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>1-Benzylcyclopropan-1-ol is an organic compound that has been shown to be a reactive intermediate in the mechanistic pathway of bond cleavage. It can be formed from diketones by ring opening and subsequent protonation. The functional groups on 1-Benzylcyclopropan-1-ol are mainly electron donating and electron withdrawing, which gives it the capability to form covalent bonds with electron rich and electron poor molecules, respectively.</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-Hydroxyquinoline-4-carboxamide is a diastereomer of the natural product quinoline, which is found in plants. This compound has been shown to have anti-inflammatory effects and may be a potential drug for arthritis due to its ability to inhibit prostaglandin synthesis. The ring structure of this compound is related to other biologically active natural products, such as the isatins, which are also found in plants. 2-Hydroxyquinoline-4-carboxamide is synthesized by a photocycloaddition reaction with an aromatic amide. This reaction mechanism was first proposed by E. J. Corey and co-workers in the 1970s and later confirmed by D. M. Evans and coworkers in 2007.</p>

<p>Imidazo[1,2-a]pyridine-2-carbohydrazide is a synthetic compound that is used as an enhancer in organic synthesis. It has been shown to produce bathochromic shifts in the UV-visible spectra of ethyl esters and to be useful for identifying c. parapsilosis, a fungus that causes a form of erythema toxicum in infants. The anticancer activity of this compound has been demonstrated in vitro against cancer cells from different species, including human breast cancer cells. This anticancer activity may be due to its ability to inhibit microsporum and t. rubrum growth by inhibiting protein synthesis or DNA replication. Imidazo[1,2-a]pyridine-2-carbohydrazide is also capable of binding to DNA through hydrogen bonding interactions with the amine group on the N7 position of guanine residues and with the carbonyl group on the C5</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>