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>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>Versatile small molecule scaffold</p>

<p>4-Aminobutane-1-sulfonic acid is a drug that has been shown to inhibit the growth of cancer cells in vitro. It binds to sulfonic acid groups, which are found on the surface of many cancer cells, and inhibits cell growth by preventing the formation of hydrogen bonds between water and proteins. The affinity of 4-aminobutane-1-sulfonic acid for different tissues has been quantified using human lung tissue. This drug may be a promising therapeutic agent for cancer because it can be used at low concentrations. It has been shown to have an anticancer effect on A549 cells in vitro. Nuclear magnetic resonance spectroscopy was used to investigate the binding mode of 4-aminobutane-1-sulfonic acid with respect to its parameters such as activation energies and distances.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-(Quinolin-2-yl)acetonitrile is an acceptor molecule in the nitrobenzene oxidation scheme. It has a nitro group, which is converted to a chiral chromophore by diethyl etherate. This compound also has oxygen atoms that can act as nucleophiles and activated malonate anions. 2-(Quinolin-2-yl)acetonitrile is an alkylating agent that is used for the synthesis of chiral compounds.</p>

<p>Versatile small molecule scaffold</p>

<p>(-)-Menthone is a plant metabolite that is found in peppermint and other mint oils. It can be synthesized by the action of caffeic acid esterase on menthol, which is also present in peppermint oil. (-)-Menthone has been shown to inhibit the enzyme activities of human pathogens such as Salmonella typhimurium, Escherichia coli, and Shigella sonnei. (-)-Menthone also has genotoxic activity and has been shown to cause chromosome breaks in human lymphocytes. The reaction mechanism of (-)-menthone involves an intramolecular hydrogen transfer from one carbon atom to another. X-ray diffraction data from (-)-menthone crystals show a phase transition temperature of approximately -5°C for the molecule.</p>

<p>Versatile small molecule scaffold</p>

<p>5-Nitropyrimidine is a chemical with antiviral properties. It inhibits the synthesis of new viruses by reacting with malonic acid, which is an intermediate in the virus's life cycle. 5-Nitropyrimidine has also been shown to have anti-malarial and anti-parasitic properties. This compound binds to amines and inhibits their production, which may be due to its ability to react with dialkylamino groups in proteins. 5-Nitropyrimidine has been found in humans and animals, but not plants or fungi.</p>

<p>Versatile small molecule scaffold</p>

<p>4-Aminothieno[2,3-d]pyrimidine is a potent inhibitor of the P-glycoprotein multidrug transporter. It has been shown to inhibit chloride transport in the kidney and gastrointestinal tract. 4-Aminothieno[2,3-d]pyrimidine also inhibits the function of amine oxidase, which is involved in the metabolism of endogenous compounds such as catecholamines and serotonin. This drug may also be effective against cancer cells. The mechanism of action for this drug is not well understood but it has been shown to have an effect on DNA replication and repair by inhibiting phosphorous acid and formamidines. 4-Aminothieno[2,3-d]pyrimidine can produce crosslinking between DNA strands that leads to chain termination or intramolecular hydrogen transfer with formamidines. This process produces formaldehyde, which can react with other molecules to produce crosslinks between</p>

<p>4-Hydrazinothieno[2,3-d]pyrimidine is an anti-cancer drug that is activated by xylene. It is used in the treatment of bowel disease and cancer. 4-Hydrazinothieno[2,3-d]pyrimidine has been shown to have antibacterial properties against Gram-positive bacteria and may be effective as a topical agent for skin infections. This drug also has platelet activating properties, which are mediated through the p2y12 receptor. This receptor is involved in inflammatory bowel disease, as well as other tissues such as the brain and heart. 4-Hydrazinothieno[2,3-d]pyrimidine may be useful in treating cancer because it inhibits the production of TNF-α (tumour necrosis factor alpha) which leads to tumor growth inhibition.</p>

<p>2-(5-Amino-3-phenylpyrazol-1-yl)ethanol is a chemical compound that is used in the preparation of mezlocillin, an antibiotic medicine. It is also used as a raw material for the production of ampicillin sodium by crystallization with sodium hydroxide. 2-(5-Amino-3-phenylpyrazol-1-yl)ethanol has been shown to inhibit bacterial growth by binding to penicillin binding proteins, which prevents the formation of an antibiotic inhibitor complex with enzymes involved in cell wall synthesis, inhibiting protein synthesis and cell division.</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-Methylbenzyl mercaptan is a heterocyclic compound that is found in the sulfoxides and azides classes. It can be synthesized by treating 2-methylbenzaldehyde with trifluoromethanesulfonic acid or trifluoroacetic acid. The chloride yields are high and the reaction is catalysed by aluminum chloride, triethylamine, or zinc chloride. This compound can be converted to a bioconjugate through ring-opening reactions with carboxyamide groups, which are present on proteins in mammalian cells. The bioconjugate can then be used as a fluorescent probe to detect the presence of specific proteins in living cells.</p>

<p>Versatile small molecule scaffold</p>

<p>1,3-Diphenylpropan-1-ol is a benzyl alcohol derivative. It is a white solid that can be used as a dehydrogenation agent for the synthesis of chalcone derivatives. It has been used as an intermediate in the synthesis of other organic compounds and has been detected in the reaction solution by thin layer chromatography. 1,3-Diphenylpropan-1-ol is also involved in the catalytic transfer of acetylacetonate to benzaldehyde or benzoic acid. The resulting anion can be neutralized with hydrochloric acid to produce benzyl alcohol or reacted with sodium hydroxide to produce dihydrochalcone.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>N-benzylsulfamide is a synthetic cannabinoid derivative that is activated by hydrochloric acid in the stomach. It is an agonist of the cannabinoid receptor, which is found in the brain and nervous system. N-benzylsulfamide has been shown to produce muscle relaxation by increasing potassium efflux from muscle cells and decreasing calcium influx, leading to decreased contractions. N-benzylsulfamide has also been shown to have anti-inflammatory effects. It inhibits prostaglandin synthesis by inhibiting cyclooxygenase activity, thus reducing inflammation. The molecule also binds to benzodiazepine receptors and can be used as a treatment for seizures or convulsions.</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-2-phenylethan-1-one is a synthetic compound that can be obtained by the ring opening of an epoxide. It has two carbonyl groups, two aldehyde groups, and one fluorine atom. This molecule can be synthesized in high yields and has been shown to react with nucleophiles due to its electrophilic nature. 1-Cyclopropyl-2-phenylethan-1-one reacts with chlorine atoms or chlorine ions to form 1-(chloromethyl)cyclopropane or 1-(chloromethyl)cyclobutane respectively. The regiospecificity of this reaction is determined by the stereochemistry of the cyclopropane ring.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Hydroxy-N-phenylbenzamide is an organic solvent that is used as a potentiator in hexane. This compound has been shown to have potentiating effects on the solubility and volatility of hexane, which are important for industrial applications. 4-Hydroxy-N-phenylbenzamide also has carcinogenic properties, which may be due to its ability to induce DNA transfer reactions with nitro groups or due to its ability to react with chloride ions in the presence of human colon carcinoma cells. The carcinogenic effects of this compound are not limited to humans; it also induces cancerous transformation in mice. Impurities found in this compound include 5-hydroxytryptamine (serotonin) and carboxyamide (NH2CONH2).</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-Phenyl-2,3-dihydropyridazin-3-one is a natural product that has been found in the human liver. It is also an organic solvent that is used in pest control to kill insects and spiders. 2-Phenyl-2,3-dihydropyridazin-3-one is a model system for studying cancer, as it has been shown to induce tumor formation in animals. It is also active against cervical cancer cells at low concentrations and induces apoptosis at high concentrations. This compound can be used as a potential therapeutic agent for the treatment of cancer in humans.</p>