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1-Methyl-N-(9-methyl-9-azabicyclo[3.3.1]non-3-yl)-indazole-3-carboxamide is a chemical inhibitor of the 5HT2 receptor, which is responsible for regulating nausea and vomiting. It has been shown to have antiemetic properties, and can be used in chemotherapy to control nausea and vomiting. The 5HT2 receptor is coupled to Gs proteins and inhibits adenylyl cyclase activity, while 1MMAI binds to the 5HT2A receptor and blocks serotonin from binding. This prevents serotonin from activating Gq protein receptors, which are involved in the generation of intracellular calcium concentrations that lead to neurotransmitter release. 1MMAI also inhibits the activation of phospholipase C by serotonin, resulting in decreased levels of diacylglycerol (DAG) and inositol triphosphate (IP3). These changes inhibit plate

<p>Isoquinoline is a heterocyclic organic compound that can be synthesized by the asymmetric addition of hydrochloric acid to an isoquinol. It has been shown to inhibit the enzyme DPP-IV, which is involved in the degradation of glucagon-like peptide-1 (GLP-1). Isoquinoline is also a potent antagonist of the NMDA receptor, and has been shown to have anti-inflammatory properties in HLA-60 cells. This drug is soluble in organic solvents and forms crystalline polymorphs. Isoquinoline has been used in polymerase chain reactions as a hydrogen bond donor.</p>

5-Acetylindoline is a tetracyclic compound that belongs to the family of phenanthridones. It has been synthesized by rationalizing the tetrahydropyridine, tetrahydroquinoline, and amine coupling reaction. The 5-acetylindoline molecule contains a phenolic group and is related to sulphones or diazonium salts. This compound can be made into a cyclization product by reacting with diazonium salts.

<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-Bromo-1H-imidazole is an environmental pollutant that has been detected in the atmosphere, water, and soil. It is used as a pesticide and has been found to be an impurity in biphenyl. 2-Bromo-1H-imidazole can be used as a substrate for the Suzuki coupling reaction or as a starting material for the synthesis of imidazole derivatives. The compound spontaneously fragments under acidic conditions to form nitric acid and hydrogen bromide. 2-Bromo-1H-imidazole has been shown to inhibit hepatitis C virus (HCV) replication and induce cancer cell apoptosis in vitro.<br>2-Bromo-1H-imidazole is also known to cause DNA fragmentation in cells through oxidation by reactive oxygen species or through spontaneous decomposition of the molecule into acid, bromine radicals, and ammonia.</p>

<p>1,3-Dipropylxanthine is a congener of caffeine. It is a nonselective adenosine receptor antagonist that binds to the adenosine receptors in the kidney. 1,3-Dipropylxanthine has been shown to increase renal blood flow and increase urine output. This drug may be used as a mobilisation agent for patients who are bedridden or have limited mobility. It should not be given to patients with heart disease or high blood pressure. 1,3-Dipropylxanthine has also been shown to inhibit the binding of pyrimido [1,2-a]benzimidazole (PPIM) and furyl derivatives to the adenosine receptor.</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.

<p>1,5-Dimethyl-1H-indole-3-carbaldehyde is a useful building block for organic synthesis. It is an important reagent for the synthesis of complex compounds and it has been used as a versatile building block in organic chemistry. This compound can be used as a starting point for the preparation of other chemicals, such as pharmaceuticals, pesticides, and dyes. 1,5-Dimethyl-1H-indole-3-carbaldehyde is also a fine chemical that has been used for research purposes. There are no known commercial uses for this compound.</p>

<p>Xanthotoxol is a naturally occurring furanocoumarin, which is derived from various plant species, primarily within the Apiaceae family. This compound exhibits its biological activity through several mechanisms, including the inhibition of enzyme pathways, modulation of signaling pathways, and interaction with cellular proteins, impacting various physiological processes.</p>

<p>Quinoline-2,8-diol is a bacterial strain that can be used to remove fatty acids from wastewater. The recombinant cytochrome P450 in this strain can degrade fatty acids, which are carcinogenic and have been shown to cause hepatic steatosis. In addition, the quinoline-2,8-diol strain has shown an ability to inhibit xenograft tumor growth in mice by activating cytochrome P450 and inducing apoptosis. This bacterial strain also has the potential to produce xanthurenic acid from tyrosine. Xanthurenic acid is toxic and has been shown to inhibit polymerase chain reaction (PCR) amplification of DNA. Quinoline-2,8-diol may be used as a model for experimental studies of xanthurenic acid's effects on energy metabolism and DNA synthesis.</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>Yellow dye used in food industry</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>

<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>Boc-(3S)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid is an amino acid that has the δ-opioid receptor antagonist activity. It can be synthesized by a stepwise synthesis with an asymmetric center. The δ-opioid receptor antagonist activity of Boc-(3S)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid was found to be comparable to naloxone in terms of affinity constants and functional groups.</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>2,9-Diphenyl-1,10-phenanthroline is a yellow crystalline compound. This molecule has been shown to be an effective anticancer drug and is used in the study of ultrafast electron reduction. It exhibits photophysical properties that are dependent on its coordination geometry and the surrounding environment.<br>2,9-Diphenyl-1,10-phenanthroline is a coordination complex that can be synthesized by electropolymerization of copper complexes with phenanthrolines. The polymer film has been shown to have high stability constants and is resistant to water or organic solvents.</p>

<p>6-Iodoisatin is a potential anticancer agent that has been shown to inhibit the growth of murine melanoma cells in vitro. The mechanism of action is not yet fully understood, but it seems that 6-iodoisatin may inhibit the synthesis of melanin and its cross-coupling reaction. This compound also exhibits affinity for tumour cells and can be radiolabeled with a radionuclide such as iodine-131 (I) or iodine-123 (I). 6-Iodoisatin has been shown to have a high biodistribution profile in mice. It accumulates in melanoma tumours at an amount that is ten times higher than that observed in other tissues.</p>

<p>3-Methyl-3,8-diaza-bicyclo[3.2.1]octane dihydrochloride is a high quality reagent that is useful as an intermediate in the synthesis of complex compounds and as a reagent for fine chemicals. 3-Methyl-3,8-diaza-bicyclo[3.2.1]octane dihydrochloride can be used as a versatile building block in the synthesis of speciality chemicals and research chemicals. It can also be used to synthesize a variety of reaction components, such as amines, carboxylic acids, alcohols, amides, and nitriles.</p>

<p>Dichloro[9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene]palladium(II) is a fine chemical that can be used as a building block in the synthesis of compounds with diverse structures. It is a research chemical and reagent that has been found to be useful in the synthesis of complex organic compounds. This compound is also versatile enough to be used as an intermediate or scaffold in the synthesis of many different types of organic compounds.</p>

<p>Quinoline-5-carboxylic acid is a peroxide that is produced by the oxidation of quinoline derivatives. Quinoline-5-carboxylic acid has been shown to have antibacterial activity, and it also has affinity values for chloride ions. The chemical isomers of quinoline-5-carboxylic acid are called quninolines, which are produced by the hydrolysis of quinoline-5-carboxylic acid. Quinolines can be obtained by the oxidation of aniline. Quinolines have been shown to catalyze reactions with carbonyl groups in organic molecules, such as the reaction between an alkoxycarbonyl group and a hydroxyl group to form an aldehyde or ketone. Kinetic data for this reaction was obtained using titration calorimetry.</p>

Please enquire for more information about 5,6-Diaminobenzimidazole dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>6-Bromo-2,3-dihydro-1H-indole is a natural product that has been shown to inhibit cancer cell growth in vitro. In the presence of 6-bromoindole, cells are unable to proliferate and undergo apoptosis. This compound also shows anti-cancer activity against human leukemia cells. The mechanism of action for this molecule is not yet known but may be related to its ability to activate the caspase enzyme family or its ability to bind to DNA. 6-Bromoindole has been shown to have anti-inflammatory properties through inhibition of prostaglandin synthesis in animal models.</p>

<p>4-Bromo-5-methyl-1H-indole-2,3-dione is a synthetic molecule that has been shown to have neuroprotective effects. It inhibits the production of proinflammatory cytokines, such as tnf-α and il-6, by binding to survivin. 4Bromo-5 methyl 1Hindole 2,3 dione also binds to the viral capsid protein and blocks virus infection. This compound has been shown to inhibit viral replication in vitro as well as provide protection against alphavirus infection in mice.</p>

<p>Boc-L-indoline-2-carboxylic acid is a high quality, versatile building block that can be used as a reagent or intermediate in organic synthesis. It is used as a research chemical and has potential applications in the development of new drugs. Boc-L-indoline-2-carboxylic acid is a complex compound that reacts with nucleophiles to form valuable products. It also has the ability to bind to metal ions such as copper, zinc, and nickel. This product can be used in reactions involving amines, alcohols, amides, phenols, carboxylic acids, sulfonic acids, and other compounds.</p>

<p>3-Quinuclidinone hydrochloride is an organic compound that is used as a reagent in organic synthesis. It is synthesized by the acylation of 3-quinuclidinol with ethyl bromoacetate in the presence of a base. This reaction occurs in an isolated yield, and the product can be purified by rotary evaporation. 3-Quinuclidinone hydrochloride has a high affinity for GABA receptors, which are found on nerve cells in the brain and inhibitory neurons throughout the body. The binding of 3-quinuclidinone hydrochloride to these receptors leads to a decrease in neuronal excitability. This drug also has been shown to have effects on motor function, including a positive effect on motor performance when tested using a rotarod test. The rate of this reaction can be increased by adding chloride or sodium carbonate as a catalyst and by increasing the reaction time. Substrate binding plays an important</p>

<p>3-Chloroisoquinoline is a thiolate, which is a reactive chemical group. 3-Chloroisoquinoline has been shown to react with trifluoromethanesulfonic acid to form a compound with biological properties. The amide and palladium complexes of 3-chloroisoquinoline have been prepared in the past. Additionally, the two isomers of 3-chloroisoquinoline are known as the halides and magnetic resonance spectroscopy of this compound has been studied. Structural isomers and functional groups of 3-chloroisoquinoline have also been studied in detail. Tautomers and lactams are structural isomers of 3-chloroisoquinoline that have also been researched extensively. Finally, trifluoroacetic acid reacts with 3-chloroisoquinoline to form an ester product.</p>

<p>7-Methylisatin is a natural product that is used in clinical settings as an acridone. It has been shown to have potent antifungal and insecticidal activities. 7-Methylisatin is also a potent antagonist of the nicotinic acetylcholine receptor (nAChR) and binds to the receptor with high affinity. It also inhibits the production of nitric oxide (NO), which is important for maintaining vascular homeostasis and inhibiting pain. 7-Methylisatin has been shown to be an efficient method for plutella xylostella larvae, which can lead to significant reductions in caterpillar populations. This natural product can be synthesized by a number of methods, including ammonolysis, reaction system, or mass spectrometry assays.</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>6-Fluoroindole-3-acetic acid is a molecule that has been synthesized by the reaction of 6-fluoroindole with acetic anhydride. When mixed with acetonitrile, the fluorescence of 6-fluoroindole-3-acetic acid can be seen in the solution. The fluorescence intensity is proportional to the concentration of this molecule. 6-Fluoroindole-3-acetic acid is used as a template molecule for fluorescence labeling experiments. It interacts with hormones and can be used to identify their conformations and interactions. This compound has been shown to have anticancer properties in mice, and it may also be effective against cancer cells in humans. It has also been shown to inhibit the growth of pisum sativum (pea).</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>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>6-Aza-5-methyl-1H-indazole is a chemical compound that acts as a building block for the synthesis of pharmaceuticals and other compounds. It is used in research for the development of new drugs, such as antihypertensive agents, antibiotics, and immunosuppressants. 6-Aza-5-methyl-1H-indazole has been shown to be an effective intermediate in the synthesis of many complex compounds, including cephalosporins, penicillins, carbapenems, and aminoglycosides. This versatile reagent can be used to synthesize a wide variety of organic compounds.</p>

<p>5-Fluoro-1-Methyl-1H-Indole-3-Carbaldehyde is a high quality chemical that is used as a reagent, an intermediate for the synthesis of pharmaceuticals, and in the production of fine chemicals. 5FMICA is also a useful scaffold for developing valuable building blocks. This chemical has been shown to be a versatile building block for the synthesis of complex compounds. 5FMICA can be used as a reaction component for the preparation of speciality chemicals and research chemicals.</p>

2,2'-Bipyridine-6,6'-(1H,1'H)dione is a high-quality compound that is used as a reagent to provide a variety of useful compounds. This compound can be used as a building block for various chemical syntheses or as a component in many reactions. It is also a versatile building block and can be used in the synthesis of other compounds. 2,2'-Bipyridine-6,6'-(1H,1'H)dione has been shown to be an effective intermediate for organic synthesis.

<p>2-Amino-5(6)-benzoylbenzimidazole is an antifilarial and anthelmintic drug that belongs to the benzimidazole class. It is used for the treatment of filarial infections in humans, including lymphatic filariasis, which is caused by worms transmitted by mosquitoes. 2-Amino-5(6)-benzoylbenzimidazole has low bioavailability due to its poor water solubility. The drug can be administered orally or topically and is metabolized in the liver. The metabolites are excreted in urine as glucuronides and sulfates.</p>

<p>1,2,3,4-Tetrahydrocyclopenta[b]indole is a synthetic drug that has been shown to be an effective antidepressant in animal models of depression. It has also been shown to inhibit the replication of HIV and Hepatitis C virus in cell culture. It is thought that 1,2,3,4-tetrahydrocyclopenta[b]indole's anti-depressant effects are due to its ability to block the α2-adrenergic receptor and cholinergic receptors. The drug also inhibits the synthesis of amines including serotonin, dopamine and noradrenaline. This compound may be used as a treatment for depression because it does not have any significant side effects on the central nervous system or other organs.</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>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>

7-Chloroquinoline-3-carboxylicacid (7CQCA) is a synthetic compound that has been shown to have regulatory, immunomodulatory, and anticancer properties. It is a potent inhibitor of mammalian DNA polymerase beta and it has been shown to induce apoptosis in human prostate cancer cells by inhibiting the production of cAMP. 7CQCA also inhibits the proliferation of mouse CD1 leukemia cells in vitro and induces apoptosis in these cells. The compound was found to be more effective when used with other agents such as triticum aestivum extract, which may be due to its synergistic interaction with these compounds.

<p>Acridone is a potent antimicrobial agent that inhibits bacteria by binding to the duplex DNA. Acridone has been shown to have inhibitory properties against wastewater treatment, which may be due to its ability to bind with the bacterial dna and inhibit the replication of bacterial cells. Acridone also has genotoxic activity, as it has been shown to react with nuclei in carcinoma cell lines and cause DNA strand breakage. Acridone is a fluorescent probe that can be used for electrochemical impedance spectroscopy (EIS). It binds to the complementary sequence of double-stranded DNA and causes an increase in the impedance of a solution when exposed to an electric current. This property can be used for analytical methods such as gel electrophoresis or chromatography.</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>This is a quinoline derivative that has been shown to have inotropic and cardioprotective effects. It has been shown to increase the duration of action potentials and contractions in isolated heart muscle, as well as to improve the function of the heart by reducing the rate of myocardial oxygen consumption. 6-Hydroxy-3,4-dihydro-1H-quinoline-2-one has been shown to have anti-inflammatory properties and may be useful for treating respiratory diseases such as asthma. This compound is also used as a precursor for some pharmaceutical drugs, including chloroquine, mefloquine, amodiaquine, and primaquine. The compound is metabolized into conjugates that are recycled back into the body or excreted in human urine; this process is regulated by the balance between conjugation reactions and hydrolysis reactions.</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>2,2'-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>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>2-Dimethylamino-6-hydroxypurine is a biochemical that belongs to the group of purines. It is a methylated form of 2,6-diaminopurine and has been shown to be an antigenic product in wheat germ. 2,6-Diaminopurine is involved in the synthesis of protein and other biomolecules by transferring methyl groups from S-adenosyl methionine to amino acid side chains. This gene product is also involved in enzyme preparations and reactions that are related to the biochemical properties of mammalian cells. The methyltransferase enzyme catalyzes the reaction mechanism for 2,6-dimethylamino-purine. 2,6-Dimethylamino-purine has been shown to have anticancer effects on various types of cancer cells with modifications on their DNA.</p>

<p>2-(2-Aminophenyl)benzimidazole is a synthetic compound with the chemical formula C8H6N2. It has an intramolecular hydrogen bond and reacts with salicylaldehyde to form 2-aminobenzimidazole, which is a reaction product. 2-(2-Aminophenyl)benzimidazole may be used as an antimicrobial agent, but it also has other uses such as a reagent in organic synthesis. It is soluble in water and can be obtained through liquid chromatography.</p>

<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>

<p>(1R,3S,5S)-3-(3-Isopropyl-5-methyl-4H-1,2,4-triazol-4-yl)-8-azabicyclo[3.2.1]octane is a versatile building block that can be used in the synthesis of complex compounds. It is a reagent and speciality chemical with applications in research or as a useful intermediate in the synthesis of other chemicals. (1R,3S,5S)-3-(3-Isopropyl-5-methyl-4H-1,2,4-triazol-4-yl)-8-azabicyclo[3.2.1]octane is also a useful scaffold for the synthesis of other compounds with specific properties such as high quality and usefulness as reaction components.</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>6-Bromo-2-(4-bromophenyl)-indole is a fine chemical with CAS No. 28718-96-9 that can be used as a versatile building block for the synthesis of complex compounds, useful scaffold for research chemicals, and reaction component for speciality chemicals. This compound has high quality and is a reagent in the synthesis of other compounds.</p>

<p>2-Amino-6-iodopurine is an analog of the purine nucleoside guanine, which has been used to synthesize a variety of boronic acids. The most common use for 2-amino-6-iodopurine is in the synthesis of benzylboronic acid, which can be used as an organometallic reagent in organic synthesis. This compound also has dehydrogenase activity and has been shown to catalyze the conversion of benzoic acid to benzaldehyde, mediated by NADH. 2-Amino-6-iodopurine is found in the biosynthesis of ribonucleotides and deoxyribonucleotides, where it reacts with chloride ions and phosphate groups to form adenylate and xanthosine monophosphates.</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>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>

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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>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>

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<p>Please enquire for more information about 4-(2-(4-Bromophenyl)-6,6-dimethyl-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>Please enquire for more information about 3-((4-Methoxyphenyl)methylene)-1,4-dihydro-4-thiaquinolin-2-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

Please enquire for more information about 5-methyl-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

<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>

Please enquire for more information about 3-(2-(4-Bromophenyl)-6,6-dimethyl-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

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>Please enquire for more information about 1-(2-Chloropropanoyl)indoline including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<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>

<p>Please enquire for more information about 3-(3,4,5-Trimethoxybenzoylhydrazidyl)-2-oxoindoline including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 3-(4-Bromophenyl)-5-(hydroxyimino)-7,7-dimethyl-6,7,8-trihydrocinnoline including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Applications 5-Nitroisoindoline is used as a reagent in organic synthesis of several compounds including that of biphenylcarboxamidoisoindoline derivatives, which act as apolipoprotein B secretion inhibitors, and of benzenesulfonamides which may act as antipsychotic agents.<br>References Yamada, H., et al.: Preparation of biphenylcarboxamidoisoindoline derivatives as apolipoprotein B secretion inhibitors, WO Patent 2002014277, Feb 21, 2002; Cooper, D., et al.: Preparation of benzenesulfonamides as antipsychotic agents, WO Patent 2003068732, Aug 21, 2003;<br></p>

<p>Stability Store under Argon<br>Applications 3,6-Thioxanthenediamine-10,10-dioxide (cas# 10215-25-5) is a compound useful in organic synthesis.<br></p>

<p>Stability Hygroscopic<br>Applications 2,4-Dichloro-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidine hydrochloride (cas# 1187830-76-7) is a useful research chemical.<br></p>

<p>Applications Bicyclo[4.1.0]Heptane-7-Carboxylic Acid (cas# 41894-76-2) is a useful reagent for the heteroatom-​directed C-​H borylation of cyclopropanes and cyclobutanes.<br>References Murakami, R., et al.: Chem. Eur. J., 20, 13127 (2014)<br></p>

<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>