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>3-Chloro-4-iodoaniline is an activated, synthetic chemical that is used in the preparation of a variety of chemicals. 3-Chloro-4-iodoaniline can be prepared by the reaction of chloroacetic acid with nitrobenzene and hydrochloric acid. The compound may be purified by vacuum filtration and recrystallization from water. It is also a precursor to other chemicals that are used in the production of polyhalogenated aromatic compounds. 3-Chloro-4-iodoaniline has been found to react with amines and form the corresponding amides, which may be useful for chemical synthesis.</p>

<p>Versatile small molecule scaffold</p>

<p>N-Boc-2-hydroxymethylmorpholine is a potent inhibitor of tyrosine kinase and has been shown to inhibit the activity of the enzyme. It is also an effective inhibitor of metaperiodate oxidation, which plays a role in the metabolism of tyrosine. The compound inhibits the binding of chiral benzyl compounds to receptor tyrosine kinases and is used for research purposes.</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>(1S)-1-(3-Chlorophenyl)ethanol is an optically pure chiral molecule. It is a homochiral molecule with a non-selective carbonyl group. The molecule can be prepared by the reaction of 3-chlorobenzaldehyde and methanol in the presence of pyridine. Diffraction experiments were performed on single crystals of (1S)-1-(3-chlorophenyl)ethanol to determine the optimal conditions for its crystallization. These experiments revealed that (1S)-1-(3-chlorophenyl)ethanol has a high degree of symmetry, which makes it suitable for use in optical applications.</p>

<p>tert-Butyl 5-formylthiophene-2-carboxylate is an acylguanidine that has been shown to have a high affinity for bone, mediating its effects on osteoporosis. This compound is selective for bone and inhibits the activity of steroid sulfatase, which is responsible for breaking down steroids in the body. It is also lipophilic and can penetrate into the cell membrane, where it binds to the receptor sites of cyclic AMP and blocks their activation by acetylcholine or other substances. This results in a decrease in calcium uptake into cells, reducing skeletal breakdown and enhancing bone formation. Structurally, tert-butyl 5-formylthiophene-2-carboxylate contains a thiophene ring that provides it with this selectivity.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2,5-Dioxopyrrolidine-1-carbonitrile is a ligand that binds to boronic acids and is used in the synthesis of drug molecules. The synthesis of 2,5-dioxopyrrolidine-1-carbonitrile requires the reaction of a pyridine ring with an aryl boronic acid, followed by hydrolysis to release the lactam. This synthetic process can be modified to produce amines.</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-Cyclopropyl-1H-imidazole is an antifungal agent that has been shown to be active against candida. It acts by inhibiting the synthesis of ergosterol, which is essential for fungal cell membranes. Its activity against Candida albicans was shown in a gas phase study and also in a conformational analysis. 1-Cyclopropyl-1H-imidazole has been found to be active against other fungi including Trichophyton mentagrophytes and Aspergillus niger. This triazole derivative inhibits the growth of bacteria by binding to the cytochrome P450 system and preventing the production of ergosterol, which is essential for fungal cell membranes.</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-Dimethyl-2-[(2-oxopropyl)sulfanyl]-1H-imidazol-3-ium chloride is a cationic salt that inhibits the enzyme acetylcholinesterase.</p>

<p>5-Bromo-6-hydroxypyrimidine-4-carboxylic acid is a homologous organic acid that is used as a pharmaceutical preservative. It is most commonly found in acidic pharmaceutical formulations. 5-Bromo-6-hydroxypyrimidine-4-carboxylic acid inhibits the growth of bacteria and fungi by acting as an enzyme inhibitor. The inhibition of enzymes such as lactamase, which breaks down the lactam ring in penicillin, prevents bacterial and fungal growth by preventing them from breaking down their natural cell walls. 5-Bromo-6-hydroxypyrimidine-4-carboxylic acid has also been shown to have potent anticancer activity in the lab setting, although the clinical significance of this has not yet been determined.</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>6-Benzyl-2,6-diazaspiro[3.4]octane is a viscous liquid with a molecular weight of 594. It is an oil-in-water emulsifier that is used in cosmetics as a viscosity agent, thickener, and emulsifier. It has been shown to be effective as a surfactant and yield high levels of polymers in the range of 1000 to 5000 microns. 6-Benzyl-2,6-diazaspiro[3.4]octane is also effective as an anionic or cationic polymer that can be used for micronization.br&gt;br&gt;<br>This product is not intended for use in pharmaceuticals.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Methyl-2,7-diazaspiro[4.4]nonane is a substance that has been found to inhibit the production of proteins that are involved in neurodegenerative diseases. It also has shown the ability to prevent protein misfolding and can be used as a pharmaceutical agent for Tourette syndrome, Alzheimer's disease, Parkinson's disease, and Huntington's disease. 2-Methyl-2,7-diazaspiro[4.4]nonane is an enantiomer that has been shown to have antidepressant properties in animal models.</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>

<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>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>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>