Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-(Benzyloxy)benzohydrazide is a new, potent and selective inhibitor of candida glabrata and cryptococcus neoformans. It has been shown to inhibit the growth of cancer cells in vitro and can be used to rationalize the anticancer properties of formamide. This compound inhibits chloride ion uptake in tuberculosis bacteria, which may be responsible for its antifungal activity. 4-(Benzyloxy)benzohydrazide has been synthesized by reacting benzaldehyde with hydrazine hydrate in the presence of a base, such as sodium bicarbonate or potassium carbonate. The reaction occurs at temperatures between room temperature and 120°C. The product is purified by recrystallization from water or acetone, or by column chromatography on silica gel using chloroform-methanol (1:1) as eluent.</p>

<p>Versatile small molecule scaffold</p>

<p>7-Fluorochromone-2-carboxylic acid is an enantiomer of 2-fluorochromone. It is a potent compound that has been shown to have significant reduction in the activity of the channel protein. This drug is orally active and is selective for animal models over other animals, such as rats and mice. 7-Fluorochromone-2-carboxylic acid binds with high affinity to the amine group of the chiral center of the class A GABAA receptor and exhibits potency by inhibiting amino acid uptake into cells in culture.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about 1-Bromobicyclo[1.1.1]pentane including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Versatile small molecule scaffold</p>

<p>4-Bromobenzofuran is a heterocycle that has electron donating properties. It is a benzofuran with a bromine atom in the 4-position, which is activated and can be used as an intermediate for pharmaceuticals. The heterocycle has been shown to have medicinal properties, including anti-inflammatory, antibacterial, and antifungal activities. 4-Bromobenzofuran is also used as a starting material in the synthesis of other heterocycles such as furan, pyrrole, thiophene and benzene. Furfural and bromoform are two derivatives of 4-bromobenzofuran.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Amino-3-(2-bromophenyl)propanoic acid hydrochloride is a cell biology research tool. It is an inhibitor of ion channels and ligand for the receptor. 2-Amino-3-(2-bromophenyl)propanoic acid hydrochloride is soluble in water, which makes it suitable for use in pharmacological research and as an activator of antibodies.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Bromo-3-methoxybenzyl bromide is a ligand that binds to the 5-HT1A receptor. It has been shown to bind to the serotonin transporter and inhibit uptake of serotonin into the brain, as well as antagonize 5HT1A receptors. This drug has also been shown to be an optimization for 5HT1A receptor agonists, with potential therapeutic applications for disorders such as depression, anxiety, and insomnia.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Chloroquinolin-3-ol is an orally active, organic solvent-free, synthetic drug that is a basic compound. It has been shown to have anti-inflammatory properties and can be used for the treatment of inflammatory diseases such as rheumatoid arthritis. The drug has also been shown to be effective against autoimmune diseases such as type 1 diabetes mellitus. 2-Chloroquinolin-3-ol is an analogue of quinolinic acid, which is found in plants and animals. 2CQOL binds to chloride channels on the surface of cells, which prevents the influx of chloride ions into the cell and leads to cytotoxicity.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-Azido-4-ethylbenzene is a chemical compound that is synthesized from 1-azido-2,4-dibromobenzene and an alkylating agent. It reacts with triflates to produce the corresponding aziridines. The synthesis of 1-azido-4-ethylbenzene can be achieved by using photoreduction or cross coupling reactions. This compound is used in the synthesis of diarylamines and aziridinium salts.<br>1-Azido-4-ethylbenzene can be synthesized from 1,2,3,4,5,6-(dibromomethyl)benzene and an alkylating agent (e.g., ethyl bromide). It reacts with triflates to produce the corresponding aziridines. The synthesis of 1-azido-4-ethylbenzene can also be achieved by using photore</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>8-Aminoquinoline is an antimalarial drug that is used to treat and prevent malaria in adults and children. It inhibits the polymerase chain reaction, which is a technique used in molecular biology to amplify DNA sequences. 8-Aminoquinoline has been shown to be effective against various species of Plasmodium, including chloroquine-resistant strains. 8-Aminoquinoline has a safety profile that includes pharmacokinetic properties, an inhibitory effect on intravascular hemolysis, and a low risk of redox potential in plasma concentrations. The drug also has anti-inflammatory properties due to its ability to inhibit the synthesis of prostaglandins by inhibiting cycloxygenase activity.br&gt;br&gt;<br>br&gt;br&gt;8-amino-1h-quinolin-2-one is a member of the class of quinoline compounds with broad spectrum activity against malaria and other infectious diseases caused by protozoan parasites</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Dithiocarbamates are compounds that inhibit the growth of fungi by inhibiting enzymes within the cell, such as carbonic anhydrase and acetylcholinesterase. Dithiocarbamates have been shown to be synergistic with other fungicides, leading to a more rapid and effective killing of fungi. N-(2,6-Dimethylphenyl)-2-methoxyacetamide is a dithiocarbamate that has been shown to be effective against resistant strains of fungi, such as Fusarium oxysporum. It is soluble in water and can be used as a soluble salt or as a soluble salt in combination with other fungicides.</p>

<p>Methyl 3-methylquinoline-2-carboxylate is a ketone that is used in the synthesis of nothapodytine and mappicine. It can be synthesized by condensation of methyl 2-chloroquinoline-4-carboxylate with methyl 3,4,5,6-tetrahydropyridine-2,4-dicarboxylate. The reaction sequence includes an acid catalyzed reaction to produce the desired product. Methyl 3-methylquinoline-2-carboxylate is also used as a precursor for synthesizing pyridones and ring systems. It can be deprotected by hydrolysis or oxidation to produce the desired products.</p>

<p>1,3-Dihydro-1-hydroxy-2H-benzimidazol-2-one is a sodium salt that is used as an antifungal agent. It has been shown to be fungistatic against Microsporum canis and Trichophyton mentagrophytes with low toxicity to humans. The synthesis of 1,3-Dihydro-1-hydroxy-2H-benzimidazol-2-one involves the reaction of 2,4,6,-triaminopyrimidine with formaldehyde and sodium hydroxide in water. This synthesis requires a high degree of skill because of the difficult conditions it requires.</p>

<p>Versatile small molecule scaffold</p>

<p>6-Bromo-2,3-dimethoxybenzaldehyde is a quinone that has been used for the synthesis of x-ray crystallography. It is an olefination agent, which also has been used in palladium-catalyzed cross-coupling reactions. 6-Bromo-2,3-dimethoxybenzaldehyde has been used in organic chemistry as a modular building block and has also been used as a reagent in cross-coupling reactions with bromohydrins. 6-Bromo-2,3-dimethoxybenzaldehyde can be purified by recrystallization from methanol and ether.</p>