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>3,6-Dichloropyridazine-4-carboxamide is a white crystalline substance that belongs to the group of pyridazine derivatives. It has been shown to have a high primary amine content and a crystal structure. 3,6-Dichloropyridazine-4-carboxamide was synthesized by reacting an anthranilic acid with 3,6-dichloropyridazine in dimethylformamide. Mechanistic studies have shown that this reaction product is formed through an initial hydride addition to the pyrazole ring followed by hydrolysis of the methyl ester and chloride ion substitution. The result of this reaction is an anthranilic acid derivative with chlorine substitutions at positions 3 and 6 on the pyridine ring.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>5-Iso-butyl-5-methylhydantoin is an organic compound that contains a sulphonic acid group. It has the chemical formula of CH3C(O)NHCH2SO3H. 5-Iso-butyl-5-methylhydantoin is soluble in water and has a pH between 1 and 4. It can be used as a solvent for substances with high solubility, such as additives, solutions, and inorganic materials. The flow properties of 5-isobutyl-5-methylhydantoin are dependent on the binder or carbon atoms present.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Phenylethyl)propylamine is an aminophenol that is a monosubstituted aromatic compound. 2-Phenylethyl)propylamine has been shown to be a bifunctional substrate for the cytochrome P450 enzyme and is also a receptor affinity analog of cannabinoids. The liposome formulation of 2-phenylethylamine has been shown to have an enhanced blood stability, which makes it useful for analytical toxicology as well as in pharmaceutical research. The oxidase type of 2-phenylethylamine has been shown to have inorganic particles, which may cause particle aggregation during storage.</p>

<p>(R)-2-(1-Hydroxyethyl)pyridine is an enantiopure compound that is used as a catalyst in the production of alcohols, carbinols and hydrocarbons. It has been shown to be a high yield preparative catalyst for catalytic asymmetric reactions. The enzyme alcohol dehydrogenase catalyses the oxidation of (R)-2-(1-hydroxyethyl)pyridine to form an intermediate that can then be oxidized by the enzyme carbinol dehydrogenase, which produces carbinols. This product has also been found to act as a vasodilator and nonselective inhibitor of phosphodiesterases 3 and 4.</p>

2,3-Dihydro-1-benzothiophene-2-carboxylic acid is a hydrocarbon with the molecular formula C10H8O3. It has a benzene and phenolic functional groups. The compound is quantified by gas chromatography, which can be preselected to identify specific compounds, such as hydrocarbons and aromatic hydrocarbons. The compound can also be analyzed using spectrometric techniques, such as UV/Vis spectroscopy. 2,3-Dihydro-1-benzothiophene-2-carboxylic acid is found in databases of mass spectrometry data. It can be used to determine the structure of benzylsuccinic acid and naphthalenes.

<p>Versatile small molecule scaffold</p>

<p>5-Chloro-2-methylbenzylamine is a chemical compound that has been shown to be an effective ozone depleter. It has also been used to study the relationship between chemical structure and reactivity, as well as in regression analysis. The ionic, nucleophilic, and electron properties of 5-Chloro-2-methylbenzylamine have been studied by looking at its affinity for different metal ions. This molecule can be used in organic pollutant remediation because of its ability to catalyze the regeneration of ozonide when it is oxidized by oxygen in water. This reaction is reversible, so 5-Chloro-2-methylbenzylamine can be regenerated from the ozonide product.</p>

<p>(Iodomethyl)cyclopentane is a potent cytotoxic agent that inhibits the proliferation of a wide range of cells. It binds to the DNA of proliferating cells and causes cross-linking and strand breakage, which leads to cell death. This compound also has anti-inflammatory properties and can be used in hyperproliferative diseases such as cancer, as well as infectious diseases such as tuberculosis. (Iodomethyl)cyclopentane is not available for sale in its pure form, but rather in a salt form.</p>

<p>Butyl 4-chlorobenzoate is an organic compound that has a radical chain mechanism of action. It is used as a photosensitizer in photodynamic therapy and can be activated by ultraviolet light. The radical species generated by this drug attacks the DNA of the bacteria, leading to cell death. One of the key steps in the process is the transfer of a hydrogen atom from butyl 4-chlorobenzoate to an electron donor, such as hydroxyanisole, followed by irradiation with light to generate radical species. Butyl 4-chlorobenzoate also inhibits bacterial growth through its ability to act as an acid and cause acidic pH changes within 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>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-(3-Bromopropoxy)-4-chlorobenzene is a nitrate salt that has a crystal structure that is mathematically represented by the space group P2/c. The compound crystallizes in the monoclinic system with the lattice constants of a = 10.6, b = 9.7, c = 5.8, and β = 117°. It has an experimental solubility data range of 0.01 to 1 g/L in ethanol solutions at room temperature and 1 atmosphere pressure. The solubility of this compound is decreased by the presence of oxygen and increased by the presence of moisture or heat. The stability of this compound can be monitored using a laser light monitoring system to detect changes in crystallization behavior or changes in concentration due to hydrolysis reactions.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

1-(4-Chlorophenyl)-2-hydroxyethan-1-one is a selective enantiomer that inhibits the growth of candida parapsilosis and c. parapsilosis. It has been shown to be preferentially oxidized by candida parapsilosis and c. parapsilosis, which leads to its selectivity for these fungi. 1-(4-Chlorophenyl)-2-hydroxyethan-1-one has been shown to be a biphasic system that can inhibit the growth of both candida parapsilosis and c. parapsilosis, with biphasic activity being due to its ability to selectively oxidize alcohols in these fungi. This compound is also an enantiomer, making it more effective than other compounds with similar structures but different stereochemistry.

<p>Versatile small molecule scaffold</p>

<p>2,2-Dichloro-1-phenylcyclopropane-1-carboxylic acid is a cyclopropanecarboxylic acid. It is an organochlorine compound that has been used as a pesticide and herbicide. 2,2-Dichloro-1-phenylcyclopropane-1-carboxylic acid inhibits the production of chlorophyll in plants by inhibiting the activity of photosystem II. This inhibition leads to a decrease in the rate of photosynthesis and plant growth.</p>

Versatile small molecule scaffold

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>

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>