Composés polycycliques

1H-Indazole-5-boronic acid is a potent compound that belongs to the class of indazole compounds. It has been shown to inhibit protein phosphorylation and induce morphological changes in cells. This compound also inhibits the activity of a number of different cellular enzymes, including protein phosphatases, protein kinases, and protein tyrosine phosphatases. 1H-Indazole-5-boronic acid has been shown to be a promising lead compound for the discovery of novel inhibitors of these enzymes.

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Applications 2-(Chloroacetyl)isoindoline was used in the reaction with potassium thiocyanate to synthesize N-​(α-​Thiocyanatoacetyl)​indolines, which is useful as agricultural fungicides. References Richter, S.: U.S. (1975), US 3929830 A 19751230.

Applications 3-(quinolin-2-yl)propanoic acid (cas# 39111-94-9) is a useful research chemical for biological study. In particular it has been used in identifying structure-activity relationship of HDAC6 zinc-finger ubiquitin binding domain inhibitors. References Ferreira, F., et al.: J. Med. Chem, 61, 4517 (2018)

Applications Indole analogue; shows pharmacological activity. References Mohammadi, M., et al.: Science, 276, 955 (1997), Bramson, H., et al.: J. Med. Chem., 44, 4339 (2001), Lane, M., et al.: Cancer Res., 61, 6170 (2001), Yu, B., et al.: Biochem. Pharmacol., 64, 1091 (2002),

Phenanthrenequinone is a redox potential inhibitor that binds to the catalytic site of the enzyme. It is an inhibitor with a redox potential of -0.4 V (vs Ag/AgCl). Phenanthrenequinone has been shown to be toxicologically safe in human serum and has no carcinogenic potential. The reaction mechanism is not well understood, but it may be due to hydrogen bonding interactions with the enzyme active site.

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2-Amino-1H-isoindole-1,3(2H)-dione is a reactive compound that can be prepared by the reaction of sodium salts with aniline. It is a valuable intermediate used in the synthesis of various organic compounds. The 2-Amino-1H-isoindole-1,3(2H)-dione molecule has two functional groups: sulfoxide and aziridino. This compound exhibits anticancer activity against carcinoma cell lines. It also has been shown to repair genes damaged by cancer cells and inhibit their growth.

The optimal reaction conditions for the acylation of 5-bromoindole with 2,2,2-trichloroethyl chloroformate are a mixture of methanol and sodium hydroxide solution. Reaction products include 2-chloro-5-(trichloromethyl)quinoline and the quinoline derivative 1-(2,2,2-trichloroethyl)-1H-imidazole. UV absorption spectra of these products have been recorded in the range of 200 to 400 nm. The reaction is successfully monitored by following changes in the NMR spectrum. The liquid chromatography method is based on a reverse phase column and detection at 220 nm.

8-Methyl-isoquinoline (8MI) is a chiral molecule that has two different enantiomers, the R and S forms. The R form is optically active and the S form is not. 8MI has been shown to have a regioselective reaction with acidic solutes in the presence of aluminum oxide. When exposed to an acidic environment, 8MI reacts in an atropisomeric fashion and forms benzyne. This reaction occurs when 8MI dissolves in water or alcohols. In addition, 8MI has been shown to have triazine properties due to its three alkyl groups on the benzene ring.

6-Nitroindazole is an antibacterial agent that inhibits the growth of bacteria by binding to bacterial DNA and blocking DNA synthesis. 6-Nitroindazole has been shown to induce tumor cell apoptosis in mouse cancer models. This drug also has anti-inflammatory properties, as it inhibits prostaglandin synthesis by inhibiting cyclooxygenase activity.

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Applications 3-Azabicyclo[3.3.0]octane Hydrochloride is a reactant in the preparation of substituted pyrimidines derivatives as novel hedgehog signaling pathway inhibitors. References Xin, M. et al.: Med. Chem. Res., 23, 3784 (2014); Xin, M. et al.: Bioorg. Med. Chem. Lett., 24, 983 (2014);

6-Hydroxy-4-methylcoumarin is a chemical compound that serves as a lactone derivative. It is commonly derived from synthetic sources through various organic reactions involving resorcinol and ethyl acetoacetate. The compound functions primarily through its ability to absorb ultraviolet light and fluoresce, making it highly valuable in spectroscopic analyses. This compound finds extensive applications in chemical and biological research. Its fluorescent properties are exploited in the development of various assays, including enzyme activity studies and cellular imaging. Additionally, 6-hydroxy-4-methylcoumarin can be used as a starting material for synthesizing more complex coumarin-based molecules, which may serve diverse roles such as anticoagulants or other pharmaceutical agents. Researchers also explore its potential antioxidant and antimicrobial activities, contributing to the study of oxidative stress and microbial resistance mechanisms. Overall, 6-hydroxy-4-methylcoumarin is a crucial tool in scientific investigation, providing insights into molecular interactions and enabling the development of novel therapeutic compounds.

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Oxypeucedanin hydrate acetate is a furanocoumarin, primarily classified as a phytochemical. It is derived from various plant sources, particularly from species in the Apiaceae family, such as Peucedanum and Angelica. These compounds are typically isolated through advanced extraction and chromatographic techniques. The mode of action of oxypeucedanin hydrate acetate involves the inhibition of cytochrome P450 enzymes, which play a pivotal role in the metabolism of drugs within the liver. This compound can influence the pharmacokinetics of co-administered pharmaceuticals and is thereby of significant interest to pharmacologists and toxicologists. In research, oxypeucedanin hydrate acetate has been investigated for its potential applications in cancer therapy, owing to its ability to induce apoptosis in certain cancer cell lines. Additionally, it is studied for its antimicrobial properties and its role in modulating cellular oxidative stress responses. These attributes make it a valuable subject in the exploration of new therapeutic agents and in understanding herb-drug interactions within complex biological systems.

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L-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid is a structural formula for an organic compound. It is produced by the biotransformations of several medicines and solutes. A chemoenzymatic process was used to produce L-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid. This reaction yielded 0.03 grams in 2 hours at a temperature of 50 degrees Celsius with a refluxing system. The diameter of the particles produced was 1 micrometer and it had an organic chemist particle size distribution that ranged from 0.1 to 20 micrometers. L-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid is used as a reagent in chromatographic reactions.

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Gatifloxacin intermediate

4-(2-Pyridyl)imidazole is an imidazole with two pyridine rings. It is a weak chelating agent that forms complexes with metal ions, such as copper and iron. The enthalpy of the reaction between 4-(2-pyridyl)imidazole and copper(II) ion was determined calorimetrically using a stepwise method. The enthalpy of the reaction between 4-(2-pyridyl)imidazole and iron(III) ion was determined by calorimetric studies. The structure of 4-(2-pyridyl)imidazole was confirmed by X-ray crystallography.