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>1,2,3,4-Tetrahydroquinolin-3-ol is a stabilizer that can be used to prevent or slow down the polymerization of epoxy resins. It can also be used as an intermediate in the synthesis of other organic compounds. 1,2,3,4-Tetrahydroquinolin-3-ol has been shown to react with amines and nucleophiles to form new compounds. It has also been shown to stabilize proton transfer reactions. This compound is also capable of reacting with inorganic acids to form ring-opening polymers.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Methyl (2R)-2-amino-3-(4-hydroxyphenyl)propanoate is a linker that binds to the nuclear hormone receptors found in cancer cells. It has been shown that this molecule has anticancer activity in animals, but its efficacy has not been evaluated in humans. Methyl (2R)-2-amino-3-(4-hydroxyphenyl)propanoate is a stereoselective agent, which means it selectively binds to one of two mirror images of the same molecule. The molecule was originally synthesized for use as an estrogen receptor antagonist but also shows affinity for progesterone and androgen receptors. This linker is being investigated as a potential drug for the treatment of hormone receptor positive glioma, prostate cancer, and breast cancer.</p>

<p>1-(4-Bromophenyl)-3,3-dimethylurea is a growth regulator that belongs to the heterocycle pyrazole derivative. It binds to the cytochrome P450 enzyme and inhibits the production of proteins vital for cell division, leading to cell death by inhibiting the production of proteins vital for cell division. 1-(4-Bromophenyl)-3,3-dimethylurea has been shown to inhibit methionine adenosyltransferase and suppress DNA methylation. This drug also has a toxic effect on respiratory system cells, which may be due to its ability to induce apoptosis.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-[(4-Nitrophenyl)sulfanyl]acetic acid is a colorless liquid with a boiling point of 168°C. It is soluble in water, glycol, and ether, but not in ethanol. 2-[(4-Nitrophenyl)sulfanyl]acetic acid has been shown to be an acceptor for borate, forming the perborate ion. It also reacts with glycol to form the glyoxalate ion. The compound has been shown to react with nitric acid and ethylene glycol to form nitroethane and acetic acid molecules. This reaction is catalyzed by hydrogen bonding between the oxygen atoms of acetic acid and nitric acid, which causes an electron transfer from nitric acid to acetic acid molecules. This process results in reactive species that can then react with other substances such as hydrogen bonds or peracetic acid.</p>

<p>Versatile small molecule scaffold</p>