Pharmaceutical Standards

Please enquire for more information about (NZ)-4-chloro-N-[1-[2-(4-nitrophenyl)ethyl]piperidin-2-ylidene]benzenesulfonamide 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'-Dihexyl-2,2'-bithiophene including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 1-(2-Aminoethyl)-3-Phenylurea Hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 17-Hydroxy-19-nor-17alpha-pregna-4,6-dien-20-yn-3-one acetate including the price, delivery time and more detailed product information at the technical inquiry form on this page

2,4,4’-Trichlorobiphenyl is a polychlorinated biphenyl congener. It has been shown to have an adverse effect on the central nervous system, causing neurotoxicity. 2,4,4’-Trichlorobiphenyl has been used as a model system for the study of the effects of environmental toxins on mitochondrial membrane potential and lipid peroxidation. 2,4,4’-Trichlorobiphenyl binds to fatty acids in mitochondria and inhibits fatty acid β-oxidation. The inhibition of fatty acid oxidation leads to increased levels of protocatechuic acid in the serum and liver tissue. 2,4,4’-Trichlorobiphenyl has also been found to be toxic to aquatic organisms such as fish and shrimp at low concentrations.

1,3-Dihydroxy-2-naphthoic acid is an organic compound that belongs to the binaphthyls. It is a white solid that can be obtained by reacting naphthalene with inorganic phosphite in the presence of acidic potassium carbonate. This reaction system produces 1,3-dihydroxy-2-naphthoic acid and potassium biphosphite as byproducts. The reaction time depends on the concentration of reactants. 1,3-Dihydroxy-2-naphthoic acid has acidic properties and can be used as a catalyst for chemical reactions involving carboxylic compounds. This compound has been shown to be effective at treating abdominal pain caused by intestinal inflammation or infection with a carbon source such as carbohydrates (e.g., glucose) or fats (e.g., oleic acid).

(±)-3-Methyl-2-oxovaleric acid is a fatty acid that is found in the mitochondria of liver cells and other tissues. It is an intermediate in the citric acid cycle and can be converted into acetyl-CoA, which is used for energy production. (±)-3-Methyl-2-oxovaleric acid has been shown to cause necrotic cell death when it binds to the mitochondrial membrane potential and causes a loss of ATP production. This results in a lack of energy for the cell, leading to cell death. (±)-3-Methyl-2-oxovaleric acid has also been shown to inhibit protein synthesis by decreasing uptake and increasing creatine kinase activity. This inhibition leads to decreased body formation and tissue culture growth in vitro. In vivo, (±)-3-Methyl-2-oxovaleric acid causes primary sclerosing cholangitis, a disease characterized by inflammation of bile ducts that

Valeric acid is a fatty acid that is used in the manufacture of polymers. Valeric acid can be synthesized from caproic acid, which is found in palm oil and coconut oil. Valeric acid has been shown to inhibit the activity of nicotinic acetylcholine receptors at low concentrations and to have an inhibitory effect on the ryanodine receptor at high concentrations. Valeric acid also has a matrix effect on analytical methods such as gas-liquid chromatography, which has been modeled using polymer compositions.

L-Aspartic acid alpha-tert-butyl ester is a synthetic amino acid that can be used as a substrate for the synthesis of L-cysteine in the presence of selenomethionine. This compound is an auxotroph and cannot be synthesized by the body, so it must be obtained through diet or supplementation. It has been shown to have anti-cancer properties, which may be due to its role in regulating cell proliferation, apoptosis, and angiogenesis. L-Aspartic acid alpha-tert-butyl ester may also inhibit colon cancer cells by preventing them from recycling proteins. This compound was shown to inhibit HCT116 human colon cancer cells in both experimentally and computationally studies. Additionally, this molecule was seen to induce tumor regression in mice with colitis by inhibiting eukaryotic protein synthesis. This inhibition was found to be mediated through a trifluoromethyl group on the molecule's

2-Bromo-3'-hydroxyacetophenone is a molecule that has been shown to be cytotoxic and effective in inhibiting the growth of cancer cells. 2-Bromo-3'-hydroxyacetophenone inhibits the production of kynurenine, an amino acid that is used in the production of proteins, by competitively binding to the enzyme IDO1. This binding prevents the conversion of tryptophan into kynurenine, leading to cell death. The cytotoxicity of 2-bromo-3'-hydroxyacetophenone was also confirmed by testing its ability to inhibit cellular interaction with human erythrocytes (blood cells) and by measuring its effects on crystallography efficiency.

单酚香气;胶粘剂;密封剂;抗氧化剂;消毒剂

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

Please enquire for more information about Tadalafil impurity B including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-(4-Chlorophenyl)glutaric acid is a subunit of lanthanide complexes. It has been synthesized from cinchona alkaloids and single-crystal x-ray diffraction data obtained in the absence of ligands. 3-(4-Chlorophenyl)glutaric acid is a desymmetrization reagent and has been shown to be an effective ligand for lanthanide complexes. This compound has the potential to form impurities during the synthesis process, which can lead to morphological changes, luminescence, or high-performance liquid chromatography interference.

Please enquire for more information about Ibuprofen Sorbitol Ester - (Mixture of Diastereomers) including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about rec Human Growth Hormone (expressed in E.coli) including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-(4-Nitrophenoxy)aniline is a synthetic drug that is used as a substrate for the cytochrome P450 system. It has been shown to be metabolized by the liver in two steps, forming reduction products and interacting with thiourea. This drug also has functional groups which are active in the group p2 of the periodic table, such as diphenyl ethers and aminophenols. 4-(4-Nitrophenoxy)aniline can be used to probe the interaction between an enzyme and its substrate.

2-Naphthol is an organic compound with the chemical formula C10H7O. It is a derivative of naphthalene, and is produced by the condensation of two molecules of malonic acid in the presence of a reducing agent such as sodium borohydride. 2-Naphthol is used as a pesticide and as a chemical intermediate in the production of other chemicals. 2-Naphthol has been shown to be toxic to humans and animals; it may cause liver damage, kidney damage, and skin irritation. The acute oral LD50 for rats is 690 mg/kg body weight. 2-Naphthol binds to cell receptors that are involved in a variety of physiological processes including heme transport, phagocytosis, oxidative burst, chemotaxis, and respiratory burst. This binding inhibits these functions leading to cell death.