Amides

2-Chloro-N-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)acetamide (CPA) is a chemical compound that belongs to the class of phenyl pyrazoles. It has a thermal stability and is soluble in organic solvents. CPA crystallizes in the monoclinic system with the space group P21/c, with the following unit cell parameters: a = 8.943(4) Å, b = 7.878(3) Å, c = 17.834(6) Å, α = 90°, β = 112° and γ = 90°. In this crystal structure, there are two molecules of chloride per molecule of CPA. The crystal x ray diffraction pattern showed that this compound forms dimers in solution at room temperature and can be dissolved

<p>Trifluoromethanesulfonamide is a strong acid that has been shown to inhibit the proteolytic activity of human secretase. It binds to a specific site on the enzyme and prevents it from cleaving the substrate. This inhibition slows down the progression of Alzheimer's disease, Parkinson's disease, and other related disorders. Trifluoromethanesulfonamide has also been shown to bind to metal hydroxides, such as iron hydroxide, which may be due to its ability to form hydrogen bonds with these metals. Structural analysis reveals that trifluoromethanesulfonamide contains a pyrazole ring and two chlorine atoms, one in the para position and one in the meta position.</p>

2-Hydroxy-N-(1-phenylpropan-2-yl)acetamide is a versatile building block that can be used as a reagent or research chemical. This compound is an intermediate in the synthesis of many other organic compounds and has been shown to be useful for the production of pharmaceuticals, agrochemicals, and other industrial chemicals. The CAS number for this compound is 99985-83-8.

<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>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>3-Chlorobenzamide is an analytical reagent that is used for the separation and purification of organic compounds. It has been shown to be a catalyst for the reaction system in the dehydration of amides, amido, and halides. 3-Chlorobenzamide has also been suggested as a possible environmental pollutant due to its catalytic properties and ability to react with monoxide. The correlations between 3-chlorobenzamide concentrations in air and soil have also been studied extensively.</p>

<p>1H-Imidazole-2-carboxamide is a purine derivative that can inhibit the activity of certain molecules. It has been shown to have an inhibitory effect on the metabolism of fatty acids and metabolism disorders, as well as the physiological effects of insulin resistance. The molecule also inhibits uptake and cross-linking in cells, which may be useful in treating cancer or other metabolic disorders.</p>

<p>2-Amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide is an anticancer agent that inhibits the synthesis of proteins required for cell division. It has been shown to have anticancer activity and efficacy in vitro studies against human cancer cells, such as HCT116. This compound also induces apoptosis in infected cells by binding to viral particles and inducing the release of chloride ions. 2-Amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide has been found to be effective against influenza virus and particle production by inhibiting neuraminidase activity.</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>N-[(8-Fluoro-2,3-Dihydro-1-Methyl-5-Phenyl-1H-1,4-Benzodiazepin-2-Yl)Methyl]-3-Furancarboxamide is a hydrophobic, implanting drug with an iontophoresis device. It has been shown to have therapeutic effects in cancer. The drug is a targetable molecule that can be used for diagnostic purposes and the treatment of various cancers. N-[(8-Fluoro-2,3-Dihydro-1,5 -Phenyl 1H -1,4 Benzodiazepin 2 Yl) Methyl] 3 Furancarboxamide has been shown to inhibit cell proliferation by blocking the synthesis of proteins required for DNA replication and also inhibits the activity of protein kinase C.</p>

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<p>N-(5-Bromoacetamidylpentyl) acrylamide is employed in the synthesis of substrates used for nucleotide sequence determination, covalently linked to polymer coatings such as poly(N-(5-azidoacetamidylpentyl)acrylamide-co-acrylamide) (PAZAM). Polynucleotide-binding substrates find application as molecular arrays and flow cells.</p>

Please enquire for more information about (3-(2,6-dichlorophenyl)-5-methylisoxazol-4-yl)-N-(2-indol-3-ylethyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

<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>

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<p>3-Amino-4-chlorobenzamide is an organic compound that belongs to the class of aminobenzoic acids and is used as a coupling agent in organic synthesis. It reacts with aryl halides or halides to form 3-amino-4-chlorobenzonitrile, which can be converted into anilines by heating with ammonia and ammonium chloride. This reaction has been shown to be reversible with heat. 3-Amino-4-chlorobenzamide is also used as a water absorber in paper products, such as diapers and sanitary napkins.</p>

<p>4-(Chloromethyl)-N,N-dimethylbenzamide is a versatile building block that can be used in the synthesis of various complex compounds. It is a versatile intermediate and can be used in reactions as a reagent or building block. 4-(Chloromethyl)-N,N-dimethylbenzamide is also a high-quality chemical with a CAS number of 121083-51-0. The compound has many applications, including being useful as a reaction component or scaffold for research chemicals and speciality chemicals.</p>

<p>Please enquire for more information about N-(2-Indol-3-ylethyl)(4-(trifluoromethoxy)phenyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>N-[6-Chloro-5-(2-methoxyphenoxy)-(2,2-bipyrimidine)4-4-yl]-(1,1-dimethylethyl)-benzenesulfonamide is a reagent that can be used as a reaction component in the synthesis of complex compounds. It has high quality and is a versatile building block for the synthesis of speciality chemicals. N-[6-Chloro-5-(2-methoxyphenoxy)-(2,2-bipyrimidine)4-4-yl]-(1,1-dimethylethyl)-benzenesulfonamide is also a useful intermediate in the synthesis of fine chemicals.</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>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>

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<p>3-(Bromomethyl)benzamide is a versatile building block that can be used in the synthesis of a variety of complex compounds. It is also useful as a research chemical and as a reagent. 3-(Bromomethyl)benzamide can be used to produce useful intermediates and reaction components. This compound has been shown to be useful as scaffolds for synthetic organic chemistry.</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>1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-heptadecafluoro-N-methyloctane-1-sulfonamide is a perfluorinated sulfonate that is used as a surfactant in wastewater treatment and to package food. This compound is not water soluble and requires an organic solvent to dissolve it. It has been shown that the use of 1HFAFMS can reduce the amount of phosphates in packaging materials by up to 50%. 1HFAFMS also has been found to be safe for humans and does not accumulate in the environment. It does not bioaccumulate and is rapidly excreted through urine.</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>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>

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<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>

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>Anthranilamide is used for non-selective, efficient fluorescent labelling of glycans.</p>

<p>This is a high quality reagent, complex compound, useful intermediate, and fine chemical. It is also a useful scaffold and can be used as a reaction component in the synthesis of speciality chemicals. The CAS number for this compound is 3873-79-8. <br>[[Category:Chemical Compounds]]</p>

<p>Please enquire for more information about (2-Aminophenyl)-N-((3,4-dimethoxyphenyl)methyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>4-Hydroxyphenylacetamide is a natural product that has been shown to have antibiotic properties. It inhibits the growth of bacteria by inhibiting the synthesis of p-hydroxybenzoic acid, which is an essential precursor for the biosynthesis of aromatic amino acids and other important compounds. 4-Hydroxyphenylacetamide also inhibits dopamine oxidation, which may lead to its anti-infective properties. The biological properties of 4-hydroxyphenylacetamide have been studied using electrochemical impedance spectroscopy (EIS) on bacterial strains and in vitro studies on P. aeruginosa. This compound is not metabolized by microorganisms and does not mineralize or react with oxygen at physiological pH levels. It can be used as a pharmaceutical dosage form for treatment of infectious diseases.</p>

<p>Hydroxyflutamide is an anti-androgen drug that belongs to the group of nonsteroidal anti-androgens. It has been shown to bind to the androgen receptor with high affinity and inhibit the growth of cancer cells in vitro. Hydroxyflutamide also has a strong antitumor response in vivo, which is due to its ability to inhibit cellular proliferation by binding to DNA polymerase during replication. The drug may also have some activity as an antineoplastic agent because it inhibits the growth of prostate cancer cells. However, hydroxyflutamide has never been tested on humans or animals, so its effects are unknown.</p>

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<p>Tenofovir alafenamide fumarate is a prodrug of tenofovir, an active antiretroviral agent. Tenofovir binds to the viral polymerase and blocks the synthesis of viral DNA. Tenofovir alafenamide fumarate is a prodrug that undergoes hydrolysis to form tenofovir. It has been shown to inhibit growth factor-β1, which may reduce the risk of opportunistic infections in people with HIV or AIDS. Tenofovir alafenamide fumarate has also been shown to be effective as an antiviral prophylaxis when used in combination with other drugs for active antiretroviral therapy.</p>

<p>2-Amino-N-methylbenzamide is a benzodiazepine receptor antagonist that has been shown to inhibit the proliferation of cancer cells in vitro. 2-Amino-N-methylbenzamide binds to the benzodiazepine receptor, which is found in cell nuclei and is involved in controlling the process of cell division. Benzodiazepines are a class of drugs that work by increasing the activity of GABA, which reduces neuronal excitability. 2-Amino-N-methylbenzamide prevents this activity by binding to the benzodiazepine receptor, preventing GABA from binding to its receptors and thereby inhibiting neuronal excitability. This drug has also been shown to inhibit cancer growth through an anthranilic acid derivative, methyl anthranilate. Methyl anthranilate inhibits DNA synthesis and induces apoptosis in cancer cells, leading to cell death.</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-[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>Coconut diethanolamide is a chemical substance that is used as a test compound in carcinogenesis studies. It is a fatty acid and a fatty alcohol, and it has been shown to promote the growth of cancer cells. Coconut diethanolamide has not been found to be an allergen, but it has shown carcinogenic potential. The bioassay for long-term exposure to coconut diethanolamide showed epidermal hyperplasia in mice.</p>

<p>Inducer of apoptosis; NF-κB activator; PP2A modulator</p>

<p>3-Bromobenzamide is an amide compound, which is a functional group. It has a molecular weight of 273.3 g/mol and three amine groups. The 3-methoxybenzamide moiety in the molecule can be protonated, which provides the hydration of the molecule and increases its solubility in water. This molecule also has a dipole moment due to the presence of two amide groups.<br>The synthesis of 3-bromobenzamide starts with the reaction between 3-aminobenzoic acid and benzoyl chloride to form 3-benzoyloxybenzoic acid. This is then reacted with ammonia to form 3-aminobenzamide. Finally this is converted into 3-bromobenzamide by reacting it with bromine in the presence of potassium carbonate as a catalyst. <br>This molecule is used as an inhibitory compound for mammalian cell proliferation, specifically for cancer cells</p>

<p>2-Methoxy-5-(2-oxopropyl)benzenesulfonamide is a metal catalyst that can be used in the synthesis of tamsulosin hydrochloride, an alpha blocker that is used to treat benign prostatic hyperplasia. It catalyzes the reaction between 2-methoxybenzenesulfonyl chloride and 3-amino-1,2,4-triazole. The industrial importance of this compound is due to its ability to be used as a catalyst for various chemical reactions.</p>

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<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>

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