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>2,2-Dimethylpropane-1-sulfonamide is a macrocyclic compound that has antiviral activity. It reacts with hydrogen peroxide to form a serine protease inhibitor. The reaction system consists of 2,2-dimethylpropane-1-sulfonamide, serine protease and polyelectrolyte. This reaction system is efficient in the synthesis of tripeptides and nitrogen atoms containing chromene. The biological properties of this compound have been shown to inhibit the hepatitis virus in cell culture and can be used as an antiseptic agent for wounds. 2,2-Dimethylpropane-1-sulfonamide inhibits the activity of NS3 protease from some strains of Hepatitis C virus (HCV) by binding to the active site and blocking the access to substrate. The NS3 protease is a serine protease that cleaves HCV polyprotein into individual proteins, such as NS4A</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>(E)-1-Bromo-4-(2-nitroprop-1-en-1-yl)benzene is an organic compound with a benzene ring. It is stabilized by the dihedral angle and has a crystal structure. The condensation reaction of ethyl nitrite and 1,2-dibromoethane was found to produce (E)-1-bromo-4-(2-nitroprop-1-en-1-yl)benzene. This compound is used in the synthesis of other chemicals, such as azo dyes.</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-Cyano-3-phenylbutanoic acid is a chiral organic compound with two stereogenic centers. The molecule can be synthesized by the hydrolysis of racemic 4-cyano-3-phenylbutanoic acid or by the optically catalyzed desymmetrization of (S)-trans,trans-2,4,6-trimethylcyclohexanone. This compound has been used as an additive to produce homochiral products in chemical reactions and as a catalyst for enantioselective reactions.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>(S)-1-(2-Chlorophenyl)ethanol is a substrate for the enzyme dehydrogenase, which catalyzes the conversion of (R)-1-(2-chlorophenyl)ethanol to (R)-1-(2-chlorophenyl)propanol. The reaction time for this reaction is dependent on the concentration of the substrate, with high concentrations of (S)-1-(2-chlorophenyl)ethanol requiring a longer reaction time. The product, (R)-1-(2-chlorophenyl)propanol, is an organic chemical that can be used as a model system for studying other reactions involving alcohols. This compound has been shown to be reactive in biological systems and has been found to have symptoms similar to those of Parkinson's disease in mice.</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-Amino-1H-indole-3-carbonitrile is a nucleoside analog used as a precursor for the synthesis of other biologically active compounds. 2-Amino-1H-indole-3-carbonitrile has been shown to be capable of forming hydrogen bonds with nucleic acid bases, which can lead to changes in conformation and chain length. This leads to changes in the spectra of these compounds, allowing them to be identified.<br>2AICC is prepared from indolium salt and carbon tetrachloride by reaction with ammonia gas. The reaction takes place in an ice bath with stirring and produces a white solid that can be purified by recrystallization or column chromatography.</p>

<p>Versatile small molecule scaffold</p>

<p>3-Hydroxy-3-phenylpentanamide is a chiral molecule that has been found to produce neurotoxic effects in rats. 3-Hydroxy-3-phenylpentanamide binds to the benzodiazepine binding site on the GABA receptor and produces a neurotoxic effect. The neurotoxicity of this drug was studied using x-ray crystallography and it was found that 3-hydroxy-3-phenylpentanamide binds with high affinity to the gamma amino butyric acid (GABA) receptor, which causes an increase in chloride ion flow into the neuron and can lead to death of the neuron. This compound also has a halogen substituent at C3, which may be responsible for its toxicity. 3-Hydroxy-3-phenylpentanamide is an enantiomer that is not present in nature and is produced synthetically by reacting phenylacetonitrile with hydroxylamine followed by chlorination. It has</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-bromo-1,3-thiazol-5-yl)methanamine is a ring system that contains a phthalimide and thiazole. It has a planar molecular geometry. The methoxy group is located on the left side of the molecule, which creates a dihedral angle of about 60°. The two bromine atoms are on opposite sides of the molecule and are separated by 2.6 Å. This ring system reacts readily with nucleophiles to form covalent bonds.</p>

<p>2-Bromo-5-(bromomethyl)thiazole is an industrial chemical that belongs to the tribromide class of compounds. It is used as a solvent in organic reactions and can be prepared by reacting sodium borohydride with 2-bromothiazole. The preparation process includes recrystallization from acetonitrile and dihedral rotation with potassium carbonate and phthalimide.<br>2-Bromo-5-(bromomethyl)thiazole has been shown to react with fluoride ions to form a borohydride ion, which is then able to abstract a hydrogen atom from a molecule of water to produce hydrogen gas.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>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>

<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-(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>

<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>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>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>

<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>