Amino Acids (AA)

<p>4-Methoxyphenyl isocyanate (4MPIC) is a reactive organic compound that is used in the synthesis of polymers. 4MPIC reacts with amines to form amides, and can be used as a photophysical probe to study reaction mechanisms. It has been shown to react with hydroxy groups in polymers and form an insoluble polymer. 4MPIC also has antibacterial activity, although it is not active against all bacteria. This compound also reacts with chlorine atoms to form heterocycles, which are efficient for the synthesis of pharmaceuticals.</p>

<p>2-(4-methoxyphenyl)ethyl]methylamine is a pharmacological agent that inhibits protein synthesis. It has been shown to have an optimum concentration of 1 μM, with maximal inhibition at 10 μM. 2-(4-methoxyphenyl)ethyl]methylamine binds to the basic amino acid residues of proteins and inhibits the activity of eosinophil cationic protein, which is responsible for histamine release. 2-(4-Methoxyphenyl)ethyl]methylamine has also been shown to reduce the activity of epidermal growth factor, which is responsible for cell proliferation and differentiation. The drug has been demonstrated to be an effective inhibitor of activated eosinophils, but not normal cells. 2-(4-Methoxyphenyl)ethyl]methylamine may be used as a treatment for chronic asthma patients who suffer from eosinophilic inflammation in their</p>

<p>Apixaban is a novel, orally active, and selective factor Xa inhibitor. It is the first oral anticoagulant that has been developed to inhibit both free and clot-bound thrombin. Apixaban binds reversibly to the active site of factor Xa and inhibits factor Xa-mediated conversion of prothrombin to thrombin, resulting in an increased concentration of prothrombin in blood. Apixaban also inhibits the activity of thrombin-activated protein C (APC) that degrades fibrin clots by proteolytic cleavage of fibrinogen. This drug has a crystalline form with a particle size between 10 and 100 μm.</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>Please enquire for more information about 4-Methyl-2-piperidin-4-yl-1,3-benzoxazole 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-(4-Methoxyphenyl)-2-(1-hydroxycyclohexyl)ethylamineHydrochloride 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 6-methyl-2-thioxo-4-(3,4,5-trimethoxyphenyl)-1,2,3,4-tetrahydropyrimidine-5-carboxylate 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 L-Methionine-methyl-13C,methyl-D3 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ile-Ile-OH is a zwitterion that is the product of an enzyme serine protease. It has been shown to exhibit serine protease activity against corynebacterium, and it can be used for the production of active enzymes such as corynebacterium glutamicum. Ile-Ile-OH is synthesized from serine and hydrochloric acid in a reaction catalyzed by the enzyme serine protease. The rate of this reaction depends on pH and temperature, which causes the conversion of ile-ile to ile-ole at higher temperatures. Ile-Ile-OH exhibits conformational properties that are similar to those found in natural amino acids, which may be due to its zwitterionic nature. This compound also has protonation properties that have been shown to be important for uptake assays in L6 cells.</p>

<p>Methyl 2-methylpropanimidic acid hydrochloride is a neutralizing agent that can be used to react with water, acids, and bases. It has been shown to react with gaseous compounds at temperatures as high as 200°C. Methyl 2-methylpropanimidic acid hydrochloride is soluble in organic solvents such as alcohols, ethers, and acetone and can be used to prepare esters by reacting with the corresponding alcohol or phenol. In addition, it has been shown to interact with haloalkyl groups and oxazinones. This compound also has nod-like receptor binding properties that have been shown to play a role in mediating the transport of organic solutions into cells. A receptor protein that reacts with methyl 2-methylpropanimidic acid hydrochloride has been identified in some organisms. The stereostructure of this compound resembles that of triazines and other organometallic compounds.</p>

<p>Timapiprant is an amide that acts as a selective inhibitor of the prostanoid receptor CRTH2, which is involved in regulating the inflammatory response. Timapiprant inhibits skin eosinophilia, which is associated with inflammatory skin diseases such as atopic dermatitis and psoriasis. It has been shown to be safe in clinical trials and has a good safety profile. The drug's mechanism of action may be due to its ability to inhibit the production of IL-4 and IL-13 by Th2 cells and its ability to inhibit lung function. Timapiprant has shown efficacy in treating allergic rhinitis, asthma, chronic obstructive pulmonary disease, erythema multiforme, pyoderma gangrenosum, and other types of inflammatory skin diseases.</p>

<p>Please enquire for more information about 3-[4-(2-Chlorophenyl)-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-2-yl]-2-propyn-1-ol 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 Ne-(trimethyl)-L-lysine chloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-[1-(4-Fluorophenyl)propan-2-Yl]-N-methylprop-2-Yn-1-amine is a synthetic molecule that has been shown to be an inhibitor of the enzyme nitroethane reductase. This drug is also capable of inhibiting the activity of other enzymes and is being investigated for its potential use in the treatment of various types of cancer. N-[1-(4-Fluorophenyl)propan-2-Yl]-N-methylprop-2-Yn-1-amine inhibits nitroethane reductase by binding reversibly to the active site and competitively inhibiting the substrate. The potency of this drug against nitroethane reductase has been shown to be increased by alkylation.br&gt;<br>The inhibition of nitroethane reductase by N-[1-(4-fluorophenyl)propan-2-Yl]-</p>

<p>1,3-Diethyl-8-phenylxanthine is a p2y receptor antagonist that inhibits bacterial growth by interfering with the energy metabolism of the cell. It is an analytical reagent that can be used to measure specific DNA sequences and has been shown to have genotoxic effects on cultured human cells. 1,3-Diethyl-8-phenylxanthine has also been shown to inhibit the growth of infectious bacteria such as staphylococcus aureus and Mycobacterium tuberculosis in vitro. This compound may be used as a potential biomarker for the identification of antimicrobial peptides that are active against Mycobacterium tuberculosis in humans.</p>

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

<p>Z-D-Lys(Boc)-OH is a synthetic peptidomimetic that has been shown to selectively kill cancer cells. Z-D-Lys(Boc)-OH binds to the lysine residue on the target cell surface, which is not present in normal cells. This binding inhibits serine protease activity and disrupts the synthesis of peptides, which are essential for cellular function. The electron microscopic images show that this compound causes an enhancement of biological function in human pathogenic chlamydia.</p>

<p>Please enquire for more information about L-Glutamic acid gamma-tert-butyl ester alpha-amide 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'-Methylene bis[theobromine] 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 Boc-2-cyano-D-phenylalanine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-D-Glu-OMe is a synthetic amino acid that is used as an antibacterial agent. It inhibits bacterial cell wall synthesis by binding to the enzyme murein. H-D-Glu-OMe has been shown to have antimicrobial activity against Escherichia coli and Pseudomonas aeruginosa, with minimal side effects on mammalian cells. The uptake of H-D-Glu-OMe into bacteria is dependent on the concentration of glutamic acid in the extracellular environment; this uptake also leads to an increase in intracellular glutamate levels, which activates nociceptive neurons in the brain. The following product description was generated: Rifapentine Rifapentine is an anti-tuberculosis drug that belongs to the class of rifamycins. It is the most active of the rifamycins for the treatment of tuberculosis. Rifapentine</p>

<p>Please enquire for more information about Dimethyl (2R,3R)-2,3-O-(1-Phenylethylidene)-L-tartrate 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 (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 5-Methyl-4H-1,2,4-triazole-3-sulfonyl chloride 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 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>The N-alpha-Boc-L-tryptophan N-alpha-carboxy anhydride is a postulated intermediate in the ring opening of the ester of tryptophan. The kinetics of this reaction, which is influenced by the basicity and acidity of the environment, have been studied using techniques such as crystal violet, formamide and radiolabeling.</p>

<p>5-[3-Methoxy-4-(4-methoxy-benzyloxy)-benzyl]-pyrimidine-2,4-diamine is a monoclonal antibody that blocks the signal of CTLA-4, a receptor on T cells. It has been shown to be effective in inhibiting skin cancer and primary breast cancers. This drug also has immunomodulatory effects and can be used to treat autoimmune diseases. 5-[3-Methoxy-4-(4-methoxy-benzyloxy)-benzyl]-pyrimidine-2,4-diamine binds to ctla-4 with high affinity and specificity, preventing the interaction of ctla-4 with its ligands such as CD80 (B7.1) and CD86 (B7.2). This prevents the activation of T cells by antigen presenting cells and suppresses the immune response.</p>

<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>

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

<p>1-O-Hexadecyl-2-O-acetyl-sn-glycero-3-phosphocholine is a phospholipid that is synthesized in the liver and has been shown to be a pressor agent. This drug has shown hypotensive effects in animal models, likely due to its ability to inhibit platelet aggregation and activate platelets. The mechanism of action of 1-O-hexadecyl 2-O-acetyl sn glycero 3 phosphate choline may be through inhibition of lipoxygenase and acetylcholine release, as well as an increase in tissue plasminogen activator (tPA) and plasminogen activator inhibitor (PAI).</p>

<p>4-Phenylphenol is a phenolic compound that is used in the synthesis of other compounds. 4-Phenylphenol was found to react with rat liver microsomes and showed a hydroxyl group as its reactive site. 4-Phenylphenol also inhibited the activities of enzymes such as diazonium salt, sodium carbonate, monoclonal antibodies, analytical methods, light emission and p-hydroxybenzoic acid. The reaction mechanism of 4-Phenylphenol involves hydrogen bonding with human serum biphenyl.</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>Please enquire for more information about (1R,2S)-2-[N-Benzyl-N-(mesitylenesulfonyl)amino]-1-phenyl-1-propanol 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 1,1,1-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>Please enquire for more information about Z-Glu(OtBu)-OH 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-Bromo-1-methyl-1H-imidazole 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-Methylpiperidinyl-2-methyl benzilate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Z-NH-PEG8-CH2COOH 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-PEG8-CH2COOH 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>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 Boc-(S)-3-amino-3-(2-methoxyphenyl)propionic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1,3-Dimethoxy-2-(2-methoxyphenoxy)propane-1,3-diol (DMMP) is a natural product with antioxidant properties. It has been shown to be a potent inhibitor of the epidermal growth factor receptor (EGFR), and also inhibits the activity of the response elements for EGFR. DMMP is also a potent inhibitor of proliferation in human cancer cells and can inhibit the growth of tumour cells that are resistant to methotrexate. DMMP is a precursor to protocatechuic acid, which has been shown to have anti-herpes virus effects. DMMP has been shown to decrease the rate of second order reactions through its ability to react with carbonyl groups on proteins. This reaction leads to an increase in stability and decreases the rate of protein degradation by proteases. A mutant strain was found that can produce this compound without any external stimulus, making it ideal for use as an antibiotic against bacterial</p>

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

<p>Fmoc-β-azidoalanine is a cyclic peptide that is synthesized by the Fmoc solid phase peptide synthesis method. It is used as a model for serine proteases, and its ability to bind to other molecules has been shown using molecular modelling and validation. Fmoc-β-azidoalanine has an acidic side chain that can form a disulfide bond with cysteine residues on proteins. This property allows it to be used in crystallography and chemical biology studies. The molecule can also be used in the study of human serum biomolecules.</p>

<p>4-Iodo-2-methoxypyridine-3-carboxaldehyde is a disubstituted compound that has insulin-like properties. It inhibits the activity of the insulin receptor, which may contribute to its insulin-like growth factor effects. This inhibitor also targets the protein kinase, which is responsible for the response of cells to insulin. 4-Iodo-2-methoxypyridine 3 carboxaldehyde has been shown to inhibit IGF1R and malonate ion, and it may have potential as an oral treatment for diabetes.</p>

<p>Charybdotoxin is a peptide toxin that is found in scorpion venom. It acts as a potent inhibitor of the adenylyl cyclase, which is an enzyme that catalyzes the formation of cAMP from ATP. Charybdotoxin binds to the cavity of the enzyme and blocks access to ATP, preventing the accumulation of cAMP. This inhibition leads to a decrease in calcium ions in cells, and thus causes relaxation of smooth muscle tissue. Charybdotoxin has been shown to cause relaxation of bowel disease in mice by inhibiting contraction of intestinal muscle tissue. Charybdotoxin also has been shown to have therapeutic effects on pluripotent cells such as miapaca-2 cells by increasing their ability to form new blood vessels.</p>

<p>Iodosulfuron-methyl sodium is a herbicide that inhibits the activity of lipid-metabolizing enzymes in plants. It inhibits the action of phosphatases, which are enzymes that catalyze hydrolysis of phosphoric acid esters, and can be used to control weeds. Iodosulfuron-methyl sodium has been shown to have synergistic interactions with other herbicides, such as 2,4-D or dicamba. The effective dose for this product varies depending on the plant species and type of soil.</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>4'-[[1,4'-Dimethyl-2'-propyl(2,6'-bi-1H-benzimidazol)-1'-yl]-methyl]-1,1'-biphenyl-2-carboxylic acid 1,1-dimethylethyl ester (DMBPC) is a drug substance that is used in the manufacture of solid oral dosage forms. It has been shown to be present at low levels as an impurity in other drug substances. The presence of this impurity has been shown to cause problems with the chromatographic and hplc methods used for its quantification. The following are some important aspects of DMBPC: A. Impurities: The purity of DMBPC is 98%. The impurity profile includes 6% 2-propylbenzimidazole (2PB), 3% 4'-[[2-(6' -methoxycarbony</p>

<p>Please enquire for more information about Ethyl 3-{[(1E)-(dimethylamino)methylene]amino}-5-methoxy-1-methyl-1H-indole-2-carboxylate 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 tert-Butyl-n-(6-methoxy-3-pyridyl)carbamate 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 nintedanib</p>

<p>3-Methyl-2-phenylmorpholine hydrochloride (3MPH) is a phenmetrazine derivative that has been used in animal studies to study the effects of plant metabolism on sensor and analytical methods. 3MPH has shown toxicity in rats, as well as some physiological effects such as increased heart rate, ataxia, and sedation. This compound is also a pharmacological agent that can be used for chromatographic analysis. 3MPH is metabolized by the liver into dopamine which can cause renal cell cancer in mice. A biological sample is required for this compound.</p>

<p>Please enquire for more information about N-Boc-b-alanine ethyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Biphenyl-4-yl)-5-(4-tert-butylphenyl)-4-phenyl-4H-1,2,4-triazole is a small molecule that interacts with and inhibits transcriptional regulatory protein complexes. This interaction disrupts the normal function of proteins that regulate transcription and leads to cellular transformation. Biphenyl-4-yl)-5-(4-tert-butylphenyl)-4-phenyl-4H-1,2,4--triazole has been shown to inhibit the production of proinflammatory mediators in macrophages and cause regression of atherosclerotic lesions in mice. The molecular mechanism by which biphenyl--5-(4--tert--butylaniline) 4--phenyltriazole exerts its effects is not well understood but may involve direct binding to DNA or indirect effects due to changes in gene expression.</p>

<p>Please enquire for more information about 2-Valeryl-17'-estradiol 17-valerate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Phenylisobutyric acid is a colorless to white crystalline solid with a molecular weight of 218.29 g/mol and a melting point of 120-122 °C. It is soluble in water, but not in alcohol or ether. 2-Phenylisobutyric acid is used as an intermediate for pharmaceutical preparations and as a reagent for organic synthesis. It is also used to produce thiomorpholine, which has been shown to have anti-inflammatory properties and can be used in the treatment of bowel disease. Thiomorpholine reacts with acylation agents such as phosphorus pentachloride to form esters that are useful pharmaceuticals, including corticosteroids. 2-Phenylisobutyric acid has been shown to inhibit insulin resistance by reacting with reactive sites on the insulin receptor, thus preventing the binding of insulin molecules to their receptors on cells.</p>

<p>4-Methylimidazole is a chemical with the molecular formula CH3NH2. It is an aromatic amine that forms in the body as a byproduct of histidine metabolism. 4-Methylimidazole has been shown to have carcinogenic potential and can be found in high concentrations in human liver cells. This chemical is also present in cigarette smoke and has been detected at levels up to 1,000 times higher than normal in lung cancer tissue samples. 4-Methylimidazole may be used for analytical purposes such as determining matrix effects or sample preparation techniques.</p>

<p>Please enquire for more information about 2-Cyano-N-cyclohexyl-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 4,5-Dihydro-5a-methoxy D-(-)-norgestrel 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-Butoxycarbonyl)-4-methylpiperidine-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Chloro-2-methyl-3-isothiazolone (CMIT) is a highly water-soluble apoptotic agent and preservative with numerous applications. It is used in anti-microbial coatings, latex formulations, hydraulic fracturing fluids, pesticides and cosmetics. CMIT in conjunction with 2-methyl-4-isothiazolin-3-one (MIT) is marketed as Kathon. CMIT is also an allergen. CMIT is active against gram-positive and gram-negative bacteria, yeasts and fungi. CMIT is believed to form mixed disulfides with protein thiol groups which then undergo thiol-disulfide exchange reactions to give mixed protein thiol disulfides leading to cell apoptosis and necrosis.</p>

<p>Please enquire for more information about H-Cys-Glu-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>Please enquire for more information about 17a-Methyl-4-[(phenylthio)methyl]testosterone 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 5-Chloro-2-hydroxy-2-methoxycarbonyl-1-indanone 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 Methyl 4,5-dimethoxy-1-methyl-1H-indole-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Trans-beta-Methylstyrene is an inorganic acid that has been shown to be carcinogenic to animal tissue. It is a reactive compound that can undergo chemical reactions with other substances, such as hydroxyl groups, and can form adducts by reacting with nucleophilic groups. Trans-beta-Methylstyrene can react with human liver DNA and tumor cells in the presence of enzymes. The reactive properties of this compound have been used for analytical methods such as particle ionization and chemical ionization. Trans-beta-Methylstyrene has also been found to inhibit the activity of certain enzymes, including squamous carcinoma, which may be due to its ability to inhibit the production of prostaglandins from arachidonic acid.</p>

<p>R-2-Methylaziridine is a diastereomer of R-Methylaziridine. The diastereomers are chiral and have different chemical properties. R-2-Methylaziridine has been synthesized by the reaction of an epoxide with methyl iodide, which produces a mixture of isomers. The compound is optically pure when the reactants are used in an equimolar ratio. <br>R-2-Methylaziridine has two rotational constants and a spectrum that can be used to identify it. It also chelates metals such as copper, zinc, and nickel with its nitrogen atom. This compound is used in organic synthesis as a ligand for metal complexes, which includes asymmetric hydrogenation reactions.</p>

<p>Z-NH-PEG3-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-PEG3-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>2-(2-Methyl-1H-imidazol-1-yl)ethanol is a synthetic intermediate that has been used to synthesize antibiotics and antiviral agents. It has a terminal half-life of about 2 days and its pharmacokinetics are linear with an oral dose range from 10 to 100 mg/kg. The fruit extract of Camptotheca acuminata contains alkaloids, which can be converted into 2-(2-methyl-1H-imidazol-1-yl)ethanol by alkalization. 2-(2-Methyl-1H-imidazol-1-yl)ethanol is effective against hordeolum, acne, and infectious diseases caused by viruses such as herpes simplex. This drug has antibacterial properties and can be used in the treatment of bacterial infections such as staphylococcal skin infections, streptococcal throat infections, or gonorrhea. Dehydration is an</p>

<p>Please enquire for more information about H-Gln-pNA trifluoroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Methylnicotinic acid methyl ester is a synthetic chemical compound that belongs to the isomer family. It has been used in the synthesis of cocaine and isomers, as well as in the modification of drugs. 2-Methylnicotinic acid methyl ester can be synthesised from 2-methylpyridine and formaldehyde via the method of methylmagnesium iodide. 2-Methylnicotinic acid methyl ester has been shown to be a potent inhibitor of human platelet aggregation, which may be due to its structural similarity to nicotine.</p>

<p>N-Acetyl-L-proline is a metabolite of proline that has been shown to have a role in the development of metabolic disorders. It is an amide that has a hydroxyl group and a protonated nitrogen atom. N-Acetyl-L-proline is present in a model system that can be used to study the frequency shift phenomenon. This compound also undergoes michaelis–menten kinetics, which are used to describe enzyme activity and the velocity of reactions with high concentrations of substrate. N-Acetyl-L-proline has been found to have protease activity and intramolecular hydrogen bonding. It also forms hydrogen bonds with other molecules, such as fatty acids, which are involved in conformational properties.</p>

<p>H-Pro-AMC hydrobromide salt is an enzyme that belongs to the family of proteases. H-Pro-AMC hydrobromide salt has been shown to have carboxypeptidase activity, which cleaves peptides at the C terminus of a single amino acid. It has also been shown to interact with other enzymes and proteins, such as recombinant proteins and enzymes from the ubiquitin-proteasome system. This enzyme's ability to cleave peptides at the C terminus of a single amino acid makes it useful for protein sequencing. H-Pro-AMC hydrobromide salt has also been sequenced and found to share homology with other proteases, such as subtilisin E.</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>Clobetasol propionate is an organic acid with a chemical structure that is stable in pharmaceutical preparations. It is used to treat inflammatory skin disorders such as psoriasis and atopic dermatitis. Clobetasol propionate is an impurity of clobetasol, which has been shown to be chemically stable in preparations. The clobetasol propionate compound has been found to be more potent than other topical corticosteroids for the treatment of plaque psoriasis and atopic dermatitis.</p>

<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>Lys-Bradykinin is a peptide that is a member of the group of kinins. It has been shown to be effective at inhibiting the activity of kallikrein, which is an enzyme that converts kininogen to bradykinin. This inhibition lowers the levels of bradykinin in the blood and may be used as a diagnostic tool for identifying diseases such as congestive heart failure, pulmonary edema, and acute renal failure. Lys-Bradykinin can also be used as a model system for studying kinins and their biological effects on various systems. For example, it has been shown to have natriuretic properties in humans by increasing levels of erythropoietin and ANP.</p>

<p>6-Methoxypyridine-2-boronic acid is a boronate ligand that can be used to form coordination complexes with metals. It has been shown to interact with silver ions, which are the most effective ligands for enhancing the fluorescence of organic dyes. 6-Methoxypyridine-2-boronic acid is able to rigidify organic molecules by binding to their steric and electronic properties, making them more resistant to photodegradation. This property makes it an excellent candidate for the use in the development of fluorescent labels in analytical chemistry.</p>

<p>4-Methylcatechol is a plant compound that has been shown to have neurotrophic and anticarcinogenic properties. It is a natural product that can be found in the bark of the cinchona tree, and it has been used as an additive in skin care products for its antioxidant properties. 4-Methylcatechol has been shown to have anti-inflammatory effects and inhibit the growth of cancer cells in vitro. It also shows potential for the treatment of diabetic neuropathy, due to its ability to inhibit acetylcholine esterase activity. 4-Methylcatechol is a neurotrophic factor that affects cell nuclei and protein synthesis. This compound acts by binding with DNA, preventing DNA polymerase from adding new bases during replication. This effect inhibits RNA synthesis, which leads to cell death after prolonged exposure. In addition, 4-methylcatechol may be carcinogenic when administered orally or topically on skin cells in vivo or when applied ex</p>

<p>Please enquire for more information about tert-butyl (2S)-2-Methyl-4-oxopiperidine-1-carboxylate 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-Ile-Asn-OH trifluroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>DL-2-Aminoadipic acid is a metabolite of the amino acid lysine, which is found in many protein-containing foods. It is also synthesized from glutamate, which is an excitatory neurotransmitter and a major regulator of neuronal function. This compound has been shown to have potential as a biomarker for metabolic disorders. DL-2-Aminoadipic acid has been shown to bind to penicillin-binding proteins (PBPs) in the bacterial cell wall and disrupt its formation, leading to the inhibition of peptidoglycan synthesis. DL-2-Aminoadipic acid may also be involved in regulating gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter that inhibits the release of excitatory neurotransmitters. DL-2-Aminoadipic acid has also been shown to inhibit HIV infection by binding to lysine residues on the virus envelope protein gp120.</p>

<p>5-Hydroxyethyl-4-methylthiazole (5HET) is a chemical that has been shown to inhibit the growth of some wild-type strains of bacteria. It has been found to bind to the bacterial cell membrane and prevent the transport of nutrients into the cell. This leads to a decrease in ATP synthesis and metabolic disorders. 5HET also inhibits caproic acid oxidation, which may be related to its cytosolic Ca2+ response. 5HET binds with high affinity to DNA and RNA, making it an excellent candidate for use in biochemical experiments involving these biomolecules. The binding site for 5HET is not yet known, but it is hypothesized that this compound interacts with nucleic acids by electrostatic interactions or hydrogen bonding.</p>

<p>Please enquire for more information about Tetrakis[N-phthaloyl-(S)-phenylalaninato]dirhodium Ethyl Acetate Adduct including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(2S,3S)-5-[2-(Dimethylamino)ethyl]-3-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-1,5-benzothiazepin-4-one hydrochloride is a racemic mixture of two enantiomers. It is a prodrug that is hydrolyzed to its active form, diltiazem. The drug has been shown to be effective in the treatment of hypertension and angina pectoris. (2S,3S)-5-[2-(Dimethylamino)ethyl]-3-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-1,5-benzothiazepin-4-one hydrochloride has been shown to inhibit the activity of the enzyme phosphodiesterase which breaks down cyclic AMP. This inhibition results in an increase in levels of</p>

<p>Cyclo(-Arg-Gly-Asp-D-Phe-Cys) acetate salt is a peptide that has been modified to be an active targeting agent. It is an amphipathic molecule that can be used to deliver therapeutic agents specifically to cancer cells. Cyclo(-Arg-Gly-Asp-D-Phe-Cys) acetate salt is conjugated to a drug and is taken up by cells through the process of endocytosis. Once inside the cell, the drug is released and binds with the cell membrane, which leads to cell death. The uptake of this peptide has been shown to be pH dependent; it is taken up more readily in acidic environments than in neutral or alkaline environments. This peptide has also been shown to have cytotoxic effects on both MFC7 cells and rat liver cells.</p>

<p>2-Methylnicotinamide is an amide that is used to treat inflammatory bowel disease. It inhibits the production of glutamate and aspartate, which are neurotransmitters that are involved in the inflammation process. 2-Methylnicotinamide has been shown to have a protective effect on renal function by reducing blood flow to the kidneys, thereby decreasing renal damage caused by glutamate and aspartate. This drug also has anticancer properties, which may be due to its ability to inhibit viral replication and reduce the incidence of cancer in animals. 2-Methylnicotinamide has not yet been tested on humans, but it is thought to be safe for use in pharmaceutical dosages.</p>

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

<p>4-(4-Hydroxymethyl-3-methoxyphenoxy)-butyric acid (HMPA) is a synthetic compound that is used in the production of butyric acid. It is also used as a reagent in the preparation of enzymes and enzyme preparations, such as serine proteases. HMPA has been used as an intermediate in the synthesis of ribulose, which is a sugar molecule found in plants. The structure of this compound can be determined by FTIR spectroscopy and by X-ray crystallography. HMPA has been shown to have hydrogen bonding between its molecules, which may account for its stability. Hydrogen bonding accounts for the solidity of this compound and its resistance to heat and solvents.</p>

<p>L-Phenylalanine b-naphthylamide is a phenylalanine derivative that can be used as an indicator for the detection of Clostridium, 2-naphthylamine, and other anaerobes. This compound is a chromogenic substrate that reacts with amino groups in amino acids and amides in peptides to form a variety of color products. The condensation of phenylalanine with 2-naphthylamine is catalyzed by enzymes found in clostridia. When L-phenylalanine b-naphthylamide is incubated with tissue from animals or humans, it produces a pink coloration that indicates the presence of clostridia. The aerobic conditions necessary for this reaction are also found in the environment and within the body.</p>

<p>L-threo-droxidopa is a prodrug that is hydrolyzed in the liver to L-3,4-dihydroxyphenylalanine (L-DOPA) and then metabolized by dopamine β-hydroxylase to form dopamine. This drug has been shown to be effective for the treatment of Parkinson's disease. The long-term efficacy of this drug is unknown, but it has been shown to be safe and well tolerated for up to six months. L-threo-droxidopa has also been shown to be effective in lowering systolic blood pressure in patients with mild hypertension. The side effects of this drug include symptoms such as nausea, vomiting, dizziness, headache, and insomnia. However, these side effects are often transient and do not require discontinuation of treatment with this medication. There are no known interactions between L-threo-droxidopa and other drugs or foods. Pharmacological</p>

<p>Please enquire for more information about 4-Amino-1-Boc-piperidine-4-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Methyl-2-hexanamine hydrochloride is a synthetic amide that is used as a solvent in laboratories. It is a psychoactive substance and has been found to be an inhibitor of serotonin uptake, which may be related to its ability to inhibit the function of the serotonin transporter. The amount of 4-methyl-2-hexanamine hydrochloride absorbed by the body varies depending on how it is taken. When taken orally, 4-methyl-2-hexanamine hydrochloride enters through the digestive tract and reaches high levels in the blood stream. When taken intravenously, it enters the bloodstream directly and can reach higher concentrations in the blood. When inhaled, 4-methyl-2-hexanamine hydrochloride can enter into the lungs at high concentrations and then is absorbed into the bloodstream. 4-Methyl-2-hexanamine hydrochloride also degrades quickly in natural environments due to its biodegradable properties.</p>