Amides

<p>Applications 5-Amino-2-chlorobenzenesulfonamide (cas# 2015-19-2) is a compound useful in organic synthesis.<br>References Somers, F., et al.: Pharm. Pharmacol. Commun., 6, 89 (2000), D'Ambrosio, K., et al.: J. Med. Chem., 51, 3230 (2008),<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>Applications 4-Ethynyl-N-ethyl-1,8-napthalamide is a chemical reagent used in the synthesis of fluorescent thalidomide and fluorogenic probes.<br>References Kampmann, S. et al.: Tetrahedron 71, 8140 (2015);<br></p>

<p>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.<br>References Olszewska, T., et al.: Tetahedron., 69, 474 (2013);<br></p>

<p>Stability No Data Availabe<br>Applications 2-(4-phenyl-1,3-thiazol-2-yl)acetamide (cas# 58351-19-2) is a useful research chemical.<br></p>

<p>Applications Used in the preparation of homobifunctional rhodamine for labeling proteins.<br>References Corrie, J. et al.; Bioconjugate Chem. 9, 160 (1998)<br></p>

<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 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-Isobutylsorbamide shows antitubercular activity towards mycobacterium strains. It is a derivative of Sorbic Acid (S676890), a naturally occurring organic compound first isolated from unripe berries and used as a food preservative and as an inhibitor of Clostridium Botulinum bacteria in meat products.<br>References Gupta, O. et al.: Bull. Med. Ethno-Bot. Res., 1, 99 (1980); Van, M.C., et al.: Int. J. Food. Microbiol., 160, 124 (2012); Li, J., et al.: J. Am. Soc. Mass. Spec., 23, 1625 (2012);<br></p>

<p>Applications Tosyl Brinzolamide is a derivative of Brinzolamide (B677601) which is a carbonic anhydrase inhibitor and an antiglaucoma agent.<br>References Silver, L.H., et al.: Am. J. Ophthalmol., 126, 400 (1998);Davies, N., et al.: Clin. Exp. Pharmacol. Physiol., 27, 558 (2000); Stave, J., et al.: Ophthalmologe, 99, 276 (2002);<br></p>

<p>Applications N-Cyclopropyl 5-bromonicotinamide<br></p>

<p>Stability Hygroscopic<br>Applications is a novel lipid-soluble, thiol-redox antioxidant and heavy metal chelator.<br></p>

<p>Applications N-allyl-2-chloro-acetamide (cas# 13269-97-1) is a useful research chemical.<br></p>

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

<p>Applications 2-Amino-N,N-dimethylbenzenesulfonamide is an intermediate used to prepare LDK378 as potent and selective anaplastic lymphoma kinase inhibitor.<br>References Marsilje, T., et al.: J. Med. Chem., 56, 5675 (2013)<br></p>

<p>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.<br>References Shireman, B. T., et al.: Bioorg. Med. Chem. Lett., 18, 2103 (2008);<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,N'-(1,2-DIHYDROXYETHYLENE)BISACRYLAMIDE (cas# 868-63-3) is a useful research chemical.<br></p>

<p>Applications (E)-N-(2-((7-nitrobenzo[c][1,2,5]oxadiazol-4-yl)amino)ethyl)-4-oxo-4-phenylbut-2-enamide is a useful research chemical.<br></p>

<p>Applications N-[4-Cyano-3-(trifluoromethyl)phenyl]-2-oxopropanamide (cas# 87310-69-8) is a compound useful in organic synthesis.<br></p>

<p>Applications 2-HYDROXY-N,N-DIMETHYLACETAMIDE (cas# 14658-93-6) is a useful research chemical.<br></p>

<p>Applications 2-tert-Butylbenzenesulfonamide can be used as reactant in preparation of benzimidazole derivatives for inhibiting neoplastic cells.<br>References Sperl, G., et al.: U.S., US 6348032 B1 20020219 (2002)<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>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>7-Phenylacetamide-3-chloromethyl-3-cephem-4-carboxylic acid diphenylmethyl ester is an organic solution that is used in the detoxification of chemical substances. It has a hydroxyl group and is soluble in nonpolar solvents. 7PAMC has been shown to be effective against bone lesions caused by acylation reactions. This drug also binds to the enzyme called cytochrome P450, which is involved in the metabolism of many drugs. It also inhibits bacterial growth by binding to DNA gyrase and topoisomerase IV, enzymes that maintain bacterial DNA integrity. The particle size of this drug is small, with a diameter of less than 10 microns. 7PAMC has a viscosity of 1 cps at 25°C and a melting point of 129°C.</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>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.</p>

<p>Dopamine (D2) receptor antagonist</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>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>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>