Composti policiclici

5,6-Dichloroisatin is an electron-deficient molecule that can be synthesized by the reaction of isatin with dichloroacetic acid in the presence of a base. This compound has been shown to have regiospecificity and yields depending on the conditions used during its synthesis. 5,6-Dichloroisatin is a precursor for many compounds including isatins and other intermediates.

Imperatorin is a furanocoumarin compound, which is a natural product primarily isolated from plants in the Apiaceae family, such as Angelica dahurica and Citrus species. This compound is characterized by its unique chemical structure that includes a furan ring fused to a coumarin backbone. Imperatorin exerts its biological activities through multiple modes of action, including the modulation of enzymatic activity, interference with cellular signaling pathways, and binding to specific biological targets.

Indole-5-carboxylic acid ethyl ester is a formamide activated analog of piperidine. It is an effective antibacterial agent against Staphylococcus aureus. Indole-5-carboxylic acid ethyl ester inhibits the growth of bacteria by binding to the extracellular surface and interfering with cell membrane permeability. The compound also has anti-cancer properties, and may be used in pharmaceuticals as a pyrazole derivative.

1-Benzyl-1H-indole-2-carboxylic acid is a molecule that binds to chemokine receptors and has been used in screening assays as a chemical probe of chemokine receptor binding. It has been shown to be an antagonist of the CXCR3 receptor, with high affinity and selectivity. 1-Benzyl-1H-indole-2-carboxylic acid is also an antagonist of the CCR5 receptor, with low affinity. This compound was discovered by screening for novel antagonists of chemokines.

7-[(Dimethylamino)methyl]-2,2,4-trimethyl-1,2-dihydroquinolin-6-ol is a chemical compound that belongs to the group of fine chemicals. It is a versatile building block and useful intermediate for research chemicals. 7-[(Dimethylamino)methyl]-2,2,4-trimethyl-1,2-dihydroquinolin-6-ol is also a speciality chemical with high purity and quality. CAS No. 300690-44-2

Noreleagnine is a natural compound that is used to inhibit the replication of viruses. It has been shown to bind to dopamine receptors in the brain, which may be responsible for its cytotoxic effects on mouse tumor cells. Noreleagnine can also be used as a sample preparation agent because it can produce light emission and biological properties that are similar to those of dopamine. This drug is synthesized using an asymmetric synthesis and sodium carbonate. A number of methods have been developed for the synthesis of noreleagnine, including ester hydrochloride and electrochemical detector.

Indole-3-acetone is a nitrogen nucleophile that has been used in the synthesis of amino acids. Indole-3-acetone has also been shown to inhibit the oxidation of primary amines and chloride by oxidases, which play a role in the physiology of plants. It also inhibits hydroxylase and pyrylium, which are enzymes involved in plant metabolism. Indole-3-acetone is found in dietary sources such as cabbage, cauliflower, celery, and spinach.

7-Deazaxanthine is a purine derivative that has been shown to have antiangiogenic properties. It inhibits the growth of cancer cells by inhibiting the synthesis of vascular endothelial growth factor (VEGF), which is a potent angiogenic factor. 7-Deazaxanthine also binds to the VEGF receptor, preventing it from binding to VEGF. The x-ray crystal structures and kinetic data for 7-deazaadenosine suggest that this compound may be an inhibitor of hydrogen bonding interactions between amino acids in protein molecules, leading to its antiangiogenic activity. 7-Deazaxanthine does not prevent the activation of tyrosine kinases or phosphatases. In addition, this compound has been shown to inhibit the proliferation of breast cancer cells in culture and in vivo studies using mouse models. This drug also has glycosidic bond, which can result in a variety of chemical structures due to different types of glycos

5-Benzyloxyindole-3-glyoxylamide is a versatile building block that can be used in the synthesis of complex compounds. It has been shown to have a high quality and is useful as a reagent for research purposes. 5-Benzyloxyindole-3-glyoxylamide can be used as a reaction component and is useful as an intermediate in organic synthesis. 5BIGA has CAS number 22424-62-0 and is also known as 3-(benzyloxy)-5-(2,2,2-trifluoroethoxy)indole glyoxamide.

Please enquire for more information about 3-(3,4-dimethoxyphenyl)-4-(hydroxyimino)-1,6,6-trimethyl-5,6,7-trihydro1H-indazole including the price, delivery time and more detailed product information at the technical inquiry form on this page

6-Bromoindole-2-carboxylic acid is a useful building block that can be used in the synthesis of complex compounds. This chemical is also a versatile intermediate for research chemicals and pharmaceuticals. 6-Bromoindole-2-carboxylic acid is often used as a reaction component for organic syntheses, such as the manufacture of reagents and other specialty chemicals.

2-Methylindole is a reactive molecule that can undergo electrophilic substitution at the 2-position. It reacts with a variety of nitrogen nucleophiles, acylating them at the 2-position. These reactions are catalyzed by enzymes such as carbonyl reductase and methyl ketone reductase. The reaction mechanism is not yet fully understood, but it has been proposed that it proceeds through an acylation reaction between two molecules of 2-methylindole to form a linear product. The regiospecificity of this reaction has been demonstrated in vivo using a model system.

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7-Methylindole-3-acetic acid is a metabolite of indomethacin. It is excreted in the urine and has been found to be present in the tissues of monkeys. 7-Methylindole-3-acetic acid is excreted by the kidneys and it is not known how much of this compound is reabsorbed into the body. 7-Methylindole-3-acetic acid can be metabolized to form other metabolites, including 2,4,5,6 tetrahydropyridine (2,4,5,6 THP), which has been shown to produce DNA damage in rats. The metabolites are then excreted from the body through urination and feces.

Ethyl 2-hydroxy-5,6,7,8-tetrahydroquinoline-3-carboxylate is a fine chemical that is used as a building block in the manufacture of other compounds. It is also used as a reagent and speciality chemical. Ethyl 2-hydroxy-5,6,7,8-tetrahydroquinoline-3-carboxylate is an intermediate that can be used to produce other compounds. It can be used as a reaction component or useful scaffold for complex molecules.

9-Fluoro-10,13,17-Trimethyl-2,3,4,5,6,7,8,11,12,14,15,16-Dodecahydro-1H-Cyclopenta[a]Phenanthrene-3,11,17-Triol is a synthetic nucleic acid molecule that can be used for diagnostic purposes. It has been shown to bind to the nucleic acid of human cells. This nucleic acid binds to the antibodies in order to detect and identify different types of RNA sequences. 9F18TMTD has also been shown to target specific sites on the DNA molecule and can be used as a probe for detecting specific sequences of DNA. The synthetic process starts by reacting an aromatic compound with methanol in the presence of a base catalyst to form an intermediate product. The intermediate is then oxidized with nitric acid and hydrogen peroxide in order form the final product.

3-Trichloroacetylindole is an indole derivative that is a hydrogen bond donor. It is a pharmacological agent that has been shown to have antitumor and antiproliferative activities. The crystal structure of 3-trichloroacetylindole has been determined and the interaction with solvent molecules studied. It was synthesized from indole-3-carboxylic acid, which was converted to the hemihydrate form by reacting with butyl lithium in ether. 3-Trichloroacetylindole is a 5-HT4 receptor antagonist, and it also inhibits the synthesis of serotonin and dopamine.

Diuretic; cardiac stimulant; smooth muscle relaxant; bronchodilator

Oxypeucedanin is a furanocoumarin compound, which is derived from various plant sources, most notably those in the Apiaceae family such as Peucedanum and Angelica species. It functions primarily as a photoreactive agent, capable of interacting with DNA under ultraviolet (UV) light through a process called photoactivation. Upon UV exposure, it forms covalent bonds with DNA, leading to cross-linking that can disrupt cellular functions.