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>1,3-Dihydro-2,1-benzisothiazole 2,2-dioxide is a chemical compound that has been synthesized to be used as a pharmaceutical. It has the following characteristics: cyclization, amidation, and unsubstituted. The synthesis of this chemical is done through a synthetic process where it is coupled with an FT-IR and then sulfited. This product also reacts with sodium sulfite and chloride in a cyclization reaction.</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>7-(Methylsulfanyl)heptanoic acid is an alkaloid that is found in the bark and leaves of the tree Dictyocarpus heptacarpus. It is a racemic mixture of diptocarpiline and diptocarpidine. This alkaloid has shown to have sulfide and diptocarpidine as its main constituents. 7-(Methylsulfanyl)heptanoic acid has been shown to be effective against tuberculosis, but it does not show antimicrobial activities against gram-positive bacteria such as Staphylococcus aureus or Streptococcus pyogenes.</p>

<p>Versatile small molecule scaffold</p>

<p>Ethyl 3-bromo-1,2-oxazole-4-carboxylate is a reactive compound that can react with bromonitrile to form an isoxazole. It reacts with other dipolarophiles such as dimerization of bromonitriles to give the desired product in high yield. This compound can also be used for the synthesis of 1,3-dipolar cycloadducts. The active compounds are often used as starting materials for the synthesis of other organic compounds.</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>4-[(tert-Butyldimethylsilyl)oxy]aniline is a structural analog of the anti-hepatitis drug thalidomide. It has been shown to have antiviral activity against HIV, Hepatitis C and SARS. This compound has high affinity for the viral capsid protein and prevents viral assembly by inhibiting the production of progeny virions. 4-[(tert-Butyldimethylsilyl)oxy]aniline also has anti-inflammatory effects that are similar to those of thalidomide and can be used as a lead compound in the search for new drugs to treat hepatitis B infections.</p>

<p>Versatile small molecule scaffold</p>

<p>2-(1-Piperazinyl)benzonitrile is a neuroprotective drug that has been shown to be effective in the treatment of neuropathic and traumatic brain injury. It is a dopamine receptor agonist that binds to the d4 receptor, which is found in high concentrations in the central nervous system. 2-(1-Piperazinyl)benzonitrile enhances dopamine release by increasing calcium levels in cells, which leads to increased dopamine production and improved cognitive function. This drug also prevents neuronal death by preventing oxidative stress and apoptosis. The synthesis of this molecule can be achieved through solid-phase synthesis or chloroformate coupling reactions.</p>

<p>3-Methoxy-1H-pyrazolo[3,4-d]pyrimidin-4-amine is a soluble guanylate cyclase (sGC) inhibitor that inhibits the production of cyclic guanosine monophosphate (cGMP) in smooth muscle cells. 3MPPD inhibits intracellular cGMP and therefore causes the blood vessels to relax, which leads to an increase in blood pressure. This inhibition is selective for sGC, as it does not inhibit adenosine kinase or other intracellular enzymes. 3MPPD also has a contractile effect on vascular smooth muscle cells, which may be due to its ability to inhibit calcium release from intracellular stores. The maximal response of 3MPPD was found using mesenteric vascular strips in vitro, where it was shown to produce a concentration-dependent relaxation of VSMCs. In addition, this drug is able to reduce the severity of injury caused by a balloon</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>[(1,3,4-Thiadiazol-2-yl)amino]formonitrile is a cytostatic agent that inhibits the synthesis of cellular proteins. It has been shown to be effective against influenza virus and some other viruses. [(1,3,4-Thiadiazol-2-yl)amino]formonitrile also has anti-inflammatory properties and can be used as a diagnostic agent for tissue culture. This drug binds to DNA at the nucleotide level and prevents the formation of protein by inhibiting RNA synthesis in cells. It has been shown to be effective against tissue culture cells infected with hepatitis B virus or influenza A virus. [(1,3,4-Thiadiazol-2-yl)amino]formonitrile is reconstituted in water or DMSO before use in experiments with animals such as mice (CD1 strain).</p>

<p>(2-Bromoethynyl)tris(propan-2-yl)silane is a synthetically useful compound that has been used in the synthesis of amines, as well as in the preparation of triazoles. It can be used to produce chaperones and antitumoural drugs, such as solvents and palladium-catalyzed cross-coupling reactions. This compound is an efficient source of ethynyl groups for cross-coupling reactions with a wide range of amine partners. The ring-opening reaction of this compound with pyrroles provides two equivalents of propargyl alcohols, which can then be converted into an array of products including amino acids and pharmaceuticals.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>