Building Blocks

<p>2-Methylcyclohexane-1-carbonitrile is a phenoxide that is formed by the reaction of silicon and carbon. It has an empirical formula of C6H4O2NSi and a molecular weight of 122.14 g/mol. 2-Methylcyclohexane-1-carbonitrile has been found to yield a variety of products, including carbons, phenol, and cyclohexanol.</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-Chloro-5-ethylpyridine is a chemical compound that belongs to the class of heterocyclic compounds. It is used as a catalyst in catalytic reduction and metabolic rate studies. This compound has been found to increase the production of flavopereirine, an important intermediate in the metabolism of plant polyphenols. 2-Chloro-5-ethylpyridine has also been shown to have an agonistic effect on the long term treatment of diabetes mellitus type 2. This agent has been shown to optimize yields and reduce hypoglycemic effects in animal models.</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>Octahydro-2H-1,3-benzoxazine is a biomolecule that has been found in nature. It is an unsymmetrical molecule with a hydroxyl group at the terminal position on one of the six carbon atoms. Octahydro-2H-1,3-benzoxazine can be synthesized by metathesis reactions. This molecule can also undergo enantiospecific metathesis reactions and stereoselective carbinol additions.</p>

<p>Octahydroindolizin-2-ol is a bacteriostatic agent that inhibits the synthesis of RNA and DNA, which in turn prevents protein synthesis. It has been shown to be effective against fungus and lactam, as well as unraveling ribonucleotide chains. The chemical analysis of this compound shows that it contains an n-oxide group and a methoxy group. Octahydroindolizin-2-ol is extracted from the Oxytropis plant and has been found to be endophytic (living inside plants). This compound also has anti-viral properties, which are due to its ability to inhibit viral transcription by binding to viral RNA polymerase. Octahydroindolizin-2-ol is chemically related to swainsonine, a toxin produced by the endophytic fungus</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>3-Phenylpropane-1-sulfonamide is a synthetic drug that binds to the receptor tyrosine kinases and blocks the receptor system. It has been shown to be effective in reducing tumor growth in mice, although its mechanism of action remains unclear. 3-Phenylpropane-1-sulfonamide has also been shown to reduce cancer metastasis in mice. This drug binds to the quinoline derivatives and cyclic ligand, which are involved in hyperproliferative disorders such as cancer. 3-Phenylpropane-1-sulfonamide is also known for its ability to inhibit tumor cell proliferation by blocking hyperfunction through inhibition of receptor tyrosine kinases.</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>

2,3-Dihydro-1,4-benzodioxine-6-sulfonamide is a pyruvate kinase inhibitor that has been shown to modulate the activity of this enzyme in human cancer cells. The inhibition of this enzyme leads to an accumulation of pyruvate and a decrease in ATP, which causes cell death by apoptosis. 2,3-Dihydro-1,4-benzodioxine-6-sulfonamide has also been shown to have anticancer activity against several types of cancer cells. It is not active against bacteria such as Mycobacterium tuberculosis and Clostridium perfringens.

Versatile small molecule scaffold

<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>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Decahydroquinoxalin-2-one is a mitochondrial membrane potential stabilizer. It binds to the imine moiety of the mitochondrial membrane and prevents collapse of the mitochondrial membrane potential, which is essential for cell survival. Decahydroquinoxalin-2-one also has an antiproliferative effect on cancer cells. The proapoptotic activity of decahydroquinoxalin-2-one has been shown in some studies; however, this activity has not been demonstrated in all cases, suggesting that it may have other mechanisms of action. Decahydroquinoxalin-2-one is currently being studied as a possible treatment for cancer and Parkinson’s disease.</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>2-Pyridin-2-yl-cyclopropanecarboxylic acid is a chemotype that belongs to the class of echs. It has been shown to regulate the expression of genes in the erythroid lineage and inhibit Keap1. 2-Pyridin-2-yl-cyclopropanecarboxylic acid has been shown to bind to erythrocyte proteins and act as an anti-oxidant. This molecule has also been found to interact with proteins such as glutathione reductase, cytochrome P450, and glutathione S transferases. 2-Pyridin-2-yl-cyclopropanecarboxylic acid disrupts homoeostasis by regulating the levels of cytoprotective agents such as heme oxygenase 1 and prostaglandins. The therapeutic effect of this molecule is currently being researched for use in medicinal treatments.</p>

<p>3,4-Dihydro-2H-1,4-benzoxazine-2-carboxylic acid is a chemical compound that is used in the synthesis of esters. It can be used to separate mixtures of compounds in liquid chromatography and reversed phase liquid chromatography. This chemical compound has been shown to have adrenolytic properties, which are due to its ability to modify the activity of the alpha and beta adrenergic receptors. 3,4-Dihydro-2H-1,4-benzoxazine-2-carboxylic acid inhibits lipogenesis by inhibiting enzymes that catalyze this process.</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>3-Amino-4-methyl-pyridazine is a pyridazine molecule that has analgesic properties. This drug is used in population studies to investigate the effects of nitrogen atom substitution on the pharmacological activity of carrageenans and betaines. 3-Amino-4-methyl-pyridazine has been shown to be an analog of cinnoline, which is a member of the quinone class of compounds. The crystal structure and diffraction techniques have been determined for 3-aminopyridine using single crystal x-ray diffraction. The structure was determined by a molecular replacement method with a difference in formula weight of 0.01%.</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>

3-Azabicyclo[4.3.1]decan-4-one is a lactam that contains 4 rings and 10 carbon atoms. The molecule can exist in two geometries, which are both optimized for the lowest energy conformations. This compound has a multicyclic ring system with three azabicyclo[4.3.1]decane rings and one decan ring, which is attached to the nitrogen atom of the amide group. 3-Azabicyclo[4.3.1]decan-4-one has been shown to bind lanthanides and shift their spectral properties, as well as undergo conformational changes when reacting with reagents such as hydrogen cyanide or ammonia gas, indicating that it may be a useful substrate for theoretical studies of lanthanide coordination chemistry and mechanisms of catalysis by metal complexes in organic synthesis.br>br> br>br>

<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>

Methyl 2-amino-3-hydroxy-4-methoxybenzoate is a synthetic compound that is an isomeric mixture. It has been shown to be active against gram-negative bacteria and soil bacteria, which are both gram-negative. Methyl 2-amino-3-hydroxy-4-methoxybenzoate has also been shown to have activity against Staphylococcus aureus and gram negative bacterium. This substance's mechanism of action may be due to its ability to inhibit the enzyme enoyl reductase, which is involved in fatty acid synthesis and cell membrane integrity.

<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>2-Amino-2-methyl-1-propanol is a chemical compound with the molecular formula CH(NH)CH(OH)CH(OH). It is also known as 2-amino-2-phenylpropan-1-ol. This compound has been shown to be effective in the uptake of fatty acids and can be used in the production of coatings and polymers. The viscosity of 2-amino-2-methylpropane 1,3 diol is lower than that of other similar compounds due to its primary alcohol structure. This chemical is not readily polymerized, but can react with chloride ions to form chlorinated derivatives.</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<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>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>