Building Blocks

<p>Versatile small molecule scaffold</p>

<p>2-Cyclohexylpropane-1,3-diol is a substrate for porcine pancreatic lipase. It is hydrolyzed by this enzyme, which is stereoselective and enantioselective. 2-Cyclohexylpropane-1,3-diol also has properties that are similar to angiotensin, a peptide that is secreted by the human body. This substance can be used as a solvent for other organic compounds in chemical reactions.</p>

<p>2-Benzylpropane-1,3-diol is an intermediate in the synthesis of desymmetrization. It can be used to synthesize β-amino acids by acetylation and chemoenzymatic methods. The binding constants for 2-benzylpropane-1,3-diol with porcine pancreatic lipase were determined using a kinetic study. A molecular modeling study was conducted to gain insight into the binding properties of 2-benzylpropane-1,3-diol with porcine pancreatic lipase. The molecular modeling study revealed that 2-benzylpropane-1,3-diol binds to the active site of porcine pancreatic lipase and stabilizes the enzyme's structure.</p>

<p>Versatile small molecule scaffold</p>

<p>6,6-Dimethyloxan-2-one is a chemical compound that has been shown to have anti-inflammatory properties. It does this by inhibiting the production of prostaglandins. This compound has also been shown to inhibit the growth of bacteria and fungi. Telomeres are protein structures located at the end of chromosomes that protect the chromosome from degradation. 6,6-Dimethyloxan-2-one is found in telomeres and may be involved in the protection of these structures. Telomeres are important for protecting cells and preventing them from becoming cancerous or dying prematurely. The mechanism by which 6,6-Dimethyloxan-2-one inhibits bacterial growth is not yet fully understood but it may involve its ability to bind to ligands and c–h bonds on bacterial cell membranes. It is also believed that this compound can bind to rotigotine, which is a dopamine receptor agonist used in Parkinson's disease treatment, and may have an</p>

<p>Versatile small molecule scaffold</p>

<p>2,3,5,6-Tetramethylbenzoic acid (TMB) is a white crystalline solid that is soluble in organic solvents and slightly soluble in water. It is used as a precursor for the manufacture of dyes, pharmaceuticals, and other organic compounds. TMB has been shown to be an effective catalyst for the use of malonic acid as a substrate. The active site of TMB is acidic and it has been shown to catalyse the reaction between malonic acid and carbon tetrachloride with a dipole moment. TMB also interacts with functional groups such as methylene chloride, chloroform, methanol and benzene.</p>

<p>2,6-Dimethylpyridine-3,5-dicarboxylic acid is a stabilizer that can be used to stabilize peptidomimetic molecules. It has been shown to be effective in the stabilization of peptides and proteins. The stability of 2,6-dimethylpyridine-3,5-dicarboxylic acid is due to its ability to form hydrogen bonds with neighboring molecules. This compound also has the ability to chelate metals such as copper and zinc. 2,6-Dimethylpyridine-3,5-dicarboxylic acid has been shown to inhibit syneresis in aqueous systems which may be due to its ability to form hydrogen bonds with water molecules. 2,6-Dimethylpyridine-3,5-dicarboxylic acid has also been found to have diffraction patterns that are similar to those of cellulose acetate butyl ether</p>

<p>8-hydroxy-quinoline-5-carbaldehyde (8HQ) is a quinoline derivative that can bind to metal ions. It has antiviral properties and can be used to treat HIV, Hepatitis B and C, as well as influenza. 8HQ is synthesized by the reaction of sodium salts and 5-hydroxy-2,4-quinolinediol in aqueous solution at pH 11. The reactants are coordinated with the metal ion before the addition of trifluoroacetic acid. Computational methods have been employed to study this process.</p>

<p>2-(1H-Indol-3-yl)propanoic acid is a chemical that is a derivative of indole-3-acetic acid. It is used as an additive in cosmetics and hair products to impart color.</p>

<p>Versatile small molecule scaffold</p>

<p>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-Hydroxy-4-iodobenzamide is a hydroxamic acid that is used in organic synthesis for the formation of alkenylations, carboxylates and amides. It reacts with formamide to yield formyl groups. The activated hydroxamic acid undergoes reductive elimination to produce an amine group. N-Hydroxy-4-iodobenzamide has been shown to react with biomolecules such as proteins and nucleic acids. Mechanistic studies have shown that this reaction proceeds through a formyl intermediate, which can be reduced by formaldehyde or sodium borohydride.</p>

<p>3-Bromo-N-hydroxybenzamide is an extractive that is used as a solvent. It has been shown to have a high absorptivity, which makes it useful for spectrophotometric measurements of toluene. 3-Bromo-N-hydroxybenzamide also chelates metals and can be used in the spectrophotometric determination of metal ions.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>6-Chloropiperonyl alcohol is a metabolic byproduct of the insecticide 2,4-dimethylbenzyl alcohol and the acid ester of piperonylic acid. It can be found in urine. 6-Chloropiperonyl alcohol is a metabolite of a variety of drugs including acetaminophen, chloramphenicol, ethionamide, and nitrofurantoin. 6-Chloropiperonyl alcohol also has an insecticidal effect as it disrupts the insect's nervous system by inhibiting acetylcholinesterase in the insect's body.</p>

<p>Versatile small molecule scaffold</p>

<p>4-Octanoylphenol is a synthetic compound that binds to the beta subunit of protein kinase C. It is used as a research tool for cell biology, pharmacology, and protein interactions. 4-Octanoylphenol is an activator of ion channels and can be used in the study of ligand-receptor interactions. The antibody cross-reactivity with this product has been shown to be low.</p>

<p>Versatile small molecule scaffold</p>

<p>4-Nitrophenyl-N-benzylformamide is a heterocycle that is a reactive, biomolecular building block with reactive groups. It has been shown to react with primary alcohols and amines to form mesoporous silica materials. This compound reacts with chlorides in the presence of phosphine to form 4-nitrophenylchloroformate. The product is an acylating agent that can react with amides or thiocarbamates to form amide or thiocarbamic esters respectively.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Methyloctanenitrile is an oxime that can be hydrocyanated to produce a regioselective addition product. This reaction is catalyzed by the presence of hydroxylamine, which acts as a ligand in the transition state. The reaction proceeds with anti-markovnikov selectivity, which is due to the hydroxyl group on the methyl group. This reaction has been optimized for frequency and rates of reaction, and can be used with aldoximes as well.</p>

<p>Versatile small molecule scaffold</p>

<p>N-Benzoyl-N-methylglycine is a chemical compound that is used as an intermediate for the production of pharmaceuticals and skin care products. It can be synthesized from hippuric acid or benzoic acid, which are found in urine samples. N-Benzoyl-N-methylglycine has been shown to have a kinetic rate of cleavage of amides with a bond adjacent to the carbonyl group. This compound also has an intermolecular hydrogen bonding interaction with hippuric acid and a transfer reaction with chloride ions. The N-benzoyl derivatives of N-methylglycine can be separated by chromatography into two isomers, one being more reactive than the other. The perchlorates anions can replace the chloride ion in this compound, leading to different profiles and properties.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1,1,3-Trichloro-1-propene is a chlorinated hydrocarbon with a chemical formula of CCCH. It is used in the production of isomers of 1,2-dichloroethane and 1,1-dichloroethene. It has been shown to be genotoxic in vitro. The peroxides and hydrogen chloride produced from this compound are unstable and can lead to carcinogenic effects.</p>

<p>2-(Methylamino)-3-phenylpropanoic acid is a proton ionophore that inhibits the growth of bacteria by binding to amine groups in cell walls. 2-(Methylamino)-3-phenylpropanoic acid has been shown to inhibit the growth of tumor cells by preventing ATP production. It binds to lysine residues on the bacterial cell wall and blocks the proton channel, which prevents the accumulation of protons inside the cell and leads to a loss of energy production. This agent also inhibits protein synthesis in eukaryotic cells by inhibiting messenger RNA (mRNA) function. 2-(Methylamino)-3-phenylpropanoic acid has been used as a model system to study biochemical properties of amines and tetracycline resistance in corynebacterium glutamicum.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>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-Methyl-1-benzofuran-5-carboxylic acid is a synthetic compound that has been shown to induce apoptosis in human malignant melanoma cells. It inhibits the proliferation of these cells and induces cell death by an apoptotic mechanism. 3-Methyl-1-benzofuran-5-carboxylic acid has anti-proliferative effects on a variety of human malignant cells including those from breast, colon, and prostate cancers, as well as those with leukemia. Cell death was induced in all cases by an apoptotic mechanism. Addition of the compound to cultured cells at concentrations below its IC50 value resulted in a dose dependent inhibition of cell proliferation.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>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-Fluoro-2-iodonaphthalene is a reagent that is used for the cleavage of 1,4-cis-bonds. It has been shown to react with aryl halides in the presence of aluminium and lithium to form 1-fluoro-2-(aryl)naphthalenes. This reaction can be done selectively in the presence of other substituents. The fluorine atom in this compound can also be substituted with chlorine or bromine.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>