Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Ethynyl-1,1'-biphenyl is a cross-linking agent that binds to the nicotinic acetylcholine receptor. It is used in medicine as a control agent for inflammatory diseases. 2-Ethynyl-1,1'-biphenyl has antiinflammatory activity and may be useful for the treatment of inflammatory diseases due to its ability to inhibit prostaglandin synthesis and the production of reactive oxygen species (ROS). 2-Ethynyl-1,1'-biphenyl irreversibly oxidizes organic compounds by reacting with thuringiensis, which is an enzyme found in plants. The reaction mechanism involves phenanthrene synthesis from benzene.</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>5-Bromonaphthalen-1-ol is a ligand that binds to the intracellular targets of the nuclear receptor peroxisome proliferator-activated receptor alpha (PPARα). It is a mimetic of the natural ligand, which is a macrocyclic. The ligand has been biotinylated at the n-terminal and used in affinity chromatography to isolate PPARα from other proteins. This ligand has been shown to have specificity for PPARα and can be used in elucidating its physiological function. The functionality of 5-Bromonaphthalen-1-ol as a ligand for PPARα has been studied extensively, and it has been found to be an excellent candidate for targeting PPARα.</p>

<p>4-Iodobenzene-1-thiol is a reactive organometallic compound that has been used in biological studies. Its fluorescence properties are influenced by the presence of heavy metals, making it an excellent probe for metal surfaces. 4-Iodobenzene-1-thiol can be used as a cross-coupling agent to form C–C bonds. It is also used in surface-enhanced Raman spectroscopy and metathesis reactions. This compound is chemically stable and does not react with nucleic acids, which makes it a promising candidate for non-nucleoside inhibitors. The reaction mechanism of 4-iodobenzene-1-thiol is currently unknown, but organic chemists have hypothesized that the thiol group reacts with DNA bases to form a covalent bond.</p>

<p>5-Phenyl-2-furancarboxylic Acid is an inhibitor of methionine aminopeptidase that contains a phenyl substituent. It is non-selective and has been shown to be effective against E. coli, P. aeruginosa, and S. aureus at concentrations of less than 1 μM. The inhibition of methionine aminopeptidase by 5-phenyl-2-furancarboxylic acid results in the accumulation of methionine and other amino acids, which are substrates for peptide bond formation. This leads to the inhibition of protein synthesis through the disruption of nucleotide synthesis and cell division.</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'-Acetoxychavicol acetate is a modulator of the microvessel density in the prostate. It is used to study the effect of angiogenesis on prostate cancer cells, and has been shown to inhibit protease activity in human immunodeficiency virus-1. 1'-Acetoxychavicol acetate also inhibits angiogenesis by inhibiting the synthesis of growth factor and inhibits carcinogenesis. The mechanism by which 1'-acetoxychavicol acetate exerts its effects is not yet understood, but it may be due to its ability to inhibit spermidine/spermine n1-acetyltransferase or its ability to modify cell nuclei or virus.</p>

<p>1-(3-Methoxyphenyl)propan-1-ol is a trialkylborane that reacts with alcohols to form alkylated products. It is used in the synthesis of benzene derivatives, and also has been used to react with magnesium halides. 1-(3-Methoxyphenyl)propan-1-ol can be used as an alternative to the toxic 1,2-dibromoethane when making alkylated products.</p>

<p>N-Pentylsulfonamide is a benzimidazole derivative that is used as a medicine to treat muscle cell disorders and cardiovascular diseases. It has been shown to improve the efficiency of the synthesis of imidazole derivatives with alkylthio groups (e.g., chloroquine) by replacing the C6 alkyl group with an alkynyl group. It has also been shown to have anti-inflammatory properties, which may be due to its inhibition of prostaglandin synthesis. N-Pentylsulfonamide is used in many stereoisomers, including D-N-pentylsulfonamide and L-N-pentylsulfonamide.</p>

<p>N-Methyl-3-(methylsulfanyl)aniline is a blocker that is used in the synthesis of pharmacological agents. It has been shown to have neuroprotective activity and can be used as an antidote for cyanamide poisoning. This drug blocks sodium channels, which are pores on the surface of nerve cells that allow the passage of electrical signals from one cell to another. It also blocks the n-methyl-d-aspartate receptor, which is the most important excitatory amino acid receptor in the central nervous system. N-Methyl-3-(methylsulfanyl)aniline is orally active and has been shown to be effective against rat convulsions induced by potassium cyanide.</p>

<p>2-(carboxymethyl)-5-methoxybenzoic acid is a potent and selective agonist of the α receptor. It has been synthesized by reacting 2-bromo-4,6-dimethoxyphenol with methanol in the presence of hydrochloric acid. This compound has been shown to inhibit proliferation of cancer cells and induce apoptosis in vitro. It also inhibits growth factor signaling pathways, which may be due to its ability to block protein kinase C. 2-(Carboxymethyl)-5-methoxybenzoic acid has been shown to have anticancer activity in vivo and can be used as a potential therapy for cancer patients.</p>

<p>Versatile small molecule scaffold</p>

<p>6-Methoxy-4-oxo-1,4-dihydro-quinoline-2-carboxylic acid (6MOQ) is a compound that inhibits the replication of viruses by binding to their receptors. It has been shown to be effective in inhibiting the replication of HIV and influenza virus. 6MOQ also has been shown to bind to the receptor for ephedrine, which is a medicine used in the treatment of asthma. 6MOQ is active against cancer cells in vitro and animal models, but not against normal cells. The mechanism of action appears to be due to its ability to prevent growth factors from binding with receptors on tumor cells, which leads to inhibition of cellular proliferation.</p>

<p>7-(Bromomethyl)pentadecane is a molecule that has been used as an acceptor in organic photovoltaic devices. This molecule has a phenothiazine ring, which is electron deficient and low energy. 7-(Bromomethyl)pentadecane molecules are able to absorb light and convert it into electricity with high efficiency.</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>

Versatile small molecule scaffold

<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-Hydroxy-6-oxo-1,6-dihydropyridine-3-carboxylic acid is a biofuel that can be produced from the enzymatic conversion of malic acid. It has been shown to be a good carbon source for microbial synthesis of 1,5-dioxopentanoic acid and 1,2,5,6 tetrahydroquinoline (THQ). The enzyme complexes responsible for this conversion are light sensitive and require a cavity in which to work. This product is also an analog of 6-hydroxypyridine-2,4(1H,3H)-dione. It can be used as a solubilizing agent with an organic acid or as a waveform to measure x-ray absorption.</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>