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>2-Benzoylpyrimidine is a surfactant that has been shown to have anti-inflammatory properties. It has also been shown to be cytotoxic and antiproliferative, but it is not active against the growth of cancer cells. It is a fluoropyrimidine compound that has been synthesized in the laboratory by combining an aromatic hydrocarbon with a nitrogen atom. 2-Benzoylpyrimidine was originally developed as a pesticide, but its use in agriculture has declined due to environmental pollution concerns. 2-Benzoylpyrimidine can be found as an organic solvent.</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>

Versatile small molecule scaffold

<p>2-Amino-4-bromobenzamide is a ring-opening reaction system that is used in the synthesis of isatins. It has been shown to be an efficient and rapid method for the synthesis of this class of heterocyclic compounds. The oxidative nature of this reaction makes it useful for generating reactive intermediates, which can be used for further transformations.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Phenoxy-1-(pyrrolidin-1-yl)ethan-1-one is a novel compound that has been shown to inhibit the replication of viruses. It binds to the virus's RNA polymerase and prevents translation. 2-Phenoxy-1-(pyrrolidin-1-yl)ethan-1-one can be used as a diagnostic tool for infectious diseases, such as bacterial vaginosis. This drug has also been shown to have antiinflammatory properties, which may be due to its ability to inhibit cjun N terminal kinase (JNK). The compound is metabolized in mammalian cells by cytochrome P450 enzymes. It has also been shown to cause body fat mass loss in humans and mice with metabolic disorders.</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>N1-(5-Bromo-2-pyridinyl)-N2,N2-dimethyl-1,2-ethanediamine is a potent inhibitor of PI3K and p38 MAPK. It also has anti-inflammatory properties through the inhibition of alveolar macrophages. This compound can be used to treat idiopathic pulmonary fibrosis and chronic obstructive pulmonary disease (COPD), both of which are caused by the excessive accumulation of extracellular matrix proteins. N1-(5-Bromo-2-pyridinyl)-N2,N2-dimethyl-1,2-ethanediamine is also an important intermediate in the synthesis of other compounds that have been shown to be potent modulators for Alzheimer's disease and cancer.</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Furo[3,2-b]pyridine-2-carboxylic acid is a borohydride diester with the molecular formula CHB(OCH)CHB(OH)COOH. It is created by the decarboxylation of furopyridine (a compound of the class of furopyridines), followed by hydrolysis and cyclization. It can be synthesized by reacting ethyl bromoacetate with phosphoric acid and then hydrolyzed to yield a hydroxy derivative. Furo[3,2-b]pyridine-2-carboxylic acid is used in organic chemistry as an intermediate for other compounds, such as pharmaceuticals and pesticides.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Benzyl-2-azabicyclo[2.2.1]hept-5-ene is a reactive molecule that belongs to the class of carbocyclic nucleosides. It reacts with a variety of functional groups, including amide groups and iminium groups, which makes it a useful monomer for peptidomimetic synthesis, as well as copolymerization with other monomers. This compound yields high molecular weight polymers with amide and iminium functionalities in good yield, making it an attractive polymer candidate for drug delivery and biomedical applications.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Methyl 2-{[(tert-butoxy)carbonyl]amino}propanoate is a chiral compound that has been synthesized in a gramicidin-based process. This process was optimized to yield the desired stereoselectivity and enantiopurity. The synthesis of Methyl 2-{[(tert-butoxy)carbonyl]amino}propanoate involves a three step reaction that starts with the condensation of L-alanine and methyl 2-(2,4,6-trimethoxyphenyl)acetate. In the second step, an aminoester intermediate is formed by reacting this condensation product with tert-butyl bromoacetate. The final step involves the hydrolysis of this aminoester intermediate to form Methyl 2-{[(tert-butoxy)carbonyl]amino}propanoate. Methyl 2-[(tert-but</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>

Versatile small molecule scaffold

<p>The compound 5H,6H,7H-Pyrrolo[1,2-a]imidazol-7-ol is a chiral molecule that has been synthesized and characterized. It has shown to be an effective catalyst for the activation of alkenes and isatin. The reactivity of this compound is due to its dinuclear nature, which allows for two different reactive sites to come in contact with the substrate. The first site is the azomethine nitrogen, which reacts with electrophiles to form nitrenium ions. The second site is the dimeric macrocycle, which reacts with nucleophiles such as water or alcohols to form imidazolidinones. This reactivity makes this compound useful in organic synthesis because it can activate both alkenes and azomethines.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>