Polycyclic Compounds

<p>8-Aminopurine is an aminopurine that is used as a research tool in magnetic resonance spectroscopy. The proton magnetic resonance spectrum of 8-aminopurine shows two characteristic peaks at 3.0 and 4.2 ppm, which are assigned to the aminopurine tautomers (3-HPA, 4-HPA). The kinetic stability of 8-aminopurine in water is pH dependent and has been shown to be strongly dependent on the presence of aldehyde oxidase (AO) activity. AO activity can be inhibited by the addition of dimethylformamide or other non-specific inhibitors such as 2,6-dichloroisonicotinic acid.</p>

<p>(8S,10S,11S,13S,14S,16S)-9-Fluoro-11-Hydroxy-10,13,16-Trimethyl-17-Methylsulfanylcarbonyl-3-Oxo-6,7,8,11,12,14,15,16-Octahydrocyclo penta[a]Phenanthren-17-Yl) Acetate is a fatty acid ester that is used as a pharmaceutical preparation. It has been shown to be an effective treatment for the muscle wasting disease myotonic dystrophy and has been approved by the FDA. (8S,10S,11S,13S,14S,, 16 S)-9 - Fluoro - 11 - Hydroxy - 10 , 13 , 16 - Trimethyl - 17 - Methylsulfanylcarbonyl - 3 - Oxo - 6 , 7 , 8 , 11</p>

<p>6-Methoxyindole is an acetate extract of the plant 5-methoxyindole. It has been shown to be a 5-HT1A receptor agonist in animals, and has been shown to have cardiac effects in rats. 6-Methoxyindole is also used as a precursor for the synthesis of diphenylacetylindoles. 6-Methoxyindole is one of the molecules that can be recombined to form a batcho-leimgruber indole (BLI).</p>

<p>3-Cyano-7-ethoxycoumarin is a specialized fluorescent probe, which is a synthetic organic compound designed for use in biochemical assays. This compound is sourced from the broader family of coumarins, which are known for their versatile fluorescence properties. The mode of action of 3-Cyano-7-ethoxycoumarin involves its ability to exhibit strong fluorescent emission when excited by specific wavelengths of light, making it a valuable tool for monitoring biochemical reactions and interactions.</p>

<p>Rutaretin is a polyphenolic compound, which is a derivative of natural flavonoids extracted from plant sources. It functions primarily as an antioxidant by scavenging free radicals and inhibiting oxidative stress at the cellular level. Its molecular structure allows it to interact with reactive oxygen species, mitigating the damaging effects on cellular components such as DNA, proteins, and lipids.</p>

<p>Isatin dianilide is an organic compound with the chemical formula C8H6N2O. It is a white solid that is soluble in water, ethanol and acetone. Isatin dianilide can be synthesized by reacting phenylacetic acid with ammonia and formaldehyde. Isatin dianilide has been shown to have efficient oxidation reaction with Baeyer-Villiger oxidation, which makes it suitable for industrial use. Isatin dianilide also has biological activities such as inhibition of aminopeptidase N and aminopeptidase M, which are enzymes involved in protein synthesis. Yields of isatin dianilide are high because it can be produced from the commercially available compounds isatin and amidine.</p>

<p>2-Methyl-5-nitroimidazole, also known as menidazole, is an impurity of metronidazole, which is used as an antibacterial and antiprotozoal medication in the treatment of infections, including rosacea. 2-Methyl-5-nitroimidazole is a derivative of nitroimidazole and has potential antimicrobial and antitrichomonal activities. Its synthesis can be achieved using various methods, including nucleophilic reaction, ester derivatives, reaction with metronidazole, and substitution reactions. Several derivatives of 2-Methyl-5-nitroimidazole have been synthesized and tested for their antibacterial, antifungal, and antitrichomonal activities. Both 2-Methyl-5-nitroimidazole and its derivatives have potential applications as antimicrobial and antitrichomonal agents.</p>

<p>5-Bromoindole-3-carboxaldehyde is a water molecule that has been crystallized in the form of an amide. It is a chemical substance with asymmetric synthesis and significant antifungal activity. 5-Bromoindole-3-carboxaldehyde is active against some strains of the fungus Candida albicans and has been shown to inhibit the growth of kidney cells. This molecule also binds to the neurokinin 1 receptor and is used as a probe for fluorescence studies. The efficient method for synthesizing 5-Bromoindole-3-carboxaldehyde includes using silico analysis to confirm the structure on a computer, then performing an asymmetric synthesis with an acid catalyst to produce this compound.</p>

<p>6-Bromo-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one is a versatile building block that can be used in a variety of chemical reactions as an intermediate. It is also useful in the synthesis of a variety of compounds, such as pharmaceuticals and research chemicals. 6-Bromo-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one is an organic compound with a molecular formula of C8H5BrN4O. It has an mp of 152°C and decomposes to form nitrogen gas and carbon monoxide at higher temperatures.</p>

<p>1-Methyl-1H-indole-2,3-dione is a chemical compound that belongs to the class of indole derivatives. It can be synthesized by reacting 2,3-dihydroxybenzaldehyde with 2,2'-azobis(2-amidinopropane) dihydrochloride and methyl iodide in the presence of copper (II) acetate. This reaction mechanism is similar to that of other reactions involving an intramolecular hydrogen transfer. The binding constants for 1-methyl-1H-indole-2,3-dione are very high and this compound has been shown to inhibit herpes simplex virus replication in vitro. 1MIDD binds to the active site of tryptophan fluorescence and synchronous fluorescence proteins. 1MIDD also binds to copper ions in a coordination geometry that is similar to that found for other compounds containing a carbonyl group.</p>

<p>5-Amino-1-phenylpyrazole-4-carboxamide (APC) is a synthetic compound that has been shown to have potential as an antitumor agent. This compound has been shown to inhibit the growth of cancer cells in vitro, with cytometric analysis showing that it inhibits DNA synthesis and cell proliferation. It also has antibacterial activity, which may be due to its ability to inhibit bacterial DNA gyrase and topoisomerase IV. APC has been found in wastewater at concentrations of 2.6 μg/L, indicating that it is currently being produced and used for industrial purposes. APC can be synthesized by reacting 1-(3-aminopropyl)piperazine with 3-(2H)-furanone and triethylamine to form 5-amino-1-[(2H)-pyridin-2-yl]pyrazole-4-- carboxylic acid chloride, which can then</p>

<p>4-Chloroindole-3-acetic acid is a plant hormone that belongs to the group of auxins. It has been shown to stimulate root formation in plants by increasing the amount of auxin present in the plant's tissues. 4-Chloroindole-3-acetic acid is an intramolecular hydrogen donor and can form hydrogen bonds with other molecules. It also has a receptor binding site and cyclic peptide backbone, which allow it to act as a transcription factor or enzyme inhibitor. This molecule has been shown to be an optimum concentration for root formation in physiology experiments, and can be used as a model system for auxin research.</p>

<p>4,4',6,6'-Tetramethyl-2,2'-bipyridine (TMTB) is a small molecule that can be used as an efficient and cost-effective catalyst for the production of hydrogen from water. TMTB is able to transform solar energy into chemical energy by converting light absorbed in a semiconductor material to an electric current. TMTB has been shown to improve the efficiency of solar cells by boosting the performance of the catalysts that drive chemical reactions in the devices. This effect was found to be synergistic with other materials such as graphene oxide and tungsten disulfide. In addition, TMTB nanoparticles were shown to have a normalizing effect on the charge density in photoelectrochemical cells, which may lead to improved stability and durability.</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>7-Ethoxycoumarin is a fluorescent substrate used in biochemical research, which is derived synthetically. It undergoes biotransformation primarily via oxidative dealkylation, catalyzed by cytochrome P450 enzymes, resulting in the formation of 7-hydroxycoumarin. By monitoring the fluorescent 7-hydroxycoumarin, researchers can assess enzymatic activity and study metabolic pathways.</p>

<p>Scopolin is a coumarin glucoside, which is derived from the plant secondary metabolism. It originates predominantly from species within the Solanaceae family, including tobacco and potato plants. Its biosynthesis involves the conversion of scopoline, a precursor molecule, through glucosylation. This process is catalyzed by glucosyltransferases, which facilitate the attachment of a glucose moiety.</p>

<p>8-Aminoquinoline is a fluorescent probe that is used to detect the presence of nitrite ions in biological samples. It is used in electron paramagnetic resonance (EPR) experiments and can be used as a chemical inhibitor of cytochrome P450 enzymes. 8-Aminoquinoline has been shown to have minimal toxicity in animal models. It has been shown to inhibit the growth of Leishmania, an organism that causes leishmaniasis, by arresting protein synthesis at the ribosome level. The drug interactions of 8-aminoquinoline have not been well studied, but it may be necessary for patients to avoid other drugs that are metabolized by cytochrome P450 enzymes when taking this agent.</p>

<p>Radiosensitiser in hypoxic tumours</p>

<p>1-Benzyl-3-hydroxy-1H-indazole is a hydrophilic matrix that can be used to deliver drugs. The hydrophilicity of the matrix allows it to dissolve in water and form a paste when mixed with water. The drug or drug formulation is dispersed within the paste and delivered to the site of action by the matrix. 1-Benzyl-3-hydroxy-1H-indazole has shown inhibition of inflammation, which may be due to its ability to inhibit prostaglandin synthesis. 1BHI can also be used for electroreduction reactions, such as reduction of metal ions, at temperatures ranging from -10°C to +20°C.</p>

<p>Synthon for preparation of cholinergic receptor ligands; hypotensive</p>

<p>Substrate for dealkylase.</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-Bromo-1H-indole-6-carbonitrile is a versatile building block that can be used in the synthesis of complex compounds and research chemicals. 4-Bromo-1H-indole-6-carbonitrile is a reagent in the production of speciality chemicals, and is also used as an intermediate to produce other compounds. This compound is useful as a starting material for the synthesis of pharmaceuticals, agrochemicals, and perfumes. It has been shown to be an effective scaffold for the construction of heterocycles.</p>

<p>(-)-Oxypeucedanin is a natural furanocoumarin, which is a type of organic compound. Furanocoumarins are derived from specific plants and are known for their complex structures and biological activities. (-)-Oxypeucedanin is sourced primarily from plants belonging to the Apiaceae family, such as Peucedanum species.</p>

<p>Fraxidin is a naturally occurring compound, specifically an O-methylated coumarin, which is derived from certain plant sources such as the fruits of the ash tree. It is primarily obtained through the processing of various plant materials within the Rutaceae family. The mode of action of Fraxidin involves the inhibition of oxidative damage due to its capacity to scavenge free radicals, thus leading to potential antioxidant properties in biological systems.</p>

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

<p>5-Nitro-1,10-phenanthroline is a coordination compound that belongs to the group of p2. It has been shown to have low toxicity and can be used as an ancillary ligand in coordination chemistry. 5-Nitro-1,10-phenanthroline has been used as a synchronous fluorescence probe for amines and is also useful for kinetic studies due to its high stability and sensitivity. FTIR spectroscopy has shown that this compound binds to glyoxal at neutral pH; it may also react with reactive oxygen species such as superoxide, hydrogen peroxide, or hydroxyl radicals.</p>

<p>2-Mercapto-5-benzimidazole sulfonic acid sodium salt dihydrate is a molecule that can be used in devices. It has been shown to reversibly change the morphology of a monolayer and to generate asymmetric structures. 2-Mercapto-5-benzimidazole sulfonic acid sodium salt dihydrate can be used to generate fluorescent emulsions, which are systems where the magnetic particles are suspended in an oil droplet and illuminated by light of an appropriate wavelength. The molecules that make up 2-Mercapto-5-benzimidazole sulfonic acid sodium salt dihydrate have been shown to function as acceptors for molecular orbitals, which are wave functions that describe electron distribution around the atomic nucleus. These properties make it a promising candidate for use in microscopy techniques, such as scanning tunneling microscopy (STM) or atomic force microscopy (AFM).</p>

<p>5-Aminoindole is a hydrogen bond acid. It has been shown to have an optimum concentration of 0.1 mM in the presence of 0.2 mM potassium chloride and 2 mM magnesium chloride, which is similar to the pH range for biological systems. 5-Aminoindole also acts as a competitive inhibitor of quinoline derivatives, such as chloroquine and hydroxychloroquine, which are used in the treatment of malaria and rheumatoid arthritis. The compound has been shown to be active against primary cells grown in culture, including mouse erythrocytes and human hepatocytes. When used with agarose gel electrophoresis or electrochemical impedance spectroscopy, 5-aminoindole shows excellent selectivity for kinases over other enzymes. 5-Aminoindole is not reactive under physiological conditions because it does not have any redox potentials that can be measured by Langmuir adsorption isother</p>

<p>5-Methoxy-2-methylindole is an organic solvent that has been shown to have a wide range of bioactive properties. It is used in the production of acetylcholine, which is an important neurotransmitter. 5-Methoxy-2-methylindole also reacts with chloride ions, which may be an important factor when considering the life cycles and bioactive substances of this molecule. The reaction yield depends on the pH of the solution. 5-Methoxy-2-methylindole can undergo chlorination reactions to form polychlorinated derivatives, which are used as petrochemicals. This molecule also has retinoid properties and can act as a proton donor or acceptor depending on whether it is protonated or deprotonated.</p>

<p>Isatin bis-cresol is a silicon-containing compound that can be used as a viscosity modifier and stabilizer in polymers. Isatin bis-cresol has shown resistance to degradation by water, alkali, and acid. It also has a high formation rate and can be used for the production of functionalized polymers such as polycarbonates or phosphonium salts. Isatin bis-cresol is insoluble in water but soluble in organic solvents, which makes it an ideal candidate for use in transesterification reactions. Isatin bis-cresol contains three functional groups: phenolic (OH), carboxylic acid (COOH), and alcohol (OH).</p>

<p>Bis(2,2'-bipyridine)-4'-methyl-4-carboxybipyridine-ruthenium N-succinimidyl ester-bis(hexafluorophosphate) is a molecule that inhibits the activity of matrix metalloproteinases. It binds to the active site of the enzyme and blocks its activity. This drug has been shown to be effective in inhibiting the activity of MMPs in cells, but not in tissue culture because it does not cross cell membranes. Bis(2,2'-bipyridine)-4'-methyl-4-carboxybipyridine-ruthenium N-succinimidyl ester-bis(hexafluorophosphate) has also been shown to have a low detection limit and can detect low levels of matrix metalloproteinase activity in cells.</p>

<p>2,2'-Bipyridine-6,6'-dicarboxylic acid is a molecule that has an acidic functional group. It has been found to have a molecular weight of 220.2 g/mol and is soluble in water at elevated temperatures. 2,2'-Bipyridine-6,6'-dicarboxylic acid has been shown to be photoprocessable in the presence of sodium carbonate as a catalyst. The reaction rate can be increased by adding a diluent to the solution or by using linear models.</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>Please enquire for more information about Nordalbergin including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>MAO inhibitor; neuro-protective and cognitive enhancement effects</p>

<p>5-Fluoro-N,N-Dimethyl-1H-Indole-3-Ethanamine is a psychedelic drug with affinity for the serotonin 5HT2A receptor. It has been shown to interact with a diversity of ion channels and transporters. The affinity of 5FEDME for the 5HT2C receptor may also be normalizing. This drug has been shown to be an agonist at the 5HT2A receptor, which may contribute to its psychedelic effects.</p>

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

<p>Indole-3-acetyl-L-tryptophan is a water soluble anion that can be used as a recovery agent in the analysis of salicylic acid. It has been shown to quantitatively recover ammonium formate, which is an indicator for the presence of salicylic acid in a sample. Indole-3-acetyl-L-tryptophan also has been shown to quantitatively recover indole-3-acetyl-l -aspartic acid, which is another indicator for the presence of salicylic acid in a sample. Indole-3-acetyl L tryptophan can also be used to quantify and identify indoles. This compound has been proposed as a possible regulatory molecule for abscisic acid, which regulates plant growth and seed germination. Indole 3 acetyl tryptophan can also be used to measure the level of salicylic acid in plants and plant extracts by using UV spectrosc</p>

<p>3-Carbethoxyquinuclidine is an antihistaminic drug that belongs to the class of quinuclidines. It is used in research and has been shown to have a pharmacological effect on the central nervous system, including inhibition of histamine release. 3-Carbethoxyquinuclidine has been found to be anti-inflammatory and analgesic. It also inhibits prostaglandins and other mediators of inflammation, such as leukotrienes, thromboxanes, and platelet activating factor. 3-Carbethoxyquinuclidine is hydrolyzed by acid or alkaline conditions, but can be recrystallized from boiling methanol or ethanol.</p>

<p>2,2'-Bipyridine-5,5'-dicarboxylic acid is an algal metabolite that has been shown to have a glucose sensor function. It is synthesized by Chlorella and other green algae in response to light and high concentrations of glucose. This compound can be used as a linker for the immobilization of fluorescent probes or luminescent probes. It also has a catalytic subunit that can be used in oxidation reactions at low temperatures with chloride as the oxidant. 2,2'-Bipyridine-5,5'-dicarboxylic acid is chemically stable and does not react with chloride or ligands. It can also be used as an oxidation catalyst for reactions at high temperatures.</p>

<p>5-(5-Chloro-2-hydroxyphenyl)-1-phenylpyrazole is a useful intermediate for the synthesis of complex compounds. It is also used as a reagent and a speciality chemical in research. 5-(5-Chloro-2-hydroxyphenyl)-1-phenylpyrazole has a CAS number of 36124-03-5. This chemical is soluble in organic solvents such as benzene, chloroform, dichloromethane, tetrahydrofuran, and toluene.</p>

<p>Benzo[c]phenanthrene is a polycyclic aromatic hydrocarbon that has been shown to have carcinogenic properties in rats. It is also a potential mutagen and can cause DNA damage by forming intramolecular hydrogen bonds with guanine residues in DNA duplexes. These adducts are detected in tumor cells of rats treated with benzo[c]phenanthrene, as well as in human liver cells and mouse liver tumor cells. Benzo[c]phenanthrene can be activated by cytochrome P450 enzymes to form reactive metabolites, which bind covalently to DNA, proteins, and other cellular macromolecules. Benzo[c]phenanthrene has been shown to cause cancer in mice when given orally or injected into the peritoneal cavity. This chemical has also been found to cause liver cell necrosis in rats, at doses of 25 mg/kg body weight.</p>

<p>8-Hydroxy-2-quinolinecarbonitrile is an uncomplexed ligand that can be used for the synthesis of metal complexes. 8-Hydroxy-2-quinolinecarbonitrile is insoluble in most solvents, including water, and has a high melting point. This compound can be synthesized from acetonitrile and primary amines by condensing with formaldehyde. It is not possible to catalyze this reaction, as it does not undergo homolysis or heterolysis reactions. The uncomplexed ligand has been shown to bind to metal ions such as copper and silver. Its diffraction pattern was found to have a polynuclear nature with a number of diffraction peaks within the range of 5–9 Å.</p>

<p>4,4' -Bis(N,N-dimethylamino)-2,2' -bipyridine (DMAB) is a ligand that is used in electrochemical studies. It has been shown to have ancillary properties, which means that it does not interact directly with the substrate but modifies its environment. DMAB can form a complex with the proton at the electrode surface and x-ray crystal structures have been obtained for this interaction. These structures demonstrate that DMAB binds to the tetrazole ring of pyridine and stabilizes the molecule by increasing its redox potentials.</p>

<p>7-Chloro-2H-pyrido[3,2-B]-1,4-oxazin-3(4H)-one is a chemical which is used as a reagent and building block in the synthesis of more complex compounds. It has been reported to be an intermediate for the production of pharmaceuticals and agrochemicals. The compound can also be used as an intermediate for the synthesis of other valuable chemicals such as pesticides and dyes. 7-Chloro-2H-pyrido[3,2-B]-1,4-oxazin-3(4H)-one has a CAS number of 205748-05-6.</p>

<p>Umbelliferone-3-carboxylic acid is a coumarin derivative, which is a type of natural or synthetic organic compound often utilized in biochemical research. It is sourced from modifications of natural coumarins, which are typically isolated from plants belonging to the Apiaceae family, such as parsley, celery, and carrots. This compound functions by interacting with cellular enzymes, providing a fluorescent probe that aids in the investigation of enzymatic activities and pathways.</p>

<p>Monomethyl triazeno imidazole carboxamide (MTIC) is a drug that is used to treat cancer. It has been shown to inhibit the proliferation of tumor cells and induce apoptosis by inhibiting the expression of proteins, such as Bcl-2, which are involved in regulating mitochondrial membrane potential. MTIC has also been shown to inhibit protein synthesis and cell signaling pathways, such as the PI3K/Akt pathway. The use of MTIC for diagnosis purposes can be achieved using electrochemical impedance spectroscopy. A concentration–time curve can be obtained by incubating a biological sample with MTIC and measuring cell response using an impedance spectrophotometer. The clinical properties of MTIC include its ability to be administered orally or intravenously, have low toxicity, and inhibit the growth of tumor cells in vivo and in vitro.</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>(1S,4S)-1,7,7-Trimethyl-3-(Trifluoroacetyl)Bicyclo[2.2.1]Heptan-2-One is a white solid with a melting point of -76.8°C and a boiling point of 265°C at 10 mm Hg. It has the following functional groups: particle, luminescent, lanthanide, stabilizer, ligand, voltammetry, thermally stable and has nmr spectra that show light emission and coordination chemistry. This compound is a sulfoxide but can also be considered to be a phosphine or an amine depending on its structural features. The compound's nature is dependent on the temperature and pressure as well as the solvent it is being dissolved in.&gt;&gt;END&gt;&gt;</p>

<p>7-(Cyanomethoxy)indole is a versatile building block that can be used as a scaffold for the synthesis of complex molecules. It has been used as an intermediate in organic synthesis and as a reaction component for the preparation of useful compounds. 7-(Cyanomethoxy)indole is also known to have high quality and is widely used in research laboratories.</p>

<p>N-Amino-2-methylindoline HCl is an organic chemical compound that belongs to the class of acylating agents. It is a colorless solid that is soluble in water and methanol. The compound has been used in the acylation reaction with triethylamine and chloride to synthesize dioxane. N-Amino-2-methylindoline HCl is also a substance that can be found in nature, such as in the leaves of plants. Organic chemistry deals with the study of compounds and their reactions, which includes N-Amino-2-methylindoline HCl and its uses.</p>

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

<p>2-(3-Hydroxypropyl)benzimidazole is a chloroform extract of the bark of the tree, Pongamia pinnata. It has been shown to have antibacterial and antitumor activity. 2-(3-Hydroxypropyl)benzimidazole has been found to be active against methicillin-resistant Staphylococcus aureus (MRSA), showing strong inhibitory effects on bacterial cell growth in vitro. The mechanism of action may be due to its ability to bind to DNA and RNA, preventing transcription and replication. 2-(3-Hydroxypropyl)benzimidazole also inhibits protein synthesis by binding to ribosomes and interfering with the function of enzymes that are involved in this process such as cytochrome c reductase, glutathione reductase, and 3-ketoacyl coenzyme A thiolase.</p>

<p>6-Chloro-3-indolyl 1,3-diacetate is an aglycone that is used as a chromogenic substrate for the detection of bacteria. It reacts with specific enzymes in the bacterial cell wall to produce a red or pink color. 6-Chloro-3-indolyl 1,3-diacetate is used as a diagnostic tool to identify bacteria and has been shown to be excreted in urine.</p>

<p>Please enquire for more information about 7,7-Dimethyl-2,5-dioxo-1,2,5,6,7,8-hexahydroquinoline-3-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Benzyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid is a versatile building block that can be used in the synthesis of fine chemicals and pharmaceuticals. It is used as a precursor to other compounds such as 2-benzylisoquinoline and 2-(2'-benzyloxy)benzoic acid. It is also used as a reagent for various research purposes.</p>

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

<p>Thiamine sulfate inner salt is a hyaluronic acid that is used in skin cancer treatment. It has been shown to have antimicrobial properties, which may be due to its ability to disrupt the cell membrane. Thiamine sulfate inner salt has also been shown to increase the germination rate of damaged seeds and can be used as a stabilizer for carrageenan. This compound is an acidic substance with a pH of 2-3. It is soluble in water and hydrochloric acid and reacts with magnesium salts, ethylene diamine, diamine tetraacetic acid, and antimicrobial peptides.</p>

<p>4-Bromomethyl-2(1H)-Quinolinone is a chemical compound that is used in the calibration of an HPLC system. It has been shown to be linear over a wide range of concentrations. The detection wavelength is at 230 nm, and the flow rate is 1 mL/min. The average response for 4-bromomethyl-2(1H)-quinolinone was found to be approximately 0.7 AUFS with a standard deviation of 0.3 AUFS.</p>

<p>L-Octahydroindole-2-carboxylic acid is a basic structure that is used in the industrial preparation of a number of chemical compounds. It is also used for the synthesis of L-(2S,3aS,7aS)-octahydroindole-2-carboxylic acid (LOTSC) and its ester hydrochloride salt. The kinetic energy of this molecule has been studied by measuring it's rate of reaction with cyclohexane ring. The inhibition study was done on lung cells to study the effects of LOTSC on growth factors and showed that this molecule inhibited the release of bradykinin B2, which is a peptide secreted by lungs. The pharmacokinetic properties have been studied in rats and shows that it has higher bioavailability than other molecules in this class.</p>

<p>7-Bromo-1,2,3,4-tetrahydroquinoline is a high quality reagent that is an intermediate for the synthesis of heterocycles. It is useful as a building block for the synthesis of complex compounds. 7-Bromo-1,2,3,4-tetrahydroquinoline has been used as a useful scaffold in the synthesis of novel and versatile molecules with biological activity. This compound can be used as a reaction component in organic chemistry and can also be used to produce speciality chemicals and research chemicals. CAS No. 114744-51-3</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>The 4-cyanoindole is a fluorescent molecule that binds to proteins and affects protein homeostasis. It has been shown to bind to the sodium salt form of proteins, which are typically found in human liver cells. The binding of 4-cyanoindole to these proteins leads to its reduction by borohydride and fluorescence resonance energy transfer (FRET) between the molecule and the protein. This binding can be detected using a fluorescence lifetime spectroscopy technique, which detects changes in the fluorescence's lifetime as well as intensity. The binding of 4-cyanoindole to proteins has been shown to have anti-cancer properties. It has also been used for detection of monoclonal antibodies against cancer cells or for fluorescent labeling of cancer cells for immunofluorescent microscopy.</p>

<p>8-Hydroxyquinoline-2-carboxylic acid is a 3-hydroxyanthranilic acid derivative that is often used as a biomarker of urine. The 8OHQA can be synthesized from 3-hydroxyanthranilic acid by the action of xanthine oxidase and hydrogen peroxide, and it has been shown to be an inhibitor of protein synthesis. This inhibition may be due to its ability to form hydrogen bonds with the hydroxyl group on the ribose side chain and its ability to coordinate with metals. 8OHQA has been shown to have anti-inflammatory effects in bladder cancer cells, which may be due to its ability to inhibit prostaglandin synthesis.</p>

<p>2-Methylindole is a reactive molecule that can undergo electrophilic substitution at the 2-position. It reacts with a variety of nitrogen nucleophiles, acylating them at the 2-position. These reactions are catalyzed by enzymes such as carbonyl reductase and methyl ketone reductase. The reaction mechanism is not yet fully understood, but it has been proposed that it proceeds through an acylation reaction between two molecules of 2-methylindole to form a linear product. The regiospecificity of this reaction has been demonstrated in vivo using a model system.</p>

<p>Noreleagnine is a natural compound that is used to inhibit the replication of viruses. It has been shown to bind to dopamine receptors in the brain, which may be responsible for its cytotoxic effects on mouse tumor cells. Noreleagnine can also be used as a sample preparation agent because it can produce light emission and biological properties that are similar to those of dopamine. This drug is synthesized using an asymmetric synthesis and sodium carbonate. A number of methods have been developed for the synthesis of noreleagnine, including ester hydrochloride and electrochemical detector.</p>

<p>Fluorescent dye used in diagnostic culture media</p>

<p>5-Hydroxyoxindole (5HO) is a naturally occurring molecule that is found in oxindole and other indoles. It has been shown to have regulatory effects on inflammatory diseases, notably in the treatment of colitis. 5HO possesses significant cytotoxicity against carcinoma cells and also has radical scavenging activity. This compound can be synthesized using a solid-phase synthesis method. The presence of 5HO in skin cells has been correlated with the production of skin pigment called melanin. In addition, this molecule has been shown to bind to picolinic acid, which may contribute to its anti-inflammatory properties. 5HO is also present in neurologic disorders such as Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis.</p>

<p>Glycocoumarin is a phytochemical compound that is primarily categorized as a bioactive flavonoid. It is derived from Glycyrrhiza uralensis, commonly known as liquorice, a plant renowned for its diverse pharmacological properties. The mode of action of glycocoumarin involves the modulation of various biological pathways, including its potential to influence inflammatory responses and antioxidant activity. This compound is known to interact with cellular signaling mechanisms, which could mediate its effects on immune modulation and cellular protection.</p>

<p>Indole-4-Carboxylic acid is a molecule that belongs to the group of indole carboxylic acids. It is an organic compound that has a dipole moment and isomers. Indole-4-carboxylic acid can be synthesized by the saponification of indole-7-carboxylic acid, which has two functional groups: a hydroxy group and an amide group. The molecule has a chemical structure with an amide bond between the carboxyl and amino groups at one end, which forms a protonated amide. This protonated amide also has two orientations: trans and cis. The trans orientation is found in human cytochrome P450 and other proteins, while the cis orientation is found in enzymes such as tryptophan synthase, indoleamine 2,3 dioxygenase, or tyrosine hydroxylase.</p>

<p>2-Azaspiro[3.3]heptane HCI is a fine chemical that has many uses in research, manufacturing, and other industries. It is a versatile building block that can be used as an intermediate or reaction component for the synthesis of organic compounds. 2-Azaspiro[3.3]heptane HCI is also a speciality chemical because it has many applications in the pharmaceutical and agrochemical industries. This compound can be used as a reagent for the determination of carboxylic acids, alcohols, and amines by paper chromatography and high performance liquid chromatography (HPLC). 2-Azaspiro[3.3]heptane HCI is also useful in the synthesis of peptides and other complex compounds, such as diazepam.</p>

<p>3,3'-Diindolyl is a molecule that belongs to the class of oxindoles. Oxindoles are bioactive molecules that are formed by the reduction of 3,3'-dihydroxyindole (oxindole). The borohydride reduction of 3,3'-dihydroxyindole yields 3,3'-diindolyl. It has been shown to have anti-inflammatory properties and can be used for the treatment of inflammatory diseases such as congestive heart failure. 3,3'-Diindolyl is also an acidic compound and therefore can be used as an acidic buffer in pharmacopeia. It reacts with peroxide to form an aldehyde after oxidation. This reaction is catalyzed by sodium borohydride reduction or hydrogen peroxide. The borohydride reduction of 3,3'-diindolyl yields 2-hydroxy-1-(2-hydroxyethyl) indole (oxindole).</p>

<p>Acetyl columbianetin is a natural compound, which is a type of secondary metabolite derived primarily from plant sources. This compound is part of a broader category of phytochemicals known for their diverse bioactive properties. Acetyl columbianetin is specifically sourced from certain species within the Apiaceae family, commonly found in traditional medicine.</p>

<p>Isoscopoletin is a naturally occurring coumarin derivative, which is typically sourced from various plants, including some medicinal herbs. This compound is found in a variety of plant species, where it plays a role in the plant's defense mechanisms against pathogens. It is known for its characteristic chemical structure that belongs to the coumarin family, which is widespread in the plant kingdom.</p>

<p>N,N'-Thiocarbonyldiimidazole is a potent inhibitor of the enzyme acetylcholinesterase. It is used in research as an inhibitor molecule for receptor activity and to study the mechanism of action of other drugs. N,N'-Thiocarbonyldiimidazole inhibits the production of ester hydrochloride by rat liver microsomes and muscle cell proliferation. In addition, this compound has been shown to be a protonophore that can transport protons across membranes without energy input. This can be done through Langmuir adsorption isotherm and electrochemical impedance spectroscopy.</p>

<p>3,4-Dihydro-2(1H)-quinolinone is a potent inhibitor of dopamine β-hydroxylase and is used as a model system to study the pharmacokinetic properties of carbostyril. It has been shown that 3,4-dihydro-2(1H)-quinolinone binds to the chloride ion in the active site of dopamine β-hydroxylase. This binding prevents the formation of a complex with the enzyme's substrate, which is required for catalysis. 3,4-Dihydro-2(1H)-quinolinone also interacts with the alkynyl group on dopamine and competitively inhibits its metabolism by monoamine oxidase (MAO).</p>

<p>1H-Indoline-3-carboxylic acid is a molecule with the chemical formula C8H6N2O2. It is an aromatic carboxylic acid and one of the three enantiopure isomers of indoline. 1H-Indoline-3-carboxylic acid has two tautomers, cis (cis) and trans (trans). The stereoisomer cis is found in nature, while trans can be synthesized. 1H-Indoline-3-carboxylic acid can be cleaved to form phenylacetic acid and benzoic acid in reactions catalyzed by acids at high temperatures. Kinetic studies have shown that 1H-indoline-3-carboxylic acid undergoes biotransformation to form methylbenzene, ethylbenzene, propylbenzene, butylbenzene, pentylbenzene and hexylbenzene.</p>