Eterocicli con ossigeno (O)

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This compound is a potent and selective agonist for the human mineralocorticoid receptor (hMR). It increases the serum concentration of cortisol, which is an anti-inflammatory hormone. This agent has been shown to increase systolic pressure in humans and has been used as a research tool in the study of congestive heart failure. The nasal drug inhibits the activation of the inflammatory response by inhibiting histamine release from mast cells. Potassium [2-[3-Bromo-5-[(5-carbamoyl-4-cyclopropyl-2-ethylimidazol-1-yl)methyl]-1-benzofuran-2-yl]phenyl]-(trifluoromethylsulfonyl) azanide (CGP7930) has also been shown to be effective at increasing glomerular filtration rate and diastolic blood pressure.

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Please enquire for more information about 5-Cyanobenzofuran-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-[6-(Bis(Carboxymethyl)Amino)-5-[2-[6-(Bis(Carboxymethyl)Amino)-2,3-Difluorophenoxy]Ethoxy]-2-Benzofuran-1-Yl]-1,3-Oxazole-5-Carbox ylic Acid (CAF01) is a small molecule that has been shown to have neuroprotective effects in animal models of stroke. It prevents neuronal death by inhibiting the release of glutamate and cytosolic calcium levels. CAF01 also inhibits intracellular calcium overload and mitochondrial membrane potential. It protects cells from ischemic brain damage by maintaining the function of neurons and ATP production. CAF01 is a high resistance compound with good bioavailability in vivo.br> br> CAF01 is being developed as a treatment for stroke patients who are at high risk of recurrent stroke or death due to cerebral infar

5-(4-((3-Chloro-4-((3-fluorobenzyl)oxy)phenyl)amino)quinazolin-6-yl)furan-2-carbaldehyde is a heterocyclic compound that has been used to study protein tyrosine kinase activity. This drug binds to the active site of the enzyme and inhibits its function by forming an irreversible covalent bond with the enzyme's reactive cysteine residue, which prevents the transfer of phosphate groups from ATP to the substrate (tyrosine).

Applications (5-Amino-2-butyl-3-benzofuranyl)[4-[3-(dibutylamino)propoxy]phenyl]methanone is an intermediate used in the synthesis of dronedarone hydrochloride (I), a class III antiarrhythmia drug for the prevention of cardiac arrhythmias such as atrial fibrillation. References Mali, A. C., et al.: Org. Proc. Res. Dev., 17, 863 (2013)

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Stability Volatile Applications It is an ideal marker for detecting cigarette smoke. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Spitzer, W., et al.: Clin. Invest. Med., 13, 17 (1990), Alonso, M., et al.: Anal. Bioanal. Chem., 396, 2989 (2010),

Please enquire for more information about 2-Ethyl-3-methyl-1-benzofuran-5-amine 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-Dibenzo[b,d]furan-2-ylethyl)amine 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 4-Chloro-5-fluoro-7-(2-beta-C-methyl-beta-D-ribofuranosyl)-7H-pyrrolo[2.3-d]pyrimidine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about [(1S,2R)-3-[[(4-Nitrophenyl)sulfonyl](2-methylpropyl)amino]-2-hydroxy-1-phenylmethyl)propyl]carbamic acid, (3S)-tetrahydro-3-furanyl ester 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-(Methoxymethylene)-2(3H)-benzofuranone including the price, delivery time and more detailed product information at the technical inquiry form on this page

3H-Spiro[Isobenzofuran-1,4'-piperidine] hydrochloride is a high quality reagent that is used as a complex compound for the synthesis of various fine chemicals. It has been shown to be an excellent building block for drug discovery and development. 3H-Spiro[Isobenzofuran-1,4'-piperidine] hydrochloride is available in bulk quantities and can be shipped worldwide. This chemical is also used as a reaction component in the synthesis of various speciality chemicals. 3H-Spiro[Isobenzofuran-1,4'-piperidine] hydrochloride is versatile and can be used in reactions with different functional groups.

2-Heptylfuran (2HF) is a volatile oil that is found in many plants, animals, and foods. 2HF has been shown to have antiviral and antioxidant properties. It also has been shown to inhibit the growth of herpes simplex virus in animal models. 2HF inhibits lipid peroxidation by reacting with free radicals and other reactive oxygen species in the cell membrane and tissues. This compound also has been shown to protect against oxidative stress-induced apoptosis, which may be due to its ability to inhibit the activation of caspases 8 and 9, as well as inhibiting inflammatory cytokines such as tumor necrosis factor-α (TNF-α). 2HF may also be involved in the metabolism of fatty acids by competing with enzymes for substrate binding sites. 2HF can react with fatty acid substrates to form reaction products that are active against tumor cells and may contribute to carcinogenesis.

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Please enquire for more information about Dihydro-3-(3-pyridoyl)-2-(3H)-furanone including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications 2-Phenylfuran (cas# 17113-33-6) is a useful research chemical.

5-Phospho-beta-D-arabinofuranosyl-1-(5-fluorouracil) (5FUA) is a synthetic compound used in chemotherapy. It is the first of a new type of anticancer agent that inhibits the synthesis of RNA and DNA. 5FUA has been shown to be effective against animal tumors, but it has not been tested for use in humans. 5FUA selectively inhibits the enzyme ribonucleotide reductase, which converts ribonucleotides into deoxyribonucleotides. The resulting lack of DNA prevents cell division and leads to cell death.

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Please enquire for more information about 4-Methoxy-1-benzofuran-6-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Furan-2-boronic acid is a reaction intermediate in the Suzuki coupling reaction, which is a cross-coupling reaction between an organoboron compound and an organic electrophile. Furan-2-boronic acid can be used as a chiral auxiliary to generate optically pure products. Furan-2-boronic acid has been shown to react with amines and other activated carboxylic acids to form amides, which are bioactive molecules. Furan-2-boronic acid can also be used in asymmetric synthesis reactions. This product's fluorescence properties make it useful for detection of boronate esters and other boron compounds in biochemical studies.

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Intermediate in the synthesis of afatinib

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N-[(1S)-1-[[[(4S,7R)-Hexahydro-7-methyl-3-oxo-1-(2-pyridinylsulfonyl)-1H-azepin-4-yl]amino]carbonyl]-3-methylbutyl]-2-benzofurancarb oxamide is a drug that is used to treat bone cancer and cancer. It has been shown to have long term efficacy on the reduction of tumor size and the prevention of recurrence. The diagnostic properties of this drug are due to its ability to bind to collagen in the tumor tissue. The pharmacokinetic properties of this drug include a rapid absorption rate, low volume of distribution, high clearance rate, and a long half life. N-[(1S)-1-[[[(4S,7R)-Hexahydro-7-methyl-3-oxo-1-(2-p

Please enquire for more information about (2,5-Dimethoxy-2,5-dihydrofuran-2-yl)methanol including the price, delivery time and more detailed product information at the technical inquiry form on this page

Tetrahydro-a-(1-naphthalenylmethyl)-2-furanpropanoic Acid 2-(Diethylamino)ethyl Ester is a fatty acid analog that has antimicrobial properties. It is used in the treatment of bone cancer, and can be used to diagnose and treat other diseases such as glomerular filtration rate, receptor binding, and malonic acid. Tetrahydro-a-(1-naphthalenylmethyl)-2-furanpropanoic Acid 2-(Diethylamino)ethyl Ester binds to receptors on cells, which leads to an increase in the amount of monoamine neurotransmitters released by the cells.

Please enquire for more information about 6-[1-[(tert-Butyldimethylsilyl)oxy]ethyl]-7-oxo-3-(tetrahydro-3-furanyl)-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylicacid 2-pro penylester including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about [1,1'-Biphenyl]-4-carboxylic acid[3ar-[3aa,4a(E),5b,6aa]]-4-[4-(3-chlorophenoxy)-3-oxo-1-butenyl]hexahydro-2-oxo-2H-cyclopenta[b]fur an-5-ylester 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 4-(1-Benzofuran-2-yl)pyrimidin-2-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Methyl-1-benzofuran-2-carbohydrazide is a molecule that has been shown to inhibit the growth of bacteria by binding to their DNA. It is an analog of pyrazole and has been shown to have antimycobacterial activity against Mycobacterium tuberculosis and Mycobacterium avium complex. 3-Methyl-1-benzofuran-2-carbohydrazide inhibits bacterial growth by preventing the replication and transcription of DNA, which results in inhibition of protein synthesis. It is also used as an antibacterial agent for the treatment of tuberculosis.

6-Methoxy-3-methyl-1-benzofuran-2-carboxylic acid is an organic compound with a molecular formula of C12H8O4. It has a melting point of 207°C, and it is soluble in acetonitrile and acetone. The crystal structure for 6-methoxy-3-methylbenzofuran is shown below. The x-ray diffraction pattern for 6-methoxybenzofuran is shown below. 6 - Methoxy - 3 - methyl - 1 - benzofuran - 2 - carboxylic acid fluoresces with emission maxima at 440 nm and 459 nm in the presence of light (λ = 514 nm). The maximum solubility of the compound in solvents such as ethanol, methanol, acetone, and acetonitrile are listed below: Ethanol: 0.0359 g/L

Please enquire for more information about 5-Methyl-2-(trifluoromethyl)-3-furansulphonyl chloride 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 N,N-Diethyl-N'-[1-(7-methoxy-1-benzofuran-2-yl)ethyl]ethane-1,2-diamine including the price, delivery time and more detailed product information at the technical inquiry form on this page

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5-Amino-4-cyano-2-methyl-furan-3-carboxylic acid ethylester (5ACMC) is an amide that inhibits the growth of cancer cells. It has been shown to be active against pancreatic cancer cell lines and cancer cells from human patients. 5ACMC also inhibits lipid kinase activity and Pi3K, which are proteins involved in the formation of new blood vessels. 5ACMC has anti oncogenic properties, which may be due to its ability to inhibit the growth of cancer cells by binding to the active site of lipids kinase proteins.

2,2-Dimethyl-5-(1-methylprop-1-enyl)tetrahydrofuran is a compound that is used in coatings and foodstuff. It has synergistic effects when combined with other compounds such as citric acid, hydrogen peroxide, or terpineol.

Please enquire for more information about N-(3-Nitrodibenzo[b,d]furan-2-yl)acetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications 2-((Methyldisulfanyl)methyl)tetrahydrofuran is a useful compound in organic chemistry.

1-Methyl-2-nitro-3-(tetrahydrofuran-3-yl)methyl)guanidine (1MNTG) is a pesticide that is used to control pests. It has been shown to be highly resistant to degradation by cytochrome P450, which may cause chronic exposure and/or analytical problems. 1MNTG has also been shown to cause genetic damage in bacteria, as well as enzyme activities in the liver and kidneys of rats exposed for short periods of time. 1MNTG has been shown to be an agonist of toll-like receptor 4, which can lead to health effects such as inflammation and have been shown to affect biochemical processes in vitro.

3-Formylfuran-2-boronic acid is a molecule that can reversibly form an imine with primary amines. 3-Formyl group and fluorophore are the main features of this molecule. The fluorescent properties of 3-formyl group have been extensively studied by functional theory, structural studies and kinetic experiments. The study of these properties has led to the discovery of new fluorescent probes for use in biochemical studies. 3-Formyl furan also interacts with anthracene and other heterocycles by binding constants. These interactions were studied using quantum chemical calculations.

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6-Bromo-3H-isobenzofuran-1-one is a selective solvent that can be used to extract 5-bromophthalide from an organic reaction mixture. It is also used in the preparation of anhydrides. 6-Bromo-3H-isobenzofuran-1-one reacts with acidifying agents, such as sulfuric acid or hydrochloric acid, to produce crystalline solids. The extraction of 5-bromophthalide can be accomplished by adding a solution of the 6-bromo compound to the reaction mixture and extracting it with ether.

2-(2-Pentenyl)furan is an odoriferous compound that is found in plants, animals, and dietary products. It is a volatile compound with a strong garlic-like odor. The 2-(2-pentenyl)furan molecule consists of two isoprene units linked together by a double bond. This compound can be used as a marker for the plant species Acacia spp., which has been shown to have anti-inflammatory properties. 2-(2-Pentenyl)furan may be formed by lipid peroxidation of polyunsaturated fatty acids during the process of cooking. This process can also produce other compounds such as 4-hydroxyoctanoic acid (4HOA), 4-hydroxypentanoic acid (4HPPA), and 3,4-dihydroxypentanoic acid (3,4DHPPA). These compounds are also found in various food products such as milk, eggs,

9-(β-D-xylofuranosyl)guanine (9XG) is a trifluoride. It is an antiviral agent that inhibits the growth of herpes virus, in particular by methylating guanosine to 9-methylguanosine in the viral DNA. 9XG binds to the viral DNA and prevents its replication through the inhibition of RNA synthesis. The drug is active against many different types of viruses and has been shown to be effective against tissue cultures infected with herpes virus. 9XG is synthesized from guanosine and boron trifluoride etherate, which are reacted at -78 degrees Celsius for three days. This yields a mixture of compounds with various peracylation groups, which are then separated by chromatography.

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