Heterocycles with Sulphur (S)

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3-acetylbenzo[b]thiophene is an isomeric molecule that has been shown to inhibit the reuptake of dopamine by binding to the dopamine transporter. It has a high affinity for the dopamine transporter, and has been shown to be selective for this receptor. 3-acetylbenzo[b]thiophene is not toxic in mice at doses up to 150 mg/kg, and has a safety profile similar to placebo. This drug can be administered orally, which makes it more convenient than other drugs with similar pharmacokinetic properties (e.g., amphetamine). The optical properties of this compound make it suitable for confocal microscopy. 3-acetylbenzo[b]thiophene also reacts with camphor, a chemical in plants such as cinnamon and bay leaves, with photoexcited fluorescence and chemoenzymatic reactions.

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3,4-Dichlorothiophenol is a chemical compound that belongs to the group of reactive compounds. It can be used as a chemical intermediate for the synthesis of other organic compounds. 3,4-Dichlorothiophenol is an inhibitor of methylating enzymes such as glyoxalase I and II and glyceraldehyde-3-phosphate dehydrogenase. This inhibition leads to the accumulation of methylglyoxal and 3-deoxyglucosone in cells, which are potent inhibitors of protein glycosylation. 3,4-Dichlorothiophenol also inhibits nucleophilic attack on DNA by epoxide hydrolases such as epoxide hydrolase 1 and 2. This inhibition results in the accumulation of reactive metabolites that are covalently adducted with DNA bases.

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Please enquire for more information about Ethyl 2-amino-4-(3,4-dichlorophenyl)thiophene-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 4-Chlorothiophen-2-boronic acid, pinacol ester 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-Amino-4-(4-Fluorophenyl)thiophene-3-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Pentylthiophene is a synthetic compound that has been shown to have magnetic properties. It can be extracted from a sample using solid phase microextraction techniques. 3-Pentylthiophene can be analyzed by optical techniques, such as infrared spectroscopy, ultraviolet spectroscopy and fluorescence spectroscopy. This compound can also be analyzed by ionizing techniques, such as electron spin resonance (ESR) and nuclear magnetic resonance (NMR). 3-Pentylthiophene is soluble in organic solvents and has an optimum temperature of 50°C. It is a light blue solid with a melting point of -37°C. The compound has optical properties that are polychromatic, with peaks at 290 nm and 310 nm.

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Please enquire for more information about 1-Boc-4-(carboxythiophen-2-yl-methyl)-[1,4]diazepane including the price, delivery time and more detailed product information at the technical inquiry form on this page

Oripavine is a naturally occurring alkaloid that can be synthesized from 2,2-bromoethane and potassium carbonate. It has been used for the treatment of Parkinson's disease. Oripavine is an intermediate in the synthesis of rotigotine, a dopamine agonist used to treat Parkinson's disease. The reaction mechanism involves the addition of bromine to 2,2-bromoethane followed by hydrochloric acid treatment to form oripavine. The reaction proceeds with the formation of hydrogen chloride and potassium bromide. The product can then be reacted with a Grignard reagent or allyl group to produce rotigotine.

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

Please enquire for more information about (2E)-3-[2,2'-Bithiophen]-5-yl-2-cyano-2-propenoic 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-methyl-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 7-Methyl-4,5-dihydrothieno[2,3-e][1]benzothiophene-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Methyl3-methylthiophene-2-carboxylate is a nicotinic acetylcholine receptor agonist. It is a structural analogue of acetylcholine and has been shown to be effective in treating corneal epithelial defects caused by chemical substances. Methyl3-methylthiophene-2-carboxylate has also been shown to have anticancer activity, as well as an anti-malarial activity. The safety profile of this drug has not yet been determined.

Please enquire for more information about N-Butyloxycarbonyl-3-[7-(imidazol-1-ylmethyl)indan-4-yl]-5-isobutylthiophene-2-sulfonamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

2,5-Bis(5-tert-butyl-2-benzoxazolyl)thiophene (purified by sublimation) is a high purity compound that is used primarily as a precursor to make other chemicals. It can be used to form polymers and cationic surfactants. 2,5-Bis(5-tert-butyl-2-benzoxazolyl)thiophene (purified by sublimation) has been shown to inhibit the activity of enzymes such as fatty acid synthase and lipoxygenase. The inhibition of these enzymes leads to the suppression of inflammatory responses in the body. In addition, this compound can be used in analytical methods for determining the concentration of coumarin derivatives in samples with fluorescence.

4-(Trifluoromethoxy)thiophenol is a compound that has been shown to have antioxidant properties. It has been shown to scavenge free radicals and chelate metal ions, which can be toxic to cells. 4-(Trifluoromethoxy)thiophenol has been shown to inhibit the growth of bacteria, fungi, and viruses in laboratory studies. This compound also has antimicrobial activity against methicillin-resistant Staphylococcus aureus (MRSA). The biological activity of 4-(trifluoromethoxy)thiophenol is due to its ability to cleave DNA strands by donating electrons and hydrogen atoms. 4-(Trifluoromethoxy)thiophenol also exhibits radical scavenging activity, which may be due to its ability to produce hydrogen peroxide from peroxides through a reaction with superoxide anions.

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4-Methylthiophenylboronic acid is a synthetic compound that is used as a building block in supramolecular chemistry. It has been shown to inhibit the growth of cancer cells and has been used in the synthesis of selenium compounds that have anticancer activity. The conductances of 4-methylthiophenylboronic acid have been studied in detail, and it was found to be a molecule with an unusual structure. This molecule has also been found to bind to chloride ions, making it useful in controlling the pH of water. 4-Methylthiophenylboronic acid is also an effective inhibitor of COX-2, which may lead to its use as a treatment for inflammatory diseases such as arthritis.

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Methyl 2-amino-4-ethyl-5-methylthiophene-3-carboxylate is a potential pharmacokinetic. It has been shown to have a good pharmacokinetic profile and an allosteric modulator activity in vitro. Methyl 2-amino-4-ethyl-5-methylthiophene-3-carboxylate can bind to the cannabinoid receptor type 1 (CB1), which is a G protein coupled receptor that inhibits cAMP production. This may lead to agonism of the CB1 receptor, which could be useful for treatments of pain, inflammation, or mood disorders.

Please enquire for more information about 4,6-Dihydrothieno[3,4-b]thiophene-2-carboxylic Acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Applications 5-Bromo-2-thiophenecarboxaldehyde is used in biological studies as anti-inflammatory and anti-tumor activity of the marine mangrove Rhizophora apiculata. References Prabhu, V.V., et al.: J. Immunotoxicol., 9, 341 (2012);

2-Ethynyl-3-hexylthiophene is a terminal organic molecule. It has the ability to catalyze cross-coupling reactions, which are stepwise reactions that involve the coupling of two or more electrophiles with an electron donor. 2-Ethynyl-3-hexylthiophene can catalyze the reaction of amines and halides in the presence of organometallic reagents such as phosphines and hydrocarbon groups. In these reactions, the hydrogen atom of an amine is replaced by a halide. The product can be obtained in high yield through electrochemical studies. 2-Ethynyl-3-hexylthiophene also has the ability to couple with sulfoxides. This reaction is irreversible and it is not possible to synthesize this compound from its components.

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5-Morpholin-4-ylthiophene-2-carbaldehyde (MT) is a novel anticancer agent that has been shown to have potent cytotoxicity against cancer cells. It interacts with the cancer cell membrane, which results in the disruption of the membrane and leads to the release of cytochrome C from the mitochondria into the cytosol. MT also inhibits tumor growth by inhibiting protein synthesis and inducing apoptosis. MT has been shown to be effective against breast adenocarcinoma in animal studies and human cancer cell lines in vitro. This drug has also been found to have a synergistic effect when used with tamoxifen for breast cancer treatment.

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Benzo[b]thiophene-2-carboxaldehyde is a compound that has optical properties with a dihedral angle of 90°. This compound also has a functional group of imine, which can be found in the amino acid histidine. Benzo[b]thiophene-2-carboxaldehyde has been shown to have cancer inhibiting properties by targeting the protease activity of at1 receptors. It inhibits the synthesis of protein and RNA by binding to them and preventing their production. This compound also inhibits the activity of proteases, which are enzymes that break down proteins. Benzo[b]thiophene-2-carboxaldehyde is synthesized through metathesis reactions, which are reactions that involve the exchange of atoms between two compounds. The yield is isolated at about 95%.

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2-(2-Nitroanilino)-5-methylthiophene-3-carbonitrile is a crystalline compound that belongs to the group of small molecules. It has a molecular weight of 153.2 g/mol and a melting point of 281 °C. The compound has three different crystalline forms, including a monoclinic form, which is thermodynamically stable at room temperature. 2-(2-Nitroanilino)-5-methylthiophene-3-carbonitrile can be used as a model system for studying influenza virus and as an inhibitor of influenza virus replication. 2-(2-Nitroanilino)-5-methylthiophene-3-carbonitrile also inhibits the activity of carbamazepine, which is an anti epileptic drug, by binding to its active site on the molecule.

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