Building Blocks

<p>Used with EDC for carboxyl-foot printing studies of proteins</p>

<p>Gallic acid anhydrous is a compound that is found in plants and has antioxidant properties. Gallic acid anhydrous can be used as a model system for the study of electrochemical impedance spectroscopy. It has shown to have anti-cancer activity in vitro, but not in vivo, against squamous carcinoma cells. In addition, gallic acid anhydrous has been shown to inhibit oral pathogens and to scavenge anion radicals. Gallic acid anhydrous may have structural similarities to procyanidin B4, which is important for its antioxidant activity.</p>

<p>5-Carboxyvanillin is the oxidation product of isoeugenol and p-hydroxybenzoic acid. It can be produced by reacting these two compounds with a peroxide in an oxidizing reaction. The reaction products include 5-carboxyvanillic acid, which can be hydrolyzed to vanillin. 5-Carboxyvanillin is a white crystalline solid with a chemical nature similar to that of vanillin. It has been shown to have antimicrobial properties against tissues, such as guinea pig ileum and rat liver, but not against bacterial cultures. This compound may also be used in pulping processes for the production of paper or cellulose fibers.</p>

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

<p>Fmoc-Pro-Gly-Gly-OH is a synthetic peptide that is used in the manufacture of bivalirudin, an anticoagulant. It is a large molecule that can be dissolved in water or acetonitrile. The impurities may include ammonium and acetate ions. Fmoc-Pro-Gly-Gly-OH is insoluble in trifluoroacetic acid and trifluoroacetic acid/ammonium acetate mixture, but can be recrystallized from these solvents. The lyophilized product should be stored at 4°C to avoid hydrolysis. Polypeptides are not stable under acidic conditions, so care must be taken when handling this material.</p>

<p>2-Fluoro-3-methylbenzoic acid is a high quality, versatile building block that has been shown to be an effective reagent for the synthesis of complex compounds. It is also a useful intermediate in the synthesis of fine chemicals and speciality chemicals. This compound can be used as a reaction component for many chemical reactions, such as the formation of new bonds and the removal of protecting groups. As a versatile building block, 2-fluoro-3-methylbenzoic acid is an important starting material for synthesizing a number of natural products, pharmaceuticals, and other organic compounds.</p>

<p>3-Fluoro-4-hydroxyphenylacetic acid is a fluorinated aromatic compound that has been shown to have serotonergic, dopaminergic and noradrenergic actions. 3-Fluoro-4-hydroxyphenylacetic acid has been shown to interact with the serotonin receptor 5HT2A in cell culture and in vivo, as well as with the dopamine receptor DRD2. This compound also interacts with the eschscholtzia receptor. 3-Fluoro-4-hydroxyphenylacetic acid is biosynthesized from 5-hydroxyindoleacetic acid (5HIAA).</p>

<p>4-Fluoro-3-hydroxybenzoic acid is a colorless solid that can be produced through the sulfonation of 4-fluorophenol with sulfuric acid. This process usually takes place in two steps: first, the phenol is refluxed with sulfur trioxide and then aqueous potassium hydroxide is added to the mixture. The reaction produces a sulfite salt, which is then treated with sodium sulfite to produce the desired acid. 4-Fluoro-3-hydroxybenzoic acid can also be synthesized by adding sulfur dioxide to an aqueous solution of 3% hydrogen peroxide and adding potassium hydroxide dropwise until effervescence ceases. This method produces an insoluble precipitate, which is filtered out and washed with water. The product can then be purified by recrystallization from hot water or by washing with ether.</p>

4-Formylcinnamic acid is a molecule that is produced by the condensation of benzaldehyde and formic acid. The nmr spectra of 4-formylcinnamic acid show that it has a structure with two aromatic rings. It has been shown to activate Toll-like receptor 4 (TLR4) in human liver cells. The radiation induced photochemical properties of this molecule have been studied using x-ray diffraction data and the hydrochloric acid decoupling technique. This molecule has also been shown to suppress tumor xenografts in mice and primary cells in vitro, which may be due to its ability to inhibit cellular proliferation and induce cell death by apoptosis.

<p>4-Fluoro-3-methoxyacetophenone is a chemical compound that can be used as a building block for the synthesis of other organic compounds. It is also a useful intermediate for the production of pharmaceuticals, pesticides, and fragrances. 4-Fluoro-3-methoxyacetophenone has been shown to react with various reagents including amines, alcohols, and thiols. This chemical is water soluble and can be stored at room temperature.</p>

<p>4-Fluoro-2-methoxybenzaldehyde (4FMBA) is a potential PET radioligand that binds to the serotonin 5-HT2A receptor. 4FMBA has been shown to be an efficient and selective 5-HT2A antagonist with low molecular weight and high affinity. The binding of 4FMBA to the serotonin 5-HT2A receptor can be inhibited by ketanserin, which is a nonselective 5-HT2A antagonist. This drug may be used for cancer diagnosis, as it has a low detection limit and can detect endogenous serotonin in the brain. It also shows anti-depressant properties, which may be due to its ability to bind to the orthosteric site of the serotonin 5-HT2A receptor.</p>

<p>5-Fluoro-3-methylindole is a reactive compound that is not soluble in water. It has a molecular weight of 288.5 and an ionization potential of 7.8 eV. 5-Fluoro-3-methylindole can act as a potent antagonist by binding to the pharmacophore, which is the three hydrogen bonding sites on the benzodiazepine receptor. This drug has been shown to be reactive with halides, nitro, and magnesium, as well as with some endogenous compounds such as nitroarenes and amides. 5-Fluoro-3-methylindole also reacts with fluorescence ligands and transfer agents.</p>

5-Carboxyvanillic acid is a chemical compound that belongs to the class of organic compounds known as carboxylic acids. It is also called o-vanillin, and it has a molecular weight of 116.19 g/mol. 5-Carboxyvanillic acid is one of the main ingredients in natural vanilla flavour. The hydroxyl group on the 5th carbon atom of this molecule reacts with a proton, which results in an addition reaction mechanism. The reaction proceeds through two steps: first, protonation occurs at the 5th carbon atom; second, deprotonation occurs at the 4th carbon atom. This chemical compound can be found as a white crystalline solid and as a volatile oil.

<p>5-Fluoro-2-methylbenzoic acid is a synthetic compound that has antiviral potency against the influenza A virus. It is the active form of 5-fluoro-2-methylbenzoyl chloride, which is synthesized from a Grignard reagent and an asymmetric synthesis. 5-Fluoro-2-methylbenzoic acid has been shown to have anticancer properties in vitro, which may be due to its ability to inhibit cancer cell growth through interaction with chloride channels. This drug also inhibits the activity of dehydrogenases, which are enzymes that catalyze the oxidation of various substrates by reducing them.</p>

4-Fluoro-1-butanol is a gaseous protonated fluorine compound. The proton is transferred from the hydrogen to the fluorine, resulting in an intramolecular hydrogen bond. 4-Fluoro-1-butanol has been shown to undergo conformational changes due to the substituent effects of other atoms on its molecules. This molecule has been shown to be able to orient itself in different ways, depending on the experimental parameters and conditions that are used. 4-Fluoro-1-butanol has also been shown to have a strong hydrogen bond with other molecules such as water, which may be due to its ability to form a stable H···O hydrogen bond with a strong donor atom (fluorine).

<p>Fmoc-L-m-Tyrosine is a reagent that is used in organic synthesis. It is a complex compound that can be synthesized from m-tyrosine and t-butyl bromoacetate. Fmoc-L-m-Tyrosine is also a useful intermediate for the preparation of other compounds, such as pharmaceuticals and agrochemicals. It has been shown to be a fine chemical that has a wide range of applications in the field of biotechnology and pharmaceuticals. Fmoc-L-m Tyrosine is also a versatile building block with many possible reactions, making it an excellent candidate for research chemicals, including speciality chemicals. The CAS number for this compound is 204384-71-4 and it's molecular weight is 262.3 g/mol.br&gt;</p>

<p>6-Oxo DL-norleucine, formate salt is an anti-inflammatory agent that has been shown to reduce the symptoms of inflammatory bowel disease. It is a prodrug that is converted in vivo to 6-oxo DL-norleucine, its active form. This drug inhibits the activity of enzymes involved in metabolic pathways including ester hydrolysis and dinucleotide phosphate metabolism. 6-Oxo DL-norleucine has also been shown to inhibit the production of inflammatory mediators such as prostaglandin E2 (PGE2), leukotriene B4 (LTB4), and reactive oxygen species (ROS) in human serum. The mechanism by which this drug exerts its effects is not yet fully understood but may be due to inhibition of p. pastoris, a fungus that can cause opportunistic fungal infections.</p>

<p>Fmoc-Ala-OH is a bioactive molecule with a molecular weight of 195.2 Daltons. It has been shown to have receptor activity and cyclic peptide properties. Fmoc-Ala-OH is soluble in chloroform and methanol, but insoluble in water. It can be used as a substrate for the chemical ligation reaction, which involves the joining of two peptides by forming an amide bond between their carboxyl groups. This process is known as "Fmoc chemistry". Fmoc-Ala-OH has also been shown to have anti-inflammatory effects in animal models of autoimmune diseases such as rheumatoid arthritis and multiple sclerosis.</p>

5-Formylindole is a non-selective and irreversible inhibitor of protein α, which is the catalytic subunit of the enzyme AMP-activated protein kinase. It binds to the hydroxyl group at position Cys177 in the ATP binding pocket of protein α, thereby inhibiting its activity. 5-Formylindole has been shown to inhibit tumor growth in xenografts and also inhibits fat accumulation in 3T3-L1 preadipocytes by inhibition of fatty acid synthesis. This compound has also been used to study molecular modeling in order to understand hydrogen bond interactions between aldehyde groups and intramolecular hydrogen. The genus that this compound belongs to is stilbene derivatives.

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