Hétérocycles soufrés (S)

Please enquire for more information about 5-Acetyl-4-bromothiophen-2-boronic acid 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-Amino-6-tert-butyl-N-(2-methoxyphenyl)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Acetylthiophene is an organic compound with the chemical formula CH3C6H2S. It is a white solid that is soluble in water and alcohols, but not in ethers or chloroform. 3-Acetylthiophene has been shown to inhibit cell growth through competitive inhibition of the cationic surfactant cetrimide, which blocks the formation of micelles and destabilizes the cell membrane. This process causes DNA oxidation and leads to the production of reactive oxygen species such as hydrogen peroxide. 3-Acetylthiophene also inhibits metal ion-catalyzed reactions by competing with them for binding sites on functional groups.

Please enquire for more information about Methyl 2-amino-5-ethyl-4-phenylthiophene-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Methoxythiophenol is a reactive oxygen species (ROS) that is produced by the interaction of hydroxyl groups with an intramolecular hydrogen. It has been shown to have cytotoxic effects in tissues and has been used as an experimental treatment for cancer. The compound also functions as an antioxidant, which prevents the oxidation of other molecules. 2-Methoxythiophenol can also be used to prevent damage caused by ROS in animals. 2-Methoxythiophenol may cleave bonds, such as those found between gold nanoparticles and acetonitrile molecules. This reaction yields active oxygen, which can be used to produce radicals that are highly reactive and able to oxidize organic materials or bond with protonated molecules, leading to their destruction.

Please enquire for more information about Methyl 2-amino-4,5,6,7,8,9-hexahydrocycloocta[b]thiophene-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

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.

3-Heptylthiophene is a building block for organic synthesis. It can be converted to thiophene-3-carboxylic acid, which can be used to synthesize polymers and other organic materials. 3-Heptylthiophene has been shown to have optical properties such as spin resonance, techniques such as gel permeation chromatography, and x-ray diffraction study. This compound has also been shown to be soluble in organic solvents such as chloroform and carbon nanotube. 3-Heptylthiophene is also a low molecular weight compound with a melting point of 130 degrees Celsius.

Please enquire for more information about 2-Amino-6-(1,1-dimethylpropyl)-N-phenyl-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide 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-Chlorothiophen-3-boronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

2,3,5,6-Tetrabromo-thieno[3,2-b]thiophene is a processable brominated polymeric material that can be used in transistors and other electronic devices. It has been shown to be suitable for use in the fabrication of organic field effect transistors (OFETs) with good performance characteristics. 2,3,5,6-Tetrabromo-thieno[3,2-b]thiophene has been successfully synthesized by a variety of routes including the addition of bromine to thiophene followed by quaternization with dialkyl halides or diketones. This compound has also been used as an ingredient in copolymers such as poly(thiophene-2,5-diyl)-co-(poly(ethylene glycol)) and poly(ethynyl methacrylate).

Please enquire for more information about N-(3-Aminophenyl)thiophene-2-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

RITA is a novel compound that has been shown to have anticancer activity in vivo in a rat model. RITA is a small molecule with high potency and low toxicity. It binds selectively to the α subunit of the enzyme topoisomerase II, which is involved in DNA replication and repair. RITA has been shown to induce apoptosis in cancer cells by pro-apoptotic proteins such as Bax and Bak. These proteins are known for their ability to induce apoptosis by increasing mitochondrial membrane permeability, inhibiting mitochondrial functions, or destabilizing the mitochondrial membrane potential. The compound class of RITA is not yet known, but it has been shown to be chemically stable at physiological pH levels and does not require metabolic activation for its cytotoxicity. The pharmacokinetics of this drug have also been studied in human liver cells and humans, indicating that this drug may be able to cross the blood-brain barrier.