Building Blocks

<p>Versatile small molecule scaffold</p>

<p>2-Tridecyloxirane is a diagnostic agent that is used to identify hydroxy groups in collagen. It reacts with the hydroxyl group on collagen, forming an acyl chloride intermediate. This intermediate can be detected using a gas chromatography technique. The biodegradability of 2-tridecyloxirane has been studied and found to be dependent on the environment in which it is released. It was found to have a half-life of around 4 days in water, but up to 8 months in soil. The viscosity of 2-tridecyloxirane has been shown to decrease as the temperature increases, with the highest rate of change at temperatures above 150°C. This chemical has also been shown to react with primary amines and alicyclic compounds, such as ebola virus.</p>

<p>4-Chloro-2-oxo-2H-chromene-3-sulfonyl chloride is a heterocyclic compound with significant biological activity. It is a salmonicida that kills bacteria by inhibiting the enzyme adenosine triphosphate (ATP). 4-Chloro-2-oxo-2H-chromene-3-sulfonyl chloride has been shown to have significant activity against Staphylococcus aureus, Streptococcus pneumoniae, and Streptococcus pyogenes. This drug also inhibits the growth of Pseudomonas aeruginosa and Escherichia coli.</p>

<p>2,3-Diaminopropionic acid monohydrobromide is a dibenzoylated derivative of 2,3-diaminopropionic acid. It has been shown to be an antibacterial agent. The compound inhibits bacterial growth by binding to the ribosomal protein L5 and blocking the synthesis of proteins necessary for cell division. 2,3-Diaminopropionic acid monohydrobromide has also been found to have neuropathic effects in animals. This compound can be extracted from plants such as lathyrus and eluted with ethanol or hydrobromide.</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>

Versatile small molecule scaffold

<p>Bicyclo[2.2.2]octan-2-ol is an antiplasmodial agent that is used to treat malaria caused by Plasmodium falciparum and P. vivax. It binds to the parasite's heme, preventing its conversion of heme to protoporphyrin IX and blocking the synthesis of ATP, leading to cell death. Bicyclo[2.2.2]octan-2-ol has also been shown to be effective against multiresistant strains of plasmodium and has a low toxicity in humans. This substance can be synthesized by epimerization of 2-(bromomethyl)cyclohexanol with maleic anhydride or 2-benzoylcyclohexanol with benzoic acid. The yields from these reactions are low, but the product can be easily tracked due to its distinctive chemical properties (e.g., high boiling point</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>6,7-Dichloro-2,3-dihydro-1H-indole-2,3-dione is a drug that is used to treat high blood pressure. It is a potent inhibitor of the enzyme phosphodiesterase (PDE), which breaks down cyclic adenosine monophosphate (cAMP). 6,7-Dichloro-2,3-dihydro-1H-indole-2,3-dione inhibits PDE and increases the concentration of cAMP in cells. This increase in cAMP leads to an increased effect of the neurotransmitter acetylcholine on the heart and blood vessels. 6,7-Dichloro-2,3-dihydro-1H-indole--2,3--dione also increases calcium binding to membrane receptors and increases membrane hyperpolarization. These changes lead to an increase in nω--nitro--</p>

<p>1-(4-Chlorophenyl)-2-methylpropan-1-one is a phenyl ester that is used as an intermediate in the synthesis of other compounds. 1-(4-Chlorophenyl)-2-methylpropan-1-one can be synthesized by reacting potassium t-butoxide with diethyl succinate, followed by reaction with isopropyl alcohol. This process will result in the production of 1-(4-chlorophenyl)-2-methylpropan-1-one and potassium t-butoxide. The compound can also be synthesized by condensing naphthalene, diethyl ether, and isopropanol. This process will produce the same product but with a different reactant order.</p>