Amides

<p>N-(2-indol-3-ylethyl)benzamide (4-AIBA) is a functional, health functional food. It has shown anticancer activity in a human colon carcinoma cell line, and it inhibits the production of nitrous oxide from inducible nitric oxide synthase, which is important for tumor invasion. 4-AIBA also inhibits tyrosinase activity, an enzyme that is involved in melanin synthesis. This inhibition may be beneficial to skin conditions such as acne or pigmentation disorders. The compound also inhibits the degranulation of mast cells and stimulates cell proliferation in rat mesenteric lymph nodes.</p>

<p>2-Chloro-N-(4-chlorophenyl)propanamide is an acetanilide that is used as a research chemical in the preparation of other compounds. It also has been used to synthesize chloroacetanilides and chloroanilides. 2-Chloro-N-(4-chlorophenyl)propanamide can be prepared by reacting 4-chloroaniline with acetic anhydride and potassium chloride in a basic solution. The reaction will take place at room temperature, but will produce a greater yield when heated to 40°C for 1 hour. This compound can be used as a starting material for the synthesis of other compounds, such as chlorinated analogues of acetaminophen (paracetamol).</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>2-Amino-5-chlorobenzenesulfonamide is a synthetic chemical that is used in the manufacture of amides and diazoxide. It is also found naturally in humans as a metabolite of the amino acid histidine. 2-Amino-5-chlorobenzenesulfonamide has been shown to be a potent receptor for the modulation of acetylcholine release by binding to muscarinic receptors, including M1 and M2 subtypes, and inhibiting the enzyme hydrolysis of acetylcholine. This chemical has been shown to be chemically stable at pH 5 or higher, and it has been found to be resistant to hydrolysis by enzymes such as esterases, glucuronidases, glutathione reductase, and cytochrome P450. 2-Amino-5-chlorobenzenesulfonamide is also an enantiomer that can bind to collagen in the human</p>

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<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>Rink amide PEGA resin is a cation-exchange resin that has been modified with poly(ethylene glycol) and poly(ethylene oxide). It binds to calcium ions, which are required for cell division. Activated resins can be used in animal diagnostic tests to measure blood glucose levels or as an adsorbent for the removal of heavy metals from drinking water. Rink amide PEGA resin can be used to modify polymer conjugates and assay biological properties, such as cancer cells or solid-phase synthesis.</p>

<p>4-Chloro-3-nitrobenzamide (4CNBA) is a potent inducer of hepatic drug metabolizing enzymes. It reacts with methyl cinnamate to form the 4-chloro-3-nitrobenzamide methyl ester and chloride ions. This reaction is catalyzed by copper, which binds to the 4CNBA molecule. The chloride ion then displaces water from the ester, producing a nitroso intermediate. This intermediate breaks down into an unstable nitrite, which in turn reacts with hydrogen peroxide to form a hydroxylamine intermediate. Hydroxylamine can then react with sulfhydryl groups to produce reactive thiols that are responsible for the induction of detoxification enzymes in the liver.<br>4CNBA has been shown to be toxic at high concentrations and is rapidly detoxified by Phase II enzymes such as glutathione S transferase, UDP glucuronosyltransferase, and N-acetyl</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>N-Phenylhydrazinecarbothioamide is a chemical compound that is used in wastewater treatment. It is an organic molecule that is composed of hydrophobic and hydrophilic parts. The hydrophobic part, which contains the phenyl group, binds to the hydrophobic region of the cell membrane and causes the cell to lyse. The hydrophilic part has an affinity for water and can be used as an electrode material in electrochemical impedance spectroscopy. N-Phenylhydrazinecarbothioamide also has been shown to have antibacterial properties against human pathogens, including Mycobacterium tuberculosis, Clostridium perfringens, and Escherichia coli O157:H7. The compound has been shown to inhibit cervical cancer cells by inhibiting protein synthesis through inhibition of ribosomal activity and fragmentation assay analysis showed that N-phenylhydrazinecarbothioamide binds to copper ions at a coordination geometry of</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-Chloro-5-nitrobenzene sulfonamide (2CNS) is a glycol ether that has been shown to inhibit the activity of carbonic anhydrase. It has been shown to be a competitive inhibitor of the enzyme, and can be used as a lead compound for developing new drugs. 2CNS has been shown to inhibit an anhydrase that is found in bacteria, such as Streptococcus pneumoniae, Haemophilus influenzae, and Staphylococcus aureus. This inhibition causes increased levels of hydrogen ions in the bacterial environment, which leads to the acidification of their surroundings. 2CNS also inhibits chloride ion uptake in these bacteria.<br>2CNS's pharmacophore includes two aromatic hydrocarbon rings with at least one hydrogen bond acceptor group on each ring. This pharmacophore is responsible for its inhibition of carbonic anhydrase and chloride ion binding site.</p>

<p>N-(Phenylsulfonyl)palmitamide is a versatile building block that can be used to create complex compounds for research. CAS No. is 527-87-2 and it is a reagent and speciality chemical with high quality. It is also useful as a reaction component in the synthesis of other compounds, or as a scaffold for the synthesis of new derivatives.</p>

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<p>2-Veratramide is a drug that belongs to the group of amides. It is a highly soluble, water-soluble and lipophilic molecule. The molecular modeling study revealed that it has a hydroxyl group in its structure and a hydrogen bond with the intramolecular hydrogen atom. 2-Veratramide has been observed to inhibit protein synthesis and cellular proliferation by binding to cancer cells or inflammatory cells. It also binds to dopamine receptors, inhibiting uptake of dopamine and subsequent activation of downstream signaling pathways. 2-Veratramide is an inhibitor of nitric oxide synthase (NOS), which plays an important role in inflammation, vascular tone, neurotransmission, and cell proliferation.<br>2-Veratramide inhibits NOS by competitively binding to the heme moiety at the active site of the enzyme, thereby blocking access to substrate arginine.</p>

<p>N-[2-(2,3-Dimethoxyphenyl)ethyl]-2-chlorobenzamide is a versatile building block that can be used as a reaction component and reagent. It is an intermediate in the synthesis of pharmaceuticals and fine chemicals and has been shown to be useful in the synthesis of complex compounds. This compound reacts with nucleophiles, such as amines and alcohols, by replacing the chloride group with a variety of functional groups. The product is then hydrolyzed to release the original reactant. N-[2-(2,3-Dimethoxyphenyl)ethyl]-2-chlorobenzamide has a CAS number of 320576-19-0 and can be found at ChemDiv.com.</p>

<p>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.</p>

<p>3-Oxo-2-phenyl butanamide is an amphetamine that has been shown to be a potential marker for wastewater. 3-Oxo-2-phenyl butanamide is one of the many intermediates in the synthesis of amphetamine from phenylacetone and can be found in wastewater as an impurity. This compound has also been used as a marker for wastewater treatment malfunctioning. 3-Oxo-2-phenyl butanamide is excreted into the environment through urine, and its presence can be measured in water samples by gas chromatography/mass spectrometry or liquid chromatography/mass spectrometry.</p>

<p>2-Chloro-4-nitrobenzamide is a drug that belongs to the sulfa drugs. It has been shown to be effective in treating autoimmune diseases, particularly bowel disease and inflammatory bowel disease. 2-Chloro-4-nitrobenzamide inhibits the synthesis of fatty acids by blocking the enzyme acetyl CoA carboxylase, which is involved in the formation of long chain fatty acids. This drug also has immunosuppressive activities, which may be due to its ability to block T cell proliferation. 2-Chloro-4-nitrobenzamide is used as a chemical intermediate for antibiotics such as maduramicin ammonium and salinomycin sodium. It is also used as a dietary supplement or pharmaceutical dosage form for cardiac glycoside drugs such as digoxin.</p>

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<p>Quinfamide is a polyunsaturated compound that contains a cevimeline hydrochloride molecule. It is used to treat bowel disease, usually in combination with other drugs. Quinfamide has been shown to have specific treatment effects on the symptoms of inflammatory bowel disease (IBD) when given at doses of 400-800 mg per day for up to 12 weeks. This drug can also be used as an analog for 5-membered heteroaryl compounds, such as benzalkonium chloride, which are also used to treat bowel disease. Quinfamide has been shown to have anti-inflammatory properties and may work by inhibiting fatty acid synthesis or by reducing the number of neutrophils in the gut.</p>

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<p>5-(Acetylamino)-N,N'-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-1,3-benzenedicarboxamide is a reactive iodinated contrast agent that is used in the diagnostic imaging of body cavities and blood vessels. It can be prepared by the acetylation of 5-(acetylamino)naphthalene-2,3-diol with 2,4,6-triiodobenzene dicarboxylic acid using an alkali metal as a base. The yields for this reaction are dependent on the type of solvent used. This chemical has two functional groups: an amide and an acetate group. It reacts with iohexol to form a radiocontrast product that contains both iodine and propanediol. This process is industrially carried out by mixing 5-(acetylamino)naphthalene-2,</p>

<p>Solid phase peptide anchor; tool for the Fmoc solid phase synthesis of peptide amides.<br>100-200 mesh. 1% DVB, substitution range 0.3-0.6 meq/g</p>

<p>2,6-Dichlorobenzamide is a chemical compound that belongs to the group of organochlorine compounds. It is soluble in water and has been shown to be an effective treatment for metal contamination in groundwater. 2,6-Dichlorobenzamide reacts with metal ions at the surface of cells by forming an insoluble metal chloride complex that accumulates inside the cell and leads to cell death. 2,6-Dichlorobenzamide has been shown to be toxic to bacteria, particularly gram-positive bacteria such as Staphylococcus aureus and Bacillus subtilis. This compound also binds to bacterial membrane lipids with high affinity constants. This activity may be due to its ability to form lipid hydroperoxides and free radicals.</p>

<p>N-Allyl-N-(4-cyano-2-chlorophenyl)acetamide is a high quality reagent that has been used as an intermediate in the synthesis of fine chemicals, useful scaffolds and building blocks. It is also a versatile building block that can be used to synthesize high quality compounds with a wide range of functionalities. N-Allyl-N-(4-cyano-2-chlorophenyl)acetamide is a speciality chemical that can be used for research purposes. This compound has been shown to produce reactions with other compounds, such as nitrobenzene, to generate useful products.</p>

<p>Lacosamide is a drug that is used for the treatment of epilepsy. It has been shown to inhibit neuronal death in vitro and in animal models, and has been extensively studied for its potential benefits in the treatment of bowel disease. The mechanism of action for lacosamide involves inhibition of the transport of neurotransmitters from the synaptic cleft by binding to the neuronal sodium channels and increasing their recovery rate. Lacosamide has also been found to affect energy metabolism by inhibiting the activity of mitochondrial enzymes such as matrix effect and complex I/III.</p>

<p>Hydroxy tolbutamide is a drug with an unknown mechanism of action. It has been shown to inhibit the transcription-polymerase chain reaction and human serum in vitro. This drug may be used as a marker for renal disease, as it has been shown to increase the level of magnesium in urine and reduce the rate of protein synthesis in rat liver microsomes. Hydroxy tolbutamide also inhibits receptor activity, which may be due to its ability to inhibit the metabolic rate.</p>

<p>N-(2-indol-3-ylethyl)-3-phenylprop-2-enamide is a serotonin analog that has been shown to inhibit the production of tryptophan decarboxylase in organisms. This compound has also been shown to be an inhibitor of the biosynthesis of p-coumaric acid, which is involved in the synthesis of lignin, phytoalexins, and other phenolic compounds. N-(2-indol-3-ylethyl)-3-phenylprop-2-enamide may be useful as a fungicide against pyricularia or as an antimicrobial against microbial infections.</p>

<p>N-[(4-Amino-2-methylpyrimidin-5-yl)methyl]formamide (NAMPT) is a triazolo compound that inhibits the ATP binding cassette transporter and blocks the uptake of uridine and pyrimidine compounds. It also inhibits inorganic pyrophosphatase, which is an enzyme that catalyzes the hydrolysis of pyrophosphate to inorganic phosphate. NAMPT has been shown to be a substrate for hypochlorous acid production in neutrophils, suggesting it may play a role in the regulation of oxidative stress. Chemical biology studies have demonstrated that NAMPT plays a physiological function as an intermediate in vitamin B1 biosynthesis.</p>

<p>Avanafil is a drug that can be used as a treatment for male erectile dysfunction. It works by inhibiting the production of PDE5, which is an enzyme that regulates the levels of cGMP in the penis. Avanafil has been shown to be effective when taken at a dose of 100 mg; this is because it takes about 30 minutes for avanafil to reach its peak level. Avanafil has a chemical stability that is greater than 12 hours, with an average lifespan of 24 hours. The drug also has no major drug interactions and does not inhibit any other drugs from working.</p>

<p>Intermediate in the synthesis of vildagliptin</p>

<p>Morpholine-4-carboxamide is a polymerase chain inhibitor that inhibits the activity of DNA polymerases. It binds to the DNA template strand and prevents the enzyme from adding nucleotides to the primer strand, thereby inhibiting DNA synthesis. Morpholine-4-carboxamide has shown efficacy in treating hyperproliferative diseases such as cancer cells and psoriasis. This drug has been shown to inhibit caspase activation and histone protein acetylation, which may be related to its anti-cancer properties. Morpholine-4-carboxamide also binds to cannabinoid receptor 2 (CB2) and may have therapeutic effects on inflammatory diseases such as psoriasis and arthritis.</p>

<p>N-[4-[1-(2-Fluorobenzyl)-3-butyl-2,6-dixo-2,3,6,7-tetrahydro-1H-purin-8-ylmethyl]phenyl]acetamide is a fine chemical with a diverse range of potential applications. It can be used as a versatile building block in the synthesis of complex compounds and is useful as a reaction component or reagent. Its CAS number is 628279-07-2.</p>

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<p>2-Amino-N-methylbenzamide is a benzodiazepine receptor antagonist that has been shown to inhibit the proliferation of cancer cells in vitro. 2-Amino-N-methylbenzamide binds to the benzodiazepine receptor, which is found in cell nuclei and is involved in controlling the process of cell division. Benzodiazepines are a class of drugs that work by increasing the activity of GABA, which reduces neuronal excitability. 2-Amino-N-methylbenzamide prevents this activity by binding to the benzodiazepine receptor, preventing GABA from binding to its receptors and thereby inhibiting neuronal excitability. This drug has also been shown to inhibit cancer growth through an anthranilic acid derivative, methyl anthranilate. Methyl anthranilate inhibits DNA synthesis and induces apoptosis in cancer cells, leading to cell death.</p>

<p>2-Chloro-N-(3,5-dichlorophenyl)acetamide is a stabilized, crystalline compound. It has a planar structure with an amide bond and hydrogen bonds. The 2-chloro group is bonded to the nitrogen atom of the acetamide group. The 3,5-dichlorophenyl group is bonded to the carbon atom of the acetamide group. The chlorine atoms are in a planar configuration with adjacent chlorine atoms forming a skeletal arrangement. This chemical is used as an intermediate for other compounds.</p>

<p>3-Aminobenzamide is a drug that has been shown to be effective in the treatment of temozolomide-induced neuronal death. 3-Aminobenzamide inhibits the synthesis of ATP and blocks its binding to the atp-binding cassette transporter, which prevents the transport of this nucleotide into cells. This results in cell death due to insufficient energy metabolism and inability to repair DNA damage. 3-Aminobenzamide also increases production of reactive oxygen species, which are involved in reperfusion injury and myocardial infarcts. 3-Aminobenzamide is used as a model system for studying DNA repair and energy metabolism.</p>

<p>Sodium diformylamide is a chemical compound that belongs to the class of amides. It has been shown to inhibit the activity of a number of enzymes including alkanoic acid, inorganic acid, and amide. It has also shown promising results in the prevention and treatment of metabolic disorders such as hepatitis. The asymmetric synthesis of this compound is achieved through the use of trifluoroacetic acid and nitrogen atoms. The biological properties of sodium diformylamide have not yet been fully researched but it has been found to have integrin receptor-binding properties.</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>N-[(3S)-2,5-Dioxotetrahydro-3-furanyl]-2,2,2-trifluoroacetamide is a boronic acid that has been used to synthesize polymers. This compound is of interest for the synthesis of hydrophobic amino acids such as threonine and lysine. The high yield and functionalisation of this molecule make it deserving of further investigation.</p>

<p>N-Benzylbenzamide is a molecule that contains an amide group, which is considered to be a hydrogen bond acceptor. The amine group of this compound can also act as a hydrogen bond donor. It has been shown to inhibit the activity of tyrosinase, which is an enzyme responsible for the production of melanin in melanocytes. N-Benzylbenzamide has been shown to have a molecular mechanism similar to that of hydroquinone and other phenolic compounds. In addition, it has been found to decrease microvessel density and inhibit the growth of cancer cells in vitro. This compound is not yet approved for use as a drug but may be used in future research studies as an alternative treatment for cancer.</p>

<p>L-alanine-β-naphthylamide is an amino acid that is synthesized by the action of β-Naphtholactamase on l-alanine. It is used as a substrate for enzyme studies and to determine the uptake of substances by cells. L-Alanine-β-naphthylamide has been shown to inhibit the activity of some enzymes, such as aminopeptidases and peptidases. The inhibition may be due to its ability to bind to lysine residues in the active site of these enzymes. This amino acid also inhibits the growth of bacteria at neutral pH and has a bacteriostatic effect at a pH range from 4.5 to 5.5.</p>

<p>5-Methyl-2-nitrobenzamide is a compound that has antiproliferative activity and is used as an anticancer drug. This drug inhibits the polymerization of the protein tubulin in cancer cells, thereby inhibiting cell division. It also inhibits the growth of certain tumor cell lines in vitro. 5-Methyl-2-nitrobenzamide was found to inhibit the proliferation of human ovarian carcinoma cells by binding to DNA, preventing transcription and replication of genetic information. In addition, this agent binds to tubulin and prevents its polymerization, leading to inhibition of cell division.</p>

<p>2,5-Dichlorobenzamide is a halogenated compound that inhibits topoisomerase and proteasome activity. It has been shown to be cytotoxic against cancer cells in vitro. 2,5-Dichlorobenzamide can also inhibit the growth of tuberculosis bacteria and may be used as an operational agent for weed control. The safety profile of this drug has not yet been fully determined. 2,5-Dichlorobenzamide is available in two crystalline forms, both of which are active with different degrees of potency.<br>2,5-Dichlorobenzamide is a hybridization inhibitor that inhibits the enzyme DNA gyrase and proteasome activity. It binds to bacterial 16S ribosomal RNA and inhibits protein synthesis, leading to cell death by inhibiting the production of proteins vital for cell division.</p>

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<p>6-Methylnicotinamide is a transport inhibitor that prevents the uptake of fatty acids and growth factors into cells. It has been shown to inhibit the activity of glutamate receptors by blocking the interaction between these receptors and their binding partners, which are called co-agonists. 6-Methylnicotinamide has also been shown to inhibit the synthesis of virus proteins in vitro and in vivo. There is a lack of evidence on its safety profile. 6-Methylnicotinamide may be used to treat hepatitis C and colorectal carcinoma.</p>

<p>N'-(2-Cyano-4-fluorophenyl)-N,N-dimethylimidoformamide is a high quality, reagent that is useful for the synthesis of complex compounds. It can be used as a fine chemical and speciality chemical in research and development. The CAS number for this compound is 1017082-62-0. N'-(2-Cyano-4-fluorophenyl)-N,N-dimethylimidoformamide has shown to be a versatile building block for the synthesis of novel compounds that are not commercially available. This product is suitable for use in reaction components as well as being an intermediate for the synthesis of other compounds.</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>Please enquire for more information about N-((4-(2-Furylcarbonyl)piperazinyl)thioxomethyl)benzamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N,N'-Dimethyl benzamide (DMAB) is an aryl halide that reacts with hydrogen to form the corresponding carbonyl group. The reaction solution of DMAB and hydrogen gas produces a chemical structure that resembles a hydrogen bond. DMAB has been shown to have anti-inflammatory effects in animals with inflammatory diseases. It has also been studied for its ability to inhibit the formation of amyloid plaque, which is associated with Alzheimer's disease. In addition, DMAB has been shown to have therapeutic effects against boron nitride and amides.<br>The crystal structure of DMAB can be found in both crystalline polymorphs: monoclinic and triclinic. The triclinic form is stable at room temperature and pressure, while the monoclinic form is only stable at higher temperatures. The monoclinic form is more soluble than the triclinic form, as it contains fewer hydrogen bonds between</p>

<p>Please enquire for more information about N-(4-(4-bromophenyl)-2,5-thiazolyl)hexanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-[6-Chloro-5-(2-methoxyphenoxy)-(2,2-bipyrimidine)4-4-yl]-(1,1-dimethylethyl)-benzenesulfonamide is a reagent that can be used as a reaction component in the synthesis of complex compounds. It has high quality and is a versatile building block for the synthesis of speciality chemicals. N-[6-Chloro-5-(2-methoxyphenoxy)-(2,2-bipyrimidine)4-4-yl]-(1,1-dimethylethyl)-benzenesulfonamide is also a useful intermediate in the synthesis of fine chemicals.</p>

<p>Dodeca 2E,4E,8Z,10E,Z-tetraenoic acid isobutylamide (DETBA) is a versatile building block that is used in the synthesis of natural products and pharmaceuticals. DETBA can be used as a reaction component in organic synthesis to form complex compounds such as polyesters, polyamides, polyurethanes, and polyimides. It also has high quality and can be used in research or speciality chemical applications.</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>

Please enquire for more information about 2-Chloro-N-(2-fluorophenyl)propanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>2-Piperazin-1-ylacetamide hydrochloride is a drug that binds to the protein PCSK9, which transports cholesterol into cells. It blocks the transport of cholesterol and therefore lowers the level of cholesterol in blood. 2-Piperazin-1-ylacetamide hydrochloride is used for the treatment of bowel disease, atrial fibrillation (a type of irregular heartbeat), congestive heart failure, and as an anti-viral agent. This drug has been shown to reduce levels of LDL cholesterol by up to 60%. 2-Piperazin-1-ylacetamide hydrochloride has also been shown to be effective against cancers such as prostate cancer and inflammatory bowel disease.</p>

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<p>(2R)-1-(Phenylmethyl)-N-[3-(spiro[isobenzofuran-1(3H),4'-piperidin]-1-yl)propyl-2-pyrrolidinecarboxamide HCl is an endogenous opioid that has been shown to have antidepressant-like effects. It can bind to γ-aminobutyric acid (GABA) receptors, catecholamine receptors, and nociceptin receptors. This drug also has anti-cancer properties and may be used for the treatment of autoimmune diseases. The interaction of this drug with other drugs is not well understood, but it has been shown to modulate the effects of opioids and increase the aversive nature of some substances.</p>

<p>Homoveratramide is a synthetic drug that is used as an antibacterial agent. It has a broad spectrum of activity against bacteria, fungi, and protozoa. Homoveratramide has been shown to be effective against both Gram-positive and Gram-negative bacteria, including Staphylococcus aureus, Streptococcus pneumoniae, Escherichia coli, Salmonella enterica, Pseudomonas aeruginosa, and Klebsiella pneumoniae. Homoveratramide inhibits the synthesis of DNA by binding to the enzyme ribonucleotide reductase. This produces a bacteriostatic effect on the cell by halting DNA replication and transcription.</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>Nipecotamide is a water-soluble drug that inhibits the activity of α1-acid glycoprotein, which is a blood protein that regulates the concentration of hydrogen ions in the body. It has been shown to inhibit the growth of amyloid protein and decrease camp levels in erythrocytes. Nipecotamide is used as an inhibitor for infectious diseases, such as leprosy, tuberculosis, and malaria. The chemical structure of nipecotamide contains nitrogen atoms and an amide bond with carbonyl oxygens. It is also an inhibitor binding to hydrochloric acid and hydrogen bonds with amide groups.</p>

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

<p>Piperazinophenylacetic acid benzylamide hydrochloride is a versatile building block that can be used in the synthesis of complex compounds for research and development. It is a reagent for the preparation of speciality chemicals and also a useful intermediate for the synthesis of reaction components. Piperazinophenylacetic acid benzylamide hydrochloride is a high quality, commercially available chemical that can be used as a scaffold for the preparation of new chemical compounds.</p>

<p>2,3-Diaminobenzamide is a synthetic aromatic compound that is used as a radiation stabilizer. It is also an effective antimicrobial agent with reactive properties against bacteria and fungi. 2,3-Diaminobenzamide has been shown to have anti-cancer properties and can be used to treat inflammatory diseases such as rheumatoid arthritis or ulcerative colitis. The intramolecular hydrogen bond between the amide group and the benzene ring in 2,3-diaminobenzamide contributes to its stability and biological activity.</p>

<p>Pantethine is a dietary supplement, which is a derivative of pantothenic acid, sourced from vitamin B5. As a biologically active compound, it undergoes conversion to pantetheine, which then forms coenzyme A (CoA) and acyl-carrier proteins. This conversion is critical, as CoA is an essential cofactor involved in numerous biochemical reactions that are integral to fatty acid metabolism, among other processes.</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>

<p>3-Bromobenzamide is an amide compound, which is a functional group. It has a molecular weight of 273.3 g/mol and three amine groups. The 3-methoxybenzamide moiety in the molecule can be protonated, which provides the hydration of the molecule and increases its solubility in water. This molecule also has a dipole moment due to the presence of two amide groups.<br>The synthesis of 3-bromobenzamide starts with the reaction between 3-aminobenzoic acid and benzoyl chloride to form 3-benzoyloxybenzoic acid. This is then reacted with ammonia to form 3-aminobenzamide. Finally this is converted into 3-bromobenzamide by reacting it with bromine in the presence of potassium carbonate as a catalyst. <br>This molecule is used as an inhibitory compound for mammalian cell proliferation, specifically for cancer cells</p>

<p>Coconut diethanolamide is a chemical substance that is used as a test compound in carcinogenesis studies. It is a fatty acid and a fatty alcohol, and it has been shown to promote the growth of cancer cells. Coconut diethanolamide has not been found to be an allergen, but it has shown carcinogenic potential. The bioassay for long-term exposure to coconut diethanolamide showed epidermal hyperplasia in mice.</p>

<p>4-Chloro-3,5-dinitrobenzamide is a bifunctional molecule that contains a chlorine atom. It has been found to react with dipolar solutes as well as vicinal dioxan arylation. The nucleophilic amide group is also labile and can be hydrolyzed by strong acids or bases. The electron lone pair of the chlorine atom in 4-chloro-3,5-dinitrobenzamide can be used for electrophilic substitution reactions with aromatic rings or amines. This molecule has been found to undergo an arylation reaction with imidazole in the presence of dioxan solvent at room temperature.</p>

<p>Please enquire for more information about (3-(2,6-dichlorophenyl)-5-methylisoxazol-4-yl)-N-(2,5-dimethoxyphenyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Hydroxyphenylacetamide is a natural product that has been shown to have antibiotic properties. It inhibits the growth of bacteria by inhibiting the synthesis of p-hydroxybenzoic acid, which is an essential precursor for the biosynthesis of aromatic amino acids and other important compounds. 4-Hydroxyphenylacetamide also inhibits dopamine oxidation, which may lead to its anti-infective properties. The biological properties of 4-hydroxyphenylacetamide have been studied using electrochemical impedance spectroscopy (EIS) on bacterial strains and in vitro studies on P. aeruginosa. This compound is not metabolized by microorganisms and does not mineralize or react with oxygen at physiological pH levels. It can be used as a pharmaceutical dosage form for treatment of infectious diseases.</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>2,2-diphenyl-N,N-dimethylpropeneamide (DPPA) is a disulfide compound that has photolytic, thermolytic and modelling properties. DPPA can be used to produce alkylcobalt complexes with various substituents at the α position of the phenyl ring. The lactam structure of DPPA has been shown to undergo thermolysis at temperatures of 250°C in a vacuum. Cinnamic acids have been shown to form lactams with DPPA as well as cinnamic acid derivatives. Molecular modelling studies have been conducted on 2,2-diphenyl-N,N-dimethylpropeneamide and its molecular interactions with styrene and amido groups.</p>

<p>μ-opioid receptor agonist; calcium channel inhibitor; anti-diarrheal</p>

<p>6-Aminonicotinamide is an experimental drug that has shown promising results in animal studies. This compound may be useful for the treatment of cancer, due to its ability to inhibit reactive oxygen species and maintain mitochondrial membrane potential. 6-Aminonicotinamide also has a protective effect against radiation-induced cell damage, as it prevents oxidative injury to DNA and protein. In addition, 6-aminonicotinamide can stimulate the proliferation of pluripotent cells, which are cells that have the ability to differentiate into any type of cell in the body. Finally, this compound was shown to have antitumor effects by inhibiting squamous carcinoma tumor growth in experimental models.</p>

<p>2,5-Dimethoxybenzamide is a potent inhibitor of the enzyme DECATENASE. This enzyme plays an important role in the biosynthesis of the aromatic amino acids phenylalanine and tyrosine. 2,5-Dimethoxybenzamide has been shown to have anticancer activity in vitro and in vivo. Remoxipride is a synthetic drug that competitively inhibits the action of benzodiazepines on GABA receptors by binding to them with high affinity. It was developed as an antipsychotic agent but was never marketed for this indication due to its adverse effects on motor coordination. Remoxipride has also been shown to have estrogenic activity, which may be due to its ability to bind with high affinity and inhibit the enzyme aromatase, which converts testosterone into estradiol.</p>

<p>4-Cyanobenzamide is a naphthalene derivative that is both reactive and intramolecular. It has been shown to react with the amino group of peptides, forming a ruthenium complex. The functional groups are acceptors and donors that can be used in assays for the detection of anions or cations. 4-Cyanobenzamide reacts with water to release hydrogen gas, which can be used to measure its hydration ability. This compound has been synthesized using solid-phase synthesis and it has amide bonds that vibrate at a specific frequency.</p>

<p>Cyclotheonamide A is a cyclopeptide, which is a type of secondary metabolite composed of non-standard amino acids arranged in a cyclic structure. It is naturally sourced from marine sponges, particularly Theonella sp., which are known for their rich and diverse repertoire of bioactive compounds. Cyclotheonamide A functions through the inhibition of serine proteases, a class of enzymes that play a significant role in numerous biological processes, including digestion, immune response, and blood coagulation.</p>

<p>5-Amino-1,3,4-thiadiazole-2-sulfonamide is a chemical compound that inhibits the growth of skin cancer cells. It has inhibitory properties against choroidal neovascularization induced by dorzolamide hydrochloride and other pharmacological agents. 5-Amino-1,3,4-thiadiazole-2-sulfonamide has also been shown to have antiangiogenic activity in vitro and in vivo assays. 5ATTS inhibits the growth of bacteria and fungi by inhibiting fatty acid synthesis. The drug also has been shown to be effective in treating diabetic neuropathy and fluorescein angiography associated with itchy eyes.</p>

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

<p>4-Methoxybenzenecarbothioamide is a urea nitrogen analogue that inhibits the synthesis of urea and other nitrogenous compounds. It is an inhibitor of the enzyme pyruvic transaminase, which converts pyruvate to alanine. The drug is also an inhibitor of the enzyme lactam synthetase, which catalyzes the formation of lactams from amino acids. This activity results in decreased production of cancer cells and renal toxicity. 4-Methoxybenzenecarbothioamide has been shown to have anticancer activity in vitro against a number of human cancer cell lines, including A549 lung carcinoma cells and MCF-7 breast cancer cells.</p>

<p>Please enquire for more information about (2,6-difluorophenyl)-N-(2-indol-3-ylethyl)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 hydrochloride is a high quality, reagent, complex compound, useful intermediate, fine chemical. It has CAS No. 1449108-90-0 and is used as a research chemical and building block in the synthesis of other compounds. (E)-N-(3-Methylaminopropyl)-2-thiopheneacrylamide hydrochloride can be used as a versatile building block in organic synthesis reactions and is an important reaction component for the preparation of speciality chemicals.</p>

<p>C2 dihydroceramide is a lipid that belongs to the group of sphingolipids and is involved in neuronal death. It is a precursor for ceramide, which can also induce apoptosis. C2 dihydroceramide has been shown to inhibit axonal growth by interfering with the polymerase chain reaction, as well as inducing autophagy through toll-like receptor 4 signaling. This lipid has also been shown to inhibit intracellular Ca2+ levels, mitochondrial functions, and bowel disease. C2 dihydroceramide was identified in HL-60 cells and may be used as an analytical method for detecting other sphingolipids.</p>