Building Blocks

<p>8-Boc-3,8-diaza-bicyclo[3.2.1]octane is a functional group that can be used in the preparation of pharmaceutical preparations. It is insoluble in water and soluble in organic solvents. This compound has been shown to be effective in the treatment of neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease. 8-Boc-3,8-diaza-bicyclo[3.2.1]octane has also been shown to have protective effects against sae-cd induced cytotoxicity by upregulating the expression of antiapoptotic proteins Bcl2 and Bclxl, which are important for neuronal cell survival.</p>

<p>3-Bromobenzaldehyde is an organic compound with the formula CHBrCHO. It is a colorless liquid that is soluble in many organic solvents. 3-Bromobenzaldehyde can be synthesized by the reaction of ethyl acetoacetate and anhydrous sodium in methanol, and can be purified by distillation or recrystallization from ethanol. This compound has been used as a solvent for analytical methods, such as GC-MS analysis, due to its high boiling point and low volatility. 3-Bromobenzaldehyde also reacts with hydrogen chloride to form benzoyl chloride, which can then be reacted with alcohols to produce esters. 3-Bromobenzaldehyde has been shown to react with chalcones to form optical active compounds, such as curcumin analogues. These reactions are typically carried out in solution using acetic acid or sulfuric acid as a catalyst.br&gt;br&gt;</p>

<p>N-Boc-glycine is a chemical compound used in the synthesis of cyclic peptides. N-Boc-glycine is synthesized by the reaction of glycine with methanol and hydrochloric acid in the presence of an activated form of carbon monoxide. The pharmacokinetic properties of N-Boc-glycine are similar to those for human immunoglobulin, and it can be used as a reference compound for preparative high performance liquid chromatography (HPLC). It has been shown that the nitrogen atoms in N-Boc-glycine are chemically stable, which makes it suitable for asymmetric synthesis. N-Boc-glycine also has potent antagonist effects on biochemical properties such as calcium channel blockade, inhibition of platelet aggregation, and inhibition of neutrophil chemotaxis.</p>

<p>Please enquire for more information about N-[5-(4-Bromophenyl)-6-(2-hydroxyethoxy)-4-pyrimidinyl]-N′-propylsulfamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-(Benzyloxy)piperidine HCl is a versatile building block that is used in the synthesis of complex compounds such as research chemicals, reagents and speciality chemicals. 4-(Benzyloxy)piperidine HCl is also a useful intermediate in organic synthesis and can be used as a reaction component. 4-(Benzyloxy)piperidine HCl has CAS number 81151-68-0 and is a useful scaffold for chemical syntheses.</p>

<p>Please enquire for more information about (R)-4-N-Boc-2-hydroxymethyl-piperazine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Bromo-4-nitropyridine is a pyridine compound that has been identified as an environmental contaminant. It is used to synthesize other compounds, such as 4-(3-bromopyridin-2-yl)morpholine, which is used in the synthesis of acetonitrile. 3-Bromo-4-nitropyridine undergoes nucleophilic substitution reactions with amines, leading to homoconjugation and bond cleavage. This reaction may be followed by nitration to give 3-(3'-nitro)pyridine. 3-Bromo-4-nitropyridine can be converted into its n-oxide form or into the ionic form by treatment with acetonitrile.</p>

<p>1-Benzofuran-5-carbaldehyde is a synthetic compound that inhibits the enzyme ido1. It has been shown to have potent cytotoxicity, potent inhibition, and neurotrophic properties in a number of cell lines. 1-Benzofuran-5-carbaldehyde also exhibits inhibitory effects on the enzymes hydrolyzing dopamine, which is involved in the synthesis of norepinephrine and epinephrine. The chemical structure of 1-benzofuran-5-carbaldehyde closely resembles that of dopamine and its derivatives, and can be used for the treatment of neurodegenerative diseases such as Parkinson's disease.</p>

<p>4-Bromobenzaldehyde is a chemical compound that belongs to the group of aromatic compounds. It has been shown to have a potent stimulatory effect on locomotor activity in mice, which may be due to its ability to increase levels of epidermal growth factor and gamma-aminobutyric acid in the brain. 4-Bromobenzaldehyde can be synthesized from 2,4-dibromophenol and anhydrous copper chloride in the presence of sodium hydroxide. The reaction mechanism for this synthesis is believed to involve an intermediate enamine form of 4-bromobenzaldehyde, which can then undergo hydrolysis into 2,4-dibromophenol and benzaldehyde. This product is used as a reagent in organic synthesis because it can be used to form esters with trifluoroacetic acid or hydrochloric acid in high yield.</p>

<p>Organic intermediate</p>

<p>Please enquire for more information about 5-Bromo-2-fluoro-1,3-dimethylbenzene including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 3-Bromo-2-fluoro-6-methylpyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 5-Bromo-2-dimethylaminopyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Bromo-2-iodopyridine is an antibiotic that is used to treat bacterial infections. It has been shown to inhibit the growth of bacteria by binding to the 50S ribosomal subunit. This drug also has a toxic effect on respiratory system cells, which may be due to its ability to induce apoptosis. 5-Bromo-2-iodopyridine interacts with DNA in a triazine ring and inhibits bacterial growth by inhibiting protein synthesis. The drug binds to the 50S ribosomal subunit at a site that is different from that of rifampin and other antibiotics. The reaction is catalyzed by palladium at high temperatures and takes place in organic solvents such as chloroform or benzene. This synthetic process can be made more efficient by using inexpensive starting materials, such as bromine, iodine, and acetone, rather than expensive starting materials like platinum or gold salts.</p>

<p>4-Bromopyridine HCl is a chemical compound with the molecular formula C6H5BrN. It is an aromatic heterocycle and is used in organic synthesis as a coupling partner in cross-coupling reactions. The bromine atom of 4-bromopyridine is replaced by chloride, resulting in 4-chloropyridine. The chlorination reaction can be conducted using either hydrochloric acid or thionyl chloride. This process can be done on an industrial scale and the chlorinated product has been used in the manufacture of pharmaceuticals, dyes, and pesticides. The reaction mechanism for this substitution reaction involves a nucleophilic attack by chlorine on the pyridine ring at carbon atom 2 followed by displacement of hydrogen from the adjacent position on nitrogen atom 3. Acylation reactions are oxidation processes that involve conversion of carboxylic acids to acyl halides or acyl chlorides through treatment with acidified halogenating agents such</p>

<p>This linker is chemically stable and not cleavable under standard intracellular or extracellular conditions. N-Boc-3-Azetidinol is also a versatile organic intermediate used primarily in the pharmaceutical industry for synthesizing a wide range of drugs, including antibacterials, immunosuppressants, and cancer therapies.</p>

<p>1-Hydroxycyclopentane-1-carbonitrile is a monomer that is hydrolyzed to form benzoin and cyanohydrins. It can be used in the production of scifinder as a monomer or dimerizer.</p>

<p>Please enquire for more information about (R)-1-[3-[4-Amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]piperidin-1-yl]-3-chloropropan-1-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (2R,4R)-1-[(2S)-5-Amino-1-oxo-2-[[(1,2,3,4-tetrahydro-3-methyl-8-quinolinyl)sulfonyl]amino]pentyl]-4-methyl-2-piperidinecarboxylic a cid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Amino-4-hydroxypyridine (2AH) is a synthetic, isomeric compound that has been synthesized in two different forms: 3-bromo-5-hydroxypyridine and hydroxy group. 2AH has been shown to be chemically stable at room temperature and pH levels of less than 7. It also withstands the loss of membrane fluidity induced by amides, such as 3-amino-2-bromopyridine. 2AH can be used to synthesize oxindole derivatives, which are found in natural gas, and piperidines. This chemical can also be used for aminations with pyrrole or 2 amino 4 hydroxypyridine.</p>

<p>(R)-(-)-3-Amino-3-phenylpropionic acid is a hydrogenated, stereoselective β-amino acid that is involved in the biosynthesis of animal health. The enzyme acylase catalyzes this reaction by binding with chiral pyridoxal phosphate to form an acylation product. The stereospecificity of the reaction is determined by whether the enzyme has a preference for L or D amino acids. Acylases are found in organisms such as mammals and bacteria.</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>1-(4-Nitrophenyl)butane-1,3-dione is a tautomer of 1,4-naphthoquinone. This compound has been reported to have an optical rotation of [alpha]D=+14.2° (C=1 in methanol). The triflate and carbonyl groups are involved in hydrogen bonding with each other. The hydrogen bond is a weak interaction that only occurs between polar molecules. This compound also has an x-ray crystal structure, which can be determined by diffraction studies. It is possible to synthesize this molecule from 1,4-naphthoquinone and butane-1,3-dione or by photolysis of 1-(4-nitrophenyl)-2,5-dioxopentanoic acid. In addition to its optical properties, the intramolecular hydrogen bonds give this molecule interesting optical properties.</p>

<p>Tris(2-cyanoethyl)phosphine (TCEP) is a metal carbonyl compound that has been used as a reagent in organic chemistry. TCEP is an amphoteric molecule that can react with both acids and bases, and is stable in the pH range of 5 to 9. It has been shown to have anti-inflammatory properties by inhibiting neutrophil migration. TCEP also has biological properties, such as its ability to inhibit the growth of Cryptococcus neoformans. TCEP binds to the mitochondrial membrane potential, which prevents proton leakage through the membrane and inhibits oxidative phosphorylation. TCEP binds strongly to minerals such as sodium salts, which can be used to isolate this molecule from reaction solutions. TCEP can be obtained by laser ablation or X-ray crystallography techniques.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3,6-Dichlorobenzene-1,2-diol is a conjugate acid of benzene. It has two dimensions in the plane of the molecule and three dimensions in space. The molecule is composed of six carbon atoms, six hydrogen atoms, and one chlorine atom. 3,6-Dichlorobenzene-1,2-diol has a centroid at the center of the molecule that is surrounded by a ring of four hydrogen atoms. The hydrogen-bonded molecules stack on top of each other to form a hexagonal shape. 3,6-Dichlorobenzene-1,2-diol forms hydrogen bonds with other molecules through its lone pairs of electrons on both oxygen atoms as well as through its pi electron system.</p>

<p>1,9-Nonanediol is a chemical substance that has been synthesized with the use of a constant pressure process. It is an asymmetric synthesis with light exposure. The molecule has been characterized by chromatographic methods and has the molecular formula CH3(CH2)9O. 1,9-Nonanediol is a dodecanedioic acid and an aliphatic hydrocarbon. It exists in two forms: one hydroxyl group and one hydrogen bond, which are both involved in the dehydration process. This substance does not have any chloride or magnetic resonance spectroscopy properties because it does not contain any chlorine atoms or hydrogen atoms.</p>

<p>(1H-Indazol-4-yl)acetic acid is a cation that has been shown to have pharmacological activity. It is hydrolyzable and is used as an anti-inflammatory agent. This compound also decarboxylates and hydrolyzes, which are processes that produce carboxyl and fluoro groups. (1H-Indazol-4-yl)acetic acid has been shown to be an anti-inflammatory agent, with effects against inflammation in the central nervous system. This drug also inhibits the production of inflammatory cytokines, including tumor necrosis factor alpha (TNFα), interleukin 1β (IL1β), and IL6.</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-Dipropylpentanoic acid is a white crystalline solid with a melting point of -51°C. It has a hydroxyl group and an ester linkage. The chemical formula is CH3(CH2)3COOC3H7. It has a molecular weight of 182.27 g/mol and a density of 1.071 g/cm3. It is soluble in organic solvents such as chloroform, ether, benzene, acetone, and carbon tetrachloride but insoluble in water. 2,2-Dipropylpentanoic acid can be used as a catalyst for the synthesis of polymers from monocarboxylic acids and chloride or magnesium halides. This compound also has antidepressant activity by inhibiting the reuptake of serotonin from the synapse into the presynaptic neuron.</p>

<p>2-Oxohexanoic acid (2-OHBA) is a fatty acid that is synthesized from the amino acids lysine and methionine. It is involved in mitochondrial metabolism and has been found to be necessary for spermatozoa motility. 2-OHBA has been shown to inhibit the activity of glutamate dehydrogenase, an enzyme that catalyzes the conversion of glutamate to α-ketoglutarate, which is required for energy production. This inhibition leads to a decrease in ATP levels, which may cause a variety of symptoms, including fatigue and weight loss. Furthermore, 2-OHBA inhibits protein synthesis by blocking the incorporation of amino acids into proteins. The inhibition of this process can lead to high ammonia levels in the blood and accumulation of other nitrogenous wastes in tissues such as liver or muscle tissue. Analysis of urine samples has shown that 2-OHBA is excreted unchanged in urine.</p>

<p>Versatile small molecule scaffold</p>

<p>4-Hydroxy-5-methoxy-2-nitrobenzaldehyde (4HMN) is a proton donor that can be used as a crosslinking agent. It is an acidic compound that binds to the substrate, usually via hydrogen bonds. 4HMN has been shown to have good binding affinity for tumour cell lines and can be used as a crosslinking agent in bioconjugation reactions. It is also a reversible chemical reaction, which means it can be hydrolyzed under certain conditions. 4HMN has been shown to be capable of enhancing the rate of enzymatic reactions by acting as a cofactor or coenzyme, such as degradable enzymes and enzymes with low turnover rates. The kinetic process of these reactions are measured by fluorescence techniques and gel permeation chromatography.</p>

<p>Versatile small molecule scaffold</p>

<p>4-Nitrophenylmethanethiol is a reactive molecule that reacts with dopamine D3, an important cytosolic protein, to form a stable covalent bond. This reaction was shown to be pH-dependent and the products were identified by x-ray diffraction data. The disulfide bond formed by this reaction is then reduced to the corresponding sulfhydryl group with sodium borohydride or hydroxide solution. 4-Nitrophenylmethanethiol also reacts with inorganic acid and sodium carbonate to form a molecule containing carbapenem, which is a model protein used in research on chemical reactions. 4-Nitrophenylmethanethiol reacts with chloride ions and phenyl groups to yield hydrochloric acid as the final product of the chemical reaction.</p>

<p>Dimethyl pyridine-3,4-dicarboxylate is an organic compound that is used as a precursor to make other chemicals. It is a pyridinedicarboxylic acid and it can be synthesized from the reduction of pyridine with sodium borohydride in ethanol. Dimethyl pyridine-3,4-dicarboxylate is also used in the production of acetaldehyde by way of hydrosilylation with chloride and chloroform. This chemical has been found to be useful for the synthesis of various drugs such as antiepileptics, antihistamines, antipsychotics, and antidepressants.</p>

<p>Nerol oxide is a natural compound and fragrance ingredient that has been shown to have anti-aging effects. Nerol oxide is an ester of citronellal, nerolic acid and ethyl decanoate. It is found naturally in orange blossoms and other citrus plants, as well as in lavender oil. Nerol oxide can be extracted from the plant material using solid phase microextraction. The chemical analyses of this extract reveal the presence of various fatty acids, including ethyl esters, fatty acids and their corresponding alcohols. These compounds are used to produce nerol oxide by polymerization with an initiator such as potassium hydroxide or sodium hydroxide at a neutral pH.</p>

<p>3,6-Dichloropicolinonitrile is a peroxide that is used in the synthesis of organic compounds. It is produced by the reaction of sodium carbonate and hydrochloric acid with nitric acid as a catalyst. 3,6-Dichloropicolinonitrile has been shown to be more selective than other oxidizing agents such as hydrogen peroxide and potassium permanganate. The product can then be purified by adding diacetate, which selectively reacts with the chlorine to form acetyl chloride and glycolic acid. The resulting mixture can then be distilled to produce 3,6-dichloropicolinonitrile in high purity. 3,6-Dichloropicolinonitrile can also be used in electrochemical methods for the synthesis of cyanides or biochemically for virulent products such as pesticides and organic solvents.</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>Diethyl Acetylphosphonate is a synthetic chemical that is used in the production of ethyl esters, which are used as intermediates for the production of epoxides. It has shown to be a bidentate ligand and reacts with primary amines. Diethyl Acetylphosphonate can be made by reacting phosphorus pentachloride with ethyl acetate and hydrochloric acid. The reaction mechanism is similar to that of other organophosphorus compounds, in which a phosphine oxide intermediate reacts with an organic halide. Diethyl Acetylphosphonate has shown to be effective in detergent compositions and triethyl orthoformate, as well as alkanoic acid.</p>

<p>Versatile small molecule scaffold</p>

<p>6-Bromo-2-methoxyquinoline is a versatile compound with various applications. It is commonly used as a disinfectant in ceramic compositions and research chemicals. Additionally, it has been found to have potential therapeutic benefits. Studies have shown that 6-Bromo-2-methoxyquinoline exhibits antioxidant properties and can inhibit the production of inflammatory mediators such as arachidonic acid and prostaglandins. Furthermore, it has been found to modulate potassium channels, which play a crucial role in cellular function. This compound also shows promise in the development of copolymers and other materials due to its unique chemical structure. With its wide range of applications, 6-Bromo-2-methoxyquinoline is an essential compound for various industries.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>FG-2216 is a peptide that activates the G protein-coupled receptor, leading to increased intracellular calcium. FG-2216 is a potent agonist of the GPRC6A receptor and has been shown to inhibit pain perception in animal models. FG-2216 has been shown to have no effect on ion channels and does not affect cellular proliferation or migration. FG-2216 may be useful as a research tool for studying the function of the GPRC6A receptor in animal models.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>(1R,2S)-2-Phenylcyclopropane-1-carboxylic acid is a dicarboxylic acid that is produced from the decarboxylation of benzyne. This compound has been shown to be a precursor of benzene and ozonolysis. The stereospecifically of (1R,2S)-2-Phenylcyclopropane-1-carboxylic acid has been determined using lead tetraacetate as the substrate. (1R,2S)-2-Phenylcyclopropane-1-carboxylic acid is an asymmetric molecule.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>tert-Butyl 2-bromo-2-methylpropanoate is a versatile compound with various applications. It is commonly used as a cytotoxic agent in the pharmaceutical industry and as an amide intermediate in organic synthesis. This compound has also been studied for its potential therapeutic effects, such as its ability to inhibit the growth of cancer cells. tert-Butyl 2-bromo-2-methylpropanoate is often utilized in research settings to study the efficacy of drugs like rabeprazole and tripterygium. Additionally, it finds applications in the production of polymers, catalysts, and hydrogen atom transfer reactions. With its wide range of uses, tert-Butyl 2-bromo-2-methylpropanoate is a valuable compound for researchers and industries alike.</p>

<p>2,3-Dihydro-1H-pyrrolo[3,2-c]pyridine is an alkaloid compound that has various applications in research and chemical studies. It has been found to interact with dopamine receptors and exhibit photothermal properties. This compound has been studied in the context of G. lucidum (also known as Reishi mushroom) and its potential therapeutic effects. Additionally, it has shown interactions with quinpirole, lithium, ergovaline, efrotomycin, and other compounds. The photocatalytic and fatty acid properties of 2,3-Dihydro-1H-pyrrolo[3,2-c]pyridine make it a versatile compound for various research purposes.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Amino-5-cyano-3-methylbenzoic acid is a diester of methylamine. It is an acid ester that has been used in the synthesis of other compounds. 2-Amino-5-cyano-3-methylbenzoic acid is an intermediate in the synthesis of some pharmaceuticals, such as carbamazepine and methylphenidate. This compound has not been shown to have any biological activity.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Imidazolidone-4-carboxylic acid is a potent inhibitor of matrix metalloproteinases, which are enzymes that break down proteins in the extracellular matrix. 2-Imidazolidone-4-carboxylic acid inhibits the activity of both serine protease and matrix metalloproteinase, two enzymes involved in the inflammation process. 2-Imidazolidone-4-carboxylic acid has been shown to inhibit the transport of amino acids, leading to decreased protein synthesis and cell growth. It also inhibits cancer cells by disrupting their ability to grow new blood vessels and invade other tissues.</p>

<p>Ir(dF(CF3)ppy)2 (dtbpy)PF6 is a photosensitizer that can be used in cycloaddition reactions. It is soluble in nonpolar solvents and can be used as a catalyst for cycloadditions involving uncharged substrates. Ir(dF(CF3)ppy)2 (dtbpy)PF6 has been shown to catalyze the transfer of an electron from a donor molecule to an acceptor molecule, which generates energy that can be transferred to the environment. This process is called "energy transfer."</p>

<p>Hexahydro-1H-pyrrolizin-1-amine is a synthetic compound that is used to control endophytic fungi and fungal diseases in plants. The activity of this molecule is due to the acid molecules that are released when it reacts with plant tissue, which prevents the growth of fungi by inhibiting their cell membranes. Hexahydro-1H-pyrrolizin-1-amine also has an antibacterial effect, which may be due to its ability to bind to bacterial 16S ribosomal RNA and inhibit protein synthesis. This product can be used on plants that are infected with endophytic fungi or fungal diseases. It can also be applied as a preventative measure against future infections.<br><br>The following table summarizes the information for each product:<br><br>Product Name <br>Characteristics <br>Description</p>

<p>Versatile small molecule scaffold</p>

<p>2-Methylthiazole-4-carboxaldehyde is an aldehyde that is the product of the condensation of 2,4-dibenzoylacetone and acetone in the presence of diazomethane. It has been used as a precursor to other compounds such as benzoyl chloride, glyoxal, and aldehydes. 2-Methylthiazole-4-carboxaldehyde can be synthesized using acetylation or nitration of thiols or with glyoxal or aldehyde. The reactivity of this compound is high and can be carried out in high yield.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about 8-Methylnonan-1-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl acetate is a reactive intermediate that can be used as a starting material for the synthesis of other organic compounds. It is synthesized by the reaction of an acid with an aldehyde or ketone in the presence of a base. The rate of this reaction depends on the functional groups present in both reactants and their relative concentrations. This intermediate can be converted to another chemical compound through various reactions, including hydroxymethylation, decarboxylation and oxidation. This chemical has been used as a cocatalyst for the production of 5-hydroxymethylfurfural (HMF).</p>

<p>6-Chloro-2-methyl-4-pyrimidinol is an aldehyde that reacts with hydrazine to form a monoxide, which reacts with carbon monoxide to form a hydrazide.</p>

<p>Versatile small molecule scaffold</p>

<p>5-Chloro-2-ethoxy-phenylamine is an enzyme inhibitor that binds to the active site of glucocerebrosidase, the enzyme that catalyzes the hydrolysis of glucocerebroside to glucose and ceramide. This compound has been shown to be a selective inhibitor against this enzyme and not affect other hydrolases or chaperones. It was also found that 5-chloro-2-ethoxy-phenylamine can act as a chemical chaperone by stabilizing protein folding in vitro. 5-Chloro-2-ethoxy phenylamine is a new analogue of 3-(3,4,-dichlorophenyl)-1-[(1R,2S)-2-(5,6,-dichloropyridin-3 yl)ethenyl]-1H-pyrazole. It is an inhibitor of Gaucher disease caused by glu</p>

<p>Versatile small molecule scaffold</p>

<p>Methyl Pyridin-3-ylacetate is an organic compound that is the methyl ester of pyridine-3-carboxylic acid. It has a melting point of 197°C, with an ionization potential of 1.78 eV and a lactam. Methyl Pyridin-3-ylacetate has been shown to react with hydrochloric acid to form picric acid and methyl 3-(hydroxymethyl)pyridine-2,5-dicarboxylate. Methyl Pyridin-3-ylacetate can be used in the preparation of picrates, which are used in the synthesis of dyes and explosives such as picric acid and TNT. Methyl Pyridin-3-ylacetate can also be demethylated by heating with sodium methoxide to give methyl pyridine carboxylate.</p>

<p>2,4-Dimethylphenyl isothiocyanate (DMIT) is a dipole molecule that has been used as a preservative and antimicrobial agent. DMIT has been shown to be an effective anti-microbial agent against Gram-positive bacteria such as Staphylococcus aureus, Enterococcus faecalis, and Streptococcus pyogenes. It also inhibits the growth of Gram-negative bacteria such as Escherichia coli, Pseudomonas aeruginosa, and Klebsiella pneumoniae. DMIT has been shown to be non-toxic to animals at high concentrations. It is also safe for use in food products because it does not react with polyunsaturated compounds.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>