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>3-{[(2-Fluorophenyl)sulfanyl]methyl}-1-benzofuran-2-carboxylic acid is a synthetic peptide that has been shown to inhibit the activity of several ligands. It also has an activating effect on some receptors. 3-{[(2-Fluorophenyl)sulfanyl]methyl}-1-benzofuran-2-carboxylic acid is a research tool for studying protein interactions, receptor activation and ion channels. This peptide is not intended for therapeutic use.</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>The 4-(3,4-Difluorophenyl)-1,2-dihydrophthalazin-1-one is a synthetic compound. It is a sugar modified with fluorination and glycosylation. The chemical structure of this product can be found in the Chemical Abstracts Service (CAS) registry.</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>7-Bromo-1H-indene is a chemical compound that is synthesized by dehydration of propionic acid. 7-Bromo-1H-indene is a processable compound that can be used as an intermediate in the industrial production of various products. Dehydration, chlorination, and alkene formation are factors that lead to the synthesis of 7-bromo-1H-indene. The industrial synthetic method for the production of this product yields a high yield with a low cost.</p>

<p>2-Cyclohexylpropan-2-ol is a solvent that belongs to the group of primary alcohols. It is used for the dilution of biomolecules and as a solvent for organic reactions. 2-Cyclohexylpropan-2-ol has been shown to have a major effect on the solvation properties of hydroxyl groups in acidic environments. The hydroxyl group can be removed by photoexcitation or by reacting with an electrophilic reagent such as ozone, nitrous acid, or peroxy acids. The kinetic study of 2-cyclohexylpropan-2-ol was carried out in water at 37°C and showed that it has a low molecular weight and is rapidly hydrolyzed by alkaline solutions.</p>

<p>(4-Methoxy-pyridin-2-yl)-methanol is a nucleophile that can be used in the preparation of phosphorothioates and triphosphates. It is also used to synthesize oligonucleotides, which are biomolecules used to probe the structure of DNA. This compound has been shown to have high yields and is exothermic, making it a good candidate for catalysis. The chemical properties of (4-Methoxy-pyridin-2-yl)-methanol make it an excellent nucleophile with a strong affinity for phosphorous, which makes it useful in the synthesis of phosphorothioates and triphosphates.</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-Chloro-3-nitropropane is a compound that has been synthesized from ethylene diamine and yields amide, ethylene, and alkali metal. 1-Chloro-3-nitropropane is used as an intermediate in the production of hydrochloride salts of phosphorus pentoxide. This substance reacts with chlorine to produce phosphonitriles, which are intermediates for the synthesis of nitronates. The synthesis of 1-chloro-3-nitropropane was mechanistically studied by refluxing chlorination agents with phosphorus pentoxide.</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',4'-Dimethoxyacetoacetanilide is a disubstituted dicarbonyl compound that is synthesized by acetoxylation of 2,4-dimethoxybenzaldehyde. The equilibrium between the two forms can be shifted to favor one form through the addition of reagents, such as dimethylformamide or dicarbonyl compounds. The oxidation of 2',4'-dimethoxyacetoacetanilide with hydrogen peroxide yields 2,4-dihydroxydiphenylmethane, which can undergo hydrolysis with hydrochloric acid to yield phenol.</p>

<p>Versatile small molecule scaffold</p>

<p>2-(1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl)butanal is an antibacterial agent that belongs to the group of aminoglycosides. It is a synthetic compound that has shown antibacterial activity against gram positive and gram negative bacteria. 2-(1,3-Dioxo-2,3-dihydro-1H-isoindol-2-)butanal binds to the 30S ribosomal subunit of bacteria and inhibits protein synthesis by inhibiting the translocation of tRNA from the A site to the P site on the ribosome. This compound also prevents bacterial cell wall synthesis by binding to peptidoglycan precursors in the cell wall and inhibiting transglycosylation reactions.</p>

<p>1H-2-Benzothiopyran-4(3H)-one 2,2-dioxide belongs to the group of ketones and isomers. It has an electrophilic character and a nucleophilic character. The tautomerization of this molecule was studied by computational methods. The reactivity of 1H-2-Benzothiopyran-4(3H)-one 2,2-dioxide towards nucleophiles was studied experimentally by using reagents such as hydrogen bond donors, hydrogen bond acceptors, oximes and zwitterions. The conformations of the molecule were analyzed with single crystal x-ray diffraction experiments to find out the most stable conformation for each isomer.</p>

<p>3-N-Propoxypropylamine is an alkyl ether that is synthesized from propylamine. The chemical structure of 3-N-Propoxypropylamine has a low molecular weight and contains acidic functional groups. This compound can be used in the synthesis of other drugs, such as alkanolamide derivatives. 3-N-Propoxypropylamine can also be used to deaminate histidine residues, which are found in proteins, and this property makes it useful for culture cell experiments.</p>

<p>Phenoxybutanamine is a pharmaceutical preparation that contains 4-phenoxybutan-1-amine. It is used for the treatment of inflammatory diseases and bowel disease. Phenoxybutanamine may be prescribed as an antiinflammatory or immunosuppressant agent. This substance is also used to treat tumour necrosis factor-α (TNF-α) mediated inflammatory diseases, such as bowel disease. Phenoxybutanamine may be synthesized by reacting phenol with butylamine and hydrochloric acid. It is an aliphatic hydrocarbon with a carboxy group and a fluorine atom on the side chain. Phenoxybutanamine can inhibit the proliferation of cells in vitro, which may be due to its ability to inhibit protein synthesis in these cells.</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-Methoxypyridine-2-carboxaldehyde (4MPCA) is a chemical with antihistaminergic properties that can be used as a histamine antagonist. 4MPCA is synthesized from the reaction of 4-methoxypyridine, formaldehyde, and chloroacetic acid. The compound has been shown to inhibit the H2 receptor at concentrations of 1 x 10 M. It also has been shown to possess antiproliferative activity in tumor cell lines. This compound is unique because it contains a heterocyclic moiety in its structure and can be used in cross-coupling reactions.</p>

<p>3-Amino-3-phenylpropanenitrile is a monocarboxylic acid derivative. It is synthesized by reacting acrylonitrile with an excess of benzonitrile in the presence of a base, followed by treatment with an oxidizing agent. 3-Amino-3-phenylpropanenitrile has been shown to undergo protonation and form an amide linkage with dimethylformamide, which may be useful for preparative purposes. The compound class includes other compounds such as benzamide, 2-aminoethanol, and 2-aminophenol.</p>

<p>2-Amino-2-phenylacetonitrile is a chiral compound that has been shown to be effective in the treatment of inflammation in the bowel. It has been shown to be effective against inflammatory bowel disease, which is a chronic inflammatory condition of unknown origin that affects the large intestine. 2-Amino-2-phenylacetonitrile inhibits neutrophil migration and reduces proinflammatory cytokines, such as tumor necrosis factor (TNF)-α and interferon (IFN)-γ. The drug may also have an effect on apoptosis protein expression. The drug is well tolerated with minimal side effects and can be used in patients with diabetes suffering from diabetic neuropathy. 2-Amino-2-phenylacetonitrile has pharmacokinetic properties that make it suitable for oral administration, while its hydrochloric acid solubility makes it well suited for use in the bladder. The drug's redox potentials are low</p>

<p>4-Amino-2-isopropylphenol is a phenolic compound that is used in the synthesis of esters. It reacts with carboxylic acids to form an acylation product, which is selective for hydroxy groups. 4-Amino-2-isopropylphenol can be used as a solvent for phenolic compounds such as resorcinols and hydroquinones. This reagent also selectively reacts with organic solvents preferentially to hydroxy groups on the same molecule. The regioselective reaction of 4-amino-2-isopropylphenol is due to its steric hindrance by the substituent on the isopropyl group.</p>

<p>4-Amino-2-bromophenol is a homolytic, alkaline, nitrate, oxidative, evolution, pyridinecarboxylic, alkylation, chloroplasts, aminophenols, oxidative decarboxylation, acyl chlorides and catalyzed by photosynthesis. 4-Amino-2-bromophenol is used in the preparation of acyl chlorides and catalyzed by photosynthesis. It is also used in the synthesis of azo dyes. 4-Amino-2-bromophenol hydrolyzes in an alkaline solution to form 4-aminobenzoic acid and bromine water. This reaction can be reversed by adding acid to the solution.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Chloro-1,2-dimethoxybenzene is a ligand that binds to the active site of acetylcholinesterase. It is used in synthetic chemistry as a precursor for acridone and dimethoxyacridone. 4-Chloro-1,2-dimethoxybenzene has been found to have antioxidant properties and may be used as an antioxidant. This substance may also act as a potential antioxidant by protecting lipids against oxidation.</p>

<p>3-(Phenylcarbamoyl)benzoic acid (PCBA) is a molecule that is used in different fields of research, including mass spectrometry and diagnostic medicine. It has been shown to have properties that can be used for the diagnosis of Parkinson’s disease. The chemical structure of PCBA includes a carboxylic acid group and an aromatic ring with three hydroxyl groups. PCBA can be synthesized from phenylacetic acid by decarboxylation, elimination, or ortho-elimination reactions. This molecule has two possible isomers: 4-hydroxy-3-(phenylcarbamoyl)benzoic acid and 3-hydroxy-4-(phenylcarbamoyl)benzoic acid. PCBA may be used as a diagnostic agent for Parkinson’s disease because it can form molecular ions with m/z values of 302, 268, and 204, which are diagnostic for this</p>

<p>4-(Phenylcarbamoyl)benzoic acid is a metabolite of all-trans-retinoic acid that has been shown to induce promyelocytic leukemia in human cells. It binds to cellular retinobenzoic acid receptors, which are proteins that regulate cellular differentiation and apoptosis. The binding of 4-(phenylcarbamoyl)benzoic acid to these receptors leads to the inhibition of cellular proliferation and the induction of apoptosis in promyelocytic leukemia cells. 4-(Phenylcarbamoyl)benzoic Acid also inhibits the metabolism of retinoids by inhibiting the enzyme retinol dehydrogenase, thereby increasing the levels of all-trans-retinoic acid. This leads to an increased activity of retinoic acid on its receptor.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Bromo-4,5-dimethoxyaniline is a chemical compound that is used to optimize the synthesis of antimalarial agents. It has been shown that 2-bromo-4,5-dimethoxyaniline can be used as an efficient and selective synthetic intermediate for the preparation of benzene derivatives with biological properties. This chemical compound has been shown to be a mediation agent in biological systems and is also responsible for cross-coupling reactions between carbazoles and acridinium. The method for preparing this chemical compound involves a two step process involving alkylation and hydrolysis. The first step involves the preparation of dimethylformamide by reacting methyl iodide with formaldehyde in methanol. In the second step, acetyl chloride reacts with 2-bromoethanol in DMF to produce 2-bromo-4,5-dimethoxyaniline.</p>