Compuestos policíclicos

<p>Applications 3-Hydroxyindole is a mutation product of toluene-4-monooxygenase (T4MO), that gets spontaneously converted to indigo. Used in the preparation of indolyl-oxadiazoles with anticonvulsant activity.<br>References Rajak, H. et al.: Int. J. Pharm. Sci. Nanotech., 2, 661 (2009); McClay, K. et al.: Appl. Environ. Microbiol., 71, 5476 (2005); Berry, A. et al.: J. Ind. Microbiol. Biotech., 28, 127 (2002)<br></p>

<p>Applications 1-Ethyl-2,3,3-trimethylindolenium-5-sulfonate (cas# 146368-07-2) is a compound useful in organic synthesis.<br></p>

<p>Applications 2,2':6',2''-Terpyridine (cas# 1148-79-4) is a useful research chemical.<br></p>

<p>Applications 2-Chloro-6-[N,N-di(2-hydroxybenzyl)amino]-9-isopropylpurine (cas# 1076199-83-1) is a compound useful in organic synthesis.<br></p>

<p>Applications Indole-3-acetamide is a compound that is converted to indole-3-acetic acid by indole-3-acetamide hydrolase in auxin biosynthesis in plants.<br>References Mano, Y., et al.: J. Exp. Bot., 61, 25 (2010)<br></p>

<p>Applications 2-Amino-6-hydroxy-8-mercaptopurine (cas# 6324-72-7) is a compound useful in organic synthesis.<br></p>

<p>Applications trans-Indole-3-acrylic Acid is a regent used as a matrix for MALDI-TOF mass spectroscopy in order to characterize polyphenols.<br>References Madrigal-Carballo, S., et al.: Int Food Res J, 20, 2023-2034 (2013)<br></p>

<p>Applications 6,7-Dimethoxyisoquinoline is used as an organocatalyst in the chemoselective O-tert-butoxycarbonylation of phenols.<br>References Saito, Yukako, et al.: Tetrahedron Let., 51(52), 6915-6917 (2010)<br></p>

<p>Applications 3,4-DIHYDRO-2H-PYRIDO[1,2-A]PYRIMIDIN-2-ONE (cas# 5439-14-5) is a useful research chemical.<br></p>

<p>Applications 2,2,4-Trimethyl-1,2,3,4-tetrahydroquinoline is a reagent in the synthesis of tetrahydroquinoline sensitizers used for dye-sensitized solar cells. 2,2,4-Trimethyl-1,2,3,4-tetrahydroquinoline is also a reagent in the preparation of tetra- and pentacyclic derivatives of phenothiazinium photosensitizers which are used as photoantimicrobial agents.<br>References Hao, Y., et al.: Tetrahedron, 68, 552 (2012); Wainwright, M., et al.: Dyes Pigments, 91, 1 (2011)<br></p>

<p>Applications Ethyl Indole-3-acetate is a compound used in the synthesis of 9H-Pyrrolo[1,2-α]Indoles via Michael Addition-Condensation with α,β-Unsaturated Ketimines.<br>References Zhang, M., et al.: J. Heterocyclic Chem. (2016)<br></p>

<p>Applications 4,4'-Di-tert-butyl-2,2'-bipyridine acts as a reagent in the preparation, antiproliferative and cytotoxic activity of apoptotic ruthenium nitrogen heterocyclic complexes via combinatorial library synthesis.<br>References Mulcahy, S. P., et al.: Dalton Trans., 39, 177 (2010)<br></p>

<p>Applications Indole-3-acetonitrile is an indole derivative involved in the biosynthesis of the plant hormone indole acetic acid (I577340) via the indole-3-acetaldoxime pathway.<br>References Kong, W., et al.: Plant Cell Physiol, 56, 715-726 (2015)<br></p>

<p>Applications 5,6-Dihydroxyindole is an intermediate in melanogenesis, the production of melanin which is found in our skin, eyes, hair, and inner ear.<br>References S. Ito., et al.: Photochem. Photobiol., 84, 582-92 (2008);<br></p>

<p>Applications Indazolone derivative.<br></p>

<p>Applications 8-Hydroxyquinoline (cas# 148-24-3) is a compound useful in organic synthesis.<br></p>

<p>Applications 1,1’-Bicyclohexyl is a hydrocarbon component present in diesel fuel.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Patino, P. et al.: Energy. Fuel., 16, 1470 (2002); Shokri, S. et al.: Chem. Tech., An Ind. J., 1, 119 (2006);<br></p>

<p>Applications 3-(Bromomethyl)-2-cyclopropyl-4-(4-fluorophenyl)quinoline is used to prepare artificial HMG-CoA reductase inhibitors. It is also used to synthesize pitavastatin calcium via stereoselective Wittig olefination reaction.<br>References Hiyama, T., et al.: Bull. Chem. Soc. Japan, 68, 364 (1995); Fabris, J., et al.: Synth., 44, 1700 (2012)<br></p>

<p>Applications Isoquinoline-5-sulfonic Acid (cas# 27655-40-9) is a compound useful in organic synthesis.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br></p>

<p>p-Nitrobenzyl 6-(1'-hydroxyethyl)-azabicyclo(3.2.0)heptane-3,7-dione-2-carboxylate is a drug substance that is used in the manufacture of carbapenem antibiotics. It can be detected by a chloride ion chromatographic method, and the detection limit is 0.5 mg/L in the presence of zinc powder as a modifier. This material is used to prepare carbapenems using an analytical method that includes reaction monitoring by optical rotation, diastereomer chromatography, and transfer.</p>

<p>Quinolin-4-ylboronic acid is a heterocyclic compound with two nitrogen atoms that are attached to the ring by means of carbonyl groups. This compound is a precursor in the synthesis of the drug dorsomorphin, which is used for pain relief. It also has an important role in pharmacokinetics because it can be used as a marker for estimating blood levels of other drugs. Quinolin-4-ylboronic acid yields an active form, quinolin-4-yl boronic acid, when reacted with piperazine in basic conditions. The drug ldn-193189 is a derivative of this active form and has been evaluated as a potential drug for treating osteoporosis and cancer.</p>

<p>5-Formylindole is a non-selective and irreversible inhibitor of protein α, which is the catalytic subunit of the enzyme AMP-activated protein kinase. It binds to the hydroxyl group at position Cys177 in the ATP binding pocket of protein α, thereby inhibiting its activity. 5-Formylindole has been shown to inhibit tumor growth in xenografts and also inhibits fat accumulation in 3T3-L1 preadipocytes by inhibition of fatty acid synthesis. This compound has also been used to study molecular modeling in order to understand hydrogen bond interactions between aldehyde groups and intramolecular hydrogen. The genus that this compound belongs to is stilbene derivatives.</p>

<p>5,6-Difluoroindole is a chemical compound that has been studied in biological and chemical research. It is an analog of the neurotransmitter serotonin, which binds to the 5-HT2C receptor and activates phospholipase C (PLC) to produce inositol triphosphate (IP3). This compound may be useful for the treatment of neurodegenerative diseases such as Alzheimer's disease. 5,6-Difluoroindole has been shown to block the activity of acetylcholinesterase (AChE), which is an enzyme that breaks down acetylcholine. This leads to an increase in acetylcholine levels and a decrease in AChE activity. The reaction mechanism for this process is not known.</p>

<p>5-Methoxy-2,3-dihydroindoline is a methoxy compound that is substituted with a methyl group. It has been shown to be an effective hydrogen transfer agent in cyclopentenone reactions, and can also be used as a sensor for nitroaromatic compounds. 5-Methoxy-2,3-dihydroindoline can be synthesized by the reaction of methoxylated aniline with sodium ethoxide in acetonitrile. This reaction produces the desired product in high yield (70%), and it can also be used for the methylation of secondary amines in good yield (80%). 5-Methoxy-2,3-dihydroindoline is potently active when titrated against benzo[a]pyrene.</p>

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

<p>4'-(4-Methylphenyl)-2,2':6',2''-terpyridine (TPEN) is a chemical compound with anti-cancer properties that has been shown to induce apoptosis in cancer cells. TPEN also inhibits the growth of tumor cells by interacting with mitochondria and inducing mitochondrial dysfunction. TPEN synergistically induces death in neuronal cells when combined with other agents that are known to cause neuronal cell death. In vivo studies have shown that TPEN produces neuroprotective effects at normoxic temperatures, but can be toxic at hyperthermic temperatures.</p>

<p>Methyl (1R,2S,3S,5S)-3-(4-fluorophenyl)-8-[(E)-3-iodoprop-2-enyl]-8-azabicyclo[3.2.1]octane-2-carboxylate is an imaging agent that is used to diagnose and treat bowel diseases. It has pharmacokinetic properties that allow for a more accurate diagnosis of eye disorders and bowel disease. Methyl (1R,2S,3S,5S)-3-(4-fluorophenyl)-8-[(E)-3-iodoprop-2-enyl]-8-azabicyclo[3.2.1]octane-2-carboxylate is a DPPIV inhibitor that modulates the dopamine transporter in the brain by binding to its extracellular site of action on dopamine transporter proteins and blocking the reuptake of dopamine into the pres</p>

<p>Indole-3-carboxaldehyde is a chemical compound that is used as an antimicrobial agent. The biological properties of this compound are not well studied, but it has been shown to be effective against bacteria and fungi. Indole-3-carboxaldehyde has been shown to inhibit the enzyme activity of sodium carbonate, which is involved in the production of lactic acid in bacteria. This effect may contribute to its antibacterial activity. Indole-3-carboxaldehyde is also a potential anticancer agent because it can bind to toll-like receptor 4 (TLR4). Indole-3-carboxaldehyde reacts with sulfa drugs through a mechanism similar to the reaction between hydrogen peroxide and potassium permanganate. It has been shown that indole-3-carboxaldehyde can be used as a pesticide for plants and as an electrochemical impedance spectroscopy probe for histological analysis.</p>

<p>4-Methylindole-3-carboxaldehyde is a lipophilic extract that inhibits the growth of fungi. It has been shown to be effective against phytopathogenic fungi, and it has been used as an antibiotic in the treatment of bacterial infections. 4-Methylindole-3-carboxaldehyde is an analog of streptochlorin, which inhibits protein synthesis by binding to the ribosome. This leads to cell death by inhibiting the production of proteins vital for cell division. 4-Methylindole-3-carboxaldehyde also has antifungal activity against Candida albicans and Trichophyton mentagrophytes.</p>

<p>3-Amino-5-nitroindazole is an anticancer drug that inhibits the growth of cancer cells. It has been shown to inhibit the growth of cancer cells by blocking the synthesis and repair of DNA, leading to cell death. 3-Amino-5-nitroindazole also blocks the production of new proteins, which are needed for cell division. This drug also acts on pathways that are important for tumor development and progression, such as signaling pathways and transcription factors. This compound has been shown to be selective against human squamous cell carcinoma cells and has been studied in combination with other anticancer drugs in clinical trials.</p>

<p>4,4'-Bis(bromomethyl)-2,2'-bipyridine is a cyclic molecule that can be synthesized by the reaction of 4-bromo-2,2'-bipyridine with a brominating agent. It is used as a precursor to ruthenium catalysts in organic synthesis, and as an additive in dendrimers. The compound has been shown to have light absorption properties and can be used in photovoltaics and electropolymerization.</p>

<p>2,4-Dihydroxyquinoline is a malonic acid derivative that is used as an antimicrobial agent. It is a diazonium salt that can be synthesized from 2-chloro-4-nitrobenzene and malonic acid. The reaction mechanism for this compound involves the formation of a diazo intermediate, which reacts with the amine to form a quinoline. This compound has been shown to have antibiotic properties and is able to inhibit the growth of bacteria such as Salmonella typhi, Mycobacterium tuberculosis, Escherichia coli, and Staphylococcus aureus. 2,4-Dihydroxyquinoline has also been shown to have anticancer activity in vitro on human liver cells (HepG2) and human hepg2 cells.</p>

<p>6-Bromo-2-oxindole is a crystalline compound with a molecular formula of C10H6BrO. It has been shown to have a high efficiency in the production of butyric acid and other organic acids. 6-Bromo-2-oxindole is also used in electron microscopy studies as an electron acceptor, and can be used for producing polymers with crystalline structures and dihedral angles. The compound has been shown to inhibit the growth of breast cancer cells by preventing the synthesis of mda-mb-231 breast cancer cells. It also has been shown to inhibit the production of isoindigo and morphology.</p>

<p>4,4'-Dinitro-2,2'-bipyridine-N,N'-dioxide is a fine chemical with a high quality. It is a versatile building block with a wide range of applications in research and as a reagent. The compound is used in the synthesis of organic compounds and many other products. This product can be used as an intermediate for the production of more complex compounds or scaffolds. 4,4'-Dinitro-2,2'-bipyridine-N,N'-dioxide has been shown to be useful in the synthesis of pharmaceuticals and agrochemicals.</p>

<p>4,6-Dimethoxyindole is a molecule that can be used as an amide or chloride. The molecular modeling study indicated that the 4,6-dimethoxyindole is hydrophobic and has a molecular weight of 164.4 g/mol. In the acetylation reaction, the 4,6-dimethoxyindole was synthesized with an acetyl group on one side of the molecule and an acetate group on the other side of the molecule. This molecule has shown to have anticholinesterase activity in vitro and can be used as an antibiotic. The synthesis of this molecule was confirmed by X-ray diffraction analysis, which showed that it had a crystal structure with two molecules in space group P2(1)2(1).</p>

<p>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</p>

<p>6-Chloro-7-iodo-7-deazapurine is a nucleoside analogue that is synthesized by a cross-coupling reaction between 6-chloro-2,4(1H,3H)-pyrimidinedione and 7-iodo-7-(trifluoromethyl)purine. 6CIDP has been shown to inhibit growth of epidermal cells at concentrations as low as 0.1 µM, with cytostatic effects seen at 10 µM. 6CIDP has also been shown to potently inhibit the replication of the human papilloma virus in vitro and in vivo. 6CIDP is currently being investigated for the treatment of AIDS and other viral infections. The molecular modeling studies on this compound have revealed that it may be a potent inhibitor of the epidermal growth factor receptor (EGFR).</p>

<p>2-Methyl-1,10-phenanthroline is a bidentate ligand that can be used as a catalyst in some organic reactions. It has been shown to selectively inhibit the activity of the enzyme carbonic anhydrase. This drug is also able to bind to metal ions with nitrogen atoms, such as copper and zinc, which may be useful for cancer treatments. 2-Methyl-1,10-phenanthroline has also been shown to have anti-tumor activity in prostate carcinoma cells when used as a ternary complex with hypophosphorous acid and anhydrase.</p>

<p>5-Chloro-3-methyl-1H-indole-2-carboxylic acid (5CMC) is a versatile building block and research chemical. It has been shown to be an effective intermediate for the synthesis of many complex compounds with interesting pharmacological properties. 5CMC is also used as a speciality chemical in the production of pharmaceuticals, agrochemicals, and other chemicals. The compound is a fine chemical that can be used in various research and industrial applications.</p>

<p>9-Hydroxyxanthene is a natural drug that has been used in traditional Chinese medicine for treating a variety of diseases. It is extracted from Rhizoma Gastrodiae and Angelicae Dahuricae. 9-Hydroxyxanthene has shown to be effective against various metabolic disorders, including insulin resistance, hyperlipidemia, and diabetes. The mechanism of action of 9-hydroxyxanthene is not known but it is thought to be due to its ability to activate the immune system by transferring reactions and promoting the production of antibodies. 9-hydroxyxanthene also shows anti-inflammatory effects by inhibiting the production of prostaglandins and leukotrienes. 9-hydroxyxanthene can also inhibit angiotensin II, which may reduce high blood pressure and congestive heart failure.</p>

<p>10-(2,5-Dihydroxyphenyl)-10H-9-oxa-10-phospha-phenanthrene-10-oxide is a synthetic compound that has an orange color and a molecular weight of 568. It is soluble in chloroform, ethanol, acetone, ether and benzene. The compound does not react with water or hydrochloric acid. It has been shown to have synergistic interactions with chloride and glycol ethers. 10-(2,5-Dihydroxyphenyl)-10H-9-oxa-10-phospha phenanthrene 10 oxide can be synthesized using a polymeric matrix as the reaction medium.</p>

<p>4,4'-Dinitro-2,2'-bipyridine is a dihedral molecule that is used in biosensors to detect nitro compounds. It is synthesized by the reaction of osmium tetroxide with pyridine. The transfer of electrons from the pyridine ring to the osmium atom results in an oriented molecule with a positive charge on one end and a negative charge on the other end. This orientation can be reversed by oxidation. 4,4'-Dinitro-2,2'-bipyridine has been shown to react with monoalcohols and nucleophiles such as water to form covalent bonds. It also reacts with radiation, which may account for its use in dosimeters for measuring radiation exposure.</p>

<p>Daphnetin dimethyl ether is a synthetic chemical compound, which is a derivative of the naturally occurring coumarin scaffold. It is primarily sourced through chemical synthesis rather than extraction from natural compounds, allowing for precise control over purity and structural modifications that are otherwise challenging to achieve through natural means.</p>

<p>6-Chloro-5-ethylisatin is a fine chemical that can be used as a building block for making other compounds, including pharmaceuticals and bioactive agents. It is also a versatile building block that can be used in the synthesis of many different types of compounds. 6-Chloro-5-ethylisatin is an intermediate, which means it is a substance that is used to make other substances. It can also act as a reagent in reactions and as a scaffold for complex molecules.</p>

<p>Impurity found in Primaquine diphosphate</p>

<p>6-Methylmercaptopurine is an important metabolite of 6-methylmercaptopurine, which is a vital component of the nucleotide synthesis pathway. It is used in analytical methods to determine levels of nucleotides, as well as in biological studies for its effect on autoimmune diseases. 6-Methylmercaptopurine can inhibit replication by inhibiting the methyltransferase enzyme.</p>

<p>7-Methylcoumarin is an organic compound classified as a coumarin derivative, which is sourced from various plants and synthesized chemically. Its basic structure consists of a benzopyrone, with a methyl group at the seventh position on the coumarin core, distinguishing it from naturally occurring coumarins.</p>

<p>N-(4-Hydroxyphenyl)-5-methyl-2-1H-pyridone is a molecule that is found in plasma samples and has been shown to inhibit the growth of cells. It is a potent inhibitor of tubulointerstitial injury, which is the most common type of kidney disease. The mechanism of this drug has been shown to involve the inhibition of primary amino acid uptake. This compound also inhibits urea synthesis and decreases plasma concentrations by increasing the rate of elimination. In addition, it has been shown to have an inhibitory effect on growth factors such as EGF, bFGF, IGF-1, and PDGF. N-(4-Hydroxyphenyl)-5-methyl-2-1H-pyridone can be synthesized by heating at high temperatures (thermally activated).</p>

<p>8-HQ, liberated by enzymatic activity, is a strong metal chelator and forms insoluble, grey precipitates with several metal cations such as Fe3+</p>

<p>2-Acetamido-6-chloropurine (2ACAP) is a nucleophilic agent that inhibits cancer cells by binding to the enzyme cholinesterase. It is used in the treatment of T-cell leukemia and herpes simplex virus. 2ACAP binds to the amine group of cholinesterase, which prevents it from breaking down acetylcholine. This inhibition leads to accumulation of acetylcholine, which has been shown to induce apoptosis in k562 cells. The molecular modeling study showed that 2ACAP binds to both chlorine atom and benzyl groups in the active site of cholinesterase. 2ACAP also has a potent inhibitory effect on cancer cell proliferation and can be used as an anti-cancer agent for many types of cancers including colon, breast, and prostate cancer.</p>

<p>Lauryl isoquinolinium bromide is a pyridinium cationic surfactant that is used as a diagnostic agent and pharmaceutical preparation. It is also used as an antimicrobial agent in liquid chromatography, which is a technique to separate chemical compounds. Lauryl isoquinolinium bromide has been shown to be effective against Gram-positive bacteria such as Staphylococcus aureus and Enterococcus faecalis, and Gram-negative bacteria such as Pseudomonas aeruginosa. Lauryl isoquinolinium bromide has also been shown to be effective against yeast such as Candida albicans. Lauryl isoquinolinium bromide is not effective against viruses or fungi. This agent can be used to enhance the permeability of membranes during cross-linking reactions between polymers.</p>

<p>4,5-Dichloroisatin is a versatile building block that can be used as a reagent for research and as a speciality chemical. It is also useful in the synthesis of complex compounds. 4,5-Dichloroisatin is a high quality compound with a CAS number of 1677-47-0. This compound is not intended for use in humans or animals.</p>

<p>5-Cyano-1H-indole-2-carboxylic acid is a high quality reagent that is used as an intermediate in the synthesis of complex compounds. It can also be used as a building block for the synthesis of speciality chemicals and research chemicals. The versatile nature of this compound makes it useful as a reaction component in the synthesis of many different types of compounds, including fine chemicals and pharmaceuticals. 5-Cyano-1H-indole-2-carboxylic acid is available commercially with CAS No. 169463-44-9.</p>

<p>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.</p>

<p>Isoquinoline-4-carbaldehyde is an aldehyde chemical that has been synthesized in the laboratory. It is a chiral molecule with one asymmetric carbonyl group. Isoquinoline-4-carbaldehyde is a potential precursor to naphthyridine, which can be used as a building block for the synthesis of natural products. Isoquinoline-4-carbaldehyde has been shown to have phosphine properties, and it can be used as a ligand in transition metal complexes. The molecule has been shown to exist in two forms, which coexist in equilibrium and can undergo interconversion.</p>

<p>5-Iodoindole is an organic compound that is used as a nematicide. It has been shown to have cytostatic effects on the growth of human pathogens, juveniles, and model systems. 5-Iodoindole inhibits the production of reactive amines and pyridine in vivo. It also inhibits glutamine metabolism by competitive inhibition at the glutamate dehydrogenase enzyme. 5-Iodoindole also has hemolytic activity and is able to induce transcriptomic changes in P. aeruginosa cells.</p>

<p>Please enquire for more information about 3-(4-ethoxyphenyl)spiro[1,3-thiazolidine-2,3'-indoline]-4,7-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>6-Mercaptopurine is a purine analog that suppresses the production of white blood cells by inhibiting the enzyme thiopurine methyltransferase. It has been used to treat bowel disease and also for long-term suppression of the immune system in patients with autoimmune diseases. 6-Mercaptopurine is metabolized to 6-mercaptopurine, which is then converted to dinucleotide phosphate (dNTP) by group P2 enzymes. This conversion allows 6-mercaptopurine to inhibit dNTP synthesis and cell division. The effects of 6-mercaptopurine are potentiated when given in conjunction with azathioprine, another drug that inhibits purine metabolism. 6-Mercaptopurine is not active against human serum albumin or erythrocytes because it cannot be cleaved into an active form by these proteins. However, it does inhibit enzyme activities such as DNA polymerase, RNA polymerase, and protein</p>

<p>7-Azaindole is a reactive chemical that has been shown to be effective in the treatment of skin cancer, as well as hepatic steatosis. The compound can promote the transfer of hydrogen atoms and form a dimer with protonated nitrogen. 7-Azaindole reacts rapidly with nucleophiles such as amines, alcohols, and thiols to form covalent bonds. The reaction mechanism is characterized by an initial protonation step followed by nucleophilic attack or hydrogen transfer from the nucleophile to 7-azaindole. Kinetic studies have demonstrated that the rate of this reaction depends on the concentration of both reactants.</p>

<p>7-Fluoroisatin is a crystalline compound that can exist as two different polymorphs. The metastable form of 7-fluoroisatin has been shown to have low energy vibrations and hydrogen bonding interactions, which are responsible for the intermolecular hydrogen bonding. 7-Fluoroisatin also has a tautomeric form that exists as a hydrochloride salt, which is not stable in the solid state. The protonated form of 7-fluoroisatin has been shown to be an excellent hydrogen bond acceptor, with the ability to stabilize long range interactions.</p>

<p>2,4-Dihydroxy-6-methoxyquinoline is a compound that exhibits antifungal properties. It has been shown to have activity against Aspergillus flavus, Aspergillus fumigatus, Candida albicans and other fungi. 2,4-Dihydroxy-6-methoxyquinoline also inhibits the growth of E. coli and A. aureus in vitro. Elemental analysis showed that this compound possesses antibacterial properties and can inhibit the growth of Staphylococcus aureus.</p>

<p>1-Acetyl-5-bromoindole is a high quality reagent that is useful as an intermediate in the synthesis of a wide range of complex compounds. It can be used as a speciality chemical for research purposes or to make other chemicals. 1-Acetyl-5-bromoindole is also needed for the synthesis of indoles, which are useful scaffolds and building blocks in organic chemistry. This compound can be used to form reactions with other chemical compounds and can be used to create versatile building blocks.</p>

<p>N-Nitroso-3-azabicyclo[3.3.0]octane is a nitrosating agent that can be used for the determination of gliclazide in pharmaceuticals and other applications. It is synthesized by reacting 3-azabicyclo[3.3.0]octane with sodium nitrite in an alkaline environment, followed by hydrolysis with hydrochloric acid. Nitrosation reactions are usually slow, but N-nitroso-3-azabicyclo[3.3.0]octane has been shown to have a fast reaction kinetics, which makes it useful for the determination of gliclazide in pharmaceuticals and other applications. The product is analyzed using chromatographic techniques such as high performance liquid chromatography (HPLC) or gas chromatography/mass spectrometry (GC/MS). The product was found to be linear over the range of 0–</p>

<p>7-Nitroindole-2-carboxylic acid is a molecule that has been shown to inhibit the activity of cytidine deaminase, an enzyme involved in the synthesis of DNA. This drug also inhibits the replication of dna and can be used for the treatment of cancer. 7-Nitroindole-2-carboxylic acid binds to basic proteins and has a helical structure. The affinity constants for this compound have not been reported, but it is thought that hydrogen bonding interactions are involved in its binding.</p>

<p>6-Methyl-2,2':6',2''-terpyridine is a versatile building block that can be used in the synthesis of complex compounds. It is a fine chemical and is sold for research purposes only. 6-Methyl-2,2':6',2''-terpyridine has been used as a reagent or speciality chemical in the manufacture of pharmaceuticals, agrochemicals, and other organic compounds. This compound also has potential use as an intermediate in the synthesis of other useful compounds or scaffolds.</p>

<p>5,7-Dibromo-8-hydroxyquinoline is a cytotoxic agent that has been shown to inhibit the growth of xenograft tumor cells. It was found to be effective in inhibiting the mitochondrial membrane potential and decrease the rate of cell proliferation. 5,7-Dibromo-8-hydroxyquinoline also showed significant cytotoxicity against carcinoma cell lines, with no effect on normal human fibroblast cells. The drug is an organophosphate compound that inhibits fatty acid synthesis by binding to an enzyme involved in fatty acid biosynthesis. This inhibition causes diarrhoea and sodium salt loss. 5,7-Dibromo-8-hydroxyquinoline can be extracted from hydrochloric acid through a solvent extraction process.</p>

<p>Indole is a nitrogen-containing heterocyclic aromatic organic compound. Copper chloride in the presence of trifluoroacetic acid and indole gives rise to an indolenine derivative, which reacts with nitrogen atoms to form a copper nitride. This reaction is used as a model system for biological properties of indole. Indolenine has been shown to have bone cancer prevention and treatment effects in mice, and may also be beneficial in autoimmune diseases and metabolic disorders, due to its ability to inhibit toll-like receptor signaling pathways. The wild-type strain has shown resistance to antibiotics, which can be overcome by using mutant strains that are resistant to antibiotic treatments.</p>

<p>4,4'-Dihydroxy-2,2'-bipyridine is a metallo-organic compound that can be used as a homogeneous catalyst for the oxidation of hydroxyl groups. It is also used in cancer research because it has been shown to inhibit tumor cell proliferation and induce apoptosis. 4,4'-Dihydroxy-2,2'-bipyridine is an activated form of 2,2'-bipyridyl with a hydroxyl group on its ortho position. It can be prepared by reacting bromine with the metal salt of 2-hydroxybenzaldehyde in the presence of sodium hydroxide. This reaction produces two products: 4,4'-dihydroxy-2,2'-bipyridine and 2-bromoethanol. The deuterium isotope is used for nuclear magnetic resonance spectroscopy studies because it has a spin quantum number of one and does not cause chemical shift</p>

<p>7-Hydroxyquinoline-(1H)-2-one is a quinoline derivative that binds to epidermal growth factor (EGF) receptors. It has been shown to inhibit the chloride current in neurons, which may be due to its ability to bind to the dopamine receptors in these cells. 7-Hydroxyquinoline-(1H)-2-one also inhibits DNA and protein synthesis by binding to nucleophilic nitrogen atoms and protonated nitrogen atoms, respectively. It has been shown to have an inhibitory effect on cancer cell growth in control experiments. This drug is not active against normal cells because it does not bind well to them. 7-Hydroxyquinoline-(1H)-2-one binds with high affinity to piperazine and this interaction can be used as a fluorescent probe for the presence of quinoline derivatives.</p>

<p>5-Hydroxy-6-methoxyindole-carboxylic acid (5-HMICA) is a molecule that is found in the pericardium and urine of patients with cancer. 5-HMICA has been shown to suppress tumor growth and activate cell mediated cytotoxicity in vitro. It also induces T helper type 1 (Th1) immune responses, which are associated with the production of cytokines such as interferon gamma and tumor necrosis factor alpha.</p>

<p>6-Benzylamino-7-deazapurine is a drug that has been shown to be effective in the treatment of pancreatic cancer. It is a monomer that reacts with nucleophiles such as 6-mercaptopurine, which are present in the human lung. The reaction generates an exergonic molecule that can be used to generate ATP and regenerate NAD+ during irradiation. This process has been observed using kinetic studies on human colon adenocarcinoma cells. 6-Benzylamino-7-deazapurine can also react with triazole compounds to form a linker and increase the rate of polymerization. The optimization of this reaction time could lead to more efficient cancer treatments.</p>

<p>4,6-Dichloro-1H-indole-2-carboxylic acid ethyl ester is a synthetic compound that functions as an agonist of the indole 2 receptor. It has been shown to have affinity for cortical and brain membranes, with a greater affinity for acidic regions of the membrane. 4,6-Dichloro-1H-indole-2-carboxylic acid ethyl ester is also capable of binding to the indole 2 receptor and activating it. The carboxyl group in this compound is substituted with benzene rings, which are connected by a moiety containing two carboxylic groups. 4,6-Dichloro-1H-indole-2-carboxylic acid ethyl ester was synthesised from 1H -indole acetic acid and chloroethane in four steps.</p>

<p>Betamethasone is a corticosteroid that is used to treat inflammation, ankylosing spondylitis, and rheumatoid arthritis. It has been shown to have efficacy in the treatment of pediatric patients with asthma, as well as animal models of cardiac arrest and stroke. Betamethasone has also been shown to be effective in the treatment of potassium ion-associated death due to cardiac arrhythmia or repolarization abnormalities. This drug can be administered orally or topically; it binds to the glucocorticoid receptor on cells and modulates gene transcription. The primary mechanism of action for betamethasone is not fully understood but may involve inhibition of protein synthesis and suppression of inflammatory cells.</p>

<p>Tetraethyl 2,2'-bipyridine-4,4'-diylbisphosphonate is a chemical that is used as an intermediate in the synthesis of other fine chemicals. Tetraethyl 2,2'-bipyridine-4,4'-diylbisphosphonate can be used as a building block for synthesis of more complex compounds with high chemical and biological activity. Tetraethyl 2,2'-bipyridine-4,4'-diylbisphosphonate can also be used to synthesize speciality chemicals or research chemicals. This compound has many versatile uses due to its ability to react with different substances to form new chemical compounds.</p>

<p>6-Amino-9H-purine-9-propanoic acid is an acid lactam that belongs to the class of dihedral molecules. It is a colorless solid that crystallizes in plates, which have been shown to have a strong affinity for ammonium ions. 6-Amino-9H-purine-9-propanoic acid has been shown to be a substrate for the enzyme purine nucleoside phosphorylase, which catalyzes the phosphorolysis of nucleosides with the release of inorganic phosphate and ribose 5'-phosphate. The molecule can also react with electron radiation to form gamma rays, which may lead to its use as a molecular probe.</p>

<p>3-(4-Fluorobenzoyl)-6-Methoxy-2-Methyl-1H-Indole-1-Acetic Acid is a prodrug that is metabolized to 6-fluoro-3,4 dioxo tamoxifen in the liver. It has been shown to have anticholinergic, cytosolic calcium and c1-4 alkyl properties. 3-(4-Fluorobenzoyl)-6-Methoxy-2-Methylindole Acetic Acid also has a basic group, cyclopentane ring, and pyridine ring.</p>

<p>Quinolin-2-yl-methylamine is an amine that is used in the synthesis of other compounds. It can be prepared by protonation of quinoline with methylamine, followed by crystallization. The yield of this reaction is dependent on the purity of the starting materials and the reaction conditions. This compound has a molecular weight of 169.07 g/mol and a melting point at 217 °C. The infrared spectrum for Quinolin-2-yl-methylamine shows peaks at 2900 cm−1, 1670 cm−1, and 1590 cm−1. It also has x-ray crystallography data (space group P21/c).</p>

<p>5-Methylindole-2-carboxylic acid (5MICA) is a synthetic compound that has been shown to be cytotoxic in vitro. It has been shown to inhibit the growth of multiple cancer cell lines, including hepatoma cells, and is currently being studied as a potential anticancer drug. 5MICA inhibits the synthesis of protein and RNA by binding to the ribosome. This inhibition leads to cell death by apoptosis. 5MICA also exhibits an antimicrobial effect against opportunistic fungal pathogens such as Candida albicans, Aspergillus fumigatus, and Cryptococcus neoformans. The mechanism for this inhibition is unknown but may involve inhibition of protein synthesis or other cellular processes.</p>

<p>Apterin is a naturally occurring compound, classified as a coumarin derivative, which is isolated from members of the Apiaceae family. Its source is primarily derived from plant species known for their therapeutic properties.</p>

<p>Intermediate in the synthesis of nintedanib</p>

<p>5-Hydroxy-2-methylindole is a product that transfers serotonin and melatonin, which are neurotransmitters. It can be used in animal studies to investigate the effects on cancer cells and its potential as an anti-cancer agent. 5-Hydroxy-2-methylindole can also be used to stabilize nitro compounds, such as TNT and RDX, by inhibiting the oxidation of these substances. This compound has been shown to have antiviral properties against HIV and HSV and may also have potentials for treating Alzheimer's disease. 5-Hydroxy-2-methylindole is synthesized by reacting indole with hydrogen peroxide in the presence of a halogeno (e.g., chlorine) or ferrous salts. The reaction rate of this synthesis depends on the concentrations of these reactants.</p>

<p>Furil is a pharmaceutical preparation used for the treatment of metabolic disorders, such as hypertension and diabetes. Furil is an inhibitor of the enzyme acyl coenzyme A: diacylglycerol acyltransferase-2 (DGAT-2) which catalyses the formation of triacylglycerols from diacylglycerol and free fatty acids. Furil has been shown to have potent inhibitory activity against DGAT-2, with an IC50 value of 0.5 μM. Furil also inhibits the enzyme phosphodiesterase 4B (PDE4B), which plays a role in signal transduction and inflammation. Furil can be synthesized by reacting hydrogen chloride with 2-bromoacetophenone in a nonpolar solvent to form 2,4-dichlorobenzoyl chloride, followed by reaction with 3-furancarboxylic acid in methanol to produce furil. Furil</p>

<p>Halquinol, a mixture of 5,7-dichloro-8-quinolinol, 5-chloro-8-quinolinol, 7-chloro-8-quinolinol and 8-hydroxyquinoline, is an important intermediate in organic synthesis. It has been used as a reagent in the synthesis of a variety of complex compounds. Halquinol has also been used as a building block for the synthesis of many other chemical products. The CAS number for halquinol is 806769-4.</p>