Amino Acids (AA)

<p>Bz-Phe-Val-Arg-pNA·HCl is an antibacterial agent that inhibits the synthesis of bacterial cell wall peptidoglycan by binding to the enzyme UDP-N-acetylmuramyl-L-alanyl-D-glutamate synthase. This compound has been shown to inhibit the growth of Gram negative bacteria and atypical bacteria, such as Staphylococcus aureus and Enterococcus faecalis. Bz-Phe-Val-Arg has also been shown to have immunomodulatory properties, which may be due to its ability to modify cellular immunity.</p>

<p>BOC-D-Ser-OH is a synthetic amino acid with an acetylated serine side chain. It is used in the synthesis of glycosidic bonds. BOC-D-Ser-OH reacts with sodium hydrogen carbonate to form the sodium salt of D-serine, which can be used to produce glycoconjugates or as a model protein. The reaction yield is low and can be improved by adding acetyl groups to the substrate, such as galactose. Glycosidic bonds are formed by transfer reactions between nucleophilic hydroxyl groups on sugar molecules and electrophilic amino groups on proteins. The glycoconjugates produced by this reaction have been shown to have anticancer activity in animal models.</p>

<p>4-Phenoxybutyric acid is a molecule that is produced by filamentous fungi. It has been shown to inhibit the growth of many bacteria, including Staphylococcus aureus, Salmonella typhimurium, and Enterobacter aerogenes. 4-Phenoxybutyric acid binds to the receptor on the surface of the bacterial cell membrane and prevents it from functioning correctly. It also prevents the production of proteins necessary for growth and survival. This inhibition leads to a loss of energy in the cell, which eventually leads to death. The molecule has been shown to be effective in inhibiting bacteria even if they are resistant to antibiotics. 4-Phenoxybutyric acid has been shown to be more efficient than other methods for microbial biotransformation, such as dispersive solid-phase extraction or liquid-liquid extraction.</p>

<p>2-Methyl-3,5-dinitrobenzonitrile is a nitro compound that is used as a coccidiostat in the poultry industry. It inhibits the development of coccidiosis in chickens by preventing the growth of protozoa. 2-Methyl-3,5-dinitrobenzonitrile binds to DNA and RNA and prevents protein synthesis, thereby inhibiting cell division and causing death. This drug has been shown to be an analog of benzene, hexane, and pyridine. The structural analysis of this molecule reveals that it contains two nitro groups attached to a benzene ring. One nitro group is located on each methyl group. The hydrogen atoms are replaced by fluorine atoms with one hydrogen atom being replaced by chloride atom. The other nitro group is located on the 3rd carbon on the right side of the benzene ring. This molecule also contains three chlorine atoms which are attached to two adjacent carbons</p>

<p>Please enquire for more information about 4-(N-Methylamino)phenylboronic acid pinacol ester 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 1-Hexyl-4-phenylpiperazine 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 1-(4-Amino-3,5-dichloro-phenyl)-2-bromo-ethanone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Bromo-4-methyl-1,3-thiazole is a diazotization agent that reacts with nitrogen and forms a terminal nitro group. This reaction system is used in the formation of diazo compounds and the synthesis of dyes. 2-Bromo-4-methyl-1,3-thiazole can be used to generate nitrogen oxide, which is a precursor for the manufacture of various types of nitro compounds. It also reacts with metal oxides to produce metal nitrates.</p>

<p>Please enquire for more information about (R)-(-)-2-Methylglutaric Acid 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-(Dimethylamino)-1-(1-methyl-1H-indol-2-yl)prop-2-en-1-one 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 rac-N-ethyl-4-methyl cathinone hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Boc-Dap (Z)-OH is a tert-butyl ester of dipeptide that has been synthesized as a mimetic of the natural amino acid L-dap, which is an important component of the precursor molecule for the synthesis of polyamides. The Boc-Dap (Z)-OH is synthesized by reacting dodecane with a mixture of t-Boc protected α,α'-diaminoethane and t-Boc protected N,N'-diisopropylcarbodiimide hydrochloride. This reaction produces Boc-Dap (Z)-OH in high yield with an excellent purity.</p>

<p>The liposome is a spherical lipid bilayer that encloses an aqueous interior. It is used in the treatment of hyperproliferative diseases, such as cancer, and infectious diseases. The lipid bilayer membrane of the liposomes are made up of phospholipids, mostly phosphatidylcholine, with cholesterol or other molecules added to increase stability. The liposome is composed of two layers: the external layer which includes the phosphate head groups and hydrophilic polymers, and the internal layer which includes the hydrophobic fatty acid tails. Liposomes can be manipulated to target specific cells by adding proteins to either side of the membrane. These proteins are called targeting factors and they usually bind to receptors on the surface of cells that have particular features (e.g., CD4+ T-cells). This drug is toxic because it causes significant cytotoxicity when exposed to various types of cells at a concentration greater than 1 mM. There is significant</p>

<p>Please enquire for more information about Boc-L-Lys(Me)2-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Tetradecafluoro-2-methylpentane is a fluorinated hydrocarbon that is used in synthetic chemistry. It has been shown to inhibit the growth of cancer cells and leaves. Tetradecafluoro-2-methylpentane has also been shown to be an anthropogenic emission and may contribute to global warming. The chemical is classified as a cyclic hydrocarbon, which means it contains two or more rings of carbon atoms. Cyclic hydrocarbons are generally toxic because they disrupt normal cellular function through interference with cell membranes, protein synthesis, and DNA replication.</p>

<p>Please enquire for more information about 1-N-Boc-pyrrolidine-3-(S)-methylcarboxylate 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 1-tert-Butyl 2-methyl 4-oxopiperidine-1,2-dicarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Methylbenzenesulfonamide is a chemical compound that has been shown to induce apoptosis in bladder cancer cells. It is an acid conjugate of the drug 2-methylbenzene-1,4-sulfonamide and it can be used for the treatment of bladder cancer. The compound binds to the apoptosis protein and inhibits its function, leading to cell death. The cytotoxic effects of 2-methylbenzenesulfonamide have been shown in short term toxicity studies in rats. In long term animal studies, this compound showed no adverse effects on the liver or kidneys, but did show some indication of reproductive toxicity. 2-Methylbenzenesulfonamide is not mutagenic and does not affect male fertility when given orally at doses up to 2000 mg/kg body weight for 90 days. 2-Methylbenzenesulfonamide binds to receptors on the surface of cancerous cells and induces apoptosis by inhib</p>

<p>4-Methoxyphenylacetylene is a phosphane that has been extensively studied for its reactivity in cross-coupling reactions with electron-deficient olefins. 4-Methoxyphenylacetylene has been shown to react with chlorides and form an intermediate chloride, which reacts with an olefin to form an ether. X-ray crystal structures of the reaction mechanism have been determined. The transfer mechanism involves nucleophilic attack of chloride on the phosphorus atom followed by elimination of hydrogen chloride from the phosphorus. The reaction product is an ether.</p>

<p>Please enquire for more information about 2-(Chloromethyl)-3-(2-methoxyphenyl)quinazolin-4(3H)-one 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-Homoleucine HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Rac-prolinol is a picolinic acid derivative that has been shown to inhibit the production of pyrrolidinecarboxylic acid in the form of l-tartaric acid. This inhibition is due to the formation of a hydrogen bond with the hydroxyl group on the substrate molecule, which prevents its conversion into pyrrolidinecarboxylic acid. Rac-prolinol has also been shown to inhibit collagen production in cells. Rac-prolinol binds to receptors that are involved in regulating cell proliferation and differentiation, including transforming growth factor beta receptor and epidermal growth factor receptor. It inhibits collagen synthesis by acting as a competitive inhibitor of proline hydroxylase, an enzyme responsible for catalyzing proline into hydroxyproline. The molecule also inhibits DNA synthesis by binding to the erythrocyte membrane skeleton and blocking ATP synthesis.</p>

<p>Please enquire for more information about 3-(4-Methyl-1,4-diazepan-1-yl)propanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Haloxyfop-P-methyl is a herbicide that inhibits the growth of Gram-positive bacteria by inhibiting protein synthesis. Haloxyfop-P-methyl has been shown to inhibit the production of inflammatory genes in hispidum, an experimental bacterial strain. This herbicide also has an inhibitory effect on testicular cells and animals, which may be due to its ability to interfere with the production of prostaglandins. It is used for weed control in cereals such as triticum aestivum and lc-ms/ms method for plant analysis. The chemical structure of haloxyfop includes a methyl group and two oxyfluorine groups. Haloxyfop-P-methyl is soluble in n-dimethyl formamide (DMF) and fluoresces under UV light.</p>

<p>Please enquire for more information about N-Boc-erythro-L-beta-methylphenylalanine 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 rac-4'-Methyl ketoprofen 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 Acetyl-ACTH (3-24) (human, bovine, rat) 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 (S)-1,2,3,4-Tetrahydro-5-methoxy-N-propyl-2-naphthalenamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Methylcyclopropane-1-carboxylic acid is a reactive, stereoisomeric amide with an alkaline metal. It can be prepared by the reaction of methoxide and nitrobenzene in the presence of a base such as potassium hydroxide. 1-Methylcyclopropane-1-carboxylic acid has been shown to have potent antitumor activity against solid tumors in vivo. This compound was also shown to inhibit the growth of human prostate cancer cells in vitro. Additionally, 1-methylcyclopropane-1-carboxylic acid has been shown to inhibit the generation of reactive oxygen species (ROS) from xylene and other aromatic hydrocarbons, which may be due to its ability to nitrosylate these compounds and prevent them from reacting with oxygen.</p>

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

<p>2-Ethyl-2-phenylmalonamide (2-EPMA) is a metabolite of primidone that acts as an inhibitor of glutamate dehydrogenase and may be used in the treatment of epilepsy. It has been shown to be effective in treating seizures caused by carbamazepine, phenobarbital, or phenytoin. 2-EPMA is also used to measure enzyme activities in serum, which can be used as a diagnostic tool for liver diseases. 2-EPMA is typically prepared for use as an enzyme inhibitor by diluting it with high salt or human serum. This compound may have carcinogenic potential and should not be administered with single doses greater than 100 mg/kg body weight. 2-EPMA interacts with many other drugs such as phenobarbital, phenytoin, and carbamazepine.</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>Z-NH-PEG6-CH2CH2COOH is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. Z-NH-PEG6-CH2CH2COOH is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.</p>

<p>4-Chloro-6-methylnicotinic acid (4C6MNA) is a chemical substance that is used in the study of plant leaves and their permeability. This substance has been found to be an excellent indicator of chlorophyll content, as it stains leaf cells with a green color. 4C6MNA is taken up by healthy plant cells and mitochondria, where it binds to the chromophore molecule in the mitochondria. The binding of 4C6MNA to the chromophore molecule leads to the production of fluorescence, which can be detected via microscopy. This substance has been used for laser microbeam studies on natural leaves and tobacco plants.</p>

<p>Please enquire for more information about D-Glyceric acid calcium dihydrate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H2N-PEG12-OH is a PEG polymer categorised as monofunctional (OH-PEG-X). Used as a linker, H2N-PEG12-OH is used to attached PEG to proteins, peptides, oligonucleotides, nanoparticles and small molecules via pegylation, a bioconjugation technique.</p>

<p>N-Ethyl-N-[(Heptadecafluorooctyl)sulphonyl]glycine is a high-concentration environmental pollutant that has been detected in the environment and human blood plasma. This chemical is a member of the class of polyfluoroalkyl substances (PFASs), which are used as surfactants in many industrial processes, including the manufacture of paper, textiles, and paints. PFASs are also present in foods such as meat, butter, and eggs. N-Ethyl-N-[(Heptadecafluorooctyl)sulphonyl]glycine has been shown to have trophic effects on invertebrates and can be measured using a triple-quadrupole mass spectrometer with reaction monitoring. This chemical is not suspected to be carcinogenic or toxic to humans because it does not react with DNA or proteins. The health effects of this substance are still</p>

<p>H-Arg-Gln-OH is a growth factor that has been shown to be effective in the genetic ablation of mice. This growth factor is taken up by cells via receptor activity and stimulates DNA synthesis and cell division. H-Arg-Gln-OH has been shown to be successful in the treatment of congenital heart disease. The onset latency is site specific and low energy, which means that it can be used for noninvasive treatments.</p>

<p>3-Methyl-p-anizaldehyde is a vanillyl alcohol, which is a natural compound that can be found in vanilla beans. It has been used in the synthesis of vanillic acid and lactams. 3-Methyl-p-anizaldehyde has been shown to react with alkyl halides to form alkylated products. These reactions are catalyzed by an enzyme called alcohol dehydrogenase. This enzyme binds to the hydroxyl group on the 3 position of the vanillin molecule, which is then oxidized to form a functional group called an acetate ester. The reaction occurs at low temperatures and can result in optical activity if it produces a chiral product. 3-Methyl-p-anizaldehyde also reacts with ecteinascidins, which are marine natural products that have potent cytotoxic properties against cancer cells.</p>

<p>Please enquire for more information about N-alpha-Z-L-lysine benzyl ester benzenesulfonate 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 1-Boc-4-aminopiperidine-4-carboxylic acid 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 Ethyl 1-N-Boc-3-oxopiperidine-4-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Phenyl-1H-pyrazole-4-carbaldehyde is an antibacterial agent that has been shown to have bactericidal activity against bacteria. It inhibits the growth of bacteria by binding to the pyrazole ring in the bacterial cell wall and blocking the formation of a hydrogen bond. 1-Phenyl-1H-pyrazole-4-carbaldehyde has been shown to be effective against methicillin resistant Staphylococcus aureus (MRSA) and Ciprofloxacin resistant Pseudomonas aeruginosa isolates, but not against Mycobacterium tuberculosis or Mycobacterium avium complex.</p>

<p>Please enquire for more information about 1-Methyl-2-(piperazin-1-ylcarbonyl)-1H-indole hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 1-[2-(5-Methyl-1H-indol-3-yl)ethyl]-5-oxopyrrolidine-3-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

Indene-1-methanamine is a drug that has been used for the treatment of neurologic disorders and is an ester of aliphatic hydrocarbons. It has been shown to have antidepressant effects in animal models, which may be due to its ability to bind to 5-HT1A receptors. Indene-1-methanamine also has antimicrobial properties and can be used for treating bladder infections as well as cancer. This drug binds to the quinolizine site on bacterial DNA gyrase, which inhibits DNA synthesis and leads to cell death.

<p>Please enquire for more information about N6-(1-Deoxy-D-fructos-1-yl)-N2-[(phenylmethoxy)carbonyl]-L-lysine 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 H-Leu-2-chlorotrityl resin 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 1-(5-Methyl-1,2,4-oxadiazol-3-yl)cyclohexanamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 1-[(1-Methyl-1H-pyrazol-4-yl)methyl]piperazine 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 (S)-5,6,6a,7-Tetrahydro-6-methyl- 4H-dibenzo[de,g]quinoline-10,11-diol hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Z-L-leucine-N-hydroxysuccinimide ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Methyl-1,3-dihydro-2H-imidazol-2-one is a chemical compound with the formula CHN. It has been used as a precursor to other compounds and can be prepared by reaction of methanol with chlorine or chloramine. 1,3-Dihydroimidazole reacts with UV light to generate photoproducts that contain pyrimidine or pyridinium rings. It is also reactive with chloride ion and can be used as a raw material for organic synthesis. 1,3-Dihydroimidazole can also be synthesized from chlorinated methanesulfonate esters.</p>

<p>(R)-3-Methylmorpholine is a potent inhibitor of phosphoinositide 3-kinases (PI3Ks) that have been implicated in the development and progression of cancer. It inhibits the PI3Ks at low concentrations, which may result in cell death. This drug also has an anti-inflammatory effect on cancer cells by inhibiting the production of lipids that promote inflammation. The pharmacokinetic properties of (R)-3-methylmorpholine include oral absorption, with a half-life of about 2 hours. In addition, it is well tolerated and does not cause any adverse side effects such as nausea or vomiting.</p>

<p>Please enquire for more information about 1,1,1-Trichloro-3-(1-methyl-1H-benzimidazol-2-yl)propan-2-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methionine sulfoxide is a methionine that has been oxidized to methionine sulfoxide. Methionine sulfoxides are produced through protein oxidation, which is the chemical process of reacting with oxygen in the air or other compounds to form an organic peroxide and superoxide radical. Methionine sulfoxides are found in proteins and are formed as a result of oxidative stress on cells and tissues. The rate constant for the conversion of methionine to methionine sulfoxide is 0.01983 min-1 at pH 7, 25°C. There are two methods of detection: chemiluminescence method and chromatographic analysis. In addition, methionine sulfoxides have natural antioxidant properties that can be used to treat diseases such as Alzheimer's disease and Parkinson's disease, as well as cancer treatments. Methionine sulfoxides have been shown to have a significant effect on wild-type strains of bacteria, reducing their growth rates</p>

<p>Please enquire for more information about 5-(5-Chloro-1-methyl-1H-benzimidazol-2-yl)pentanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Methylthio-4-hydroxypyrimidine is a protonated thione that inhibits the growth of bacteria, including Streptococcus faecalis. It has been shown to have an inhibitory effect on UV absorption and halide ions, such as mercury chloride. 2-Methylthio-4-hydroxypyrimidine is an analog of pyrimidine nucleosides and has a constant and regiospecific synthesis. The compound has also demonstrated antibacterial activity against bacteria, such as Staphylococcus aureus, Enterobacter aerogenes, Pseudomonas aeruginosa, Proteus vulgaris, Salmonella typhimurium, Escherichia coli, and Shigella flexneri.</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>Please enquire for more information about 5-Boc-octahydro-pyrrolo[3,4-c]pyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-(2-Methoxybenzyl)piperazine (1-MBP) is a multitarget drug that has been shown to have medicinal properties. It inhibits the cholinergic system, which is involved in memory and cognition, as well as pathways such as the inflammatory response and amyloid production. 1-MBP has been shown to inhibit acetylcholinesterase, an enzyme that breaks down acetylcholine, thus increasing the amount of acetylcholine available for signaling. 1-MBP also inhibits cholinesterase, which increases the amount of acetylcholine in the brain. This drug may have synergistic effects with other drugs for Alzheimer's disease, such as donepezil and tacrine. 1-MBP has been used in optimization studies to find new potential treatments for Alzheimer's disease by targeting different aspects of its pathogenesis.</p>

<p>Cyclo(-Gly-L-Phe) is a cyclic peptide with hydroxyl group at the C-terminal. It has been shown to have high uptake and cytotoxicity in intestinal cells. The uptake of Cyclo(-Gly-L-Phe) was found to be reversed phase high performance liquid chromatography (RP-HPLC). Cyclo(-Gly-L-Phe) is also cytotoxic to coryneform, caco2, and HeLa cells and inhibits cellular protein synthesis through inhibition of ribosome function.</p>

<p>Tyrosinase protein:<br>Peptide Tyrosinase (Asp371) – HLA-A*0201 (YMDGTMSQV) is a human tyrosinase-derived (369-377) peptide by posttranslational conversion of the sequence YMNGTMSQV. Tyrosinase is an oxidase membrane-bound protein. Tyrosinase play a key role in the melanin synthesis pathway. Tyrosinase is presented on the surface of HLA-A*02:01 melanomas and also expressed in melanocytes. Tyrosinase has been still suggested to be a tumor antigen and might be implicated in improvement of immunotherapeutic strategies such as for efficient anticancer vaccine development.<br>Applications of Peptide Tyrosinase (Asp371) – HLA-A*0201 (YMDGTMSQV):<br>Peptide Tyrosinase (Asp371) – HLA-A*0201 (YMDGTMSQV) is used to stimulate specific cytotoxic T lymphocytes (CTL) in PBMCs and then to analyze CTL response especially the cytokine production by ELISPOT assay. Peptide Tyrosinase (Asp371) – HLA-A*0201 (YMDGTMSQV) is also involved in experimental therapies of metastatic melanoma by allogeneic hematopoietic stem cell transplantation. In fact, cytotoxic T cells were generated from peripherical blood mononuclear cells (PBMCs) of HLA-A*02:01 healthy donors after being stimulated by injection of Asp371 antigen (2). This strategy raises issues which concern the graft versus tumor (GvT) effect and graft versus host disease (GvHD).</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>Please enquire for more information about 1-(3-Methoxyphenyl)piperazine dihydrochloride 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 (2S,3S,5S)-5-[(N-Formyl-L-leucyl)oxy]-2-hexyl-3-hydroxyhexadecanoic acid 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 6-Bromo-3-phenylquinazoline-2,4(1H,3H)-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-[4-(2-Methylpropenyl)phenyl]propionic acid is an analgesic and antipyretic agent. It has been shown to have antiinflammatory properties, which are mediated through inhibition of prostaglandin synthesis. This agent binds to the enzyme cyclooxygenase and inhibits the biosynthesis of prostaglandins that are responsible for inflammation. 2-[4-(2-Methylpropenyl)phenyl]propionic acid also has optical antipyretic activity, which may be due to its ability to inhibit the release of prostaglandins from arachidonic acid in the hypothalamus. The optical antipyretic activity is most likely due to the enantiomers that this drug contains. 2-[4-(2-Methylpropenyl)phenyl]propionic acid has a pharmacologic profile that includes analgesic and antipyretic activities.END&gt;&gt;</p>

Please enquire for more information about Fmoc-4-(3-carboxymethyl-2-keto-one-benzimidazolyl)piperidine including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>Please enquire for more information about N-Pyrazinylcarbonyl-L-phenylalanine methyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Cys(Me)-OH is an organosulfur compound that contains a sulfhydryl group. It is used as a model system for the study of the p2 group of compounds in nitrogen chemistry and enzyme activity. H-Cys(Me)-OH has been shown to have anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis. The compound also exhibits carcinogenic potential, as it induces mitochondrial membrane depolarization and kidney bean necrosis in rats when administered at high doses.</p>

<p>2-Methyl butyric acid is a fatty acid that is produced by the fungus Monascus purpureus. 2-Methyl butyric acid has been shown to inhibit the activity of a number of enzymes in gland cells, including proteases, lipases, and amylases. This effect may be due to its ability to inhibit lipid peroxidation. Further research into the metabolic profiles of 2-methyl butyric acid has shown that it inhibits the activity of enzymes involved in fatty acid synthesis and metabolism, such as tiglic acid synthase and ketoacyl CoA reductase. It also shows some potential as a solid catalyst for kinetic studies.</p>

<p>Please enquire for more information about 2-Phenylpropan-1-amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 4-Chloro-2-methylbenzenesulfonyl chloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Acetyl-L-isoleucine is a molecule that has been shown to inhibit the dehydrogenase enzyme. It can be synthesized from acetyl chloride and isomers of L-isoleucine in the presence of a metal catalyst, such as trifluoromethanesulfonic acid. Acetyl-L-isoleucine can also be used in protein synthesis and hydrolysis reactions. The ability of this molecule to bind to metal ions may also account for its antioxidant properties.</p>

<p>Please enquire for more information about 2-(2-Methyl-1H-indol-3-yl)ethanamine oxalate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Methyl-5H-dibenzo[a,d]cycloheptene-5-propylamine hydrochloride (NMBPD) is a drug with anti-inflammatory properties that belongs to the class of tricyclic antidepressants. It has been shown to have synergistic effects with synthetic matrix in vitro. This drug also has receptor activity and can be used to treat infectious diseases such as HIV and tuberculosis. NMBPD is excreted in the urine, which can lead to kidney fibrosis. The drug is metabolized by α1-acid glycoprotein, which may be related to its potential adverse effects on the liver and kidneys. The analytical method for quantification of NMBPD includes gas chromatography with mass spectrometry detection (GC/MS).</p>

<p>Please enquire for more information about 17,21Dihydroxy-16beta-methylpregna-1,4,9(11)-triene-3,20-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(±)-N-Methyl-p-methoxyamphetamine (MEM) is a synthetic cannabinoid that is used as an ingredient in the manufacture of designer drugs. MEM can be detected by gas chromatography and mass spectrometry, although it is not possible to distinguish MEM from other synthetic cannabinoids by these methods. MEM produces no significant adverse effects on human liver, but may have serious adverse effects on the heart and blood vessels. The drug can be found in urine samples with a chemical ionization detector or electrochemical detector. <br>The analytical method for MEM detection is based on liquid chromatography-tandem mass spectrometry (LC/MS/MS). The LC/MS/MS technique separates and identifies compounds by creating ions through the use of an electric field. This method has been shown to accurately detect MEM, while also eliminating false positives due to its specificity.</p>

<p>Please enquire for more information about D,L-Alanosine sodium 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 4-Amino-2-methylphenylboronic acid, pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-(2-Aminopropyl)-2-methoxybenzenesulphonamide is a trimethyl derivative of the aminopropyl group. It is used as a reagent to introduce hydroxymethyl groups into organic compounds. 5-(2-Aminopropyl)-2-methoxybenzenesulphonamide reacts with hydrochloric acid and an organic solvent in the preparation process. In the Friedel-Crafts reaction, 5-(2-Aminopropyl)-2-methoxybenzenesulphonamide reacts with d-alanine to form an optical isomer, which can be converted to its racemic form by ammonolysis. This compound is also used as a prostatic agent and an amide in the synthesis of benzene and phenoxymethyl alcohols.</p>

<p>Please enquire for more information about (5-Methoxy-1-methyl-1H-benzimidazol-2-yl)methanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Methylaniline is a chemical compound that is used in the treatment of wastewater. It can be synthesized by reacting acetaldehyde with ammonia and ethyl chloride. The adsorption of N-methylaniline onto a Langmuir monolayer was studied using electrochemical impedance spectroscopy (EIS). The kinetic energy of N-methylaniline molecules was found to be lower than water vapor molecules, which may explain its high detection sensitivity.</p>

<p>Please enquire for more information about 1-(1,1-Dimethylethyl) hydrogen N-[20-(1,1-dimethylethoxy)-1,20-dioxoeicosyl]-L-glutamate 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 H-Leucinol-2-chlorotrityl resin including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,5-Dibromo-3-methylthiophene is a small molecule that has been shown to have anti-bacterial properties. It reacts with the bacterial cell membrane, disrupting the bacteria's ability to function and causing it to die. 2,5-Dibromo-3-methylthiophene can be used as an antibacterial agent in medicine or cosmetics. The chemical structure of 2,5-dibromo-3-methylthiophene is similar to that of oxadiazole and 5H-[1]benzothiazol[5,4,-d][1,2]oxazole and it has been shown that these compounds can also be used for antibacterial purposes. The anti-bacterial activity of 2,5-dibromo-3-methylthiophene is due to its functional groups which are reactive with metal ions such as Cu(II) and Fe(III).</p>

<p>3-Methylphenethylamine is a synthetic amine that is used in the production of 3-methylphenethylamine hydrochloride. It has been shown to have a wide range of pharmacological effects, including increasing blood pressure, heart rate, and respiration. This drug also has an antitussive effect and can be used to treat asthma symptoms. 3-Methylphenethylamine can be synthesized by reacting phenylethylamine with formaldehyde and hydrogen chloride gas in the presence of alcohol or sodium hydroxide solution.</p>

<p>2-Methoxy-5-methylsulfonylbenzoic acid is an organic compound that can be used as a pharmaceutical intermediate. It has been used to synthesize diagnostic agents and drugs such as isradipine and sarpogrelate hydrochloride. 2-Methoxy-5-methylsulfonylbenzoic acid is also used as an intermediate in the synthesis of bortezomib, a drug that inhibits the proteasome. This product contains impurities that may interfere with its use as a pharmaceutical preparation. The flow rate of this product is sensitive to changes in temperature and pressure.</p>

<p>2-Methyl-5-benzothiazolol is a compound that has photophysical properties. It is soluble in organic solvents and can be used in techniques such as photochemical, fluorescence, crystallography, and MALDI-TOF. 2-Methyl-5-benzothiazolol has been shown to inhibit the formation of amyloid fibrils in the brain microvasculature endothelium of mice. This drug also inhibits the production of cyclotriphosphazene from bacteria. 2-Methyl-5-benzothiazolol can be synthesized from cyclotriphosphazene with benzaldehyde and methylamine. 2-Methyl-5-benzothiazolol has been shown to have anti cancer activity by inhibiting cell proliferation through apoptosis induction. It can also inhibit viral replication by interfering with viral protein synthesis at concentrations below those needed for inhibition of host cell</p>

<p>2-(2-Methoxyphenoxy)ethanol (2-MPE) is a metabolite of propanediol, which is a precursor in the synthesis of polyurethanes. 2-MPE can be oxidized by monooxygenases to form syringyl and other reactive metabolites. Basic hydrolysis may also produce monomers such as phenols, alcohols, and carboxylic acids. Syringyl is one of the metabolic products of 2-MPE, which has been shown to be resistant to degradation by basidiomycete fungi.</p>

<p>Please enquire for more information about 5[(R)-(2-Aminopropyl)]-2-methoxybenzenesulfonamide hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (S)-1-Z-2-tert-butyl-3-methyl-4-imidazolidinone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Indole-3-acetyl-L-phenylalanine is a plant growth regulator that inhibits the transport of auxin in the plant. It is used as a regulatory agent to inhibit the growth of plants by interfering with their natural regulatory mechanisms. Indole-3-acetyl-L-phenylalanine is an effective inhibitor of auxin transport and has been shown to have an inhibitory effect on plant growth. This compound also binds to acid conjugates, which are found in plants, and blocks their ability to bind to auxin receptors, preventing them from activating the cell's responses. This inhibition leads to decreased cell division and reduced root growth.</p>

<p>Please enquire for more information about 5-Bromo-2-methoxyphenethylamine hydrobromide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>