Amides

<p>Tiaramide hydrochloride is a nonsteroidal anti-inflammatory drug that inhibits the production of prostaglandins. It has been shown to have an anti-inflammatory activity in bowel disease and inflammatory bowel disease, which may be due to its ability to inhibit the production of prostaglandin synthesis. Tiaramide hydrochloride is also a coumarin derivative that can form an n-oxide on exposure to air or light. It has been used in tissue culture experiments as a nanoparticulate composition, where it was found to have a dose-dependent effect on cell viability and proliferation. Tiaramide hydrochloride has been used in sample preparation for human serum and rat liver microsomes, where it showed a hydroxyl group that binds with fatty acids.</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>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>

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

<p>4-Benzylpiperazine-1-carboximidamide sulfate is a versatile building block that can be used in the synthesis of complex compounds. It is a useful intermediate that can be used in the production of research chemicals and speciality chemicals. 4-Benzylpiperazine-1-carboximidamide sulfate is also an excellent reagent for reactions involving complex substrates, such as high quality and useful scaffolds.</p>

<p>N-[2-Iodoethyl]trifluoroacetamide is a reactive alkylating agent that is used in the synthesis of biologically active molecules. It reacts with lysines, tryptic and other amino acids to form covalent bonds, which can be cleaved by hydrolysis. The compound also reacts with sulfhydryl groups to produce sulfonium ions, which react with the thiol group at position C6 on the sarcoplasmic reticulum Ca2+ -ATPase to inhibit muscle contraction. N-[2-Iodoethyl]trifluoroacetamide has been shown to cause allergic reactions in rats, mice, and guinea pigs. This drug has also been observed to have an effect on the central nervous system when administered at high doses.</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>

<p>4-Hydroxy-3,5-dimethoxybenzamide is a phenolic compound that is soluble in organic solvents. It has been shown to bind to fatty acid sequences and neutral polypeptides in the presence of an acidic or basic environment. 4-Hydroxy-3,5-dimethoxybenzamide has also been shown to have catalytic activity, which may be due to its ability to form a polymeric matrix with other compounds.</p>

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<p>Sulfacetamide sodium monohydrate is a sulfa drug that is used in the treatment of infections caused by bacteria that are sensitive to sulfonamides. It is also used to reduce the symptoms of rosacea, a skin condition. Sulfacetamide sodium monohydrate inhibits microbial growth by disrupting microbial fatty acid synthesis and inhibiting bacterial growth through various mechanisms including hydrolysis by hydrochloric acid, metabolic disorders, or changes in water permeability. It has been shown to be an effective treatment for congestive heart failure due to its ability to increase the thickness of the glomerular basement membrane and inhibit erythrocyte adhesion. This drug is also useful as a topical agent for treating mild cases of radiation dermatitis and has high values as an anhydrous sodium sulfate substitute for wastewater treatment.</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>

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<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>3-[(Aminocarbonyl)amino]-5-[4-(morpholin-4-ylmethyl)phenyl]thiophene-2-carboxamide is a chemical inhibitor that inhibits the activity of kinases. It has been shown to be cytotoxic against cancer cells and to induce apoptosis through a number of different mechanisms. 3-[(Aminocarbonyl)amino]-5-[4-(morpholin-4-ylmethyl)phenyl]thiophene-2-carboxamide binds to DNA and induces DNA repair, which can lead to cell death. This drug also has an anti-inflammatory effect, which may be due to its ability to inhibit pro-inflammatory cytokines such as TNFα and IL1β.</p>

<p>N-[4-[1-(2-Fluorobenzyl)-3-butyl-2,6-dixo-2,3,6,7-tetrahydro-1H-purin-8-ylmethyl]phenyl]acetamide is a fine chemical with a diverse range of potential applications. It can be used as a versatile building block in the synthesis of complex compounds and is useful as a reaction component or reagent. Its CAS number is 628279-07-2.</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>Cecropin A (1-7)-Melittin A (2-9) amide trifluoroacetate salt is a cecropin-melittin hybrid peptide that has been immobilized on cellulose nanofibers for use as an antimicrobial. It has been shown to have strong antimicrobial activity against bacillus subtilis, and the immobilization process ensures that the peptide is not released from the surface of the material. The process of coating with nanopaper and then applying the peptides provides a stable surface with high antimicrobial activity. The synthetic peptides are synthesized by solid phase synthesis using Fmoc chemistry and purified by preparative HPLC.</p>

<p>2-Chloro-5-(2,3-dihydro-1-hydroxy-3-oxo-1H-isoindol-1-yl)-benzenesulfonamide is a drug that belongs to the class of sulfonamides which is used in pharmaceutical formulations. It has been shown to have potent antihypertensive effects, and it also lowers blood pressure by inhibiting an enzyme called carbonic anhydrase. 2CCHIB binds to the chloride channel in kidney tubule cells and prevents the reabsorption of chloride ions in these cells. This leads to more water being excreted from the body, which reduces blood volume and pressure. The low density lipoprotein (LDL) cholesterol levels are also reduced when this drug is taken orally. 2CCHIB increases high sensitivity C reactive protein (hsCRP), a marker for inflammation, but it can also have antioxidant effects.</p>

<p>L-Aspartic acid beta-naphthylamide is a dietary amino acid that is metabolized to oxaloacetate in the liver. This metabolite is then converted to aspartate and glutamate, which are both important for brain functions. L-Aspartic acid beta-naphthylamide has been shown to have regulatory effects on peptide hormones, such as inhibiting the synthesis of angiotensin II and vasopressin in rats. L-Aspartic acid beta-naphthylamide also has anti-cancer properties, which may be due to its ability to inhibit the growth of cancer cells by hydrolyzing proteins and enzymes involved in fatty acid synthesis.</p>

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<p>N-Phenylhydrazinecarbothioamide is a chemical compound that is used in wastewater treatment. It is an organic molecule that is composed of hydrophobic and hydrophilic parts. The hydrophobic part, which contains the phenyl group, binds to the hydrophobic region of the cell membrane and causes the cell to lyse. The hydrophilic part has an affinity for water and can be used as an electrode material in electrochemical impedance spectroscopy. N-Phenylhydrazinecarbothioamide also has been shown to have antibacterial properties against human pathogens, including Mycobacterium tuberculosis, Clostridium perfringens, and Escherichia coli O157:H7. The compound has been shown to inhibit cervical cancer cells by inhibiting protein synthesis through inhibition of ribosomal activity and fragmentation assay analysis showed that N-phenylhydrazinecarbothioamide binds to copper ions at a coordination geometry of</p>

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

<p>Lacosamide is a drug that is used for the treatment of epilepsy. It has been shown to inhibit neuronal death in vitro and in animal models, and has been extensively studied for its potential benefits in the treatment of bowel disease. The mechanism of action for lacosamide involves inhibition of the transport of neurotransmitters from the synaptic cleft by binding to the neuronal sodium channels and increasing their recovery rate. Lacosamide has also been found to affect energy metabolism by inhibiting the activity of mitochondrial enzymes such as matrix effect and complex I/III.</p>

<p>N-Allyl-N-(4-cyano-2-chlorophenyl)acetamide is a high quality reagent that has been used as an intermediate in the synthesis of fine chemicals, useful scaffolds and building blocks. It is also a versatile building block that can be used to synthesize high quality compounds with a wide range of functionalities. N-Allyl-N-(4-cyano-2-chlorophenyl)acetamide is a speciality chemical that can be used for research purposes. This compound has been shown to produce reactions with other compounds, such as nitrobenzene, to generate useful products.</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>Quinfamide is a polyunsaturated compound that contains a cevimeline hydrochloride molecule. It is used to treat bowel disease, usually in combination with other drugs. Quinfamide has been shown to have specific treatment effects on the symptoms of inflammatory bowel disease (IBD) when given at doses of 400-800 mg per day for up to 12 weeks. This drug can also be used as an analog for 5-membered heteroaryl compounds, such as benzalkonium chloride, which are also used to treat bowel disease. Quinfamide has been shown to have anti-inflammatory properties and may work by inhibiting fatty acid synthesis or by reducing the number of neutrophils in the gut.</p>

<p>N-[3-(3-Dimethylamino-1-oxo-2-propenyl)phenyl]-N-ethylacetamide is a high quality, complex compound that is useful as a reagent, intermediate, and building block. The CAS number for this product is 96605-66-2. This product has shown to have use in the synthesis of fine chemicals and research chemicals. It is a versatile building block that can be used as a reaction component.</p>

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<p>2-Amino-3-benzoylbenzeneacetamide is an ophthalmic drug that has significant cytotoxicity. It is used to treat inflammation of the retina and macula, as well as other diseases of the eye such as uveitis. 2-Amino-3-benzoylbenzeneacetamide is a nonsteroidal anti-inflammatory drug (NSAID) that inhibits prostaglandin synthesis by blocking cyclooxygenase. This agent has been shown to be effective in reducing pain and inflammation in animal models, but there are no studies on its side effects or analytical methods for detection. There are also no studies on the effectiveness of this drug for treating uveitis.</p>

<p>Metformin is an antidiabetic drug that is used to treat type 2 diabetes. It works by increasing insulin sensitivity and decreasing glucose production in the liver. Metformin does not cause low blood sugar in people with diabetes, but it can lower blood sugar in those without the condition. Metformin is available as metformin hydrochloride and has a molecular weight of 314.5 g/mol. Metformin is excreted primarily through the kidneys, with less than 10% of a dose being excreted unchanged in the urine. Excipients include acetonitrile, which is used as an organic solvent for liquid drug products; impurities may be present due to incomplete synthesis or purification processes; and animal studies are performed to assess safety and efficacy of drugs that may have adverse effects on humans.<br>Metformin has been shown to decrease blood sugar levels in animals through its antidiabetic potential, but there are no studies showing its effect on humans with type</p>

<p>Acetamide is an acyclic nucleoside phosphonate with a basic structure. Acetamide is metabolized to the corresponding ester hydrochloride, which has been shown to inhibit the polymerase chain reaction. This inhibition may be due to the effector proteins that are inactivated by acetamide, or it could be due to radiation-induced changes in the amide bond of the enzyme. Acetamide and its ester hydrochloride have been shown to inhibit skin cancer cells and carcinoma cell lines.</p>

<p>Avanafil is a drug that can be used as a treatment for male erectile dysfunction. It works by inhibiting the production of PDE5, which is an enzyme that regulates the levels of cGMP in the penis. Avanafil has been shown to be effective when taken at a dose of 100 mg; this is because it takes about 30 minutes for avanafil to reach its peak level. Avanafil has a chemical stability that is greater than 12 hours, with an average lifespan of 24 hours. The drug also has no major drug interactions and does not inhibit any other drugs from working.</p>

<p>4-Bromobenzamide is an amide with a hydrogen bond that inhibits the activity of proteases. It has been shown to inhibit the activity of cathepsin C and chymotrypsin in vitro, as well as the proteolytic activity of elastase. 4-Bromobenzamide also has a covalent inhibition effect on protein synthesis. This inhibitor is capable of reducing the levels of glutathione reductase, cytochrome P450, and mycobacterium in cell culture. In addition, 4-bromobenzamide has been shown to have acute toxicities in mice and rats when administered at high doses. However, it does not show any toxic effects on healthy mice or rats when administered at low doses.</p>

<p>Anthranilamide is used for non-selective, efficient fluorescent labelling of glycans.</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>N-(2-indol-3-ylethyl)-3-phenylprop-2-enamide is a serotonin analog that has been shown to inhibit the production of tryptophan decarboxylase in organisms. This compound has also been shown to be an inhibitor of the biosynthesis of p-coumaric acid, which is involved in the synthesis of lignin, phytoalexins, and other phenolic compounds. N-(2-indol-3-ylethyl)-3-phenylprop-2-enamide may be useful as a fungicide against pyricularia or as an antimicrobial against microbial infections.</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>Indapamide is an antihypertensive drug that inhibits the activity of the enzyme carbonic anhydrase, which is involved in the conversion of carbon dioxide to bicarbonate. It is used to treat high blood pressure and congestive heart failure. Indapamide has been shown to be effective in reducing oxidative injury to red blood cells and preventing cardiovascular events such as stroke and heart attack. Indapamide also has a long-term efficacy with no withdrawal symptoms or rebound hypertension when it is discontinued.</p>

<p>Propiolamide is a sulfoxide-substituted diphenyl compound that inhibits the growth of cancer cells. It is an irreversible inhibitor of the enzyme, protein kinase C, which has been shown to be involved in the regulation of cell proliferation and differentiation. Propiolamide also inhibits the production of estrone sulfate by inhibiting mitochondrial superoxide production. The hydrochloric acid-catalyzed reaction solution can be prepared using anhydrous sodium as a reducing agent and chemical stability can be achieved by using palladium as a catalyst.</p>

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

<p>3,5-Dinitrobenzamide is a sulfa drug that inhibits the growth of bacteria by inhibiting 3-dehydroquinate synthase (EC 4.2.1.23) and 3-dehydroquinate dehydratase (EC 4.2.1.46). The enzyme catalyzes the conversion of 3-dehydroquinic acid to quinic acid, which is an intermediate in the biosynthesis of benzoic acid from glucose. This inhibition occurs because 3,5-dinitrobenzamide forms a glycosidic bond with Cys34 in these enzymes, which prevents their function. This drug has been shown to have significant cytotoxicity against human pathogens and model organisms such as Salmonella typhimurium and Escherichia coli, but not against Saccharomyces cerevisiae or Candida albicans.</p>

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

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<p>Agonist of D2 dopamine receptors</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>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>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-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>Please enquire for more information about D-Valine amide hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>