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>

Versatile small molecule scaffold

<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>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>Benzyl(ethyl)nitrosoamine is a nitrosamine that is classified as a Group 2A carcinogen. It has been shown to cause liver damage in mice, which may be due to its ability to metabolize into hepatotoxic metabolites. Benzyl(ethyl)nitrosoamine has phototoxic effects and will produce reactive oxygen species (ROS) when exposed to light. This reaction is enhanced by the presence of nitrogen dioxide (NO2), nitrous acid (HNO2), or nitric acid (HNO3). The compound produces photochemical reactions with biomolecules such as proteins, nucleic acids, lipids, carbohydrates, and other organic substances. Nitrosamines are also known to have mutagenic effects on DNA and RNA synthesis.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-(3-Chloro-phenyl)-oxirane is a reactive molecule with the chemical formula C6H4ClO2. It is an epoxide that can be obtained by ring-opening of acetone cyanohydrin. 2-(3-Chloro-phenyl)-oxirane has been used as a glycosidic bond in the synthesis of α-amino acid derivatives and as a substrate for ring opening polymerization. This compound is also used to study the mechanism of enantioselective reactions, such as kinetic and thermodynamic studies, which can lead to the development of new methods for producing enantiopure compounds.<br>2-(3-Chloro-phenyl)-oxirane has been shown to inhibit growth in E. coli K12 and S. typhimurium at concentrations between 10 and 100 μM; it also inhibits growth in ovary cells at concentrations between 5 and 50 μM. The inhibition of bacterial</p>

<p>2-(3-Nitrophenyl)oxirane is an oxidase inhibitor that inhibits the activity of many oxidases, including monoamine oxidases and aldehyde oxidases. It has been shown to inhibit the oxidative deamination of dibenamine, which is catalyzed by dehydrogenase. 2-(3-Nitrophenyl)oxirane also reacts with metal ions such as copper and zinc, forming a complex that can be reduced back to the parent compound by acceptor molecules such as NADH or glutathione. 2-(3-Nitrophenyl)oxirane binds to receptors in the brain and other organs and may inhibit neurotransmitter release from nerve endings.<br>2-(3-Nitrophenyl)oxirane inhibits acid production by inhibiting the activity of acid cholinesterase, which breaks down acetylcholine at synapses. The resulting accumulation of acetylcholine leads to paralysis of muscles in voluntary muscles (e</p>

<p>Versatile small molecule scaffold</p>

<p>2-Methyl-decahydroquinoline is a chemical compound of the quinoline group. It is a colorless solid that can be prepared by reacting carbon disulfide with chloroacetanilides in the presence of hydrochloric acid. The reaction mechanism of 2-methyl-decahydroquinoline is based on the substitution of chlorine by hydrogen, which produces an alkylthio group. This compound can be used to treat wastewater and has been found to have growth regulatory properties when used as an alkylsulfonyl fluoride reagent. It also has been shown to be a potential intermediate for the synthesis of thiocarbamates, oxime derivatives, and c1-c4 haloalkyls.</p>

<p>1-Bromo-2-naphthoic acid is a tetronic acid with an antiproliferative effect. It has been shown to inhibit the enzyme IDO1, which is involved in the production of interferon gamma and other cytokines. 1-Bromo-2-naphthoic acid is also a potent inhibitor of cancer cells and leukemia cells, and has been shown to be cytotoxic at low concentrations. This drug inhibits the growth of tumor cells in vivo by preventing the division of cancer cells.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2,5-Dicyanopyridine is a ligand that can form coordination complexes with metal ions. It has been shown to form a trimeric structure in nonpolar solvents. 2,5-Dicyanopyridine is also able to act as a substrate for the hydroxy group and cyclopenta ring cleavage of epoxides. The unpaired electron on the nitrogen atom in 2,5-dicyanopyridine makes it an excellent nucleophile in nature. This property may be used to convert feedstock into valuable products such as ammonia or ethylene oxide.</p>

<p>3-Bromo-4,5-dimethoxybenzoic acid is an ether that is used in the synthesis of bromophenols. It can be prepared by reacting bromonaphthalene with sodium methoxide in methanol. 3-Bromo-4,5-dimethoxybenzoic acid has a methyl ether side chain. The compound is also known as bromophenol and it is a polysiphonia extract. This compound reacts with phenols to form ethers and the reaction product can then be purified by crystallization or vacuum distillation.</p>

<p>Methyl 2-hydroxy-2-phenylpropanoate is an organic compound that contains a nitrogen atom. It is the product of the reaction between Grignard reagent and alkynyl group. This reactive chemical can be used in agricultural chemistry as a fungicide. Methyl 2-hydroxy-2-phenylpropanoate also has a functional group and can be used as an analog for other compounds, such as oxazolidinones and alkynyl amines. Methyl 2-hydroxy-2-phenylpropanoate may be synthesized by reacting methyl 2-chloroacetoacetate with hydroxylamine. The nitrogen atoms on this molecule are important for the formation of bonds with other molecules, which is why it is so reactive. Methyl 2-hydroxy-2-phenylpropanoate has been shown to inhibit collagen production in plants and to have receptor activity against fungi.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>N-(1,3-Dioxaindan-5-ylmethylidene)hydroxylamine is a chemical compound that is used as an intermediate in the synthesis of other compounds. It has been shown to increase tyrosinase activity and inhibit tyrosinase production in vitro. N-(1,3-Dioxaindan-5-ylmethylidene)hydroxylamine is also an aldoxime, which reacts with aluminium to form an insoluble aluminium hydroxide precipitate. This reaction can be used to precipitate aluminum from solution. Reaction with sodium carbonate forms an insoluble sodium carbonate precipitate, which can be useful for removing residual aluminum after precipitation. The reaction of N-(1,3-dioxaindan-5-ylmethylidene)hydroxylamine with propionate or methyl ethyl chloride produces a polymerized product and piperonal respectively. Reaction of this compound with benzoic acid yields the</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Methyl 6-sulfanylhexanoate (MSH) is a diphenylacetylene derivative that has been shown to be able to form a chemical bond with gold nanoparticles. MSH can be synthesized by the reaction of sulfur, ammonia, and methyl alcohol in an ionic liquid, followed by phase transfer catalytic reduction. This compound has been shown to act as a functional group for the synthesis of amides and sulfides. MSH also has the ability to absorb infrared light due to its thiolate functional group. In addition, MSH is able to function as a hydrogen-bonding donor or acceptor in chemical reactions, which can be useful for sensors or indicator compounds.</p>

<p>5-Bromo-4-phenyl-1,3-oxazole is a marine sponge metabolite that has been found to have a 5-membered dihedral ring with a bromine and phenyl group. It is an organic compound that is used as a chemical building block in the synthesis of other compounds called multidrugs. The anticancer activity of 5-bromo-4-phenyl-1,3-oxazole has been demonstrated by chemists in the laboratory. This molecule has also been shown to be active against cancer cells in organisms such as rats and mice. 5-Bromo-4-phenyl-1,3 -oxazole is not effective against all types of cancer, but it has shown efficacy against certain cancers such as those found in the breast and colon.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Furan-2-carbonyl azide is an azide with a hydroxyl group that is synthesized by the reaction of ethylene diamine and methyl ethyl carbonyl chloride. Furan-2-carbonyl azide has been shown to be a potent immunosuppressant in rats, inhibiting the proliferation of T cells and B cells in vitro. It also causes cardiac arrhythmia in mice. Furan-2-carbonyl azide can be used for the synthesis of other compounds through cross-coupling reactions or as a reagent for phosphite formation.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Methoxyphenylisocyanide is a functional group that is used as a ligand in coordination chemistry. It can be synthesized by reacting phenylisocyanide with formaldehyde and potassium hydroxide. 2-Methoxyphenylisocyanide is a molecule that can coordinate to metal ions such as copper, zinc, nickel, palladium, and platinum. The reaction solution of 2-methoxyphenylisocyanide with hydrogen chloride produces an acid molecule. This chemical has demonstrated the ability to enhance the activity of myeloid-derived suppressor cells in mice injected with cancer cells via a supramolecular interaction between the 2-methoxyphenylisocyanide and the myeloid cell membrane.</p>

<p>2-Formyl-6-methylbenzoic acid is an additive that is used in organic chemistry. It can be used as a reactant to form isoindolinones, which are tetracyclic and tricyclic compounds. This product is efficient and can be used for the synthesis of bromides and catalysts. 2-Formyl-6-methylbenzoic acid has been shown to react with hydrazides to produce allyl compounds. This chemical also reacts with bromides or catalysts to produce chemistry, such as organic chemistry.</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-Phenylpentan-3-one is a monoterpene hydrocarbon found in lavandula angustifolia that has anxiolytic properties. It is also an antinociceptive and nociceptive agent. 1-Phenylpentan-3-one binds to the GABA receptor, which inhibits the release of glutamate, resulting in decreased nerve activity. Clinical studies have shown that 1-phenylpentan-3-one can be used to treat anxiety disorders. Dopamine has been shown to bind to the same site as 1 phenylpentan 3 one, suggesting that this terpenoid may play a role in brain functions by affecting dopamine levels. Extracellular concentrations of 1 phenylpentan 3 one are high enough to be detected with mass spectrometry, suggesting that it may have potential use as a neuroprotective drug for brain injuries. Gamma-terpinene has been shown to inhibit the growth of cancer cells</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-(2-Hydroxyethyl)-2,6-dimethoxyphenol is a phenolic compound that can be extracted from the bark of the Indian tree Terminalia arjuna. The extract has been used in traditional medicine for centuries to treat diabetes and cancer. In vitro studies have shown that this extract inhibits the activity of viruses, including HIV, with a mechanism of action similar to that of indinavir. 4-(2-Hydroxyethyl)-2,6-dimethoxyphenol also has an antioxidant effect and stimulates the production of glutathione reductase and superoxide dismutase by cells in culture. 4-(2-Hydroxyethyl)-2,6-dimethoxyphenol is used as an herbal drug in India and research has found it to be hepatoprotective when administered orally to rats.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Methyl-1-(p-tolyl)-2-propanol is a chemical compound that belongs to the group of alcohols. It is an organic compound that can be used as a solvent or a raw material in the synthesis of other chemicals. 2-Methyl-1-(p-tolyl)-2-propanol has been found to be safe for use in dermatology and toxicology, although there are some cases of sensitization. This chemical is not classified as hazardous and does not pose any substantial risk to human health. It exhibits no functional groups, but does contain two benzene rings and one alcohol group. 2-Methyl-1-(p-tolyl)-2-propanol has been found to be useful in the treatment of dermatologic conditions such as dry skin, eczema, psoriasis, acne, and pruritus.</p>

<p>2,4-Bis(tert-butyl)-6-bromophenol (2,4-BBP) is a ligand that binds to copper and forms an electron transfer complex. It has been shown to form radical species in the presence of proton and hydrogen. The crystal structure of the copper complex has been determined by x-ray diffraction. The ligand can be debrominated with electrochemical methods and the resulting product can be identified by nmr spectroscopy or absorption spectroscopy. The phenoxy group is well known for its ability to form a thiolate bond with hydrogen peroxide. 2,4-BBP has also been shown to have metal ion binding properties as well as anti-inflammatory activities.</p>

<p>Versatile small molecule scaffold</p>