Amides

<p>Lacosamide is an antiepileptic drug that has been shown to be bioequivalent to the reference product, Gabapentin. Lacosamide binds to voltage-gated sodium channels and is thought to have a similar clinical profile as Gabapentin. It is used in the treatment of partial seizures (with or without secondary generalization) and adjunctive therapy for generalized seizures in adults and children aged 2 years or older. Lacosamide can interact with other drugs, such as gabapentin, by increasing their serum concentrations. This interaction may lead to adverse effects such as dizziness and confusion. Lacosamide plasma concentrations are measured using LC-MS/MS methods after a two-way crossover study in healthy human volunteers. This study also showed that lacosamide is excreted unchanged in urine samples at a rate of about 50% over 24 hours, indicating that it does not undergo extensive metabolism in humans.</p>

<p>Ceramide is a group of sphingolipids that are found in the outermost layer of cells. Ceramides have been shown to be important for maintaining cell structure and function, as well as regulating cellular processes such as apoptosis, insulin resistance, and inflammation. A ceramide profile can be used to identify an individual's risk for developing certain conditions such as cardiovascular disease, chronic kidney disease, or cancer. In addition to its role in cell biology, ceramide has been shown to increase insulin sensitivity in animals by increasing glucose uptake in adipocytes. Ceramides are also produced by the body from other lipids such as cholesterol or fatty acids. They are found in various tissues and organs including the brain, skin, lungs, and gut.</p>

<p>Please enquire for more information about N-(5-bromo-pyridin-2-yl)-2,2-dimethyl-propionamide 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-[4-Amino-3-(trifluoromethyl)phenyl]-2-methylpropanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Carisoprodol Related Compound AMeprobamate is a carbamate derivative used as an anxiolytic drug.</p>

<p>L-Alanine amide hydrobromide is a carboxylic acid that can be used as an antibacterial agent. It reacts with the amino group of l-tyrosine and alkylsulfonyl groups to form an amide. L-Alanine amide hydrobromide has been shown to inhibit bacterial growth in vitro, and it also has anti-inflammatory properties. The antibacterial activity of L-alanine amide hydrobromide is activated by reaction time, which may be due to its ability to react with the basic proteins found in bacteria. This drug also interacts with vinyl alcohol, which may be important for its immobilized application.</p>

<p>Please enquire for more information about N-(1,2,3,4-Tetrahydro-7-methoxy-1-oxo-2-naphthalenyl)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 N-(4-Chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-2-yl)pivalamide 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-Chloro-N-(3-cyano-4,5-dimethylthien-2-yl)acetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Methoxy-N-methylacetamide is a nucleophilic amide that can be synthesized by the reaction of acetamide with methylmagnesium chloride. It has been used to synthesize an enantiopure derivative of 2-aminopropanol, which is used in the synthesis of potent antitumor agents. N-Methoxy-N-methylacetamide has shown potent anticancer activity in mice and rats. This molecule exhibits a carbonyl group that can act as an enolate, which is a reactive intermediate within chemical reactions. The nucleophilic attack on this carbonyl group leads to intramolecular hydrogen transfer, producing a more stable product.</p>

<p>Please enquire for more information about N-(p-Hydroxyphenethyl)-N-(3-hydroxy-4-methoxybenzyl)formamide 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 (R)-Dragonfly N-trifluoroacetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N,N-Dimethyl decanamide is a fatty acid ester that is used as an amide with sodium carbonate and tebuconazole to form a particle. The particle has a diameter of about 0.5 microns and is thermally stable. N,N-Dimethyl decanamide can be used for the removal of organic substances from water by absorption onto the particle surface. It has been shown to be more efficient than other amides in removing these substances from water.</p>

<p>Please enquire for more information about N-Methyl-2-[[3-[(1e)-2-(2-pyridinyl)ethenyl]-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-yl]thio]benzamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Bromoacetamide is a reactive chemical that can react with the sodium channel to produce a postulated effect. It has been shown to inhibit the kinetics of the sodium channel in whole-cell voltage clamp experiments. This inhibition is reversible and does not depend on the pH of the solution. Bromoacetamide has been shown to have an irreversible inhibition on potassium channels, which may be due to its ability to form covalent bonds with sulfhydryl groups. Bromoacetamide also inhibits voltage-gated calcium channels, but at a slower rate than it does for sodium channels. N-Bromoacetamide has been shown to be effective in pharmacological treatments for epilepsy, myasthenia gravis, and multiple sclerosis.</p>

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

<p>7-Phenylacetamide-3-chloromethyl-3-cephem-4-carboxylic acid diphenylmethyl ester is an organic solution that is used in the detoxification of chemical substances. It has a hydroxyl group and is soluble in nonpolar solvents. 7PAMC has been shown to be effective against bone lesions caused by acylation reactions. This drug also binds to the enzyme called cytochrome P450, which is involved in the metabolism of many drugs. It also inhibits bacterial growth by binding to DNA gyrase and topoisomerase IV, enzymes that maintain bacterial DNA integrity. The particle size of this drug is small, with a diameter of less than 10 microns. 7PAMC has a viscosity of 1 cps at 25°C and a melting point of 129°C.</p>

<p>Please enquire for more information about 2-(Diethylamino)-N-(2,4-dimethylphenyl ) acetamide HCl 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-Ethyl-1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluoro-N-(2-hydroxyethyl)Hexane-1-sulfonamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Methyl picolinamide is a novel anticancer agent that inhibits the activity of BCR-ABL kinase. It has been shown to be effective against human colon cancer cells (HCT116) and breast cancer cells (MCF-7). N-Methyl picolinamide binds to the ATP binding site of BCR-ABL kinase, inhibiting its enzymatic activity. The compound also binds to annexin II and blocks cell cycle progression at G2/M phase. The chemical structure of N-Methyl picolinamide includes an amide group, which may lead to low bioavailability. This drug has significant inhibitory activities against nitrogen atoms and inhibition constants for both the A and B forms of the enzyme.</p>

<p>N-Cyanobenzenecarboximidamide hydrochloride (NCBCH) is an intermediate for the synthesis of azomethine dyes. It can be used to produce azo dyes with a methoxy group at the 3 position and a hydrogen atom at the 4 position. NCBCH is also an excellent substrate for chemical reactions involving fragmentation, extraction, or elimination. NCBCH can be synthesized from methyl ether and benzonitrile in the presence of benzamidine. The product is then treated with methanol to give a tautomeric mixture of benzyl and methyl ether.</p>

<p>(S)-(+)-2-Phenylglycine amide is a racemic mixture of the (R) and (S) enantiomers. It is an inhibitor of the enzyme, racemase, which converts one type of amino acid to another. This inhibition prevents allergic reactions that can be caused by acylation reactions or ph profiles in the body. The amino acid composition of this drug is unique because it contains an ester hydrochloride group, which does not exist in other drugs. The kinetic and thermodynamic properties of (S)-(+)-2-phenylglycine amide have been studied extensively, but there are no reports on its ability to inhibit inflammatory diseases. However, it has been shown that the β-amino acid in this drug can inhibit amide hydroxamic acids and stereoselective hydroxamic acids.</p>

<p>Benzenesulphonamide is a biologically active compound that has been shown to bind to an integrin receptor, which mediates the attachment of leukocytes to the endothelium. It also binds to a basic protein found in human immunoglobulin. Benzenesulphonamide has been shown to have cytotoxic effects on synchronous fluorescence cells and can be used for the treatment of bowel disease. This drug has also been shown to be toxic in vitro and in vivo, with a moderate acute oral toxicity and low chronic oral toxicity. Benzenesulphonamide has been shown to act as a surfactant by binding with sodium dodecyl sulfate (SDS), which is commonly used in detergents, disinfectants, shampoos, soaps, and other household products. The biological properties of benzenesulphonamide are not well-known due to its low solubility in water.</p>

<p>2-Oxo-3-hydroxy-N-methyl-N-propyl D-lysergamide (2OMD) is a metabolite of the drug lysergic acid diethylamide (LSD). It can be detected in urine, blood, and saliva. The detection time in urine is approximately 3 hours after ingestion. 2OMD can be found by chromatography techniques, such as thin layer chromatography or high performance liquid chromatography. It can also be detected using mass spectrometric techniques, such as gas chromatography/mass spectrometry or liquid chromatography/mass spectrometry. 2OMD can also be detected in urine samples by calibrations with standards of known concentration and by the use of analytical methods such as gas chromatography/mass spectroscopy.</p>

<p>2-(4-Aminophenoxy)acetamide is a chemical compound that belongs to the class of acetamides. It is used in the production of polyester fibers and dyes. 2-(4-Aminophenoxy)acetamide is a colorless, crystalline solid that has not been identified in nature.</p>

<p>N-[4-(1-Allyl-3-butyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-8-ylmethyl)phenyl]acetamide (NUAA) is an antiinfective agent that has been shown to be effective against typhimurium. It inhibits bacterial growth by binding to the light chain of the monoclonal antibodies. NUAA is also able to inhibit uptake of iron in E. coli K12 and human cells. The mechanism for this inhibition is not well understood but may be related to its ability to bind iron homeostasis proteins or its oxidation catalyst activity.</p>

<p>Please enquire for more information about 3-Amino-2-hydroxy-N,N-dimethylbenzamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Thionicotinamide is a drug that belongs to the group of ethionamide. It is a synthetic compound with synergistic activity against tuberculosis bacteria. Thionicotinamide inhibits bacterial growth by binding to mycolic acid, which is a component of the cell wall. Thionicotinamide also has conformational properties, which inhibit the enzyme activities. This drug also interacts with other drugs, such as ethionamide, and may have an effect on the metabolism of these drugs in humans. Thionicotinamide binds to lipids and reduces the activity of enzymes that are involved in lipid synthesis. The nitrogen atoms of thionicotinamide bind to four oxygen atoms from two molecules of glycol ethers in a 1:1 ratio. This binding leads to the formation of hydrogen bonds between these molecules, resulting in an increase in kinetic energy for these reactions and improved structural analysis for this molecule.</p>

<p>Please enquire for more information about 16-Phenoxy tetranor pgf2alfa cyclopropyl methylamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Oxamide is a chemical compound with the molecular formula CHNO. It is a white solid that is moderately soluble in water and alcohol, but not in ether. Oxamide has been shown to have antioxidative properties and to inhibit the formation of reactive oxygen species. This drug also has an effect on thermal expansion and on the blood flow rate in human serum.</p>

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

<p>N-Acetylglycinamide is an amide that is structurally similar to the amino acid glycine. It has been shown to have anti-inflammatory properties by inhibiting prostaglandin synthesis in vitro. In vivo, N-acetylglycinamide is metabolized and excreted as the non-polar solvents n-acetylglycine and chloride. This amide is soluble in non-polar solvents such as chloroform, dichloromethane, or ether. N-acetylglycinamide also has a pairwise orientational order with respect to solvent molecules and exhibits a low degree of hydrogen bonding interactions with water molecules.</p>

<p>2-Chloro-N-(2-oxotetrahydro-3-thienyl)acetamide is a chemical compound that is used as an intermediate in the synthesis of other organic compounds. The impurities are minimized by using organic solvents such as acetone, pyridine, and tetrahydrofuran. The product can be precipitated by adding sodium carbonate or potassium carbonate to the solution, or it can be crystallized from a mixture of methanol and water. 2-Chloro-N-(2-oxotetrahydro-3-thienyl)acetamide is also soluble in ethers such as erdosteine and acetonitrile, which can be used to remove the last traces of water.</p>

<p>Please enquire for more information about 2-Bromo-N,N-dimethylisonicotinamide 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 4-Hydrazino-N-methyl benzene methanesulfonamide, hydrochloride (1:1) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-(6-Phenylhexyl)-5-chloro-1-naphthalenesulfonamide is a dibutyryl camp analog that has been shown to inhibit the L-type calcium channel in a dose-dependent manner. It has an effect on both spermatozoa and glioma cells, with its most significant effect being inhibition of the intracellular calcium ion. This drug inhibits the growth rate of these cells, which may be due to its ability to activate adrenergic receptors and cause increased intracellular calcium ion levels. N-(6-Phenylhexyl)-5-chloro-1-naphthalenesulfonamide also slows the cycle of the cell, which may be due to a kinetic effect.</p>

<p>Please enquire for more information about (9Z)-N-[(3-Methoxyphenyl)methyl]-9-octadecenamide 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,N-bis(2-Chloroethyl) benzenesulfonamide 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 4-(Aminomethyl)-N-Methylbenzenesulfonamide 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-[(1S)-1-(Aminocarbonyl)propyl]-4-chlorobutanamide 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 (Nle 8·18,Tyr34)-pTH (7-34) amide (bovine) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>PAR-2 (6-1) amide is a proteolytic enzyme that is activated by inflammatory stimuli. It has been shown to be a major contributor to the pathogenesis of inflammatory bowel disease, and is found in neurons, the bowel, and pancreatic acinar cells. PAR-2 (6-1) amide activates proteases such as trypsin and chymotrypsin and also functions as an antimicrobial peptide. Activation of PAR-2 (6-1) amide leads to the cleavage of proteins at specific sites on their amino acid chains. This cleavage can lead to changes in protein conformation or function. PAR-2 (6-1) amide has been shown to increase endothelial cell proliferation and inhibit bacterial growth, but does not have any effect on cultured normal human skin fibroblasts.</p>

<p>Please enquire for more information about (Asn10,Leu11,D-Trp12)-pTH-Related Protein (7-34) amide (human, mouse, rat) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>L-trans-Epoxysuccinyl-Ile-Pro-OMe propylamide is a pharmacological agent that inhibits the toll-like receptor 4 signaling pathway. L-trans-Epoxysuccinyl-Ile-Pro-OMe propylamide has been shown to cause caspase independent cell death by inducing cathepsin and iron homeostasis. The drug also causes polymerase chain reaction inhibition and neuronal death in vivo.</p>

<p>4-Amino-6-chloro-1,3-benzenedisulfonamide is a natural substance that has been used in Chinese medicine preparations for the treatment of cardiac problems. It belongs to the class of organic compounds called benzenedisulfonamides. 4-Amino-6-chloro-1,3-benzenedisulfonamide is produced by the bacterial enzyme aminase from amino acid and benzoic acid. The adsorption mechanism of 4-Amino-6-chloro-1,3-benzenedisulfonamide is not fully understood, but it is believed that the benzyl groups are key players in this process. The high affinity of 4-Amino-6-chloro1,3 benzenedisulfonamide to proteins may be due to its ability to form hydrogen bonds with protein side chains, such as serine or threonine residues. 4 Amino</p>

<p>Galanin (2-11) amide trifluoroacetate salt H-Trp-Thr-Leu-Asn-Ser-Ala-Gly-Tyr-Leu-Leu is a galanin analog and a ligand for the galanin receptor 1. It has affinity for the receptors in the brain, which are involved in cognition, and is used to study Alzheimer's disease. Galanin (2-11) amide trifluoroacetate salt H-Trp-Thr-Leu-Asn-Ser -Ala -Gly -Tyr -Leu -Leu is a member of the family of neuropeptides and neuromodulators that regulate nerve injury and alzheimer's disease.</p>

<p>Kemptamide is a peptide that has been shown to have cytotoxic and anti-proliferative effects on renal cancer cells. It is a synthetic analogue of an endogenous peptide, Lys-Lys-Arg-Pro-Gln-Arg-Ala-Thr-Ser-Asn-Val-Phe, that is found in porcine kidney. Kemptamide’s cytotoxic activity may be due to its ability to inhibit the activity of phosphatases. Kemptamide also has regulatory properties and can modulate the expression of genes that are involved in cell growth and apoptosis. This peptide has been shown to be reactive with kidney cells, which may lead to its therapeutic effect on renal cancer.</p>

<p>Please enquire for more information about 1-Methyl-4-nitro-1H-pyrazole-3-carboxamide 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 Phenylacetyl-(D-Arg2·28,p-chloro-Phe6, Homoarg 9·29,Tyr(Me)10, Abu 15, Nle 27)-GRF (1-29) amide (human) 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 3-[[[2-[(Aminoiminomethyl)amino]-4-thiazolyl]methyl]sulfinyl]-N-(aminosulfonyl)propanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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

<p>N-2-[(2-bromo-4,6-dinitrophenyl)azo]-5-(diethylamino)phenyl]acetamide (NBDPA) is a yellowish solid that is soluble in water. It has a molecular weight of 308.3 and chemical formula C14H21BrN2O4. NBDPA is used as an analytical reagent for the kinetic data of liver cells and in wastewater treatment. This compound has been shown to exhibit carcinogenic potential in rats, causing genetic damage to the DNA of liver cells and kidney tissue. NBDPA has also been shown to be toxic to fish embryos and larvae, with significant effects on the development of larvae at high concentrations.</p>

<p>Please enquire for more information about Sorbin (147-153) amide (porcine) trifluoroacetate salt 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 Mca-(endo-1a-Dap (Dnp))-TNF-a (-5 to +6) amide (human) trifluoroacetate salt 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 (Nle 27)-GRF (1-29) amide (human) 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 Osteostatin amide trifluoroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Growth hormone-releasing factor (GRF) is a peptide fragment of amino acids 1–2 from GHRH (growth hormone-releasing hormone). This 1-29 region is the shortest fully functional fragment of GHRH. GRF is also known as sermorelin. Sermorelin binds to the growth hormone-releasing hormone receptor (GHRH-R), and acts as a surrogate for GHRH, causing growth hormone secretion.human: H-YADAIFTNSYRKVLGQLSARKLLQDIMSR-NH2rat:        H-HADAIFTSSYRR I LGQLYARKLLHEIMNR-NH2</p>

<p>Benzamidine is a benzamidase inhibitor that competitively binds to bacterial enzymes such as metalloendopeptidases and matrix metalloproteinases. It inhibits the degradation of collagen, resulting in a higher concentration of soluble extract. This drug also has an effect on spermatozoa, which may be due to its ability to inhibit bacterial enzymes that are involved with uptake and preload. Benzamidine has been shown to have a pH optimum of 8-9 and is most active at this pH range.</p>

<p>Please enquire for more information about N-(2-Amino-ethyl)-2-(benzyl-phenyl-amino)-acetamide 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 Apelin-36 (1-16) amide (human) trifluoroacetate salt 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 GLP-1 (7-36)-Lys(biotinyl) amide (human, bovine, guinea pig, mouse, rat) trifluoroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Hexahydroisonicotinamide (HNI) is a potent amyloid protein inhibitor that is structurally related to picolinic acid. HNI has been shown to be effective in the treatment of infectious diseases caused by bacteria, such as diazonium salt-resistant strains of Pseudomonas aeruginosa and Enterobacter cloacae. Hexahydroisonicotinamide is also active against methicillin-resistant Staphylococcus aureus (MRSA), which may be due to its structural similarity to picolinic acid. The molecular weight of HNI is 587.6, with a molecular formula of C9H11N3O2. It has been shown that hexahydroisonicotinamide inhibits the transfer reaction between an amide and piperidinium, as well as the phosphorylation of proteins by enzyme kinases. This drug binds to hydrated biphenyl molecules and inhibits their</p>

<p>Protease-activated receptor 1 (PAR-1) selective activating peptide, TFA salt. 98%.</p>

<p>Please enquire for more information about (D-Arg6,Asn10)-MCH (6-16) amide (human, mouse, rat) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Dynorphin A (1-11) amide trifluoroacetate salt is a modified form of the opioid peptide dynorphin, which is a natural ligand for kappa-opioid receptors. It has affinity for the surface receptors and can be used to study the modifications that occur in cell function. Dynorphin A (1-11) amide trifluoroacetate salt has been shown to decrease cell function when it interacts with these surface receptors, which are found in brain homogenates and other tissues. Dynorphin A (1-11) amide trifluoroacetate salt also has an effect on brain cells, which may be due to its ability to alter conformational changes in proteins by binding to them. This can lead to alterations in the structure of certain enzymes or receptor proteins.</p>

<p>Please enquire for more information about (Tyr36)-pTH-Related Protein (1-36) amide (chicken) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>LymnaDFamide-1 is a neuropeptide that belongs to the family of c-terminal peptides. It is a dipeptide with a sequence of L-Pro-Tyr-Asp-Arg-Ile-Ser-Asn-Ser-Ala-Phe. This peptide was found in the nervous system of invertebrates, where it is believed to play an important role in the regulation of neurotransmitter release. In mammals, LymnaDFamide has been detected in the brain and in the gallbladder. It may be involved in regulating feeding behavior and gastric motility.</p>

<p>6-Aminopicolinamide is a metabolite of nicotinamide, which can be found in the urine of humans and animals. 6-Aminopicolinamide has been shown to have anti-leukemic activity against experimental leukemias in animals. The mechanism of action is not well understood but may involve inhibition of nucleotide synthesis or the inhibition of dehydrogenase activity. Clinical trials are underway to determine its efficacy as an anti-tumor agent.</p>

<p>L-Glutamic acid alpha-amide is an ester hydrochloride that is a tissue culture amide. It is a cyclic peptide analog and a hydroxyl group. L-glutamic acid alpha-amide has been shown to inhibit the inflammatory response in the bowel disease, Crohn's disease, by blocking the toll-like receptor 4 and 5. This drug also inhibits protein synthesis, which may be due to its ability to bind to fatty acids, thereby inhibiting the production of proteins vital for cell division.</p>

<p>Please enquire for more information about Beta-Casomorphin (1-5) amide (bovine) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Adamantane is a cyclic hydrocarbon with 18 carbon atoms. It is a colorless, crystalline compound that is soluble in organic solvents. Adamantane has been used as an anti-influenza drug for the treatment of pandemic influenza. Adamantane binds to the virus and inhibits its ability to bind to the host cell surface receptor, preventing viral entry into the cell. Adamantane has been shown to be effective against both influenza A and B viruses in animal studies. Adamantane also has an inhibitory effect on amine metabolism and aryl halide reactions, which may be due to its hydrogen bond forming abilities.</p>

<p>4-Amino-N-(4-methylpyrimidin-2-yl)benzenesulfonamide (AMBPS) is a sulfonamide antimicrobial agent that belongs to the group of sulfa drugs. It is a potent inhibitor of tetracycline resistance in bacterial cells, and has been shown to be effective against infectious diseases such as tuberculosis, leprosy and pneumonia. AMBPS has also been used in wastewater treatment and biological studies with high values. This drug binds to sulfamerazine, which inhibits bacterial growth by inhibiting RNA synthesis. The hydrogen bonding interactions between AMBPS and sulfadiazine are thought to be responsible for the effects on congestive heart failure.</p>

<p>Please enquire for more information about Gastric Inhibitory Polypeptide (6-30) amide (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Hydroxy-2-phenyl-acetamide is a metalloprotease inhibitor that binds to the active site of the enzyme, thereby preventing it from binding with its natural substrate. This drug has been shown to inhibit the production of TNF-α in mice with autoimmune diseases and may be able to inhibit other proinflammatory mediators. N-Hydroxy-2-phenyl-acetamide has been shown to bind to a water molecule and an aliphatic hydrocarbon in order to form a hydrogen bond. This coordination complex inhibits the activity of matrix metalloproteinases, which are enzymes that break down collagen, elastin, and other proteins in the extracellular matrix. N-Hydroxy-2-phenyl-acetamide is not active against acid complexes or tnfα.</p>

<p>N,N-Bis(2-hydroxyethyl)dodecanamide is a surfactant that is used in the treatment of wastewater. It has been shown to be effective at removing p-hydroxybenzoic acid from water and at reducing the concentration of this compound in the environment. N,N-Bis(2-hydroxyethyl)dodecanamide also has antimicrobial properties and synergizes with other antimicrobial agents to provide a more potent effect than when it is used alone. This surfactant has been shown to have an effect on congestive heart failure by blocking the action of angiotensin II receptors.</p>

<p>Please enquire for more information about Phenylacetyl-(D-Arg2·28,p-chloro-Phe6,Arg9, Abu 15, Nle 27, Homoarg 29)-GRF (1-29) amide (human) 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 Antho-RPamide III·HCl Pyr-Val-Lys-Leu-Tyr-Arg-Pro-NH2·HCl 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 Tyr-Amyloid P Component (27-38) amide trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>He-LWamide II is a neuropeptide that is found in the hydrozoa, cnidarians, and anthozoa. It is an endogenous hormone that is produced by the planula stage of development. He-LWamide II inhibits muscle contractions and can be used as a model system for studying the effects of neuropeptides on invertebrate development. The developmental effects of this peptide have been studied in animals and humans, including its role in regulating the maturation of eggs and spermatozoa. He-LWamide II also has inhibitory effects on the nervous system and muscles.</p>

<p>Salicylamide is a drug that is used as an analgesic, antipyretic, and anti-inflammatory agent. It is also used to treat bowel disease, including ulcerative colitis and Crohn's disease. Salicylamide has been shown to inhibit the activity of enzymes such as cyclooxygenase-2 (COX-2) and 5-lipoxygenase (5-LOX), which are responsible for the production of inflammatory mediators. Salicylamide also inhibits copper chloride induced synchronous fluorescence in rat colon cells. Salicylamide also binds to human serum albumin and other nitrogen atoms, which can be measured using chemiluminescence methods. Salicylamide may also have properties that make it useful for the detection of cancerous tumors in the colon. Salicylamide can be detected using electrochemical impedance spectroscopy by measuring its resistance at different frequencies when a voltage is applied across a cell containing sal</p>

<p>Parathyroid hormone-related protein (PTHrP) is a peptide hormone produced by the parathyroid gland that functions as a phosphatase, inhibiting alkaline phosphatase. It also has an inhibitory effect on osteoclastic bone resorption and stimulates osteoblastic bone formation. PTHrP has been shown to be useful in treating osteoporosis and Paget's disease. It also has been used in conjunction with dexamethasone to treat patients with malignancies of the head and neck. PTHrP is an inhibitor of protein kinase A and phosphodiesterases, which are enzymes that regulate cellular processes such as proliferation and differentiation.</p>

<p>Please enquire for more information about PAR-3 (1-6) amide (mouse) trifluoroacetate salt 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 (D-Phe5,Cys6·11,N-Me-D-Trp8)-Somatostatin-14 (5-12) amide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Dynorphin A (1-10) amide H-Tyr-Gly-Gly-Phe-Leu-Arg-Arg-Ile-Arg-Pro-NH2 is an analog of dynorphin A. It is a peptide that has been shown to be effective in reducing blood pressure and stress levels in animals. Dynorphin A (1-10) amide H-Tyr-Gly-Gly-Phe-Leu-Arg - Arg - Ile - Arg - Pro - NH2 also has analgesic properties and may be useful for the treatment of cardiac diseases.</p>

<p>2-Chloroacetamide is a quaternary ammonium compound that is used as an intermediate in the synthesis of other organic compounds. It has been reported to have anticancer activity and has been studied for use as a herbicide in agriculture. The vibrational, turbidimetric method, amide, and sample preparation are all instrumental in determining the reaction mechanism of 2-chloroacetamide. This molecule has also been studied using FT-IR spectroscopy and molecular modelling techniques. The hydrogen bond is integral to its optical properties and can be determined by nmr spectra.</p>

<p>PAR-4 (1-6) amide (mouse) trifluoroacetate salt H-Gly-Tyr-Pro-Gly-Lys-Phe-NH2 trifluoroacetate salt is a guanine nucleotide binding protein that belongs to the PAR family of proteins. It is expressed in wild type mice and binds to the cytosolic calcium, which regulates polymerase chain reaction. PAR-4 (1-6) amide (mouse) trifluoroacetate salt H-Gly-Tyr-Pro-Gly-Lys-Phe NH2 trifluoroacetate salt can be used as a potential drug target for epidermal growth factor. It has been shown to activate transcription polymerase chain and transcriptase polymerase chain during transcriptional regulation of messenger RNA.</p>

<p>Please enquire for more information about Propionyl-Amyloid b-Protein (31-34) amide 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 TRAP-14 amide trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Clopamide is a diuretic drug that belongs to the group of protein genes. It is used in the treatment of chronic heart failure, low-density lipoprotein cholesterol and infectious diseases. Clopamide has been shown to increase the glomerular filtration rate by inhibiting the sodium citrate enzyme, which is involved in the formation of urine from blood plasma. This drug also reduces blood pressure by blocking angiotensin II receptors on vascular smooth muscle cells. Clopamide does not have any significant interactions with other drugs, although caution should be exercised when using it with cardiac drugs due to its effects on blood pressure.</p>

<p>Please enquire for more information about PAR-2 (6-1) amide (human) trifluoroacetate salt 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 Cecropin A (1-8)-Melittin (1-18) amide 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 Nociceptin (1-13) amide trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>