Building Blocks

<p>Versatile small molecule scaffold</p>

<p>N-(2,2-Dimethylpropyl)aniline is a heterocyclic compound that belongs to the class of amines. It is used in the synthesis of polymers and copolymers, such as polycarbonate plastics, polyurethane elastomers, and polyester fibers. N-(2,2-Dimethylpropyl)aniline can be used as a catalyst for cross-coupling reactions and also has been shown to catalyze x-ray crystallography studies. This product has also been shown to have carbamate and amide properties.<br>N-(2,2-Dimethylpropyl)aniline is an intermediate in the production of anilines from benzene derivatives with dimethylformamide or carbonyldiimidazole. It has also been shown to react with alcohols or phosphites to form esters or phosphoramides, respectively.</p>

<p>2-Iodo-N-phenylacetamide (2IA) is a chemical that binds to the substrate binding site of the enzyme. It has been shown to have pro-inflammatory cytokine activity in vitro and in vivo. 2IA is a member of a class of compounds that are able to inhibit chronic viral infections by inhibiting the production of pro-inflammatory cytokines. The chemical diversity of 2IA is due to its functional groups, which include an electrospray ionization quadrupole, a phosphate group, and a disulfide bond. 2IA also has been shown to inhibit phosphorylation reactions in biochemical pathways.</p>

<p>Versatile small molecule scaffold</p>

<p>3,4-Dihydro-2H-1,5-benzodioxepine is a chalcone that has been shown to have organic and inorganic acid properties. It is a natural product that has been shown to inhibit the growth of bacteria. The ultraviolet absorption properties of 3,4-dihydro-2H-1,5-benzodioxepine are due to its conjugated double bond system. This compound is an amide and contains a hydroxyl group and a chloride ion. 3,4-Dihydro-2H-1,5-benzodioxepine also has the ability to bind with amino groups on proteins. <br>3,4-Dihydro-2H-1,5 benzodioxepine can be found in plants such as "Achillea millefolium" (Yarrow).</p>

<p>4-Phenylbut-3-ynoic acid is a mixture of two stereoisomers that are obtained by the reaction of but-3-yne with phenylhalide. The mixture is used as a ligand in asymmetric synthesis and catalytic reactions. 4-Phenylbut-3-ynoic acid is also used as a reagent in organic syntheses, such as alkenylations, to produce an optically pure alkene product. 4-Phenylbut-3-ynoic acid has been shown to be selective for the desired stereoisomer.</p>

<p>N-Propargylphthalimide is a supramolecular compound that has been shown to have antiinflammatory properties. It inhibits the production of prostaglandin E2 (PGE2) in human neutrophils, which can be caused by inhibiting the activity of acetylsalicylic acid (ASA). N-Propargylphthalimide has also been observed to inhibit tyrosinase and amine oxidase, which may be due to its ability to form hydrogen bonds with the enzyme's active site. N-Propargylphthalimide has not yet been tested on animals or humans.</p>

<p>Versatile small molecule scaffold</p>

<p>1-Chloro-3,4-methylenedioxybenzene is an organic solvent used in the treatment of various inorganic compounds. The solvent is used to dissolve inorganic compounds that are insoluble in water and other solvents. 1-Chloro-3,4-methylenedioxybenzene can be used as a dehydrating agent or additive to remove water from organic substances such as coal tar or oils. It is also used as a catalyst for alkylation reactions and has been shown to inhibit the growth of bacteria by binding to DNA. This product has been demonstrated to have anti-inflammatory properties.</p>

<p>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>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Dichloro-1,3,4-thiadiazole is a dipole molecule with a nitrogen atom in the center of two chlorine atoms. It has a molecular electrostatic potential of -0.6 and an efficiency of 73%. Dichloro-1,3,4-thiadiazole is a polar molecule that can be described by three geometries: amide, dimethylformamide, and chlorine. The geometry of dichloro-1,3,4-thiadiazole is optimized using parameters such as the distance between two chlorine atoms (-2.8) and the distance between two nitrogen atoms (1.7).</p>

<p>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>