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>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>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>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>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>Azidocyclohexane is an unsymmetrical azide that is used in pharmaceutical preparations. It is a non-selective cation, which means it can bind to both positive and negative ions. Azidocyclohexane has been shown to have a chemokine receptor activity, which may be related to its immunosuppressive effects on autoimmune diseases. Azidocyclohexane also has been found to inhibit the binding of adenosine receptors in cancer cells, which may lead to cancer cell death. In addition, azidocyclohexane may also be effective in treating inflammatory bowel disease due to its anti-inflammatory properties.</p>

<p>Versatile small molecule scaffold</p>

<p>4-Iodobenzyloxybenzene is an organic compound with a molecular formula of C6H5OHO. It is an aromatic hydrocarbon that can be used as a monomer for supramolecular chemistry. 4-Iodobenzyloxybenzene can also be used to introduce a clickable group to other molecules and is capable of forming nanowires in the presence of aluminium. The diameter of these nanowires can be controlled by changing the concentration of aluminium ions and temperature. This product has been shown to form complexes with water molecules, chloride, and halides.</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-(Piperidin-2-yl)acetic acid hydrochloride is a research chemical that is used in the synthesis of esters, solvents and other organic compounds. It is also used as a solvent in the production of pharmaceuticals. 2-(Piperidin-2-yl)acetic acid hydrochloride can be obtained by chemoenzymatic reactions or by alcoholysis of methyl esters. This compound has been shown to have the ability to act as a lipase inhibitor.</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-Bromo-3-chloro-2-hydroxybenzaldehyde is a potent regulator of microglia, a type of immune cell. It has been shown to be neuroprotective in the presence of radiation and activated TNF-α, by decreasing necrosis and inflammation. This compound is also capable of inhibiting the production of IL-1β and IL-6 from human monocytes, which may be due to its hydrophobic properties. 5-Bromo-3-chloro-2-hydroxybenzaldehyde has been shown to suppress the development of experimental sclerosis in rats. The mechanism for this effect is unknown, but it may be due to its ability to inhibit the activation of proinflammatory genes such as p65 nuclear translocation or nuclear factor kappa B (NFκB).</p>

<p>Ethyl 1-Piperidinepropionate is an organic compound that is an electron donor. It has an average molecular weight of 170.1 g/mol and a sensitivity to radiation. Ethyl 1-Piperidinepropionate can be used as a polymerization initiator for the preparation of polymers with a patterning ability. This compound is also used to produce dyes, flavours, perfumes, and pesticides.</p>

<p>Versatile small molecule scaffold</p>

<p>8-Chloro-6-methylquinoline is a heterocyclic compound with the structure of an indole. This compound has been shown to selectively dehydrogenate cyclohexanones and transiminate indoles. 8-Chloro-6-methylquinoline is also capable of dehydrochlorinating indoles and tetrahydroquinolines, as well as azaheterocycles. The sequence in which these reactions occur can be controlled by the substitution of chlorine atoms at different positions on the ring.</p>

<p>8-Ethylquinoline is a chemical compound that is classified as an organometallic. It reacts with trifluoroacetic acid to give 8-ethyltrifluoromethylquinoline, which can undergo reductive elimination to form 8-ethylquinoline. 8-Ethylquinoline has been used in the synthesis of azobenzene derivatives, including a luminescent n-oxide and various quinolines. The structural studies of 8-ethylquinoline have been carried out by nmr spectroscopy. The compound has also been shown to be useful for the preparation of terminal alkynes, tetrachloropalladate ions, and constant potential 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>Versatile small molecule scaffold</p>

<p>Silver trifluoromethanesulfonate is a chemical that is used in the manufacture of 1-bromo-2-propanol. When it reacts with hydroxyl groups, it forms an anhydrous sodium salt that can be used to inhibit population growth. Silver trifluoromethanesulfonate has been shown to have an inhibitory effect on human serum and postharvest populations of bacteria by reacting with the hydroxyl group in the enzyme population growth. Chemical ionization mass spectrometry (CI-MS) has been used to identify the aromatic hydrocarbon produced during this reaction. The mechanism for this reaction is thought to be due to hydrogen bonding between silver trifluoromethanesulfonate and the hydroxyl group.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Tert-Butyl hydroxy(methyl)carbamate is a linker that has been used in the synthesis of a number of pharmaceuticals including the anti-inflammatory drug celecoxib. It is an intermediate in the synthesis of several drugs, such as erythromycin, cefuroxime, and amoxicillin. Tert-Butyl hydroxy(methyl)carbamate can be activated to form reactive carbonyl groups by treatment with reagents like diazoethane or oxalyl chloride. These carbonyl groups can then react with nucleophiles like hydroxide ion to produce tert-butyl hydroxy(methyl)carbamate derivatives. Tert-Butyl hydroxy(methyl)carbamate reacts with bacterial cells by binding to purine bases on the ribosome. This binding prevents protein synthesis and cell division, leading to cell death.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>(2S)-1-Acetyl-N-methylpyrrolidine-2-carboxamide is a functional theory that has been shown to be able to form an intramolecular hydrogen bond. This compound's crystal x-ray diffraction study showed the presence of a water molecule, which helps to stabilize the molecule. The molecule was found to interact with a nonpolar solvent, such as chloroform, through a hydrogen bond. The computational method used for this study was DFT (density functional theory). The hydroxymethyl group on the 1st carbon atom forms a hydrogen bond with the oxygen atom on the 2nd carbon atom and also interacts with the chlorine atom on the 3rd carbon atom.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>7-Methoxy-2-methyl-3-phenyl-4H-chromen-4-one is a fungal metabolite that can be found in plants such as soybeans, peanuts, and peas. It also exists in human urine. 7-Methoxyisoflavone can inhibit the growth of fungi by inducing DNA damage. This compound has been shown to exhibit estrogenic activity and may have anticarcinogenic properties. 7-Methoxyisoflavone can also act as an inhibitor of the enzyme cyclopium and demethylase, which are responsible for the conversion of methoxyisoflavones into their corresponding phenolic acids.</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>3-Methyl-3-phenylpiperidine is a tertiary amine that contains a quaternary carbon. It has three different conformers, which can be determined by the presence of trifluoromethanesulfonic acid. The tertiary amine has two hydrogen atoms on the nitrogen atom and one hydrogen atom on the methyl group. 3-Methyl-3-phenylpiperidine is stable at room temperature in ethanol and preferentially reacts with sodium borohydride to form sodium N-(3-methyl-3-phenylpiperidinium) borohydride. This compound also has an electron withdrawing substituent, so it will have a higher thermodynamic stability than benzene or pyridinium salts.</p>