Building Blocks

<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>

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>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>4-Methylquinoline-2-carboxaldehyde is a formylating agent that is used in the synthesis of heterocycles. It has been shown to react with methanol and mediated by oxidative conditions to produce formaldehyde. This reagent can be used for the functionalization of biomolecules by reacting with amines, thiols, and hydroxyl groups. 4-Methylquinoline-2-carboxaldehyde can also be used for the oxidative coupling of phenols and naphthols. The functional group on this compound is a carboxylic acid (-COH).</p>

<p>8-Thia-4,6-diazatricyclo[7.5.0.0,2,7]tetradeca-1(9),2(7),5-trien-3-one is a synthetic antifungal molecule with inhibitory properties against the growth of fungi. This compound inhibits the biosynthesis of ergosterol, an essential component of the fungal cell membrane, by inhibiting the enzyme squalene epoxidase. 8-Thia-4,6-diazatricyclo[7.5.0.0,2,7]tetradeca-1(9),2(7),5-trien-3-one has been shown to be effective in killing Candida albicans and other species of pathogenic fungi in cell culture and animal models.</p>

<p>Versatile small molecule scaffold</p>