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>2-[(2,6-Dimethylmorpholin-4-yl)methyl]aniline is a research tool that can be used as an activator or ligand for receptors and ion channels. It has been shown to inhibit the activity of ion channels by binding to them and altering their function. 2-[(2,6-Dimethylmorpholin-4-yl)methyl]aniline has also been shown to inhibit the activity of protein kinase C (PKC) in cell culture. 2-[(2,6-Dimethylmorpholin-4-yl)methyl]aniline has been used extensively in pharmacology and cell biology research.</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>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>5-(2-Bromo-5-fluorophenyl)-1,3,4-oxadiazol-2-amine is a synthetic monosaccharide that is used as a building block in the synthesis of complex carbohydrates. It is also used in fluorination reactions and click chemistry. This compound can be used as a methylating agent to produce 5-(2-bromo-5-fluorophenyl)furan.</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>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>3-Methoxy-4-[(methylcarbamoyl)methoxy]benzoic acid is a methylated, custom synthesized and click-modified oligosaccharide with a high purity. It is used in the synthesis of polysaccharides and saccharides. The modification of this chemical can be done at the monosaccharide level or even at the glycosylation level. This product has been fluorinated to increase its activity.</p>

<p>Versatile small molecule scaffold</p>

<p>2-[1-(5-Bromothiophen-2-yl)-N-methylformamido]acetic acid is a peptide that was originally identified in the venom of the spider Agelenopsis aperta. It has been shown to be an activator of ion channels and is used as a research tool to study their functions. This peptide binds to receptors on cells, thereby inhibiting the action of ligands, which may be useful for pharmacology.</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>5-Ethynylpyridine-2-carboxylic acid is a ligand with a pyridine ring. It binds to the pyridyl subunit of proteins, such as phosphoglycerate kinase and ATP synthase. This compound coordinates with metals to form complexes. It has been used to synthesize other compounds, including benzoate and nitrate salts, which have yielded luminescent frameworks.</p>

<p>Methyl 5-ethynylpyridine-2-carboxylate is a ligand that binds in the active site of many enzymes. It can enhance the activity of these enzymes and also change their conformations. Methyl 5-ethynylpyridine-2-carboxylate interacts with four subunits to form a tetradentate framework, which is responsible for this molecule's ability to bind to any type of ligand. This enhancement effect is reversible, and it can be reversed by oxidizing methyl 5-ethynylpyridine-2-carboxylate with nitric acid. The yield of methyl 5-ethynylpyridine-2-carboxylate depends on the reaction conditions and the type of arylacetylene used. Methyl 5-ethynylpyridine-2-carboxylate has been shown to be an effective ligand with a high emission yield when using 1,3</p>

<p>[(4-Methylquinolin-2-yl)sulfanyl]acetic acid is a chemical intermediate that is used in the synthesis of other organic compounds. It can be obtained by reacting acrylonitrile with potassium permanganate in water, followed by hydrolysis of the resulting manganese dioxide to give [(4-methylquinolin-2-yl)sulfanyl]acetic acid. This intermediate can also be synthesized from chloroacetic acid and ethyl bromoacetate, which are then converted to allyl bromide by reaction with potassium. The allyl bromide is then reacted with methyl methacrylate in the presence of amide to produce [(4-methylquinolin-2-yl)sulfanyl]acetic acid.</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>3-Ethyl-2-propyl-1H-indole is an indole that can be used as a synthetic intermediate. It can also be used in nucleophilic substitution reactions to produce functionalized indoles. 3-Ethyl-2-propyl-1H-indole is nontoxic and does not react with most functional groups. This chemical is a good nucleophile and reacts regioselectively with electron deficient or neutral substrates to generate substituted indoles.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Bis(furan-2-yl)methanone is a furyl compound that is activated by trifluoromethanesulfonic acid. It has been shown to be an effective dose for the treatment of bacterial infections that are resistant to erythromycin and other antibiotics. Bis(furan-2-yl)methanone is used in veterinary medicine to treat infections caused by bacteria such as Escherichia coli, Proteus mirabilis, Klebsiella pneumoniae, and Streptococcus agalactiae. This drug has been shown to be active against Gram-positive bacteria, including Bacillus cereus, Clostridium perfringens, Clostridium tetani, Staphylococcus aureus, Streptococcus pyogenes, and Streptococcus pneumoniae.</p>

<p>3-Methylenebicyclo[3.3.1]nonan-7-one is a chiral molecule that has been synthesized as a racemic mixture of two enantiomers. This compound is an amine with a hydroxy group and an isopropyl side chain. It has been shown to have anti-inflammatory properties, which may be due to its ability to inhibit cyclooxygenase and lipoxygenase activity. 3-Methylenebicyclo[3.3.1]nonan-7-one also has antiviral properties, which are due to its inhibition of protein synthesis in viruses by blocking the activity of ribonucleotide reductase, an enzyme required for nucleic acid synthesis. The reaction mechanism involves the formation of a covalent bond between the amantadine and the active site of ribonucleotide reductase through either radical or hydrogen atom transfer mechanisms.</p>

<p>Versatile small molecule scaffold</p>

<p>4-Amino-2,3,6-trimethylphenol (4ATMP) is a halogenated phenol that has been used as a developer in the production of silver halide photographic emulsions. It interacts with hydrogen chloride to form a gaseous product and can be used as an indicator for the presence of chlorine gas. 4ATMP is also known to react with formaldehyde and acetaldehyde to produce formic acid and acetic acid respectively. 4ATMP is most commonly prepared by reacting phenol with diethylaminopropyl chloride in the presence of hydrogen chloride gas.</p>

<p>2-Phenoxyethyl)amine hydrochloride is a chlorinated, industrial, synthetic chemical used as a reaction solvent. It can be derived from cyclohexylamine and ethanolamine by reacting with phenol. The reaction product is then hydrolyzed to produce 2-phenoxyethyl)amine hydrochloride.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>