenamide 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-L-isoleucineamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>6-Chloro-3,4-dihydro-3-(a-methylbenzyl)-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide is an active metabolite of the drug benzbromarone. It is primarily administered as a diuretic to treat high blood pressure and congestive heart failure. The pharmacodynamics of this drug are related to its ability to inhibit the activity of sodium channels in vascular smooth muscle cells and thereby reduce the force of contraction and relax the vessel wall. 6CBDMTD has shown an increase in glomerular filtration rate in patients with congestive heart failure. This drug also decreases the plasma concentration of fatty acids by inhibiting the formation of lipoprotein particles. 6CBDMTD has been shown to be effective at lowering diastolic and systolic blood pressure levels in patients with hypertension.</p>