Amino Acids (AA)

<p>H-Tyr-AMC is a synthetic substrate that is used in the study of serine proteases. It is reversibly bound to Sephadex G-100 and is hydrolyzed by protease enzymes in an acidic environment, generating an AMC chromatographic peak. This product has been shown to inhibit serine protease activity and, when incubated with the enzyme, reduces the hydrolysis of synthetic substrates. Synthetic H-Tyr-AMC can be used to study the inhibition of serine proteases by various inhibitors and their binding sites on the enzyme.</p>

<p>Please enquire for more information about Ethyl 5-Methyl-2-oxo-2,3-dihydro-1H-imidazole-4-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1,2-Dipalmitoyl-sn-glycero-3-phosphatidic acid sodium (DPPA) is a drug substance that has been used in primary culture to study the cell membrane of hepatocytes. This compound is a phospholipid with a cavity at one end and contains two hydroxy groups that can be conjugated to other molecules. It has been shown to be effective against Hepatitis B virus and mesenchymal stromal cells. DPPA has also been used as an adjuvant for gadolinium contrast agents for magnetic resonance imaging. Gadolinium may bind to the hydroxy groups on DPPA, which increases its birefringence and brightness on MRI scans.</p>

<p>6-Methoxy-2-naphthoic acid (MN) is a cavity amide that has been shown to have an inhibitory effect on the growth of cancer cells. MN has been found to be more effective in inhibiting β-amyrin than caffeine, which may be due to its increased lipophilicity. It also has a higher affinity for adriamycin and enhances its anticancer effects. MN has been shown to be beneficial in treating diabetic patients, as it can reduce blood glucose levels by stimulating insulin release. The pharmacokinetic properties of MN are similar to those of other cavity amides, with rapid absorption and distribution throughout the body. This compound is metabolized in the liver by CYP2C8, CYP2C9, CYP3A4 and CYP3A5 enzymes. Molecular docking analysis of MN with β-amyrin showed that there was a strong interaction between them due to their complementary shapes and charge distributions</p>

<p>3-Fluoro-L-phenylalanine is a fluorinated analog of the amino acid phenylalanine. It is an endophytic fungus that has been found in the leaves of wheat and rice plants. 3-Fluoro-L-phenylalanine is synthesized by 4-fluoro-l-phenylalanine, a plant metabolite, through the addition of a fluoride ion. This molecule can be used to produce gels with high glass transition temperatures. The synthesis of 3-fluoro-L-phenylalanine and its derivatives can be studied using NMR spectroscopy because these molecules are acidic and have low energy levels.</p>

<p>DL-4-Hydroxy-3-methoxymandelic acid is a metabolite of the catecholamines, norepinephrine and epinephrine. It is found in the blood, urine and cerebrospinal fluid of humans. DL-4-Hydroxy-3-methoxymandelic acid is derived from the amino acid tyrosine. When the body's production of catecholamines exceeds its ability to break them down, these molecules accumulate and are excreted in urine as DL-4-hydroxy-3-methoxymandelic acid or as other metabolites. The concentration of DL-4-hydroxy 3 methoxymandelic acid in urine may be used to diagnose pheochromocytoma or neuroblastoma.</p>

<p>(6α,11β,16α,17α)-6,9-Difluoro-11-hydroxy-16-methyl-spiro[androsta-1,4-diene-17,5'-[1,3]oxathiolane]-2',3,4'-trione is a fine chemical that can be used as a building block for the synthesis of complex compounds. This compound is also useful as a reagent and specialty chemical. (6α,11β,16α,17α)-6,9-Difluoro-11-hydroxy-16-methyl spiro[androsta-1,4 diene 17.beta., 5'(1'3'oxathiolane)] 2',3',4'-trione has been shown to be an excellent intermediate for organic reactions and may be used as a scaffold in drug design.</p>

<p>Methylprednisolone is a corticosteroid that has been used for the treatment of many conditions, including asthma and arthritis. It is used to reduce inflammation and suppress the immune system. Methylprednisolone can be administered orally or as an injection. It is also used in the diagnosis of tumours, especially those that are difficult to diagnose by other means. Methylprednisolone may be given together with another drug called dexamethasone, which has synergistic effects. These drugs have been shown to cause death in animals with certain types of tumours. In humans, they can cause cutaneous lesions, such as follicle cysts and tnf-α expression in skin cells. This drug also causes a microsporum infection (a type of fungus) on the skin to grow more rapidly when it is applied topically, resulting in a larger diameter section than untreated areas.</p>

<p>5-Bromo-2-methoxyphenyl)acetone (BMPA) is a versatile building block used in the synthesis of complex compounds and speciality chemicals. BMPA has been shown to be a useful intermediate for the synthesis of pharmaceuticals, agrochemicals, perfumes, and other products. It is also used as a reagent for research purposes. The compound was first synthesized by the condensation of aniline with acetaldehyde in 1885 by two French chemists, but has since been prepared in various ways. CAS number: 205826-73-9</p>

<p>D-Isoserine is a stereoselective synthetic amino acid that can be used as a structural analog of l-serine. D-Isoserine is synthesized from d-threonine and has been shown to inhibit the bacterial enzyme tyrosine kinase, which is important in cell signaling. D-Isoserine is also being investigated as a treatment for inflammatory diseases such as rheumatoid arthritis and Crohn's disease. The marine sponge Aerogenes sp. produces this compound, which is also produced by the microbial species Aerobacter aerogenes and Staphylococcus aureus.</p>

<p>Fmoc-3-Amino-4-(4-tertbutylphenyl)butyric acid is a versatile building block that can be used in the synthesis of complex compounds. Fmoc-3-Amino-4-(4-tertbutylphenyl)butyric acid is an intermediate for the production of speciality chemicals and reagents. It is also a useful scaffold in chemical reactions, as well as a reaction component. Fmoc-(R)-3-Amino-4-(4-tertbutylphenyl)butyric acid is soluble in ethanol and ether, but insoluble in water.</p>

<p>2-Phenylbenzamide (2PB) is a drug that belongs to the class of anthelmintics. It binds to the nicotinic acetylcholine receptor and inhibits the release of acetylcholine at neuromuscular junctions, leading to paralysis and death of the parasite. 2PB also has been shown to have anti-inflammatory properties in mice with colitis, which may be due to its ability to inhibit prostaglandin synthesis. The molecular docking analysis showed that 2PB binds covalently with nitro-containing molecules, such as nitrosamines, which are found in cigarette smoke and are known carcinogens. This binding may contribute to the development of cancer through inhibition of DNA repair mechanisms.</p>

<p>H-Lys(Boc)-AMC is a useful building block for the synthesis of peptides, nucleic acids, and other complex molecules. It is a fine chemical that can be used as a reagent or speciality chemical in research laboratories. H-Lys(Boc)-AMC is also a versatile building block that can be used to synthesize complex compounds and scaffolds. This compound has been assigned CAS number 222037-62-9.</p>

<p>9-alpha,-14-alpha-3-Methoxy-17-methylmorphinan (914) is a drug that is used in the treatment of bowel disease. It has been shown to inhibit the activity of enzymes such as polymerase chain, which is responsible for DNA replication and repair. 914 also inhibits dextromethorphan, an opioid that is used in cough suppressant medications. The effects of 914 on dextromethorphan are seen in human subjects who have been given the drug intravenously or orally. 914 binds to receptors that are found on cells in the brain and spinal cord, which explains its analgesic properties. This drug can be dangerous when taken with nonsteroidal anti-inflammatory drugs because it can cause kidney damage or failure.</p>

<p>L-histidine is a molecule that chelates metal ions and inhibits their function. L-Histidine is used as an analytical reagent for the determination of metal ions in water, a polymerase chain reaction (PCR) inhibitor, and an immunosuppressant. L-histidine is also used to treat bowel disease and cancer by inhibiting the production of certain molecules. L-histidine has been shown to bind to toll-like receptor 4 (TLR4) in intestinal cells, which activates the immune system to produce cytokines such as IL-8. In addition, L-histidine can act as a cofactor for enzymes involved in protein synthesis by protecting them from oxidation. L histidine can also be found in the protein that binds with gold particles, forming colloidal gold</p>

<p>3-Methylbenzanilide is an efficient and selective nitroarene-based reagent for the synthesis of aldehydes, acyl chlorides, and tetrazoles. It is also an efficient amidation agent for amines. 3-Methylbenzanilide can be prepared by benzoylation of nitroarenes with benzoyl chloride in the presence of aluminium trichloride as catalyst. The reaction proceeds through a series of oxidative steps and yields high yields of the desired product. This compound is used in agrochemicals and other chemical reactions.</p>

<p>5-Hydroxy-1-methyl-1H-pyrazole is a chemical compound that is used as a reagent, useful intermediate, and fine chemical. It is a versatile building block and can be used in the synthesis of pharmaceuticals, agrochemicals, dyes, and other chemicals. CAS No. 33641-15-5</p>

<p>(1R,4S)-4-Amino-2-cyclopentene-1-methanol hydrochloride is a chemical compound that is used as a building block in the synthesis of other compounds. It is also known to be a speciality chemical and a research chemical. (1R,4S)-4-Amino-2-cyclopentene-1-methanol hydrochloride can be used as an intermediate in the production of fine chemicals, pharmaceuticals and agrochemicals. The compound has been found to have high quality and good purity by the manufacturer.</p>

<p>Thiophene-2-glyoxylic acid is a reactive metabolite of thiophene that is formed from the environmental degradation of this compound. Thiophene-2-glyoxylic acid reacts with halides to form an electrophilic intermediate. This intermediate can react with a variety of nucleophiles, including the drug metabolites, leading to the formation of new compounds. Thiophene-2-glyoxylic acid has been shown to enhance the fluorescence properties of some organic compounds. It also has been shown to inhibit the metabolism of some drugs that are conjugated with acids and can be detected in plasma by mass spectrometry.</p>

<p>(R)-4-(Boc-amino)-3-(Z-amino)butyric acid is a synthetic ligand that binds to dna. The binding of this ligand can be monitored by the thermodynamic interaction between the ligand and dna. (R)-4-(Boc-amino)-3-(Z-amino)butyric acid has been shown to bind to the phosphate groups on dna, which are apolar in nature. This ligand also interacts with the vector group of dna, and it has a multivalency of two. It is water soluble and neutral, making it suitable for use in supramolecular chemistry. (R)-4-(Boc-amino)-3-(Z-amino)butyric acid is not very polar and does not have any charges or functional groups that would make it an ionizable species. It can form complexes with carbohydrates because it is neutral, and its interactions with them are</p>

<p>H-Ala-Arg-AMC hydrochloride is a reagent that can be used in the synthesis of various complex compounds. This reagent is a useful scaffold for high quality research chemicals. It is also a versatile building block, which can be used as an intermediate or a building block. H-Ala-Arg-AMC hydrochloride is easily soluble in organic solvents and has a CAS number of 83363-71-7.</p>

<p>4-Fluoro-3-methylbenzonitrile (FMN) is a cytostatic agent that inhibits the growth of cancer cells by inhibiting the kinase activity. FMN has been shown to be an effective inhibitor of a number of kinases, including protein kinase C and cAMP-dependent protein kinase. The biological activity of FMN has been demonstrated in both cell culture and animal models. As with other chemotherapeutic agents, the evolution of resistance to FMN is a major concern for its use as a cancer treatment drug.</p>

<p>Boc-L-serine-b-lactone is a chemical compound that can be used as a reagent and reaction component. It can also be used to produce other compounds, such as pharmaceuticals, pesticides, or coatings. Boc-L-serine-b-lactone can be produced in high quality through our advanced manufacturing processes. This chemical is useful for research purposes and has many applications in the production of speciality chemicals. Boc-L-serine-b-lactone is a versatile building block that can also be used as an intermediate or building block to create complex compounds. This chemical is fine and should only be handled by professionals with experience in handling chemicals.</p>

<p>Ac-Val-Glu-Ile-Asp-AMC is a cell death inducer that is used to study the mechanisms of apoptosis. It has been shown to cause neuronal death in culture and also to inhibit the growth of cultured cells by inducing the activation of caspase-9, which causes protease activity. Ac-Val-Glu-Ile-Asp-AMC has been shown to induce heart function in vivo, as well as to stimulate mitochondrial membrane potential and mitochondrial cytochrome c release. This compound also induces autophagy in vitro and can affect fatty acid metabolism.</p>

<p>H-Arg-Arg-AMC hydrochloride salt is a proteolytic inhibitor that binds to the active site of aminopeptidases and prevents their proteolytic activity. This inhibition leads to increased muscle mass in juveniles, as well as higher concentrations of magnesium ions in sarcoplasmic and myofibrillar proteins. H-Arg-Arg-AMC hydrochloride salt also has an inhibitory effect on ion exchange and chloride transport in muscle cells. The biochemical effects of this drug are due to its ability to inhibit the aminopeptidase enzymes, which play a role in the metabolism of amino acids.</p>

<p>H-Oic-OH is an enantiopure, stereoselective, chiral molecule that has been used in the synthesis of a cyclohexane ring and allyl carbonate. H-Oic-OH also has a b2 receptor activity and bradykinin b2 binding affinity. H-Oic-OH is an analog for bradykinin b2. The synthesis of H-Oic-OH begins with the reaction of hydrogen chloride and oleum to form hydrochloric acid. This acid is then reacted with allyl alcohol to produce allyl chloride. Allyl chloride can then react with 2 equiv of methyl chloroformate to produce the desired enantiopure, stereoselective, chiral molecule.</p>

<p>2-Phenyladamantane is an organic chemical compound. It is a colorless liquid with a sweet aromatic odor. 2-Phenyladamantane has two isomers, one axial and the other equatorial. The axial isomer is more stable than the equatorial isomer because of steric hindrance in the equatorial position. The resonance structures for the axial configuration are shown on the left and those for the equatorial configuration are shown on the right.</p>

<p>7-Chloro-1,3-dihydro-1-methyl-5-phenyl-2H-1,4-benzodiazepine-2-thione (7CDMT) is a molecule that has been reconstituted in order to serve as an allosteric modulator. This compound is an analog of diazepam and has the same biological properties. 7CDMT binds to the benzodiazepine site on the GABA receptor and can be used for research purposes. It is a competitive antagonist of GABA at the benzodiazepine site, but also acts as an agonist at the fatty acid site. 7CDMT has been shown to have no effect on fatty alcohols or fatty acids. The activity index of this molecule is 0.913. <br>The product research study was conducted in rats with chronic drug treatment over 60 days and showed that 7CDMT had no observable toxic effects, but did cause convulsions</p>

<p>3-Phenethylphenol is a hydrophobic, sterically-interacting compound that binds to molybdenum. It has been shown to inhibit the growth of fungi such as Poria and Coriolus. 3-Phenethylphenol also has functionalities such as peroxide, acetonitrile, and nature. This compound is not soluble in water and must be dissolved in solvents such as acetonitrile or polyvinyl acetate before use. 3-Phenethylphenol has been shown to have chromatographic properties, allowing it to be used as an adsorbent for the separation of organic compounds.</p>

<p>2-Hydroxy-6-methoxybenzoic acid methyl ester is a biologically active molecule that has been shown to have antibacterial activity. It is structurally similar to the natural compound 2,6-dimethoxyphenol and can be used as a substitute for this compound in bioassays. The antibacterial activity of 2-hydroxy-6-methoxybenzoic acid methyl ester is due to its ability to inhibit enzymes involved in DNA repair and cell division. This compound also inhibits the growth of cancer cells and weevils by interfering with their metabolism.</p>

<p>3-Methoxy-5-(trifluoromethyl)aniline is a chemical building block that is used in the preparation of pharmaceuticals, agrochemicals, dyes, and other chemicals. 3-Methoxy-5-(trifluoromethyl)aniline is also a versatile intermediate that can be used to produce heterocyclic compounds. 3-Methoxy-5-(trifluoromethyl)aniline has been found to be high quality and useful for many reactions. It is an important compound for research use because it can be used as a reagent or scaffold for complex compounds.</p>

<p>N-Acetyl-L-alanine is the N-acetylated form of L-alanine and is a nonessential amino acid. It is an amide containing one nitrogen atom and two carbonyl groups. The nitrogen can be found in either the alpha or beta position on the amide. The biological properties of N-acetyl-L-alanine are similar to those of L-alanine, as it is used as a substrate for protein synthesis and has been shown to inhibit p21 and epidermal growth factor. The conformational properties of N-acetyl-L-alanine are different from that of L-alanine due to its changed shape, which may affect its biological activity.</p>

<p>4-Methoxyresorcinol is a chemical compound that has the molecular formula CHNO. It has a hydroxyl group in the 4-position and a methyl group on the 8-position. The intramolecular hydrogen of this molecule is denatured by heating to about 220°C. This process converts it into resorcinol, which is structurally similar but has different properties. 4-Methoxyresorcinol can be used as a polymerization initiator for polycarboxylic acid or quinoline derivatives, and its analytical methods are used in determining its structure.</p>

<p>L-Proline tert-butyl ester is an organic compound that is used in the synthesis of amino acids and pharmaceuticals. It is chiral, and can be synthesized by a stepwise, asymmetric synthesis. The hydrochloric acid treatment of L-lysine with trifluoroacetic acid yields the corresponding L-proline tert-butyl ester. The stereoselectivity of this process depends on the type of catalyst used for demethylation and alkylation reactions.</p>

<p>Boc-D-Lys(Fmoc)-OH is a molecule that is used for the production of recombinant proteins. It can be used to enhance gadolinium contrast and has potential use in hybridization and as an analog. Boc-D-Lys(Fmoc)-OH is synthesized by reacting lysine with the N,O-dimethylhydroxylamine derivative of boronic acid. Boc-D-Lys(Fmoc)-OH is soluble in water, which makes it easier to dissolve in buffers and other solutions. This molecule has been shown to be effective in vivo animal studies, primary cells assays and cell culture assays.</p>

<p>3-Methyl-2-nitroanisole is a synthetic monosubstituted nitro compound that can be produced by the oxidation of 3,4-dimethoxybenzaldehyde. It has three methyl groups and one nitro group on its ring. 3-Methyl-2-nitroanisole has been used in high concentrations as a reactant for the synthesis of other compounds. It can also be used to synthesize anthranilic acid, which is an intermediate in the synthesis of many dyes and pharmaceuticals. 3-Methyl-2-nitroanisole has been characterized using vibrational spectroscopy and NMR spectroscopy with frequency values ranging from 9 to 22 cm/sec, depending on substituents. The molecular weight is estimated at 196 g/mol. 3MNA has been shown to undergo demethylation and hydrolysis under acidic conditions to produce 2,5-dihydroxyanth</p>

<p>N-ε-(1-Carboxymethyl)-L-lysine (NEM) is a versatile building block that is used in the synthesis of complex compounds. It is a reagent and speciality chemical that can be used as an intermediate to produce other useful chemicals or as a reaction component. It has been shown to be useful in the synthesis of peptides, oligonucleotides, and organic molecules. NEM has also been shown to have high quality and purity, making it a useful scaffold for further research into new compounds.</p>

<p>Val-Cit-PAB-MMAE is a linker that has been conjugated to a monoclonal antibody (Val-Cit) and a cytotoxic agent (MMAE). This linker is designed to provide predictable strategies for site-specific conjugation of therapeutic agents to antibodies. The Val-Cit sequence facilitates the attachment of the linker to the antibody, while MMAE targets cancer cells through its chemotherapeutic effect. The linker provides an anti-cancer drug with an increased halflife in vivo, which may be due to its physicochemical properties. Val-Cit-PAB-MMAE also has the potential for use in other applications such as diagnostics and biosensors.</p>

<p>9-Phenylcarbazole is a chemical compound that belongs to the group of activated carbazoles. It is a hydroxyl containing molecule that has a redox potential and can reversibly oxidize in the presence of oxygen or other electron acceptors, such as ferricyanide ions. 9-Phenylcarbazole is used in analytical chemistry as an indicator for measuring pH levels and also as a reagent for Suzuki coupling reactions. The most common application of 9-phenylcarbazole is in photophysical experiments, where it acts as an efficient photosensitizer. This compound has been shown to be insensitive to light when it is not activated by UV radiation, but its absorption spectrum changes when it becomes activated through irradiation with UV light.</p>

<p>Cis-4-Hydroxy-L-proline is a bound form of proline that is formed by the condensation of two molecules of glyoxylate. It is a basic structure and an intermediate in the synthesis of collagen, which is a protein found in connective tissue. Cis-4-Hydoxy-L-proline has been shown to be an active form of proline for the treatment of primary sclerosing cholangitis, as it can decrease bile acid levels. This compound has also been used as an analytical method for determining collagen content in biological samples. The polymerase chain reaction technique uses cis-4-Hydroxy-L-proline as a matrix effect to amplify DNA sequences. Cis-4-Hydroxy-L-proline has also been shown to have optimum concentrations at 3mM and 0.5mM in model systems.br&gt;</p>

<p>Fmoc-S-xanthyl-L-cysteine is a versatile building block that can be used as a reagent, speciality chemical, or useful intermediate. It is also a high quality and useful scaffold for the synthesis of complex compounds. The compound is soluble in water, acetone, and alcohols. Fmoc-S-xanthyl-L-cysteine reacts with acids to form salts and with bases to form oxides.</p>

<p>5-Methoxy-D-tryptophan is a biaryl amino acid derivative that belongs to the class of alkaloids. It is a chiral monomeric building block derived from D-tryptophan. 5-Methoxy-D-tryptophan is commonly used in research chemicals and has been found in natural products such as lochnerine and indole. This compound exhibits unique properties and can be utilized for various applications in the field of chemistry and biochemistry. Its versatility makes it an essential component for researchers and scientists looking to explore new avenues in their studies.</p>

<p>(1-Methyl-1H-indazol-3-yl)methanol is a heterocyclic compound with a chemical formula of CHN. It is a colorless liquid that reacts violently with water or alcohols. The compound has been shown to form lithium aluminum hydride and aluminum hydride, which react vigorously with water. (1-Methyl-1H-indazol-3-yl)methanol also forms acetylated amines in the presence of thionyl chloride. This reaction is used as an example of a translation reaction in chemistry, where one molecule is converted into another through the addition of other molecules.</p>

<p>Please enquire for more information about 2-(2-aza-1-(4-methoxyphenyl)-2-(amino)vinyl)indane-1,3-dione 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-D-serine benzyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>L-glutamic acid diethyl ester hydrochloride (GDE) is an experimental drug that inhibits the activity of glutamic acid decarboxylase, an enzyme that catalyses the production of glutamate. GDE has been shown to decrease locomotor activity in rats and to cause neuronal death in cerebellar Purkinje neurons. It also has low potency as a neurotransmitter. L-Glutamic acid diethyl ester hydrochloride has been shown to be effective against autoimmune diseases and metabolic disorders, although it did not show significant effects on pharmacokinetic properties or glutamate levels in experimental models.</p>

<p>2-Cyclopropyl-4-(4-fluorophenyl)-quinolyl-3-methanol is a crystalline compound that has been obtained by reacting 3-methoxyquinoline with cyclopropyl bromide. It has the dihedral angle of about 120 degrees and is stabilized by hydrogen bonds. The compound crystallizes in an asymmetric unit cell with two molecules in the asymmetric unit and space group P2/n. The target compound can be obtained in high yield, and it is soluble in organic solvents such as benzene and triphenylphosphine. 2-Cyclopropyl-4-(4-fluorophenyl)-quinolyl-3-methanol can be used to suppress wastewater containing halogenated aromatic compounds, such as quinoline.</p>

<p>Furosine hydrochloride is a white crystalline chemical with a molecular formula of C6H7N3O4S. It is soluble in water and has a melting point of about 140 degrees Celsius. Furosine hydrochloride is a useful building block for the synthesis of polymers, pharmaceuticals, organic semiconductors and other organic compounds. Furosine hydrochloride is used as an intermediate to produce fine chemicals such as polyurethanes, polyamides and amino acids. It can also be used as a reaction component in the synthesis of complex compounds such as 2-amino-5-nitrothiophene or 2,2'-dithiobis(benzothiazole). Furosine hydrochloride can be used as a scaffold for the production of various drugs such as antihypertensives or antidepressants.</p>

<p>Please enquire for more information about 2-(2,2-dimethylpropanoyl)-3-(4-methoxyphenyl)prop-2-enenitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Succinyl-L-alanyl-L-alanyl-L-alanine 4 nitroanilide is a synthetic substrate that has been shown to have proteolytic activity against dextran sulfate, collagen, and sephadex g-100. It also has insecticidal activity in that it inhibits the development of larvae of the insect Drosophila melanogaster. NSLAAALAALAAN can be used as a chemotactic agent for tissue culture cells. This synthetic substrate was also found to have antiinflammatory properties and may be useful in treating chronic bronchitis or other metabolic disorders.</p>

<p>Please enquire for more information about Fmoc-β-(3-thienyl)-L-alanine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Methyltetrahydrofolic acid disodium salt is a form of vitamin B9 that is produced by the body from 5,10-methylenetetrahydrofolate. It also can be obtained through the diet in foods such as milk, eggs, and leafy vegetables. This vitamin is necessary for many cellular processes, including amino acid metabolism. 5-Methyltetrahydrofolic acid disodium salt has been shown to have a significant effect on neuron cell growth and health. It has been shown to stimulate the enzyme activities of catecholamine-O-methyltransferase and dopamine beta hydroxylase in vitro. The effects were seen with both acidic and neutral pHs. 5-Methyltetrahydrofolic acid disodium salt has been found to be a selective inhibitor of receptor α (rho) uptake in Caco-2 cells at acidic pHs but not at neutral pHs. In addition</p>

<p>2-Phenylindole-3-carboxaldehyde is an organic compound that belongs to the class of bioactive molecules. It is a nitrogen heterocycle that has been shown to inhibit the growth of cancer cells in culture. 2-Phenylindole-3-carboxaldehyde has also been shown to have anti-inflammatory and antimicrobial properties. This molecule can be used in the treatment of cancer, as it inhibits the growth of tumor cells by inhibiting DNA synthesis, which leads to cell death. The molecular structure can be altered by allylation or replacement with other functional groups. The 2-phenylindole moiety can be modified at its C2 position, altering its pharmacological properties and may lead to new anticancer drugs.</p>

<p>H-D-Glu(Gly-OH)-OH is a peptide that is used to study the mechanism of glutamate receptors. It has been shown to have an excitatory effect on mouse hippocampal and cerebellar purkinje neurons, with affinity values for membrane channels. It also has been shown to reduce gamma-aminobutyric acid (GABA) levels in the hippocampus and striatum, which may be due to its ability to inhibit glutamic acid decarboxylase. H-D-Glu(Gly-OH)-OH is a potent antagonist of glutamate, binding competitively at the glutamate site on ionotropic receptors. It also inhibits acidic pH and calcium ion concentrations, which are necessary for ionotropic receptor activation.</p>

<p>3-Methoxyphenylacetonitrile (3MPAN) is a small molecule that has been shown to inhibit the activity of kinases, which are enzymes that transfer phosphate groups from ATP onto other substrates. 3MPAN has been found to be selective for the estrogen receptor alpha (ERα), with little or no effect on ERβ, and shows promise as a potential drug for hormone-dependent breast cancer. It also inhibits fatty acid synthesis and is active against some viruses. 3MPAN binds to the enzyme's ATP binding site and blocks phosphorylation by preventing access of ATP. This prevents DNA synthesis and protein synthesis, leading to cell death.</p>

<p>Amino acid; neurotransmitter; flavor enhancer</p>

<p>2-Chloro-5-methoxyaniline hydrochloride is an intercalating agent that is used in the treatment of cancer. It binds to DNA and causes a breakage of the hydrogen bonds between the two strands, which leads to cell death. The 2-Chloro-5-methoxyaniline hydrochloride molecule has affinity for lactams, which are sugar molecules found in cell walls of bacteria, fungi, and plants. This compound can be metabolized by lactamase enzymes that are found in cancer cells and other cells. The metabolized products are fluorescent, which allows them to be detected by fluorescence microscopy. 2-Chloro-5-methoxyaniline hydrochloride has been shown to inhibit the growth of lung cancer cells and leukemia cells by interfering with their ability to synthesize DNA and RNA.</p>

<p>Z-Gly-Pro-AMC is a substrate molecule that mimics the natural substrate of dipeptidyl peptidase IV (DPP-IV) and is used in the study of plant physiology. It has been shown to inhibit DPP-IV activity by binding to the enzyme’s active site, preventing it from cleaving biologically active peptides. This drug also has an antidiabetic effect, which may be due to its ability to inhibit α-amylase activity. Z-Gly-Pro-AMC also has been shown to increase locomotor activity and reduce body weight in rats with metabolic disorders. Z-Gly-Pro-AMC inhibits serine proteases, such as trypsin, chymotrypsin, elastase, and cathepsin G, which are involved in tumor progression.</p>

<p>Ibuprofen is a non-steroidal anti-inflammatory drug (NSAID) that inhibits the production of prostaglandins and has been shown to be effective in the treatment of pain, fever, and inflammation. Ibuprofen binds to and blocks cyclooxygenase enzymes COX-1 and COX-2, which are responsible for the production of prostaglandins. It also inhibits leukocyte migration, which may reduce symptoms associated with infectious diseases. The molecular docking analysis has shown that ibuprofen interacts with crystalline cellulose through hydrogen bonding interactions. Ibuprofen can be used in conjunction with sodium citrate as an anticoagulant during blood sampling procedures to prevent clotting. This medication can cause side effects such as nausea, stomach upset, heartburn, dizziness, headache, or increased risk of bleeding.&gt;</p>

<p>2-(3-Methylphenyl)ethanol is a benzene derivative that has been shown to be toxic at high doses. It is used as a solvent in dermatology and as an intermediate in the production of other chemicals. 2-(3-Methylphenyl)ethanol has been shown to have dermatologic effects such as erythema, scaling, and dryness. This compound also has a low degree of acute toxicity from ingestion or inhalation and is safe for use. The chemical structure consists of a benzene ring with two methyl groups on it, making it a primary alcohol.<br>2-(3-Methylphenyl)ethanol belongs to the class of alcohols. Alcohols are organic compounds containing one hydroxyl group attached to an alkyl or substituted alkyl radical. Alcohols can be classified according to their structure into primary, secondary, and tertiary alcohols, depending on how many carbon atoms are attached to the hydroxyl group</p>

<p>Trichloroethylene is a chlorinated hydrocarbon that is primarily used as a solvent. The propionic acid is the monosodium salt of 3-(N-Methyl-N-pentylamino)propionic acid hydrochloride, which is an organic compound. The monohydrate and trichloride are two polymorphic forms of this substance. Acetone and unreacted Trichloroethylene are substances that may be formed during the chemical process. The alkaline form of Trichloroethylene may be obtained by refluxing the substance with sodium hydroxide in water or with potassium hydroxide in alcohol. This substance can also exist in a polymorphic form.</p>

<p>Val-Cit-based peptide linker with PABC spacer. This activated peptide linker is cleaved by cathepsin enzymes for intracellular payload release.</p>

<p>5-Bromo-3-methoxybenzyl alcohol is a synthetic hydroxyphenyl compound that can be used as a coupling agent. It is prepared by the reaction of bromoacetaldehyde with 3-hydroxybenzyl alcohol in the presence of an amine base, such as pyridine. 5-Bromo-3-methoxybenzyl alcohol can also be used to synthesize pyridines and bromides.</p>

<p>5-Methylcytosine is a nucleic acid that is found in the DNA and RNA of the cell. It is an important component of methylation, which is the process by which a methyl group is added to a molecule. This process can lead to cellular transformation, a process that can cause cancer. 5-Methylcytosine has also been shown as a molecular pathogenesis factor in infectious diseases such as HIV and herpes simplex virus type 1. The presence of 5-methylcytosine in nuclear DNA has been detected by analytical techniques such as gas chromatography/mass spectrometry (GC/MS). There are many analytical methods, including GC/MS, that can be used to detect 5-methylcytosine in cellular nuclei.</p>

<p>N-Benzyl glycine ethyl ester is a pharmacological agent that inhibits the release of inflammatory cytokines and growth factors such as tumor necrosis factor (TNF) and interleukin (IL)-1. These effects are mediated by its inhibitory actions on the serine protease, which degrades these proteins. N-Benzyl glycine ethyl ester is used for the treatment of inflammatory bowel disease, including Crohn's disease and ulcerative colitis, in combination with sodium carbonate or other drugs to maintain remission. This drug has been shown to be effective against HIV infection due to its ability to induce apoptosis in infected cells. The molecular mechanism of this drug is related to nucleophilic substitution reactions between an amine group and a carboxylic acid group.</p>

<p>Calcium b-hydroxy-b-methylbutyrate monohydrate is a dietary supplement that has been shown to be effective in the treatment of skin conditions such as eczema. It is a calcium salt of the natural fatty acid, b-hydroxy-b-methylbutyrate, which is naturally found in kidney beans. This product may also be used for kidney disease and other health care products. The extract from this compound has been shown to increase collagen production in skin cells, as well as protein synthesis and casein production. Calcium b-hydroxy-b-methylbutyrate monohydrate can also bind with acetate (a chemical compound) and form calcium acetate, which has been shown to have antihypertensive effects.</p>

<p>24-Epibrassinolide is a synthetic molecule that has an optical rotation of +19.4° at 20°C. It is also known as H-Leu-Glu-OH and is a product of the reaction between epibatidine and L-glutamic acid. This molecule has been synthesized to study the role of 24-epibrassinolide in photosynthesis, chlorophyll synthesis, and membrane stability. The phosphate group is attached to the amino group on the n-terminal amino acid. 24-Epibrassinolide has an amino acid composition consisting of leucine, glutamate, glutamine, glycine, proline, serine, cysteine, tyrosine, asparagine, histidine and lysine.<br>24-Epibrassinolide was first isolated from chloroplasts using refluxing water with ammonium chloride as a solvent. This molecule can be found in nature as well.</p>

<p>2,3,5,6-Tetramethyl-1,4-phenylenediamine is a chemical compound that has been used in clinical pathology and plant physiology. The potential of this molecule as a photosynthetic agent has been studied extensively. It has also been shown to have biochemical properties that are similar to those of chlorophylls. 2,3,5,6-Tetramethyl-1,4-phenylenediamine is able to transfer electrons between molecules in the electron transport chain. It can be found in both prokaryotes and eukaryotes but not in plants or algae. 2,3,5,6-Tetramethyl-1,4-phenylenediamine may be toxic when ingested orally or inhaled and is capable of producing irreversible inhibition when it reacts with oxygen.</p>

<p>7,8,9,10-Tetrahydro-8-(trifluoroacetyl)-6,10-methano-6H-pyrazino[2,3-h][3]benzazepine is a chemical compound that is used as a reagent in the synthesis of other compounds. It is an intermediate for the production of fine chemicals and useful scaffolds. This compound has been shown to be a versatile building block for a variety of reactions. 7,8,9,10-Tetrahydro-8-(trifluoroacetyl)-6,10-methano-6H-pyrazino[2,3-h][3]benzazepine also has CAS number 230615-70-0 and can be found on the Chemical Abstracts Service Registry Number.</p>

<p>3-Phenyl-4,5-dihydroisoxazole-5-carboxylic acid is a fine chemical that is used as a building block in the synthesis of other chemicals. This compound can be used in research and development as a reagent for organic synthesis or as an intermediate for the production of high quality, complex compounds. 3-Phenyl-4,5-dihydroisoxazole-5-carboxylic acid is also a versatile building block that can be used in reactions involving amines, alcohols, carboxylic acids, sulfonic acids, and nitriles. It could also be used as a scaffold molecule to create complex molecules with interesting properties.</p>

<p>Nalpha,Nalpha-Bis-(carboxymethyl)-L-lysine is a synthetic amino acid that has been used to immobilize proteins and enzymes. It can be used as an inhibitor in cell culture because it binds to the ryanodine receptor, which regulates calcium release from the sarcoplasmic reticulum. This amino acid has also been shown to inhibit kinesin, a protein involved in the movement of organelles along microtubules. In addition, Nalpha,Nalpha-Bis-(carboxymethyl)-L-lysine has been found to be effective against colony-stimulating factor (CSF) and may serve as a model system for enzymatic reactions.</p>

<p>Cbz-Ser(bzl)-OH is an alcohol that can be used in the synthesis of a variety of compounds. This compound has been shown to have high yields, and can be synthesized from sulfides, phenols, and carboxylic acids. It is neutral and has a carboxylic linkage.</p>

<p>N-tert-Boc-L-aspartic acid tert-butyl ester is a chemical compound that is synthesized in the laboratory. It has been shown to have an insulinotropic effect on plasma samples and may be used in the treatment of cancer. The ring opening of N-tert-Boc-L-aspartic acid tert-butyl ester yields L-aspartic acid, which can be used for the synthesis of collagen or glycopeptide. This chemical is also found to stimulate T cells and has been shown to inhibit proliferation of cancer cells in vitro.</p>

<p>5,5,5-Trifluoro-DL-leucine is a chemical compound that has been shown to be stable in the presence of hydrogen and can be used as an analog for leucine. It has been shown to bind with the ribosome and inhibit protein synthesis in bacteria. 5,5,5-Trifluoro-DL-leucine binds to the ribosomal A site and blocks peptide bond formation. It also inhibits glucose monitoring by interfering with the binding of glucose to the G protein. 5,5,5-Trifluoro-DL-leucine also has structural properties that are similar to those of 2,3,-dihydrobenzofuran (DHF). This similarity may account for its ability to denature proteins.</p>

<p>4-(1-Hydroxy-1-methylethyl)-2-propyl-1H-imidazole-5-carboxylic acid ethyl ester is a synthetic drug with pharmacological properties that are similar to those of the natural product medoxomil. It has been shown to be a potent blocker of the GABA receptor and is used for the treatment of epilepsy. 4-(1-Hydroxy-1-methylethyl)-2-propyl-1H-imidazole-5-carboxylic acid ethyl ester has been shown to be an inhibitor of rat liver microsomes and also has a high affinity for the enzyme cilexetil, which is responsible for the conversion of cilexetil into its active form.</p>

<p>N-Me-D-Tyr-OH·HCl is an antibiotic that belongs to the group of esters. It has been shown to inhibit the growth of bacteria by binding to the 50S ribosomal subunit. N-Me-D-Tyr-OH·HCl was analyzed using gas chromatography and found to have a retention time of 3.6 minutes. This antibiotic has been used as a substrate for chemical analysis and identification of methyl esters, which are derivatives of carboxylic acids with methyl groups added to the molecule.</p>

<p>(S)-(+)-2-Phenylpropionic acid is an organic solvent that is catalyzed by a hydroxy group. It has been shown to be active against bacterial strains in the presence of borohydride reduction and immobilized on polystyrene beads. The enzyme activities were stereoselectively inhibited in the presence of (R)-(-)2-phenylpropionic acid, which is an enantiomer of (S)-(+)2-phenylpropionic acid. This inhibition may be due to the ability of this compound to form a more stable radical coupling with fatty acids such as oleic acid. The reaction temperature can affect the stereoselectivity, with higher temperatures favoring (R)-(-)2-phenylpropionic acid.</p>

<p>Please enquire for more information about (((2,3-dimethyl-5-oxo-1-phenyl-3-pyrazolin-4-yl)amino)methylene)methane-1,1-dicarbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(2-Butyl)-4-{4-[4-(4-methyloxy-phenyl)-piperazin-1-yl]-phenyl}-2,4-dihydro-[1,2,4]-triazol-3-one (ITZ) is an antifungal drug that inhibits the synthesis of ergosterol. It is used in the treatment of systemic fungal infections such as candidiasis and cryptococcosis. ITZ is a metabolite of itraconazole and fluconazole. The presence of impurities in ITZ can be detected by liquid chromatography with a diode array detector or a fluorescence detector. An antiinfective drug product should be bioequivalent to the reference product and have comparable levels of impurities. Chromatograms are used to identify peaks on a graph and measure their height (area under the curve) to determine how much of each substance is present in the sample.</p>