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>Ethyl 3-amino-4,6-dimethylthieno[2,3-b]pyridine-2-carboxylate is a heterocyclic compound that is used as a reagent in organic synthesis. It is a polyfunctionalized heterocycle that contains an ethyl ester and an acid ethyl ester moiety. The compound can be prepared by the reaction of thiophene with nitromethane and ethyl iodide followed by hydrolysis.</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>2-Hydroxy-4-(phenylmethoxy)benzoic Acid Methyl Ester is a benzene derivative that inhibits the binding of xanthones to the benzene ring in a variety of ways. This compound is formed by reacting phenol with methyl benzoate in the presence of acid and heat. The low energy ligand inhibits the binding of xanthones to benzene by forming hydrogen bonds, covalent bonds, or van der Waals forces with the anion. 2-Hydroxy-4-(phenylmethoxy)benzoic acid methyl ester has shown anti-inflammatory properties, which may be due to its ability to inhibit leukocyte adhesion at inflammatory sites.</p>

<p>Bromocycloheptane is a c6 alkyl that functions as an uptake inhibitor. It is used in the synthesis of other organic compounds, such as imidazole derivatives. Bromocycloheptane has been shown to inhibit uptake in the brain and consequently reduce infarctions in animal models of Alzheimer's disease. Bromocycloheptane inhibits uptake by blocking the function of the carrier protein, which carries neurotransmitters from synapses to axons and dendrites. Bromocycloheptane binds to magnesium ions, which are necessary for hydrolysis of ATP and therefore for uptake into cells. The magnesium ion is found in many enzymes involved in cellular processes, including those that produce ATP, so bromocycloheptane may interfere with cell function by interfering with these enzymes. This drug also blocks the production of lactam, a precursor molecule to GABA, which can be synthesized by glutamic acid decarboxyl</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>1-(Dimethylsulfamoyl)imidazole is a chemical compound that belongs to the class of heterocycles. It has been shown to inhibit the activity of two enzymes, which are xanthine oxidase and nitric oxide synthase. 1-(Dimethylsulfamoyl)imidazole is synthesized by reacting 2-aminothiophene with methyl sulfonyl chloride in tetrahydrofuran. The yield of this reaction is low, which may be due to the imidazole ring being a poor nucleophile in this reaction. This chemical has been shown to have an inhibitory potency against xanthine oxidase and nitric oxide synthase, which may be due to its functional groups or dimethylformamide solvate state. The mechanism for 1-(dimethylsulfamoyl)imidazole's inhibition of these enzymes is not yet known.</p>

<p>Versatile small molecule scaffold</p>

<p>4-(3-Methoxypropyl)-4H-1,2,4-triazole-3-thiol is a sulfuric acid derivative of 4H-1,2,4-triazole-3-thiol. It is an efficient and potentiodynamic polarizer that can be used to measure the concentration of copper ions in solution. This agent has been shown to have synergistic effects with copper ions and can be used as an analytical tool for cyclic voltammetry.</p>

<p>Versatile small molecule scaffold</p>

<p>Tetramethyl-1,3-cyclobutanediol is a diacid that can be used as a monomer for the production of polyesters. It has conformational properties that are different from other diols. Tetramethyl-1,3-cyclobutanediol is soluble in hydrochloric acid and reacts with coatings containing dibutyltin oxide to produce residues. This chemical also reacts with copper oxide, resulting in the formation of copper cyclohexanol and dibutyltin oxide. Tetramethyl-1,3-cyclobutanediol is able to react with carboxylic acids to form esters. This compound has been shown to be employed in the synthesis of polycarboxylic acids such as adipic acid and sebacic acid. Tetramethyl-1,3-cyclobutanediol has been used in the production of polyester resins by reacting with ethylene glycol and tere</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>Methyl 2,2-dichloro-1-methylcyclopropanecarboxylate is a cyclic compound with an effective rate of 11.6 s−1. It has been shown to be an effective catalyst for the electrochemical reduction of anthracene and other aromatic compounds in metallocomplexes. The catalytic activity of Methyl 2,2-dichloro-1-methylcyclopropanecarboxylate is dependent on the concentration and type of anion present in solution. In homogeneous systems, this compound is catalytically active for the electrochemical reduction of radical anions and polarographic oxidation of pyridine. This chemical also shows high electrochemical reductive activity towards palladium.</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>