Building Blocks

<p>Versatile small molecule scaffold</p>

<p>3-[(2-Methoxyphenyl)sulfamoyl]-4-methylbenzoic acid is a chemotherapeutic agent that is used to treat cancer. It is an analogue of the natural amino acid tyrosine and inhibits protein synthesis by methylation of the N-terminal amine group. 3-[(2-Methoxyphenyl)sulfamoyl]-4-methylbenzoic acid has been shown to inhibit the growth of cancer cells in vitro, in animals and humans. The drug has been used to treat leukemia, lymphoma, prostate cancer, and other cancers. 3-[(2-Methoxyphenyl)sulfamoyl]-4-methylbenzoic acid also has a variety of applications as a reagent for chemical modification of proteins and polysaccharides.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-[(4-Benzylpiperazin-1-yl)sulfonyl]benzoic acid is a potent and selective inhibitor of the human T cell receptor alpha/beta heterodimer. This inhibitor binds to the peptide binding site of the T cell receptor beta chain, thereby blocking the interaction between the T cell receptor beta chain and its ligand. 3-[(4-Benzylpiperazin-1-yl)sulfonyl]benzoic acid is a high purity research tool that can be used in Cell Biology, Peptides, Pharmacology, Ligand, Activator or Ion channels research. It has been shown to inhibit ion channel activity in some types of cells but not others. The IC50 value for inhibition of ion channel activity is approximately 0.5 μM.</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>5-Bromo-furan-2-carboxylic acid is an estrogen receptor modulator that binds to the estrogen receptor and exerts estrogenic effects. This compound, also known as Bracinostat, has been shown to inhibit the growth of breast cancer cells in vitro by binding to the estrogen receptor. It acts as a prodrug for benzoxazole analogues, which are active forms of 5-Bromo-furan-2-carboxylic acid. The analogues are capable of inhibiting DNA synthesis, protein synthesis, and cell growth. They have been shown to be effective in treating prostate cancer, breast cancer, ovarian cancer, and endometrial cancer.</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-{4,6-Dimethyl-3,7,8,10-tetraazatricyclo[7.4.0.0,2,7]trideca-1,3,5,8,10,12-hexaen-5-yl}-N-[3-(methylsulfanyl)phenyl]propanamide is a chemical compound that has been shown to be an inactivator of glycolysis and is being studied for its potential use as a cancer therapy. It is also being researched for its potential to treat inflammatory diseases and type 2 diabetes. 3-(4,6-dimethyl-3,7,8,10 tetraazatricyclo[7.4.0.0 2 7]trideca 1 3 5 8 10 12 hexaen 5 yl) N (3 methylsulfanyl) phenyl propanamide is structurally related to the heter</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>5-(2,4-Dimethylphenyl)-1,3,4-oxadiazol-2-amine is a potent and selective small molecule antagonist of the N-methyl-D-aspartate receptor (NMDAR). It inhibits the neurotoxic effects of glutamate on neurons in vitro. This compound has been used as a research tool to study the role of NMDA receptors in neuronal cell death and to investigate the development of novel therapies for Alzheimer's disease. 5-(2,4-Dimethylphenyl)-1,3,4-oxadiazol-2-amine binds to the NMDAR at a site distinct from that occupied by MK801 and other channel blockers.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-(2-Methylpropoxy)benzonitrile (BMB) is a chemical compound that is synthesized by the bromination of 2-methylpropylbenzene with bromine and potassium bromide. It is used in medicinal preparations as an intermediate for the synthesis of febuxostat, an antihypertensive agent. BMB has been shown to have oxidative properties, which may be due to its ability to form hydroperoxides from peroxide radicals in alkaline solution. The hydrolysis of BMB occurs readily in water or alcohols and leads to the formation of methyl benzoate and hydrogen chloride.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Aminobenzamide oxime is a covalent binding agent that is used to quantify the amount of dopamine in biological samples. 4-Aminobenzamide oxime reacts with dopamine to form a cyclic compound, which can be detected electrochemically by cyclic voltammetry. The current generated when the aminobenzamide oxime binds to dopamine is proportional to the concentration of dopamine in the sample. This process has been shown to be selective for dopamine, as it does not react with other compounds such as serotonin or norepinephrine.</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>Cyclobutanone is a cyclic ketone that is used as a reagent in organic synthesis. It can be converted to the corresponding oxime by treatment with hydroxylamine. The oxime then reacts with an ester to form the corresponding ester of cyclobutanone. Cyclobutanones are also used as coupling agents for amines, alcohols, and carboxylic acids.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>N-(4-bromobenzenesulfonyl)acetamide is a carbonyl compound that contains an arylsulfonyl group. The molecule attacks the electron-rich double bond of benzene, leading to the formation of two molecules of benzenesulfonic acid. This compound has been studied using spectroscopy and theoretical calculations, which have shown that the activation energies are low and that the anion has a strong interaction with the carbonyl oxygen atom.</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-(5-Ethylthiophene-2-carbonyl)benzoic acid is a ketone that is used in the synthesis of pharmaceuticals, dyes and other organic compounds. 2-(5-Ethylthiophene-2-carbonyl)benzoic acid has been shown to have antioxidant 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>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>Methyl 2,2-dimethoxycyclobutane-1-carboxylate is an ethyl methyl compound that is not reactive and unreactive. It's a regioselective oxidative process in which the methyl group is removed from the carbon atom adjacent to the carboxyl group. The product of this reaction is an ethyl methyl ketone, which is then scissioned by electron transfer to form a cyclopropane. This reaction can be used in the synthesis of cyclopropanes for use in chemical reactions that require this type of functionality.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>