Polycyclic Compounds

Please enquire for more information about 7-Chloro-2-(2,4-dimethylphenyl)-8-methylquinoline-4-carbonyl chloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications 5-Fluoroindole-3-butyric Acid is used in preparation of Aminochroman and Aminotetralin derivatives, which are useful in the treatment of serotonin-mediated disorders. References Hatzenbuhler, N., et al.: PCT Int. Appl., (2005);

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Please enquire for more information about tert-Butyl 6-bromo-1-oxo-3,4-dihydroisoquinoline-2(1H)-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Lactone

Please enquire for more information about 5,5'-Bis(trifluoromethyl)-2,2'-bipyridyl 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-Chloro-7-methyl-3-(5-methyl-1,2,4-oxadiazol-3-yl)quinoline including the price, delivery time and more detailed product information at the technical inquiry form on this page

(±)-Decursinol (3',4'-dihydro-3'-hydroxy-Xanthyletin) is a natural product from Angelica gigas.

Please enquire for more information about 1-Acetyl-6-nitro-1,2,3,4-tetrahydroquinoline including the price, delivery time and more detailed product information at the technical inquiry form on this page

In this experimental study, 7-Bromo-5-methylindoline-2,3-dione has been shown to interact with a square of rotations. It was found that 7-Bromo-5-methylindoline-2,3-dione interacts with the square in a monolithic way. The experimental study showed that the molecule is not affected by the rotation and is unaffected by the shape of the square.

Please enquire for more information about Methyl 7-cyclopropyl-1-ethyl-2-mercapto-4-oxo-1,4-dihydropyrido[2,3-d]pyrimidine-5-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 8-Bromoquinoline-3-carboxylic 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 tert-Butyl 6-(hydroxymethyl)-1H-indole-1-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

N-Formylindoline is an organic compound that reacts with formamide in the presence of a strong acid to produce N-formylglycine. It can be used as a formylating agent, which is a chemical compound that contains the formyl group (HC=O). This reaction occurs at room temperature and does not require an acid catalyst, unlike other reactions that form amides. Formylation is a reaction in which the formyl group replaces one or more hydrogen atoms on carbon atoms of an organic molecule. N-Formylindoline has been shown to react with tripeptides and carbon tetrachloride to produce endoplasmic reticulum peptides. The reaction system for this process includes mammalian cells and plates (96 well) for assays.

Please enquire for more information about 3-(Pyrido[2,3-e]pyrrolo[1,2-a]pyrazin-6-ylthio)propanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications 3-Amino-3-benzyl-3,4-dihydroquinolin-2(1H)-one

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Lactone

Please enquire for more information about 5-Methoxy-1H-indazole-3-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Chloropyrido[3,4-d]pyrimidine is a heterocyclic compound that belongs to the pyrimidine family. It can be synthesized by reacting 2-chloro-3-nitropyridine with potassium tert-butoxide in an aqueous solution of ethanol. 4-Chloropyrido[3,4-d]pyrimidine can be converted into other heterocycles by different methods and has been used as a synthon for many other pyrimidines. This functional group has five members, which are interconnected by single bonds and form a ring system with alternating single and double bonds. The 5 atoms of this ring system are arranged in the shape of a pyramid (trigonal). There are two isomers: 4-(2,6) and 4-(2,5).

2-[3-(S)-[3-(2-(7-Chloro-2-quinolinyl)ethenyl)phenyl]-3-hydroxypropyl]benzoic acid methyl ester is a synthetic compound that can be used as a reagent in the synthesis of polynucleotides and polypeptides. It can also be used as an inhibitor of ketoreductase, which is an enzyme involved in the synthesis of fatty acids and ketones. 2-[3-(S)-[3-(2-(7-Chloro-2-quinolinyl)ethenyl)phenyl]-3-hydroxypropyl]benzoic acid methyl ester has been shown to inhibit the growth of wild type and mutant strains of E. coli. The molecular weight of this compound is 439.

Please enquire for more information about 1-Benzyl-3-hydroxy-1H-indazole sodium salt including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Isoquinoline-7-carboxylicacid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Borabicyclo[3.3.1]nonane is a functional group that has been used in the synthesis of α-pinene and other terpenoids. Borabicyclo[3.3.1]nonane can be synthesized by reacting α-pinene with methoxy groups and amines at high temperatures in the presence of a catalyst, such as boron trifluoride etherate. The reaction mechanism involves an elimination reaction followed by an addition reaction to form a lactam ring, which is then hydrolyzed to release 9-borabicyclo[3.3.1]nonane. This functional group has been used for the synthesis of α-pinene, which is a monoterpene found in pine needles and oil from turpentine trees, among other sources. The structural analysis shows that these molecules are linear chains with reactive sp2 hybridized carbons and hydroxyl groups on one end and alk

Please enquire for more information about 4-Chloro-2,6-bis(trifluoromethyl)quinoline including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications 6-Chloro-4-(2-cyclopropylethynyl)-3,4-dihydro-3-(phenylsulfonyl)-4-(trifluoromethyl)-2(1H)-quinolinone is an intermediate in the synthesis of novel quinolinones as HIV-1 reverse transcriptase inhibitors. References Patel, M., et al.: Bioorg. Med. Chem. Lett., 11, 1943 (2001);

Please enquire for more information about 5-Methoxy-1,2,3,4-tetrahydroquinoline 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 2-(3-Morpholin-4-ylpropyl)-1-oxo-1,2,3,4,5,6-hexahydro-3a,5-epoxyisoindole-7-carboxylic 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 1-(Methylsulfonyl)indoline-5-carboxylic 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 1-Ethyl-3,4,5,6-tetrahydro-1H-azepino[5,4,3-cd]indole including the price, delivery time and more detailed product information at the technical inquiry form on this page

Indoline-2-carboxylic acid is a photophysical molecule with an absorption maximum at 518 nm. It has been shown to inhibit the activity of enzymes such as cyclooxygenase, lipoxygenase, and monoamine oxidases. This compound has been found to be effective in the treatment of cancer cells. Indoline-2-carboxylic acid is also used in pharmaceutical preparations, where it binds to enantiomers of other molecules and inhibits their biological activity. Indoline-2-carboxylic acid reacts with hydrochloric acid to form allyl carbonate and amide.

Please enquire for more information about Methyl 3-formyl-6-methyl-1-(4-vinylbenzyl)-1H-indole-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Aminoquinoline-2-one is a nonsteroidal anti-inflammatory drug that has tuberculostatic activity. It binds to the nitrogen atoms of the enzyme dihydropteroate synthase, which is involved in the synthesis of folic acid and DNA. This leads to an increase in reactive oxygen species and inflammation, which causes disease activity. 4-Aminoquinoline-2-one has been shown to be synergistic with monoclonal antibodies when used as a treatment for inflammatory diseases. In order for 4-aminoquinoline-2-one to be taken up by cells, it must bind to cellular uptake proteins through hydrogen bonds or disulfide bonds.

Please enquire for more information about 7-Amino-1(2h)-isoquinolinone including the price, delivery time and more detailed product information at the technical inquiry form on this page

(9R,11S,14S,16R,17R)-6,6,9-Trifluoro-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl-8,11,12,14,15,16-hexahydro-7H-cyclopenta[a]phenanthrene 3-one is a congestive heart failure drug that belongs to the group of cardiotonic drugs. It has high resistance to elution and is used in the diagnosis of autoimmune diseases. (9R,11S) 6-(1′Hexahydrocyclohexa[b]pyrrolo[2′1′b]indolizinium bromide) is a nitrogenous compound that has been employed as a pharmaceutical preparation for the treatment of cardiac disorders. The biological properties of (9R) 11-(2′Hydroxyacetyl

Please enquire for more information about (R)-1,2,3,4-Tetrahydro-3-isoquinolinecarboxylic acid methyl ester hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Aminoquinoline is a chemical compound that inhibits the activity of the epidermal growth factor receptor (EGFR). It is a potent inhibitor of cell proliferation and has been shown to have antitumour activity. 3-Aminoquinoline has been shown to inhibit the proliferation of carcinoma cell lines. This drug binds to the EGFR receptor, preventing it from activating downstream signalling pathways that control cell growth. 3-Aminoquinoline also has biological properties, including matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, analytical chemistry, sample preparation, and Suzuki coupling reaction. The molecule is structurally analyzed using chemical structures and structural analysis techniques such as thermodynamic data or proton NMR spectroscopy. 3-Aminoquinoline also interacts with sugars through hydrogen bonding and oligosaccharides. These interactions are found to be high in value in some cases.

Please enquire for more information about 1-Isobutyrylindoline-5-carboxylic 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 3-(Pyrrolidin-1-ylcarbonyl)quinolin-2-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-Bromo-7-methyl-1H-indole-2,3-dione is a lead compound that inhibits the inosine monophosphate (IMP) deaminase enzyme. This compound is an inhibitor of the IMP deaminase enzyme and has been shown to reduce viral load in HIV patients. 5-Bromo-7-methyl-1H-indole-2,3-dione has been studied as a potential treatment for other diseases such as mycophenolic acid renal toxicity and inflammatory bowel disease. This molecule is a regiospecific inhibitor of the IMPDE4 protein with IC50 values of 0.5 μM and 2 μM for the wild type and mutant forms respectively.

Please enquire for more information about 4,4'-Dithio-2,2'-bipyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 8-Methyl-2-(4-methylphenyl)quinoline-4-carboxylic 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 8-N-Boc 2-Oxo-8-Azabicyclo[3.2.1]Octane-6-Carboxylic Acid Methyl 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 (R)-2-Tetrahydroisoquinoline acetic acid hydrochloride 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 (6-Methyl-5-quinolinyl)boronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Phenylpyrazole is a phenylpyrazole compound that binds to the GABA receptor, which is a ligand-gated ion channel and chloride channel. 3-Phenylpyrazole has been shown to bind to the human serum albumin as well as nitrogen atoms in the ryanodine receptor. In vitro assays have been used for light emission and gamma-aminobutyric acid assay, showing that it can be used in insect resistance. It has also been shown to inhibit acute toxicities such as hydrogen bond binding, bound form and matrix effect.

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2-Bromopurine is an analog of the naturally occurring purine, adenine. It has been shown to be a potent inhibitor of DNA synthesis in both bacterial and mammalian cells. 2-Bromopurine has been shown to react with hydrophobic amino acids, such as methionine and tryptophan, in proteins to form crosslinks that inhibit protein synthesis. 2-Bromopurine is effective against tuberculosis and has been used for the treatment of this disease since the 1950s.

1,2,3,4-Tetrahydropyrido[2,3-b]pyrazine is a ligand that binds to the h3 receptors of the brain. It has been shown that this ligand inhibits the chloride channel in animals and humans. 1,2,3,4-Tetrahydropyrido[2,3-b]pyrazine is used as a starting material for the synthesis of other ligands with different chemical groups. It can be synthesized by reacting 2-chloroethyl nitrobenzene with ethyl acetate and hydrochloric acid.

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Phenanthrene-2-carbaldehyde is a linear range aromatic hydrocarbon. It is used in the manufacture of dyes, pharmaceuticals, and pesticides. It has been detected in environmental pollutants such as diesel exhaust and cigarette smoke. Phenanthrene-2-carbaldehyde has been found to be homologous to other phenanthrene derivatives with respect to its chemical structure and toxicity. It has been shown to cause dyslipidemia and increase urinary creatinine levels.

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