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>Versatile small molecule scaffold</p>

<p>The Suzuki coupling reaction is a chemical reaction that forms new carbon-carbon bonds by the action of an organometallic catalyst and a boron compound. The process is named after the Japanese chemist Akira Suzuki who first reported it in 1979. The reaction has been shown to be successful with a wide variety of boronic acids, including 2-bromo-5-cyclopropylpyridine, which can be obtained from cyclopropylboronic acid. This coupling has been optimized for high yields under mild conditions with organic solvents such as tetrahydrofuran or dichloromethane.</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>1,8-Naphthyridine-3-carbonitrile is a compound that has been shown to have significant antiproliferative activity. The molecular modelling of the 1,8-naphthyridine-3-carbonitrile showed that it has an active methylene group and is acidic in nature. It also has significant neuroprotective properties and can be used to treat inflammatory diseases due to its ability to inhibit the production of proinflammatory cytokines. This drug also has anticancer activity as it inhibits cancer cell lines by modulating signal transduction pathways. 1,8-Naphthyridine-3-carbonitrile is also known to inhibit the growth of carcinoma cells by inhibiting DNA synthesis and protein synthesis.</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-Fluoro-7-nitro-2,3-dihydro-1H-indole is a chemical compound that can be synthesized in the laboratory. The synthesis proceeds by reacting 4-fluoroindole with sodium hydroxide and anhydride in a trichloromethane solution containing sodium cyanoborohydride. This chemical compound has not been shown to have any specific biological activity.</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>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>3-(3-Iodophenyl)propanoic acid is a molecule that has been shown to accumulate in the brain and muscle. It is an unlabeled analog of fluoroacetate, a compound that is used as a diagnostic agent for cancer. Fluoroacetate has been shown to be effective against brain tumors, although it cannot be used as a therapeutic agent due to its severe side effects. 3-(3-Iodophenyl)propanoic acid has not been studied in detail yet, but it has been found to accumulate in tumor tissue and may be useful for the diagnosis of cancer.</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>Imidazo[4,5-c]pyridin-2-amines are a class of compounds that have shown anticancer activity in vitro and in vivo. They are structurally related to the azepines and can be synthesized from 1H-imidazo[4,5-c]pyridine-2-carboxylic acid. Imidazo[4,5-c]pyridin-2-amines may inhibit cancer cell proliferation by inhibiting the activity of matrix metalloproteinases (MMPs) and may also inhibit the synthesis of DNA and RNA. Several members of this class of compounds have been shown to be potent inhibitors of human cancer cells in vitro and in vivo.</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>1-Bromo-4-(bromomethyl)-2-chlorobenzene is a brominating agent that can be used for the preparation of alkyl halides. It reacts with sodium hydride to give the corresponding sodium alkoxide, which can be hydrolyzed to give an alcohol. The reaction product is then treated with methoxy or chloro groups, giving a 1-bromo-3-methoxy-2-chlorobenzene or 1-bromo-3-chloro-2-chlorobenzene respectively. This compound can also be used as an inhibitor in organic synthesis reactions involving hydrolysis and reductive dehalogenation.</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>5-[(3-Methoxyphenyl)amino]-1,3,4-thiadiazole-2-thiol (MTT) is an elastomer that is used for surface modification and as a monomer. It has been shown to be a conditioner for polyethylene terephthalate (PET), polyurethane, and polyvinyl chloride (PVC). MTT has also been used in the preparation of organic halide polymers. This polymer can be prepared by radical polymerization with hydroxyl groups on the backbone. The hydroxyl group can react with the active hydrogen of an ester to produce an alcohol or amine. The product of this reaction is called an organohydrogenpolymer. If this polymer is a hydroxyl copolymer, it can be modified by the addition of functional groups such as carboxylic acids or amines.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>