Aminoácidos (AA)

<p>Please enquire for more information about 3-Amino-6-bromo-2-methylquinazolin-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 1-(4-Chlorophenyl)-3-(4-methylphenyl)-1H-pyrazole-5-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Acetyl-L-proline methyl ester is a conformationally restricted chiral compound. It is an ester of the amino acid L-proline and acetyl chloride. The conformational restriction in this molecule may be due to the interaction between the amide group and the methyl ester side chain. This chemical is used in collagen production as well as a theoretical model for other molecules with similar structural properties. Acetyl-L-proline methyl ester has been shown to have anti-inflammatory properties, which are thought to be due to its ability to stabilize collagen fibers and inhibit the formation of matrix metalloproteinases.</p>

<p>2-Hydroxy-4-methylquinoline is an organic compound that has a chelate ring. It is soluble in deionized water and reacts with metal ions to form a fluorescent product. The molecule also has antibacterial activity, which may be due to its ability to inhibit the growth of bacteria by acting as a metal ion chelator. 2-Hydroxy-4-methylquinoline can react with halides and ammonium persulfate to form isomeric products, such as 4,5-dihydroxyquinoline, which have been shown to have antimicrobial properties. 2-Hydroxy-4-methylquinoline can also react with phosphorus oxychloride and alkylating agents such as chloroethane or chloroform to form substituted derivatives.</p>

<p>3-Chloro-4-methylaniline is a chemical compound with a chlorinated aromatic ring. It is a metabolite of the herbicide atrazine, which has been found to produce toxic effects in humans and animals. 3-Chloro-4-methylaniline has been shown to disrupt energy metabolism in mammalian cells through its interaction with mitochondrial respiratory chain complexes I and II. This compound has also been found to cause tubule cell death in the kidneys of rats, as well as liver lesions in mice.</p>

<p>(1R,2R)-Boc-aminocyclopentane carboxylic acid (BCPC) is a high quality, reagent, and useful intermediate. It is a versatile building block that can be used as a speciality chemical or research chemical. BCPC has been shown to react with amines to form ureas, with nitriles to form oxazolidines, and with epoxides to form aziridinones.</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>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>Please enquire for more information about [(5-Methyl-4-phenyl-4H-1,2,4-triazol-3-yl)thio]acetic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Methyl-O-methyl-L-tyrosine hydrochloride (NMT) is an organic compound that is synthesized from D-alanine. It has been shown to inhibit the production of didemnin, a protein that regulates the cell cycle, in mcf-7 cells. NMT has also been shown to stop the growth of human breast cancer cells and increase the lifespan of mice with cancerous tumors. NMT is a macrocyclic molecule, which means it has a ring structure made up of at least six atoms. The conformation of this molecule may be cyclic or linear.</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>Please enquire for more information about 4-Bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Methyl-1,3-oxazole (5MOX) is a chiral molecule that belongs to the class of polyatomic compounds. It has an aldehyde functional group and is used as a precursor for pharmaceuticals, agrochemicals, and other organic compounds. 5MOX can be accessed through dehydration of ethyl acetate or benzene. The compound crystallizes in a different form depending on the temperature at which it is cooled. At room temperature, it forms crystals similar to those of covid-19 pandemic, while at higher temperatures it forms crystals with methyl groups on one side. 5MOX has been shown to inhibit neprilysin, an enzyme that degrades amyloid beta peptide in Alzheimer’s disease patients and mice models. This property makes 5MOX an attractive candidate for treating Alzheimer’s disease.</p>

<p>Homoglutathione is a glutathione analog that contains an extra b-alanine residue. Homoglutathione has been shown to be a potent inhibitor of fatty acid synthesis. It inhibits the activity of the enzyme, acetyl-CoA carboxylase, which catalyzes the conversion of acetyl-CoA to malonyl-CoA. Homoglutathione also binds to and inhibits cytoplasmic proteins, such as glutamine synthetase and glutamate synthase. The binding of homoglutathione to these proteins prevents the formation of the active site by preventing the hydrogen bonding between amino acid residues. This process is important in energy metabolism because it regulates the production of ATP from ADP and phosphate.</p>

<p>1-Benzyl-4-phenylpiperazine is a type of phenylpiperazine that has hydroxy, phenyl ring, alkylthio, naphthyl and dopamine. It is an agonist for the D2 receptor and a specific ligand for the serotonin 5HT1A receptor. 1-Benzyl-4-phenylpiperazine has been shown to be effective in treating depression and psychotic depression. This drug can also be used as a substance in research on the neuropsychology of depression.</p>

<p>The drug, 10-[2-(1-methyl-2-piperidinyl)ethyl]-2-(methylthio)-10H-phenothiazine hydrochloride (CGP 46660), is a competitive antagonist at the human histamine H3 receptor. It has been shown to bind to the histamine H3 receptor in the range of 0.001 to 1 μM and is selective for this receptor over other receptors. CGP 46660 is an optical sensor that can be used in titration calorimetry experiments to measure changes in heat production when it binds to histamine H3 receptors. The drug also has been shown to inhibit guanine nucleotide-binding protein (G protein) signaling pathways and brain functions such as memory formation, learning, and attention span. These effects were demonstrated in humans by measuring EEG activity. The optimum concentration of CGP 46660 for these effects was found to be between 0.01 and 10 μM.</p>

<p>D,L-Threo-b-hydroxy aspartic acid is a stereoselective synthetic amino acid that has been used to study the uptake and hydrolysis of D,L-threo-b-hydroxy aspartic acid by rat brain synaptosomes. It has also been used in the synthesis of an L-alanine analogue with the same stereochemistry at the chiral center. The stereoselective synthesis of this compound is achieved by epimerization reaction using d-alanine as a starting material. Threo bhda has been shown to inhibit glutamate release from neurons and stimulate GABA release in synaptosomes, which may be due to its ability to bind to ion channels. Threo bhda has also been found to inhibit the binding of radioactive thymidine to calf thymus DNA with a high degree of stereoselectivity.</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>Please enquire for more information about 5-(3-Methylphenyl)-1,3,4-oxadiazol-2-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Z-L-Asp-OH is a protease inhibitor that inhibits the activity of serine proteases, including trypsin and chymotrypsin. Z-L-Asp-OH binds to the active site of these enzymes and prevents them from cleaving their substrates. The optimal pH for this enzyme is 8.0, which corresponds to its maximum level of activity. Z-L-Asp-OH also has apoptotic activities in cells by causing cellular pathway changes, leading to cell death via programmed cell death or apoptosis. This agent is activated by hydrolysis at ester linkages and polymerizes into films in aqueous solution at physiological pH. It has been shown to inhibit the growth of human ovarian carcinoma cells in vitro, but not normal cells.</p>