Amides

<p>Diacetone acrylamide is a chemical compound that has the molecular formula C3H6O2N2. It is a colorless liquid with a low boiling point and an unpleasant odor. Diacetone acrylamide has been used as an intermediate in the production of polyvinyl acetate. It can also be used as an additive to rubber, plastics, and other materials. The thermal expansion coefficient of diacetone acrylamide is similar to that of polyvinyl chloride and polystyrene, making it a useful material for constructing models of those substances.</p>

<p>1-Methyl-nicotinamide iodide is a drug that has been used in clinical trials for the treatment of type 2 diabetes mellitus. It is thought to work by increasing the sensitivity of cells to insulin, which may be related to its ability to bind to protein amide groups and form hydrogen bonds with the amino acid side chains. The compound also has been shown to increase the activity of the enzyme glycogen synthase in rats. 1-Methyl-nicotinamide iodide is soluble in water and human serum, and shows low solubility in ethanol. It has not been studied in humans, but animal studies have shown that it can be absorbed orally and metabolized into hippuric acid, which is excreted as a metabolic product through urine. Animal studies also showed that 1-methyl-nicotinamide iodide inhibits glucose production by pancreatic beta cells, which may lead to an increased insulin response after eating.</p>

<p>Beta-naphthamide is an inhibitor binding to the dinucleotide phosphate (DNP) in bacterial cells. This binding prevents the enzyme from carrying out its normal function, which is the production of ATP, and it also inhibits various other enzymes. Beta-naphthamide inhibits the growth of Gram-positive bacteria by inhibiting their cell wall assembly and also has a bactericidal effect on Gram-negative bacteria. Beta-naphthamide has been shown to be active against multidrug efflux pump proteins that are present in Gram-negative bacteria, such as Escherichia coli. DNP is a receptor for dopamine and beta-naphthamide inhibits dopamine receptors in mammalian cells, which may lead to Parkinson's disease. Beta-naphthamide has been shown to inhibit the polymerase chain reaction (PCR) mechanism by binding to DNA polymerase. Beta-naphthamide binds to receptors on trigeminal nerve endings, which leads to paralysis of</p>

<p>2-Amino-5-fluorobenzamide (2AFB) is a compound that has been shown to have neurotoxic properties. 2AFB is a ring-opening agent, which means it can open the six-membered ring of aromatic compounds such as benzene or pyridine. 2AFB also has affinity for metal ions and therefore can be used in magnetic separations. The reaction system of 2AFB includes an enzyme, pentylenetetrazole (PTZ), that catalyzes the reaction between 2AFB and its substrate, 4-nitrophenol (4NP). This reaction produces free radicals that react with oxygen to produce peroxides. These peroxides are then detected by a chemiluminescence assay. In this way, the amount of 2AFB and 4NP can be measured quantitatively.<br>2AFB also has antioxidant properties, which may be due to its ability to scavenge free radicals from</p>

<p>4-Butoxyphenyl)acetamide is a synthetically produced chemoattractant that is used in vitro to study the migration of cells. It is soluble in non-polar solvents and can be expressed from many organisms, including bacteria and plants. 4-Butoxyphenyl)acetamide has been shown to induce cell movement by binding to the G protein coupled receptor that stimulates the release of calcium ions from intracellular stores. This molecule also has photophysical properties, which have been studied in rat liver microsomes and hydrochloric acid, hydroxamic acids, and spermatozoa. 4-Butoxyphenyl)acetamide can be absorbed from the intestine into plasma, where it binds to odorant receptors on sensory neurons in the nose. These receptors are also found in plant physiology, where they are responsible for detecting chemicals that attract pollinators such as bees or insects.</p>

<p>(1E)-N',2-Dihydroxyethanimidamide (DHEEA) is a versatile building block in organic synthesis. It is an important intermediate in the synthesis of various drugs, such as metoprolol, amlodipine, and clomiphene. DHEEA is also used as a reagent in organic chemistry for the preparation of other compounds and as a research chemical. The compound has CAS No. 73728-45-7 and can be purchased from chemical suppliers or synthesized by reacting formaldehyde with ethanolamine.</p>

<p>Erucamide is a fatty acid amide that is a natural compound and part of the biochemical composition of microbial organisms. Erucamide has been shown to have antimicrobial activity against Gram-positive bacteria but not against Gram-negative bacteria. The mechanism by which erucamide kills bacteria is unknown, but it may be due to its hemolytic activity or its ability to inhibit protein synthesis. Erucamide is resistant to hydrolysis by trifluoroacetic acid and glycol ester, which makes it difficult for microbes to metabolize it.</p>

<p>Ropivacaine is a local anaesthetic of the amino ester group that is used to provide relief from pain caused by surgery or other medical procedures. It is a potent inhibitor of the enzyme activity of cholinesterases, which are enzymes responsible for the degradation of acetylcholine. Ropivacaine also inhibits the activity of cardiac Na+/K+ ATPase and Na+-Ca2+ exchanger, thereby reducing the excitability and contractility of heart muscle. This drug has shown pharmacokinetic properties in maternal blood that are similar to those observed in plasma, indicating that it can cross the placenta. Ropivacaine has been shown to have bactericidal effects against bacterial strains such as Escherichia coli and Staphylococcus aureus. In addition, ropivacaine has been shown to inhibit colorectal adenocarcinoma cells in vitro and in vivo. Levobupivacaine</p>

<p>4-(Aminomethyl)benzenesulfonamide acetate is a biocompatible polymer that is used in the treatment of infectious diseases. It has antibacterial efficacy against a range of microorganisms, including methicillin-resistant Staphylococcus aureus and Pseudomonas aeruginosa. This polymer binds to sulfadiazine and antimicrobial peptides, which then act as antimicrobial agents. 4-(Aminomethyl)benzenesulfonamide acetate also exhibits good chemical stability in vivo and has been shown to inhibit the growth of skin cells.</p>

4-(tert-Butyl)benzenesulfonamide is a pyrimidine derivative that has an affinity for metal ions and can be used as a catalyst. It is insoluble in water but soluble in acetonitrile and other organic solvents. This compound is a strong oxidant when it reacts with ethylene, styrene, or propyl gallate. 4-(tert-Butyl)benzenesulfonamide has been shown to be highly reactive with the oxygen in air, leading to the formation of 4-dimethylaminobenzoic acid, formyl group, and phosphorus oxychloride.

<p>4-Trifluoromethylbenzene-1-carbothioamide (4FBA) is a non-toxic, organosulfur compound that is found in the fructus of Aurantii or Garcinia mangostana. 4FBA inhibits oxidant enzymes by reacting with their sulfhydryl groups and, as a result, prevents oxidation of other molecules. It has been shown to have antioxidant properties and inhibitory activity against two important enzymes that are involved in the progression of oxidative stress and inflammation. 4FBA has also been shown to be an effective inhibitor of chloride channels which may provide therapeutic potential for diseases such as sclerosis.</p>

<p>2-Iodo-N-phenylbenzamide is a palladium compound that inhibits bacterial growth by binding to DNA and preventing transcription. The drug binds to the DNA as a monomer, but also forms polymeric matrixes with other drugs. 2-Iodo-N-phenylbenzamide has been shown to have genotoxic effects on subtilis and methicillin resistant Staphylococcus aureus (MRSA) in vitro, which may be due to its ability to form crosslinks between adjacent strands of DNA. 2-Iodo-N-phenylbenzamide has been shown to be an effective anti-bacterial agent against MRSA, methicillin resistant coagulase negative staphylococci and erythromycin resistant strains of Streptococcus pyogenes.</p>

<p>N-Methyl-N-(1-naphthyl)-2-bromobenzamide is a high quality reagent that is used as a complex compound. It has CAS No. 74881-58-6 and it can be used as a useful intermediate, fine chemical or speciality chemical. N-Methyl-N-(1-naphthyl)-2-bromobenzamide is also a versatile building block that is used in reactions to synthesize other compounds.</p>

<p>Gly-pro-4-methoxy-beta-naphthylamide is a synthetic substrate that is used to measure the activity of human plasma phosphatases. Gly-pro-4-methoxy-beta-naphthylamide is synthesized in an organic solvent and then reacted with diazonium salt to form a glycosylated aminophosphonic acid. The product is purified by chromatography and identified by mass spectrometry. Gly-pro-4-methoxy beta naphthylamide has been shown to inhibit the growth of cancer cells in vitro, as well as having antiinflammatory properties. This drug also has been shown to be effective in treating patients with severe hyperbilirubinemia who are undergoing hematopoietic stem cell transplantation.</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>N-[3-(Diethylaminomethyl)-4-hydroxyphenyl]acetamide is a molecule that has been shown to have acetylcholine esterase (AChE) inhibitory activity. It binds to the active site of AChE, preventing it from breaking down acetylcholine, leading to the accumulation of this neurotransmitter. The inhibition of AChE by N-[3-(Diethylaminomethyl)-4-hydroxyphenyl]acetamide prevents muscle contraction and leads to paralysis and death by asphyxiation. This drug has been used in the treatment of sarin gas poisoning. The molecular structure of N-[3-(Diethylaminomethyl)-4-hydroxyphenyl]acetamide is similar to that of pyridinium chlorides, which are used for synthesizing nerve agents such as sarin and soman. This drug also has a proton</p>

<p>4-Iodo-N-(4-methoxyphenyl)-N-methylbenzamide is a useful scaffold that can be used in the synthesis of complex compounds. It is also a versatile building block and has been found to be useful as an intermediate and building block. 4-Iodo-N-(4-methoxyphenyl)-N-methylbenzamide is a fine chemical with CAS No. 320734-40-5. This reagent is high quality, research chemicals, and can be used in the synthesis of speciality chemicals.</p>

<p>Boc-L-leucine N,O-dimethylhydroxamide is a chemical compound with CAS number 87694-50-6. It is a white crystalline solid and has a molecular weight of 144.17 g. This product is soluble in water and ethanol, but insoluble in ether. Boc-L-leucine N,O-dimethylhydroxamide can be used as a reaction component or reagent for organic synthesis, including research chemicals and speciality chemicals. It can also be used as an intermediate for the production of complex compounds and fine chemicals.</p>

<p>2-Chloro-N-(hydroxymethyl)acetamide (2CHAA) is an inhibitor that has been shown to be effective against a number of infectious diseases. 2CHAA inhibits the growth of bacteria by inhibiting the synthesis of proteins from RNA. This drug is also active against viruses, including herpes simplex virus and human immunodeficiency virus type 1, as well as fungi, such as Aspergillus niger. 2CHAA has no genotoxic effects in humans, but it does have carcinogenic potential and can cause allergic reactions. It also reacts with strong acids to form toxic compounds.</p>

<p>3-(Aminomethyl)-N,N-dimethylbenzamide (DMBA) is a compound that can be used as a chemical marker for the identification of bacteria. It has been tested on an automated DNA sequencer and found to be effective in identifying different strains of bacteria. DMBA is applied to plates containing bacterial colonies and then contacted with a device containing the sequence analyzer. The analyzer measures the amount of DMBA that binds to the bacterial colony and generates a profile of the colony's DNA. This information can then be used to identify the bacterial colony type.</p>

<p>2-Chloro-N,N'-di-p-tolylbenzamide is a fine chemical that is used in the synthesis of complex compounds. It has a wide range of applications, including research chemicals and reagents. This compound is also a useful building block for the preparation of high quality pharmaceuticals and speciality chemicals. 2-Chloro-N,N'-di-p-tolylbenzamide may be used as a reaction component or scaffold in organic synthesis.</p>

<p>N-(4-Butylphenyl)acetamide is a reactant that can be used in the production of other chemicals. It is an intermediate for the synthesis of a wide range of organic compounds, which makes it a useful building block. N-(4-Butylphenyl)acetamide has been shown to have antihistamine and anti-inflammatory properties. It is also known as acetanilide or 4-butylaniline. This chemical has CAS number 3663-20-5 and a molecular weight of 150.06 g/mol.</p>

<p>2,2-Dimethylthiopropionamide is an organic compound with the chemical formula C4H7NOS. It is a nucleophilic, unsymmetrical, n-benzyltrifluoroacetamide that is soluble in chloroform and reacts with nucleophiles to give products of desulfurization. 2,2-Dimethylthiopropionamide has been shown to react with electron-deficient amines such as azetidine and elucidate their structures. The reaction of 2,2-Dimethylthiopropionamide with chloroformate gives a dipole product and can be analysed by infrared spectroscopy.</p>

<p>Thiophene-2-carboxamide is a synthetic chemical that is an inhibitor of the efflux pump, receptor activity, and recombinant cytochrome p450. It has been shown to be effective against colorectal carcinoma cells in vitro and in vivo. Thiophene-2-carboxamide also inhibits the mitochondrial membrane potential and hydrogen bond formation. This compound has potent inhibitory activity for the enzyme synthetase, which may be a potential drug target for cancer treatment. Nitrogen atoms are present in this molecule.</p>

<p>N,N'-Ethylenebis(iodoacetamide) is a molecule that binds to peptides and is used in cancer research. It has been shown to inhibit the growth of leukemia cells by inhibiting the synthesis of DNA. N,N'-Ethylenebis(iodoacetamide) has been shown to be an active analog for artemisinin, a drug used for malaria prophylaxis, and podophyllotoxin, a natural product used for the treatment of cancer. The molecule also inhibits cancer cell proliferation through its effects on protein synthesis.</p>

<p>L-Isoleucine amide hydrochloride is a high quality reagent that is useful as an intermediate, fine chemical or speciality chemical. It can be used to synthesize compounds with a wide range of properties and uses. L-Isoleucine amide hydrochloride can be used in research for the development of new drugs or other chemicals. The versatility of this reagent makes it a useful building block for reactions involving amino acids, peptides, nucleosides, and carbohydrates.</p>

<p>Methyl 2-naphthylbenzoate is a high quality reagent that is used as a complex compound, useful intermediate and speciality chemical. It is also a useful building block for the synthesis of other compounds. The CAS number 74881-61-1 identifies Methyl 2-naphthylbenzoate as a fine chemical with an interesting scaffold. This chemical is suitable for research purposes and versatile in its use as a reaction component.</p>

<p>Orazamide is a piperazine derivative that is used in the treatment of high blood pressure. It works by binding to the skeleton and the liver, preventing the accumulation of sodium and chloride ions. This results in a decrease in blood pressure. Orazamide has been shown to decrease insulin resistance and also has an important role in the prevention of symptoms such as edema, headache, dizziness, nausea, vomiting, and fatigue. It also has a diuretic effect on the kidneys with sodium citrate as its main excipient. The chlorine atom binds to the heterocycle group to form a coordination complex that can bind to heme proteins, thus inhibiting its function.<br>Orazamide is an analog of chlorothiazide with a chlorine atom replacing one oxygen atom on the heterocycle group.</p>

<p>L-Valinamide hydrochloride is an amide with a reactive group. It binds to the CB2 receptor and the CB1 receptor, which are found in the brain and immune system. L-Valinamide hydrochloride has been shown to have anti-inflammatory effects in animal models of inflammatory diseases, such as rheumatoid arthritis. L-Valinamide hydrochloride has also been shown to be a synthetic cannabinoid that inhibits pain transmission by binding to the same receptors as delta-9 tetrahydrocannabinol (THC), one of the active components of cannabis.</p>

<p>N-(4-Cyano-2-chlorophenyl)acetamide is a versatile building block that is used in the synthesis of complex compounds. N-(4-Cyano-2-chlorophenyl)acetamide has been shown to be a useful intermediate in the synthesis of important compounds such as 4-aminoantipyrine, 4,5-dichloroanthranilic acid and 2,6-dichloropurine. This chemical has also been found to be an effective reagent for the preparation of other chemicals.</p>

N-Benzyltrifluoroacetamide is an amide that inhibits the activity of the enzyme fatty acid synthase, which catalyzes the synthesis of fatty acids. It has been shown to be effective against a number of cancers and has been used in the treatment of patients infected with HIV. N-Benzyltrifluoroacetamide is active against a range of cancer cell lines, including breast, pancreatic, ovarian, prostate, and colorectal carcinomas. Its mechanism of action is not known but may involve inhibition of protein synthesis or induction of apoptosis.

<p>N-alpha-[2,4-Dinitro-5-fluorophenyl]-D-alanine amide is a potential drug for the treatment of cancer. It has been shown to be effective in inhibiting the proliferation of human prostate carcinoma cells in culture. This compound is a potential anticancer drug that binds to DNA and inhibits topoisomerase II, which is an enzyme involved in DNA replication. The mechanism of action of this drug was studied using methods such as optimization, isomers, plates, trifluoroacetic acid, tautomers, amino acid analysis and nanomolar concentrations. N-alpha-[2,4-Dinitro-5-fluorophenyl]-D-alanine amide has also been shown to inhibit cyanobacteria growth.</p>

<p>2-Amino-4,5-dimethoxybenzamide is an anticancer agent that inhibits the epidermal growth factor receptor tyrosine kinase. It binds to the linker region of the epidermal growth factor receptor and prevents autophosphorylation. 2-Amino-4,5-dimethoxybenzamide has shown in vitro cytotoxic activity against testicular cancer cells and acute lymphoblastic leukemia cells. 2-Amino-4,5-dimethoxybenzamide is a synthetic compound that has been shown to have bioisosteric properties with other growth factors such as epidermal growth factor.</p>

2-Bromo-N-(4-methoxyphenyl)-N-methylbenzamide is a fine chemical that is used in the synthesis of other chemicals. It is also a reagent and a speciality chemical, which can be used as a reaction component or as an intermediate in the synthesis of other compounds. 2-Bromo-N-(4-methoxyphenyl)-N-methylbenzamide can be used to make a wide variety of compounds, including polymers and pharmaceuticals. This compound has been shown to be useful for the synthesis of polycarbonates, polyurethanes, polyesters, polyamides, and polystyrenes.

<p>N-(2-Chlorophenyl)benzamide is a phenanthridone that reacts with chlorides in the presence of anilines to form singlet carbonyls. The photocyclization of these carbonyls yields an electron-deficient product that can be converted to a reactive electrophile by the addition of chlorine. This electrophilic species reacts with electron-rich aromatic compounds, such as phenols and benzene, to produce substitution products. The reaction rate for this process is dependent on the isotope effect, which is the change in reactivity due to changes in the mass number of atoms. The use of deuterium chloride instead of hydrogen chloride provides a kinetic isotope effect, which enhances the reaction rate.</p>

<p>2-(Indenylamino)acetamide, hydrochloride salt is a potential drug that is an uptake inhibitor. It prevents the uptake of dopamine in the brain and has been shown to be neuroprotective in animal research. It also has potential to treat diabetic neuropathy, inflammatory diseases, and pain. The kinetic properties of this drug were studied using rat striatal cells. 2-(Indenylamino)acetamide, hydrochloride salt inhibits the transport of dopamine into these cells by blocking the movement of dopamine from outside the cell to inside the cell. This drug could potentially be used for treatment of Parkinson's disease or other conditions involving dopaminergic dysfunction.</p>

<p>2-Chloroacetamide is a useful building block that can be used to synthesize a variety of compounds. This chemical is also a versatile intermediate and can be used in the preparation of fine chemicals, research chemicals, and speciality chemicals. It is also a reaction component that can be used in the synthesis of complex compounds. 2-Chloroacetamide has been shown to have high quality properties and is often used as a reagent.</p>

<p>Adamantyl-2-chloroacetamide is an analog of adamantyl acetamide and has been shown to be a potent inhibitor of Mycobacterium tuberculosis. Adamantyl-2-chloroacetamide inhibits the growth of Mycobacterium tuberculosis by inhibiting the synthesis of DNA, RNA, and protein. This compound also shows selectivity for Mycobacterium tuberculosis over other bacteria such as Escherichia coli. Adamantyl-2-chloroacetamide may have a role in the treatment of tuberculosis because it can inhibit the synthesis of DNA, RNA, and protein in Mycobacterium tuberculosis while leaving these functions intact in other bacteria.</p>

<p>3,5-Diacetoxybenzamide technical is a solvent that can be used in organic synthesis. It is soluble in hydrochloric acid and has a boiling point of 210 degrees Celsius. 3,5-Diacetoxybenzamide technical is soluble in water and has an LD50 (lethal dose) of over 5 g/kg when administered orally to pigs. 3,5-Diacetoxybenzamide technical is also used as a reagent for the preparation of peracetates and esters of aromatic ketones. This product can be used as a reaction medium for lipase or porcine pancreatic lipase. It is also used in the manufacture of pharmaceuticals, fragrances, dyes, herbicides and pesticides.</p>

<p>2-Iodo-N-methyl-N-phenylbenzamide is a cyclised molecule that has been synthesized by intramolecular arylation and reductive cyclisation. 2-Iodo-N-methyl-N-phenylbenzamide can be used as an industrial catalyst for the production of phenols, benzaldehydes, and indoles. The catalytic activity of 2-Iodo-N-methyl-N-phenylbenzamide is high, with yields of up to 99%. This molecule is recyclable because it can be easily regenerated from the crude product. It also has high catalytic activity due to its cyclic structure.</p>

<p>1-Butyl-3-methylimidazolium dicyanamide is an ionic liquid that is a colorless, volatile liquid. It is a hydrophobic compound that has been shown to have a high thermal expansion coefficient and a low viscosity. This compound has been shown to form stable complexes with many metals and nonmetals, such as lithium, sodium, silver, copper, gold, palladium, nickel, cobalt and zinc. 1-Butyl-3-methylimidazolium dicyanamide has been used for solvent extraction of metals and as an electrolyte in electrochemical studies. The solubility of this compound in water has been found to be dependent on the concentration of the hydrogen bond acceptor sites on the surface of the solute molecule.</p>

1-Methyl-N-(9-methyl-9-azabicyclo[3.3.1]non-3-yl)-indazole-3-carboxamide is a chemical inhibitor of the 5HT2 receptor, which is responsible for regulating nausea and vomiting. It has been shown to have antiemetic properties, and can be used in chemotherapy to control nausea and vomiting. The 5HT2 receptor is coupled to Gs proteins and inhibits adenylyl cyclase activity, while 1MMAI binds to the 5HT2A receptor and blocks serotonin from binding. This prevents serotonin from activating Gq protein receptors, which are involved in the generation of intracellular calcium concentrations that lead to neurotransmitter release. 1MMAI also inhibits the activation of phospholipase C by serotonin, resulting in decreased levels of diacylglycerol (DAG) and inositol triphosphate (IP3). These changes inhibit plate

<p>1-Z-N'-Hydroxypropanimidamide is a novel anion that has been shown to inhibit the proliferation of human cancer cells. It binds to the cholinergic receptor subtype and inhibits the uptake of acetylcholine, which leads to a reduction in the production of nitric oxide. 1-Z-N'-Hydoxypropanimidamide also inhibits the growth of Mycobacterium tuberculosis and possesses antimycobacterial activity. This compound is a ligand that binds bidentate to both DNA and RNA molecules and inhibits chemokine signaling.</p>