Amides

<p>2,3-Diaminobenzamide is a synthetic aromatic compound that is used as a radiation stabilizer. It is also an effective antimicrobial agent with reactive properties against bacteria and fungi. 2,3-Diaminobenzamide has been shown to have anti-cancer properties and can be used to treat inflammatory diseases such as rheumatoid arthritis or ulcerative colitis. The intramolecular hydrogen bond between the amide group and the benzene ring in 2,3-diaminobenzamide contributes to its stability and biological activity.</p>

<p>4-Iodobenzenesulphonamide is a drug with antifungal and anticancer activity. The compound has been shown to inhibit the growth of cancer cells in vitro. It also has an antifungal effect in vitro, which is most likely due to its ability to inhibit the synthesis of ergosterol, a component of the cell membrane. 4-Iodobenzenesulphonamide may be used for the treatment of cervical cancer and vulvovaginal candidiasis. This drug does not show any serious side effects, but it has been shown to have some adverse effects on liver function tests and red blood cells.</p>

<p>2-Chloro-5-nitrobenzene sulfonamide (2CNS) is a glycol ether that has been shown to inhibit the activity of carbonic anhydrase. It has been shown to be a competitive inhibitor of the enzyme, and can be used as a lead compound for developing new drugs. 2CNS has been shown to inhibit an anhydrase that is found in bacteria, such as Streptococcus pneumoniae, Haemophilus influenzae, and Staphylococcus aureus. This inhibition causes increased levels of hydrogen ions in the bacterial environment, which leads to the acidification of their surroundings. 2CNS also inhibits chloride ion uptake in these bacteria.<br>2CNS's pharmacophore includes two aromatic hydrocarbon rings with at least one hydrogen bond acceptor group on each ring. This pharmacophore is responsible for its inhibition of carbonic anhydrase and chloride ion binding site.</p>

<p>Please enquire for more information about N-(4-(4-bromophenyl)-2,5-thiazolyl)hexanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>6-Hydroxy-N,2-dimethylbenzofuran-3-carboxamide is a fine chemical which is used as a building block in the synthesis of complex compounds. It can be used as a reactant in various reactions, such as Friedel-Crafts reactions and cycloadditions. This compound has been shown to be a useful intermediate for the synthesis of various heterocyclic compounds and scaffolds for drug development. 6-Hydroxy-N,2-dimethylbenzofuran-3-carboxamide has CAS number 638217-08-0 and is readily available in high quality.</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>

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<p>4-Chloro-3-nitrobenzamide (4CNBA) is a potent inducer of hepatic drug metabolizing enzymes. It reacts with methyl cinnamate to form the 4-chloro-3-nitrobenzamide methyl ester and chloride ions. This reaction is catalyzed by copper, which binds to the 4CNBA molecule. The chloride ion then displaces water from the ester, producing a nitroso intermediate. This intermediate breaks down into an unstable nitrite, which in turn reacts with hydrogen peroxide to form a hydroxylamine intermediate. Hydroxylamine can then react with sulfhydryl groups to produce reactive thiols that are responsible for the induction of detoxification enzymes in the liver.<br>4CNBA has been shown to be toxic at high concentrations and is rapidly detoxified by Phase II enzymes such as glutathione S transferase, UDP glucuronosyltransferase, and N-acetyl</p>

<p>(2R)-1-(Phenylmethyl)-N-[3-(spiro[isobenzofuran-1(3H),4'-piperidin]-1-yl)propyl-2-pyrrolidinecarboxamide HCl is an endogenous opioid that has been shown to have antidepressant-like effects. It can bind to γ-aminobutyric acid (GABA) receptors, catecholamine receptors, and nociceptin receptors. This drug also has anti-cancer properties and may be used for the treatment of autoimmune diseases. The interaction of this drug with other drugs is not well understood, but it has been shown to modulate the effects of opioids and increase the aversive nature of some substances.</p>

<p>Homoveratramide is a synthetic drug that is used as an antibacterial agent. It has a broad spectrum of activity against bacteria, fungi, and protozoa. Homoveratramide has been shown to be effective against both Gram-positive and Gram-negative bacteria, including Staphylococcus aureus, Streptococcus pneumoniae, Escherichia coli, Salmonella enterica, Pseudomonas aeruginosa, and Klebsiella pneumoniae. Homoveratramide inhibits the synthesis of DNA by binding to the enzyme ribonucleotide reductase. This produces a bacteriostatic effect on the cell by halting DNA replication and transcription.</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>4-Amino-N-((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-N-isobutylbenzenesulfonamide is an amide that is used to treat HIV infections. It has been shown to have potent anti-viral activity against HIV infected cells in the laboratory and can inhibit the replication of HIV by interfering with the virus's ability to use the reverse transcriptase enzyme. 4ABAB has been shown to bind to the enzyme ribonuclease H (crth2), which is responsible for breaking down viral RNA. This binding prevents crth2 from cleaving viral RNA, thus inhibiting DNA synthesis and preventing cell death. 4ABAB also interferes with a hydrogen bond between ethyl group and the hydroxyl group on crth2, leading to a decrease in activity.</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>Please enquire for more information about LL-37 amide trifluoroacetate 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-(2,5-dimethylphenyl)(3-chlorobenzo[b]thiophen-2-yl)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-(2-(3,4-dimethoxyphenyl)ethyl)(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>Nonafluorobutanesulfonamide (NFBS) is a volatile organic solvent that is used in the manufacture of coatings and other organic chemicals. It has been shown to have a high vapor pressure, which makes it useful for drying solvents. NFBS is also used as an intermediate in the production of fluorinated acrylates and methacrylates. NFBS reacts with styrene monomers to form ionic forms, and can be converted to its neutral form by reaction with acrylonitrile or acrylates. Nonafluorobutanesulfonamide has been shown to cause liver cancer in rats, but this effect has not been observed in humans.</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>The Val-Cit-PAB linker is an activated peptide linker that is cleaved by cathepsin B. It enables the selective intracellular release of attached drugs in ADC applications.</p>

<p>Please enquire for more information about 2-Chloro-N-(2-fluorophenyl)propanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N,N'-Dimethyl benzamide (DMAB) is an aryl halide that reacts with hydrogen to form the corresponding carbonyl group. The reaction solution of DMAB and hydrogen gas produces a chemical structure that resembles a hydrogen bond. DMAB has been shown to have anti-inflammatory effects in animals with inflammatory diseases. It has also been studied for its ability to inhibit the formation of amyloid plaque, which is associated with Alzheimer's disease. In addition, DMAB has been shown to have therapeutic effects against boron nitride and amides.<br>The crystal structure of DMAB can be found in both crystalline polymorphs: monoclinic and triclinic. The triclinic form is stable at room temperature and pressure, while the monoclinic form is only stable at higher temperatures. The monoclinic form is more soluble than the triclinic form, as it contains fewer hydrogen bonds between</p>

<p>N-[(8-Fluoro-2,3-Dihydro-1-Methyl-5-Phenyl-1H-1,4-Benzodiazepin-2-Yl)Methyl]-3-Furancarboxamide is a hydrophobic, implanting drug with an iontophoresis device. It has been shown to have therapeutic effects in cancer. The drug is a targetable molecule that can be used for diagnostic purposes and the treatment of various cancers. N-[(8-Fluoro-2,3-Dihydro-1,5 -Phenyl 1H -1,4 Benzodiazepin 2 Yl) Methyl] 3 Furancarboxamide has been shown to inhibit cell proliferation by blocking the synthesis of proteins required for DNA replication and also inhibits the activity of protein kinase C.</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>Modulator of CFTR channel in cystic fibrosis models</p>

<p>(S)-2-Aminobutyramide hydrochloride is a strong acid that can be used in the synthesis of other compounds. It is made by dissociating acetic acid with hydrogen chloride, or by reacting ammonia with hydrochloric acid. (S)-2-Aminobutyramide hydrochloride is also known as 2-aminobutyric acid dihydrochloride and protonated aminobutyric acid. It can be used to synthesize many other compounds, including amino acids, pharmaceuticals, and polymers. The virulent properties of this compound make it useful for industrial purposes.</p>

<p>Inhibitor of carbonic anhydrase</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>Phenylmethanesulfonamide is a chemical compound that has been shown to inhibit the proliferation of cancer cells in vitro. This drug has also been shown to be effective in reducing inflammatory diseases, such as arthritis and asthma, which may be due to its ability to inhibit prostaglandin synthesis. Phenylmethanesulfonamide has shown anti-inflammatory properties, which may be due to its inhibition of prostaglandin synthesis.</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-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>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>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-[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>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>3-(4-Hydroxyphenyl)propionamide is a heparinoid that is found in exudates, such as urine and saliva. It has significant cytotoxicity against the cell line Hepg2. 3-(4-Hydroxyphenyl)propionamide inhibits protein synthesis by binding to lectins and stabilizing them on the surface of the cells. This stabilizing effect blocks the lectin-carbohydrate interaction that leads to cellular activation and inflammation. 3-(4-Hydroxyphenyl)propionamide also has an anti-aging effect, which may be due to its ability to enhance chloride ion flow in biological tissues.</p>

<p>Gly-pro-4-methoxy-β-naphthylamide hydrochloride is a fine chemical that is useful as a versatile building block and intermediate. It is a research chemical that has been used in the production of other compounds, such as drugs, pesticides, and dyes. This compound is also used to synthesize certain polymers and plastics. Gly-pro-4-methoxy-β-naphthylamide hydrochloride has CAS number 100929-90-6, but it can be found under many other names including 4-(2′,5′dimethylphenyl)-1-(2′hydroxyethyl)piperazine (CAS 105999).</p>

<p>Please enquire for more information about 2-(2,4-dichlorophenoxy)-N-(2-(3,4-dimethoxyphenyl)ethyl)ethanamide 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-((3,4-dimethoxyphenyl)methyl)(3-(2-chlorophenyl)-5-methylisoxazol-4-yl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<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>

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<p>a-[2-(Diisopropylamino)ethyl]-a-phenyl-2-pyridineacetamide is a hydrogen bond donor. It has been shown to have cytotoxicity in vitro, with parameters that can be used for accurate prediction of descriptors. These descriptors are informative and insightful, which can be used for regression analyses and linear regression methods. The pharmacokinetic properties of a-[2-(Diisopropylamino)ethyl]-a-phenyl-2-pyridineacetamide have been studied in humans and have shown linearity between dose and plasma concentration.</p>

<p>2-Phenyl-2-(2-piperidyl)acetamide is an enantiomeric amide that can be used as a chiral building block for the synthesis of other organic compounds. It is synthesized by reacting phenylacetic acid with piperidine. 2-Phenyl-2-(2-piperidyl)acetamide is a primary amide and has been shown to have analgesic properties.</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>

<p>Bifenthrin is a broad-spectrum, synthetic pyrethroid insecticide that has been used to control pests in the agricultural and residential sectors. It is applied as a spray or dust on plants and animals. Bifenthrin is highly toxic to mammals, with an oral LD50 of less than 10 milligrams per kilogram of body weight in rats and mice. The acute toxicity can be attributed to its ability to inhibit protein synthesis by binding to the cholinesterases, which are found in high concentrations in mammalian tissues.</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>

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<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>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>

<p>N-(3-Aminopropylmethacrylamide HCl is a water-soluble optical sensor that has been used in the field of bioanalysis. This compound has been shown to react with propranolol hydrochloride and produce a fluorescent product. The fluorescence intensity depends on the concentration of propranolol hydrochloride, which can be measured using an optical detector. N-(3-Aminopropylmethacrylamide HCl is synthesized from trifluoroacetic acid and 3-aminopropylamine using a solid-phase synthesis technique. This compound has also been used as a ligand for affinity chromatography and as a template molecule in nonsteroidal anti-inflammatory drug research.</p>

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