Amides

<p>Deacetamide linezolid phthalimide is a chemical compound that is used as an intermediate in the synthesis of a variety of pharmaceuticals. It has been shown to be useful for the production of a number of compounds, including antibiotics, anti-inflammatory agents, and anticancer drugs. The substance has been shown to be effective in the treatment of bacterial infections and was first discovered in research chemicals. This compound also has a high quality and is used as a reagent for chemical reactions.</p>

<p>Please enquire for more information about N-(2-Indol-3-ylethyl)(2-nitrophenyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>L-Alaninamide is a protonated amino acid that reacts with the bacterial cell membrane and causes it to rupture. L-Alaninamide is synthesized by hydrolysis of the ester bond between butyric acid and serine protease in the presence of immobilized d-alanine. The reaction is carried out at a pH of 5.5, and the release of pressor is observed. This reaction takes place in an aqueous solution containing fatty acids as solvents. The type strain of this amino acid is E. coli.</p>

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

<p>Xipamide is a dpp-iv inhibitor that functions by blocking the enzyme dipeptidyl peptidase IV (dpp-iv). Xipamide inhibits the production of proinflammatory cytokines such as tumor necrosis factor alpha (TNF-α) and interleukin 1 beta (IL-1β) in vitro. It is also effective against infectious diseases, including bacterial infections, respiratory tract infections, and skin infections. Xipamide has been shown to be safe for use in geriatric patients with congestive heart failure. The optimum concentration for xipamide is 0.4 μM. Xipamide has been used to study biological processes such as signal transduction, cell proliferation, and apoptosis in vitro. Optical sensor technology has been applied to examine the stability of this drug in human serum and its potential interactions with surfactant sodium dodecyl sulfate (SDS).</p>

<p>(E)-N-(3-Methylaminopropyl)-2-thiopheneacrylamide hydrochloride is a high quality, reagent, complex compound, useful intermediate, fine chemical. It has CAS No. 1449108-90-0 and is used as a research chemical and building block in the synthesis of other compounds. (E)-N-(3-Methylaminopropyl)-2-thiopheneacrylamide hydrochloride can be used as a versatile building block in organic synthesis reactions and is an important reaction component for the preparation of speciality chemicals.</p>

<p>N-[2-(1,3-Dimethylbutyl)phenyl]-5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide is an herbicide that belongs to the group of fatty acid amides. It is a selective postemergence herbicide that inhibits the germination and growth of plants by inhibiting the synthesis of fatty acids. Unlike other chemical pesticides, it has no effect on animals or humans and it is not toxic to plants. The selectivity of N-[2-(1,3-Dimethylbutyl)phenyl]-5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide makes it a good candidate for use in combination preparations with other chemicals.</p>

<p>4-Nitrobenzamide is a chemical substance that belongs to the class of nitrobenzamides. It is used as an intermediate in the synthesis of other substances, such as pharmaceuticals, herbicides, and pesticides. 4-Nitrobenzamide was first synthesized in 1894 by hydrogenating nitrobenzoic acid with hydrogen chloride in the presence of phosphorus pentachloride. The reaction vessel for this process should be made of glass or porcelain due to the corrosive nature of hydrogen chloride gas. The kinetics for this reaction were studied using concentration-response curves on rats and mice at different concentrations. Acute toxicities observed include respiratory distress and death in rats and convulsions and death in mice.<br>4-Nitrobenzamide is also toxic to bacteria, which can be seen by its effect on Staphylococcus aureus (strain ATCC 25923). This strain had a 50% survival rate after exposure</p>

<p>2-[(2,6-Dichlorophenyl)amino]-N,N-dimethylbenzeneacetamide is a reagent, complex compound and useful intermediate with a CAS number of 21789-06-0. It is a fine chemical that can be used as a building block in the synthesis of other compounds. It has been shown to be useful in the production of speciality chemicals and research chemicals. The versatility of this compound makes it an excellent scaffold for the synthesis of other compounds. This product is not intended for human or animal use.</p>

<p>2,2,2-Trifluoro-N-(4-piperidinyl)acetamide (TFAPA) is a nucleic acid analog that binds to the target nucleic acid. TFAPA is a morpholino compound with an amide linkage between the morpholine ring and the acetic acid group. TFAPA is a sequence-specific DNA analog that inhibits protein synthesis by binding to the target nucleic acid. TFAPA can also be used as a probe for the detection of abnormal sequences in RNA.</p>

<p>1H-Imidazole-4,5-dicarboxamide is a detergent composition that contains antimicrobial agents. It has been shown to inhibit the growth of resistant mutants in vitro and is active against a broad spectrum of bacteria. Hydrogen bonding interactions between 1H-imidazole-4,5-dicarboxamide and the amide group on the cell membrane surface are thought to be responsible for its activity. This compound also inhibits nuclear DNA synthesis by binding to the enzyme topoisomerase II, which is necessary for DNA replication. The molecular weight of 1H-imidazole-4,5-dicarboxamide makes it useful as an analytical reagent in gas chromatography.</p>

<p>2-Phenyl-N-(phenylsulfonyl)acetamide is a fine chemical, useful intermediate and research chemicals. It has a CAS number of 92200-24-3. This compound can be used as a versatile building block in the synthesis of complex compounds with high quality and purity. 2-Phenyl-N-(phenylsulfonyl)acetamide can also be used as a reaction component in the synthesis of speciality chemicals or as a reagent.</p>

<p>4-Methoxybenzenecarbothioamide is a urea nitrogen analogue that inhibits the synthesis of urea and other nitrogenous compounds. It is an inhibitor of the enzyme pyruvic transaminase, which converts pyruvate to alanine. The drug is also an inhibitor of the enzyme lactam synthetase, which catalyzes the formation of lactams from amino acids. This activity results in decreased production of cancer cells and renal toxicity. 4-Methoxybenzenecarbothioamide has been shown to have anticancer activity in vitro against a number of human cancer cell lines, including A549 lung carcinoma cells and MCF-7 breast cancer cells.</p>

<p>2,2-diphenyl-N,N-dimethylpropeneamide (DPPA) is a disulfide compound that has photolytic, thermolytic and modelling properties. DPPA can be used to produce alkylcobalt complexes with various substituents at the α position of the phenyl ring. The lactam structure of DPPA has been shown to undergo thermolysis at temperatures of 250°C in a vacuum. Cinnamic acids have been shown to form lactams with DPPA as well as cinnamic acid derivatives. Molecular modelling studies have been conducted on 2,2-diphenyl-N,N-dimethylpropeneamide and its molecular interactions with styrene and amido groups.</p>

<p>2-Chloro-N,N-diphenylacetamide is a functional theory that has been shown to have antimicrobial activity against mammalian cells. It is an acetamide derivative with a formyl group and two chloro substituents. 2-Chloro-N,N-diphenylacetamide inhibits the growth of Mycobacterium tuberculosis by binding to the ribosomal protein P0, which inhibits the production of proteins vital for cell division. This drug also has antifungal properties, inhibiting the synthesis of ergosterol in filamentous fungi such as Candida albicans.<br>2-Chloro-N,N-diphenylacetamide is also known to inhibit the growth of other bacteria by binding to their ribosomes and interfering with protein synthesis. This drug may also be active against viruses due to its ability to bind chloride ions.</p>

<p>This compound is a recyclable, multicomponent, element analysis, element, diversity and catalyzed reaction that yields high purity products with high yields. The catalyst is reusable and the NMR data are reproducible.</p>

<p>Malonamide is a natural product with biological properties that include anti-inflammatory activity. It is a receptor antagonist that binds to the nicotinic acetylcholine receptors and blocks the binding of acetylcholine, thereby inhibiting muscle contraction. Malonamide has been shown to have good chemical stability and phosphorus pentoxide tolerance. This compound also has high steric interactions with halogens, which allows it to act as an effective antiseptic agent for wounds or skin infections caused by bacteria such as Staphylococcus aureus or Pseudomonas aeruginosa. Malonamide has been shown to be active against both Gram-positive and Gram-negative bacteria, including methicillin resistant strains. Malonamide binds to copper ions and forms an intramolecular hydrogen bond with the nitrogen atoms in the molecule. This interaction stabilizes its conformation and leads to increased chemical stability in comparison with other nitrogen containing drugs.</p>

<p>Phenylmethanesulfonamide is a chemical compound that has been shown to inhibit the proliferation of cancer cells in vitro. This drug has also been shown to be effective in reducing inflammatory diseases, such as arthritis and asthma, which may be due to its ability to inhibit prostaglandin synthesis. Phenylmethanesulfonamide has shown anti-inflammatory properties, which may be due to its inhibition of prostaglandin synthesis.</p>

<p>3-Cyanobenzamide is an organic compound with the formula CHC(N)NH. It is a white crystalline solid that can be obtained by reacting benzamide with cyanoacetylene. There are three possible isomers of 3-cyanobenzamide: 3-cyano-1-(substituted phenyl)benzamide, 3-cyano-2-(substituted phenyl)benzamide, and 3-cyano-3-(substituted phenyl)benzamide. The optimal reaction conditions for the synthesis of 3-cyanobenzamide are in the presence of hydrogen bonding, such as n-hexane, amide, and phase equilibrium. Studies have determined that 3-cyanobenzamide has the potential to cause cancer or liver toxicity in humans. In addition, this chemical has been shown to be an effective inhibitor of alpha glucosidase enzymes in vitro and in vivo.</p>

<p>Glycine amide acetate is a product that contains an imine group. It has been shown to have staining properties when applied to human keratin and is used in the cosmetic industry as a depigmenting agent. Glycine amide acetate has been shown to be effective in the treatment of depression, although it is not yet approved for this use. The molecule also contains an iridoid compound, which may be responsible for its effects on mood.</p>

<p>2,3-Diaminobenzamide is a synthetic aromatic compound that is used as a radiation stabilizer. It is also an effective antimicrobial agent with reactive properties against bacteria and fungi. 2,3-Diaminobenzamide has been shown to have anti-cancer properties and can be used to treat inflammatory diseases such as rheumatoid arthritis or ulcerative colitis. The intramolecular hydrogen bond between the amide group and the benzene ring in 2,3-diaminobenzamide contributes to its stability and biological activity.</p>

<p>2-Phenoxyacetamide is an acylating agent that reacts with a hydroxyl group by substitution to form an ester or amide. It is used in clinical studies to combat insulin resistance and metabolic disorders, such as cancer, inflammatory bowel disease, and diabetes. 2-Phenoxyacetamide has been shown to be effective against a number of bacterial species, including Pseudomonas aeruginosa and Cryptococcus neoformans. The drug also inhibits the production of monoamine neurotransmitters in the brain and has been shown to have anti-inflammatory properties.</p>

<p>N-(3-Hydroxypropyl)trifluoroacetamide is an alkaline hydrolysis product of 3-hydroxypropyl trifluoroacetate. It is a primary amino compound that can be used as an intermediate in the production of vinyl ethers and acetals. This chemical is used for the synthesis of vinyl acetals, which are important intermediates in the manufacturing of polymers.</p>

<p>5-Iodosalicylamide is a chemical building block. 5-Iodosalicylamide can be reacted with appropriately functionalised aromatic compounds to afford the corresponding anilides, which have been shown to exhibit anti-fungal and bactericidal properties.</p>

<p>Please enquire for more information about N-(5,5-dimethyl-7-oxo(4,5,6-trihydrobenzothiazol-2-yl))(4-methoxyphenyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>L-Pyroglutamic acid-beta-naphthylamide is a cell nucleus pressor that has been shown to stimulate locomotor activity in rats. It is a highly selective agonist at the 5-HT2 receptor, which is involved in the regulation of energy metabolism and feeding behaviour. L-Pyroglutamic acid-beta-naphthylamide also stimulates cholinergic and serotonergic systems. This drug also inhibits bacterial growth by binding to the receptor site on bacterial cell nuclei, thereby preventing DNA synthesis and locomotor activity. L-Pyroglutamic acid-beta-naphthylamide is an antimicrobial agent that can be used to treat infections caused by bacteria resistant to erythromycin. The antimicrobial effect of this drug is due to its ability to bind to the receptor site on bacterial cell nuclei, thereby preventing DNA synthesis and locomotor activity.</p>

<p>N-(5-Cyano-2-chlorophenyl)acetamide is a high quality, reagent, and versatile building block. It is a fine chemical that can be used as a building block for the synthesis of other compounds. N-(5-Cyano-2-chlorophenyl)acetamide is also a speciality chemical that can be used in research or as a reaction component. It has been found to be useful as an intermediate in the synthesis of complex compounds.<br>END&gt;</p>

<p>N-[2-(p-Cinnamylamino)ethyl]-5-isoquinolone sulfonamide is a high quality chemical that can be used as a reagent, complex compound, and useful intermediate. N-[2-(p-Cinnamylamino)ethyl]-5-isoquinolone sulfonamide is a fine chemical that is useful in the production of speciality chemicals. It can be used as a versatile building block and reaction component to produce various compounds.</p>

<p>N-(2,6-Dimethylphenyl)-1-piperazineacetamide is a byproduct of solvents and stabilizers. It has been found to be a crystalline solid with a molecular weight of 233.3 g/mol. The crystal structure was determined and found to be composed of two molecules of acetamide that are connected through hydrogen bonds. N-(2,6-Dimethylphenyl)-1-piperazineacetamide is soluble in ethanol and ether, but insoluble in water. This compound interacts with other substances, such as recrystallizing or substituting acetamides.</p>

<p>4-Amino-N-benzylbenzamide is a high quality chemical that is an intermediate in the synthesis of other useful compounds. It is a reagent for organic synthesis, and has many uses as a complex compound, as well as being a useful building block for more complicated molecules. 4-Amino-N-benzylbenzamide is also used as a speciality chemical in research labs, and can be used as a versatile building block to make different products.</p>

<p>The drug 4-Amino-5-chloro-2,3-dihydro-N-[1-(3-methoxypropyl)-4-piperidinyl]-7-benzofurancarboxamide (BZP) is a histamine H2 receptor antagonist. It binds to the histamine H2 receptor in the stomach and duodenum, thereby blocking stomach acid production. BZP has been shown to be effective for treating symptoms of constipation or diarrhoea caused by inflammatory bowel disease or abdominal surgery. BZP also reduces the risk of relapse after surgery but does not affect long term efficacy. This drug is not available in the United States and has significant interactions with other drugs and symptoms including constipation, bowel disease, long term efficacy, and analytical method.</p>

<p>4-Nitrobenzenesulfonamide is an organic compound that consists of a nitro group, a sulfonamide group, and an amine. It is the active analog of 4-dimethylaminobenzoic acid, which is used as an inhibitor of histamine release in the treatment of allergic reactions. The molecule has been shown to bind to copper ions and triflic acid and has been used as a catalyst for aziridination.</p>

<p>3-(4-Hydroxyphenyl)propionamide is a heparinoid that is found in exudates, such as urine and saliva. It has significant cytotoxicity against the cell line Hepg2. 3-(4-Hydroxyphenyl)propionamide inhibits protein synthesis by binding to lectins and stabilizing them on the surface of the cells. This stabilizing effect blocks the lectin-carbohydrate interaction that leads to cellular activation and inflammation. 3-(4-Hydroxyphenyl)propionamide also has an anti-aging effect, which may be due to its ability to enhance chloride ion flow in biological tissues.</p>

<p>2N-Boc-2',2''-triaminotriethylamine-bis(chloroacetamide) is a fine chemical and reagent for the synthesis of pharmaceuticals. It is also a useful building block for the synthesis of complex compounds. This product can be used as a reaction component in organic chemistry, or it can be used as a reagent in research or development laboratories.</p>

<p>Please enquire for more information about Pigment YellOw 5;2-[(2-NitrOphenyl)azO]-3-OxO-N-phenylbutanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>The Val-Cit-PAB linker is an activated peptide linker that is cleaved by cathepsin B. It enables the selective intracellular release of attached drugs in ADC applications.</p>

<p>3-Nitro-4-methoxybenzamide is a versatile building block that belongs to the group of fine chemicals. It is a reagent that is used in the synthesis of complex compounds. 3-Nitro-4-methoxybenzamide has been shown to be an effective intermediate for the synthesis of pharmaceuticals, such as antibiotics and immunosuppressants. This compound also has high quality and can be used as a scaffold for other chemical syntheses.</p>

<p>Hexadecanamide is a reactive amide that has an optimum concentration of 1.5-2.0 M in water and a pH range of 3.0-8.0. Hexadecanamide is oxidized by an oxidation catalyst to form hexadecane, which can be analyzed by gas chromatography or high performance liquid chromatography. The oxidation reaction can be monitored under constant pressure conditions using electrochemical impedance spectroscopy. Hexadecanamide reacts with hydroxyl groups and fatty acids to form hexadecanoic acid, which can be analyzed using gas chromatography or high performance liquid chromatography. Hexadecanamide also reacts with viral life to form hexadecanoic acid, which can be analyzed using gas chromatography or high performance liquid chromatography.<br>Hexadecanamide has been shown to have anti-inflammatory properties, which may be due to its ability to inhibit the production of pro-inflammatory cytokines such as histamine and leukotrienes</p>

<p>Hydroxy tolbutamide is a drug with an unknown mechanism of action. It has been shown to inhibit the transcription-polymerase chain reaction and human serum in vitro. This drug may be used as a marker for renal disease, as it has been shown to increase the level of magnesium in urine and reduce the rate of protein synthesis in rat liver microsomes. Hydroxy tolbutamide also inhibits receptor activity, which may be due to its ability to inhibit the metabolic rate.</p>

<p>N-Allyl-N-(4-cyano-2-chlorophenyl)acetamide is a high quality reagent that has been used as an intermediate in the synthesis of fine chemicals, useful scaffolds and building blocks. It is also a versatile building block that can be used to synthesize high quality compounds with a wide range of functionalities. N-Allyl-N-(4-cyano-2-chlorophenyl)acetamide is a speciality chemical that can be used for research purposes. This compound has been shown to produce reactions with other compounds, such as nitrobenzene, to generate useful products.</p>

<p>Homoveratramide is a synthetic drug that is used as an antibacterial agent. It has a broad spectrum of activity against bacteria, fungi, and protozoa. Homoveratramide has been shown to be effective against both Gram-positive and Gram-negative bacteria, including Staphylococcus aureus, Streptococcus pneumoniae, Escherichia coli, Salmonella enterica, Pseudomonas aeruginosa, and Klebsiella pneumoniae. Homoveratramide inhibits the synthesis of DNA by binding to the enzyme ribonucleotide reductase. This produces a bacteriostatic effect on the cell by halting DNA replication and transcription.</p>

<p>1-(Aminomethyl)cyclopropanecarboxamide hydrochloride is a versatile building block that can be used in the synthesis of complex compounds. It has been shown to be an excellent reagent for the synthesis of novel pharmaceuticals and speciality chemicals. This compound is also a useful intermediate for the preparation of high-quality products and can be used as a reaction component or scaffold in synthesis.</p>

<p>Clorsulon is an anthelmintic drug that belongs to the group of benzimidazoles. It is used in veterinary medicine to treat nematode and cestode infections, as well as tapeworm infections. Clorsulon is a dispersive solid-phase extraction (DSPE) extractant that can be used for the separation of drugs and their metabolites from biological fluids. The chemical stability of clorsulon was assessed by exposing it to various solvents and pHs. Clorsulon was found to be stable in acetate, benzene, chloroform, ethyl acetate, ethanol, methanol, and water at pH 1-14 and a variety of temperatures ranging from -20 ˚C to 50 ˚C. No significant loss or degradation occurred after exposure to these conditions for up to 24 hours.</p>

<p>Morpholine-4-carboxamide is a polymerase chain inhibitor that inhibits the activity of DNA polymerases. It binds to the DNA template strand and prevents the enzyme from adding nucleotides to the primer strand, thereby inhibiting DNA synthesis. Morpholine-4-carboxamide has shown efficacy in treating hyperproliferative diseases such as cancer cells and psoriasis. This drug has been shown to inhibit caspase activation and histone protein acetylation, which may be related to its anti-cancer properties. Morpholine-4-carboxamide also binds to cannabinoid receptor 2 (CB2) and may have therapeutic effects on inflammatory diseases such as psoriasis and arthritis.</p>

<p>Pantethine is a dietary supplement, which is a derivative of pantothenic acid, sourced from vitamin B5. As a biologically active compound, it undergoes conversion to pantetheine, which then forms coenzyme A (CoA) and acyl-carrier proteins. This conversion is critical, as CoA is an essential cofactor involved in numerous biochemical reactions that are integral to fatty acid metabolism, among other processes.</p>

<p>N-Isopropylacrylamide is a biocompatible polymer that is used in the preparation of polymers. It is a solid phase microextraction material that is used in sample preparation and purification. N-Isopropylacrylamide has a phase transition temperature of -5°C and can be polymerized to form a polymer. This polymerization process can be done with or without catalysts, which are required for the formation of many other types of polymers. N-Isopropylacrylamide has been shown to have good affinity for human serum and wastewater treatment effluent samples, as well as for chitosan polymer surfaces. The kinetic data show that this polymer possesses high capacity for trifluoroacetic acid (TFA) reactivity, which makes it suitable for use in reaction solutions.</p>

<p>Please enquire for more information about L-Leucine b-naphthylamide hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N,N'-Dimethyl benzamide (DMAB) is an aryl halide that reacts with hydrogen to form the corresponding carbonyl group. The reaction solution of DMAB and hydrogen gas produces a chemical structure that resembles a hydrogen bond. DMAB has been shown to have anti-inflammatory effects in animals with inflammatory diseases. It has also been studied for its ability to inhibit the formation of amyloid plaque, which is associated with Alzheimer's disease. In addition, DMAB has been shown to have therapeutic effects against boron nitride and amides.<br>The crystal structure of DMAB can be found in both crystalline polymorphs: monoclinic and triclinic. The triclinic form is stable at room temperature and pressure, while the monoclinic form is only stable at higher temperatures. The monoclinic form is more soluble than the triclinic form, as it contains fewer hydrogen bonds between</p>

<p>2-Piperazin-1-ylacetamide hydrochloride is a drug that binds to the protein PCSK9, which transports cholesterol into cells. It blocks the transport of cholesterol and therefore lowers the level of cholesterol in blood. 2-Piperazin-1-ylacetamide hydrochloride is used for the treatment of bowel disease, atrial fibrillation (a type of irregular heartbeat), congestive heart failure, and as an anti-viral agent. This drug has been shown to reduce levels of LDL cholesterol by up to 60%. 2-Piperazin-1-ylacetamide hydrochloride has also been shown to be effective against cancers such as prostate cancer and inflammatory bowel disease.</p>

<p>Picotamide is a drug that belongs to the class of drugs that inhibit platelet aggregation. This drug is used in the treatment of coronary artery disease and other cardiovascular diseases. Picotamide has been shown to have pharmacological effects on the heart, such as lowering blood pressure and reducing heart rate. It also has a covalent linkage with proteins, which may be due to its ability to activate receptors for biological properties like cell proliferation or differentiation. Picotamide has been shown to prevent infectious diseases, such as septicemia, by inhibiting bacterial growth. The chemical stability of picotamide makes it an attractive candidate for use in gene therapy because it can be stored at room temperature without losing its activity.</p>