Amides

<p>Gly-pro-4-methoxy-β-naphthylamide hydrochloride is a fine chemical that is useful as a versatile building block and intermediate. It is a research chemical that has been used in the production of other compounds, such as drugs, pesticides, and dyes. This compound is also used to synthesize certain polymers and plastics. Gly-pro-4-methoxy-β-naphthylamide hydrochloride has CAS number 100929-90-6, but it can be found under many other names including 4-(2′,5′dimethylphenyl)-1-(2′hydroxyethyl)piperazine (CAS 105999).</p>

<p>2,4-Dichloropyrimidine-5-carboxamide is a 2,4-dichloropyrimidine derivative. It is an intermediate in the synthesis of other compounds, and can be used as a building block in the synthesis of complex compounds. It is a versatile building block that can be used to make many different products. This chemical has been shown to have high quality and is useful as a research reagent or speciality chemical. 2,4-Dichloropyrimidine-5-carboxamide is also a useful intermediate for reactions involving nucleophilic substitution reactions and can serve as a scaffold for organic synthesis.</p>

<p>Bifenthrin is a broad-spectrum, synthetic pyrethroid insecticide that has been used to control pests in the agricultural and residential sectors. It is applied as a spray or dust on plants and animals. Bifenthrin is highly toxic to mammals, with an oral LD50 of less than 10 milligrams per kilogram of body weight in rats and mice. The acute toxicity can be attributed to its ability to inhibit protein synthesis by binding to the cholinesterases, which are found in high concentrations in mammalian tissues.</p>

<p>2-((4-Methylphenyl)sulfonyl)ethanamide is an amide that has been shown to have antibacterial activity. It binds to the DNA of bacteria, inhibiting its replication and transcription. This drug also inhibits the growth of influenza virus in cell culture. 2-((4-Methylphenyl)sulfonyl)ethanamide is a sensor for chloride ions, which may be used as treatments for bacterial infections. This drug is also able to inhibit the replication of bacteria that are resistant to other antibiotics, such as penicillin. The unsaturated alkyl group on this molecule allows it to be activated by radiation treatment, which may be useful in the treatment of cancer cells or viral infections.</p>

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

<p>N-(2,6-Dimethylphenyl)-1-piperazineacetamide is a byproduct of solvents and stabilizers. It has been found to be a crystalline solid with a molecular weight of 233.3 g/mol. The crystal structure was determined and found to be composed of two molecules of acetamide that are connected through hydrogen bonds. N-(2,6-Dimethylphenyl)-1-piperazineacetamide is soluble in ethanol and ether, but insoluble in water. This compound interacts with other substances, such as recrystallizing or substituting acetamides.</p>

<p>2-Amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide is an anticancer agent that inhibits the synthesis of proteins required for cell division. It has been shown to have anticancer activity and efficacy in vitro studies against human cancer cells, such as HCT116. This compound also induces apoptosis in infected cells by binding to viral particles and inducing the release of chloride ions. 2-Amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide has been found to be effective against influenza virus and particle production by inhibiting neuraminidase activity.</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>Phthalimidoyl-N-(methyltosyl)hexanamide is a fine chemical that can be used as a versatile building block and reaction component. It is an intermediate in the production of a variety of products, including pharmaceuticals and pesticides. Phthalimidoyl-N-(methyltosyl)hexanamide is also used as a reagent for the preparation of other compounds. This compound has high purity and quality, making it suitable for research purposes. The CAS number for this compound is 183828-04-7.</p>

<p>N-(2-Piperidin-4-ylethyl)methanesulfonamide hydrochloride (MSM) is a fine chemical that belongs to the group of useful scaffolds. It is used as a versatile building block in research and can be used as a reaction component for speciality chemicals. The compound has high quality and can be used as a reagent, which is an important tool for organic synthesis.</p>

<p>5-Aminoimidazole-4-carboxamide HCl (5-AICA) is a compound that is used for the treatment of bowel disease. It inhibits the synthesis of 5'-nucleotidase and phosphoribosyl transferase, which are enzymes responsible for the conversion of nucleotide monophosphates to nucleotide diphosphates. This inhibition leads to a decrease in the amount of adenosine triphosphate (ATP) produced by cells, which may be due to its ability to inhibit ATP synthase activity. 5-AICA also has been shown to bind to DNA and inhibit transcriptional activities. The binding of 5-AICA may be due to its ability to form hydrogen bonds with guanine residues in DNA or its capability to form covalent bonds with thymidine residues in DNA. 5-AICA also has been shown to have cytotoxic effects on HL60 cells, as well as other</p>

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<p>Cecropin A (1-7)-Melittin A (2-9) amide trifluoroacetate salt is a cecropin-melittin hybrid peptide that has been immobilized on cellulose nanofibers for use as an antimicrobial. It has been shown to have strong antimicrobial activity against bacillus subtilis, and the immobilization process ensures that the peptide is not released from the surface of the material. The process of coating with nanopaper and then applying the peptides provides a stable surface with high antimicrobial activity. The synthetic peptides are synthesized by solid phase synthesis using Fmoc chemistry and purified by preparative HPLC.</p>

<p>Please enquire for more information about 2-(((2,5-dimethoxyphenyl)sulfonyl)amino)benzamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Nitrobenzenesulfonamide is an organic compound that consists of a nitro group, a sulfonamide group, and an amine. It is the active analog of 4-dimethylaminobenzoic acid, which is used as an inhibitor of histamine release in the treatment of allergic reactions. The molecule has been shown to bind to copper ions and triflic acid and has been used as a catalyst for aziridination.</p>

<p>4-Chlorocinnamide is an organochlorine compound that has been found to have antibacterial properties. It inhibits the shikimate pathway in bacteria, which is essential for bacterial growth. This molecule has been shown to bind with the cation channel of the nerve cells in the trigeminal nerve and inhibit their function. The inhibition of this channel leads to reduced sensitivity to pain. 4-Chlorocinnamide is also a precursor in the synthesis of stilbene derivatives, which are used as anticancer drugs.</p>

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<p>2-Phenoxyacetamide is an acylating agent that reacts with a hydroxyl group by substitution to form an ester or amide. It is used in clinical studies to combat insulin resistance and metabolic disorders, such as cancer, inflammatory bowel disease, and diabetes. 2-Phenoxyacetamide has been shown to be effective against a number of bacterial species, including Pseudomonas aeruginosa and Cryptococcus neoformans. The drug also inhibits the production of monoamine neurotransmitters in the brain and has been shown to have anti-inflammatory properties.</p>

<p>Pigment Orange 36 is an organic pigment with a light-emitting property. It is soluble in organic solvents, such as benzene and chloroform, but insoluble in water. Pigment Orange 36 has a polycyclic aromatic hydrocarbon structure with ester linkages between the aliphatic hydrocarbon and aromatic hydrocarbon moieties. The molecule consists of two sections: one section is soluble in organic solvents and the other section is soluble in water. The particle size of Pigment Orange 36 ranges from 0.1 to 1 micron in diameter, and it emits light when excited by UV radiation or visible light.</p>

<p>Tenofovir alafenamide fumarate is a prodrug of tenofovir, an active antiretroviral agent. Tenofovir binds to the viral polymerase and blocks the synthesis of viral DNA. Tenofovir alafenamide fumarate is a prodrug that undergoes hydrolysis to form tenofovir. It has been shown to inhibit growth factor-β1, which may reduce the risk of opportunistic infections in people with HIV or AIDS. Tenofovir alafenamide fumarate has also been shown to be effective as an antiviral prophylaxis when used in combination with other drugs for active antiretroviral therapy.</p>

<p>3-(4-Methoxyphenyl)propionamide is a compound that belongs to the group of benzene amides. It is synthesized by reacting an excess of 3-bromopropionaldehyde with an amine in the presence of sodium hydroxide. This reaction produces a mixture of products, which are separated by chromatography. The yields for this reaction are approximately 90%. 3-(4-Methoxyphenyl)propionamide has been used as a biomolecular building block, and its traceless nature makes it useful in organic synthesis.<br>3-(4-Methoxyphenyl)propionamide can be used to synthesize alkanesulfonamides and spirolactams, which are important intermediates in chemical synthesis. 3-(4-Methoxyphenyl)propionamide also reacts with phenanthridone to produce chloride derivatives and with arenes to produce linkers.</p>

<p>4-(Chloromethyl)benzamide is a potent inhibitor of cyclohexane ring formation in proteins and has been shown to be effective against bacteria, fungi, and parasites. 4-(Chloromethyl)benzamide inhibits the synthesis of proteins by targeting the active site of piperazine synthase, an enzyme involved in the production of piperazine. The carbon nanotube linker is a novel molecule that can be used for the attachment of the 4-(chloromethyl)benzamide molecule to cetirizine. In addition, 4-(chloromethyl)benzamide has been shown to have an effective dose at 0.1 μM and a half-life time of 2 hours in rats.</p>

<p>4-Iodobenzenesulphonamide is a drug with antifungal and anticancer activity. The compound has been shown to inhibit the growth of cancer cells in vitro. It also has an antifungal effect in vitro, which is most likely due to its ability to inhibit the synthesis of ergosterol, a component of the cell membrane. 4-Iodobenzenesulphonamide may be used for the treatment of cervical cancer and vulvovaginal candidiasis. This drug does not show any serious side effects, but it has been shown to have some adverse effects on liver function tests and red blood cells.</p>

<p>2-Phenylacetamide is a solvent that can be used as a component in alkylation reactions. It is commonly used as a component of chlorinated solvents and has been shown to catalyze the reaction with benzyl chloride. 2-Phenylacetamide can be used to produce solar cells by sensitizing the surface of silicon wafers with this solvent. Researchers have also studied the alkylation reaction of phenylacetamide with methyl iodide and benzyl chloride, which can be carried out at room temperature and does not require any catalyst. This reaction was found to proceed well under gas chromatographic conditions.</p>

<p>The drug 4-Amino-5-chloro-2,3-dihydro-N-[1-(3-methoxypropyl)-4-piperidinyl]-7-benzofurancarboxamide (BZP) is a histamine H2 receptor antagonist. It binds to the histamine H2 receptor in the stomach and duodenum, thereby blocking stomach acid production. BZP has been shown to be effective for treating symptoms of constipation or diarrhoea caused by inflammatory bowel disease or abdominal surgery. BZP also reduces the risk of relapse after surgery but does not affect long term efficacy. This drug is not available in the United States and has significant interactions with other drugs and symptoms including constipation, bowel disease, long term efficacy, and analytical method.</p>

<p>Chemically a chlorinated salicylanilide, niclosamide is clinically used as an anthelmintic agent. The action of niclosamide has been proven to proceed by inhibiting the STAT3 signaling pathway. Recently, niclosamide, has been considered as an antiproliferative agent in cancer treatment, e.g. melanoma and colorectal cancer. In 2021, niclosamide has been tested for the treatment of COVID-19 patients.</p>

<p>4-Fluorophenylacetic acid is a synthetic organic compound that has been used as a model system for the study of the reaction between hydrogen sulfate and hydrogen. 4-Fluorophenylacetic acid is a fluorinated analog of acetamide, which can be synthesized from sodium borohydride and hydrogen fluoride. It has been shown to inhibit the growth of Mycobacterium tuberculosis in an on-line assay and is also active against Mycobacterium avium complex. 4-Fluorophenylacetic acid also inhibits rat liver microsomes with a second order rate constant of 0.0006 M−1 s−1 at pH 7.4 and 37 °C (pH and temperature not specified). The biological properties of 4-fluorophenylacetic acid are not well understood, but it may bind to hydrophobic regions on proteins or DNA through hydrogen bonding interactions.</p>

<p>L-Pyroglutamic acid-beta-naphthylamide is a cell nucleus pressor that has been shown to stimulate locomotor activity in rats. It is a highly selective agonist at the 5-HT2 receptor, which is involved in the regulation of energy metabolism and feeding behaviour. L-Pyroglutamic acid-beta-naphthylamide also stimulates cholinergic and serotonergic systems. This drug also inhibits bacterial growth by binding to the receptor site on bacterial cell nuclei, thereby preventing DNA synthesis and locomotor activity. L-Pyroglutamic acid-beta-naphthylamide is an antimicrobial agent that can be used to treat infections caused by bacteria resistant to erythromycin. The antimicrobial effect of this drug is due to its ability to bind to the receptor site on bacterial cell nuclei, thereby preventing DNA synthesis and locomotor activity.</p>

<p>3-Amino-4-methylbenzamide is an interchemical that can be utilized to synthesize naphthol. 3-Amino-4-methylbenzamide is an amide that has been shown to have a molecular modeling structure of a conformation. The interaction of 3-amino-4-methylbenzamide with the P38 kinase enzyme has been shown to inhibit the activity of this enzyme, which may lead to its use as a drug for the treatment of inflammation.</p>

<p>2-Iodoacetamide is a synthetic retinoid that binds to the DNA of cells, altering transcription. It also has been found to be effective in treating bowel disease and has been shown to have dna binding activity. The compound was synthesized by attaching iodine molecules to acetamide. 2-Iodoacetamide targets the protein thiols on the surface of cells, which are responsible for oxidation and damage due to reactive oxygen species (ROS). This compound is metabolized by alcohol dehydrogenase and can be used as a biological sample or natural compound.</p>

<p>N-Phenylpiperidine-4-carboxamide is a drug that inhibits the production of thromboxane A2 and other substances that promote clotting. It is used to treat patients with high blood pressure, as well as for the prevention of strokes and heart attacks. N-Phenylpiperidine-4-carboxamide is an analog of biphenyl and has been shown to have antiplatelet activity in humans. This drug also inhibits soluble guanylate cyclase, which prevents platelets from sticking together and forming clots. N-Phenylpiperidine-4-carboxamide is rapidly metabolized by esterases in the human body and excreted primarily in urine. The pharmacokinetic properties of this drug are not well understood but it can be synthesized using a number of different methods involving amide bonds.</p>

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

<p>5-Benzyloxyindole-3-glyoxylamide is a versatile building block that can be used in the synthesis of complex compounds. It has been shown to have a high quality and is useful as a reagent for research purposes. 5-Benzyloxyindole-3-glyoxylamide can be used as a reaction component and is useful as an intermediate in organic synthesis. 5BIGA has CAS number 22424-62-0 and is also known as 3-(benzyloxy)-5-(2,2,2-trifluoroethoxy)indole glyoxamide.</p>

<p>3,4,5-Trimethoxybenzamide is a benzofuran that has been shown to have anti-cancer properties. It has been shown to inhibit the production of chemokines and inhibit cancer cell proliferation. 3,4,5-Trimethoxybenzamide also binds to chloride ion channels on cancer cells and blocks the influx of chloride ions into the cells. This causes an increase in intracellular pH and inhibits the formation of ATP. 3,4,5-Trimethoxybenzamide also has antiarrhythmic properties and can be used for the treatment of hypertension. It is metabolized by hydrolysis in tissues or blood pressure through piperidine formation or hydrochloric acid.</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>2-(3-Hydroxyphenyl)acetamide (2HPA) is a sulfonamidochrysoidine compound with analgesic, antipyretic and anti-inflammatory effects. It is used in the treatment of gout, rheumatoid arthritis, osteoarthritis and other inflammatory diseases. 2HPA has been shown to be effective in the treatment of pain following dental surgery. 2HPA is also used as a marker for dietary intake of sulfate and may be a useful indicator for determining the effect of changes in diet on urinary excretion rates. The elimination half-life of 2HPA is approximately 3 hours in humans. This drug can be detected in urine samples from humans within 24 hours after ingestion at concentrations that are proportional to dose.</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>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>Picotamide is a drug that belongs to the class of drugs that inhibit platelet aggregation. This drug is used in the treatment of coronary artery disease and other cardiovascular diseases. Picotamide has been shown to have pharmacological effects on the heart, such as lowering blood pressure and reducing heart rate. It also has a covalent linkage with proteins, which may be due to its ability to activate receptors for biological properties like cell proliferation or differentiation. Picotamide has been shown to prevent infectious diseases, such as septicemia, by inhibiting bacterial growth. The chemical stability of picotamide makes it an attractive candidate for use in gene therapy because it can be stored at room temperature without losing its activity.</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>Methylthioacetic acid is a weak organic acid that is used as an ophthalmic drug. When methylthioacetic acid is activated, intramolecular hydrogen bonds form between the methylthiosulfonate ion and the nitrate ion. This process requires spin resonance to take place, which can be explained by the functional theory of kinetics. The reaction of methylthioacetic acid with nitrate ions to form methylthiosulfonate ions has been shown to be rapid and reversible in both dry weight and wet weight experiments. The alkylation of methylthioacetic acid with ethyl bromoacetate has been shown to produce thermochemically stable imine and phosphate ions.</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>Dimethylmorpholine-4-carboxamide (DMMC) is an unsymmetrical, synthetic carbamate that has antiviral properties. The antiviral properties of DMMC are due to its ability to inhibit the synthesis of viral proteins by binding to a site on the enzyme RNA polymerase and blocking the formation of a functional enzyme. This agent also has been shown to inhibit the production of nitric oxide in k562 cells. DMMC is marketed for use as an insecticide, but it has not been approved for this use. In crystallography studies, DMMC was found to have high yield and low melting point.</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>L-Alaninamide is a protonated amino acid that reacts with the bacterial cell membrane and causes it to rupture. L-Alaninamide is synthesized by hydrolysis of the ester bond between butyric acid and serine protease in the presence of immobilized d-alanine. The reaction is carried out at a pH of 5.5, and the release of pressor is observed. This reaction takes place in an aqueous solution containing fatty acids as solvents. The type strain of this amino acid is E. coli.</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>Prothionamide is a drug that belongs to the group of drugs called sulfonamides. It is used to treat bowel disease by inhibiting the growth of bacteria and fungi. Prothionamide inhibits bacterial growth by binding to bacterial DNA and preventing it from synthesizing new proteins. This drug also has a matrix effect, which means that it binds to the inside of the bacterial cell wall and prevents the production of new cells, leading to cell death. Prothionamide has been shown to be effective against tuberculosis in mice, although there are few data on its use in humans. The most common side effects associated with prothionamide are nausea and vomiting.</p>

<p>2,4,6-Trimethoxybenzamide is a triggered compound that reacts with lithium to form an efficient regiospecific lithium 2,4,6-trimethoxybenzamide complex. This reaction occurs at low temperatures and has been shown to be more efficient than other methods for the synthesis of acridones. The reaction has not been shown to be reversible and requires the use of a strong base such as lithium.</p>

<p>2-Hydroxysalicylamide is a low-energy, small molecule that has shown to be an effective inhibitor of serine proteases. It binds to the active site of the protease, blocking catalysis and inhibiting the growth of cancer cells. 2-Hydroxysalicylamide has been shown to inhibit the transcriptional regulation of pro-inflammatory genes in a patterning assay and it inhibits tumor growth in a pain model. This drug also suppresses the expression of suppressor genes and can be used as an analgesic without causing side effects.<br>2-Hydroxysalicylamide is also a polarizer for tissues, meaning that it preferentially accumulates in tissues with high water content such as breast tissue. This property has been shown to be useful for imaging cancerous tumors.</p>

<p>This compound is a recyclable, multicomponent, element analysis, element, diversity and catalyzed reaction that yields high purity products with high yields. The catalyst is reusable and the NMR data are reproducible.</p>