Building Blocks

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

1-((Pyridin-2-yl)methyl)piperidin-4-one is an organic compound that can be synthesized from piperidine and malonic acid. It is an antipsychotic agent that binds to the dopamine D4 receptor, which may be responsible for its antiangiogenic properties. 1-(Pyridin-2-yl)methyl)piperidin-4-one has been shown to inhibit the growth of human umbilical vein endothelial cells in culture and to block the formation of new blood vessels, as well as to reduce the volume of existing blood vessels. This drug also has a high yield in crystallization and is easy to synthesize from commercially available starting materials.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

3-Methoxy-5-methyl-1,2-oxazole-4-carboxylic acid hydrobromide is an excitatory drug that belongs to the group of carboxylic acids. It has been shown to increase the firing rate of neurons in the cerebral cortex. 3-Methoxy-5-methyl-1,2-oxazole-4-carboxylic acid hydrobromide is used as a research tool for studying nervous system function and as a diagnostic agent for epilepsy.

Versatile small molecule scaffold

The condensation of 6-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol with a diaryl or chlorotrimethylsilane in the presence of a catalyst such as pyridine or triethylamine leads to the formation of a carbinol. The reaction is often used for the synthesis of phenols.

Versatile small molecule scaffold

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.

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.

(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.

Sodium butane-1-sulfinate is a reagent that can be used to synthesize sulfoxides, pyrrole derivatives, and other organic compounds. It is also used as a salt form for pharmaceuticals. Sodium butane-1-sulfinate may be used to produce sulfoxides, which are often used in organic synthesis because they are both reactive and unreactive. This compound has been found to be an antagonist of the CRTH2 receptor, which is involved in the production of prostaglandins that regulate inflammation.

Versatile small molecule scaffold

Versatile small molecule scaffold

N-iso-Propyl-4-methoxyaniline is a supramolecular framework that has been demonstrated to be mediated by nitrogen atoms. This framework has been shown to form when the two isomers are mixed together, which leads to the formation of an alkylation reaction. The isomerism of this compound can be quantified and is unique in that it destabilizes the molecule. X-ray crystallography has been used to study the molecular structure and elucidate the non-covalent interactions. N-iso-Propyl-4-methoxyaniline's destabilization may be attributed to its ability to form hydrogen bonds with water molecules, as well as its hydrophobic character.

Versatile small molecule scaffold

Versatile small molecule scaffold

3,4-Diaminopyrazole is a heterocyclic compound that has been used as a colorant in the textile industry. It is also known to be an effective acceptor for hydrogen bonding in human keratin. 3,4-Diaminopyrazole reacts with primary alcohols to form chalcones and the long-term exposure of this compound has been shown to cause fatty alcohols. This heterocyclic compound undergoes a bathochromic shift under UV light and can be used as a spectral marker in vitro.

Versatile small molecule scaffold

6-Propyl-5,6-dihydro-2H-pyran-2-one belongs to the class of isoquinoline alkaloids. It is found in leguminosae plants and has a strong spectrum of activity against bacteria, viruses and fungi. This compound is also used for the treatment of malaria and as an antihelminthic agent. The index of this substance is unknown, but it has been shown to have a mass spectrum that corresponds with that of prosopis. 6-Propyl-5,6-dihydro-2H-pyran-2-one is semiarid and indehiscent, with volatile fruit.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

2,4-Dibromo-1,3-oxazole is a nitro compound and an important intermediate in the synthesis of herbicides. It is also used to produce coatings and as a reagent for organic synthesis. The compound can be synthesized by the palladium-catalyzed coupling of phenyl bromides with 2,4-dichloro-1,3-oxazole. 2,4-Dibromo-1,3-oxazole has been shown to have potent horticultural activity against plant diseases caused by anions such as fusarium oxysporum. This compound has a pharmacokinetic profile that is favourable for oral administration in humans. The lysine analogues are converted into picolinic acid and then to 2,4-dibromo-1,3-oxazole in the body. The dialkylamino substituents on the molecule are believed to be responsible

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold