Amides

<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>

<p>3-Hydroxybenzamide is a potent inhibitor of the enzyme synthetase and has been shown to inhibit the synthesis of adenosine diphosphate (ADP) ribose. It has been shown to have potent inhibitory activity against the enzyme in both solid and liquid phases. 3-Hydroxybenzamide binds to the carbonyl group of ADP ribose, which prevents it from binding to ATP. This inhibition of the synthesis of nucleotides limits cell proliferation by preventing DNA replication and protein synthesis. 3-Hydroxybenzamide has also been shown to inhibit the growth of mouse leukemia cells in vitro, as well as inhibiting l1210 murine leukemia cells grown in vivo. The mechanism for this inhibition is not yet known, but may be due to its ability to bind with hydrogen bonds or intramolecular hydrogen bonds. 3-Hydroxybenzamide also has a skeleton that can be synthesized asymmetrically by using a chiral</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>

<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>(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>Chemically a chlorinated salicylanilide, niclosamide is clinically used as an anthelmintic agent. The action of niclosamide has been proven to proceed by inhibiting the STAT3 signaling pathway. Recently, niclosamide, has been considered as an antiproliferative agent in cancer treatment, e.g. melanoma and colorectal cancer. In 2021, niclosamide has been tested for the treatment of COVID-19 patients.</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>Sulphanilamide is an antimicrobial agent that inhibits the growth of bacteria by binding to their enzymes and blocking protein synthesis. In addition, sulphanilamide has been shown to inhibit the production of sulfanilamide, a potent inhibitor of tetracycline. Sulphanilamide is soluble in water and alcohol but not in organic solvents. The solubility of sulphanilamide can be increased by adding sodium salts or pH adjustment. Sulphanilamide is also used for wastewater treatment as it has inhibitory properties against sulfate-reducing bacteria. X-ray crystal structures have revealed that sulphanilamide binds to the active site of bacterial beta-lactamases through hydrogen bonds with both the NH group and the COOH group on its sulfur atom, resulting in inhibition of these enzymes. Sulphanilamide also interferes with bacterial DNA replication by inhibiting dna gyrase and topoisomerase IV. Sulphanilamide also</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>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>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>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>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>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>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>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>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>5-Amino-1,3,4-thiadiazole-2-sulfonamide is a chemical compound that inhibits the growth of skin cancer cells. It has inhibitory properties against choroidal neovascularization induced by dorzolamide hydrochloride and other pharmacological agents. 5-Amino-1,3,4-thiadiazole-2-sulfonamide has also been shown to have antiangiogenic activity in vitro and in vivo assays. 5ATTS inhibits the growth of bacteria and fungi by inhibiting fatty acid synthesis. The drug also has been shown to be effective in treating diabetic neuropathy and fluorescein angiography associated with itchy eyes.</p>

<p>3,4-Dichlorobenzamide is a synthetic opioid analgesic that binds to the μ-opioid receptor. It has a side-effect profile that is similar to other opioids, with an addiction risk and potential for abuse. 3,4-Dichlorobenzamide has been used in the synthesis of new drugs, such as phenazepam (a benzodiazepine) and etizolam (a thienodiazepine). This drug is chiral and can be synthesized in two stereoisomeric forms: 3-(+)-chloro-N-(2-chlorophenyl)benzamide and 3-(−)-chloro-N-(2-chlorophenyl)benzamide. The former form is marketed under the trade name Analgin, while the latter form is marketed under the trade name Etilex. The (+) form of this drug has a higher affinity for μ receptors than the (−) form.</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>2,4,6-Trimethoxybenzamide is a triggered compound that reacts with lithium to form an efficient regiospecific lithium 2,4,6-trimethoxybenzamide complex. This reaction occurs at low temperatures and has been shown to be more efficient than other methods for the synthesis of acridones. The reaction has not been shown to be reversible and requires the use of a strong base such as lithium.</p>

<p>N,N-Dimethylsulfamide (DMS) is a chemical compound with a molecular formula of CH3SO2NH2 that is used as an industrial solvent. It is an environmental biocide that can be used to treat wastewater and as a sample preparation agent, such as for chemical ionization in gas chromatography. DMS has been shown to have biological properties that are active against mammalian cells, but not against bacteria. This property may be due to the presence of nitrogen atoms in the molecule's structure that are capable of forming coordination complexes with metals such as copper and iron.</p>

<p>2-Chloro-4-nitrobenzamide is a drug that belongs to the sulfa drugs. It has been shown to be effective in treating autoimmune diseases, particularly bowel disease and inflammatory bowel disease. 2-Chloro-4-nitrobenzamide inhibits the synthesis of fatty acids by blocking the enzyme acetyl CoA carboxylase, which is involved in the formation of long chain fatty acids. This drug also has immunosuppressive activities, which may be due to its ability to block T cell proliferation. 2-Chloro-4-nitrobenzamide is used as a chemical intermediate for antibiotics such as maduramicin ammonium and salinomycin sodium. It is also used as a dietary supplement or pharmaceutical dosage form for cardiac glycoside drugs such as digoxin.</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>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>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>N'-(2-Cyano-4-fluorophenyl)-N,N-dimethylimidoformamide is a high quality, reagent that is useful for the synthesis of complex compounds. It can be used as a fine chemical and speciality chemical in research and development. The CAS number for this compound is 1017082-62-0. N'-(2-Cyano-4-fluorophenyl)-N,N-dimethylimidoformamide has shown to be a versatile building block for the synthesis of novel compounds that are not commercially available. This product is suitable for use in reaction components as well as being an intermediate for the synthesis of other compounds.</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>1-Methyl-1,4-dihydronicotinamide (1MDNA) is a flavine adenine dinucleotide analog that has been shown to be a potent inhibitor of the enzyme catalase. 1MDNA binds to the active site of the enzyme and prevents hydrogen peroxide from being converted into water and oxygen. This inhibition slows down or stops the reaction, which leads to reduced production of reactive oxygen species. 1MDNA inhibits other enzymes in a similar manner, including transferases and kinases. The kinetic properties of 1MDNA have been studied by performing kinetic studies on model systems at different temperatures. X-ray crystal structures have also been obtained for 1MDNA bound to catalase and ferredoxin.</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>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>6-Methylnicotinamide is a transport inhibitor that prevents the uptake of fatty acids and growth factors into cells. It has been shown to inhibit the activity of glutamate receptors by blocking the interaction between these receptors and their binding partners, which are called co-agonists. 6-Methylnicotinamide has also been shown to inhibit the synthesis of virus proteins in vitro and in vivo. There is a lack of evidence on its safety profile. 6-Methylnicotinamide may be used to treat hepatitis C and colorectal carcinoma.</p>

<p>Please enquire for more information about (4-Benzylpiperazinyl)-N-propylformamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Methyl-2-nitrobenzamide is a compound that has antiproliferative activity and is used as an anticancer drug. This drug inhibits the polymerization of the protein tubulin in cancer cells, thereby inhibiting cell division. It also inhibits the growth of certain tumor cell lines in vitro. 5-Methyl-2-nitrobenzamide was found to inhibit the proliferation of human ovarian carcinoma cells by binding to DNA, preventing transcription and replication of genetic information. In addition, this agent binds to tubulin and prevents its polymerization, leading to inhibition of cell division.</p>

<p>1-Adamantane carboxamide is a potent inhibitor of amines and its activity has been tested with a reaction solution. The chemical structure of 1-adamantane carboxamide is shown in Figure 1. This molecule also has inhibitory effects on insulin resistance and nervous system diseases. It was found to have an inhibitory effect on the enzyme DOPA decarboxylase, which is involved in the synthesis of dopamine, norepinephrine and epinephrine. The inhibition of this enzyme leads to increased levels of dopamine in the brain, which can lead to improved cognition, mood and motor skills. 1-Adamantane carboxamide also has a hydroxyl group that mimics the polarizer in biomimetic molecules.</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>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>Voltage-gated sodium channel blocker</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>2-Amino-N-[2-(2-chlorobenzoyl)-4-nitrophenyl]acetamide is a fine chemical that is used as a building block in organic synthesis. It is a versatile intermediate for the synthesis of other compounds and can be used to make a variety of useful scaffolds. 2-Amino-N-[2-(2-chlorobenzoyl)-4-nitrophenyl]acetamide has been used in research and development of pharmaceuticals, agrochemicals, herbicides, and other compounds.</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>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>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>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>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>Please enquire for more information about 2-Chloro-N-(2-ethyl-6-methylphenyl)propanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Amino-4-methylbenzamide is an interchemical that can be utilized to synthesize naphthol. 3-Amino-4-methylbenzamide is an amide that has been shown to have a molecular modeling structure of a conformation. The interaction of 3-amino-4-methylbenzamide with the P38 kinase enzyme has been shown to inhibit the activity of this enzyme, which may lead to its use as a drug for the treatment of inflammation.</p>

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

<p>Please enquire for more information about N-(4-(((2-Indol-3-ylethyl)amino)sulfonyl)phenyl)ethanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Iodoacetamide is a synthetic retinoid that binds to the DNA of cells, altering transcription. It also has been found to be effective in treating bowel disease and has been shown to have dna binding activity. The compound was synthesized by attaching iodine molecules to acetamide. 2-Iodoacetamide targets the protein thiols on the surface of cells, which are responsible for oxidation and damage due to reactive oxygen species (ROS). This compound is metabolized by alcohol dehydrogenase and can be used as a biological sample or natural compound.</p>