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>Isoquinolin-3-yl trifluoromethanesulfonate is an organic compound with a ring system, isoquinoline ring and alkyl group. It can be prepared by the reaction of an aldehyde and diamino in the presence of hydrochloric acid. The reaction mechanism is unclear, but it is thought that it proceeds through a cyclization to form a triazole intermediate. This transformation can be confirmed by adding isotopes to one of the reactants, which alters the rate of the 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>2,2-Difluoroethenyl 4-methylbenzene-1-sulfonate is a coupling reagent that is used to form terminal alkynes. It reacts with fluorescing compounds to yield 2,2-difluoroethenyl esters or thioesters and can be used as a source of terminal alkynes. This reagent has been shown to react with various aromatic compounds in the presence of base. The reaction results in the formation of a difluorinated aromatic compound and a sulfonic acid salt.</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-Indan-1-yl-piperazine is a compound that can be found in the leaves of the Piper plant, which is a genus of flowering plants. It is a neutralizing agent and has been used as an anti-depressant drug. This compound has been shown to have a condensation reaction with indanone, which is another class of compounds. This reaction yields 1,4-dihydropyridines, which are able to bind to potassium ion channels on the cell membrane and inhibit their function.</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>2-Chloro-N-phenyl-7H-purin-6-amine is a substituted purine that has been shown to have growth promoting properties in cultured callus and excised plants. It also shows cytokinin activity and betacyanin production in wheat leaves, tobacco leaves, and petunia flowers. This compound binds to the betalactamase enzyme, which degrades the antibiotic cephalosporins, causing resistance to this class of antibiotics. The biological activity of 2-Chloro-N-phenyl-7H-purin-6-amine was observed through its ability to activate nitric oxide synthase (iNOS) and inhibit protein synthesis in purified bacterial extracts.</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>4-tert-Butoxybenzonitrile is an organocatalyst that can catalyze the transformation of aryl iodides to aryl radicals, which can then react with organic substrates. It is most often used as a catalyst for the synthesis of α-amino nitriles. 4-tert-Butoxybenzonitrile can be used in the presence of copper salts and N-methylmorpholine to catalyze the reaction of aryl iodides with alcohols. Mechanistic experiments have shown that 4-tert-butoxybenzonitrile operates by radical coupling, generating an alkyl radical intermediate that reacts with the substrate.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Chloro-3-hydroxy-6-iodopyridine is an electrophile that reacts with magnesium to form a reactive intermediate. This intermediate can react with halides to form diaryl compounds and reactive intermediates, which can be used as reagents for organic synthesis. 2-Chloro-3-hydroxy-6-iodopyridine is also a low temperature reactive intermediate and it has been shown to react with sulfonates to form cycloadducts. This compound can be eliminated by reductive amination or hydrolysis, leading to yields of the desired product.</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>3-Chloromethylbenzamide is a potent inhibitor of cyclic nucleotide phosphodiesterases. It is synthesised from dimethylformamide and propenoic acid, and has been shown to be effective in the treatment of cancer. 3-Chloromethylbenzamide inhibits the activity of cyclic nucleotide phosphodiesterases, which are enzymes that break down cyclic AMP and cAMP. This inhibition leads to an increase in intracellular levels of these nucleotides, which can result in cancer cell death by apoptosis. 3-Chloromethylbenzamide has also been shown to be a potent inhibitor of hydroxymethylglutaryl coenzyme A reductase (HMGCR), which is the enzyme that catalyzes the conversion of HMG-CoA to mevalonic acid. The inhibition of this enzyme leads to decreased production of cholesterol and other steroids, as well as increased levels of meval</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>N-Butylhydroxylamine hydrochloride is an oxime derivative that has been used as a diagnostic agent for the detection of glutamate. The compound is also known to have anti-inflammatory properties and to be useful in the treatment of cancer. N-Butylhydroxylamine hydrochloride is a stereoselective compound, with its enantiomer being more biologically active than its diastereomer. It has been shown to inhibit the production of matrix metalloproteinase, which may be responsible for some of its therapeutic effects. The compound has also been shown to be effective against cardiovascular diseases and other inflammatory diseases.br&gt;<br>N-Butylhydroxylamine hydrochloride is soluble in organic solvents such as benzene or chloroform.</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>4-Nitro-1H-indol-5-ol is an oxidized form of 4-nitroindole. It is used as a medicine for the treatment of stomach ulcers and gastritis. This drug can be synthesized from nitric acid, copper, and formaldehyde. The oxidation of this molecule with m-chloroperbenzoic acid yields a carboxyl group, which is then reduced to a hydroxyl group by sodium borohydride. The formation of an anhydride with 4-aminoindole yields the final product.</p>

<p>Versatile small molecule scaffold</p>