Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3,5-Dimethylpyrazole-1-carboximidamide hydrochloride is a test compound that can be used in enzyme preparations. It inhibits glyoxalase, which is an enzyme that catalyzes the reaction of glyoxal and lysine residues, preventing the formation of advanced glycation end products. 3,5-Dimethylpyrazole-1-carboximidamide hydrochloride has been shown to be a potent inhibitor of vesicular stomatitis virus (VSV) replication with high specificity for the aminoguanidine (AGA) site on VSV RNA polymerase. The mechanism for this inhibition is not fully understood; however, it is thought to involve the primary amines on 3,5-dimethylpyrazole-1-carboximidamide hydrochloride reacting with lysine residues on VSV RNA polymerase. This binding prevents amino acid activation and subsequent incorporation into the growing viral</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Hydroxy-1,2-di-3-thienyl-ethanone is an organic compound that belongs to the group of organic molecules. It has a molecular formula of C6H5O and a molecular weight of 124.14 g/mol. The name 2-hydroxy-1,2-di-3-thienyl ethanone is also known as ethane.</p>

<p>Versatile small molecule scaffold</p>

<p>3-Pyridin-4-ylaniline is a chemotherapeutic that can be used to treat cancer. It has been shown to inhibit the growth of tumors in mice with leukemia, and it inhibits the replication of human cancer cells in vitro. The chemical structure of 3-Pyridin-4-ylaniline includes a nitrogen atom connected to an aromatic ring. The nitrogen atom is also bonded to two ligands, which are pyridazine and carbonyl groups. 3-Pyridin-4-ylaniline binds to purines, a type of molecule that are found in DNA and RNA. This binding prevents the incorporation of purines into DNA and inhibits cancer cell proliferation by blocking DNA synthesis.</p>

<p>Versatile small molecule scaffold</p>

<p>3,5-Dimethylphenyl Isothiocyanate is a sulfur analogue that has the same molecular weight and chemical properties as 3,5-dimethylthiophenol. It is used to derivatize organic compounds with thiol groups via reactions with aliphatic, aromatic, and heterocyclic systems. The enantiomer of this compound is called S-(+)-3,5-dimethylphenyl isothiocyanate.</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>3-Methylbenzamide oxime is a chemical compound that has the chemical formula C6H5N3O. It is used as a reagent in organic synthesis. 3-Methylbenzamide oxime also acts as a silver-containing oxidant, which can be used to generate hydrogen peroxide or silver oxide.</p>

<p>N-Hydroxymethyl-3-(trifluoromethyl)benzamide is an oxidative and reductive elimination agent that can be used in a variety of synthetic reactions. This compound can be used to synthesize hydroxamic acids, alkenylations, carboxylates, and other functionalized organic compounds. This compound is also useful for the preparation of aromatic carboxylic acid derivatives. The mechanism for this reaction is the hydroxamic acid formation through reductive elimination followed by the addition of an alcohol or amine. The reaction begins with the oxidative cleavage of an ester or amide bond to form a carbonyl group and a hydroxylamine moiety. The hydroxylamine then undergoes reductive elimination to yield a hydroxamic acid. This process is catalyzed by metal ions such as copper (Cu), zinc (Zn), and iron (Fe).</p>

<p>Versatile small molecule scaffold</p>