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>2-Chloro-4,5-dimethoxybenzoic acid is an organic compound that belongs to the class of aromatic compounds. It has been used in oxidation process as an intermediate for the production of a variety of chemicals. 2-Chloro-4,5-dimethoxybenzoic acid is produced by oxidation of acetophenone with nitric acid and sulfuric acid. The experimental data collected from this process has been modeled to determine the optimal conditions for synthesizing this chemical. The optimisation process was able to identify controllable factors that affect the efficiency of this synthesis, such as temperature and pressure, which can be controlled easily in a lab setting.</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>Cyclooct-4-enol is a constant, synthesize, and uptake that has been studied using X-ray crystallography. Cyclooct-4-enol is not resistant to bladder cancer cells, but is resistant to molecular imaging probes such as acetonitrile. Cyclooct-4-enol can be used as a ligand in luminescent probes to help target cancer cells. There are two strategies for cyclooct-4-enol: hypervalent and second order rate constants. Hypervalent strategy would involve changing the hydrophobic groups on the molecule so that it can be more easily absorbed by the cell membrane, while the second order rate constant strategy would involve attaching a ligand to the molecule that targets specific cancer types.</p>

<p>Versatile small molecule scaffold</p>

<p>3-Bromo-5-methoxy-1H-indole is an indole that can be synthesized in two steps from 3,4-dibromobenzene. It is a potassium salt that reacts with potassium t-butoxide to produce a mixture of potassium bis(3-bromoindolyl) and potassium bis(5-methoxyanilino). The product can be purified by recrystallization. 3-Bromo-5-methoxy-1H-indole has been used for Suzuki coupling reactions with various boronic acids or boronates.</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>Stobadine is a drug that belongs to the class of drugs that are known as dopamine agonists. It has antioxidative properties and may help to prevent oxidative injury in neurons. Stobadine also inhibits the activity of lysosomal enzymes, which are responsible for breaking down proteins, lipids, and nucleic acids. The drug also has been shown to have anti-inflammatory effects, with a potential to inhibit locomotor activity in mice. Stobadine is not used as an antibiotic or antiviral agent and does not act against any bacterial or viral pathogens. However, it has been shown to be effective against some parasitic diseases such as Trypanosoma cruzi (a protozoan parasite).</p>

<p>Versatile small molecule scaffold</p>

<p>2,2-Dimethyltetradecanoic acid is a fatty acid that is biosynthesized by the enzyme synthase from echinocandin A. It has been shown to have antifungal activity against Candida albicans and Saccharomyces cerevisiae. The ring structure of 2,2-dimethyltetradecanoic acid may be important for its chromatographic properties, as it has been shown to separate well on silica gel. This chemical is also used in chemical biology experiments because of its ability to bind to DNA. 2,2-Dimethyltetradecanoic acid binds to the guanine nucleotide binding site and inhibits transcription initiation.</p>