Amides

<p>2,2,2-Trifluoroacetamide is a chemical compound that is stable under normal conditions and can be stored for long periods of time. The compound has been shown to react with trifluoroacetic acid and in the presence of an electrochemical probe to give a redox reaction. This reaction mechanism has been studied by using pharmacokinetic properties of 2,2,2-trifluoroacetamide and its metabolites. The compound is not active against infectious diseases but may be used as a reagent in analytical methods. 2,2,2-Trifluoroacetamide has also been investigated for its ability to bind hydrogen atoms and form intramolecular hydrogen bonds with tryptophan residues in proteins.</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>Gly-pro-4-methoxy-β-naphthylamide hydrochloride is a fine chemical that is useful as a versatile building block and intermediate. It is a research chemical that has been used in the production of other compounds, such as drugs, pesticides, and dyes. This compound is also used to synthesize certain polymers and plastics. Gly-pro-4-methoxy-β-naphthylamide hydrochloride has CAS number 100929-90-6, but it can be found under many other names including 4-(2′,5′dimethylphenyl)-1-(2′hydroxyethyl)piperazine (CAS 105999).</p>

<p>3-Ethoxybenzamide is a crystalline compound that can form complexes with metal ions. It has been shown to inhibit bacterial growth by binding to the enzyme thiourea, which is essential for the biosynthesis of thiamine. 3-Ethoxybenzamide also inhibits the production of hydrogen sulfide, which is produced by bacteria and a cause of foul odors. 3-Ethoxybenzamide has been shown to have antibacterial activity against Gram-positive bacteria such as Staphylococcus aureus and Streptococcus pyogenes. 3-Ethoxybenzamide also inhibits the growth of Gram-negative bacteria such as Escherichia coli and Salmonella typhimurium. This compound has also been shown to have anti-inflammatory activities through its ability to inhibit prostaglandin synthesis in mice.</p>

<p>μ-opioid receptor agonist; calcium channel inhibitor; anti-diarrheal</p>

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<p>5-(Acetylamino)-N,N'-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-1,3-benzenedicarboxamide is a reactive iodinated contrast agent that is used in the diagnostic imaging of body cavities and blood vessels. It can be prepared by the acetylation of 5-(acetylamino)naphthalene-2,3-diol with 2,4,6-triiodobenzene dicarboxylic acid using an alkali metal as a base. The yields for this reaction are dependent on the type of solvent used. This chemical has two functional groups: an amide and an acetate group. It reacts with iohexol to form a radiocontrast product that contains both iodine and propanediol. This process is industrially carried out by mixing 5-(acetylamino)naphthalene-2,</p>

<p>4-N-Octyloxybenzamide is a fine chemical that can be used as a building block in organic synthesis, or as a reagent in research. It is available at high quality and has been shown to be versatile. The compound can also be used as an intermediate in the synthesis of other compounds and is useful for the production of pharmaceuticals, pesticides, and herbicides. 4-N-Octyloxybenzamide has CAS number 203243-94-1.</p>

<p>Non-steroidal androgen receptor antagonist</p>

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<p>N,N'-Diallyl-L-tartardiamide is a heparin-like molecule with the ability to bind calcium. It has been shown to be an effective inhibitor of antibody response in mice and can also inhibit periodate treatment of primary amino groups. N,N'-Diallyl-L-tartardiamide has a high degree of solubility in water and is soluble in organic solvents as well. It can be crosslinked to form polymeric matrices that are suitable for use in size-exclusion chromatography. N,N'-Diallyl-L-tartardiamide can also be used as a cross linking agent for agarose gels and gel matrices.</p>

<p>N-Chloro-4-toluenesulfonamide sodium (NCTS) is a disinfectant that is used to treat wastewater and as a preservative for water. It has been shown to be effective against bacteria, fungi, and viruses. NCTS is an antimicrobial agent that reacts with the matrix in which it is applied to form chloramines-T (NHClO). The chloramines-T inhibits the activity of enzymes such as those involved in DNA synthesis and protein synthesis. This reaction also generates an electric current due to the redox potentials of the reactants. The presence of aziridines in NCTS leads to crosslinking between proteins, which enhances its effectiveness as a disinfectant.<br>NCTS has been shown to have no adverse effects on human erythrocytes or DNA when used at concentrations up to 100 µg/mL.</p>

<p>3,4,5-Trimethoxybenzamide is a benzofuran that has been shown to have anti-cancer properties. It has been shown to inhibit the production of chemokines and inhibit cancer cell proliferation. 3,4,5-Trimethoxybenzamide also binds to chloride ion channels on cancer cells and blocks the influx of chloride ions into the cells. This causes an increase in intracellular pH and inhibits the formation of ATP. 3,4,5-Trimethoxybenzamide also has antiarrhythmic properties and can be used for the treatment of hypertension. It is metabolized by hydrolysis in tissues or blood pressure through piperidine formation or hydrochloric acid.</p>

<p>Voltage-gated sodium channel blocker</p>

<p>Dimethylphosphonoacetamide (DMPPA) is a phosphorus-containing compound that is used as an intermediate in the synthesis of fatty acids. DMPPA can be synthesized by the reaction of ethylene diamine and phosphorus pentoxide, which is a common reagent for preparing phosphorus compounds. The reaction mechanism has been studied using electrochemical impedance spectroscopy. This study revealed that DMPPA can be converted to a water-soluble product by treatment with water vapor or by adding cotton. In addition, the kinetic data obtained from this study showed that the reaction rate was affected by temperature and the type of solvent used. The frequency shift observed during this study indicated that nitrogen atoms are involved in the reaction mechanism.</p>

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<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>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>

<p>Furiosus is a monomeric and homodimeric protein that belongs to the group of S-adenosylmethionine synthetases. Furiosus is an enzyme that catalyzes the formation of S-adenosylmethionine from methylamine and ATP. Furiosus interacts with polymerase, subtilis, and catalysis to form a holoenzyme complex. Furiosus has been shown to have cleavage activity against peroxide and hydrogen peroxide, which is due to its ability to generate reactive oxygen species. Furiosus has also been shown to be a molecular modeling target for the development of new antibiotics.</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>

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>2-((4-Methylphenyl)sulfonyl)ethanamide is an amide that has been shown to have antibacterial activity. It binds to the DNA of bacteria, inhibiting its replication and transcription. This drug also inhibits the growth of influenza virus in cell culture. 2-((4-Methylphenyl)sulfonyl)ethanamide is a sensor for chloride ions, which may be used as treatments for bacterial infections. This drug is also able to inhibit the replication of bacteria that are resistant to other antibiotics, such as penicillin. The unsaturated alkyl group on this molecule allows it to be activated by radiation treatment, which may be useful in the treatment of cancer cells or viral infections.</p>

<p>2,5-Dimethoxybenzamide is a potent inhibitor of the enzyme DECATENASE. This enzyme plays an important role in the biosynthesis of the aromatic amino acids phenylalanine and tyrosine. 2,5-Dimethoxybenzamide has been shown to have anticancer activity in vitro and in vivo. Remoxipride is a synthetic drug that competitively inhibits the action of benzodiazepines on GABA receptors by binding to them with high affinity. It was developed as an antipsychotic agent but was never marketed for this indication due to its adverse effects on motor coordination. Remoxipride has also been shown to have estrogenic activity, which may be due to its ability to bind with high affinity and inhibit the enzyme aromatase, which converts testosterone into estradiol.</p>

<p>4-Cyanobenzamide is a naphthalene derivative that is both reactive and intramolecular. It has been shown to react with the amino group of peptides, forming a ruthenium complex. The functional groups are acceptors and donors that can be used in assays for the detection of anions or cations. 4-Cyanobenzamide reacts with water to release hydrogen gas, which can be used to measure its hydration ability. This compound has been synthesized using solid-phase synthesis and it has amide bonds that vibrate at a specific frequency.</p>

<p>Prothionamide is a drug that belongs to the group of drugs called sulfonamides. It is used to treat bowel disease by inhibiting the growth of bacteria and fungi. Prothionamide inhibits bacterial growth by binding to bacterial DNA and preventing it from synthesizing new proteins. This drug also has a matrix effect, which means that it binds to the inside of the bacterial cell wall and prevents the production of new cells, leading to cell death. Prothionamide has been shown to be effective against tuberculosis in mice, although there are few data on its use in humans. The most common side effects associated with prothionamide are nausea and vomiting.</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>2,5-Dichlorobenzamide is a halogenated compound that inhibits topoisomerase and proteasome activity. It has been shown to be cytotoxic against cancer cells in vitro. 2,5-Dichlorobenzamide can also inhibit the growth of tuberculosis bacteria and may be used as an operational agent for weed control. The safety profile of this drug has not yet been fully determined. 2,5-Dichlorobenzamide is available in two crystalline forms, both of which are active with different degrees of potency.<br>2,5-Dichlorobenzamide is a hybridization inhibitor that inhibits the enzyme DNA gyrase and proteasome activity. It binds to bacterial 16S ribosomal RNA and inhibits protein synthesis, leading to cell death by inhibiting the production of proteins vital for cell division.</p>

<p>Piperazinophenylacetic acid benzylamide hydrochloride is a versatile building block that can be used in the synthesis of complex compounds for research and development. It is a reagent for the preparation of speciality chemicals and also a useful intermediate for the synthesis of reaction components. Piperazinophenylacetic acid benzylamide hydrochloride is a high quality, commercially available chemical that can be used as a scaffold for the preparation of new chemical compounds.</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>Dodeca 2E,4E,8Z,10E,Z-tetraenoic acid isobutylamide (DETBA) is a versatile building block that is used in the synthesis of natural products and pharmaceuticals. DETBA can be used as a reaction component in organic synthesis to form complex compounds such as polyesters, polyamides, polyurethanes, and polyimides. It also has high quality and can be used in research or speciality chemical applications.</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>DL-Leucine amide hydrochloride is a fine chemical that can be used as a building block for research chemicals, as a reagent for the preparation of other compounds, and as a speciality chemical. DL-Leucine amide hydrochloride has been shown to be effective in the synthesis of complex compounds. The compound is also versatile and can be used as an intermediate or scaffold in the synthesis of other compounds. DL-Leucine amide hydrochloride is useful in reactions such as condensation, substitution, elimination, and Grignard reactions. It is also used in peptide synthesis and polymerization reactions.</p>

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<p>N-Ethylheptadecafluoro-N-[3-(Trimethoxysilyl)Propyl]Octanesulphonamide is a membrane filtration technology that is used to remove all organic and inorganic pollutants from water. It is effective for the removal of oils, pesticides, herbicides, detergents, antibiotics, and heavy metals. N-Ethylheptadecafluoro-N-[3-(Trimethoxysilyl)Propyl]Octanesulphonamide is also used to treat wastewater and surface water. This process can be used on large quantities of water with high efficiency. The use of this process can be beneficial for the health of humans, animals, and the environment.</p>

<p>Tropicamide is a cholinergic agent that is used as a short-term mydriatic, or eye dilator, for diagnostic purposes. It belongs to the group of nonsteroidal anti-inflammatory drugs and has been shown to have a stable complex with benzalkonium chloride. Tropicamide has been shown to affect the signal pathways in cells, leading to an increase in IL-2 receptor expression. This drug also affects locomotor activity and has been studied as a potential treatment for murine sarcoma virus. Tropicamide is administered intravenously and can cause side effects such as blurred vision, nausea, vomiting and convulsions. Tropicamide may be given together with phenylephrine in order to reduce these side effects.</p>

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<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>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'-Hydroxy-5'-nitrohexadecanamide is a synthetic fatty acid derivative that inhibits lysosomal hydrolase, which is an enzyme that breaks down cellular lipids. This compound can be used as a diagnostic agent for the detection of certain types of cancer. 2'-Hydroxy-5'-nitrohexadecanamide reacts with the magnesium ion in the lysosome to form an insoluble precipitate, which then settles to the bottom of the test tube, allowing for easy detection of cells with high levels of lysosomal hydrolase.</p>

<p>3-Iodobenzamide is a metalloporphyrin that is used as a research tool. It has been shown to inhibit the tyrosine kinase activity of the BCR-ABL protein and to induce apoptosis in chronic myeloid leukemia cells. 3-Iodobenzamide binds to the dopamine D2 receptor, which leads to inhibition of adenylate cyclase and decreased levels of cAMP. The binding affinity of 3-iodobenzamide for dopamine receptors and its ability to inhibit cAMP production make it an ideal candidate for use in studies on striatal membrane preparations and homogenates.</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>

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<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>

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

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<p>5-Aminoimidazole-4-carboxamide HCl (5-AICA) is a compound that is used for the treatment of bowel disease. It inhibits the synthesis of 5'-nucleotidase and phosphoribosyl transferase, which are enzymes responsible for the conversion of nucleotide monophosphates to nucleotide diphosphates. This inhibition leads to a decrease in the amount of adenosine triphosphate (ATP) produced by cells, which may be due to its ability to inhibit ATP synthase activity. 5-AICA also has been shown to bind to DNA and inhibit transcriptional activities. The binding of 5-AICA may be due to its ability to form hydrogen bonds with guanine residues in DNA or its capability to form covalent bonds with thymidine residues in DNA. 5-AICA also has been shown to have cytotoxic effects on HL60 cells, as well as other</p>

<p>Cyanamide is a nitrogen-containing organic compound that is used as a plant nutrient. It has been shown to increase the activity of enzymes in methyl ethyl x-ray crystal structures and locomotor activity in mice. Cyanamide is also used as an herbicide and chemical pesticide, with calcium as its main target. The cyanamide molecule binds to the calcium ion and undergoes a reaction mechanism that results in the release of ammonia gas, which is toxic to plants. In addition, cyanamide can cause kidney damage in humans due to its ability to inhibit protein synthesis.</p>