Building Blocks

<p>Versatile small molecule scaffold</p>

<p>3-Methoxy-4-(3-methylbutoxy)benzohydrazide is a high purity and cost-effective small molecule with an IC50 of 9.2 μM, which can be used as a research tool for studying the interaction between proteins and peptides. It has been shown to inhibit ion channels in cells, such as the nicotinic acetylcholine receptor (nAChR), and can be used as a potential therapeutic agent for treating conditions that involve excessive neurotransmitter release, such as epilepsy. 3-Methoxy-4-(3-methylbutoxy)benzohydrazide has also been shown to bind to an antibody in cell culture, suggesting that it may be useful for detecting protein expression levels in cells.</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>5-Fluoro-2-phenoxyaniline is a synthetic drug that has been shown to bind to the benzodiazepine receptor in rat brain tissue. This binding causes a decrease in cerebral blood flow, which can lead to seizure activity. 5-Fluoro-2-phenoxyaniline has also been shown to inhibit the production of inflammatory cytokines and other substances that are associated with neuroinflammation. It has not been determined whether this drug binds to any other receptors or what its target organ might be.</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>N-[(Z)-2-Nitroethenyl]acetamide is a synthetic anti-influenza drug. It has shown to be effective against influenza virus, and it is currently being optimized for use as an anti-influenza drug. N-[(Z)-2-Nitroethenyl]acetamide binds to the neuraminidase enzyme of influenza viruses, which prevents them from releasing viral particles. This drug has been shown to be effective in experiments that used nitro compounds in place of the more commonly used tetraethyl amine. The nitro group is thought to increase the rate of reaction because it is more reactive than the tetraethyl amine group. Optimization of parameters such as solvent, temperature, and concentration were required for this synthesis.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>