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>3-Aminonaphthalene-1-carboxylic acid is a pyridine derivative that is structurally similar to the sulfoxide and dimethyl sulfoxide. The linear regression of the methanol and acetonitrile solvates was found to be dependent on substituent effects. The model compounds, naphthalene and benzene, were used as substituents in this experiment. Substituent effects are seen in the form of steric hindrance, inductive effect, and resonance stabilization. 3-Aminonaphthalene-1-carboxylic acid has been shown to have a variety of uses, including use as an intermediate in the synthesis of model compound skeletons.</p>

<p>Versatile small molecule scaffold</p>

<p>The enantiomers of 1-(3-chlorophenyl)propan-1-ol are separated by a chiral column, yielding the (R)-enantiomer. The yield of the reaction is determined by the amount of oxidizing agent used to oxidize the alcohol and can be calculated by multiplying the molarity of the reactant and dividing it by the molarity of the product. The enantioselective oxidation of arylethyl alcohols with peracids in an aqueous solution was studied in this experiment. Nocardia and corallina are two examples of bacteria that produce this compound as part of their metabolism. Unreacted 1-(3-chlorophenyl)propan-1-ol can be found in ketones and carbinols, as well as other compounds containing an erythylene group.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Methyl-5-nitro-1,3-benzoxazole is a chemical compound that has been shown to inhibit the growth of wheat plants. It may have an effect on the regulation of plant growth and development. 2-Methyl-5-nitro-1,3-benzoxazole also inhibits the production of nitric oxide by activated macrophages and decreases their ability to produce cytokines. This chemical is found in soil, water, and air as well as in products such as plastics, textiles, and insulation materials. The amount of 2-methyl-5-nitro-1,3 benzoxazole present in these products is regulated by regulatory agencies to ensure safety standards are met.</p>

<p>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 3-methanesulfonamidobenzoate is an organic compound that is used as a reagent in organic synthesis. It has the chemical formula CH3O2C(CH2)2SO2CH=NOH. Methyl 3-methanesulfonamidobenzoate is a methyl ester of benzoic acid, which is also known as methyl benzoate. This compound has been shown to react with DNA, forming adducts with guanine and cytosine bases.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Methyl-2-(propan-2-yl)butanoic acid is an inhibitor of cancer, which is structurally related to sulfamic acid. It has been shown to inhibit the growth of bacteria by binding to metal hydroxides and acting as a free radical scavenger. 3-Methyl-2-(propan-2-yl)butanoic acid inhibits the protease activity of trypsin and aminopeptidase and has depressant effects on the central nervous system. This compound also inhibits serotonin reuptake in the rat brain, suggesting that it may be a potential antidepressant. 3-Methyl-2-(propan-2-yl)butanoic acid has been shown to inhibit HIV infection by blocking the activation of tnf alpha.</p>

<p>Ethyl (Benzyloxy)acetate is a β-unsaturated ketone that is used in the synthesis of peroxisome proliferators. It is also used in the asymmetric synthesis of β-unsaturated ketones. Ethyl (Benzyloxy)acetate has been shown to induce inflammation and inhibit serine protease, which may be due to its ability to bind to hydroxyl groups and heterocycles. It can also act as an anti-HIV agent by binding to the hydroxyl group of insulin, which causes insulin resistance. This compound is also used as a solvent for organic chemistry reactions, including the conversion of ethyl formate into acetic acid.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>N-Hydroxy-4-phenylbutanamide is a toolbox hydroxamic acid that has been shown to activate by reacting with the carbonyl group of an arylesterase. This reaction will generate an aldehyde, which can then undergo cyclodehydration in the presence of sodium periodate to form an alkene. The chiral nature of this molecule allows for selective activation on either the left or right side of the molecule. The aerobic conditions are required for this reaction to take place and it can be performed at room temperature. N-Hydroxy-4-phenylbutanamide is also used as a reagent in organic synthesis, crystallography, and alkene 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>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Amino-N-ethylbenzamide is a synthetic compound that is used in the synthesis of quinazolinones and other pharmaceuticals. It is also used as a reagent for selective halogenation. 2-Amino-N-ethylbenzamide can be synthesized from anthranilic acid, which is produced by the degradation of amino acids in the body, and chloroform. The chlorination of this compound yields 2-chloroamino-N-ethylbenzamide. This reaction can be done in two ways: regioselectively or regiocontrolled. Regioselective reactions are those that have a specific orientation on the benzene ring, while regiocontrolled reactions are less specific.<br>2-Amino-N-ethylbenzamide has been used to produce trifluoromethylated compounds, which are often found in pharmaceuticals such as fluoroquinol</p>

Versatile small molecule scaffold

<p>(S)-2-(3-Chlorophenyl)-2-hydroxyacetic acid is a chiral compound that has the enantiomeric form of tartaric acid. It is a racemic mixture, with one molecule having the (R) configuration and the other molecule having the (S) configuration. The (R) form is found in grapes, apples, and many other fruits. The (S) form is found in lemons, oranges, and tomatoes. This compound has been shown to be effective as an antacid for relief of heartburn and stomach acidity.</p>

<p>Versatile small molecule scaffold</p>

<p>Ethyl 2-(oxiran-2-yl)acetate is an enantiomer of ethyl 2-hydroxyacrylate that can be used as a toolbox molecule for the preparation of epoxides. It has been shown to catalyze the formation of epoxides from the corresponding alcohols and oxiranes. This compound has also been studied as a potential cholinergic agent with carbon source and in pharmaceutical preparations.</p>

<p>2-[(Phenoxycarbonyl)amino]propanoic acid is a synthetic small molecule that can be used as a research tool to study the function of ion channels. It has been shown to activate ligand-gated ion channels and inhibit voltage-gated ion channels. This compound binds to the receptor site, which results in an increase in cell permeability. 2-[(Phenoxycarbonyl)amino]propanoic acid also inhibits protein interactions by binding to a specific region of the protein surface.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>