Building Blocks

<p>Versatile small molecule scaffold</p>

<p>2-(Prop-2-en-1-ylsulfanyl)benzoic acid is a phenyl group that has the ability to form a desorption molecule. It is light resistant and photopolymerizable, which means it can be used in the production of polymers. The alkylthio group on this molecule allows for transfer and gel permeation chromatography. 2-(Prop-2-en-1-ylsulfanyl)benzoic acid also has a vinylic group, which makes it hydrosilylation crosslinkable. This makes it an excellent candidate for copolymerization and hydrosilylation.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Dimethylaminomethyl-benzoic acid hydrochloride (4DMABAH) is an antiviral agent that inhibits the replication of human immunodeficiency virus type 1 (HIV-1) by blocking the synthesis of viral DNA. 4DMABAH is a prodrug, which is metabolized to its active form, lamivudine, by esterases in the liver and other tissues. 4DMABAH has been shown to be effective against hepatitis B and C viruses in cell culture studies.</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>5-Ethynylpyridine-2-carboxylic acid is a ligand with a pyridine ring. It binds to the pyridyl subunit of proteins, such as phosphoglycerate kinase and ATP synthase. This compound coordinates with metals to form complexes. It has been used to synthesize other compounds, including benzoate and nitrate salts, which have yielded luminescent frameworks.</p>

<p>Methyl 5-ethynylpyridine-2-carboxylate is a ligand that binds in the active site of many enzymes. It can enhance the activity of these enzymes and also change their conformations. Methyl 5-ethynylpyridine-2-carboxylate interacts with four subunits to form a tetradentate framework, which is responsible for this molecule's ability to bind to any type of ligand. This enhancement effect is reversible, and it can be reversed by oxidizing methyl 5-ethynylpyridine-2-carboxylate with nitric acid. The yield of methyl 5-ethynylpyridine-2-carboxylate depends on the reaction conditions and the type of arylacetylene used. Methyl 5-ethynylpyridine-2-carboxylate has been shown to be an effective ligand with a high emission yield when using 1,3</p>