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>N-Hexylhydroxylamine hydrochloride is a metal chelator that is used to bind heavy metals in the gastrointestinal tract. It is taken as a pill, and then binds to heavy metals such as lead, mercury, and arsenic. This prevents absorption of these toxic substances into the body. N-Hexylhydroxylamine hydrochloride has been shown to be most effective when it is given at high doses (2-3 grams) and causes less side effects than other chelators. One of the side effects of N-Hexylhydroxylamine hydrochloride is an increased risk for asphyxiation due to the increased concentration of gases in the lungs. The drug also has an effect on reticulatum pigment cells in the foregut, which can cause ulcers or cancerous growths if too much hexylhydroxylamine hydrochloride accumulates there.</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>Tert-Butyl 3-iodopropylcarbamate is a monomer that possesses reactive chemical groups, such as carbonyl and iodide. It is used in the synthesis of polyamides and other molecules containing pyrrole rings. Tert-Butyl 3-iodopropylcarbamate is also used to synthesize oligonucleotides by coupling reactive groups on the nucleotide phosphoramidite monomers. This coupling reaction can be done with imidazole or tripyrrole nucleophiles. Tert-Butyl 3-iodopropylcarbamate can also be used to form heterodimeric complexes with cysteine. The tert-butyl group of tert-Butyl 3-iodopropylcarbamate is a sequence that may be removed by hydrolysis or reductive amination.</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>N-Methylindole-5-boronic acid is a regioselective antimicrobial agent that inhibits microbial growth. This compound has been shown to inhibit the growth of both Gram-positive and Gram-negative bacteria, as well as fungi, in vitro. N-Methylindole-5-boronic acid has been shown to be effective against strains of Escherichia coli, Bacillus subtilis, and Pseudomonas aeruginosa. The antimicrobial activity of this compound was tested using an X-ray analysis and was found to bind strongly to the bacterial cell wall in a regioselective manner.</p>

<p>6-Hydroxy-1H-indole-3-carbaldehyde is an anion transporter that has been experimentally shown to inhibit the transport of anions across the plasma membrane. It was found to have significant inhibitory activity against hypouricemia and acetone. The localization of 6-hydroxy-1H-indole-3-carbaldehyde in fungi is unknown, but it has been shown to function as a transporter in macrofungi. 6-Hydroxy-1H-indole-3-carbaldehyde inhibits the uptake of anions by competing with them for the active site on the transporter protein. This mechanism may be due to its ability to bind with cations, which are also transported by these transporters. 6 hydroxy 1H indole 3 carbaldehyde is active against yeast cells and also shows some inhibitory activity against human erythrocytes when high concentrations are used.</p>

<p>3-(Ethanesulfonyl)pyridine is a synthetic chemical that has two reactive chlorine atoms and one reactive fluorine atom. It is used in the reduction of alkoxides to alcohols or amines, or in the preparation of chloroformates. 3-(Ethanesulfonyl)pyridine reacts with alkyl halides and carboxylates to form sulfonium salts, which are useful for preparing organic compounds. This compound has a pyridine ring with an ethanesulfonyl group attached to it. The n-oxide of 3-(ethanesulfonyl)pyridine also exists, which is less reactive than the c1-c3 n-oxide form.</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>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Prinomastat is a small molecule that inhibits the protein MCL-1. It has been shown to inhibit tumor growth in mouse xenograft models of human breast, lung, and prostate cancer. This drug also blocks the expression of matrix metalloproteinases (MMPs), which are enzymes that break down collagen and other extracellular matrix components. Prinomastat inhibits iron homeostasis and induces apoptosis in epithelial cells, suggesting a role for this drug in the treatment of bowel diseases such as Crohn's disease.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Ethoxycyclohexan-1-ol is a volatile liquid. It is used as a solvent and chemical intermediate. It has been shown to be reactive with deuterium, trimethylsilanes, and other electron-deficient compounds. 4-Ethoxycyclohexan-1-ol also reacts with trimethylsilyl ether to form the corresponding trimethylsilyl ether derivatives. This reaction can be used for the labeling of silicon in organic syntheses. The reaction of 4-ethoxycyclohexan-1-ol with trimethylsilanes leads to rearrangement reactions that produce metastable products, which are unstable at room temperature.</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>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Tert-butyl-N-(2-methylphenyl)carbamate is a chiral hydrolysis product of isomunchnone. This compound has been shown to be an efficient carbonyl cleavage agent and can be used for the synthesis of cycloadducts, cycloadditions, and some other valuable compounds.</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>2-[(Acetylsulfanyl)methyl]butanedioic acid is a hydrazone that has shown immunizing effects against infestation by hetero-species. This drug has been shown to be microbicidal and microbicide in the treatment of certain bacterial infections, including methicillin-resistant Staphylococcus aureus and Clostridium perfringens. 2-[(Acetylsulfanyl)methyl]butanedioic acid may be used as an intermediate for the synthesis of other drugs with antimicrobial activity. This compound is synthesized from benzyl alcohol and acetone, which are both commercially available. 2-[(Acetylsulfanyl)methyl]butanedioic acid can also be attacked by microbiocidal agents such as hydrogen peroxide or chlorine gas, leading to inhibition of microbial growth.</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>

<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>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>4-Bromo-2-methyl-1,3-benzoxazole is a cyclization reaction product of palladium acetate and 4-bromo-2-methylbenzoic acid. It can be used as a substrate for the synthesis of benzoxazoles, which are biologically important heterocyclic compounds. The 4-bromo derivative is an intermediate in the synthesis of biologically active molecules such as pyrazinones, benzothiazoles, and other heterocycles. This process can be catalyzed by palladium acetate and yields a 96% yield with this method.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold