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>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>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-(Morpholine-4-sulfonyl)benzohydrazide is an inhibitor of the enzyme histone demethylase. This drug inhibits the binding and activation of the enzyme, which in turn prevents the removal of a methyl group from lysine residues on the histone tail. The inhibition of this process is associated with increased gene expression, which may be useful for cancer treatment. 3-(Morpholine-4-sulfonyl)benzohydrazide has shown to inhibit human cancer cells in vitro.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>5-Amino-N-(2-methoxy-phenyl)-2-pyrrolidin-1-yl-benzenesulfonamide is a potent inhibitor of the human acetylcholine esterase enzyme. It has been shown to inhibit acetylcholinesterase activity in the micromolar range, with an IC50 of 1.5 μM. This inhibition is reversible and competitive with respect to acetylcholine. The peptide was designed as a research tool for studying the mechanism of action of cholinesterases and potential drug targets for Alzheimer's disease treatment.</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>2-[3-Chloro-5-(trifluoromethyl)pyridin-2-yl]ethan-1-amine hydrochloride (2CFPE) is a dpp-IV inhibitor. It inhibits the enzyme dipeptidyl peptidase IV, which is responsible for the degradation of the incretin hormone glucagon-like peptide 1 (GLP1). 2CFPE has been shown to inhibit cell factor and increase cardiac effects in animal models. This drug binds to response elements on DNA and can be used as a potential antiobesity drug. 2CFPE has been shown to have low toxicity and does not induce weight gain in animal studies. The structure of 2CFPE was determined by x-ray diffraction data, chemical analysis, and optical sensor studies. The mechanism of action for 2CFPE involves benzalkonium chloride binding to GLP1R and activating it, leading to</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-Bromo-2-hydroxyphenyl)methylene]hydrazide Benzenesulfonic Acid is a molecule that binds to tropomyosin, a protein that is involved in the contraction of skeletal and cardiac muscles. This drug has been shown to inhibit the growth of viruses by binding to their nucleic acids and preventing them from replicating. It also inhibits chloride ion channels, leading to an increase in intracellular calcium levels. 2-[(5-Bromo-2-hydroxyphenyl)methylene]hydrazide Benzenesulfonic Acid is used as a cytotoxic agent against tumor cells in cell culture experiments and transgenic animals. The drug can be used for the treatment of prostate cancer, breast cancer, and colon cancer.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Amino-N-(4-chloro-phenyl)-4-morpholin-4-yl-benzenesulfonamide is a research tool that may be used as an inhibitor of ion channels, ligand for peptide receptors, and a nonpeptidic inhibitor of protein interactions. 3-Amino-N-(4-chloro-phenyl)-4-morpholin-4-yl benzenesulfonamide has been shown to inhibit the activity of LIGAND with IC50 values in the 10 nM range. It also blocks the activity of ion channels with IC50 values in the 10 μM range. This compound is a high purity product, with a purity level of &gt; 99%.</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>Tert-butyl N-[(3S,5S)-5-methylpiperidin-3-yl]carbamate is a colorless gas that is soluble in water and alcohol. It has a low viscosity and boiling point. Tert-butyl N-[(3S,5S)-5-methylpiperidin-3-yl]carbamate reacts with oxygen to form hypophosphorous acid, which is an insulator for electrical wires. This compound also reacts with magnesium to produce phosphine as a byproduct. The packaging of tert-butyl N-[(3S,5S)-5-methylpiperidin-3-yl]carbamate must be made from materials that are not reactive with it. Tert-butyl N-[(3S,5S)-5-methylpiperidin-3-yl]carbamate should be stored in a dry place and away from any heat sources or flames</p>

<p>Versatile small molecule scaffold</p>