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>4-Amino-2-mercaptobenzoic acid is an organic compound that is a ligand for the thiol group of cysteine. It binds to the amino acid histidine, which can be found in nature or unmodified in proteins. 4-Amino-2-mercaptobenzoic acid has been shown to have an electrospray ionization mass spectrometric and a spectroscopic technique to identify serum albumin after modification with this compound. This modified albumin has been used as a carrier of gold nanoparticles and other molecules. The disulfide bond between 4-amino-2-mercaptobenzoic acid and the protein can be reduced, forming covalent adducts.</p>

<p>Versatile small molecule scaffold</p>

<p>3,5-Dichlorophenyl)methanamine hydrochloride is a research tool that is used in the study of ion channels and their ligands. It is an inhibitor of ligand-gated ion channels and voltage-gated ion channels. 3,5-Dichlorophenyl)methanamine hydrochloride has been shown to interact with a receptor for acetylcholine and also inhibits the binding of peptides to the alpha subunit of protein kinase C. 3,5-Dichlorophenyl)methanamine hydrochloride is a high purity product that can be used in the study of protein interactions or as an activator to detect antibodies.</p>

<p>3-(2-Hydroxyethyl)oxolan-2-one is an organic compound that belongs to the group of alcohols and has a cycloalkyl, cyclohexanone, ester, or aryl group. It can be used for the synthesis of caprolactones and amines. The reaction of 3-(2-hydroxyethyl)oxolan-2-one with primary amines in the presence of acidic catalysts leads to the formation of acyl groups. 3-(2-Hydroxyethyl)oxolan-2-one can be used as a solvent or as a catalyst in reactions such as hydrogenation, esterification, and alkylation. It is also used as a stabilizer in plastics.</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>2,6-Dichlorophenylacetamide is an acetamide derivative with vasodilatory activity. It is a potent antihypertensive agent that can be used as a substitute for pyridazine. 2,6-Dichlorophenylacetamide also has the ability to contract vascular smooth muscle cells in vitro and in vivo. This drug has been shown to have antihypertensive effects in animal models of hypertension and to cause vasodilation in humans.</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-Amino-3,5-pyridinedicarbonitrile (APDC) is a small molecule that has been shown to bind to the adenosine A1 receptor with high affinity and selectivity. It has a molecular weight of 167.2 g/mol, a pK of 7.4 and a logP value of 2.8. APDC was first synthesized in 1963 by scientists at the National Institute for Medical Research in London. The chlorine atom is influential in the pharmacokinetics of this compound. The pharmacokinetic profile shows that APDC is poorly absorbed and eliminated quickly from the body, with an elimination half-life of 0.6 hours and an oral bioavailability of less than 1%. This drug also has multipotent effects on Alzheimer's disease, showing significant efficacy against both plaques and tangles in animal models of Alzheimer's disease.</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>