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>2-Amino-N-(quinolin-8-yl)acetamide is a fluorescent inorganic compound. It has been shown to have a high affinity for chloride, with nanotube structures that are able to bind the chloride ions by supramolecular interactions. This binding prevents the chloride from interacting with other biomolecules, such as proteins and DNA. The energy of this interaction can be measured using fluorophore spectroscopy, which can be used for bioassays and medical imaging. 2-Amino-N-(quinolin-8-yl)acetamide has also been shown to have an ability to interact with zinc ions (Zn2+) in electrospray experiments, resulting in the emission of fluorescence.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Miltefosine is a cell-toxic agent that is used to treat leishmaniasis. Miltefosine has been shown to be active against the promastigotes and intracellular amastigotes of Leishmania infantum. It also has antileishmanial activity against L. major, L. tropica, and L. mexicana, as well as against the human parasite Leishmania donovani. Miltefosine is an analog of 2-(hexyloxy)ethanol that can be conjugated with a variety of functional groups for use in drug delivery systems, such as liposomes and polymeric micelles. This agent exhibits hemolytic activity when introduced into erythrocytes in vitro, which may be due to its ability to inhibit protein synthesis at the ribosome level by binding to the 50S subunit of the ribosome's large subunit and inhibiting peptide</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Ethynyl-4-methylthiazole is a cell-based kinase inhibitor that binds to the ATP binding site on the enzyme and inhibits phosphorylation. It was shown to inhibit cell growth in vitro by interfering with the production of TGF-β, activin, and other growth factors. The inhibitory activity of 2-Ethynyl-4-methylthiazole is selective for receptor kinases and is not effective against alk5 kinase. This drug has been shown to be an inhibitor of cellular growth in vitro and may be useful for the treatment of cancer.</p>

<p>Versatile small molecule scaffold</p>