Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Butyl-2-methylphenol is a phenolic compound that is found in the essential oils of plants such as rosemary. It has been shown to inhibit the growth of animal cells, and this effect may be due to its ability to induce apoptosis. 4-Butyl-2-methylphenol also inhibits the production of basic fibroblast growth factor and epidermal growth factor by inhibiting protein synthesis and DNA synthesis. This chemical is an analog of platelet derived growth factor and has been shown to stimulate angiogenesis in vitro. 4-Butyl-2-methylphenol has been found to increase vessel density in animals when applied topically.</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>1,3,5-Trichloro-2-(chloromethyl)benzene (TCMB) is a chemical compound that inhibits the synthesis of proteins and is used in cancer therapy. TCMB has been shown to inhibit protein synthesis by binding to the polymerase chain reaction enzyme transcriptase polymerase chain reaction. It also inhibits the activity of enzymes involved in lipid metabolism, such as lipases and cholesterol esterases. The serum bilirubin levels were found to be lower in mice treated with TCMB than in those not treated with TCMB. This may be due to the ability of this drug to inhibit the enzyme fatty acid synthase, which is responsible for synthesizing fatty acids. TCMB has been shown to induce apoptosis in bladder cells, which may be due to its inhibition of DNA synthesis and repair.</p>

<p>2-Phenylcyclobutan-1-amine is a synthetic compound. It is a white crystalline solid that can be soluble in water, ethanol, and acetone. The compounds are chiral and exist as two stereoisomers: (S)-2-phenylcyclobutan-1-amine and (R)-2-phenylcyclobutan-1-amine. The two isomers have different effects on the central nervous system. The (S)-isomer is an analog of amphetamine and interacts with the serotonin receptor 5HT2A, while the (R)-isomer is an analog of methamphetamine which interacts with the dopamine receptors D1 and D2. 2-Phenylcyclobutan-1-amine has been shown to be more effective than cocaine in animal studies for Parkinson's disease treatment, but it has not been tested in humans. It also has properties that make it worthwhile for use as an insecticide or herbicide.</p>

<p>2-Phenylcyclohexanamine is a synthetic, experimental compound. It has been shown to have high energy content and the ability to cross over from the gas phase to the liquid phase. 2-Phenylcyclohexanamine can be used as a thermodynamic probe in analytical research and has an efficient method for synthesis. The synthesis of 2-phenylcyclohexanamine is done by heating 1,1-diphenyl cyclopropane with cyclohexylamine, producing a mixture that can be purified with column chromatography. The analytical methodology for this compound includes GC/MS analysis of the raw material, reaction product, and final product.</p>

<p>2'-Methoxybiphenyl-2-carboxylic acid is a benzene carboxylic acid that is used as a precursor for biphenyl-2-carboxylic acids. 2'-Methoxybiphenyl-2-carboxylic acid can be synthesized by refluxing 2'-hydroxybiphenyl with peroxides in the presence of benzene, followed by cyclisation and decarboxylation. Alternatively, 2'-methoxybiphenyl-2-carboxylic acid can be obtained by thermally decomposing 3,4,5,6-tetramethylbenzoic acid. This compound has been shown to react intramolecularly and intermediacy with triphenylene to form triphenyltetracarboxylic acids.</p>