Amidas

Applications N-Dimethyl-(furan-3-ylmethyl)carbamothioyl)methanethioamide is an intermediate used in the synthesis of 3-((Furan-2-ylmethyl)imino]-N,N-dimethyl-3H-1,2,4-dithiazol-5-amine Hydrobromide (F864125), which is an insect chemosterilant and an agrochemical.

Applications N-[1-[3-(2-Ethoxyphenyl)-2,5-dihydro-5-oxo-1,2,4-triazin-6-yl]ethyl]acetamide is an intermediate in the synthesis of Vardenafil (V098001) related compounds.
References Olszewska, T., et al.: Tetahedron., 69, 474 (2013);

Applications N-(1-Chloro-2-oxo-2-phenylethyl)benzamide is an amidophenacylating reagent used in various organic reactions, e.g. in the synthesis of thiohydantoin derivatives.
References Balya, A.G., et al.: Russ. J. Gen. Chem., 78, 1427 (2008); Belyuga, A.G., et al.: Zhurnal Organichnoi ta Farmatsevtichnoi Khimii, 2, 25 (2004)

Applications Intermediate in the production of Cyclophosphamide metabolites.
References Takamizawa, A., et al.: Chem. Pharm. Bull., 20, 1612 (1972),

Applications N-(4-Bromo-2-picolinoylphenyl)-2-chloroacetamide is a derivative of 2-(2-Amino-5-bromobenzoyl)pyridine (A601785); an intermediate in the preparation of Bromazepam (B678500).
References Panderi, I., et al.: J. Pharm. Biomed. Anal., 17, 327 (1998); El-Haj, B., et al.: J. Anal. Toxicol., 25, 316 (2001); Hansen, S., et al.: J. Pharm. Biomed. Anal., 39, 322 (2005)

Applications 3,5-Di-tert-butyl-4-hydroxybenzamide is used in the preparation of 2-(3,5-di-tert-butyl-4-hydroxyphenyl)oxazoles as anti-atherosclerotic agents.
References Steinberg, et al.: Am. J. Cardiology, 57, 16 (1986), Reaven, et al.: Arteriosclerosis and Thrombosis, 12, 318 (1992),

Applications 4-(dimethylamino)benzenesulfonamide (cas# 6162-21-6) is a useful research chemical.

Applications 2,3-Dihydroxybenzamide is a disubstituted benzamide used in the preparation of a catechol metabolite of dilevalol. 2,3-Dihydroxybenzamide is also used in the preparation of iron chelating agents.
References Tulshian, D.D. et al.: Bioorg. Med. Chem. Lett., 3, 2073 (1993); White, G.P. et al.: Brit. J. Haematol., 33, 487 (1976);

Applications Intermediate in the preparation of nitro substituted quinazolones.
References Tobe, M., et al.: Bioorg. Med. Chem., 11, 3869 (2003), Chinigo, G., et al.: J. Med. Chem., 51, 4620 (2008),

Applications N-(2-acetyl-1-benzofuran-3-yl)-2-chloroacetamide (cas# 855715-46-7) is a useful research chemical.

Applications N-(2-Hydroxyethyl)tetracosanamide acts as a crude oil emulsifier.
References Zhiqiang, J., et al.: Fami Zhu Shen., 5 (2016)

Applications N-(3-Aminopropyl)acetamide Hydrochloride salt is a salt form of N-Acetyl-1,3-propanediamine (A165390), which is an protected intermediate in the synthesis of analogs of Spermidine (S680400), an antineoplastic agent.
References Bergeron, R. et al.: J. Med. Chem, 40, 1475 (1997);

Stability Light Sensitive, Moisture Sensitive
Applications N-(Hydroxymethyl)Acrylamide (cas# 924-42-5) is a useful research chemical.

Applications N-(3-(Dimethylamino)propyl)dodecanamide is used in the study of surface chemistry and colloids as a new surfactnt for hydrate anti-agglomeration in hydrocarbon flowlines and seabed oil capture.
References Sun, Minwei, Journal of Colloid and Interface Science, 402, 312-319, (2013)

Applications 4,5-DIMETHOXY-2-NITROBENZAMIDE (cas# 4959-60-8) is a useful research chemical.

Applications 2-Amino-2-butenediamide (cas# 18486-76-5) is a compound useful in organic synthesis.

Stability Moisture Sensitive
Applications 2-isothiocyanatoacetamide (cas# 145518-36-1) is a useful research chemical.

Applications N-Cyclopropyl 5-bromonicotinamide

Applications 3-(Hydroxymethyl)Benzamide (cas# 126926-34-9) is a useful research chemical.

Applications 3,8-Diimino-4,7-dimethyl-2,4,7,9-tetraazadecanediimidamide is a useful research chemical.

Applications 2-(Methylamino)benzamide (cas# 7505-81-9) is a useful research chemical.

Applications Pivalimidamide Hydrochloride is used as a reagent in the preparation of 2-alkyl-4-aryltetrahydropyridopyrimidines and 2-alkyl-4-aryl-tetrahydropyrimidoazepines as selective 5-HT2A antagonists.
References Shireman, B. T., et al.: Bioorg. Med. Chem. Lett., 18, 2103 (2008);

Applications N-(2-(1,3-Dioxoisoindolin-2-yl)ethoxy)benzamide is an intermediate in the synthesis of Fluvoxamine Maleate (F603500), a selective serotonin reuptake inhibitor (SSRI) used as an anti-depressant. Antiobsessional.
References Claassen, V., et al.: Br. J. Pharmacol., 60, 505 (1977); Koran, L.M., et al.: J. Clin. Psychopharmacol., 16, 121 (1996); Ware, M.R., et al.: J. Clin. Psychiatry, 58, Suppl. 5, 15 (1997); Inazu, M., et al.: Neurochem. Int., 39, 39 (2001)

Applications N-benzyl-2,2-dichloroacetamide (cas# 6063-50-9) is a useful research chemical.

N-Bromoacetamide is a reactive chemical that can react with the sodium channel to produce a postulated effect. It has been shown to inhibit the kinetics of the sodium channel in whole-cell voltage clamp experiments. This inhibition is reversible and does not depend on the pH of the solution. Bromoacetamide has been shown to have an irreversible inhibition on potassium channels, which may be due to its ability to form covalent bonds with sulfhydryl groups. Bromoacetamide also inhibits voltage-gated calcium channels, but at a slower rate than it does for sodium channels. N-Bromoacetamide has been shown to be effective in pharmacological treatments for epilepsy, myasthenia gravis, and multiple sclerosis.

N-(3-Aminopropyl)acetamide is a secondary amine that is used as a reagent in the profiling of tissues. It has been shown to inhibit the growth of Thermus thermophilus and other bacteria, including Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa. N-(3-Aminopropyl)acetamide has also been shown to inhibit the growth of cancer cells in cell culture. It was found to be effective against logarithmic growth phase cells and not against stationary phase cells. However, its mechanism of action is unknown.

Thionicotinamide is a drug that belongs to the group of ethionamide. It is a synthetic compound with synergistic activity against tuberculosis bacteria. Thionicotinamide inhibits bacterial growth by binding to mycolic acid, which is a component of the cell wall. Thionicotinamide also has conformational properties, which inhibit the enzyme activities. This drug also interacts with other drugs, such as ethionamide, and may have an effect on the metabolism of these drugs in humans. Thionicotinamide binds to lipids and reduces the activity of enzymes that are involved in lipid synthesis. The nitrogen atoms of thionicotinamide bind to four oxygen atoms from two molecules of glycol ethers in a 1:1 ratio. This binding leads to the formation of hydrogen bonds between these molecules, resulting in an increase in kinetic energy for these reactions and improved structural analysis for this molecule.

2-Methylnicotinamide is an amide that is used to treat inflammatory bowel disease. It inhibits the production of glutamate and aspartate, which are neurotransmitters that are involved in the inflammation process. 2-Methylnicotinamide has been shown to have a protective effect on renal function by reducing blood flow to the kidneys, thereby decreasing renal damage caused by glutamate and aspartate. This drug also has anticancer properties, which may be due to its ability to inhibit viral replication and reduce the incidence of cancer in animals. 2-Methylnicotinamide has not yet been tested on humans, but it is thought to be safe for use in pharmaceutical dosages.

Adrafinil is a prodrug. It is primarily metabolized in vivo to modafinil, resulting in very similar pharmacological effects.

Deshydroxy bicalutamide is a ligand that has been synthesized to bind to the androgen receptor. It is an antagonist of the androgen receptor. Deshydroxy bicalutamide has been shown to inhibit cancer cell growth in prostate cancer cell lines, which is due to its ability to bind and block the ligand-binding domain of the androgen receptor. Molecular modelling has shown that deshydroxy bicalutamide binds in the hydroxyl group region of the binding site, which blocks it from binding with other ligands such as testosterone. This may lead to decreased levels of testosterone in males, leading to decreased levels of androgens in prostate cancer cells.

4-(3-Amino-2-hydroxypropoxy)phenylacetamide is a sweetener that is used as an artificial sweetener. It can be found in many foods and drinks and is often used to replace sucralose due to its lower cost. 4-(3-Amino-2-hydroxypropoxy)phenylacetamide is a white powder with a melting point of 133°C. This product has been shown to be safe for human consumption, although it may cause headaches, drowsiness, or dizziness in some people.

L-Alanine amide hydrobromide is a carboxylic acid that can be used as an antibacterial agent. It reacts with the amino group of l-tyrosine and alkylsulfonyl groups to form an amide. L-Alanine amide hydrobromide has been shown to inhibit bacterial growth in vitro, and it also has anti-inflammatory properties. The antibacterial activity of L-alanine amide hydrobromide is activated by reaction time, which may be due to its ability to react with the basic proteins found in bacteria. This drug also interacts with vinyl alcohol, which may be important for its immobilized application.

Dopamine (D2) receptor antagonist

Please enquire for more information about 4-Amino-1-Boc-piperidine-4-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Acetohexamide is a hypoglycemic drug that binds to the sulfonylurea receptor on pancreatic beta-cells and stimulates insulin release. It has been shown to have an oral hypoglycemic effect in humans, as well as in rats. Acetohexamide has been shown to inhibit the action of nonsteroidal anti-inflammatory drugs, such as indomethacin, through competitive inhibition. Acetohexamide also inhibits the enzyme activity of estradiol benzoate and acetohexamide hydrolase. This drug is not active against bacteria or fungi, but has been shown to be effective against some viruses. Acetohexamide is absorbed by the gastrointestinal tract and excreted unchanged in urine and feces. The drug does not bind to proteins and does not cross the blood-brain barrier.

Formamide is a colorless, volatile chemical compound that is most commonly used in the laboratory for the preparation of dna duplexes. It can also be used to treat bowel disease and HIV infection. It is not active against viruses or bacteria but has been shown to bind to toll-like receptors on cells. Formamide is an organic substance that exists as a gas at room temperature and pressure. Formaldehyde reacts with water in the presence of sodium carbonate to form formamide, which is soluble in water. Formamide has been used as a reaction solution for surface methodology experiments because it evaporates quickly and leaves no residue on surfaces. Formamide has been shown to inhibit epidermal growth factor (EGF) activity by binding to the EGF receptor protein and preventing its activation. This inhibition leads to decreased cell proliferation, reduced protein synthesis, and inhibition of DNA replication.

Please enquire for more information about N-(p-Hydroxyphenethyl)-N-(3-hydroxy-4-methoxybenzyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

WAY 316606 is a potent, orally administered small molecule that inhibits the Wnt signaling pathway by blocking the action of β-catenin. It has been shown to have potential for treating eye disorders, including age-related macular degeneration. This drug also has potential for treatment of cell and nervous system diseases such as Alzheimer's disease and Huntington's disease. WAY 316606 inhibits the transcriptional activity of the β-catenin/Tcf4 complex by binding to it and preventing its translocation into the nucleus. In addition, WAY 316606 prevents downstream activation of genes regulated by β-catenin signaling, including c-myc and cyclin D1. This drug also blocks growth factor receptor tyrosine kinases and monoclonal antibodies that activate these receptors.

Please enquire for more information about (R)-Dragonfly N-trifluoroacetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 2-(2,5-Dimethoxyphenyl)ethylformamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

L-Tryptophanamide hydrochloride is a fluorescent compound that belongs to the amides. It has been shown to have invertase activity and be hydrated in both isooctane and water. L-Tryptophanamide hydrochloride also has an anxiolytic effect on mice, which may be due to its ability to inhibit the production of serotonin at synapses by blocking the enzyme tryptophan hydroxylase. The drug is used for the treatment of anxiety disorders, including generalized anxiety disorder (GAD) and posttraumatic stress disorder (PTSD). This drug has a molecular profile that can be detected by fluorescence spectrometry, with an enhancement factor of 1.5-2.5.

N-[2-(1,3-Dimethylbutyl)phenyl]-5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide is an herbicide that belongs to the group of fatty acid amides. It is a selective postemergence herbicide that inhibits the germination and growth of plants by inhibiting the synthesis of fatty acids. Unlike other chemical pesticides, it has no effect on animals or humans and it is not toxic to plants. The selectivity of N-[2-(1,3-Dimethylbutyl)phenyl]-5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide makes it a good candidate for use in combination preparations with other chemicals.

N-Desmethyl loperamide is a prodrug of loperamide, which is a peripherally acting μ-opioid receptor agonist. It has been shown to be effective in reducing the uptake of radiation in wild-type mice. This drug also inhibits p-glycoprotein (p-gp), and has been shown to reduce the uptake of pyridinium ions and amide substrates. N-Desmethyl loperamide has been shown to have anticancer properties, including resistance to radiation, inhibition of tumor growth and metastasis, and induction of apoptosis, which may be due to its ability to inhibit cellular proliferation and induce cell death. The mechanism by which this drug functions is not yet clear but it may involve inhibition of the expression or function of p-gp or other efflux pumps in cells that are sensitive to these drugs.

Benzenesulphonamide is a biologically active compound that has been shown to bind to an integrin receptor, which mediates the attachment of leukocytes to the endothelium. It also binds to a basic protein found in human immunoglobulin. Benzenesulphonamide has been shown to have cytotoxic effects on synchronous fluorescence cells and can be used for the treatment of bowel disease. This drug has also been shown to be toxic in vitro and in vivo, with a moderate acute oral toxicity and low chronic oral toxicity. Benzenesulphonamide has been shown to act as a surfactant by binding with sodium dodecyl sulfate (SDS), which is commonly used in detergents, disinfectants, shampoos, soaps, and other household products. The biological properties of benzenesulphonamide are not well-known due to its low solubility in water.