Amides

<p>M04120 - 4-Methylumbelliferyl N-acetyl-beta-D-galactosaminide</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>L-Histidine beta-naphthylamide is an allosteric activator of the imidazole group of histidine. It has been shown to regulate sequences and functional groups in subtilisin. L-Histidine beta-naphthylamide binds to the benzyl ester and regulatory allosteric site on the enzyme, which is located between the active site and the substrate binding site. The binding of this molecule stabilizes a transition state intermediate that would otherwise be too reactive to form products.</p>

<p>Please enquire for more information about 1-Methylindole-3-acetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Methyl-4-nitro-3-propylpyrazole-5-carboxamide is an impurity of sildenafil, which is used as a treatment for erectile dysfunction. It has been found in the environment due to its widespread use and it can be detected using chromatographic methods. 1-Methyl-4-nitro-3-propylpyrazole-5-carboxamide binds to thiol groups and may cause male infertility in animals. The detection time for this compound ranges from 2 hours to 24 hours, depending on the detection method. This impurity also has fluorescence properties that can be detected with UV light.</p>

<p>Please enquire for more information about N-((3,4-dimethoxyphenyl)methyl)(3-(2-chlorophenyl)-5-methylisoxazol-4-yl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-[2-(2,3-Dimethoxyphenyl)ethyl]-2-chlorobenzamide is a versatile building block that can be used as a reaction component and reagent. It is an intermediate in the synthesis of pharmaceuticals and fine chemicals and has been shown to be useful in the synthesis of complex compounds. This compound reacts with nucleophiles, such as amines and alcohols, by replacing the chloride group with a variety of functional groups. The product is then hydrolyzed to release the original reactant. N-[2-(2,3-Dimethoxyphenyl)ethyl]-2-chlorobenzamide has a CAS number of 320576-19-0 and can be found at ChemDiv.com.</p>

<p>Veratramide is a levorotatory, vanillic acid that has been synthesized by hydrolysis of esomeprazole. It is an ester of vanillic acid and hydrochloric acid. The cis-isomer is the more active form. Veratramide has been shown to be a prodrug for cisplatin, which is used in the treatment of cancer. Veratramide can also be metabolized to acetyl derivatives or flavonoids such as vitexin and metformin hydrochloride, which have anti-diabetic effects. Veratramide also binds to chloride ion channels, hypervalent ions (e.g., AlCl3), and quaternary ammonium salts (e.g., tetraethylammonium chloride).</p>

<p>Please enquire for more information about 13,4-diaza-5-(tert-butyl)-2-hydroxy-7-oxotricyclo[6.4.0.0&lt;2,6&gt;]dodeca-1(8),4,9,11-tetraene-3-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-[Ethyl-[2-(3-hydroxy-2,6-dimethyl-anilino)-2-oxo-ethyl]amino]-N-(3-hydroxy-2,6-dimethylphenyl)acetamide is a reaction component that is used in the synthesis of complex compounds. It is a versatile building block and useful intermediate for the synthesis of fine chemicals. This chemical has been shown to be an effective reagent for the preparation of high quality research chemicals. CAS No. 2200280-96-0</p>

<p>3,5-Dinitrobenzamide is a sulfa drug that inhibits the growth of bacteria by inhibiting 3-dehydroquinate synthase (EC 4.2.1.23) and 3-dehydroquinate dehydratase (EC 4.2.1.46). The enzyme catalyzes the conversion of 3-dehydroquinic acid to quinic acid, which is an intermediate in the biosynthesis of benzoic acid from glucose. This inhibition occurs because 3,5-dinitrobenzamide forms a glycosidic bond with Cys34 in these enzymes, which prevents their function. This drug has been shown to have significant cytotoxicity against human pathogens and model organisms such as Salmonella typhimurium and Escherichia coli, but not against Saccharomyces cerevisiae or Candida albicans.</p>

<p>N,N'-Dimethyl-3,3'-dithiodipropionamide (DTDPA) is a strong oxidizing agent that is used as a catalyst in organic synthesis. It can be used to convert xylene and benzene into products that are less toxic and more easily removed from the environment. DTDPA can also be used to remove 2-methyl-4-isothiazolin-3-one, chloroform, and other pollutants from water. DTDPA has been shown to react with hydrogen peroxide or hydrochloric acid to produce oxygen gas and chlorine, which is an effective disinfectant against bacteria such as Staphylococcus aureus or Pseudomonas aeruginosa. This chemical also reacts with toluene or chloroform to produce peroxides which have been shown to have an anti-inflammatory effect on cells.</p>

<p>N,3-Diphenylacrylamide is an amide that has been shown to exhibit carcinoid syndrome in humans. It also inhibits the growth of some human pathogens, including viruses and bacteria, as well as some fungi. The compound is metabolized by a number of enzymes and can be found circulating in the blood. Magnetic resonance spectroscopy has been used to study the structure of this molecule, which is composed of a carbonyl group and hydrogen bond. The effective dose for N,3-Diphenylacrylamide is not known.</p>

<p>3,5-Dihydroxybenzamide is an amide derivative that has anticancer activity. This compound inhibits the growth of C. glabrata by inhibiting protein synthesis in the mitochondria and DNA replication in the nucleus. 3,5-Dihydroxybenzamide also inhibits the growth of cancer cells by binding to a molecule that is involved in cancer cell proliferation. The inhibitor molecule binds to a specific site on the molecule, preventing it from forming new cancer cells. The mechanism of action for this compound is not known, but may be due to its ability to bind with chloride ions or its ability to form supramolecular chemistry with other molecules.</p>

<p>5-Benzyloxyindole-3-glyoxylamide is a versatile building block that can be used in the synthesis of complex compounds. It has been shown to have a high quality and is useful as a reagent for research purposes. 5-Benzyloxyindole-3-glyoxylamide can be used as a reaction component and is useful as an intermediate in organic synthesis. 5BIGA has CAS number 22424-62-0 and is also known as 3-(benzyloxy)-5-(2,2,2-trifluoroethoxy)indole glyoxamide.</p>

<p>N-[1-[2-(4-Ethyl-5-Oxotetrazol-1-Yl)Ethyl]-4-Phenylpiperidin-4-Yl]-N-(2-Fluorophenyl)Propanamide is a drug that is used clinically for the treatment of depression. It is an analog of amitriptyline, an antidepressant and a tricyclic compound. N-[1-[2-(4-Ethyl-5-Oxotetrazol-1-Yl)Ethyl]-4-Phenylpiperidin-4-Yl]-N-(2-Fluorophenyl)Propanamide has been shown to increase the concentration of plasma drug levels by increasing transporter gene expression in muscle tissue. This drug also has clinical pharmacology and thermal expansion properties.</p>

<p>Cinnamamide is a natural compound that is structurally related to the amino acid lysine and has been shown to regulate skin cell proliferation. Cinnamamide has also been found to be an effective inhibitor of the mitochondrial membrane potential in human erythrocytes. It has been shown to inhibit the production of reactive oxygen species (ROS) and reverse oxidative damage in cells, which may reduce the risk of developing autoimmune diseases. Cinnamamide is also able to prevent cell death caused by epidermal growth factor (EGF) withdrawal and induce apoptosis in HL-60 cells.</p>

<p>(E)-N-(2-Chloro-6-methylphenyl)-3-ethoxyacrylamide is a reagent and research chemical that can be used as a building block in the synthesis of other compounds. It is also a versatile building block in organic chemistry. (E)-N-(2-Chloro-6-methylphenyl)-3-ethoxyacrylamide has been shown to be an effective intermediate for the synthesis of various complex compounds, such as pharmaceuticals and pesticides. This compound is also a useful scaffold for the synthesis of other fine chemicals.</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>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>L-Lysine amide dihydrochloride is a crystalline compound that is used for the treatment of tumours. It has been shown to bind to the enzyme iridoid synthase, which is involved in the formation of imines and aldehydes. L-Lysine amide dihydrochloride also inhibits the production of staining compounds, such as fluorine and heterocycles. The compound may also be used cosmetically as an anti-aging agent because it can inhibit the production of collagenase and elastase, which cause degradation of collagen.</p>

<p>4-(Chloromethyl)benzamide is a potent inhibitor of cyclohexane ring formation in proteins and has been shown to be effective against bacteria, fungi, and parasites. 4-(Chloromethyl)benzamide inhibits the synthesis of proteins by targeting the active site of piperazine synthase, an enzyme involved in the production of piperazine. The carbon nanotube linker is a novel molecule that can be used for the attachment of the 4-(chloromethyl)benzamide molecule to cetirizine. In addition, 4-(chloromethyl)benzamide has been shown to have an effective dose at 0.1 μM and a half-life time of 2 hours in rats.</p>

<p>2-Amino-5-chlorobenzenesulfonamide is a synthetic chemical that is used in the manufacture of amides and diazoxide. It is also found naturally in humans as a metabolite of the amino acid histidine. 2-Amino-5-chlorobenzenesulfonamide has been shown to be a potent receptor for the modulation of acetylcholine release by binding to muscarinic receptors, including M1 and M2 subtypes, and inhibiting the enzyme hydrolysis of acetylcholine. This chemical has been shown to be chemically stable at pH 5 or higher, and it has been found to be resistant to hydrolysis by enzymes such as esterases, glucuronidases, glutathione reductase, and cytochrome P450. 2-Amino-5-chlorobenzenesulfonamide is also an enantiomer that can bind to collagen in the human</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>2-Cyanoacetamide is an organic compound that is used in pharmaceutical preparations. It reacts with malonic acid to form a dioxime, which is a precursor of various drugs. The optimum concentration for the reaction to occur is at 10% (w/v). The reaction mechanism has not been fully elucidated and it involves the transfer of nitrogen from an amide group to a carbonyl group. 2-Cyanoacetamide has shown anti-angiogenic effects in mice by inhibiting the expression of Mcl-1 protein, which is involved in the regulation of apoptosis and inflammation. This drug also has biological functions as a precursor for dopamine, which helps regulate motor and cognitive functions.</p>

<p>Indole-3-glyoxylamide is a synthetic compound that was originally developed as a potential anti-cancer drug. It has been shown to inhibit glycogen synthase kinase 3 (GSK-3) and thereby reduce the production of proinflammatory cytokines in bowel disease. Indole-3-glyoxylamide also inhibits inflammatory bowel disease by inhibiting secretory phospholipase A2, which prevents the release of arachidonic acid from phospholipids. This synthesis is required for the production of prostaglandins and leukotrienes, which are involved in the inflammatory process. The compound has been shown to have immunomodulatory effects in chronic bronchitis, with an inhibitory effect on neutrophil chemotaxis, macrophage activity, and cytokine production. Indole-3-glyoxylamide has also been shown to be effective against cancer cells in vitro and in vivo animal models. It is metabolized through</p>

<p>N-(n-Butyl)thiophosphoric triamide is a triamide herbicide that inhibits the plant enzyme fatty acid synthase. It has been shown to inhibit the uptake of glycol ethers, such as glycol esters, into plants by acting on the glycol ester hydroxyl group. This chemical also inhibits the synthesis of fatty acids in plants and reduces lipid content in perennial ryegrass and solanum tuberosum. N-(n-Butyl)thiophosphoric triamide also inhibits nitrous oxide emissions from wastewater treatment plants.</p>

<p>a-[2-(Diisopropylamino)ethyl]-a-phenyl-2-pyridineacetamide is a hydrogen bond donor. It has been shown to have cytotoxicity in vitro, with parameters that can be used for accurate prediction of descriptors. These descriptors are informative and insightful, which can be used for regression analyses and linear regression methods. The pharmacokinetic properties of a-[2-(Diisopropylamino)ethyl]-a-phenyl-2-pyridineacetamide have been studied in humans and have shown linearity between dose and plasma concentration.</p>

<p>Please enquire for more information about N-(2-(3,4-dimethoxyphenyl)ethyl)(4-nitrophenyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>Metformin is an antidiabetic drug that is used to treat type 2 diabetes. It works by increasing insulin sensitivity and decreasing glucose production in the liver. Metformin does not cause low blood sugar in people with diabetes, but it can lower blood sugar in those without the condition. Metformin is available as metformin hydrochloride and has a molecular weight of 314.5 g/mol. Metformin is excreted primarily through the kidneys, with less than 10% of a dose being excreted unchanged in the urine. Excipients include acetonitrile, which is used as an organic solvent for liquid drug products; impurities may be present due to incomplete synthesis or purification processes; and animal studies are performed to assess safety and efficacy of drugs that may have adverse effects on humans.<br>Metformin has been shown to decrease blood sugar levels in animals through its antidiabetic potential, but there are no studies showing its effect on humans with type</p>

<p>This compound is a benzamide derivative that is oxidized by nature. It has been shown to undergo ring-opening in the presence of reducing agents, such as sodium borohydride, and yields 2-amino-4-chlorobenzaldehyde. This reaction system uses an efficient catalyst such as manganese dioxide to help speed up the rate of this reaction. The product of this reaction is then converted into a variety of isatins depending on the conditions used.</p>

<p>Please enquire for more information about 2-(((2,5-dimethoxyphenyl)sulfonyl)amino)benzamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Amino-4-chlorobenzamide is a chemical compound that has been shown to be an effective oxidant in biological systems. It is an oxidative condensation product of 4-chloro-2-nitrobenzoic acid and ammonium chloride, which is formed by the reaction of these two compounds at room temperature. The nature of the functional group on 2-amino-4-chlorobenzamide allows it to be used as a transition state analogue for the study of reactions involving amines and nitrates. This compound can also be used in experiments with isatins, due to its ability to react with ammonia hydroxide to form 2-amino-4,6 dichlorobenzamide.</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>N-alpha-[2,4-Dinitro-5-fluorophenyl]-L-valine amide is an acidic amino acid that is used as a reagent in organic synthesis. It has been shown to have amide and hydrogen bond properties. This compound has been shown to be involved in the biosynthesis of carboxylic acids and primary amino acids. It also absorbs UV light at 265 nm and can be used for determination of uv absorption using high performance liquid chromatography (HPLC).</p>

<p>N-Dechloroethyl cyclophosphamide is a metabolic inhibitor that is used in the treatment of cancer. It is classified as an alkylating agent and inhibits ribonucleotide reductase, which prevents the production of DNA, RNA, and protein. The chemical ionization technique has been used to measure the concentration of this compound in human liver and urine samples. N-Dechloroethyl cyclophosphamide can be analyzed using chromatography or mass spectrometry methods.</p>

<p>2-Amino-3-benzoylbenzeneacetamide is an ophthalmic drug that has significant cytotoxicity. It is used to treat inflammation of the retina and macula, as well as other diseases of the eye such as uveitis. 2-Amino-3-benzoylbenzeneacetamide is a nonsteroidal anti-inflammatory drug (NSAID) that inhibits prostaglandin synthesis by blocking cyclooxygenase. This agent has been shown to be effective in reducing pain and inflammation in animal models, but there are no studies on its side effects or analytical methods for detection. There are also no studies on the effectiveness of this drug for treating uveitis.</p>

<p>Inhibitor of carbonic anhydrase</p>