Compostos Policiclícos

<p>6-Fluoro-5-Methyl-2-[(5-Methyl-1H-Imidazol-4-Yl)Methyl]-2,3,4,5-Tetrahydro-1H-Pyrido[4,3-b]Indol-1-One is a drug that belongs to the class of fatty acid esters. It has been shown to be effective in clinical trials for the treatment of symptoms of dry eye syndrome. 6FMETI has a low safety profile and does not cause any adverse effects in humans. The drug can be administered by intravenous injection or oral administration and has a long elimination half life of 36 hours. 6FMETI is metabolized by hydrolysis to its active form, 5FMTI, which is then conjugated with glucuronic acid or methyl glutaryl coenzyme A to form an inactive metabolite. This drug also has good pharmacokinetic properties</p>

<p>Indole-3-acetic acid hydrazide is a molecule that has been shown to inhibit the activity of enzymes such as phosphofructokinase, pyruvate kinase, and lactate dehydrogenase. The compound also inhibits hemolytic activity by binding to the red blood cell membrane and inhibiting the enzyme NADH oxidoreductase. Indole-3-acetic acid hydrazide has been shown to bind to divinylbenzene with a hydrogen bond. The compound is also able to inhibit fatty acid synthesis through its interaction with the fatty acid synthase enzyme. In addition, indole-3-acetic acid hydrazide can be used as an inhibitor of SplA2 in cells.</p>

<p>5-Fluoroindole-3-acetic acid is a fluorine-containing drug that inhibits the transport of indoleacetic acid (IAA), an auxin, in the peo-iaa system. It has been shown to inhibit cancer cell growth and induce apoptosis in a variety of tumour cells. 5-Fluoroindole-3-acetic acid can be used as a chemotherapeutic agent for cancers such as bladder, breast, and prostate cancers. This drug also activates enzymatic reactions by introducing fluorine atoms into reaction sites.</p>

<p>Oroselol is an innovative beta-adrenergic blocker, which is a synthetic derivative with unique cardiovascular targeting properties. It is sourced from engineered chemical synthesis, utilizing advanced molecular design to enhance selectivity for beta-adrenergic receptors. The mode of action of Oroselol involves competitive antagonism of beta-1 and beta-2 adrenergic receptors, leading to a decrease in heart rate and myocardial contractility. This blockade of adrenergic stimulation results in reduced cardiac output and lower blood pressure.</p>

<p>7-Ethylindole is a fatty acid with a cationic surfactant that belongs to the group of mesoporous materials. It has been synthesized by using chromatographic method and sample preparation techniques. The synthetic process is based on the protonation of 7-ethylindole. It undergoes dehydrogenation and activation energy, which is programmed in copper chromite. The chemical compositions are chloride, hydrogenated, and activated 7-ethylindole.</p>

<p>4-Benzyloxyindole-2-carboxylic acid is a synthetic intermediate. It can be prepared from the hydrazide by reaction with benzaldehyde and subsequent reduction. The carboxylic acid moiety of 4-benzyloxyindole-2-carboxylic acid reacts with an electron source to form a class of compounds that can be used as synthetic intermediates. The diazonium salts formed in this process are then reacted with different electrophiles to give other useful products. 4-Benzyloxyindole-2-carboxylic acid has been used for the synthesis of many organic compounds, such as active compounds, intermediates, and synthetic intermediates, by spectroscopic techniques.</p>

<p>5,6-Dihydroxy-1H-indole-2-carboxylic acid (5,6 DHICA) is a photosensitizing agent with a long detection time. It has been used in the treatment of cervical cancer and skin cancer. 5,6 DHICA is an inhibitor of tyrosinase, which is responsible for the synthesis of melanin. 5,6 DHICA prevents the conversion of dopachrome to eumelanin by binding to the active site of tyrosinase and inhibiting its activity. This makes it an important drug for the treatment of hyperpigmentation disorders such as vitiligo and melasma.</p>

<p>7-Methoxycoumarin is a fluorescent compound, which is a derivative of coumarin. It is synthesized through chemical modification processes of natural coumarin, typically sourced from plant extracts of the Apiaceae and Rutaceae families.</p>

<p>Dihydro coumarin is a cyclic organic compound, which is a derivative of coumarin primarily obtained through synthetic processes. It possesses the characteristic odor reminiscent of freshly mown hay, contributing to its widespread application in various industries. The primary mode of action of dihydro coumarin involves its role as a fragrance and flavoring agent, capitalizing on its aromatic profile to enhance products’ sensory attributes.</p>

<p>8-Nitroquinoline is a nitrogenous compound that has been used as an inhibitor of Leishmania, a parasite that causes leishmaniasis. 8-Nitroquinoline inhibits the growth of Leishmania by inhibiting the enzyme hepg2, which is involved in the synthesis of lipids and cholesterol. The inhibition of this enzyme leads to the accumulation of malonic acid, which inhibits the production of ATP. This inhibition may lead to cell death or inhibitory effects on other enzyme activities. 8-Nitroquinoline has been shown to be effective against Leishmania parasites in vivo.</p>

<p>5-Acetylindole is a synthetic compound that has been shown to have anticancer activity. It inhibits the growth of cancer cells by disrupting their mitochondria, which leads to cell death. 5-Acetylindole was synthesized in an attempt to increase the anticancer efficacy of indole compounds and acetylation of indole rings was found to be an effective strategy for this purpose. Acetylation of the 5 position on the indole ring leads to a more potent antiproliferative agent with decreased potential for resistance development. This compound has been shown to disrupt cellular function in k562 cells, leading to cell death.</p>

<p>6-Cyanoindole is a synthetic compound that has been shown to have functional properties. It binds to the receptor of the chemokine, which is a type of protein that regulates inflammatory responses. It also inhibits the activity of coagulation factors, which are proteins involved in blood clotting. 6-Cyanoindole has been shown to inhibit cancer cell growth and induce apoptosis (cell death) in a number of cancer cell lines. The fluorescence properties and lifetimes of 6-cyanoindole have been studied extensively. It has also been used as a monomer in copolymerization reactions and is used as an intermediate in the synthesis of 6-bromoindole.</p>

<p>3,4-Dihydroisoquinolin-1(2H)-one is a potent antagonist of the histamine H1 receptor and has been shown to be safe in animal studies. 3,4-Dihydroisoquinolin-1(2H)-one has also shown efficacy in treating inflammatory diseases, such as asthma and arthritis. This compound was recently tested for its potential to diagnose cancer by targeting the tumor microenvironment. The compound was found to bind to trifluoromethanesulfonic acid (TFMS) with high affinity and selectivity. TFMS is an emerging therapeutic target for cancer therapy because it is highly expressed in the tumor microenvironment and can act as a proton donor for drug delivery systems. 3,4-Dihydroisoquinolin-1(2H)-one has also been observed to have low toxicity profiles in preclinical models, but more research is needed before it can be used clinically.</p>

<p>5-Chloroindole-3-Carboxylic Acid is a ring system that is a dimer of two indole rings and one carboxyl group. It has the ability to form hydrogen bonds with itself, which allows it to stack together in an orderly manner. The carboxyl group on the 5-chloroindole-3-carboxylic acid molecule can form hydrogen bonds with water molecules due to its electronegativity. This property enables 5-chloroindole-3-carboxylic acid molecules to be soluble in water, which is why it is used for water treatment and as a corrosion inhibitor.</p>

<p>4,6-Difluoroisatin is a chemical that is useful in the synthesis of complex compounds. It has been used as a reagent for the preparation of 4,6-difluoropyridinium salts and as a reaction component in the synthesis of polymers. 4,6-Difluoroisatin is also one of the building blocks in the synthesis of a number of other compounds. This chemical has been shown to be an effective scaffold for peptides and proteins.</p>

<p>6-Mercaptopurine is an antigen binding molecule that is biocompatible with the human body. It binds to 6-mercaptopurine and inhibits the oxidation of proteins. The inhibition of protein oxidation has been shown to decrease disease activity in patients with inflammatory bowel disease. 6-Mercaptopurine also inhibits the production of inhibitor molecules, which are responsible for the development of cardiac effects such as arrhythmias and cardiomyopathy. 6-Mercaptopurine has inhibitory properties against polymerase chain reactions, which may be due to its ability to bind with protein thiols at high rates.</p>

Please enquire for more information about 3-Methylthio-1,2,4-triazino[5,6-b]indole including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-Nitroindole is a chemical used in wastewater treatment. It is an electron acceptor that can be used to reduce the cost of the process. 5-Nitroindole has significant cytotoxicity and polymerase chain activity in human pathogens, such as Escherichia coli, Salmonella enterica, Staphylococcus aureus, and Mycobacterium tuberculosis. The drug is stable under aerobic conditions and has shown no significant cytotoxicity to mammalian cells. 5-Nitroindole has been shown to hybridize with DNA duplexes containing guanine bases and form covalent bonds in a model system. The drug also has been shown to be present in colonies of colony-stimulating factor (CSF) cells that are found in the blood stream of healthy individuals.

<p>5-Methoxyindole-3-carboxaldehyde is a molecule that belongs to the genus of indolequinones. It has been shown to have potent inhibitory activity against prostate cancer cells, and also has anti-cancer properties. 5-Methoxyindole-3-carboxaldehyde inhibits the proliferation of cancer cells by inducing apoptosis in prostate cancer cells. 5-Methoxyindole-3-carboxaldehyde also suppresses the growth of cervical cancer cells and breast cancer cells. This molecule binds to the hydrogen bond sites on DNA, which may be one reason for its anti-cancer properties. The molecule is fluorescent and can be used as a marker for detecting cancers or other diseases in living tissue.</p>

<p>9-Methylxanthine is a purine alkaloid that is structurally related to caffeine. It is used as a bronchodilator and to treat cardiac arrhythmias. 9-Methylxanthine has been shown to have an effect on the rate of DNA replication by binding to the enzyme xanthosine phosphorylase, which converts xanthosine monophosphate (XMP) to xanthosine diphosphate (XDP). The drug's effect on other nucleobases, such as adenosine monophosphate (AMP), cannot be ruled out. 9-Methylxanthine also has a strong affinity for macrochelates, which are compounds that contain chelating agents with a large number of ethylenediaminetetraacetic acid (EDTA) groups. This property is due to the high number of nitrogen atoms in the molecule and its ability to form hydrogen bonds between water molecules</p>

<p>Plant hormone; auxin; inducer of root development; used in plant rooting</p>

<p>Plant hormone of the auxin class; promotes root growth</p>

(8S,9R,10S,11S,13S)-9-Fluoro-11-Hydroxy-10,13-Dimethyl-1,2,6,7,8,11,12,14,15,16-Decahydrocyclopenta[a]Phenanthrene-3,17-Dione is a corticosteroid that is used in the treatment of inflammatory diseases. It has been shown to have immunosuppressive and antiinflammatory effects in animals. The drug is metabolized by cytochrome P450 enzymes to produce the active form prednisolone. Prednisolone binds to glucocorticoid receptors and blocks the production of inflammatory leukotrienes. The drug also inhibits neovascularization and ophthalmic disorders.

<p>Pyrazolo[1,5-a]pyrimidine-3-carboxylic acid is a pyrimidine analog and an electron transfer agent. It is a potent inhibitor of the enzyme dehydrogenase, which catalyzes the conversion of nicotinamide adenine dinucleotide (NAD) to nicotinamide adenine dinucleotide phosphate (NADP). Pyrazolo[1,5-a]pyrimidine-3-carboxylic acid has been shown to have anti-inflammatory properties and also inhibits the production of b-raf protein. This drug has also been shown to be a potent inhibitor of mitochondrial electron transport in cancer cells. Pyrazolo[1,5-a]pyrimidine-3-carboxylic acid binds to the metal centers in mitochondria, thereby inhibiting oxidative phosphorylation and reducing ATP synthesis. This ultimately leads to cell death by apoptosis.</p>

<p>4,5-Dimethoxyindole is a chemical compound that has been shown to exhibit radical scavenging activity. It is an inhibitor of integrase, which are enzymes involved in the integration of viral DNA into host cell chromosomes. This compound has been synthesized and its optical properties have been studied. The synthesis of 4,5-dimethoxyindole derivatives has also been investigated using molecular modeling. Schrodinger software was used to predict the geometry of these synthesized derivatives. These studies suggest that 4,5-dimethoxyindole may be a potential anti-cancer agent due to its ability to inhibit cancer cell growth and induce apoptosis.</p>

<p>4-Benzyloxyindole-2-carboxylic acid ethyl ester is a cyclic compound that has been synthesized through an intramolecular carboxylate cyclization. This class of compounds are known for their ability to form propargylic analogues, which have the potential to be used as anticancer drugs. The compound was first reported in 1969 by Schardt and co-workers and was found to have activity against leukemia cells. It has been shown to undergo a series of cyclizations, which are triggered by the presence of oxygen or other electron acceptors.</p>

<p>4'-Hydroxy-2,2':6',2''-terpyridine is a molecule with the molecular formula C24H22N4O8. It is an organic compound that belongs to the group of heterocycles. It has been found to be a ligand for metal ions and has been shown to interact with particles at temperatures below 20°C. 4'-Hydroxy-2,2':6',2''-terpyridine crystallizes in two polymorphs: tetragonally (alpha) at room temperature and trigonally (beta) at temperatures below 20°C. The alpha form has been observed to undergo a photophysical reaction as it absorbs light and emits light in the ultraviolet region of the spectrum.</p>

<p>Isopteryxin is a natural compound classified as a furanocoumarin, which is primarily derived from plants in the Apiaceae family, such as various species of Angelica. It is synthetically produced or extracted from these botanical sources using advanced chromatographic techniques. The mode of action of Isopteryxin involves interactions with cellular and molecular targets through its capability to intercalate with DNA and modulate enzyme activity. This confers notable biological activities, including antimicrobial, antifungal, and potentially anticancer effects. It may inhibit certain cell signaling pathways, thus influencing cellular processes such as apoptosis and proliferation.</p>

<p>The 6-Acetyl-7-methylpyrazolo[1,5-α]pyrimidine-3-carboxylic acid is a fine chemical that belongs to the group of speciality chemicals. It is an intermediate that can be used in research or as a building block for more complex compounds. This compound has been shown to have many useful properties, including its versatility as a scaffold and its ability to react with other compounds. The 6-Acetyl-7-methylpyrazolo[1,5-α]pyrimidine-3-carboxylic acid is also considered high quality and can be used in reactions related to the production of pharmaceuticals, agrochemicals, polymers and dyes.</p>

<p>3-Acetylindole is a dibenzopyran compound that has been shown to have anti-inflammatory properties. 3-Acetylindole inhibits the acylation reaction of arachidonic acid with coenzyme A and thereby blocks the production of prostaglandin E2. This compound also binds to the benzene ring, which may be due to its acidic nature. 3-Acetylindole has been shown to inhibit T-cell leukemia and other cancers in animal models. It has also been shown to inhibit the growth of cancer cells in culture by blocking DNA synthesis and inhibiting proliferation. The binding constants for this compound have been determined by x-ray crystal structures and protonation studies.</p>

<p>6-Methoxyindole-2-carboxylic acid (6MI) is a potent inhibitor of the enzyme catechol-O-methyltransferase (COMT). This inhibition prevents the conversion of catecholamines, such as dopamine and norepinephrine, to their corresponding methylated products. COMT inhibitors are used clinically to treat Parkinson's disease and other diseases that result from excessive levels of these neurotransmitters. 6MI is also an effective inhibitor of tyrosinase activity in vitro. It has been shown to inhibit the synthesis of melanin by melanocytes and inhibits the production of eumelanin, which is responsible for black or brown skin pigments. The inhibitory potency of 6MI was found to be greater than that for kojic acid, arbutin, and hydroquinone. Optimization studies showed that 6MI was most potent at a concentration of 1 mM and had an IC50 value of 0.3 mM in</p>

<p>4-Nitroimidazole has a redox potential that is well suited to the reduction of nitro groups. It is an antimicrobial agent that inhibits the growth of microorganisms by inhibiting DNA synthesis. 4-Nitroimidazole can be used for the treatment of infectious diseases such as tuberculosis, leprosy, and brucellosis. In rat liver microsomes, 4-nitroimidazole reacts with NADPH to produce a nitro group and an imidazole ring with a new configuration. The reaction mechanism is based on electron transfer from NADPH to the nitro group in 4-nitroimidazole via a series of reactions that involve cytochrome P450 enzymes. This reaction has kinetic energy and matrix effects that affect its pharmacokinetics and pharmacodynamics.</p>

<p>6-Carboxyindole is an indole that binds to the IL-17A receptor, which leads to the production of pro-inflammatory cytokines. It has been shown to be involved in autoimmune diseases and other inflammatory conditions. 6-Carboxyindole can be used as a probe for studying the biology of IL-17A, by binding to it and inhibiting its effects. The chemical structure of 6-carboxyindole is also useful for diagnostic purposes, as it can bind to antibodies and antigens for detecting infectious diseases or other biological processes. 6-Carboxyindole can be used in the treatment of heart tissue by binding with monoclonal antibodies that are specific for cardiac proteins such as myosin light chain kinase.</p>

<p>5,12-Dibutylquinacridone is an electron acceptor that is used as a monomer in cationic polymerization. It can be polymerized with acrylates to form polymers that have high fluorescence and photopolymerizable properties. 5,12-Dibutylquinacridone has shown to be reactive with epoxides and diene compounds, which are typically used as monomers in the synthesis of polymers. This chemical has been studied for its use in solar cells and photocurrent generation. The electron spin resonance technique has been used to study the chemical's photophysical properties.</p>

<p>7-Fluorooxindole is an alkylating agent that can be used in the synthesis of oxindoles. This compound can be prepared by aldol condensation reaction with butyllithium, followed by alkylation with bromides or iodides. The use of 7-fluorooxindole and its derivatives has been optimized to yield high yields. The optimal conditions for this reaction are deprotonation with an organometallic reagent, such as butyllithium, followed by alkylation with bromides or iodides.</p>

<p>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.</p>

<p>1-Acetyl-5-bromoindoline is an organic compound with the formula CH3COCH2CH(Br)CH2NH. It is a colorless solid that is soluble in organic solvents. The compound undergoes several reactions, including chloromethylation, amination, and hydrogenation. 1-Acetyl-5-bromoindoline can be used as a precursor to other compounds through catalytic hydrogenation or deprotection of alcohols. This compound has been shown to be an effective catalyst for the epimerization of lactones and β-lactams, such as penicillin G.</p>

<p>1-Methylindole is a chemical compound that belongs to the group of pyrimidine compounds. It has been shown to have antibacterial activity against many types of bacteria, including methicillin-resistant Staphylococcus aureus and Clostridium perfringens. 1-Methylindole inhibits bacterial growth by binding to DNA and RNA, preventing the synthesis of proteins necessary for cell division. The high chemical stability and low redox potential make 1-methylindole an excellent candidate for use as an anticancer agent. This drug has been shown to be effective in killing cancer cells in vitro, but more research needs to be done before it can be used in vivo.</p>

<p>Please enquire for more information about 6-Aminoindoline dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl (1S,2S,3S,5R)-3-[Bis(4-fluorophenyl)methoxy]-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylate is a molecule that has been shown to bind with high affinity to the serotonin receptor and blocks dopamine uptake. This drug has also demonstrated dose-dependent locomotor activity in rats and m1 muscarinic receptor binding. Methyl (1S,2S,3S,5R)-3-[Bis(4-fluorophenyl)methoxy]-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylate is being developed for use as a diagnostic tool for detecting Parkinsonian symptoms or chemical reactions in the brain.</p>

<p>Oxyphenisatin is a non-steroidal anti-inflammatory drug that is used in the treatment of inflammatory bowel disease. Oxyphenisatin inhibits cyclooxygenase, which is an enzyme that produces prostaglandins and thromboxanes from arachidonic acid. It has been shown to have a potent effect on bowel disease and it is used for the diagnosis of liver cells. The use of oxyphenisatin as a contraceptive has been shown to be effective, with high values in both sperm motility and number. However, this drug may lead to metabolic disorders or tissue culture. Oxyphenisatin may also cause adverse effects such as diarrhea, nausea, vomiting, dizziness, headache, fatigue, or malaise.</p>

<p>A 6-chloroindole is an organic compound that contains a six-membered ring with a chlorine atom at one of the carbons. The compound is a synthetic intermediate that has been used to synthesize other molecules. It is also used in chemical reactions to introduce the phosphate group, which can be useful when studying protein–protein interactions. 6-Chloroindole has been shown to have a predictive model for identifying organic anion transporters in rat kidneys and can be used in asymmetric synthesis to produce the desired product.</p>

<p>Flucindole is a diagnostic agent that can be used to diagnose psychiatric patients. Flucindole is an antagonist at the serotonin transporter gene and has been shown to be effective in treating depression. Flucindole is a n-oxide of fluoxetine, which is an antidepressant drug. Flucindole also inhibits fatty acid synthase, which synthesizes fatty acids from acetyl-CoA. The inhibition of this enzyme leads to a decrease in the production of fatty acids and results in weight loss for obese patients.</p>

<p>5-Chloro-7-iodo-8-hydroxyquinoline is a metal chelate that has been shown to have pharmacological effects in experimental animals. It has antioxidative properties and can protect against oxidative injury. 5-Chloro-7-iodo-8-hydroxyquinoline was found to be toxic in various animal models, including the neuronal death and mitochondrial membrane potential. This toxicity may be due to its ability to inhibit the activity of DNA polymerase and protein synthesis. The compound also showed significant cytotoxicity at low concentrations, but had no significant cytotoxicity at higher concentrations. 5-Chloro-7-iodo-8-hydroxyquinoline is similar in structure to clioquinol, which has been shown to have neurotoxic effects in humans.</p>

Ethyl 5-Benzyloxyindole-2-carboxylate is a fine chemical that is used as an intermediate for the synthesis of complex compounds. It can be used as a building block for the synthesis of other chemicals, such as pharmaceuticals and pesticides. This product is also a useful reagent in research, due to its versatility.

<p>6-Bromo-4-chloroquinoline is a chemical compound with the molecular formula C8H6BrClN. It belongs to the class of heterocyclic compounds and has been used in the synthesis of other compounds, such as pharmaceuticals. 6-Bromo-4-chloroquinoline has been shown to be an effective anticancer drug, with measurable levels in the blood after oral administration. This drug interacts with hydrogen bonding interactions with thp-1 cells, which are erythrocytes derived from human peripheral blood lymphocytes. 6-Bromo-4-chloroquinoline also interacts with sodium sulfide, which is found in human liver and kidney cells. The pharmacokinetic properties of 6-bromo-4-chloroquine have been studied in rats and mice.</p>

<p>(8S,9S,11R,13S,14S,17S)-11-(2-Fluoroethyl)-13-Methyl-6,7,8,9,11,12,14,15,16,17-Decahydrocyclopenta[a]Phenanthrene-3,17-Diol is a light emitting diode (LED) that emits light in the near infrared spectrum. This LED is composed of a single layer of CdTe nanowires and has an emission wavelength of 760 nm. It also has a high quantum efficiency and low energy requirements for fabrication. The lifetime of this device is also long and its optical properties are stable over time. This device can be used to replace traditional incandescent bulbs or to emit light in specific wavelengths for biomedical applications.</p>

<p>5-Chlorooxindole is a synthetic, chemotherapeutic drug that has been shown to have anti-tumor activity in animal models. It is an oxindole derivative with the chemical formula CHNClO. The compound is synthesized by the reaction of 3,5-dichloroaniline and indole in chloroform and purified by column chromatography. 5-Chlorooxindole has shown potential as an antitumor agent because it inhibits cancer cell growth through mechanisms such as induction of apoptosis and suppression of tumor angiogenesis.</p>

<p>4-Methyl-4'-carboxy-2,2'-bipyridine is a fluorescent probe that can be used to detect the presence of hydrogen peroxide in cells. It has been shown to bind to mitochondria and liver cells. The binding constants are in the range of 10 M. When exposed to light, 4-methyl-4'-carboxy-2,2'-bipyridine emits an orange fluorescence. This chemical has been used as an oxidation catalyst for amides and as an enhancer for reactive species in kinetic experiments. It also has been shown to have proton uptake properties.</p>

<p>5-Cyanoindole-3-carboxaldehyde is an aldehyde that is used in synthesis of β-unsaturated aldehydes. It is prepared by the reaction of 3-cyanoindole with formaldehyde. 5-Cyanoindole-3-carboxaldehyde has antibacterial activity against gram positive and gram negative bacteria. It also has a high yield and can be purified by filtration or by condensation with chlorobenzene. 5-Cyanoindole-3-carboxaldehyde can be activated by irradiation, which makes it useful for the production of pharmaceuticals.</p>

<p>Skimmin is a bioactive compound, classified as a coumarin, which is derived from various plant sources, particularly the bark of certain tree species. It functions through the modulation of enzyme activity, including antioxidant and anti-inflammatory pathways, by interacting with specific cellular receptors and enzymes.</p>

Ethyl indole-4-carboxylate is an organic compound that belongs to the group of sulfonium salts. It has a ring system, an ether and a sulfone group. The chemical structure also includes two sulfones. This compound has shown nematicidal activity and can be used as a fungicide. In addition, it can be used as an intermediate in the synthesis of other compounds, such as therapeutics and fungicides.

<p>2-Phenyl-4-quinolinecarboxylic acid is a nonsteroidal anti-inflammatory drug that is commonly used to treat bronchoconstrictor response and inflammatory bowel disease. It is also an antimicrobial agent, which can be used to treat infectious diseases. The compound was found to have structural similarity to other nonsteroidal anti-inflammatory drugs, such as ibuprofen and naproxen. 2-Phenyl-4-quinolinecarboxylic acid has shown the ability to inhibit leukemia inhibitory factor (LIF) production by lymphocytes, which may have a role in the development of leukemia. This drug also possesses antioxidative properties and has been shown to have high values in group P2 polymerase chain reactions.</p>

<p>5-Benzyloxyindole-3-carboxaldehyde is a merocyanine dye that can be used as an antimycobacterial agent in cell culture. It is also fluorescent and has been shown to inhibit the growth of Mycobacterium tuberculosis. 5-Benzyloxyindole-3-carboxaldehyde has been synthesised by reacting 5,5′-dibenzoyloxydihydropyrene with indole and benzaldehyde. The hydrolysis of this compound yields the corresponding carboxylic acid and benzoic acid, which are then converted to the desired product by action of sodium ethoxide. Merocyanine dyes are characterized by a distinctive absorption band in the visible region at about 540 nm. These compounds have also been shown to inhibit renal cells, which may be due to their ability to act as nucleophiles or tautomers.</p>

<p>Pyridoxine dipalmitate is a polycarboxylic acid that is used as an antioxidant. It can be found in fruit extracts and has been shown to have antimicrobial properties. Pyridoxine dipalmitate also possesses antioxidant properties, which may be due to its ability to react with reactive oxygen species (ROS) and other free radicals. The compound has been shown to improve skin conditions and prevent damage caused by ROS. Pyridoxine dipalmitate is also used in the treatment of metabolic disorders, such as damaged cell membranes and fatty acid metabolism disorders. This compound may act as a cationic surfactant or phosphorus pentachloride.</p>

2,2'-Biquinoline-4,4'-dicarboxylic acid disodium salt is a model system for studying the sequence and hydrogen bonding interactions of polymers. It is a biocompatible polymer that has been shown to have inhibitory properties in response to atherosclerotic lesions. 2,2'-Biquinoline-4,4'-dicarboxylic acid disodium salt has shown optical properties that can be used as a signal in recording sequences. This polymerase chain reaction (PCR) substrate is able to bind with DNA and protein molecules when they are present in an appropriate buffer. The sequence of 2,2'-biquinoline-4,4'-dicarboxylic acid disodium salt is controlled by the coordination geometry of the metal ions involved in its formation.

<p>2,2'-Bipyridine-4,4'-dicarboxamide is a catalyst that can be used in a variety of reactions. It has been used as an additive to increase yields and to accelerate catalytic reactions. The compound also has the ability to oxidize picolinic acid and form formic acid. This product can be used in glycerol synthesis or hydrogen peroxide production. 2,2'-Bipyridine-4,4'-dicarboxamide is a ligand that binds to picolinic acid and peroxide ions, forming an ion pair with the peroxide ion. This complex increases the efficiency of hydrogen peroxide evolution from water by up to 100%.</p>

<p>Pyridoxal hydrochloride is a vitamin B6 metabolite. It is involved in many biochemical reactions, including trans-sulfuration, amino acid synthesis, and neurotransmitter synthesis. Pyridoxal hydrochloride has been shown to have antimicrobial activity against some bacteria species by inhibiting their enzyme activities. This compound also inhibits the growth of various fungi. The redox potentials of pyridoxal hydrochloride can be determined by titration calorimetry, which can be used to study its structural properties. In vitro experiments with cells have shown that pyridoxal hydrochloride may increase the efficiency of protein production when used during cell transfection. Toxicity studies have shown that pyridoxal hydrochloride is not toxic to humans at doses up to 2000 mg/kg body weight per day for up to 14 days.</p>

(1R,2S,3S,5S)-3-(4-Iodophenyl)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylicacid methyl ester is a molecule that has been shown to be effective in lowering the symptoms of Parkinson's disease. It also prevents the uptake of dopamine and serotonin in the brain by binding to dopamine and serotonin transporters on the cell membrane. This drug has been shown to be safe at doses up to 100 mg/kg/day in rats, but has not been tested in humans. The drug is stable in neutral pH environments and does not degrade upon exposure to light or oxygen.

<p>Fraxetin is a coumarin compound, which is a type of secondary metabolite commonly found in plants. It is principally derived from sources such as Fraxinus rhynchophylla and other related species. Fraxetin functions through various biological mechanisms, including antioxidant, anti-inflammatory, and neuroprotective activities. It accomplishes this by scavenging free radicals, modulating inflammatory pathways, and inhibiting specific enzymes associated with oxidative stress.</p>

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

<p>1-Isopropyl-3-(4-fluorophenyl)indole is a solvent that has been shown to be useful for the deuterium enrichment of carbonyl compounds. It is also used as a reagent for the Friedel-Crafts acylation and for the synthesis of 3-methoxyacrylate. The process of wastewater treatment is made more efficient by adding 1-isopropyl-3-(4-fluorophenyl)indole to chloride. This process increases yields and decreases the amount of time it takes to complete wastewater treatment. 1-Isopropyl-3-(4-fluorophenyl)indole can also be used in the synthesis of fluvastatin, an antilipidemic agent.</p>

<p>Thiamine hydrochloride is a water-soluble vitamin that belongs to the group of B vitamins. It has been used as a model system for investigating the phase transition temperature of fatty acids in biological membranes. In addition, it has been shown to enhance thermal expansion and improve chronic exposure in fetal bovine brain cells. Thiamine hydrochloride has also shown insecticidal activity against various species of insects, including the tobacco budworm and the Indianmeal moth. This drug has been found to be active against phytophagous insects that cause crop damage, such as Anthranilate and Pyridoxine Hydrochloride. Thiamine hydrochloride is involved in cellular metabolism by enhancing the conversion of l-lysine into succinic acid via an intermediate product called anthranilate. It also plays an important role in pyridoxal phosphate synthesis, which is essential for protein synthesis and tissue growth.</p>

<p>Indole-4-carboxaldehyde is a natural compound that can be found in the acetate extract of the roots of Scopolia japonica. It has been shown to have an inhibitory effect on locomotor activity and may also have an inhibitory effect on protein synthesis. The mechanism of this inhibition is not yet known, but it may be due to an intramolecular hydrogen bond or other interactions with proteins. Indole-4-carboxaldehyde has also been shown to induce apoptotic cell death in 3T3-L1 preadipocytes by inducing mitochondrial dysfunction and oxidative stress.</p>

<p>Amodiaquine is a drug that belongs to the class of antimalarial agents. It is used for the treatment and prevention of malaria caused by erythrocytic forms of Plasmodium falciparum. Amodiaquine has shown synergistic effects with other drugs, such as sulfadoxine and pyrimethamine, for the treatment of malaria due to P. falciparum. The mechanism of action of amodiaquine is not well understood, but it may involve inhibition of the Toll-like receptor. Amodiaquine has been shown to inhibit polymerase chain reaction in a concentration-dependent manner and also inhibits polymorphonuclear leucocytes, which are important in innate immunity. In addition, amodiaquine is a hypoglycemic agent and can be used for the treatment of bowel disease.</p>

<p>6-Hydroxy-7-methoxy-4-phenylcoumarin is a synthetic chemical compound classified as a coumarin derivative. Derived from natural coumarin structures, this compound is often synthesized through organic chemistry techniques involving the hydroxylation and methoxylation of coumarin backbones, with the addition of a phenyl group.</p>

<p>Please enquire for more information about 3-(4-chlorophenyl)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>5-Nitroisoquinoline is a nitro compound that has been shown to be a potential biomarker for liver disease. 5-Nitroisoquinoline is synthesized from the reaction of hydroxylamine, sodium carbonate, and nitric acid. This chemical can also be found in human liver tissue. The titration calorimetry experiments performed on 5-nitroisoquinoline showed that the compound has a high heat of formation (194.1 kJ/mol) and low enthalpy of formation (-19.6 kJ/mol). Vibrational analysis revealed that there are four nitrogens in the molecule and two nitrogen atoms per molecule. X-ray crystal structures were obtained for 5-nitroisoquinoline with different solvents and hydrogen bonding was observed in all cases. Molecular modeling showed that there are five nitro groups, which would explain the name "5-nitro." The five nitrogen atoms coordinate to form a trigonal bip</p>

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

<p>4-Azaindole is a heterocycle that is used in the synthesis of some fluorescent derivatives and as an intermediate in the preparation of other compounds. 4-Azaindole has been shown to have anti-inflammatory effects, which may be due to its ability to inhibit the production of prostaglandins by binding to the CB2 receptor. 4-Azaindole also inhibits the activation of certain neurons and blocks the release of acetylcholine from cholinergic synapses. The antifungal activity may be related to its interaction with mt2 receptors, which are involved in fatty acid metabolism. The nitrogen atoms on this compound are important for its pharmacokinetic properties, and it has been shown to affect heart function by binding to δ receptors. 4-Azaindole can also be synthesized in an asymmetric fashion using a variety of reagents.</p>

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

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

<p>Hypoxanthine is a nucleotide, which is a building block of DNA and RNA. It is a useful intermediate for the production of other chemicals and drugs. Hypoxanthine can be used as a reagent in biochemical research, to study the effects of hypoxia on cells, or as a catalyst in organic synthesis. Hypoxanthine monosodium salt is an important building block for complex compounds with many uses. It is also used as a reaction component in many chemical reactions as well as being a versatile scaffold for drug design.</p>

<p>5-Aminoquinoline (5-AQ) is a chemical compound that was originally synthesized in the 1930s. 5-AQ is a trifluoroacetic acid derivative of quinoline, which has been used as a photographic developer and an agent for the removal of silver from photographic film. This molecule also has a fluorescence property, which can be seen when irradiated by light with a wavelength greater than 350 nm. A hydrogen bond exists between the hydroxyl group and the nitrogen atom of the amine group in 5-AQ. The reaction mechanism for 5-AQ is believed to involve the diazonium salt intermediate, which reacts with silver ions to form silver diazonide and free ammonia.<br>5-AQ is insoluble in water but soluble in organic solvents such as acetone or alcohol. It reacts with trifluoroacetic acid to form a precipitate, which may be removed by filt</p>

<p>7-Chloro-4-hydroxyquinoline-3-carboxylic acid is a chemical compound that has antioxidative activity and is used in the production of various organic substances. It is synthesized by reacting ammonium nitrate with a hydroxy group, an organic solvent, and phenoxy. The resulting product can be heated to form 7-chloro-4-hydroxyquinoline, which undergoes a series of reactions to produce 7-chloro-4-(2,2,2,-trichloroethoxy)quinoline. This reaction system produces a quinoline derivative that has been shown to be expressed at high levels in phosphatidylcholine (PC) and alpha-tocopherol (a vitamin E derivative). The final product is then purified by triethyl orthoformate (TEO), which removes the sulfoxide group.</p>

<p>4-Benzyloxyindole-3-carboxaldehyde is an analog of psilocin that is synthesized by the condensation of formylbenzene with indole-3-carboxaldehyde. It has been shown to act as a formylating agent, which can be used in the synthesis of other compounds. 4-Benzyloxyindole-3-carboxaldehyde may also be converted to n-dimethyltryptamine (DMT) by oxidation and decarboxylation.</p>

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

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

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

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.

<p>Iso-oxypeucedanin is a naturally occurring furanocoumarin compound, which is isolated from various plant species, particularly those belonging to the Apiaceae family. It exhibits a range of biological activities, primarily attributable to its structural properties that allow it to interact with various molecular targets.</p>

<p>7-Methoxy-1H-indole (7MI) is a synthetic compound that exhibits anti-inflammatory activity. It is an analog of the amino acid methionine found in proteins and its synthesis involves the condensation of a chlorinated alkyl acetate with an esterified hydrazide to form the corresponding amide. 7MI has been shown to inhibit both bacterial and mammalian protein synthesis, as well as to inhibit tumor cell growth. 7MI binds reversibly to the N7 atom of the adenine base in DNA, thereby inhibiting DNA replication through inhibition of DNA polymerase.</p>