Amides

<p>Applications Sulfur trioxide N,N-dimethylformamide Complex is a reagent used to prepare aminopyridines which are inhibitors of tetrameric fructose-1,6-bisphosphatase.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Dang, Q., et al.: J. Med. Chem., 53, 441 (2010); Hebeisen, P., et al.: Bioorg. Med. Chem. Lett., 21, 3237 (2011)<br></p>

<p>Applications Precursor of Diazopropane. Carcinogen.<br>References Hecker, L.I., et al.: Cancer Res., 43, 4078 (1983),<br></p>

<p>Applications N-(2-Hydroxyethyl)pentadecanamide could acts as an inhibitor of hydrogen sulfide corrosion of steel in the system petroleum-​electrolyte.<br>References Mamedov, I. A., et al.: Korroziya i Zashchita v Neftegazovoi Promyshlennosti, 11-14 (1971)<br></p>

<p>Applications N-Phenyl 2-Bromo-5-Fluorobenzamide (cas# 949443-48-5) is a useful research chemical.<br></p>

<p>Applications 2-(2-hydroxyphenyl)acetamide (cas# 22446-40-8) is a useful research chemical.<br></p>

<p>Applications N,N-Diethyl-2-bromobenzamide (cas# 76041-86-6) is a compound useful in organic synthesis.<br></p>

<p>Stability Hygroscopic<br>Applications N-(p-Tolylsulfonylmethyl)formamide (cas# 36635-56-0) is a useful research chemical.<br></p>

<p>Applications 3-PHENYLPROPIOLAMIDE (cas# 7223-30-5) is a useful research chemical.<br></p>

<p>Applications N-(2,4-dimethylphenyl)acetamide (cas# 2050-43-3) is a useful research chemical.<br></p>

<p>Applications N-​(3-​Dibenzofuranyl)-​5-​nitro-2-​furancarboxamide is synthesized from Dibenzo[b,d]furan-3-amine (D418205), which is a building block used as a reactant in the preparation of dibenzofuryl(phosphonomethyl)alanines as endothelin converting enzyme inhibitors.<br>References De Lombaert, S., et al.: J. Med. Chem., 43, 488 (2000);<br></p>

<p>Applications o-Carbomethoxybenzyl Sulfonamide is a useful reactant in organic synthesis.<br>References Jiang, Lin, et al.: Youji Huaxue, 26(2), 203-206 (2006)<br></p>

<p>Applications N,N-Diethyl-p-toluamide, is a buildig block used in the synthesis of phthalocyanines. It can also be used in preparation of new insect repellents.<br>References Liang, J., et al.: Nongyaoxue Xuebao, Vol. 16,P: 644-650 (2014);<br></p>

<p>Stability Hygroscopic<br>Applications 4-Hydroxybenzimidamide (cas# 15535-98-5) is a useful research chemical.<br></p>

<p>Applications N,N-Diethylacetoacetamide is an intermediate in the synthesis of Phosphamidon (E/Z mixture) (P353730), an organophosphate insecticide that acts as a cholinesterase inhibitor.<br>References Jacques, R., et al.: Archiv fuer Toxikologie 18: 316 (1960); Bachmann, F.: Proc. Intern. Cong. Crop. Protection, 4th Congr., 2, 1153 (1960)<br></p>

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

<p>Applications 3,8-Diimino-4,7-dimethyl-2,4,7,9-tetraazadecanediimidamide is a useful research chemical.<br></p>

<p>Applications N-(4-amino-2-chlorophenyl)-5-chloro-2-hydroxybenzamide (cas# 10558-45-9) is a useful research chemical.<br></p>

<p>Impurity Atenolol EP Impurity A<br>Applications 4-(Hydroxyphenyl)acetamide (Atenolol EP Impurity A) is used as an intermediate for the synthesis of Atenolol (A790075) and various other organic compounds and pharmaceuticals. It is a process impurity for Atenolol (A790075)<br>References Inkum, R., et al.: Maejo Int. J. Sci. Tech., 6, 372 (2012); Pai, N.R., et al.: J. Chem. Pharma. Rsch., 4, 375 (2012); Moon, J.T., et al.: Bio-org. Medn. Chem., 20, 734 (2012);<br></p>

<p>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.<br>References Bergeron, R. et al.: J. Med. Chem, 40, 1475 (1997);<br></p>

<p>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.<br>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)<br></p>

<p>Please enquire for more information about N-(5-bromo-pyridin-2-yl)-2,2-dimethyl-propionamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-[4-(1-Allyl-3-butyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-8-ylmethyl)phenyl]acetamide (NUAA) is an antiinfective agent that has been shown to be effective against typhimurium. It inhibits bacterial growth by binding to the light chain of the monoclonal antibodies. NUAA is also able to inhibit uptake of iron in E. coli K12 and human cells. The mechanism for this inhibition is not well understood but may be related to its ability to bind iron homeostasis proteins or its oxidation catalyst activity.</p>

<p>Please enquire for more information about N-(1,2,3,4-Tetrahydro-7-methoxy-1-oxo-2-naphthalenyl)propanamide 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 Dorzolamide hydrochloride related compound A including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Oxo-3-hydroxy-N-methyl-N-propyl D-lysergamide (2OMD) is a metabolite of the drug lysergic acid diethylamide (LSD). It can be detected in urine, blood, and saliva. The detection time in urine is approximately 3 hours after ingestion. 2OMD can be found by chromatography techniques, such as thin layer chromatography or high performance liquid chromatography. It can also be detected using mass spectrometric techniques, such as gas chromatography/mass spectrometry or liquid chromatography/mass spectrometry. 2OMD can also be detected in urine samples by calibrations with standards of known concentration and by the use of analytical methods such as gas chromatography/mass spectroscopy.</p>

<p>L-Phenylalanine b-naphthylamide is a phenylalanine derivative that can be used as an indicator for the detection of Clostridium, 2-naphthylamine, and other anaerobes. This compound is a chromogenic substrate that reacts with amino groups in amino acids and amides in peptides to form a variety of color products. The condensation of phenylalanine with 2-naphthylamine is catalyzed by enzymes found in clostridia. When L-phenylalanine b-naphthylamide is incubated with tissue from animals or humans, it produces a pink coloration that indicates the presence of clostridia. The aerobic conditions necessary for this reaction are also found in the environment and within the body.</p>

<p>Please enquire for more information about N-tert-Butoxycarbonyl-L-isoleucineamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>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.</p>

<p>4-(2-Aminoethyl)benzene sulfonamide is a small-molecule drug that inhibits the activity of proteases, including serine and cysteine proteases. It has been shown to inhibit the growth of human renal cell cancer cells, as well as subcutaneous tumors in mice. 4-(2-Aminoethyl)benzene sulfonamide also inhibits the proliferation of Hl-60 cells and shows antitumor activity in a mouse model system. This drug is an inhibitor of prostaglandin endoperoxide synthase (PGHS), which is involved in tumorigenesis by causing inflammation and oxidative stress. 4-(2-Aminoethyl)benzene sulfonamide has been shown to be effective for treating colorectal adenocarcinoma, with no significant side effects on other organs.</p>

<p>Oxamide is a chemical compound with the molecular formula CHNO. It is a white solid that is moderately soluble in water and alcohol, but not in ether. Oxamide has been shown to have antioxidative properties and to inhibit the formation of reactive oxygen species. This drug also has an effect on thermal expansion and on the blood flow rate in human serum.</p>

<p>3-Bromopropionamide is an antibacterial agent that inhibits bacterial growth by blocking the synthesis of proteins. It is a synthetic amide with significant antibacterial activity against S. aureus. 3-Bromopropionamide has been shown to be effective against drug-resistant bacteria, including those that are resistant to metalloid salts or alkylene compounds. This substance also has psychomimetic effects and may be useful for studying the kinetics of protein synthesis in cells. 3-Bromopropionamide can be used as a linker to attach other molecules to proteins, which could allow them to penetrate cell membranes more easily.</p>

<p>Please enquire for more information about 4-(Aminomethyl)-N-Methylbenzenesulfonamide 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 16-Phenoxy tetranor pgf2alfa cyclopropyl methylamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>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.</p>

<p>4-Amino-N,N-dipropylbenzenesulfonamide is a molecule that has been shown to be an effective antimicrobial agent against bacteria. It inhibits the growth of bacteria by inhibiting the enzyme that catalyzes the formation of acyl radicals from alkoxy radicals and ethoxycarbonyl groups. This prevents bacterial cell membrane lipid peroxidation and thus prevents bacterial growth. 4-Amino-N,N-dipropylbenzenesulfonamide also inhibits bacterial DNA synthesis by interfering with the enzymes that synthesize nucleotides and proteins. The molecule has been shown to bind to nucleophilic sites on DNA gyrase, preventing its activity, which leads to inhibition of DNA replication. 4-Amino-N,N-dipropylbenzenesulfonamide can also bind to pyrazolyl groups on carbanion molecules and form a stable carbamate group.</p>

<p>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.</p>

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

<p>Pyridine-3-sulfonamide is a diazonium salt that has shown anticancer activity against human colon HCT116 cells. It inhibits the proliferation of leukemia cells by inhibiting the uptake of glucose, and it also has inhibitory properties on l1210 murine leukemia cells. Pyridine-3-sulfonamide binds to metal surfaces and accumulates in the cytoplasm of cancer cells, which may be due to its structural formula consisting of a pyridine group and a sulfonamide group. This compound can be used as an anticancer drug for cancer treatment.</p>

<p>L-Serine amide hydrochloride is a synthetic, anti-HIV drug that is used as an antiviral agent. It inhibits the viral life cycle by inhibiting the activity of acyclic nucleoside phosphonates, which are vital to viral DNA synthesis. L-Serine amide hydrochloride binds to the cyclopentane ring of guanosine and prevents its interaction with the enzyme ribonucleotide reductase. This binding prevents the conversion of guanosine into GTP, thereby preventing HIV from using this molecule in their life cycle. L-Serine amide hydrochloride is not active against cellular proteins or prostaglandins.</p>

<p>Please enquire for more information about 4-(2,3-Epoxypropoxy)phenylacetamide 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 (NZ)-4-chloro-N-[1-[2-(4-nitrophenyl)ethyl]piperidin-2-ylidene]benzenesulfonamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(S)-(+)-2-Phenylglycine amide is a racemic mixture of the (R) and (S) enantiomers. It is an inhibitor of the enzyme, racemase, which converts one type of amino acid to another. This inhibition prevents allergic reactions that can be caused by acylation reactions or ph profiles in the body. The amino acid composition of this drug is unique because it contains an ester hydrochloride group, which does not exist in other drugs. The kinetic and thermodynamic properties of (S)-(+)-2-phenylglycine amide have been studied extensively, but there are no reports on its ability to inhibit inflammatory diseases. However, it has been shown that the β-amino acid in this drug can inhibit amide hydroxamic acids and stereoselective hydroxamic acids.</p>

<p>2-(4-Aminophenoxy)acetamide is a chemical compound that belongs to the class of acetamides. It is used in the production of polyester fibers and dyes. 2-(4-Aminophenoxy)acetamide is a colorless, crystalline solid that has not been identified in nature.</p>

<p>Acetyl-L-alanine methyl amide is a pharmaceutical drug that is structurally similar to L-lysine. It has been synthesized as a model system for the study of receptor binding and intracellular signaling. Acetyl-L-alanine methyl amide has shown to be reactive and can form intramolecular hydrogen bonds with other molecules in the cell. This drug also reacts with microglia cells, which are responsible for clearing out dead cells and debris in the brain. Acetyl-L-alanine methyl amide is a proton donor, which may cause steric interactions with lysine residues on proteins due to their proximity within the cell. This drug also has an intermolecular hydrogen bond between its two molecules that could lead to an α subunit conformational change within the protein.</p>

<p>Please enquire for more information about N-(4-Hydroxyphenyl)-N-methylacetamide 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-Benzoyl-4-chlorophenyl)-2-chloro-N-methylacetamide 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-Methyl-2-[[3-[(1e)-2-(2-pyridinyl)ethenyl]-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-yl]thio]benzamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>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.</p>

<p>N-Acetylglycinamide is an amide that is structurally similar to the amino acid glycine. It has been shown to have anti-inflammatory properties by inhibiting prostaglandin synthesis in vitro. In vivo, N-acetylglycinamide is metabolized and excreted as the non-polar solvents n-acetylglycine and chloride. This amide is soluble in non-polar solvents such as chloroform, dichloromethane, or ether. N-acetylglycinamide also has a pairwise orientational order with respect to solvent molecules and exhibits a low degree of hydrogen bonding interactions with water molecules.</p>

<p>Please enquire for more information about 3-(2-Ethyl-1H-benzimidazol-1-yl)propanamide 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 L-Glutamic acid gamma-tert-butyl ester alpha-amide hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Beta-alanine amide HCl is a research chemical that belongs to the class of beta-amino acid derivatives. Beta-alanine amide HCl is an activator of nucleophiles and can be used in analytical chemistry as an indicator for chloride ions. It has been shown to react with asparagine, yielding beta-alanine and ammonia. The reaction system can be analysed by measuring the elimination of a hydrogen chloride ion from the beta-alanine amide HCl molecule and the subsequent increase in pH. The analytical method has also been used to measure concentrations of deamination reactions and redox potentials at high concentrations.</p>

<p>Please enquire for more information about 4-Hydrazino-N-methyl benzene methanesulfonamide, hydrochloride (1:1) 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 2-(Diethylamino)-N-(2,4-dimethylphenyl ) acetamide HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-(6-Phenylhexyl)-5-chloro-1-naphthalenesulfonamide is a dibutyryl camp analog that has been shown to inhibit the L-type calcium channel in a dose-dependent manner. It has an effect on both spermatozoa and glioma cells, with its most significant effect being inhibition of the intracellular calcium ion. This drug inhibits the growth rate of these cells, which may be due to its ability to activate adrenergic receptors and cause increased intracellular calcium ion levels. N-(6-Phenylhexyl)-5-chloro-1-naphthalenesulfonamide also slows the cycle of the cell, which may be due to a kinetic effect.</p>

<p>Carisoprodol Related Compound AMeprobamate is a carbamate derivative used as an anxiolytic drug.</p>

<p>Please enquire for more information about 2-Chloro-N-(3-cyano-4,5-dimethylthien-2-yl)acetamide 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 (9Z)-N-[(3-Methoxyphenyl)methyl]-9-octadecenamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-(2-Aminopropyl)-2-methoxybenzenesulphonamide is a trimethyl derivative of the aminopropyl group. It is used as a reagent to introduce hydroxymethyl groups into organic compounds. 5-(2-Aminopropyl)-2-methoxybenzenesulphonamide reacts with hydrochloric acid and an organic solvent in the preparation process. In the Friedel-Crafts reaction, 5-(2-Aminopropyl)-2-methoxybenzenesulphonamide reacts with d-alanine to form an optical isomer, which can be converted to its racemic form by ammonolysis. This compound is also used as a prostatic agent and an amide in the synthesis of benzene and phenoxymethyl alcohols.</p>

<p>N,N-Dimethyl decanamide is a fatty acid ester that is used as an amide with sodium carbonate and tebuconazole to form a particle. The particle has a diameter of about 0.5 microns and is thermally stable. N,N-Dimethyl decanamide can be used for the removal of organic substances from water by absorption onto the particle surface. It has been shown to be more efficient than other amides in removing these substances from water.</p>

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

<p>Fluoxetine is a potent inhibitor of the enzyme cytochrome P450 (CYP) 2C19. The inhibition of CYP2C19 by fluoxetine may lead to an increase in the plasma concentration of other drugs that are metabolized by this enzyme, such as glipizide and hydroxycyclohexyl. Fluoxetine inhibits human uric acid secretion and increases plasma concentrations of uric acid. This drug also inhibits human erythrocyte dihydropyrimidine dehydrogenase, leading to increased blood levels of pyrimidines, especially cytotoxic ones like 6-fluoro-3-indoxyl-beta-D-galactopyranoside. Fluoxetine has been shown to have a protective effect against acetaminophen toxicity in rats because it enhances the conversion of acetaminophen to its less toxic metabolite N-acetylcysteine.</p>

<p>Please enquire for more information about 4-Hydroxy-N-(2-Piperidinylmethyl)-2,5-Bis(2,2,2-Trifluoroethoxy)Benzamide 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 2-Cyano-N-cyclohexyl-N-methylacetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Lacosamide is an antiepileptic drug that has been shown to be bioequivalent to the reference product, Gabapentin. Lacosamide binds to voltage-gated sodium channels and is thought to have a similar clinical profile as Gabapentin. It is used in the treatment of partial seizures (with or without secondary generalization) and adjunctive therapy for generalized seizures in adults and children aged 2 years or older. Lacosamide can interact with other drugs, such as gabapentin, by increasing their serum concentrations. This interaction may lead to adverse effects such as dizziness and confusion. Lacosamide plasma concentrations are measured using LC-MS/MS methods after a two-way crossover study in healthy human volunteers. This study also showed that lacosamide is excreted unchanged in urine samples at a rate of about 50% over 24 hours, indicating that it does not undergo extensive metabolism in humans.</p>

<p>2-Hydroxy-N-1H-1,2,4-triazol-3-ylbenzamide is a synthetic product that is a white crystalline solid. It has a melting point of 105°C and an average particle diameter of 3.5 nm. This compound is used as a precursor to produce the peroxide 2,2'-dihydroxybenzophenone, which can be used in the synthesis of other organic compounds. It can also be used in the production of amides and quaternary ammonium salts. 2-Hydroxy-N-1H-1,2,4-triazol-3-ylbenzamide is structurally similar to hydrotalcite and hydroxyl group which are both natural products found in nature.</p>

<p>2-Methylbenzenesulfonamide is a chemical compound that has been shown to induce apoptosis in bladder cancer cells. It is an acid conjugate of the drug 2-methylbenzene-1,4-sulfonamide and it can be used for the treatment of bladder cancer. The compound binds to the apoptosis protein and inhibits its function, leading to cell death. The cytotoxic effects of 2-methylbenzenesulfonamide have been shown in short term toxicity studies in rats. In long term animal studies, this compound showed no adverse effects on the liver or kidneys, but did show some indication of reproductive toxicity. 2-Methylbenzenesulfonamide is not mutagenic and does not affect male fertility when given orally at doses up to 2000 mg/kg body weight for 90 days. 2-Methylbenzenesulfonamide binds to receptors on the surface of cancerous cells and induces apoptosis by inhib</p>

<p>L-2-Aminobutanamide is a compound that is used as an industrial preparation and as a reagent in kinetic studies. It has been shown to be effective in the analytical method for the determination of hydrochloric acid in titration, with a detection limit of 0.1%. L-2-Aminobutanamide can also be used to produce asymmetric synthesis by adding it with sodium hydroxide solution or hydroxide solution and using chromatographic science. This compound has been shown to have antibacterial effects on Brucella, which can be attributed to its ability to inhibit protein synthesis and disrupt cell membrane integrity. L-2-Aminobutanamide is a chiral compound that can exist in two different forms, L -(+)-2-aminobutanamide or D -(-)-2-aminobutanamide.</p>

<p>N-(2,3-Dihydro-1H-inden-5-yl)acetamide (DHICA) is an organic compound that is used in the synthesis of stilbazolium and trichophyton. It has been shown to be a kinetic model for photoisomerization of indene derivatives, which is important in the study of chemistry. DHICA has also been shown to be active against the violaceum fungus. The fluorescence properties of DHICA have been studied extensively and it has been found to have high quantum yields and a large number of channels.</p>

<p>Please enquire for more information about N-(4-(4-Fluorophenyl)-5-(hydroxymethyl)-6-isopropylpyrimidin-2-yl)-Nmethylmethanesulfonamide 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-(tert-Butoxycarbonyl)glycine N'-methoxy-N'-methylamide 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 Tridecafluoro-N-(2-Hydroxyethyl)-N-Methylhexanesulphonamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>C8-Ceramide is a glucosylceramide that is involved in the production of C8-ceramides. It has shown to have potent apoptosis activity and inhibit p21, an inhibitor of cell cycle progression. C8-Ceramide also has been shown to be an inhibitor of tumor necrosis factor alpha (TNF-α) induced inflammation and apoptosis in mouse tumor cells. In addition, it can induce apoptosis by inhibiting the epidermal growth factor receptor (EGFR) pathway. This polymerase chain reaction (PCR) product was found to bind to DNA in a model system using calf thymus DNA as well as bacterial DNA gyrase and topoisomerase IV enzymes.</p>

<p>D-Glutamic acid alpha-amide is a carbohydrate that has been shown to have antibiotic properties. It can be produced by chemoenzymatic synthesis and is used as an animal feed additive. D-Glutamic acid alpha-amide is a conjugate of D-glutamic acid with either glycine or beta-alanine. The residue of this compound on red blood cells is measured in order to assess the amount of D-glutamic acid alpha-amide that has been ingested. This compound has also been shown to have antigenic properties, which can elicit immune responses when injected into animals. The meningococcal vaccine that contains D-glutamic acid alpha-amide was found to be effective at stimulating an immune response in mice against meningitis caused by gram negative species, such as Neisseria meningitidis.</p>

<p>(R)-5-(2-Aminopropyl)-2-methoxybenzenesulfonamide is an amide. It is a hydrochloric acid salt that can regulate the reaction system and introduce filtration, which can be used to separate the components of the reaction system. The kinetic and chiral properties of this compound are derived from Friedel-Crafts reactions with phosphites and Friedel-Crafts reactions with d-alanine. (R)-5-(2-Aminopropyl)-2-methoxybenzenesulfonamide can also catalyze ammonolysis and catalysis with phenoxy.</p>

<p>N,N-Dimethyl-2-chloroacetamide is a chlorinated organic compound that has a reaction rate of 1.4 × 10^6. It is used as a treatment for acrylonitrile poisoning, and it is also used in the synthesis of thienopyridine and cetirizine. N,N-Dimethyl-2-chloroacetamide reacts with an amine to produce an amide; this reaction takes place in an organic solvent with a dicarboxylate, such as ethyl acetate or butyl acetate. This reaction produces a solution that is colorless to pale yellow. The time required for the reaction to complete depends on the concentration of reactants and the type of solvent used.</p>

<p>Please enquire for more information about 5-Amino-1-(4-Fluorophenyl)-1H-Pyrazole-4-Carboxamide 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-Cyano-4-oxo-4H-1-benzopyran-8-yl)-4-(4-phenylbutoxy)benzamide 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-Ethyl-1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluoro-N-(2-hydroxyethyl)Hexane-1-sulfonamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Phenylpropanamide is a chemical inhibitor that has been shown to have a protective effect against the light-induced degradation of drugs in urine samples. The compound also inhibits the hydrolysis of amides by hydrochloric acid and hydrogen bonds with the receptor binding site on human liver cells. N-Phenylpropanamide has been shown to affect cardiac function, as well as growth factor production.</p>

<p>Please enquire for more information about 5[(R)-(2-Aminopropyl)]-2-methoxybenzenesulfonamide hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>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.</p>

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