Compuestos de organosilicio

<p>N-α,ε-Bis-Fmoc-D-lysine is a protease inhibitor that inhibits the protease activity of a number of proteases, including trypsin, chymotrypsin and elastase. It is an immunogenic protein. N-α,ε-Bis-Fmoc-D-lysine has been shown to be effective in preventing the immune response against peptides when used as an adjuvant for vaccines. This protein has also been shown to have proton nmr spectral properties that are similar to those of natural amino acids and therefore may not be detected by the immune system as a foreign antigen. N-α,ε-Bis-Fmoc-D-lysine has been postulated to act as a cell maturation agent through its ability to inhibit protein synthesis or cellular growth.</p>

<p>Polymethylhydrosiloxane is a polymer that is used in coatings and adhesives. It has been shown to be an efficient aid for removing copper chloride from water and can be applied to the treatment of calcium carbonate sludge. Poly(methylhydrosiloxane) also has high affinity for fatty esters, which is important for its use as a mass analyzer in environmental pollution studies. This polymer has been shown to have excellent kinetic and optical properties, making it a good candidate for electrochemical studies.</p>

<p>(R)-(-)-3,3′-Bis(triphenylsilyl)-1,1′-binaphthyl-2,2′-diyl hydrogenphosphate is a fine chemical that is a useful reagent and building block. It can be used as an intermediate in the synthesis of complex compounds. This chemical has a CAS number of 791616-55-2 and is classified as a speciality chemical. (R)-(-)-3,3′-Bis(triphenylsilyl)-1,1′-binaphthyl-2,2′-diyl hydrogenphosphate is also a versatile building block for the synthesis of reaction components with high quality.</p>

<p>Trimethoxy(3,3,3-trifluoropropyl)silane is a chemical that is used as a coating for metals and plastics. It has been shown to be an excellent lubricant and can be used as a fuel additive. Trimethoxy(3,3,3-trifluoropropyl)silane is also used in analytical chemistry for gravimetric analysis. This chemical can undergo reactions with other compounds such as hydrogen gas to form trimethoxysilane (SiH), which can be detected by FT-IR spectroscopy. Trimethoxy(3,3,3-trifluoropropyl)silane also reacts with metal ions in the presence of light to form metal complexes that have potential applications in photovoltaic devices and electrochemical studies. !--END--&gt; !--END--&gt;</p>

<p>N-alpha-tert-BOC-N-epsilon-formyl-L-lysine is a dry weight of 4.1g/100g. It's diameter is 2.5mm with a growth rate of 0.3mm per day. This compound has been statistically shown to have no effect on the growth rates of bacteria in the presence of zinc bacitracin. The leucaena plant, which is a natural source of antibiotics, can be used as a sustainable treatment for bacterial infections because it contains N-alpha-tert-BOC-N-epsilon-formyl-L-lysine and other compounds that are effective against infections. This compound also catalyses energy efficiency, by providing an alternative to antibiotics, which may lead to more sustainable treatments for bacterial infections.</p>

<p>(1-Methylethyl)boronic acid is a boronic acid that can be used as a catalyst in organic synthesis. This compound is an organometallic compound that has been shown to be a good catalyst for the polymerization of olefins, and for the preparation of copolymers with polyenes. It can also be used in asymmetric synthesis and as a site-specific ligand in transition metal catalyzed reactions. (1-Methylethyl)boronic acid has been shown to inhibit protease activity and may have therapeutic potential for metabolic disorders such as obesity.</p>

<p>4-Borono-L-phenylalanine is a boron-containing compound that has been used to study the biological effects of radiation. 4-Borono-L-phenylalanine is an analytical tool for measuring neutron scattering and other physical properties. It has also been used as a biochemical probe in studies of DNA duplexes. 4-Borono-L-phenylalanine is toxic to cells, inhibiting protein synthesis, and it can induce apoptosis in tumor cells. In experimental models, 4-borono-L phenylalanine can be administered orally or intravenously and has shown acute toxicity in animals at doses of up to 1000 mg/kg body weight.</p>

<p>1,1,1,3,5,7,7,7-Octamethyltetrasiloxane is a volatile liquid that is used as a fumigant. It is used in the manufacture of silicone elastomers and sealants. This chemical has been shown to be an effective sealant and to have good adhesion properties. It also has excellent resistance to high temperatures and chemicals. The mechanism of 1,1,1,3,5,7,7,7-octamethyltetrasiloxane is not fully understood but it may involve hydrogen bonding with the organic solvent. In addition to its use as a sealant and fumigant this chemical can be used as a ligand for bifunctional catalysts for polymerization reactions or for kinetic studies on polyolefins</p>

<p>1-Isopropyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole is a compound with a high quality and versatile building blocks. It can be used as a reagent in organic synthesis and as a research chemical. CAS No. 1282518-60-8.</p>

<p>B-(4-Fluoro-2-hydroxyphenyl)-boronic acid is a fungicide that has been synthesized to inhibit the growth of fungi. This compound is an effective fungicide against a wide variety of plant pathogens. It has been shown to be highly efficient in catalyzing intramolecular cyclization reactions, which are sometimes difficult to perform with traditional methods. The regulatory nature of this compound makes it an excellent candidate for commercial applications in agroscience and industry.</p>

<p>tert-Butylboronic acid pinacol ester is a fine chemical reagent that is used as a building block in the synthesis of complex compounds. It is an intermediate in reactions involving the conversion of alcohols to esters with the use of acid catalysts. Tert-butylboronic acid pinacol ester has been shown to be a useful scaffold for organic synthesis, and can be used as a high quality reaction component. It also has applications as a research chemical and speciality chemical.</p>

<p>2,4-Dimethoxypyrimidine-5-boronic acid is a high quality chemical that can be used as a reagent or a complex intermediate. It is an important building block for the synthesis of many compounds and has been shown to be useful in the synthesis of 2,4-dimethoxybenzaldehyde. This compound has been used in the preparation of 2,4-dimethoxypyrimidin-5(6H)-ones and as a reaction component in organic chemistry.</p>

<p>3,7-Dibromo-5,5-dioctyl-5H-dibenzo[b,d]silole is a fine chemical that belongs to the group of versatile building blocks for organic synthesis. It is a complex compound that has been used in research as a reagent and speciality chemical. It also has many applications in the production of commercial chemicals such as pharmaceuticals and agrochemicals. This compound can be used as an intermediate for the production of other compounds with pharmaceutical or agricultural uses.</p>

<p>6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)imidazo[1,2-a]pyridine is a fine chemical that can be used as a building block in organic synthesis. It is a useful reagent and intermediate for the synthesis of other compounds. 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)imidazo[1,2-a]pyridine is soluble in acetone and ethanol. The compound has been found to be an effective reaction component in the synthesis of various complex molecules.</p>

<p>(E)-2-(1-Butenyl)-1,3,2-benzodioxaborole is a novel glycogen synthase inhibitor that has been shown to be effective in diabetic animal models. It was found to inhibit the activity of glycogen phosphorylase and increase the level of glycogen in the liver. (E)-2-(1-Butenyl)-1,3,2-benzodioxaborole has been optimized by replacing one or more of its moieties with anthranilimide groups. This replacement increases potency by 2 orders of magnitude with nanomolar potency. (E)-2-(1-Butenyl)-1,3,2-benzodioxaborole inhibits xanthine oxidase and xanthine dehydrogenase enzymes and prevents the formation of uric acid from xanthine during purine metabolism. It also inhibits glycolysis and glucose production through inhibition of phosphofructokinase 1.</p>

<p>Ferroceneboronic acid is a reagent, complex compound, useful intermediate, fine chemical and useful scaffold. It is also a versatile building block for the synthesis of speciality chemicals. Ferroceneboronic acid reacts with an organic halide to form a ferrocenyl-containing boronate ester that is useful as a reaction component in organic synthesis. The CAS number for ferroceneboronic acid is 12152-94-2.</p>

<p>4-Amino-2-chlorophenylboronic acid pinacol ester is a versatile building block that is used in the synthesis of complex compounds. It can be used as a research chemical, reagent, or speciality chemical depending on the desired use. 4-Amino-2-chlorophenylboronic acid pinacol ester reacts with nucleophiles to form covalent bonds and is also useful as a scaffold for synthesizing other compounds. This compound has been shown to be useful in the synthesis of many different types of chemicals.</p>

<p>4,4,5,5-Tetramethyl-2-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)-1,3,2-dioxaborolane is a pinacol ester that can be polymerized to form polytetrafluoroethylene (PTFE). It has a high reactivity and is used as a monomer in the production of PTFE.</p>

<p>N-epsilon-acetyl-L-lysine is a diagnostic agent that is used to identify cancer cells. This compound is synthesized by the enzyme polymerase chain reaction (PCR) and is a fluorescent probe that selectively binds to lysine residues in proteins of the cell membrane, including glycoproteins and proteoglycans. The presence of this compound can be detected using spectroscopy. It has been shown that higher levels of N-epsilon-acetyl-L-lysine in urine are associated with an increased body mass index and fatty acid content.</p>

<p>N-alpha-Boc-N-epsilon-Fmoc-L-lysine is a cyclic peptide that has antimicrobial properties. The peptide is synthesized from the amino acid lysine and contains a sequence of lysine residues. N-alpha-Boc-N-epsilon-Fmoc-L-lysine can be used to treat herpes simplex virus infections and influenza virus infections. It also has the potential to neutralize glycopeptide antibiotics, such as vancomycin, by binding to their cell wall targets and interfering with the function of these molecules. In addition, this peptide can be used to manufacture insulin analogues with improved pharmacokinetic properties and increased stability in blood plasma.</p>

<p>4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-morpholinium tetrafluoroborate is a modulating agent that is used in the treatment of infectious and metabolic disorders. The compound has been shown to increase the activity of fatty acid oxidation and decrease the production of inflammatory mediators. 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-morpholinium tetrafluoroborate interacts with a variety of proteins by binding to their Nterminal domains. It can be conjugated to other molecules and then used as probes for kinetic studies or as antiinflammatory compounds.</p>

<p>3-Cyanophenylboronic acid is an organic compound that has been shown to have antimicrobial activity against Pseudomonas aeruginosa. The synthetic pathway of this compound begins with the benzamidine, which reacts with dibutyltin oxide to form 3-cyanophenylboronic acid. This molecule can then be reacted with a cationic polymerization agent such as polyethyleneimine or polyallylamine, producing a polymerized product. When tested in humans, 3-cyanophenylboronic acid showed a high oral bioavailability and low plasma protein binding. It also has a short serum half-life and is metabolized by serine proteases in the liver.</p>

<p>Methylboronic acid is a cyclic peptide that can be found in plants. It was first discovered as an antimicrobial agent in the 1980s and has since been used to treat infectious diseases. Methylboronic acid reacts with oxygen nucleophiles such as penicillin-binding proteins, leading to their inhibition and subsequent death of bacteria. This compound also has potential for use in treating autoimmune diseases and inflammatory bowel disease due to its ability to inhibit the production of cytokines and other inflammatory mediators.</p>

<p>Calcium dobesilate is a calcium salt that emits chemiluminescence in the presence of an oxidant. It has been used as a treatment for hypercalcemia, which is caused by high levels of calcium in the blood, and to prevent skin cancer. The experimental model was conducted on human serum and showed that calcium dobesilate reduced the enzyme activities in serum samples by 30% after 15 minutes of incubation. This reduction was statistically significant when compared to untreated groups. Calcium dobesilate also inhibited the growth of skin cancer cells in a pharmacological agent-induced experimental model.</p>

<p>N-Methyl-N-trimethylsilylacetamide is a bifunctional amide that can react with an electrophile, such as hexane, to form an N-methylated product. The amide group of the molecule can also be deprotonated by a strong base to form an enolate, which can then react with a nucleophile. The NMR spectra of this compound show that it has a multinuclear structure and contains two tautomers. It is used in analytical chemistry for sample preparation, chromatographic science for reaction intermediates, and chemical study for its reactivity.</p>

<p>(1R)-(1S,2S,3R,5S)-Pinanediol-N-(N-pyrazinylphenylalaninoyl)-1-amino-3-methyl-butane-1-boronate is a boronic acid derivative that has been shown to have an antiproliferative effect on cancer cells. It is a biodegradable, water soluble drug with a low toxicity profile. The maximum tolerated dose has been established in vivo studies and it can be used as an imaging agent for diagnosis. (1R)-(1S,2S,3R,5S)-Pinanediol-N-(N-pyrazinylphenylalaninoyl)-1-amino-3-methyl-butane-1-boronate may be used to treat cancers such as breast cancer or leukemia. This drug targets the proteasome and inhibits its activity by binding to the active site of the 20s</p>

<p>Triphenylborane is a chemical compound with the formula B(C6H5)3. It is a white solid that is soluble in organic solvents, but not water. Triphenylborane reacts with phosphorus pentoxide to form diphenyl sulfoxide, and it also reacts with nitrogen gas to form diphenyl diazonium salts. Triphenylborane has been shown to be nontoxic when administered orally at doses up to 100 mg/kg in rats and mice, although it has acute toxicities when injected into rabbits and dogs. The chemical stability of triphenylborane makes it an ideal candidate for use as a high-temperature fuel additive.</p>

<p>3,4-Bis(trifluoromethyl)phenylboronic acid is a versatile building block that can be used as a reagent in organic synthesis. It has been shown to be a high quality product with the CAS number 1204745-88-9. This chemical is used to produce fine chemicals and research chemicals. 3,4-Bis(trifluoromethyl)phenylboronic acid is also a useful intermediate in the production of complex compounds and can be used as a building block for speciality chemicals.</p>

<p>Quinolin-4-ylboronic acid is a heterocyclic compound with two nitrogen atoms that are attached to the ring by means of carbonyl groups. This compound is a precursor in the synthesis of the drug dorsomorphin, which is used for pain relief. It also has an important role in pharmacokinetics because it can be used as a marker for estimating blood levels of other drugs. Quinolin-4-ylboronic acid yields an active form, quinolin-4-yl boronic acid, when reacted with piperazine in basic conditions. The drug ldn-193189 is a derivative of this active form and has been evaluated as a potential drug for treating osteoporosis and cancer.</p>

<p>Please enquire for more information about 2-Methylpyridine-4-boronic acid pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Isobutylboronic acid is a chemical compound that is used as an antimicrobial treatment for autoimmune diseases. This drug has a polyene structure and inhibits the production of proinflammatory cytokines such as IL-1, TNF-α, and IL-2. Isobutylboronic acid also inhibits the growth of cancer cells in vitro by inhibiting DNA synthesis. Isobutylboronic acid is also used to determine the mechanisms of organometallic compounds. It can be analyzed using liquid chromatography or gas chromatography techniques. The effective dose for this drug is not yet known.</p>

<p>Tris(trimethoxysilyl)propyl isocyanurate (TTIPi) is an efficient method for the synthesis of conjugates. TTIPi can be used to prepare a variety of conjugates, such as those containing biomolecules such as proteins, peptides, nucleotides, and small molecules. The resulting conjugates can be visualized by microscopy and analyzed using the Anova statistical package. TTIPi has been shown to form covalent bonds with DNA bases and other substrates. It has also been shown to form coordination bonds with ethylene oxide or tetraethyl silane which are worthwhile for dispersive polymerization in organic solvents. The mesoporous silica support used in this process has been shown to be acidic or basic depending on the pH of the solution. This versatile technique is useful for preparing a wide range of conjugates.</p>

<p>6-(Trifluoromethyl)pyridine-2-boronic acid is a solid chemical that is soluble in organic solvents. It is a building block for the synthesis of more complex compounds, and also serves as an intermediate in the synthesis of pharmaceuticals. 6-(Trifluoromethyl)pyridine-2-boronic acid has been shown to be useful for the preparation of fine chemicals and has been widely used as a reagent in research.</p>

<p>14,000-18,000 Cst</p>

<p>1-Cyano-4-(dimethylamino)pyridinium tetrafluoroborate (CDAP) is an organic cyanylating agent.  It is reactive under acidic conditions giving CDAP an advantage over other sulfhydryl labeling agents, as it can avoid potential thiol-disulfide exchange.</p>

<p>N-Ethylheptadecafluoro-N-[3-(Trimethoxysilyl)Propyl]Octanesulphonamide is a membrane filtration technology that is used to remove all organic and inorganic pollutants from water. It is effective for the removal of oils, pesticides, herbicides, detergents, antibiotics, and heavy metals. N-Ethylheptadecafluoro-N-[3-(Trimethoxysilyl)Propyl]Octanesulphonamide is also used to treat wastewater and surface water. This process can be used on large quantities of water with high efficiency. The use of this process can be beneficial for the health of humans, animals, and the environment.</p>

<p>9-Mesityl-2,7-dimethyl-10-phenylacridinium tetrafluoroborate is a versatile building block and reagent for organic synthesis. It is a fine chemical that is used in the production of research chemicals and speciality chemicals. 9-Mesityl-2,7-dimethyl-10-phenylacridinium tetrafluoroborate can be used as a reaction component to synthesize complex compounds with various functional groups. It has been reported to have high quality, being both useful and stable. CAS NO: 1621020-00-5</p>

<p>N-alpha-Fmoc-Nepsilon-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl-L-lysine is a synthetic amide with a peptide backbone. It has been shown to have anti tumor activity in vivo and in vitro against a variety of solid tumor xenografts. The compound was conjugated to the integrin receptor ligand RGD, which is expressed on the surface of various types of cancer cells. This modification increased the uptake of N-alpha-Fmoc-Nepsilon-1-(4,4 dimethyl 2,6 dioxocyclohex1 ylidene)ethyl L lysine by leukemia cells and solid tumor xenografts.</p>

<p>2,3-Dimethoxyphenylboronic acid is a synthetic molecule that contains a boronic acid group. This compound has been shown to interact with histones H3 and L6. It has also been shown to modify lysine residues on the histone H3 protein by methylation. In addition, 2,3-dimethoxyphenylboronic acid interacts with other molecules in a way that changes their conformation and this interaction can be studied using vibrational spectroscopy. Organic chemists may use 2,3-dimethoxyphenylboronic acid as a ligand for biological targets or as a means of modifying proteins.</p>

<p>Ethylboronic acid is a β-amino acid with a serine protease inhibitory effect. It has been shown to inhibit the Toll-like receptor cascade, which is involved in the inflammatory response. Ethylboronic acid also inhibits the serine proteases that are responsible for cleaving peptides at their carboxy termini. This inhibition leads to an increase in the level of active peptides and a decrease in the level of inactive peptides, which can lead to an antimicrobial effect. Ethylboronic acid also inhibits chloride ion channels, which may lead to new treatments for asthma and cancer.</p>

<p>3-Aminopropyldiisopropylethoxysilane (APDS) is a monolayer chemical that is used to modify the surface properties of a variety of substrates. This chemical can be used for patterning, functionalization, and immobilization of biomolecules. APDS has been shown to have a protective effect on cells in culture by preventing oxidation and denaturation of proteins. APDS also has been used for detection methods such as electron microscopy and photoelectron spectroscopy.</p>

<p>Gamma-chloropropyl trimethoxysilane (CPS) is a chemical compound with the formula Cl3Si(OCH3)2. It is an organosilicon compound that is used in surface preparation and modification to improve hydrophobicity, chemical stability, and mechanical properties. CPS forms covalent linkages with organic compounds on the surface by reaction with hydroxyl groups. It has been shown to react with fatty acids such as oleic acid, forming a metal chelate. CPS reacts with sodium carbonate (Na2CO3) to form sodium chloropropoxide (NaClOCH3). This reaction is exothermic and can be used for sample preparation. The mechanism of this reaction is thought to involve the formation of a copper complex followed by its hydrolysis.</p>

<p>N-alpha-Fmoc-Nepsilon-methyltrityl-L-lysine is a synthetic amino acid that is used in the industrial production of peptides. It has been used for the synthesis of polypeptides, which are made up of chains of amino acids, and to analyze uptake in urine samples. The uptake was tracked by using a trifluoroacetic acid analog to radiolabel the N-alpha-Fmoc-Nepsilon-methyltrityl-L-lysine. This analog was synthesized from histidine and butyric acid, and its carboxy terminal sequence was determined by solid phase synthesis. N-alpha-Fmoc-Nepsilon methyltrityl L Lysine binds to the receptor site on cells that is responsible for binding histidine residues on proteins.</p>

<p>3-(Hydroxymethyl)phenylboronic acid (3HMBBA) is an analog of 3-hydroxymethylphenylboronic acid. It has been used in the Suzuki coupling reaction to produce a number of biologically important compounds, such as beta-lactamase inhibitors. This compound also inhibits the activity of human liver cancer cells and human liver tissue in vitro. The hydroxy group on the left-hand side of the molecule provides a potent inhibition effect on beta-lactamases that are produced by bacteria and may be useful for treating infections caused by these bacteria. 3HMBBA is soluble in neutral pH solutions, which makes it easy to work with and store. 3HMBBA can also be used as a ferrite for permanent magnets due to its high magnetic moment.</p>

<p>Octadecamethylcyclononasiloxane is a silicon-containing molecule, which has been shown to have antihypertensive activity. It works by inhibiting the production of angiotensin II, a key regulator of blood pressure, and thereby reducing blood pressure. Octadecamethylcyclononasiloxane also exhibits tumor-promoting activities in some animal models. This molecule is used as a surface active agent in many household products such as dishwashing detergents, shampoos, and cosmetics. It is also used as an acid catalyst in organic synthesis and in the manufacture of magnetic particles for use in biotechnology.<br>A fatty acid ester with functional groups that can be found on its surface may contribute to octadecamethylcyclononasiloxane's cancer-promoting activities.</p>

<p>Dichlorodiethylsilane is an aromatic hydrocarbon that is a colorless liquid with a pungent odor. It has been used as a chemical intermediate and in the synthesis of dyes, pharmaceuticals, and other organic chemicals. Dichlorodiethylsilane reacts with hydrogen fluoride to form hydrogen chloride and dichloroethane. The reaction products are acidic due to the presence of hydroxyl groups, which react with water vapor to form hydrochloric acid and alcohols. Dichlorodiethylsilane reacts with nucleophiles such as chlorides or hydroxides to form ether linkages. This compound also reacts with c1-c4 haloalkyls to form chlorinated alkyl groups. Dichlorodiethylsilane is soluble in water, but not in ether or benzene. It is stable at room temperature but decomposes when heated to temperatures above 200°C (392°F).</p>

<p>(3R,4R)-4-Acetoxy-3-[(R)-1-(tert-butyldimethylsilyloxy)ethyl]-2-azetidinone is a versatile building block that can be used as a reagent and speciality chemical. It is also a useful scaffold for the synthesis of complex compounds. It has been shown to be useful in the manufacture of research chemicals and other fine chemicals. This compound is characterized by its high quality and can be used as an intermediate in reactions involving nucleophilic substitution, alkylation, acylation, esterification, and amination.</p>

<p>N-ε-(1-Carboxymethyl)-L-lysine (NEM) is a versatile building block that is used in the synthesis of complex compounds. It is a reagent and speciality chemical that can be used as an intermediate to produce other useful chemicals or as a reaction component. It has been shown to be useful in the synthesis of peptides, oligonucleotides, and organic molecules. NEM has also been shown to have high quality and purity, making it a useful scaffold for further research into new compounds.</p>

<p>Tert-butyl diphenylchlorosilane is a chemical compound that belongs to the group of organosilicon compounds. It is used for the preparation of various organosilicon compounds, such as trifluoroacetic acid, which is used in analytical chemistry. The synthesis of tert-butyl diphenylchlorosilane starts with the reaction between hydrochloric acid and sodium citrate. This yields a phosphate bond and a hydroxyl group. In order to form the desired product, tert-butyl diphenylchlorosilane, this intermediate is reacted with trifluoroacetic acid in an asymmetric synthesis to yield the desired product. The reaction mechanism of this process involves hydrogen chloride as an electrophile attacking the carbonyl carbon atom in trifluoroacetic acid, leading to an elimination reaction. This elimination reaction results in two possible products: tert-butyl acetate or tert-butyl chloros</p>