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>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>N-(3-Hydroxyphenyl)-2-(2-oxopyrrolidin-1-yl)acetamide is a research tool that is used as an activator or ligand to study the function of receptors, ion channels and other proteins. It binds to cell surface receptors and activates them by mimicking the endogenous ligands. This compound has been shown to be a high purity reagent with protein interactions.</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>

<p>(+)-tert-Butyl D-lactate is a cyclic ester that is found in plants and animals. It is structurally similar to the natural amino acids, L-aspartate and L-valine. (+)-tert-Butyl D-lactate has been used as an ancillary for the determination of DNA sequences and has been shown to have a ring opening reaction with amido groups. This product has also been used as feedstock for the production of lactates and as a component in copolymerization reactions. !--</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-bromo-2,5-dimethoxybenzaldehyde is a synthetic compound that is an incompletely nucleophilic anionic molecule. It has been used to advance the study of aromaticity and analyzes the spectrum of compounds. 3-bromo-2,5-dimethoxybenzaldehyde has been used in the synthesis of anthracyclines and tetracyclic antibiotics. The chemical structure of 3-bromo-2,5-dimethoxybenzaldehyde includes an aryl group at one end and a tetracyclic ring system at the other end. This chemical is not active as a chemotherapeutic agent because it does not have any biological activity.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Chloro-2,3-dihydro-1H-indol-2-one is a chiral molecule that has two different forms: the axial form and the atropisomer. This compound is a precursor to 3-chloro-2,3,5,6-tetrahydrobenzo[b]thiophene, which can be used in the synthesis of other compounds such as atropine. It has been shown that 3-chloro-2,3,5,6-tetrahydrobenzo[b]thiophene can act as an antagonist of muscarinic acetylcholine receptors. Chloride ions are required for this reaction. This compound also reacts with titanium tetrachloride and titanium metal in the presence of boron trifluoride etherate to produce axially chiral molecules.</p>