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Please enquire for more information about 7,8,9,10-Tetrahydrophenanthridine-6-thiol including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 4,6-Dimethylquinolin-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 6-Bromo-2-(3-isobutoxyphenyl)quinoline-4-carbonyl chloride 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-(3-Bromo-2,2-dimethylpropyl)-1H-isoindole-1,3(2H)-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about (R)-Boc-4-amino-5-(3-indolyl)pentanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-[2-[4-(4-Fluorobenzoyl)-1-oxidopiperidin-1-yl]ethyl]-2,7-dimethylpyrido[2,1-b]pyrimidin-4-one (7FPP) is a polyfunctional molecule that exhibits anions and cations. It is a reactive compound and has been characterized by laser spectroscopy and microprobe analysis. 7FPP has been shown to be an effective scavenger of oxygenated molecules such as peroxides, hydroperoxides, and peroxyacids. 7FPP also has the ability to desorb cations from surfaces such as aluminum oxide and silicon dioxide. Rationally designing 7FPP with different functionalities will allow for the optimization of its properties.

4-(3,5-Dichloro-4-methoxyanilino)-6-methoxy-7-[3-(4-methylpiperazin-1-yl)propoxy]Quinoline-3-carbonitrile is a hydrogen ion pump inhibitor that has been shown to provide relief from congestive heart failure and hyperproliferative diseases. It inhibits the action of the sodium/hydrogen ion exchanger in the cell membrane, preventing the movement of sodium ions into and out of cells. The compound is biocompatible with human albumin, which may allow it to be used as a drug delivery system for cancer treatments. The molecule also functions as an efficient diode when placed in water vapor, which may be useful for detecting water leaks or monitoring humidity levels.

Please enquire for more information about 1-(2-Bromo-4,5-dimethoxybenzyl)-6,7-dimethoxyisoquinoline including the price, delivery time and more detailed product information at the technical inquiry form on this page

Tricyclohexylphosphine is a compound that is used in organic synthesis to form stable complexes with reactive functional groups such as trifluoroacetic acid, glycol ethers, and sodium carbonate. The reaction solution of these compounds forms a complex with copper chloride and fluorescence probe, which can be analyzed by x-ray crystallography. The reaction mechanism of this compound involves coordination geometry and hydroxyl group. Its basic structure is a trivalent phosphorus atom coordinated to three ligands. Structural analysis of this compound has been done using kinetic data and the results have indicated that the reaction proceeds through an SN2-like mechanism.

Rac1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid is a potent inhibitor of the Mcl-1 protein. Rac1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid has been shown to inhibit locomotor activity and to have potent inhibitory activity against bacteria. Rac1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid inhibits the antimicrobial peptide LL37 by binding to its active site and prevents LL37 from binding to bacterial cells. Rac1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid also inhibits chloride ion transport in mammalian cells. This compound has low expression in mammalian cells and erythrocytes. It is not toxic to these cells as it does not bind to plasma glucose or proteins in vitro. Rac1

Please enquire for more information about 6-Cyano-2-(4-cyanophenyl)indole including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 3-Amino-4-bromo-5-phenylpyrazole including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Aminoquinoline-3-carboxamide is a chemical compound with the molecular formula CHNO. It has an alkoxide group, which is a functional group consisting of one oxygen atom attached to two hydrocarbon groups. This alkoxide reacts with potassium and alkoxides to form salts, such as potassium 2-aminoquinoline-3-carboxylate. The pyrimidine ring in this molecule can be oxidized by sodamide and carboxamide to form pyrimido derivatives. Hydride reduction of these compounds produces cyclization products. In addition, it reacts with antiallergic drugs (e.g., hydrocortisone) to produce their corresponding quinolones in nuclear reactions.

6-Hydroxyquinoline-(1H)-2-one is an organic compound that has been shown to inhibit the uptake of carbostyril by bacterial cells. This inhibition causes increased uptake of xanthurenic acid and anthranilic acid, which are two compounds that are found in wastewater treatment. 6-Hydroxyquinoline-(1H)-2-one may be a potential anticancer agent, as it inhibits the growth of astroglia cells and bladder cancer cells. It also reacts with acylation reactions to form quinolinic acid, which has been shown to have anticancer effects.

Please enquire for more information about 2-(Chloroacetyl)-8-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole 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-(4-Ethoxyphenyl)-8-methylquinoline-4-carbonyl chloride 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-Butyl-1'-methyl-1-oxo-1,4-dihydro-2H-spiro[isoquinoline-3,4'-piperidine]-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Trichloromethylazacycloheptane is a synthetic compound that has been shown to be effective in the treatment of chronic pain. It is also used as an antiglaucoma drug and to treat endometriosis. Trichloromethylazacycloheptane has been prepared by reacting malonic acid with hexane in the presence of colitis, which is a type of bowel inflammation. The chloride ion acts as a nucleophile and attacks the electron-deficient carbon atom, forming a chloroformate intermediate. This intermediate reacts with chloride ion to form 2R,5S)-2-trichloromethyl-3-oxa-1-azabicyclo[3,3,0]octane-4-one.

Please enquire for more information about 5-Iodo-1H-indazole including the price, delivery time and more detailed product information at the technical inquiry form on this page

Murralongin is a natural compound that falls under the category of sesquiterpenes, a class of terpenoids characterized by their three isoprene units. It is derived from the leaves and stems of the plant Eremophila mitchellii, a species known for its rich diversity of bioactive compounds often utilized in traditional medicine. The primary mode of action of Murralongin involves modulation of specific enzymatic pathways, potentially influencing a range of biological processes, including anti-inflammatory and antimicrobial activities. Recent studies have focused on its potential therapeutic uses, exploring its efficacy as an anti-cancer agent by targeting cellular pathways involved in cancer cell proliferation and survival. Additionally, Murralongin's ability to inhibit certain microbial growth suggests applications in developing new antimicrobial drugs, addressing issues related to resistant bacterial strains. Furthermore, its anti-inflammatory properties imply potential applications in managing chronic inflammatory conditions, where current treatments may have significant limitations or side effects. Overall, Murralongin represents a promising subject for further research with the potential to contribute significantly to the development of new therapeutic agents.

4-Chloro-6-methoxyquinolin-7-ol (CMQ) is an alkali metal that inhibits the sodium/potassium ATPase pump, which is responsible for maintaining the cell's intracellular ion balance. It was discovered in a search for compounds that inhibit this enzyme and show promise in the treatment of heart diseases. CMQ has been shown to inhibit the sodium concentration in rat hearts with no effect on potassium concentrations, which may be due to its ability to bind to sodium ions but not potassium ions. The long-term effects of CMQ on human populations are unknown, as well as its effects on genotype and parameters. CMQ also has been shown to cause drug resistance mutations in bacteria, such as methicillin resistant Staphylococcus aureus (MRSA), by increasing the mutation rate. This is due to the fact that it inhibits DNA replication and protein synthesis in bacteria cells.

Applications Quinoline-4-carboxylic acid (cas# 486-74-8) is a useful research chemical.

5-Amino-6-(methylamino)quinoline is a molecule that inhibits the enzymatic activity of tyrosine phosphatases and has been shown to inhibit the growth of typhimurium ta98, which is resistant to quinoxaline. It has also been shown to be mutagenic in vitro. 5-Amino-6-(methylamino)quinoline has an imidazole ring and is synthesized from 2-methylbenzothiazole and N,N'-dimethylethylenediamine. The synthesis of this compound takes place in two steps with the first step being an oxidative cyclization followed by a reductive amination.

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

Please enquire for more information about S[3-Indolyl]isothiuronium iodide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 7-Methoxy-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole including the price, delivery time and more detailed product information at the technical inquiry form on this page

9-Hexahydro-9-Xanthene-9-Carbohydrazide is an herbicide that inhibits the growth of dicotyledons. It has been shown to have a substituent effect on phenyl. 9HXCZ binds to the active site of the enzyme, which prevents it from catalyzing reactions that would otherwise result in the synthesis of acetyl coenzyme A (acetyl CoA). 9HXCZ also inhibits the production of glucose by inhibiting the enzyme phosphoglucomutase.

Applications Tricyclene, is one of the main constituent of many essential oils having antioxidant activities. References Tamta, A., et al.: Cogent Chemistry, Vol.2, issue1 (2016);

Applications Dichloroquinoline derivatives for use as herbicides.

Please enquire for more information about 2-(5-Chlorothien-2-yl)-6-methylquinoline-4-carboxylic 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-(2,5-Dimethylphenyl)-8-methylquinoline-4-carboxylic 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 3-(1,1-Dioxido-2H-1,2,4-benzothiadiazin-3-yl)-4-hydroxy-1-methyl-2(1H)-quinolinone including the price, delivery time and more detailed product information at the technical inquiry form on this page

1-Ethyl-1,2,3,4-tetrahydroisoquinoline is an chiral compound that can be used as a starting material for the synthesis of other compounds. It is soluble in methanol and acetonitrile. 1-Ethyl-1,2,3,4-tetrahydroisoquinoline has been shown to behave differently in different solvents. In particular, it displays different behaviours in water and methanol. This behaviour may be due to steric interactions with the solvent or the analyte.

Please enquire for more information about 2-[(1-Methyl-3-piperidinyl)thio]-3-phenylquinolineHydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Hydroxyamino-3-methyl-3H-imidazo[4,5-f]quinoline (2HAIQ) is a reactive compound that binds to DNA. It has been shown to be a potent inhibitor of the enzyme cytosolic protein kinase C, which plays an important role in regulating cellular metabolism. 2HAIQ also inhibits the activity of enzymes such as hydroxylases and polymerases. The binding of 2HAIQ to DNA is thought to inhibit transcription by preventing RNA polymerase from transcribing DNA. 2HAIQ may also inhibit replication by binding to the dinucleotide phosphate molecule, which is essential for DNA synthesis.

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

Please enquire for more information about 5-Bromo-4,4-dimethyl-1,2,3,4-tetrahydroisoquinoline 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-(2-Ethoxyphenyl)quinoline-4-carboxylic 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 1-[Chloro(phenyl)acetyl]indoline including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Benzyl 2,4-dichloro-5,6-dihydropyrido[3,4-d]pyrimidine-7(8H)-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

The modification of 1,2,3,4-Tetrahydroquinoline-8-carboxylic acid with various functional groups has been shown to be a highly efficient method for synthesizing new compounds. The modification of 1,2,3,4-Tetrahydroquinoline-8-carboxylic acid with an acid derivative results in a compound that is an effective adjuvant arthritis drug. This modification also suppresses the symptoms of arthritis and has antirheumatic properties.

Please enquire for more information about 6-Bromo-2-(3-methoxypropyl)-3-methyl-2H-indazole including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Oxindole-4-boronic acid, pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page

7-Bromoindoline is a tricyclic compound that belongs to the class of natural products. It has been used as a lead compound for drug discovery and is synthesized from an aryl halide and palladium. 7-Bromoindoline has been shown to be active against methicillin-resistant Staphylococcus aureus (MRSA) and Mycobacterium tuberculosis, with the latter being attributed to its ability to inhibit protein synthesis by binding to bacterial RNA polymerase. 7-Bromoindoline also exhibits anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis.

Please enquire for more information about 3-(3,4-Dihydroisoquinolin-2(1H)-yl)propan-1-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page

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. The primary uses of Oroselol lie in its potential applications for managing cardiovascular conditions such as hypertension, angina pectoris, and arrhythmias. Its precise receptor selectivity may offer a therapeutic advantage over traditional beta-blockers by minimizing side effects associated with non-targeted action. Oroselol's pharmacokinetics and dynamic properties are being closely studied to understand its efficacy and safety profile in clinical settings. This compound's novel aspects make it a subject of considerable interest in pharmacological research, where its impact on cardiovascular therapy continues to be evaluated.

Please enquire for more information about 4-Chloroisoindoline hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Ethyl 5-chloro-1,3-dimethyl-1H-indole-2-carboxylate 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-Pyridin-4-yl-1H-indole-3-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 8-(Bromoacetyl)quinoline HBr including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 6-Nitroindazole-3-carboxaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Methyl 6-amino-3,4-dihydroquinoline-1(2H)-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications 3-(ETHOXYCARBONYL)BICYCLO[1.1.1]PENTANE-1-CARBOXYLIC ACID (cas# 1823373-90-5) is a useful research chemical.

Quinolinium dichromate is a complex ionic compound that is formed by the reaction of picolinic acid and potassium dichromate. It is a redox catalyst, meaning it can be used to oxidize or reduce other compounds, as well as catalyzing organic reactions. Quinolinium dichromate also has some cationic surfactant properties, which allow it to act as a non-ionic surfactant in water at high concentrations. The mechanism for this surfactant activity is not fully understood, but may involve transfer reactions between the quinolinium chromophore and hydrophilic groups on the surface of the molecule.

Please enquire for more information about 5-Bromo-1-methyl-1H-indole-3-carboxylic 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 6,8-Dimethyl-2-(4-propoxyphenyl)quinoline-4-carbonyl chloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

L-(2S,3aR,7aS)-Octahydroindole-2-carboxylic acid is an opioid drug that binds to the μ-opioid receptor. It is a synthetic compound with affinity for the opiate receptors in the brain and spinal cord, which leads to its analgesic effects. L-(2S,3aR,7aS)-Octahydroindole-2-carboxylic acid has been industrially produced by cyclizing the dimethyl ester of L-tryptophan. This synthesis process can be carried out by refluxing 3-hydroxy indole with acetic anhydride and hydrochloric acid in methanol at 60°C for about 16 hours. The resulting product is then heated with concentrated hydrochloric acid until it crystallizes. The resulting product can then be recrystallized from hot water or ethanol and dried over magnesium sulphate. L-(

Please enquire for more information about Ethyl 2-methyl-2H-indazole-7-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Trans-Khellactone is a naturally occurring lactone derivative, which is isolated from plants of the Apiaceae family. This compound exhibits a variety of biological functions due to its unique chemical structure, which includes a dihydropyran ring. Trans-Khellactone's mode of action involves interacting with various cellular pathways, potentially modulating enzyme activity, receptor binding, and influencing signal transduction processes. Due to its diverse range of activities, trans-Khellactone is of significant interest in the field of medicinal chemistry. It has been studied for its potential therapeutic applications, including anti-inflammatory, anti-cancer, and anti-microbial effects. Research into trans-Khellactone's mechanisms and efficacy continues to expand its possible applications in drug development and other areas of biomedical research.

Please enquire for more information about 1-N-Cbz-1,2-dihydro-1H-spiro[indole-3,4-piperidine]HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page