Building Blocks

<p>5-[(4-Nitrophenyl)methyl]-1H-1,2,3,4-tetrazole is a transition metal complex that has been shown to be catalytic. The crystal x-ray diffraction pattern of the compound shows that it has a crystallographic space group of P2/c, with unit cell dimensions of a = 17.94 Å and c = 9.66 Å. The molecular geometry is trigonal planar with dihedral angles of 18.6° between the nitro group and the methylene group on one side and 16.5° between the methylene group on the other side. The crystal structure consists of two benzene molecules bridged by 2 nitro groups and 1 methylene group in an octahedral geometry.</p>

<p>Versatile small molecule scaffold</p>

<p>1-(3-Chloropyridin-2-yl)ethanone is an antibacterial agent that belongs to the group of organochlorine compounds. It has a bactericidal and bacteriostatic effect on a number of microorganisms, including bacteria, fungi, protozoa, and viruses. 1-(3-Chloropyridin-2-yl)ethanone is used in preparations for the treatment of wounds and skin infections as well as for disinfecting the environment. The active substances in 1-(3-Chloropyridin-2-yl)ethanone are bactericidal and bacteriostatic against a broad spectrum of microorganisms. These substances are also effective against some strains that develop resistance to antibiotics.</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

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>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

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>

<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>1-Hydroxy-6-Thioxo-1,6-Dihydropyridine-2-Carboxylic Acid is a cellular modulator that acts as a regulator of gene expression. It is an inhibitor of the myotonica chloride channel and inhibits the activity of target enzymes by binding to their active site and blocking them from performing their function. 1-Hydroxy-6-Thioxo-1,6-Dihydropyridine-2-Carboxylic Acid has been shown to be effective in controlling cardiac hypertrophy and preventing heart failure. The molecule also targets ribosomes, which are involved in protein synthesis. This drug has low expression levels in cells and is not very cell culture labile. 1HTCA binds to the ribosome and prevents protein synthesis by inhibiting peptidyl transferase activity.</p>

Versatile small molecule scaffold

<p>Methyl 2-formyl-3-hydroxybenzoate is a formylating agent that reacts with the hydroxyl group of benzene to form a methyl ester. It has been used in the production of polyphosphoric acid, and is also used in the synthesis of salicylic acid and other organic compounds. Methyl 2-formyl-3-hydroxybenzoate reacts with hexamethylenetetramine to produce hexamethylenetricarboxylic acid, which can be reacted with an alcohol to produce an ester. This reagent has been shown to have antifungal activity against Rhizoglyphus sp.</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>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>1-(2-Methoxypyridin-3-yl)ethanone is a structural analog of 2-chloropyridine. It has the same stereochemistry as 2-chloropyridine and can be synthesized from it by metallation, oxidation, or acridone synthesis. 1-(2-Methoxypyridin-3-yl)ethanone can be used as an intermediate in the synthesis of coumarins and acridones. It is also used to produce enantiomerically pure (S)-1-(2-methoxypyridin-3-yl)propanol. The optical activity of this compound was determined using a polarimeter.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

2-Bromo-3-pyridinemethanol is a heteroaryl compound that contains a pyridine ring. It is synthesized by the lithiation of 2-bromopyridine followed by intramolecular bromination with 3-bromopyridinemethanol. The methodologies for this synthesis are similar to those used in the synthesis of quinolines and pyridines. Lithiation of 2-bromopyridine at low temperature (0°C) led to the formation of 2,6-dibromopyridine, which was then reacted with 3-bromopyridinemethanol in a sequence similar to that described for the synthesis of quinoline and pyridine. This reaction yielded 2,6-dibromo-3-(2'-pyridinyl)-N,N'-dimethylethanamine. The desired product was obtained after cyclization with potassium tert

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>