Composés polycycliques

2-Hydroxy methyl imidazole is an organic compound that contains a reactive hydroxyl group. It is used as a sealant in the manufacturing of paper and textiles, as well as in the production of synthetic leather. The reaction mechanism of 2-hydroxy methyl imidazole involves the formation of an inorganic acid and copper complex. The conformational properties of 2-hydroxy methyl imidazole have been studied using covalent adducts, which are molecules with metal atoms bound to them. Magnetic resonance spectroscopy has been used to study the activation energies for 2-hydroxy methyl imidazole.

Please enquire for more information about 2-(Anilinomethyl)-1H-isoindole-1,3(2H)-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page

(S)-(-)-6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid hydrochloride is a synthetic chiral compound that is used to study the role of glyoxylate in biochemical reactions. This drug is an enolate and alkylating agent that can react with nucleophiles such as amines and thiols. It has been shown to be effective against perchlorates by hydrolyzing them into chlorine and oxygen gas. This drug has also been shown to inhibit the growth of Rhodobacter sphaeroides by inhibiting glyoxylate metabolism.

Lactone

3-Phenanthrol is a monohydroxylated polyphenol that inhibits the polymerase chain reaction by binding to the enzyme used for DNA replication. 3-Phenanthrol has been shown to inhibit several enzymes, including the sodium carbonate-dependent enzyme α-glucosidase and the acetylcholine esterase enzyme. This compound is also an analytical method used to measure renal function by measuring glomerular filtration rate in rats. 3-Phenanthrol has been shown to have a matrix effect on pharmacokinetic properties in rats, which can be explained by its hydrophobic nature. The molecular weight of 3-phenanthrol is 188.3 g/mol. It's IUPAC name is 2,4′,6′,-trihydroxybenzaldehyde and it has an anhydrous sodium salt form with a molecular weight of 192.2 g/mol.

Please enquire for more information about 8-Methyl-2-(3-propoxyphenyl)quinoline-4-carbonyl chloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

6-Methoxy-1,2,3,4-tetrahydroisoquinoline is a chiral compound that exhibits an affinity for the microtubule. It has been shown to induce neuronal cell death by inhibiting the synthesis of serotonin in the brain and blocking its reuptake. 6-Methoxy-1,2,3,4-tetrahydroisoquinoline also inhibits estrogen production and blocks the activation of estrogen receptors. This drug has been documented as being used as a transition metal catalyst in devices such as fuel cells and batteries. The hydrochloride salt form of 6-methoxy-1,2,3,4-tetrahydroisoquinoline is used to treat Parkinson's Disease. 6-Methoxy-1,2,3,4-tetrahydroisoquinoline has been documented as being used in cell death experiments with human cells and mouse neurons. This drug has also

Please enquire for more information about 2'-Cyclohexyl-1'-oxo-1',4'-dihydro-2'H-spiro[cyclopentane-1,3'-isoquinoline]-4'-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Xanthoxyletin is a coumarin, which is a type of natural organic compound commonly found in plants, particularly in the Rutaceae family. It is sourced from various plant species, including Zanthoxylum, known for their ethnobotanical uses. Xanthoxyletin functions primarily through its biochemical activity, including the inhibition of certain enzymes and modulation of cellular pathways that influence its pharmacological effects. This compound exhibits a wide range of biological properties, including antibacterial, antifungal, anti-inflammatory, and antiproliferative activities. Due to these properties, xanthoxyletin is of great interest in the field of medicinal chemistry and pharmacology. It is studied for its potential therapeutic applications, particularly in the development of new treatments for infectious diseases and inflammatory conditions. Research also explores its role in cancer research, where it may contribute to the development of novel chemotherapeutic agents. Scientists are continually exploring its bioactivity and possible synergistic effects with other compounds to enhance its efficacy and broaden its application scope.

Please enquire for more information about 3-Chloro-4-hydroxy-1-methylquinolin-2(1H)-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Peuarin including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-Fluoroquinoline is a quinoline derivative that has been shown to have tumorigenic activity in animal bioassays. In addition, 5-fluoroquinoline induced genotoxic effects in liver cells and was found to be carcinogenic in rats and mice. The mechanism of action of 5-fluoroquinoline is not yet known, but it is thought to be due to its ability to bind covalently with DNA. It also binds to RNA and protein in the cell, which may lead to inhibition of transcription or translation.

Please enquire for more information about 4-Ethyl-1,2,3,4-tetrahydropyrido[2,3-b]pyrazine including the price, delivery time and more detailed product information at the technical inquiry form on this page