Building Blocks

<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>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<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>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<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>

Versatile small molecule scaffold

<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>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>

Versatile small molecule scaffold

<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>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<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>

Versatile small molecule scaffold

<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-(Aminomethyl)cyclohexanol (1-ACOH) is a ligand that binds to the benzodiazepine receptor that has a neuroprotective effect. 1-ACOH is orally bioavailable and exhibits anticonvulsant, hypoglycemic, and anti-inflammatory activities. 1-ACOH has been shown to be a fluorescent compound with an absorption maximum at 337 nm. It can bind covalently to anions such as chloride, bromide, iodide, and fluoride via its amine group. The binding of 1-ACOH to these anions results in changes in its fluorescence properties. Deramciclane fumarate is a prodrug that undergoes hydrolysis by esterases to form dibutyl 1-(Aminomethyl)cyclohexanol (DBA). DBA is the active form of deramciclane fumarate that binds to the benzodiazepine</p>

<p>2,5-Dimethylbenzenethiol is a functionalized thiol that is used in cross-coupling reactions. It can be used to synthesize organic compounds with a wide range of structures, including alcohols, amines, carbonyls, and esters. In addition to being an efficient method for the synthesis of these compounds, this thiol has been shown to be cytotoxic against cancer cells. 2,5-Dimethylbenzenethiol has also been shown to have gas sensing properties. The synthesis of this thiol is achieved through a reaction between 2-bromobenzene and ethanethiol. This reaction produces 2-bromoethanethiol and 2,5-dimethylbenzenethiol as products. This molecule then undergoes hydrolysis in order to produce the final product. The molecular structure of this compound consists of two benzene rings connected by a carbon chain with two methyl groups on either end of the</p>

<p>1-Methyl-1H-indazole-3-carbaldehyde is a chemical compound that belongs to the family of heterocyclic compounds. It is used as a starting material for other chemicals, including hydantoins and semicarbazones. The condensation reaction between 1-methyl-1H-indazole-3-carbaldehyde and malonic acid yields hippuric acid and semicarbazone. Oximes may be prepared from 1-methyl-1H-indazole-3-carbaldehyde by reaction with sulfuric acid or dichromate.</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>1,2,3,4,6,7,8,9-Octahydrophenazine is a cyclic ether that is usually obtained by the hydrogenation of diethylene. It is used as a pharmaceutical intermediate. 1,2,3,4,6,7,8,9-Octahydrophenazine has been shown to coordinate with metal ions such as copper and copper chromite. This coordination stabilizes the molecule and prevents decomposition. 1,2,3,4-Octahydrophenazine also has anti-inflammatory properties due to its ability to inhibit prostaglandin synthesis by inhibiting enzyme activity in the cyclooxygenase pathway.</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-(4-Bromophenyl)-1,3-butanedione is a colorless liquid that has a molecular weight of 98.09 and an elemental analysis of C, H, Br, O. It is soluble in water and alcohols and has an enol form. 1-(4-Bromophenyl)-1,3-butanedione reacts with tantalum to give the tantalum salt with a molecular weight of 203.59. 1-(4-Bromophenyl)-1,3-butanedione can be used as a raw material for organic synthesis or as an intermediate for chemical reactions involving bromine or halogens.</p>

<p>2-Hydroxy-3,3-dimethylbutanoic acid is an organic compound that is used as a precursor to hypochlorite. It is synthesized by the catalytic oxidation of ethyl formate with a palladium catalyst in an alkaline solution. The resulting 2-hydroxy-3,3-dimethylbutanoic acid has a high yield and can be used as a starting material for the manufacture of sodium hypochlorite and other chlorinating agents. The optical purity of the product can be improved by using ruthenium or copper catalysts in place of palladium.</p>

<p>2-Hydroxy-2,3,3-trimethylbutanoic acid is a molecule that has been used in the synthesis of ligands and is also used to stabilize the carboxylic acid group. The protonation of this molecule leads to its acidic properties, which are useful for many purposes, including as a precursor for insect pheromones. The addition of chloride ions to 2-hydroxy-2,3,3-trimethylbutanoic acid produces an ion with a mononuclear charge that can be detected by nmr spectroscopy. This molecule forms hydrogen bonds with water molecules.</p>

<p>Spiro[4.5]decan-8-one is a phenylhydrazine that has been used in the synthesis of indole and cycloalkyl compounds. The spectra of this compound show two peaks at 6.3 and 8.7 ppm in the IR spectrum, which correspond to the C=C stretching mode for the cycloalkyl group and the C=N stretch for the phenylhydrazine moiety respectively. This structural isomer shows different chemical properties when compared to other isomers because it has a spirocyclic ring system with an 8-membered ring fused to a 10-membered ring, whereas other isomers have a 9-membered ring fused to a 10-membered ring.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Chloroquinoxaline-2-carboxylic acid (3CQC) is a halogen atom, oxadiazole, benzene, alkoxycarbonyl, alkoxy, cyano, trifluoromethyl, dihedral and halogen. 3CQC is used as a chemical intermediate in organic synthesis. It can be used as a starting material for the synthesis of other organic compounds and pharmaceuticals. 3CQC has been found to inhibit bacterial growth by inhibiting RNA polymerase. This compound also inhibits protein synthesis by binding to the ribosome's 50S subunit and prevents the production of proteins vital for cell division.</p>

<p>Versatile small molecule scaffold</p>

<p>5-Nitro-2-(morpholin-4-yl)benzoic acid is a cytotoxic agent that induces apoptosis in cells. This compound binds to tubulin and inhibits its polymerization, which leads to the disruption of microtubules. 5NMBA has potent cytotoxicity against cancer cells, including human lung cancer cells. It has been shown to be a potent inhibitor of paclitaxel polymerization, and also can disrupt the polymerization of other drugs such as colchicine and vinblastine. 5NMBA expresses itself at high levels in human lung cancer tissues and is often found in multidrug resistant tumor cells.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Propargyl benzyl ether is an organic compound with the formula CHCH=C(CH)OCH. It is a colorless liquid that has been used as a synthetic intermediate in organic synthesis. Propargyl benzyl ether has been shown to induce apoptotic cell death, which may be due to its ability to bind and inhibit the activity of pyrazole-3-carboxamide ribonucleotide transformylase, an enzyme involved in purine metabolism. This compound also induces apoptosis through the activation of caspases. The sample is pretreated before analysis by activating the cells with a solution of HCl and KOH before adding propargyl benzyl ether. Analysis is then conducted using analytical chemistry techniques such as gas chromatography or mass spectrometry. The chemical synthesis can be accomplished by reacting a β-unsaturated ketone with an acid catalyst such as HCl or acetic acid in the presence of a chelate ligand such as pyridine hydro</p>