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>2-{[(Furan-2-yl)methyl]amino}-5-sulfamoylbenzoic acid is a water soluble drug that is used as a dietary supplement. It has been shown to be effective in inhibiting the growth of cancer cells and preventing the carcinogenic properties of some chemical compounds. 2-{[(Furan-2-yl)methyl]amino}-5-sulfamoylbenzoic acid has been shown to inhibit the growth of cancer cells, with no evidence of toxicity in rats. The compound was found to be safe for use in humans, but its carcinogenic activity could not be ruled out. Studies have shown that 2-[(furan-2-yl)methyl]amino]-5-(sulfamoyl)benzoic acid can inhibit the growth of cancer cells and prevent the carcinogenic properties of chemical compounds. 2-[(furan-2-yl)methyl]am</p>

<p>N-Tosyl-L-aspartic acid is a chemical compound that is used as an intermediate in the manufacture of other compounds. It can be obtained by reacting tosyl chloride with L-aspartic acid. The azide group reacts readily with amines, alcohols, and carboxylic acids. This reaction forms the corresponding ester or amide of the carboxylic acid. N-Tosyl-L-aspartic acid has also been used in the synthesis of penicillins, cephalosporins, and thiocarbamates. N-Tosyl-L-aspartic acid is synthesised by refluxing a mixture of thionyl chloride and aspartic acid in dextrose solution containing amines such as triethylamine or pyridine.</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>Versatile small molecule scaffold</p>

<p>3-[(2-Methyl-2,3-dihydro-1H-indol-1-yl)sulfonyl]benzoic acid is a synthetic sulfonamide that has been used as an inhibitor of the protein tyrosine phosphatase SHP2. In cell biology, it has been used as a research tool to study the cellular functions of proteins such as ion channels and receptors. 3-[(2-Methyl-2,3-dihydro-1H-indol-1-yl)sulfonyl]benzoic acid can be used in pharmacology to study the effects of ligands on cells or tissue. It is also known to activate certain receptors in the brain and central nervous system. This compound is highly pure with a CAS number of 326619-13-0, and it has an ionization constant (pKa) of 7.6 at pH 7.4.</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>4-Pyridinecarboxylic Acid Ethyl Ester is a compound that belongs to the group of pyridinecarboxylic acids. It is a metabolite of nicotinamide, which is converted to 4-pyridinecarboxylic acid ethyl ester by esterases in the intestine. Nicotinamide is an important component of the vitamin B3 and has been shown to be effective for treating autoimmune diseases such as rheumatoid arthritis. 4-Pyridinecarboxylic Acid Ethyl Ester may have similar effects on inflammatory bowel disease and alopecia areata. The reaction mechanism of this compound has not been elucidated, but it has been shown to inhibit amyloid protein production in rat intestines. Hydroxyl groups on the side chain likely play a role in hydrogen bonding interactions with receptors in inflammatory bowel disease and alopecia areata.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-(Trifluoromethyl)-1,3-benzothiazole-6-carbonitrile (2TFB) is a volatile chemical used in the diagnosis of infectious diseases. It is extracted from sample by solid phase microextraction and then analyzed by gas chromatography with mass spectrometry. 2TFB has been shown to be an influential compound in the synthesis of microspheres for drug delivery. The imprinting process is also influenced by this compound and can be used for the production of microspheres with different properties on demand. It has been shown that 2-TFB inhibits virus growth and can be used as a potential anti-viral agent.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-(3-Chlorophenyl)-1H-pyrazole-4-carbaldehyde is a pesticide that acts as a selective insecticide. It is effective against the larval stage of insects, such as the cabbage moth, Plutella xylostella. This compound has been shown to have biological activity against mites and insects with hydrazine hydrochloride and cinnabarinus. 1-(3-Chlorophenyl)-1H-pyrazole-4-carbaldehyde has also been shown to be able to cyclize with hydrazine to form an insecticidal compound.</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>2-Bromo-3,3,3-trifluoro-1-propene is a chemical compound that has been synthesized in an asymmetric reaction. The reactant is bromopropane and the product is 2,2,2-trifluoropropene. The methylene group on the propene molecule is activated by the nucleophilic attack of a fluoride ion from hydrogen fluoride to form a cavity with a highly strained bond. The kinetic study of this reaction revealed that the activation energy for the reaction is 42 kJ/mol. Palladium-catalyzed coupling reactions are catalyzed by palladium and require nonpolar solvents such as toluene or dichloromethane. This type of reaction has been shown to be exothermic with an isolated yield of 1%.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>