Amino Acids (AA)

(4-Methoxybenzylidene)Malononitrile (MBN) is a small-molecule drug that inhibits the tyrosine kinase activity of basic proteins. It has been shown to inhibit neuronal death and the angiogenic process in vitro. MBN has also been shown to be an inhibitor of the polymerase chain reaction, which is used in DNA amplification. This compound binds reversibly to the enzyme and prevents it from binding to DNA, thereby inhibiting its activity.

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Please enquire for more information about 1-(4-Nitrilophenyl)-3-(4-methylbenzoyl)thiourea including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Please enquire for more information about 1-phenyl-3-methylthiosemicarbazide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 3-(4-Hydroxy-3-methoxyphenyl)-4-(4-(trifluoromethyl)phenyl)-1,2,4-triazoline-5-thione including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about (3-Aminophenyl)-N-(4-phenoxyphenyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

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2-Amino-5-methyl-4-phenylthiazole is an organic compound that is a reactive intermediate. It can be used in treatments such as second order rate constants, stabilization, and kinetic. This chemical has a dimethylamine group, which is an amine with two methyl groups attached to it. 2-Amino-5-methyl-4-phenylthiazole has chloride and thiazolone groups, which are both heterocyclic rings of carbon atoms with nitrogen and sulfur atoms attached to them. The phenyl isothiocyanate group is also a heterocyclic ring of carbon atoms with sulfur attached to it. 2-Amino-5-methyl-4-phenylthiazole has the constant of K = 1.2 x 10 M^sup -1
s^{sup -1} at 25 degrees Celsius. It reacts with acetonitrile and ethylpyridine

Please enquire for more information about 3-((4-Acetylphenyl)amino)-5-phenylcyclohex-2-en-1-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Amino-2-phenylindenone is a lactam molecule with a five-membered ring and a carbonyl group. The compound's acetylation, protonation, and skeleton are important to its structure. 3-Amino-2-phenylindenone is an aromatic compound that has two deuterium atoms. It has the chemical formula C9H6N2O2, which consists of one chloride atom and two nitro groups. 3-Amino-2-phenylindenone has three deuterium atoms that can be seen in its proton resonances at 1.5 ppm on the IR spectrum. The compound's proton resonances are at 2.8 ppm on the IR spectrum. The compound's chloroformate can be seen in its IR spectrum at 1780 cm^(-1). This molecule has no nonequivalence in its bonds because it does not have any double or

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4-oxo-5-phenyl-2,5-thiazolidinylidene)methane-1,1-dicarbonitrile is a molecule that has been shown to stabilize the phenyl ring in some experimental conditions. The intramolecular dihedral parameters of 4-oxo-5-phenyl-2,5-thiazolidinylidene)methane are not experimentally determined but can be calculated by molecular docking. Molecular docking is a technique that predicts the binding of one molecule to another by simulating the docking process. Docking simulations can be used for understanding the structure and dynamics of molecules.

Please enquire for more information about 2-amino-7-methyl-4-(2-naphthyl)-5-oxo-4,6,7,8-tetrahydro2H-chromene-3-carbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 2,4-dimethoxy-1-(2-(1-methyl(2-pyridyl))vinyl)benzene, iodide including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Please enquire for more information about 2-Chloro(3-pyridyl) 4-(5-chloro-2-methylphenyl)piperazinyl ketone including the price, delivery time and more detailed product information at the technical inquiry form on this page

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H-Glu(His-OH)-OH is a protein, which can be found in the plasma samples of patients with fatty acid metabolism disorders. It is one of the most selective markers for identifying these disorders and has been extensively used for profiling and genomic analyses. H-Glu(His-OH)-OH is also present in rat cerebral cortex and it has been shown to be statistically significantly elevated in cerebral cortex samples from patients with Alzheimer's disease. This protein has been observed to have an acidic property and can be used as a biomimetic marker. Regression analysis has shown that H-Glu(His-OH)-OH levels are correlated with the severity of neuronal damage. This protein may serve as a biomarker for different diseases, including Parkinson's disease, Huntington's disease, or amyotrophic lateral sclerosis (ALS).

2-Amino-3-bromo-5-methylpyridine is an imidazopyrazine that interacts with the magnetic field and can be used as a ligand. It has been synthesized from pyrazole derivatives and has been shown to have antimicrobial activity against Cryptococcus neoformans. 2-Amino-3-bromo-5-methylpyridine has also been shown to inhibit the growth of bacterial cells by binding to the nicotinamide adenine dinucleotide phosphate (NADP) cofactor in bacterial cells, thereby preventing ATP production. This drug is structurally related to fluoroquinolones, which are known for their antibacterial activity. 2-Amino-3-bromo-5-methylpyridine is an amido compound that ionizes in acidic environments and transfers electrons via resonance transfer. Its FTIR spectra show strong absorption bands at 3595 cm−1

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The compound trans-3-(4-methylbenzoyl)acrylic acid is a potent and selective inhibitor of serine/threonine protein kinase. It has been shown to inhibit the proliferation of eosinophils in vitro, as well as to suppress the release of leukotrienes from human mast cells. The mechanism of action is by inhibiting phosphatidylcholine-specific phospholipase C, which leads to the inhibition of protein kinase C. This inhibition prevents the phosphorylation of various proteins, including cytoskeletal proteins that are required for cell division.

Applications N,N-[Iminobis(trimethylene)]bis-D-gluconamide (cas# 86303-20-0) is a compound useful in organic synthesis.

Applications (3S)-3-Methyl-methylester Heptanoic Acid is used as a reagent in the synthesis of stereoisomers of 5,9-dimethylheptadecane, the major sex pheromone component secreted by female moths of the mountain-ash bentwing (Leucoptera scitella).
References Taguri, T., et al.: Tetrahedron Asymmetry, 23, 852 (2012)

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