Amidas

<p>2-Chloro-N-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)acetamide (CPA) is a chemical compound that belongs to the class of phenyl pyrazoles. It has a thermal stability and is soluble in organic solvents. CPA crystallizes in the monoclinic system with the space group P21/c, with the following unit cell parameters: a = 8.943(4) Å, b = 7.878(3) Å, c = 17.834(6) Å, α = 90°, β = 112° and γ = 90°. In this crystal structure, there are two molecules of chloride per molecule of CPA. The crystal x ray diffraction pattern showed that this compound forms dimers in solution at room temperature and can be dissolved</p>

<p>N-Methyl-N-vinylacetamide is a colorless liquid with a boiling point of 105.6°C. It is produced by the reaction of acetamide and vinyl chloride in the presence of hydrochloric acid, glycol ether, and methyl ethyl ketone. The viscosity of this compound is low, which makes it an ideal solvent for paints and coatings. N-Methyl-N-vinylacetamide also has genetic damaging effects and can cause mutations in bacteria that are exposed to this compound in high concentrations. This product has an unusual chemical structure due to its hydrogen bonding interactions.br&gt;br&gt;<br>br&gt;br&gt;<br>Hydrogen bonds are weak intermolecular forces between polar molecules, such as water or alcohols, that are formed by the attraction between a partially positive hydrogen atom on one molecule and the negative end of another nearby molecule. Hydrogen bonds stabilize certain molecular structures because they provide partial shielding from electrostatic interactions with</p>

<p>2-(3,4-Dimethoxyphenyl)-N-hydroxyacetamide is a versatile building block that can be used in the production of a wide range of research chemicals. It is also useful as a reagent or speciality chemical for the preparation of pharmaceuticals, agrochemicals and other industrial chemicals. 2-(3,4-Dimethoxyphenyl)-N-hydroxyacetamide is an intermediate that can be used to synthesize complex compounds such as benzodiazepines. This compound has been shown to have high quality and can be used as a reaction component in organic synthesis.<br>2-(3,4-Dimethoxyphenyl)-N-hydroxyacetamide has CAS number 33793-80-5 and its molecular weight is 237.27 g/mol.</p>

<p>2-Amino-N-[2-(2-chlorobenzoyl)-4-nitrophenyl]acetamide is a fine chemical that is used as a building block in organic synthesis. It is a versatile intermediate for the synthesis of other compounds and can be used to make a variety of useful scaffolds. 2-Amino-N-[2-(2-chlorobenzoyl)-4-nitrophenyl]acetamide has been used in research and development of pharmaceuticals, agrochemicals, herbicides, and other compounds.</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>2,2,2-Trifluoro-N-(4-piperidinyl)acetamide (TFAPA) is a nucleic acid analog that binds to the target nucleic acid. TFAPA is a morpholino compound with an amide linkage between the morpholine ring and the acetic acid group. TFAPA is a sequence-specific DNA analog that inhibits protein synthesis by binding to the target nucleic acid. TFAPA can also be used as a probe for the detection of abnormal sequences in RNA.</p>

<p>(E)-N-(2-Chloro-6-methylphenyl)-3-ethoxyacrylamide is a reagent and research chemical that can be used as a building block in the synthesis of other compounds. It is also a versatile building block in organic chemistry. (E)-N-(2-Chloro-6-methylphenyl)-3-ethoxyacrylamide has been shown to be an effective intermediate for the synthesis of various complex compounds, such as pharmaceuticals and pesticides. This compound is also a useful scaffold for the synthesis of other fine chemicals.</p>

<p>Please enquire for more information about (2,6-dioxo-4-phenylcyclohexyl)-N-(3-(trifluoromethyl)phenyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Phenylbenzamide (2PB) is a drug that belongs to the class of anthelmintics. It binds to the nicotinic acetylcholine receptor and inhibits the release of acetylcholine at neuromuscular junctions, leading to paralysis and death of the parasite. 2PB also has been shown to have anti-inflammatory properties in mice with colitis, which may be due to its ability to inhibit prostaglandin synthesis. The molecular docking analysis showed that 2PB binds covalently with nitro-containing molecules, such as nitrosamines, which are found in cigarette smoke and are known carcinogens. This binding may contribute to the development of cancer through inhibition of DNA repair mechanisms.</p>

<p>L-Lysine amide dihydrochloride is a crystalline compound that is used for the treatment of tumours. It has been shown to bind to the enzyme iridoid synthase, which is involved in the formation of imines and aldehydes. L-Lysine amide dihydrochloride also inhibits the production of staining compounds, such as fluorine and heterocycles. The compound may also be used cosmetically as an anti-aging agent because it can inhibit the production of collagenase and elastase, which cause degradation of collagen.</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>2-Phthalimidoyl-N-(methylsulfonyl)propanamide is a fine chemical that is used as a building block for research chemicals. It is a versatile intermediate that can be used as a reaction component. 2-Phthalimidoyl-N-(methylsulfonyl)propanamide has been shown to have high quality and can be used as a reagent in the synthesis of complex compounds.</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 13,4-diaza-5-(tert-butyl)-2-hydroxy-7-oxotricyclo[6.4.0.0&lt;2,6&gt;]dodeca-1(8),4,9,11-tetraene-3-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-(Aminomethyl)cyclopropanecarboxamide hydrochloride is a versatile building block that can be used in the synthesis of complex compounds. It has been shown to be an excellent reagent for the synthesis of novel pharmaceuticals and speciality chemicals. This compound is also a useful intermediate for the preparation of high-quality products and can be used as a reaction component or scaffold in synthesis.</p>

<p>Please enquire for more information about Furan-2-carboximidamide hydrochloride 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-amino-2-(4-bromo-3,5-dimethylphenoxy)ethanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Clorsulon is an anthelmintic drug that belongs to the group of benzimidazoles. It is used in veterinary medicine to treat nematode and cestode infections, as well as tapeworm infections. Clorsulon is a dispersive solid-phase extraction (DSPE) extractant that can be used for the separation of drugs and their metabolites from biological fluids. The chemical stability of clorsulon was assessed by exposing it to various solvents and pHs. Clorsulon was found to be stable in acetate, benzene, chloroform, ethyl acetate, ethanol, methanol, and water at pH 1-14 and a variety of temperatures ranging from -20 ˚C to 50 ˚C. No significant loss or degradation occurred after exposure to these conditions for up to 24 hours.</p>

<p>Please enquire for more information about N-(6-acetylbenzo[d]1,3-dioxolan-5-yl)-2-chloropropanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Tolbutamide is a drug that is used to treat diabetes mellitus type 2. It is an inhibitor of the enzyme glucokinase and thus blocks the phosphorylation of glucose, which prevents its utilization by cells. This results in a decrease of blood glucose levels, which can be useful in the treatment of diabetes mellitus type 2. Tolbutamide has shown potent apoptosis-inducing effects on human breast cancer cells and endothelial cells. These effects are thought to be due to inhibition of protein kinase C (PKC) activity by tolbutamide. Additionally, this drug inhibits insulin secretion from pancreatic beta cells and induces cytochrome P450 enzymes, which may lead to increased metabolism of other drugs.</p>

<p>2-Bromo-N,N-diethylacetamide is a chemical compound that is used as an amide. It has been shown to have anti-inflammatory properties and can be used for the treatment of inflammatory lesions. This drug also has been shown to inhibit the production of 3-bromopropylamine hydrobromide in laboratory animals. 2-Bromo-N,N-diethylacetamide binds to cellular proteins such as mt2 receptors and can be used for the treatment of nervous system diseases such as depression. The titration calorimetry shows that 2-Bromo-N,N-diethylacetamide is a good candidate for use in biomolecular applications due to its low toxicity and high thermal stability.</p>

<p>Trifluoromethanesulfonamide is a strong acid that has been shown to inhibit the proteolytic activity of human secretase. It binds to a specific site on the enzyme and prevents it from cleaving the substrate. This inhibition slows down the progression of Alzheimer's disease, Parkinson's disease, and other related disorders. Trifluoromethanesulfonamide has also been shown to bind to metal hydroxides, such as iron hydroxide, which may be due to its ability to form hydrogen bonds with these metals. Structural analysis reveals that trifluoromethanesulfonamide contains a pyrazole ring and two chlorine atoms, one in the para position and one in the meta position.</p>

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

<p>1-Naphthaleneacetamide is a plant growth regulator that belongs to the class of compounds known as auxins. It inhibits the production of chlorophyll and reduces photosynthetic activity in plants, thereby causing a decrease in chlorophyll content. 1-Naphthaleneacetamide has been shown to have genotoxic effects on human cells in tissue culture. This agent also has an effect on DNA damage and repair and can be used as an analytical method for determining the presence of surfactant sodium dodecyl (SDS) in urine samples by fluorescence spectrometry.</p>

<p>2-Amino-5-methylbenzamide (2AMB) is a potent inhibitor of the enzyme dihydropyrimidine dehydrogenase and is used in cancer research for its ability to inhibit tumor cell line growth. 2AMB has been shown to inhibit the synthesis of DNA, RNA, and protein in various human cell lines. The mechanism of this inhibition is not well understood, but it may be due to its ability to inhibit the activity of synthetases involved in nucleotide biosynthesis or by inhibiting the reaction system that converts hydration into ATP.</p>

<p>1-Methyl-1,4-dihydronicotinamide (1MDNA) is a flavine adenine dinucleotide analog that has been shown to be a potent inhibitor of the enzyme catalase. 1MDNA binds to the active site of the enzyme and prevents hydrogen peroxide from being converted into water and oxygen. This inhibition slows down or stops the reaction, which leads to reduced production of reactive oxygen species. 1MDNA inhibits other enzymes in a similar manner, including transferases and kinases. The kinetic properties of 1MDNA have been studied by performing kinetic studies on model systems at different temperatures. X-ray crystal structures have also been obtained for 1MDNA bound to catalase and ferredoxin.</p>

<p>Retinamide is a synthetic retinoid that is used for the treatment of skin cancer. It has been shown to induce apoptosis by activation of the c-jun N-terminal kinase (JNK) and p38 pathways, as well as by suppression of signaling through the phosphatidylinositol 3-kinase (PI3K)/Akt pathway. Retinamide also inhibits proliferation of HL60 cells and induces mitochondrial membrane depolarization in colon carcinoma cells. This drug has been shown to be a potent inhibitor of squamous cell carcinoma growth in vitro and in vivo, especially when combined with other chemotherapeutic agents. Retinamide has also been found to be effective against group P2 carcinomas, which are characterized by mutations in the BRAF gene.<br>Retinamide is metabolized by cytochrome P450 enzymes, leading to reactive metabolites that may cause toxic effects on cells. These metabolites can bind to DNA and cause strand breaks</p>

<p>N-(3-Hydroxypropyl)trifluoroacetamide is an alkaline hydrolysis product of 3-hydroxypropyl trifluoroacetate. It is a primary amino compound that can be used as an intermediate in the production of vinyl ethers and acetals. This chemical is used for the synthesis of vinyl acetals, which are important intermediates in the manufacturing of polymers.</p>

<p>3-Cyanobenzamide is an organic compound with the formula CHC(N)NH. It is a white crystalline solid that can be obtained by reacting benzamide with cyanoacetylene. There are three possible isomers of 3-cyanobenzamide: 3-cyano-1-(substituted phenyl)benzamide, 3-cyano-2-(substituted phenyl)benzamide, and 3-cyano-3-(substituted phenyl)benzamide. The optimal reaction conditions for the synthesis of 3-cyanobenzamide are in the presence of hydrogen bonding, such as n-hexane, amide, and phase equilibrium. Studies have determined that 3-cyanobenzamide has the potential to cause cancer or liver toxicity in humans. In addition, this chemical has been shown to be an effective inhibitor of alpha glucosidase enzymes in vitro and in vivo.</p>

<p>N-Dechloroethyl cyclophosphamide is a metabolic inhibitor that is used in the treatment of cancer. It is classified as an alkylating agent and inhibits ribonucleotide reductase, which prevents the production of DNA, RNA, and protein. The chemical ionization technique has been used to measure the concentration of this compound in human liver and urine samples. N-Dechloroethyl cyclophosphamide can be analyzed using chromatography or mass spectrometry methods.</p>

<p>N-alpha-[2,4-Dinitro-5-fluorophenyl]-L-valine amide is an acidic amino acid that is used as a reagent in organic synthesis. It has been shown to have amide and hydrogen bond properties. This compound has been shown to be involved in the biosynthesis of carboxylic acids and primary amino acids. It also absorbs UV light at 265 nm and can be used for determination of uv absorption using high performance liquid chromatography (HPLC).</p>

<p>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.</p>

<p>Please enquire for more information about N-(4-(((2-Indol-3-ylethyl)amino)sulfonyl)phenyl)ethanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,2'-(Diazene-1,2-diyl)bis(2-methylpropanimidamide) dihydrochloride (BPDC) is a synthetic compound that is used as an analytical reagent and a model system for oxidative injury. It has significant cytotoxicity on human cells in cell culture. BPDC induces oxidative damage to proteins and DNA by increasing the production of reactive oxygen species such as hydrogen peroxide, superoxide, and hydroxyl radicals. The mechanism of action is not well understood but may be due to Toll-like receptor signalling pathways. This compound has been shown to inhibit the activity of antioxidant enzymes such as glutathione peroxidase and catalase. It also inhibits the activity of proinflammatory cytokines such as IL-6 and IL-8. BPDC is being investigated for its potential use in bowel disease treatment.</p>

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

<p>3-Amino-4-chlorobenzamide is an organic compound that belongs to the class of aminobenzoic acids and is used as a coupling agent in organic synthesis. It reacts with aryl halides or halides to form 3-amino-4-chlorobenzonitrile, which can be converted into anilines by heating with ammonia and ammonium chloride. This reaction has been shown to be reversible with heat. 3-Amino-4-chlorobenzamide is also used as a water absorber in paper products, such as diapers and sanitary napkins.</p>

<p>Tropicamide is a cholinergic agent that is used as a short-term mydriatic, or eye dilator, for diagnostic purposes. It belongs to the group of nonsteroidal anti-inflammatory drugs and has been shown to have a stable complex with benzalkonium chloride. Tropicamide has been shown to affect the signal pathways in cells, leading to an increase in IL-2 receptor expression. This drug also affects locomotor activity and has been studied as a potential treatment for murine sarcoma virus. Tropicamide is administered intravenously and can cause side effects such as blurred vision, nausea, vomiting and convulsions. Tropicamide may be given together with phenylephrine in order to reduce these side effects.</p>

<p>2,6-Dimethoxy-3-nitrobenzamide is a fine chemical that is used as an intermediate in the synthesis of other compounds. This material can be used to make pharmaceuticals and research chemicals, such as antibiotics and pesticides. 2,6-Dimethoxy-3-nitrobenzamide is a versatile building block that can be used for the production of many different compounds. It has a CAS number of 55776-15-3 and has been assigned the Chemical Abstracts Service (CAS) registry number of 71887-92-8.</p>

<p>Triethylenephosphoramide (TEP) is a model system for studying the reaction mechanism of the enzyme phosphotriesterase. TEP has been used in reactions with water vapor, which causes the release of hydrogen chloride. The reaction solution is analyzed by mass spectrometry to determine the reaction products. TEP has also been shown to inhibit nitrite ion-dependent enzymes such as nitrate reductase and aminopeptidase N. TEP reacts with fluorescence probes that have been modified with response elements to detect the binding of these probes to DNA and RNA. This helps researchers identify the location of TEP in proteins and nucleic acids.</p>

<p>4-Nitrobenzamide is a chemical substance that belongs to the class of nitrobenzamides. It is used as an intermediate in the synthesis of other substances, such as pharmaceuticals, herbicides, and pesticides. 4-Nitrobenzamide was first synthesized in 1894 by hydrogenating nitrobenzoic acid with hydrogen chloride in the presence of phosphorus pentachloride. The reaction vessel for this process should be made of glass or porcelain due to the corrosive nature of hydrogen chloride gas. The kinetics for this reaction were studied using concentration-response curves on rats and mice at different concentrations. Acute toxicities observed include respiratory distress and death in rats and convulsions and death in mice.<br>4-Nitrobenzamide is also toxic to bacteria, which can be seen by its effect on Staphylococcus aureus (strain ATCC 25923). This strain had a 50% survival rate after exposure</p>

<p>Please enquire for more information about 2-Chloro-N-(2-chloro-5-nitrophenyl)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 2-Indol-3-yl-2-oxo-N-((3-(trifluoromethoxy)phenyl)methyl)ethanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Amino-N-benzylbenzamide is a high quality chemical that is an intermediate in the synthesis of other useful compounds. It is a reagent for organic synthesis, and has many uses as a complex compound, as well as being a useful building block for more complicated molecules. 4-Amino-N-benzylbenzamide is also used as a speciality chemical in research labs, and can be used as a versatile building block to make different products.</p>

<p>1-Benzyl-1,4-dihydronicotinamide is a drug that has been shown to have potential in treating metabolic disorders by restoring the balance of nitrogen atoms. It has been shown to be effective in inhibiting the production of nitric oxide and other reactive oxygen species (ROS) which are involved in the pathogenesis of inflammation, septic shock and HIV infection. 1-Benzyl-1,4-dihydronicotinamide also inhibits light emission from cells. This effect is due to its ability to reduce the concentration of NADH and ATP, which are necessary for the light emitting reaction. The drug's mechanism of action is not well understood but it may be related to its ability to block dimethyl fumarate (DMF), an inhibitor of monoclonal antibody production. The physiological function of this drug is not yet well understood but it may be related to its ability to inhibit the proliferation of human immunodeficiency virus (HIV).</p>

<p>Please enquire for more information about N-(2-Indol-3-ylethyl)(4-(trifluoromethoxy)phenyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Sulfonamidephenylhydrazine HCl is a sulfonamide that inhibits the enzyme Cox-2, which is involved in inflammation. It also has anti-inflammatory activity and has been shown to inhibit the growth of fungi. 4-Sulfonamidephenylhydrazine HCl is an antifungal agent used for the treatment of dermatophytic infections such as tinea pedis and tinea cruris. The chemical structure of 4-Sulfonamidephenylhydrazine HCl consists of a methyl sulfone group linked with a pyrazole ring and a hydrazine hydrate group. The carbonic acid moiety in this compound stabilizes the pyrazole ring by forming hydrogen bonds with the nitrogen atom and oxygen atom on either side of it. This allows for the formation of two resonance structures to be maintained, which make it more stable than other similar compounds without this moiety.</p>

<p>COX inhibitor; non-steroidal anti-inflammatory drug</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>Please enquire for more information about (3-(2,6-dichlorophenyl)-5-methylisoxazol-4-yl)-N-(4-(trifluoromethylthio)phenyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(E)-N-(3-Methylaminopropyl)-2-thiopheneacrylamide is a high quality chemical that can be used as an intermediate in the synthesis of complex compounds. It is also a useful scaffold and building block for the synthesis of speciality chemicals with versatile reactions.</p>