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>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-(2-Methoxyethyl)-5-(pyridin-4-yl)-4H-1,2,4-triazole-3-thiol is an antibacterial agent that can be used in water. It is a congener of 4-(2-hydroxyethyl)-5-(pyridin-4-yl)-4H-[1,2,4]triazole 3(2H)-thiol and has been shown to have tautomeric and vibrational properties. 4-(2-Methoxyethyl)-5-(pyridin-4-yl)-4H-[1,2,4]triazole 3(2H)thiol has been shown to be photostable and exhibits additive effects with other compounds. The molecular weight of this compound is 278.37 g/mol.</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-{[4-Ethyl-5-(furan-2-yl)-4H-1,2,4-triazol-3-yl]sulfanyl}-1-(10H-phenothiazin-10-yl)ethanone (AET) is a subunit of an ion channel inhibitor. It binds to insect odorant receptors and blocks the activation of the ion channel. AET also blocks the pyridine ring and inhibits heterologous expression in mammalian cells. AET has been shown to be toxic to insects as well as mammals. The toxicity of AET is due to its ability to inhibit ligand binding to co-receptors, which is required for neurotransmitter release.<br>AET has been shown to affect the sensitivity of an insect species towards different concentrations of phenothiazines, which are drugs commonly used in pest control.</p>

<p>Versatile small molecule scaffold</p>

<p>4-Bromo-1-(2-chloroethyl)-1H-pyrazole is a chemical substance that belongs to the group of insensitive explosives. It has been shown to be thermally and geometrically insensitive, with an x-ray structure that is square planar. The techniques used to characterize this compound include XPS, EDS, SEM, and TEM. This compound also has magnetic properties and can be used as a catalyst in Suzuki reactions. 4-Bromo-1-(2-chloroethyl)-1H-pyrazole has been shown to be an efficient photoelectron emission source for microscopy techniques such as diffraction and transfer.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>5-Ethynyl-2-methoxypyridine is a drug with analgesic, marginally anti-inflammatory and anti-pyretic properties. It has been proposed to act as an inhibitor of prostaglandin synthesis. This compound is a weak base that is poorly soluble in water and slightly soluble in ethanol. It appears to have low oral bioavailability (less than 10%) but can be taken orally with minimal side effects because it does not cross the blood brain barrier or affect the central nervous system. 5-Ethynyl-2-methoxypyridine also has cyclic pharmacophore features that are similar to those found in aspirin and other drugs used for pain relief.</p>

<p>3,5-Dicyclopropyl-1H-pyrazole is a calcium channel modulator that can be used to treat cancers. 3,5-Dicyclopropyl-1H-pyrazole is activated by the addition of a phenyl group, which helps to increase its stability. As a calcium channel modulator, 3,5-Dicyclopropyl-1H-pyrazole blocks the function of voltage gated calcium channels. This leads to decreased production of cyclic AMP and subsequently decreases levels of protein kinase A activity. It also has an effect on hematological cancers, solid tumors, and esophageal cancer. 3,5-Dicyclopropyl-1H-pyrazole has been shown in animal studies to have cytotoxic effects against solid cancer cells and esophageal cancer cells.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>6-Chloro-7-fluoroquinoxaline is a quinoxaline that has been shown to have antiviral properties, inhibiting the activity of integrase enzymes in human cells. 6-Chloro-7-fluoroquinoxaline is structurally similar to other quinoxalines, with a hydrophobic region and a quinone acceptor. The pharmacophore of this drug is believed to be the same as that of other quinoxalines, which means it binds to the enzyme's active site by inserting into its hydrophobic pocket. 6-Chloro-7-fluoroquinoxaline has been shown to inhibit HIV and other viruses as well as SARS coronavirus (SARS CoV).</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-Phenylpentan-2-amine is an organic compound with a chemical formula of C9H12N. It is an aromatic and heterocyclic amine that exhibits oxidative reactivity. 1-Phenylpentan-2-amine can be used as a substrate for coupling reactions, such as oxidative coupling and coordinating catalysts. It can also be used in the catalysis of metal catalysts to form new molecules in a reaction known as oxidative coupling.</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>