
Amidas
Foram encontrados 16483 produtos de "Amidas"
2-Methoxy-5-(2-oxopropyl)benzenesulfonamide
CAS:2-Methoxy-5-(2-oxopropyl)benzenesulfonamide is a metal catalyst that can be used in the synthesis of tamsulosin hydrochloride, an alpha blocker that is used to treat benign prostatic hyperplasia. It catalyzes the reaction between 2-methoxybenzenesulfonyl chloride and 3-amino-1,2,4-triazole. The industrial importance of this compound is due to its ability to be used as a catalyst for various chemical reactions.Fórmula:C10H13NO4SPureza:Min. 95%Cor e Forma:PowderPeso molecular:243.28 g/mol4-Benzylpiperazine-1-carboximidamide sulfate
CAS: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.Fórmula:C12H20N4O4SPureza:Min. 95%Cor e Forma:PowderPeso molecular:316.4 g/molN-Isopropylacrylamide
CAS: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.Fórmula:C6H11NOPureza:Min. 98.5 Area-%Cor e Forma:White PowderPeso molecular:113.16 g/molBenzoyl-L-tyrosine amide
CAS:Benzoyl-L-tyrosine amide is a reaction intermediate that is a competitive inhibitor of serine proteases. It binds to the active site of the enzyme and inhibits the breakdown of proteins by blocking the access of other reactants. Benzoyl-L-tyrosine amide has been shown to inhibit proteolytic activity in subtilis, an enzyme isolated from Bacillus licheniformis. The amino acid composition and binding properties are similar to those found in natural substrates. Benzoyl-L-tyrosine amide has been synthesized and its binding affinity towards histidine residues has been determined by titration calorimetry and fluorophosphate assay.Fórmula:C16H16N2O3Pureza:Min. 95%Cor e Forma:PowderPeso molecular:284.31 g/molSulfacetamide sodium monohydate
CAS: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.Fórmula:C8H10N2O3S•H2O•NaPureza:Min. 95%Peso molecular:255.25 g/mol2-Phenyl-2-(2-piperidyl)acetamide
CAS: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.
Fórmula:C13H18N2OPureza:Min. 97 Area-%Cor e Forma:PowderPeso molecular:218.29 g/mol2-Amino-N-[2-(5-methoxy-1H-indol-3-yl)ethyl]acetamide hydrochloride
CAS:2-Amino-N-[2-(5-methoxy-1H-indol-3-yl)ethyl]acetamide hydrochloride is a magnetic compound that has been shown to be an effective cancer antigen. It is a derivative of the amino acid sequence of α,β-unsaturated fatty acids and can be used as a dietary supplement. 2-Amino-N-[2-(5-methoxy-1H-indol-3-yl)ethyl]acetamide hydrochloride has been shown to bind to fatty acid receptors on the surface of antigen presenting cells (APCs). It also activates the immune system by activating APCs, which leads to the production of cytokines and chemokines. This compound has also been shown to stimulate T cells in culture, leading to activation and proliferation of tumor cells.Fórmula:C13H17N3O2·HClPureza:Min. 95%Cor e Forma:PowderPeso molecular:283.75 g/molN-(2-Indol-3-ylethyl)(4-methylphenyl)formamide
CAS:Please enquire for more information about N-(2-Indol-3-ylethyl)(4-methylphenyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this pageFórmula:C18H18N2OPureza:Min. 95%Cor e Forma:PowderPeso molecular:278.35 g/molN-alpha-Benzoyl-L-arginine amide hydrochloride
CAS:N-alpha-Benzoyl-L-arginine amide hydrochloride (BA) is a synthetic, noncompetitive inhibitor of phosphodiesterase. It has been shown to inhibit protease activity in vitro and rhizosphere enzyme activities in vivo. BA also inhibits the formation of hippuric acid from benzoic acid, which is a reaction catalyzed by the enzyme phosphatase. The kinetics of this inhibition have been studied using a number of different substrates and enzymes. BA binds to the catalytic site on the enzyme, sterically hindering binding of the substrate and preventing hydrolysis.Fórmula:C13H19N5O2·HClPureza:Min. 95%Cor e Forma:PowderPeso molecular:313.78 g/molL-Histidine β-naphthylamide
CAS: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.Fórmula:C16H16N4OPureza:Min. 95%Cor e Forma:PowderPeso molecular:280.32 g/mol(4-(2-Fluorophenyl)piperazinyl)-N-propylformamide
CAS:Produto ControladoPlease enquire for more information about (4-(2-Fluorophenyl)piperazinyl)-N-propylformamide including the price, delivery time and more detailed product information at the technical inquiry form on this page
Fórmula:C14H20FN3OPureza:Min. 95%Cor e Forma:PowderPeso molecular:265.33 g/molAZD 1152
CAS:AZD 1152 is an Aurora kinase inhibitor, which is a type of small-molecule therapeutic agent. It is derived from the pharmaceutical research conducted by AstraZeneca. Its primary mode of action involves the selective inhibition of Aurora B kinase, an enzyme crucial for the regulation of mitosis. By interfering with this enzyme, AZD 1152 disrupts the normal progression of cell division, leading to the inhibition of proliferation and induction of apoptosis in rapidly dividing cells.Fórmula:C26H31FN7O6PPureza:Min. 97 Area-%Cor e Forma:Slightly Yellow PowderPeso molecular:587.54 g/mol2-Hydroxy-5-methylbenzamide
CAS:Labetalol is a β-blocker that is used to treat high blood pressure. Labetalol hydrochloride, the active form of labetalol, is a white, crystalline compound with a melting point of 200 °C. It is soluble in water and has an acidic pH of 2. Labetalol hydrochloride is synthesized by reacting methylbenzene with labetalol, which forms intermediates such as methyl 4-hydroxylbenzoate and methyl 3-hydroxylbenzoate in the process. The intermediates are then recrystallized to form the final product. Labetalol hydrochloride undergoes thermal analysis using thermogravimetry, calorimetry, and residue analysis to determine its purity. This product also undergoes carbonaceous and oxidative analysis by GC-MS for quality control purposes.Fórmula:C8H9NO2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:151.16 g/molN-(2-Fluorophenyl)-N-[4-(4-Methyl-1,3-Thiazol-2-Yl)-1-(2-Thiophen-3-Ylethyl)Piperidin-4-Yl]Propanamide
CAS:Produto ControladoN-(2-Fluorophenyl)-N-[4-(4-methyl-1,3-thiazol-2-yl)-1-(2-thiophen-3-ylethyl)piperidin-4-yl]propanamide is a drug that is used for the treatment of cancer. This drug is hydrophobic and has a molecular weight of 455. It has been shown to be effective in treating cancer cells by binding to the cell membrane and inhibiting the proliferation of these cells. N-(2-Fluorophenyl)-N-[4-(4-methyl-1,3-thiazol-2-yl)-1-(2-thiophen-3-ylethyl)piperidin]-4-- yl]propanamide also inhibits tumor growth by reducing extracellular matrix production and inducing apoptosis in cancer cells. This drug has a fluorescent property and can be detected with an optical microscope at aFórmula:C24H28FN3OS2Pureza:Min. 95%Peso molecular:457.63 g/molN-(2-Oxo-2-phenylethyl)-N-phenylbenzamide
CAS: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).Fórmula:C21H17NO2Pureza:Min. 95%Peso molecular:315.37 g/mol3-Chlorobenzamide
CAS: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.Fórmula:C7H6ClNOPureza:Min. 95%Cor e Forma:PowderPeso molecular:155.58 g/molEliglustat
CAS:Eliglustat is an oral medication used as a substrate reduction therapy for Gaucher disease type 1, which is an inherited lysosomal storage disorder. This product is a small-molecule inhibitor derived via chemical synthesis. Its primary mode of action involves the selective inhibition of glucosylceramide synthase, an enzyme responsible for the first committed step in glycosphingolipid biosynthesis. By reducing the production of glucosylceramide, eliglustat decreases the substrate accumulation that contributes to the pathophysiology of Gaucher disease.Fórmula:C23H36N2O4Pureza:Min. 97 Area-%Cor e Forma:White PowderPeso molecular:404.54 g/mol2,2,2-Trifluoro-n-phenylacetamide
CAS:2,2,2-Trifluoro-n-phenylacetamide is a functionalized trifluoroacetic acid. It is inactive and can be used for diagnostic purposes. 2,2,2-Trifluoro-n-phenylacetamide reacts with amines to form the corresponding deuterium isotope labeled amine. The heterocyclic amines that are formed react with diazonium salt to produce an enolate anion that reacts with chloride to form the corresponding carboxylic acid derivative. The proton of the carboxylic acid leaves as a protonated ammonium ion, which is stable in alkaline solutions. Amides have a negative charge on the nitrogen atom due to its electron withdrawing properties.Fórmula:C8H6F3NOPureza:Min. 95%Cor e Forma:PowderPeso molecular:189.13 g/molN-(2-(3,4-dimethoxyphenyl)ethyl)-2-chloropropanamide
CAS:Please enquire for more information about N-(2-(3,4-dimethoxyphenyl)ethyl)-2-chloropropanamide including the price, delivery time and more detailed product information at the technical inquiry form on this pagePureza:Min. 95%Hydroxy flutamide
CAS:Hydroxyflutamide is an anti-androgen drug that belongs to the group of nonsteroidal anti-androgens. It has been shown to bind to the androgen receptor with high affinity and inhibit the growth of cancer cells in vitro. Hydroxyflutamide also has a strong antitumor response in vivo, which is due to its ability to inhibit cellular proliferation by binding to DNA polymerase during replication. The drug may also have some activity as an antineoplastic agent because it inhibits the growth of prostate cancer cells. However, hydroxyflutamide has never been tested on humans or animals, so its effects are unknown.
Fórmula:C11H11F3N2O4Pureza:Min. 98 Area-%Cor e Forma:Yellow PowderPeso molecular:292.21 g/mol
