Amides

<p>COX inhibitor; non-steroidal anti-inflammatory drug</p>

<p>Oxyclozanide is an antimicrobial agent that inhibits the enzyme activity of chitin synthase in the nematode, which is necessary for the production of chitin. This inhibition leads to disruption of the nematode's cell membrane and death. Oxyclozanide has been shown to be effective against resistant mutants, as well as synergistic with other antimicrobial agents. It is also a specific antidote for oxyclozanide poisoning.</p>

<p>Agonist of D2 dopamine receptors</p>

<p>Coenzyme B12, also known as vitamin B12, is a coenzyme that participates in the metabolism of amino acids and fatty acids. It is required for the conversion of homocysteine to methionine, which is an important step in the synthesis of S-adenosylmethionine (SAM), a major methyl donor. Coenzymes are required for many different reactions in cells, but they are not consumed during these reactions. Instead, they are regenerated and reused. Coenzyme B12 is synthesized by bacteria and archaea but not by animals. The cobalamin form of this coenzyme is made from cobaltous chloride or cobaltous sulfate and cyanide. This coenzyme has been shown to bind to riboswitches in bacteria and to ATP-binding cassette transporters in humans. Coenzyme B12 can exist in two different forms: adenosylcobalamin and methylcobalamin.</p>

<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>4-Aminobenzamide is a compound that is used as an anti-tuberculosis drug. It inhibits the activity of aminotransferase, which is an enzyme responsible for converting amino acids into other compounds. 4-Aminobenzamide has been shown to have antimicrobial properties against bacteria, fungi and protozoa. It also has a protective effect on human liver cells, but can cause damage to rat liver cells in vitro. 4-Aminobenzamide also shows some activity against microbial metabolism and can be hydrolyzed by hydrochloric acid to form phenylacetic acid and ammonia. This compound has been shown to inhibit the nervous system disease progression of Huntington's disease in mice.</p>

<p>2-Chloro-N,N-diphenylacetamide is a functional theory that has been shown to have antimicrobial activity against mammalian cells. It is an acetamide derivative with a formyl group and two chloro substituents. 2-Chloro-N,N-diphenylacetamide inhibits the growth of Mycobacterium tuberculosis by binding to the ribosomal protein P0, which inhibits the production of proteins vital for cell division. This drug also has antifungal properties, inhibiting the synthesis of ergosterol in filamentous fungi such as Candida albicans.<br>2-Chloro-N,N-diphenylacetamide is also known to inhibit the growth of other bacteria by binding to their ribosomes and interfering with protein synthesis. This drug may also be active against viruses due to its ability to bind chloride ions.</p>

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

<p>Rink amide-AM resin is a cation exchange resin that is used in peptide synthesis. It has an optimal pH range of 8-9. Rink amide-AM resin can be activated with trifluoroacetic acid or piperidine and washed with a mixture of water and methanol to remove the salt byproduct. The resin can then be used for peptide synthesis, which is typically done by adding the desired amino acids in sequence to the resin. The synthesis is stopped when the linear peptide reaches a desired length, typically 12-15 amino acids long. The linear peptides are then cleaved from the resin using trifluoroacetic acid or piperidine, depending on which activation reagent was used during synthesis. After cleavage, the linear peptides are precipitated from solution using ethanol or acetone and collected by filtration.</p>

<p>(S,E)-3-(6-Bromopyridin-2-yl)-2-cyano-N-(1-phenylethyl)acrylamide (MBI-23) is a potential antineoplastic agent that has been shown to induce regression of bladder cancer in mice. MBI-23 induces apoptosis by inhibiting the proliferation of cancer cells and inducing differentiation of cancer stem cells. It is also shown to inhibit tumor growth and progression in glioma and prostate cancer models. MBI-23 binds to the KDR receptor subtype, which is activated by organic acids and inhibited by inorganic compounds. This binding leads to constitutive activation of the KDR receptor, thereby inducing apoptosis. The tautomers and stereoisomers of MBI-23 have not been fully elucidated yet.</p>

<p>Clofenamide is a drug that is used to treat insulin resistance. It is an at1 receptor antagonist that blocks the action of histamine, which stimulates the release of insulin from the pancreas. Clofenamide has been shown to reduce systolic blood pressure in patients with autoimmune diseases and cardiac hypertrophy. It is also used for treating infectious diseases, such as pneumonia and tuberculosis. Clofenamide reduces inflammation by inhibiting inflammatory enzymes, such as butyric acid. This drug has been found to have anticancer activity in cell-based studies by inhibiting cellular proliferation and inducing apoptosis in cancer cells.</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>N-[4-(2-Hydrazino-2-oxoethoxy)phenyl]acetamide is a phenolic compound that has been shown to have an antimicrobial effect. It has been shown to have antitubercular activity against Mycobacterium tuberculosis and the ability to inhibit the growth of cancer cells in vitro. N-[4-(2-Hydrazino-2-oxoethoxy)phenyl]acetamide is also known as monastrol. The pharmacophore of this drug is based on the structure of paracetamol, which is a member of the class of drugs known as analgesics, antipyretics, and antiinflammatory agents. Paracetamol has been used for decades in humans and animals for relief from pain, fever, and inflammation. N-[4-(2-Hydrazino-2-oxoethoxy)phenyl]acetamide may be useful for treating diseases such as cancer or tuberculosis due to its antic</p>

<p>Indole-3-acetamide is an organic compound that is a component of the natural amino acid tryptophan. Indole-3-acetamide has been shown to be a potential anti-cancer drug. It inhibits prostate cancer cells and wild-type strains by inhibiting fatty acid synthase, which is an enzyme that catalyzes the synthesis of fatty acids. Indole-3-acetamide is also able to increase the production of monoclonal antibodies in mice with antigenic stimulation.</p>

<p>4-Nitrobenzamide is a chemical substance that belongs to the class of nitrobenzamides. It is used as an intermediate in the synthesis of other substances, such as pharmaceuticals, herbicides, and pesticides. 4-Nitrobenzamide was first synthesized in 1894 by hydrogenating nitrobenzoic acid with hydrogen chloride in the presence of phosphorus pentachloride. The reaction vessel for this process should be made of glass or porcelain due to the corrosive nature of hydrogen chloride gas. The kinetics for this reaction were studied using concentration-response curves on rats and mice at different concentrations. Acute toxicities observed include respiratory distress and death in rats and convulsions and death in mice.<br>4-Nitrobenzamide is also toxic to bacteria, which can be seen by its effect on Staphylococcus aureus (strain ATCC 25923). This strain had a 50% survival rate after exposure</p>

<p>2-Cyanobenzamide is a corrosion inhibitor that is used in the electrochemical industry to protect metals from corrosion. It has been shown to be suitable for use as a corrosion inhibitor in salt water and other corrosive environments. 2-Cyanobenzamide has been shown to have light sensitive properties, which is why it should not be exposed to direct light or stored in dark containers. It also inhibits enzymes that are involved in the production of reactive oxygen species (ROS) such as superoxide anion and hydrogen peroxide. The reaction of 2-cyanobenzamide with aluminium, sodium sulfide, and polymeric matrices has also been studied extensively.<br>2-Cyanobenzamide can be synthesized by reacting benzoyl chloride with ammonia and cyanogen bromide. This reaction produces a mixture of mono-, di-, tri-, and tetramers of 2-cyanobenzamide. These products can then be separated using analytical methods such as</p>

<p>Marker for Farber disease diagnosis</p>

<p>2-Amino-4-methylthiophene-3-carboxamide is a small molecule that is a potent inhibitor of the JAK2 kinase. This enzyme is associated with human fibrosis and has been shown to be involved in the development of liver fibrosis in rats. 2-Amino-4-methylthiophene-3-carboxamide inhibits the production of cytokines such as IL1α, IL6, and TNFα. It also blocks the activation of transcription factors such as NFκB, which are involved in inflammation. The compound has been shown to be orally active and has demonstrated efficacy in animal studies. Analogues have also been synthesized for this compound that show similar activity.</p>

<p>N-Methyl-N-trimethylsilylacetamide is a bifunctional amide that can react with an electrophile, such as hexane, to form an N-methylated product. The amide group of the molecule can also be deprotonated by a strong base to form an enolate, which can then react with a nucleophile. The NMR spectra of this compound show that it has a multinuclear structure and contains two tautomers. It is used in analytical chemistry for sample preparation, chromatographic science for reaction intermediates, and chemical study for its reactivity.</p>

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

<p>4-Chlorocinnamide is an organochlorine compound that has been found to have antibacterial properties. It inhibits the shikimate pathway in bacteria, which is essential for bacterial growth. This molecule has been shown to bind with the cation channel of the nerve cells in the trigeminal nerve and inhibit their function. The inhibition of this channel leads to reduced sensitivity to pain. 4-Chlorocinnamide is also a precursor in the synthesis of stilbene derivatives, which are used as anticancer drugs.</p>

<p>N-Isopropylacrylamide is a biocompatible polymer that is used in the preparation of polymers. It is a solid phase microextraction material that is used in sample preparation and purification. N-Isopropylacrylamide has a phase transition temperature of -5°C and can be polymerized to form a polymer. This polymerization process can be done with or without catalysts, which are required for the formation of many other types of polymers. N-Isopropylacrylamide has been shown to have good affinity for human serum and wastewater treatment effluent samples, as well as for chitosan polymer surfaces. The kinetic data show that this polymer possesses high capacity for trifluoroacetic acid (TFA) reactivity, which makes it suitable for use in reaction solutions.</p>

<p>N-(3,5-Dichloro-4-Pyridinyl)-2-[1-(4-Fluorobenzyl)-5-Hydroxy-1H-Indol-3-Yl]-2-Oxoacetamide is a prodrug that is metabolized to the active form in vivo. It inhibits the activity of cyclic nucleotide phosphodiesterase (PDE), an enzyme that catalyzes the conversion of cAMP to AMP and PDE, which catalyzes the conversion of cGMP to GMP. This drug has been shown to have a potent inhibitory effect on inflammatory cytokines such as IL-6 and TNFα. N-(3,5-Dichloro-4-pyridinyl)-2-[1-(4 fluorobenzyl)-5 hydroxy 1H indol 3 yl]-2 oxoacetamide has been shown to be effective for treatment of inflammatory diseases such as bronch</p>

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

<p>4-Hydroperoxycyclophosphamide (4-HPPC) is a cytotoxic agent with anti-cancer properties. It is a prodrug that is converted to 4-hydroxycyclophosphamide, the active form of the drug, by hydrolases in cells. The cytotoxicity of 4-HPPC has been demonstrated using a model system of human erythrocytes and HL60 cells. This drug also has an effect on tumor growth and metastasis, as well as on bowel disease. Rats treated with 4-HPPC showed decreased levels of blood glucose, increased glutathione peroxidase activity, and a decrease in the number of colonic tumors after only one dose. The low-dose group had improved mitochondrial membrane potential and an increase in cell factor receptor activity. These results indicate that 4-HPPC may be a useful anti-cancer compound for treating various types of cancer including colon cancer.</p>

<p>(E)-N-(3-Methylaminopropyl)-2-thiopheneacrylamide is a high quality chemical that can be used as an intermediate in the synthesis of complex compounds. It is also a useful scaffold and building block for the synthesis of speciality chemicals with versatile reactions.</p>

<p>2-Chloro-N-(2-nitrophenyl)acetamide is an antimicrobial agent that is a ligand for thionyl chloride. It has efficient methods of production and can be used as a bioactive molecule in the synthesis of aminosulfonyl chlorides, amide chlorides, or transfer chlorides. This compound reacts with gram-negative bacteria by hydrolyzing chloride ions to produce nitrosyl chloride and releasing hydrogen gas. The reaction time and functional groups are determined by the parameters chosen for the reaction. 2-Chloro-N-(2-nitrophenyl)acetamide has luminescence properties that can be exploited to detect the presence of chloride ions at low concentrations.</p>

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

<p>Eliglustat is an oral medication used as a substrate reduction therapy for Gaucher disease type 1, which is an inherited lysosomal storage disorder. This product is a small-molecule inhibitor derived via chemical synthesis. Its primary mode of action involves the selective inhibition of glucosylceramide synthase, an enzyme responsible for the first committed step in glycosphingolipid biosynthesis. By reducing the production of glucosylceramide, eliglustat decreases the substrate accumulation that contributes to the pathophysiology of Gaucher disease.</p>

<p>4-Aminothiobenzamide (4ATB) is a chemical compound that is used as an anticancer agent and an antimicrobial agent. It has been shown to have antitumor activity against human liver cancer cells and anticancer activity against human adrenergic receptor-positive lung cancer cells. 4ATB binds to the chloride ion present in the cell membrane, which prevents the influx of chloride ions into the cell. This leads to an increase in intracellular pH and disruption of cellular functions. 4ATB has also been shown to inhibit methicillin-resistant Staphylococcus aureus (MRSA) infections by inhibiting bacterial growth and reducing the production of proteins vital for cell division.</p>

<p>Dopamine (D2) receptor antagonist; 5-HT4 serotonin receptor agonist</p>

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

<p>Please enquire for more information about N-(4-(tert-Butyl)phenyl)-3-(4-chlorophenyl)prop-2-enamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Carbonic anhydrase inhibitor; anti-glaucoma agent</p>

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

<p>N-Cyclohexyl-2-benzothiazolylsulfenamide is a cross-linking agent that is used in the production of polymeric matrices. It is a multi-walled carbon molecule with an aromatic hydrocarbon cross-linker. N-Cyclohexyl-2-benzothiazolylsulfenamide reacts with fatty acids to form cationic surfactants, which can be used as antimicrobial agents. The reaction mechanism for this type of chemical reaction has been studied under constant pressure conditions and it was found that sulfur transfer occurs in the first step, followed by activation energies for the second and third steps. The diameter of the product depends on the degree of polymerization (DP).</p>

<p>N-(2-Fluorophenyl)-N-[4-(4-methyl-1,3-thiazol-2-yl)-1-(2-thiophen-3-ylethyl)piperidin-4-yl]propanamide is a drug that is used for the treatment of cancer. This drug is hydrophobic and has a molecular weight of 455. It has been shown to be effective in treating cancer cells by binding to the cell membrane and inhibiting the proliferation of these cells. N-(2-Fluorophenyl)-N-[4-(4-methyl-1,3-thiazol-2-yl)-1-(2-thiophen-3-ylethyl)piperidin]-4-- yl]propanamide also inhibits tumor growth by reducing extracellular matrix production and inducing apoptosis in cancer cells. This drug has a fluorescent property and can be detected with an optical microscope at a</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>N,N-Diethylcyanoacetamide is an organic compound that is used in the industrial production of polyurethane. It reacts with a nucleophile to form a new carbon-nitrogen bond. The reaction can be monitored in real time, and it has high specificity for the desired product. N,N-Diethylcyanoacetamide reacts with piperidine to produce a mixture of isomers in which the methyl group is attached to either the nitrogen or the oxygen atom. This mixture can be separated by crystallization, and it generates a pure product that can be used as a monocarboxylic acid.</p>

<p>C2 dihydroceramide is a lipid that belongs to the group of sphingolipids and is involved in neuronal death. It is a precursor for ceramide, which can also induce apoptosis. C2 dihydroceramide has been shown to inhibit axonal growth by interfering with the polymerase chain reaction, as well as inducing autophagy through toll-like receptor 4 signaling. This lipid has also been shown to inhibit intracellular Ca2+ levels, mitochondrial functions, and bowel disease. C2 dihydroceramide was identified in HL-60 cells and may be used as an analytical method for detecting other sphingolipids.</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-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>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>

<p>Please enquire for more information about N-(4-(4,5-dichloroimidazolyl)phenyl)(2-(4-chlorophenoxy)(3-pyridyl))formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-(2-Oxo-2-phenylethyl)-N-phenylbenzamide is a fine chemical that can be used as a versatile building block and reagent for the synthesis of complex compounds. This compound has been shown to react with both amines and alcohols in the presence of acid to produce useful products. It is also an intermediate for the synthesis of other compounds, such as pharmaceuticals, pesticides, and herbicides. N-(2-Oxo-2-phenylethyl)-N-phenylbenzamide is soluble in organic solvents and can be purified by recrystallization or column chromatography. The purity of this compound can be confirmed by nuclear magnetic resonance spectroscopy (1H NMR) or mass spectrometry (MS).</p>

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

<p>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-Methyl-N-vinylacetamide is a colorless liquid with a boiling point of 105.6°C. It is produced by the reaction of acetamide and vinyl chloride in the presence of hydrochloric acid, glycol ether, and methyl ethyl ketone. The viscosity of this compound is low, which makes it an ideal solvent for paints and coatings. N-Methyl-N-vinylacetamide also has genetic damaging effects and can cause mutations in bacteria that are exposed to this compound in high concentrations. This product has an unusual chemical structure due to its hydrogen bonding interactions.br&gt;br&gt;<br>br&gt;br&gt;<br>Hydrogen bonds are weak intermolecular forces between polar molecules, such as water or alcohols, that are formed by the attraction between a partially positive hydrogen atom on one molecule and the negative end of another nearby molecule. Hydrogen bonds stabilize certain molecular structures because they provide partial shielding from electrostatic interactions with</p>

<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>