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<p>5-Chloroindole-2-carboxylic acid is a fatty acid that is synthesized from glucose. It has been shown to have inhibitory properties against the enzyme cyclooxygenase-2 (COX-2), which may be due to its ability to suppress prostaglandin synthesis. 5-Chloroindole-2-carboxylic acid also has been shown to have anticancer properties and can inhibit cancer cell growth in vitro. The drug may also play a role in the central nervous system, as it has been shown to cause neuronal death. 5-Chloroindole-2-carboxylic acid is not water soluble, so it must be dissolved in organic solvents such as cyclohexane or chloroform before being used for chemical reactions. This drug can be used with other drugs that are coxib sensitive, such as aspirin, acetaminophen, and ibuprofen.</p>

<p>5-Amino-6-(methylamino)quinoline is a molecule that inhibits the enzymatic activity of tyrosine phosphatases and has been shown to inhibit the growth of typhimurium ta98, which is resistant to quinoxaline. It has also been shown to be mutagenic in vitro. 5-Amino-6-(methylamino)quinoline has an imidazole ring and is synthesized from 2-methylbenzothiazole and N,N'-dimethylethylenediamine. The synthesis of this compound takes place in two steps with the first step being an oxidative cyclization followed by a reductive amination.</p>

<p>7-Azaindole-3-carboxaldehyde is a molecule that belongs to the class of indoles. It has been shown to have cytotoxic activity in vitro against cancer cells and isomers have been identified. 7-Azaindole-3-carboxaldehyde has been investigated for its ability to bind to CB2 receptors, which are located on the surface of immune cells, and may be used as a lead compound for the development of novel anti-cancer drugs. 7-Azaindole-3-carboxaldehyde also binds to chloride ions, which may be important in understanding how it interacts with other compounds or proteins.</p>

<p>Methyl 4-methoxy-2-indolecarboxylate is a natural product that has been shown to have cytotoxic and anticancer activity. It was first isolated from the leaves of Picrasma excelsa, which is a plant native to Southeast Asia. Methyl 4-methoxy-2-indolecarboxylate has been found to be effective against breast cancer cell lines and human cancer cells in culture. The anticancer effects may be due to its ability to inhibit protein synthesis by inhibiting the ribosome. This compound also inhibits dehydrocrenatine, which is a precursor of the hormone crenatine, thus leading to decreased production of this hormone.</p>

<p>Suberosin is a naturally occurring sesquiterpene lactone, which is isolated from members of the Rutaceae family, such as the plant Feronia limonia. The compound exhibits diverse biological activities, primarily attributed to its complex structure that facilitates interaction with various biological targets. Suberosin's mode of action involves disrupting microbial cell membranes and interfering with critical biochemical pathways, effectively inhibiting microbial growth and propagation.</p>

<p>1,6-Dimethyl-1H-indole-3-carbaldehyde is a compound that can be used in the synthesis of many organic and pharmaceutical compounds. It is also an intermediate for the production of other chemicals. 1,6-Dimethyl-1H-indole-3-carboxylic acid has been shown to be useful as a building block in organic synthesis, due to its versatility and reactivity. The compound is also a reagent and can be used as part of research studies. This chemical has CAS number 202584-14-3.</p>

6-Methoxy-1-methyl-1H-indole-3-carbaldehyde is a high quality chemical that is used as a reagent, complex compound, useful intermediate, and speciality chemical. It is a fine chemical that has been shown to be useful as a building block in the synthesis of many other compounds. 6-Methoxy-1-methyl-1H-indole-3-carbaldehyde is also versatile and can be used in reactions involving nucleophilic substitution, reductive amination, and oxidative coupling.

<p>2,2'-Bipyridine-3,3'-dicarboxylic acid is a coordination compound that contains two carboxylic acid groups. It forms a dihydrate in water and is orthorhombic in crystal form. The molecule can be represented by the following chemical structure:</p>

<p>Xanthine is a reactive, oxidized form of purine. It is found in the human body as a product of xanthine oxidase (XO) metabolism of xanthine and hypoxanthine. Xanthine is known to have antioxidant properties and has been shown to inhibit the activity of xanthine oxidase in vitro. Xanthine, when combined with other anticancer drugs such as doxorubicin, can be used as an anticancer agent. This drug has been shown to cause oxidative injury in humans and animal models at physiological levels.</p>

<p>1-Methylindole-6-carboxylic acid is a versatile building block that is used in the synthesis of more complex compounds. It can be used as a reagent, speciality chemical, and useful building block for pharmaceuticals and other research chemicals. 1-Methylindole-6-carboxylic acid has been shown to be an effective intermediate for the production of a number of different compounds. The compound can also act as a reaction component or scaffold for chemical reactions.</p>

<p>Chelating agent used to detect aqueous copper ions by electrochemiluminescence</p>

<p>Oxythiamine chloride is a compound that binds to DNA in the nucleus of cells. It has been shown to inhibit cell growth and induce apoptosis by binding to a number of cellular molecules, including hydrogen bonding interactions with enzymes. Oxythiamine chloride also inhibits energy metabolism by inhibiting mitochondrial respiration and mitochondrial ATP production, and is toxic to cells. This drug has potent inducers, such as cell factor, which are necessary for the production of new cells. It also inhibits thiamine-dependent enzymes, such as pyruvate dehydrogenase kinase (PDK) and pyruvate dehydrogenase (PDH). The wild-type strain of Escherichia coli was used for these studies.</p>

<p>5-Methyl-2-phenyl-1H-imidazole-4-carboxylic acid (MPICA) is a potent inhibitor of xanthine oxidase. It is also an inhibitor of β-glucuronidase and enzymes that maintain the integrity of bacterial DNA. MPICA has been shown to inhibit xanthine oxidase in a dose dependent manner and can be used as a lead compound for new inhibitors of this enzyme.</p>

<p>1-Methylindole-2-Carboxylic Acid is a chemical that belongs to the group of phenylacetic acid compounds. It has been shown to inhibit lymphocyte activation and t-cell proliferation in vitro, which may be due to its ability to interfere with the production of interleukin. 1-Methylindole-2-Carboxylic Acid also has an antitumor effect on animals and can reduce the tumor burden by inhibiting DNA synthesis, protein synthesis, and mineralization. The molecular modeling studies have shown that 1-Methylindole-2-Carboxylic Acid binds in the active site of protein kinase C as a competitive inhibitor and prevents ATP from binding to the enzyme.</p>

2-Azabicyclo[2.2.1]heptane is a lactam that has been synthesized in the laboratory. The compound exhibits significant antiproliferative activity and is shown to have a stereoselective, stereogenic, nucleophilic attack on amides. 2-Azabicyclo[2.2.1]heptane has been used to study the mechanisms of neurodegenerative diseases such as Parkinson's disease and Alzheimer's disease. The conformational properties of this compound can be determined by NMR spectra, which show that it has a skeleton with significant conformational flexibility.

<p>1-Phenyl-3-oxabicyclo[3.1.0]hexan-2-one (1POX) is a monomer that belongs to the class of cyclopropane compounds and can be used in the synthesis of polymers. It has been shown to react with benzene, irradiation, monoxide, oxiranyl, acetonitrile and trimeric dyes to form reactive intermediates such as ketones and carboxylic acids. These intermediates can undergo photolysis to produce products such as ketones and carboxylic acids. The wavelength of the light used for photolysis can influence the product formation. 1POX is also a substrate for cyclopropane ring formation reactions, which are known for their high reactivity due to the stability of this ring system. The carbonyl group on 1POX is electron withdrawing and stabilizes the planar geometry of 1POX.</p>

<p>(1S,6S)-2,8-Diazabicyclo[4.3.0]nonane is a chiral compound that can be made from the reaction of an organic acid with an amino alcohol. The enantiomers of this compound have shown to be effective against methicillin-resistant Staphylococcus aureus (MRSA) and Mycobacterium tuberculosis. The synthetic process for this compound was originally developed in the 1980s by researchers at the University of Illinois. They were able to show that it was possible to make a carbonyl reduction product using imidodicarbonic acid and an organic solvent. This led to the synthesis of moxifloxacin hydrochloride, which is used as a treatment for bacterial infections such as tuberculosis or pneumonia.</p>

<p>2-Bromomethylquinoline is a quinoline derivative that has been synthesized to study the interaction between metal ions, such as copper and zinc, and chelate rings. The reaction products formed by 2-bromomethylquinoline have been shown to have antifungal activity in vitro. It has been found that the addition of a fluorescent probe can be used to detect quinoline derivatives, which fluoresce when excited with light. This makes them useful as fluorescent probes for reactions involving metal ions.</p>

5-Methoxy-3(2-aminopropyl)indole hydrochloride is a useful reagent for the synthesis of complex compounds and a versatile building block for the preparation of speciality chemicals. It is used in the production of fine chemicals, such as reagents and intermediates. This compound also has potential use as a research chemical or as a reaction component in organic syntheses.

<p>7-Bromoquinoline is a synthetic molecule that was first synthesized in the early 1980s. It is an analog of 7-bromoquinoline, which has been shown to have cytotoxic properties against cancer cells. The synthesis of 7-bromoquinoline involves a cross-coupling reaction with chloroacetonitrile and N-methylformamide. The nmr spectra for this compound are very similar to those for 7-bromoquinoine, but it lacks the secondary amine peak at δ 10.7 ppm. Primary culture cells were used to test the bioactivity of 7-bromoquinoline, and these cells were disrupted by adding trypsin after incubation with various concentrations of 7-bromoquinoline. This study showed that the quinoline derivatives had cytotoxic effects on cultured cells at low concentrations, suggesting that they may be useful as anticancer agents. Molecular modeling studies show that</p>

cis-Bicyclo[3.3.0]octane-3,7-dione (1) is a diketone that belongs to the group of epoxides. It has two functional groups, an epoxy and a ketone, which are in the trans configuration. cis-Bicyclo[3.3.0]octane-3,7-dione (1) is a reactive molecule that can form glyoxal when heated at high temperatures. cis-Bicyclo[3.3.0]octane-3,7-dione (1) can be prepared synthetically by an asymmetric synthesis with L-(+)-tartaric acid as the chiral auxiliary and glyoxal as the substrate. The reaction has been shown to proceed through an aldol cyclization and subsequent amide formation with l-(+)-tartaric acid as the chiral auxiliary and glyoxal as

<p>3-Methyl-2-hydroxy-3H-imidazo[4,5-f]quinoline is a high quality reagent that can be used as an intermediate or building block in the synthesis of other compounds. It is a fine chemical with CAS No. 144486-08-8 and can be used as a speciality chemical in research. This compound has versatile building blocks that are useful in reactions and have been shown to be a reaction component in the synthesis of various compounds.</p>

Quinolin-5-yl-methylamine is a fine chemical that is used as a research chemical. It can be used as a reagent and as a speciality chemical. This compound has a high quality and is versatile in its use. Quinolin-5-yl-methylamine can be used in the synthesis of complex compounds, such as pharmaceuticals, agrochemicals, and polymers. It is also an intermediate that can be used to create other useful compounds, such as building blocks or scaffolds. The CAS number for this compound is 58123-57-2.

<p>6-Bromo-4-chloro-1H-indazole is an organic compound that has been reported as a reaction component, reagent, and useful scaffold in the synthesis of complex compounds. It is also a speciality chemical with versatile building block and useful intermediate properties. 6-Bromo-4-chloro-1H-indazole is a fine chemical with complex structure and high purity.</p>

<p>5-Bromo-1H-indazole-3-carbonitrile is a high quality, versatile building block that can be used in the synthesis of complex compounds. It has been described as a "useful intermediate" and a "useful scaffold".</p>

<p>4-Chloro-5-ethylisatin is a fine chemical that can be used as a versatile building block in the synthesis of complex compounds. It has been shown to be a useful intermediate and reaction component for the preparation of high quality reagents. 4-Chloro-5-ethylisatin is commercially available from Sigma Aldrich, catalog number 1379340-45-0.</p>

<p>(1S,2R,3S,5R)-2-((Benzyloxy)methyl)-6-oxabicyclo[3.1.0]hexan-3-ol is a fine chemical with a CAS No. of 117641-39-1. It has been used as a versatile building block in the synthesis of complex compounds, and has also been used as a useful intermediate in the production of specialty chemicals. This compound is useful for research purposes and can be used as a reaction component in the synthesis of new compounds.</p>

<p>4-Methylindole is an anthranilic acid derivative that inhibits the polymerase chain reaction (PCR) by binding to the polymerase and preventing DNA replication. 4-Methylindole has been shown to inhibit the production of human liver proteins in vitro, but its effects on other tissues have not been determined. 4-Methylindole is a low toxicity compound that is metabolized by hydrolysis, which can be reversed with acid or base. It also binds to and irreversibly oxidizes human protein, which may be due to its reversible oxidation properties. This chemical has been found in capsicum annuum, which produces it as a natural defense against herbivores.</p>

<p>Isoquinoline-6-carbaldehyde is a fine chemical that belongs to the group of research chemicals. It can be used as a reagent for organic synthesis, a speciality chemical, or a building block in complex organic molecules. Isoquinoline-6-carbaldehyde is also an intermediate for the synthesis of many pharmaceuticals and other useful compounds. Isoquinoline-6-carbaldehyde has been shown to react with 2-aminoethanol to form (2E)-3-(4-(1,1'-biphenyl)-2-yl)butanal, which is an important reaction component in the synthesis of nitroaromatics. Isoquinoline-6-carbaldehyde is also a versatile scaffold for the synthesis of other fine chemicals.</p>

<p>2-Methylimidazole is a crystalline solid that has been used in the preparation of coordination compounds. The compound is prepared by reacting 2-methylimidazole with an appropriate metal cyanide, such as copper cyanide or nickel cyanide. The crystal structure of 2-methylimidazole shows strong hydrogen bonding interaction between the nitrogen atoms and the carboxylate groups. This compound has been used in clinical pathology to detect increased levels of ammonia, uric acid, and lactic acid in the blood. 2-Methylimidazole is not toxic to humans but has shown some toxicity to mice when injected intravenously at high concentrations. It can be used as an analytical method for determining trace amounts of chlorine in chemical compounds by way of electrochemical impedance spectroscopy (EIS).</p>

<p>Methyl 5-methoxy-2-methylindole-3-acetate is a versatile building block that can be used as a research chemical, reagent, or speciality chemical. It is also an intermediate in the synthesis of other compounds and has been shown to be useful in reactions involving nucleophilic substitution and electrophilic addition. This compound can be used as a scaffold for complex organic molecules. CAS No. 7588-36-5</p>

<p>(1,10)Phenanthrolin-5-ylamine is a sample preparation reagent that has been used in the production of polymers with redox potentials below 0.2 V. This compound is also an antimicrobial agent that has shown to be effective against bacteria and fungi. The detection sensitivity of (1,10)phenanthrolin-5-ylamine is high, making it suitable for use in human serum samples. It can be protonated by a base such as sodium hydroxide or ammonia to form its cationic form, which can then react with nucleophiles such as thiols and amines to produce an alkylating agent. It has been used in the synthesis of l1210 murine leukemia cells and has been observed to have photophysical properties that are sensitive to neutral pH levels. <br>(1,10)Phenanthrolin-5-ylamine can be used for process optimization</p>

<p>2-Chlorobenzimidazole is an analog of benzimidazole that has been synthesized by Langmuir adsorption isotherm. It is a white crystalline solid that can be dissolved in water and hydrochloric acid. 2-Chlorobenzimidazole inhibits the growth of herpes simplex virus by acting as a competitive inhibitor for the viral enzyme thymidine kinase, which catalyzes the conversion of thymine to thymidine. 2-Chlorobenzimidazole also binds to monoclonal antibodies, inhibiting their binding to their corresponding antigens. This activity may be due to its ability to bind covalently with amino groups on proteins and other molecules. Magnetic resonance spectroscopy has shown that 2-chlorobenzimidazole binds tightly with protonated (positively charged) phosphorous atoms within cells.</p>

<p>7-Deaza-6-hydroxypurine is a skeleton of nucleosides that inhibits enzymes. It has been shown to inhibit the activity of hydrochloric acid, a tumor metastasis promoter. The constant for this drug was determined using molecular modeling and inhibition constants. 7-Deaza-6-hydroxypurine has anticancer activity and can be used for the treatment of cancer. This drug is used as a noncompetitive inhibitor in which it binds to two different sites on the enzyme. It has also been shown to bind to subunits, which are parts of a protein that make up its structure, in biological studies.br&gt;<br>7-Deaza-6-hydroxypurine is an inhibitor that binds to two different sites on an enzyme. It has been shown to have anticancer activity and can be used for the treatment of cancer. This drug is used as a noncompetitive inhibitor in which it binds to two different sites on the enzyme. It</p>

<p>4,4'-Bis(methoxycarbonyl)-2,2'-bipyridine is a ligand that can be used in cross-coupling reactions. It has been shown to bind to metal ions and form complexes with the ligands. 4,4'-Bis(methoxycarbonyl)-2,2'-bipyridine has a constant value for maximizing the yield of the reaction and is luminescent. This product also has photophysical properties that allow it to be utilized in voltammetry studies. The transfer of this product can be optimized by using chromophores or catalysis. 4,4'-Bis(methoxycarbonyl)-2,2'-bipyridine provides a means for cross-coupling reactions using electrochemical studies and dichroism.</p>

6,6'-Dibromo-2,2'-bipyridine is a synthetic molecule that is used to produce amines. It can be synthesized in a cross-coupling reaction involving the reaction of an amine with bromine and a palladium catalyst. 6,6'-Dibromo-2,2'-bipyridine reacts with formaldehyde to form 2,4-diaminobiphenyls. This reaction is catalyzed by acid or base. 6,6'-Dibromo-2,2'-bipyridine has been shown to be reactive and photoexcited. Its photophysical properties make it a useful synthetic intermediate for the production of amines.

<p>Please enquire for more information about Indole-3-acetyl-L-alanine acid methyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4'-Methyl-2,2'-bipyridine-4-carboxaldehyde is a heterocyclic compound that contains a nitro group. It has the chemical formula C8H6N2O and the molecular weight of 122.15 g/mol. This compound belongs to the class of formyl compounds and it is composed of two formyl groups and one hydrogen atom. The bipyridines are linked by a methylene bridge to form a six-membered ring. The compound can be used as an intermediate for the synthesis of other organic compounds such as pharmaceuticals, dyes, water repellents, pesticides, and herbicides.</p>

<p>5-Acetoxy-6-methoxyindole is a fine chemical, useful building block, and research chemical with CAS No. 112919-69-4. It is a versatile building block and reaction component that can be used as a reagent or speciality chemical in the synthesis of other complex compounds. 5-Acetoxy-6-methoxyindole is also used as an intermediate in the synthesis of drugs and pharmaceuticals. This compound has high purity, making it a high quality product with many uses.</p>

<p>2-Phenyl-quinoline is a naturally occurring compound that exhibits antimicrobial activity. It has been shown to inhibit the growth of bacteria by interfering with the synthesis of ATP, which is necessary for bacterial cell division. 2-Phenyl-quinoline also possesses antioxidative properties and has been shown to have inhibitory effects on a number of bacterial strains. 2-Phenyl-quinoline has been shown to induce necrotic cell death in S. aureus strains, as well as anti-inflammatory and antinociceptive properties.</p>

8-Hydroxy-5-nitroquinoline-2-carbaldehyde is a high quality, versatile building block that can be used as a reaction intermediate or to synthesize heterocycles. It is also a useful scaffold for the synthesis of complex compounds. The CAS number of this chemical is 884497-63-6.

<p>6-Nitroquinoline is a nucleophilic compound that reacts with nitroalkanes to form alkyl nitrites. It undergoes a bioreductive reaction, in which it is reduced to the corresponding amine by hydrogen peroxide and ammonia. 6-Nitroquinoline contains functional groups that can act as either electron donors or electron acceptors and is therefore reactive towards other compounds. The reaction mechanism involves nucleophilic attack at the carbon atom in the ring of the 6-nitroquinoline molecule, resulting in an addition product. 6-Nitroquinoline has been shown to react with fluorophores such as fluorescein, forming a fluorescent product that can be detected by spectroscopy. This chemical can also form hydrogen bonds with other molecules, which are important for its reactivity. The reaction products of this compound are nitrite and quinolines where one or more of the nitrogens have been oxidized to nitro groups.<br>END</p>

<p>(S,S,S)-2-Azabicyclo[3.3.0]octane-3-carboxylic acid benzyl ester hydrochloride is a research chemical that can be used as a reaction component or reagent in organic synthesis. This compound is also useful in the construction of complex compounds and fine chemicals with applications including drug discovery, pharmaceuticals, agrochemicals, and polymer chemistry.</p>

<p>5-Bromo-6-chloro-1H-indole is a fine chemical that is used as a building block for research chemicals, reagents, and speciality chemicals. It is soluble in chloroform and benzene, but insoluble in water. This product can be used as a reaction component or a useful intermediate in the production of complex compounds. 5-Bromo-6-chloro-1H-indole has been reported to be an effective scaffold for the synthesis of many novel compounds with potential applications such as pharmaceuticals, agrochemicals, and dyes.</p>

<p>2-But-3-yn-1-yl-1H-isoindole-1,3(2H)-dione is a heterobicyclic compound that has antiviral properties. It is an inhibitor of the viral enzyme RNA polymerase and can be used to treat viral infections such as HIV, influenza, or herpes. 2-But-3-yn-1yl-1H-isoindole 1,3(2H)-dione has been shown to be effective in vitro against HIV and influenza viruses. It also inhibits the replication of other viruses by binding to their RNA polymerase enzymes. This drug is fluorescent and can emit light when excited with a laser or UV light. 2B3YNIDIO has been shown to fluoresce at 477 nm when irradiated with blue light.</p>

<p>1-Methyl-1,2,3,4-tetrahydroquinolin-7-amine hydrochloride (MQ) is a fluorescent probe that has been used to study the photostability of cisplatin in real time. MQ was synthesized by reacting 3-(2'-bromoacetyl)-7-methoxy-1,2,3,4-tetrahydroquinolin with 7-aminoquinaldine. The emission spectrum of MQ peaks at 615 nm and has an extinction coefficient at 615 nm of 12.5 mM/cm. This probe has been shown to be photostable for long periods of time and can be used to visualize DNA polymerase activity in living cells.</p>

Isomeric 4-methylisoquinoline is a molecule that is structurally similar to protopine and berberine chloride. It has been shown to be an effective photosensitizer for the production of reactive oxygen species (ROS) in cells, which can lead to DNA damage and cell death. The functional groups on this molecule are the chloro group, which is a halogen, and the isoquinoline ring system with two methyl groups. The chemistry of this compound involves alkylation, yielding a new compound with one less methyl group than the original molecule. This process is called enamine formation.

<p>2-Hydroxyquinoline is a coumarin derivative that has inhibitory properties against a variety of human pathogens, including the causative agent of malaria. It binds to the active site of the enzyme xanthine oxidase, which catalyzes the oxidation of hypoxanthine to xanthine and then to uric acid. 2-Hydroxyquinoline inhibits this reaction, preventing the accumulation of uric acid in the blood and urine. This compound also has potential anticancer activity due to its ability to inhibit tumor cell proliferation in human prostate cancer cells. 2-Hydroxyquinoline is metabolized by cytochrome P450 enzymes and has pharmacokinetic properties that include an inhibitory dose (ID50) of 1mg/kg.</p>

<p>5-Hydroxy-3,4-dihydro-2(1H)-quinolinone is a high quality reagent with a CAS number of 30389-33-4. It has been shown to be a useful intermediate in the synthesis of complex compounds. This compound can also be used as an important building block for the synthesis of speciality chemicals and research chemicals. 5-Hydroxy-3,4-dihydro-2(1H)-quinolinone is versatile and can be used as a reaction component in many reactions that require the introduction of oxygen into molecules.</p>

<p>4,7-Dichloroisatin is an organic compound that is synthesized by ring-opening of oxindole. It is a bifunctional molecule that can be used for the synthesis of other organic compounds. 4,7-Dichloroisatin has been found to be an efficient method for the synthesis of thiazolidinedione derivatives and can be used as a control experiment for this type of reaction. The mechanism for the reaction includes nitroaldol addition to the C=O group, followed by nucleophilic attack on the carbonyl group to form a tetrahedral intermediate. The intermediate then collapses to form a new C=N bond and release acetonitrile.</p>

<p>2-Bromoquinoline is an antimicrobial agent that binds to bacterial receptors. It is a bifunctional molecule with two reactive groups: a hydroxyl group and a nitrogen atom. 2-Bromoquinoline has been shown to inhibit the growth of various bacteria, including Mycobacterium tuberculosis, Staphylococcus epidermidis and Streptococcus pyogenes, by preventing the formation of a proton gradient across the bacterial membrane. 2-Bromoquinoline also inhibits hyperproliferative diseases such as amyloidosis in mice by binding to amyloid fibrils. This drug has been shown to cause DNA damage in mammalian cells, which may be due to its ability to form hydrogen bonds with methyl ethyl groups on DNA bases.</p>

<p>7-Methoxyquinoline is a drug that belongs to the group of histone deacetylase inhibitors. It has been shown to inhibit monooxygenase and cytochrome p-450, which are enzymes involved in the metabolism of drugs. 7-Methoxyquinoline can be used as a fluorescent probe for reactions involving histones or other proteins with similar chemical structures. It is also used as an inhibitor in biochemical assays, such as fluorometric assays. 7-Methoxyquinoline can be prepared by reacting hydrazine with methoxyacetic acid followed by hydrolysis of the resulting hydrazone. This process yields a mixture of products, some of which are substituted with methoxy groups at different positions on the benzene ring.</p>

1-Isoquinolin-1-ylmethanamine dihydrochloride is a versatile building block that can be used for the synthesis of a wide variety of compounds. It is a reagent and speciality chemical, as well as an intermediate or reaction component in the production of pharmaceuticals, agrochemicals, plastics, dyes and other chemicals. 1-Isoquinolin-1-ylmethanamine dihydrochloride has been shown to have high purity and quality.

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Decursidin is a chemical compound, classified as a coumarin derivative, which is a bioactive constituent derived from the roots of the Angelica gigas plant. This compound is prominent for its pharmacological activities, attributed to its distinct chemical structure.

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<p>5-Iodoisatin is a cross-coupling agent that has an inhibitory effect on tumor tissue. It is also used for the synthesis of conjugated drugs and pharmacological research. 5-Iodoisatin, which forms a ternary complex with copper and iodide, inhibits the growth of colorectal carcinoma cells by interfering with their DNA replication and protein production. 5-Iodoisatin can be converted to its active form through the formation of a ternary complex with copper and iodide ions. This inhibition is due to its ability to interact with DNA, RNA polymerase, and other proteins involved in transcription, translation, and replication processes. 5-Iodoisatin is metabolized through conjugation with glucuronic acid or sulfate in the liver; it binds to human mitochondrial DNA and can enter cells via passive diffusion. The carbonyl group in this drug may play an important role in its interaction with cancer cells.</p>

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<p>1-Methylisatin, 3-thiosemicarbazide (MTST) is an antimicrobial agent that has been shown to be effective against a broad range of microorganisms. MTST inhibits the growth of bacteria and fungi by binding to the fatty acid moieties of membrane lipids, which disrupts the integrity of the cell membrane. This disruption can lead to bacterial death. MTST also has antiviral properties that are due to its ability to inhibit virus replication by binding with receptor binding sites on the virus surface. 1-Methylisatin, 3-thiosemicarbazide has been shown to be an effective treatment for autoimmune diseases such as multiple sclerosis and rheumatoid arthritis in animal models.</p>

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<p>Please enquire for more information about 4-(2,6,6-Trimethyl-4-oxo-5,6,7-trihydroindolyl)benzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Oxoindoline-3-hydrazone (2OIH) is a heterocyclic compound that has been reported to have anticancer activity. 2OIH is an intramolecular hydrogen bond acceptor, which may account for its anticancer activity. It has been shown to be effective against cancer cells in mammalian cell lines and in vitro studies of human carcinoma cell lines. This compound also showed anticancer activity against bacteria such as Pseudomonas aeruginosa (P. aeruginosa) and Staphylococcus aureus (S. aureus). The geometric isomers of 2OIH have been studied using nmr spectra, and the carbonyl group has been identified as the source of its anti-cancer properties. Structural analysis has revealed that the hydroxyl group on the indole moiety is important for the anti-cancer properties of this molecule.</p>

Please enquire for more information about 2,10-diaza-5,5,13-trimethyl-9-(4-(isopropyl)phenyl)tricyclo[9.4.0.0<3,8>]pentadeca-1(11),3(8),12,14-tetraen-7-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>Applications 5-Nitro-1H-quinolin-2-one is used in the synthetic preparation of novel antileishmanial agents for Leishmania donovani promastigotes.<br>References Paloque, L., et al.: Europ. J. Med. Chem., 54, 75 (2012);<br></p>

<p>Applications (Z)-9-(2-Propen-1-ylidene)-2-(trifluoromethyl)-9H-thioxanthene is an intermediate used in the synthesis of (E/Z)-Flupentixol-d4 Dihydrochloride (F597982), which is a neuroleptic agent related structurally to thiothixene. Antipsychotic; neuroleptic agent; dopamine receptor antagonist.<br>References Nielsen, et al.: Acta Pharmacol. Toxicol., 32, 363 (1973), Post, M.L., et al.: Nature, 256, 342 (1975), Peuch, et al.: Neuropharmacology, 20, 1279 (1981),<br></p>

<p>Applications 6-Bromo-3-cyanoindole<br></p>

<p>Applications 1-Chloro-5-isoquinolinesulfonic Acid (cas# 105627-80-3) is a compound useful in organic synthesis.<br></p>

<p>Stability Hygroscopic<br>Applications 5-Amino-6-nitroquinoline is a reagent used in the synthesis of benzodiazepine sulfonamide-based bombesin receptor 3 agonists. It is also used in the synthesis of quinoxalinediones.<br>References Liu, P. et al.: ACS. Med. Chem. Lett., 2, 933 (2011); Bigge, C. et al.: J. Med. Chem., 38, 5720 (1995);<br></p>

<p>Applications Dichloroquinoline derivatives for use as herbicides.<br></p>