Carboxylic Acids

<p>Nomegestrol acetate is a nonsteroidal anti-inflammatory drug that binds to the response element of the gene, which leads to an increase in transcription. It is used in women to treat conditions such as endometriosis, menstrual disorders and breast cancer. The apoptosis pathway is activated by nomegestrol acetate by binding to the bcl-2 protein. This then causes a decrease in caspase activity, leading to cell death. Nomegestrol acetate also has been shown to have effects on ovarian activity and may be used as an analytical tool for determining the rate constant of polymerase chain reaction (PCR).</p>

<p>DL-lactic acid is a metabolic intermediate that is produced in the muscle cells during anaerobic glycolysis. It is used to treat cancer and has been shown to be effective against squamous cell carcinoma. DL-lactic acid also inhibits mitochondrial membrane potential, which may be one of the mechanisms by which it causes cell death. DL-lactic acid has been found to have antibacterial efficacy against a number of bacteria, including Staphylococcus aureus, Enterococcus faecalis, Escherichia coli, Proteus mirabilis, Pseudomonas aeruginosa, and Streptococcus pyogenes. DL-lactic acid also inhibits enzyme activities that are necessary for bacterial growth such as phosphotransferase enzymes and urease. DL-lactic acid is a metabolic intermediate that can be used to inhibit tumor growth and metastasis. DL-lactic acid also inhibits transcriptional regulation in human serum</p>

<p>Please enquire for more information about 3,6-Dihydro-4-(tributylstannyl)-1(2H)-pyridinecarboxylic acid t-butyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Methylglutaric acid is an organic compound that belongs to the group of alkanocarboxylic acids. It has been shown to reduce the formation of malonic acid, which can be toxic to the heart and cause congestive heart failure. 3-Methylglutaric acid also inhibits oxidation catalysts and increases the production of energy in cells by providing electrons. The kinetic data for 3-methylglutaric acid have been determined using a gas chromatography technique on a high-temperature conversion reactor at a pH of 7.0 with a concentration of 0.1 M potassium phosphate buffer (pH 7) and a temperature of 70°C. 3-Methylglutaric acid has been shown to inhibit monoclonal antibody cationic polymerization, which may be due to its reactive nature and its ability to donate hydrogen ions or electrons.</p>

<p>Nicotinuric acid is an endogenous metabolite of nicotinic acid, which is a cofactor for the enzyme that catalyzes the conversion of phosphoenolpyruvate to pyruvate. Nicotinuric acid has been shown to be a potential biomarker for human pharmacokinetics. It has been shown to be involved in energy metabolism and may play a role in the pathogenesis of atherosclerotic cardiovascular disease. Nicotinuric acid is also a product of the enzymatic degradation of pyrrolidinecarboxylic acid, which is found in papillary muscle cells and penicillin-binding protein. The formation of nicotinuric acid can be inhibited by nicotinic acid, pyrazinoic acid, or by inhibitors of lc-ms/ms method.</p>

<p>2-Oxovaleric acid is a monocarboxylic acid that is produced by the oxidation of 2-oxopentanoic acid. It was first discovered as an inhibitory compound for glutamate dehydrogenase, which catalyzes the conversion of glutamate to alpha-ketoglutarate. This inhibition leads to a buildup of glutamate in the cell, which can cause metabolic disorders. The importance of 2-oxovaleric acid was demonstrated using a chromatographic method on type strain cells. The electron microscopic images showed that 2-oxovaleric acid inhibited the growth of bacteria by binding to extracellular Ca2+, carbon source, and animals.</p>

<p>Please enquire for more information about 3-[(Dimethylamino)methyl]benzoic acid hydrochloride 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 tert-Butyl (1-methyl-1H-imidazol-5-yl)carbamate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methylisoxazole-4-carboxylic acid is an amide that is oxidized to form a hydroxycrotonic acid. It is found in food products, such as milk and eggs, which are rich in amino acids. Methylisoxazole-4-carboxylic acid can be converted to the corresponding hydroxycrotonic acid by deamination of alpha-ketoglutarate or by enamine formation with other amines. These processes are important for the metabolism of amino acids and the synthesis of proteins. Methylisoxazole-4-carboxylic acid has analgesic properties and has been shown to reduce cycloaddition reactions that lead to the formation of free radicals. The methyl group on this compound also allows it to act as a reducing agent, forming nitro compounds with nitrous oxide or nitric oxide and hydroxyl groups with alcohols, phenols, and pyridines.</p>

<p>Intermediate in the synthesis of vilanterol</p>

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<p>Nonafluorovaleric acid is a glycol ether that is used as a solvent and in the manufacture of fluoropolymers. Nonafluorovaleric acid is considered to be a potential biomarker for perfluoroalkyl substances, which are toxic chemicals found in many household products. It has been shown to inhibit matrix metalloproteinase activity and can be used to study autoimmune diseases. Nonafluorovaleric acid can also be used as a synchronous fluorescent probe for enzyme-linked immunosorbent assays. The toxicity of this chemical has been studied extensively and it is well known that nonafluorovaleric acid can induce enzyme induction, leading to increased production of enzymes such as cytochrome P450.</p>

<p>4-Bromo-2,5-difluorobenzoic acid is a potent inhibitor of isoforms CYP2C9 and CYP2D6. It is an acidic drug with a pKa of 3.8, which makes it ionizable in biological fluids. 4-Bromo-2,5-difluorobenzoic acid inhibits the activity of CYP2C9 and CYP2D6 by binding to the pharmacophore region of these enzymes. 4-Bromo-2,5-difluorobenzoic acid also has an isosteric functionality that increases its selectivity for CYP2C9 and CYP2D6 over other cytochrome P450 isoforms. The functional groups on 4-bromo-2,5-difluorobenzoic acid are part of the inhibitor's nature that make it selective for these two cytochrome</p>

<p>Please enquire for more information about 6a-Ethyl-chenodeoxycholic acid 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 Fmoc-(S)-3-amino-3-(2-naphthyl)propionic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>cis-4-(Hydroxymethyl)cyclohexanecarboxylicacid is a metabolite of chorismate, an intermediate in the biosynthesis of aromatic amino acids. It has been shown to have immunosuppressive activity and can be used to treat neurodegenerative diseases like cancer. cis-4-(Hydroxymethyl)cyclohexanecarboxylicacid is produced by stepwise conversion from 3-hydroxybenzoic acid with the use of organic solvents. The final product is purified by preparative chromatography and its molecular weight is determined by mass spectrometry. This compound has also been found to have anticancer properties due to its ability to inhibit protein synthesis in tumor cells.</p>

<p>Please enquire for more information about tert-Butyl 4-(4-iodophenyl)tetrahydro-1(2H)-pyrazinecarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Hydroxyquinoline-4-carboxylic acid is a carboxylate that is structurally classified as a multidrug. It has been shown to inhibit bacterial efflux pumps and target enzymes, such as cancer cells and multidrug resistant bacteria. 2-Hydroxyquinoline-4-carboxylic acid also has potent antibacterial activity against Streptococcus faecalis, an opportunistic pathogen that causes infections in the urinary tract and on skin wounds. The fluorescence properties of this compound can be used for fluorescent labeling of biomolecules or for sensing applications.</p>

<p>(R)-2-((tert-Butoxycarbonyl)amino)-3-methoxypropanoic acid (BAAM) is a potent, orally bioavailable, and pharmacokinetically well-characterized inhibitor of blood coagulation that has been shown to be effective in animal models. BAAM inhibits the activity of tissue factor (TF), an enzyme that initiates the blood coagulation cascade. TF is important for hemostasis because it is activated by contact with blood and tissue factors such as collagen or thrombin. BAAM has shown some promise as a potential treatment for thrombosis, which can lead to heart attacks and strokes.</p>

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

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<p>Cyclopropanecarboxylic acid chloride is an organic compound with a molecular formula of C3H6Cl2O. It belongs to the group of carboxylic acids and has a pyrazole ring, which is a potential drug target. Cyclopropanecarboxylic acid chloride has been found to be active against infectious diseases such as herpes, influenza, and Ebola. The mechanism of action for this compound is not yet fully understood but it has been shown to have an effect on growth factors and kinetic data.</p>

<p>(2,4-Dichlorophenoxy)acetic acid sodium salt monohydrate is a chemical that belongs to the phenoxy herbicides. It is used as a selective herbicide for control of annual and perennial grasses and broadleaf weeds in noncrop areas. This compound has been detected by gas chromatography/mass spectrometric analysis after a dispersive solid-phase extraction procedure. The target analytes were found to be acidic with an unknown molecular weight.</p>

<p>Hydrocortisone is a corticosteroid that is used to treat inflammation, allergies and skin diseases. It is also used to treat adrenal gland disorders. Hydrocortisone Acetate Impurity G (HA) is a drug that has anti-inflammatory properties, which may be due to its inhibition of prostaglandin synthesis. HA was the first hydrocortisone impurity found in prednisolone tablets. This discovery led to the development of corticosteroids and their use in medicine for the treatment of inflammation and allergies.</p>

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

<p>Bromoacetic acid is a brominated carboxylic acid that has been shown to bind to response elements and inhibit the synthesis of proteins. It has been shown to inhibit the growth of bacteria in human serum at concentrations of 1-5 mM. Bromoacetic acid also binds to metals, such as copper and zinc, and inhibits their activity. This compound has also been shown to have anti-inflammatory properties in experimental models. Bromoacetic acid is not toxic in rats, but it may cause myocardial infarction in humans.</p>

<p>(2S)-2-Amino-2-[(5S)-3-chloro-4,5-dihydroisoxazol-5-Yl]acetic acid is an inhibitor of the enzyme glutathione reductase (GR) and cytochrome P450. GR activates glutathione in cells to form a powerful antioxidant that protects against oxidative stress. (2S)-2-Amino-2-[(5S)-3-chloro-4,5-dihydroisoxazol-5-Yl]acetic acid inhibits GR and cytochrome P450 activity, leading to increased oxidative stress and neuronal death. This drug has been shown to have inhibitory properties on bowel disease by reducing the production of proinflammatory cytokines IL1β and TNFα. The compound also exhibits anti tumor response against mouse tumors by inducing apoptosis and inhibiting cell proliferation. The compound targets intracellular targets</p>

<p>Ethyl 2-amino-4-thiazoleacetate is a supramolecular molecule that has the potential to be an anticancer agent. It inhibits the growth of tumor cells by binding to tyrosinase and hydrogen-bonding with chloride ions in solution. Ethyl 2-amino-4-thiazoleacetate also binds to a metal ion, such as zinc, which is important for biological functions. When it binds to these metals, it inhibits the enzyme hepg2 cell, which is involved in the synthesis of protein from RNA. Inhibition of this enzyme leads to decreased production of cytokines, which are molecules that regulate immune responses. This drug also has inhibitory activities against oral cephalosporins when used in combination with other drugs.</p>

<p>Ethyl 2-amino-thiazole-4-carboxylate (ETAC) is an inhibitor of protein synthesis. It binds to the dna and inhibits transcription, leading to cell death by inhibiting the production of proteins vital for cell division. ETAC has been shown to have cytotoxic activity against cancer cells and hemolytic activity. It also has a strong fluorescence probe property, which may be used in cancer diagnosis. ETAC can inhibit protein synthesis in cells that are resistant to other antimicrobial agents and platinum-based chemotherapy, making it a potential treatment for these infections. The pharmacokinetic properties of ETAC are not well studied but it is excreted through urine, suggesting that it is hydrophilic and may be metabolized with glucuronidation or sulfation. The molecular modeling study suggests that the hydrogen bond between ETAC and the dna phosphate group may explain its inhibitory effects on DNA synthesis.</p>

<p>Please enquire for more information about (6-Hydroxy-2-methyl-4-oxoquinazolin-3(4H)-yl)acetic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>7-Methyluric acid is a purine derivative that is excreted in the urine. This compound can be used to measure the metabolic rate of an individual. 7-Methyluric acid reacts with caffeine to produce methylxanthines and uric acid, which are then measured by chromatographic methods. In order to measure the metabolic rate, a known amount of caffeine is given orally to Sprague-Dawley rats for a period of time, followed by measurement of 7-methyluric acid in their urine samples. The results show that the metabolic rate increases linearly with time.</p>

<p>D(+)-Lactic acid lithium salt is a dipolar molecule with an activation energy of about 44 kJ/mol. It has been studied by NMR techniques and found to have a resonance in the range of 1.8-2.0 ppm, which is characteristic of protons on the oxygen atom. The proton magnetic resonance (PMR) study showed that the d-lactate resonances were very broad and shifted to higher frequencies, whereas the l-lactate resonances were sharp and shifted to lower frequencies. This may be due to the different number of protons on each type of lactate molecule. The magnetic resonance (NMR) study showed that lithium salt was a radical with a spin density distribution around 2.6 ppm in the nmr spectrum.</p>

<p>5,6-Epoxy-13-cis retinoic acid (5,6-ER) is the most active metabolite of all-trans-retinoic acid. 5,6-ER binds to the nuclear receptor and acts as a transcription factor. It has been shown to inhibit the growth of several cancer cell lines in vitro, including T47D cells. 5,6-ER also has antacid properties and can be used for the treatment of inflammatory bowel disease. 5,6-ER is found in low concentrations in plasma and tissues and accumulates in high concentrations in rat liver microsomes. The major metabolic pathway includes hydrolysis by trifluoroacetic acid which produces 5,6 epoxyretinoyl coenzyme A (5,6 epoxyretinoyl CoA). This compound is then converted to 5,6 epoxyretinol by an unknown mechanism.</p>

<p>3,6-Dioxaoctanedioic acid is a functional group that can be found in nature and has been studied for its potential to inhibit cancer cell growth. 3,6-Dioxaoctanedioic acid is a magnesium salt that is used as an experimental drug to treat bronchial asthma. It works by interfering with the function of serine protease enzymes. In addition, this compound has been shown to have particle size and transport properties that are suitable for inhalation therapy. These properties make it an effective drug for treatment of respiratory diseases such as asthma or chronic obstructive pulmonary disease.</p>

<p>5-Ethylthiophene-2-carboxylic acid is a chemical compound that has been acetylated. It is often used as an intermediate in organic synthesis, especially as a building block for the production of pharmaceuticals and agrochemicals. 5-Ethylthiophene-2-carboxylic acid can be chromatographically separated by using strategies such as validation, algorithm, and regression. The chemical structure of this compound may be determined by using methods such as fingerprinting and gas chromatography. The structural isomers of this compound are naphthenic (5E) and butyllithium (5B). Chemists use 5E and 5B to profile the properties of this substance.</p>

<p>Boc-L-aspartic acid a-9-fluorenylmethyl ester is a synthetic compound that mimics the structure of acetylcholine. It has been shown to be an efficient method for generating pseudopeptides and cyclic peptides. This compound may be used as a surrogate for acetylcholine in virus research, since it can bind to the same receptor. Boc-L-aspartic acid a-9-fluorenylmethyl ester has also been used to generate monoclonal antibodies that are neutralizing against foot-and-mouth disease viruses.</p>

<p>Please enquire for more information about (S)-(-)-3-(Benzoylthio)-2-methylpropanoic acid 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 L-(2S,3aS,7aS)-Octahydro-1H-indole-2-carboxylic acid benzyl ester tosylate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Cacodylic acid is a white to brown crystalline powder that is soluble in water. It has been used as an analytical reagent, polymerase chain reaction (PCR) inhibitor, and skin cancer treatment. Cacodylic acid inhibits the activity of the bacterial enzyme activities in humans and other mammals. The mechanism of action of cacodylic acid is not completely understood but it appears that it binds to inorganic iron and blocks its availability for use by bacterial enzymes such as dihydropteroate synthase, which is required for DNA synthesis. This leads to cell death. Cacodylic acid has also been shown to inhibit the growth of human HL-60 cells in vitro, suggesting that it may have carcinogenic potential.</p>

<p>(4-Aminophenyl)boronic acid pinacol ester is a semiconducting material that can be used in thin film devices. It has been shown to be a good candidate for transistor and device applications due to its high yield, low cost, and high stability. This compound can also be used to modify the structure of other compounds through substitution reactions. (4-Aminophenyl)boronic acid pinacol ester has been synthesized from inexpensive starting materials, such as triphenylamine and amines.</p>

<p>Tridecanedioic Acid is a polycarboxylic acid that has reactive functional groups. It is used in detergent compositions as an inhibitor of the formation of soaps and hard water deposits. Tridecanedioic acid has been shown to inhibit pancreatitis, which may be due to its ability to inhibit the conversion of fatty acids into prostaglandins. Tridecanedioic acid also has anti-cancer properties, which have been shown in animal studies. In addition, it has broad-spectrum antimicrobial activity against gram-positive bacteria, such as Clostridium perfringens and Staphylococcus aureus. This compound inhibits protein synthesis by inhibiting enzymes belonging to the cytochrome P450 family.</p>

<p>Please enquire for more information about 5-[2-[4',5-Bis(Pyridin-2-ylsulfamoyl)biphenyl-2-yl]diazenyl]-2-hydroxybenzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate is an organic compound that can be synthesized by the reduction of 5-bromo-2-nitro pyridine with a palladium catalyst. It has been shown to inhibit the growth of cancer cells in vitro and in vivo, and is being investigated as a potential treatment for breast cancer.</p>

<p>Please enquire for more information about tert-Butyl 2-(2-chloroethoxy)acetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3,5-Di-tert-butyl-4-hydroxyphenylacetic acid (BHT) is an antiaging agent that has been used in food packaging and cosmetics. BHT is a functionalized triethoxysilane with phenyl groups attached to the silicon atoms. BHT is an antioxidant that protects against lipid peroxidation and prevents the formation of free radicals by reacting with peroxy radicals. It has been shown to have a protective effect on skin cells when applied topically. BHT also has protective effects against environmental stressors such as UV radiation, ozone, and cigarette smoke.</p>

<p>Copper acetate is a chemical compound that is composed of copper and acetic acid. Copper acetate monohydrate, the form used in this product, is an ionic salt that has the chemical formula Cu(CHCO)2. The copper atom has a coordination geometry of 4.5 and is surrounded by six oxygen atoms and two hydrogen atoms. The reaction mechanism for this compound involves methyl ethyl malonic acid as shown below: The first step in the reaction mechanism is the formation of a carbanion intermediate with the loss of a proton from one of the methyl groups on malonic acid. This carbanion attacks the copper atom to form an intermediate with two positive charges on it, which then breaks down into two molecules of malonic acid and one molecule of water. The other methyl group then reacts with another molecule of malonic acid to form methyl ethyl dicarboxylate and release another proton. This proton can be accepted by water or react with</p>

<p>Please enquire for more information about Methyl4-aminomethyl-1-boc-piperidine-4-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Tauroursodeoxycholic acid, sodium salt is a taurine-conjugated bile acid derivative, which is synthesized in the liver from ursodeoxycholic acid. It functions through its role in stabilizing the mitochondria and inhibiting apoptosis by modulating the unfolded protein response. This molecular action involves reducing endoplasmic reticulum stress, thereby providing cytoprotective effects in various cellular environments.</p>

<p>Bromosuccinic acid is a type of organic compound with the chemical formula HOCCH=CHOH. It is an ester that contains a hydroxyl group, a carboxylic acid group, and a bromine atom. Bromosuccinic acid has been shown to have biocompatible properties and can be used as a polymer for biomedical applications. It also has the ability to form covalent bonds with basic proteins due to its hydroxyl group, which is important for protein stability. Bromosuccinic acid has been shown to inhibit trypsin activity in soybean trypsin, which may be due to its disulfide bond or low energy content. This substance also reacts with malonic acid and carbonic acid, producing galacturonic acid and fatty acids respectively. Bromosuccinic acid is produced by bacteria of the genus Enterobacteriaceae and belongs to the family of short-chain fatty acids.</p>

<p>Please enquire for more information about 4-(N-Methylamino)phenylboronic acid pinacol ester 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-(3-Acetyl-1H-indol-1-yl)propanoic acid 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-[4-(3-Chlorophenyl)piperazin-1-yl]-5-oxopentanoic acid 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-(Trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]acetic acid 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-[(3,5-Dimethyl-1H-pyrazol-1-yl)methyl]-2-furoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Nitropropionic acid (3NPA) is a mitochondrial toxin that causes neuronal death by inhibiting complex enzyme activities and inducing reactive oxygen species production. 3NPA also alters mitochondrial membrane potential and induces pro-apoptotic protein expression, leading to neuronal cell death. 3NPA has been shown to be effective in the treatment of experimental models of infectious diseases, such as rat sepsis and human HIV infection, by reducing the number of activated T cells and CD4+ T cells. 3NPA also exhibits anti-inflammatory properties by inhibiting the inflammatory responses of monocytes/macrophages and neutrophils.</p>

<p>Please enquire for more information about 4-Piperazinylphenylboronic acid, pinacol ester 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 Ethyl 6-bromo-5-hydroxy-1-methyl-2-(phenylsulfanylmethyl)indole-3-carboxylate 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 4-Amino-3-(trifluoromethoxy)benzoic acid 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 4-[1-(2-Methoxyethyl)-1H-indol-3-yl]butanoic acid 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 (trans)-2-Cyclopropylvinylboronic acid pinacol ester 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 L-Glutamic acid gamma-methyl ester alpha-tert-butyl ester hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Hydantoin-5-acetic acid is a molecule that has been studied for its potential use in the stabilization of polymers and plastics. It has shown antibacterial activity against certain bacterial strains including Escherichia coli and Staphylococcus aureus. The molecule has the ability to coordinate with metal ions such as copper, zinc, and iron. The protonation state of the molecule is dependent on the pH of the environment. Hydantoin-5-acetic acid can exist in two tautomeric forms: hydantoin or 5-hydantoin. Hydantoin-5-acetic acid can be used to determine the concentration of hydrogen in proteins through chromatographic methods. This molecule also has Langmuir adsorption isotherm properties, which give it potential for use in supramolecular structures.</p>

<p>Dibromoisocyanuric Acid is an intermediate in the metabolism of fatty acids. It has been shown to inhibit fatty acid synthesis by inhibiting the transfer reactions of fatty acids from their acyl coenzyme A ester to carnitine, which is necessary for transport across the mitochondrial membrane. Dibromoisocyanuric Acid also inhibits monoclonal antibody production by monocytes and macrophages. Dibromoisocyanuric Acid may be used as a tumor suppressor in mice with tumors because it reduces gamma-aminobutyric acid levels, leading to increased locomotor activity and decreased body mass index.</p>

<p>Please enquire for more information about 4-(Methoxycarbonyl)bicyclo[2.1.1]hexane-1-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Diisopropylammonium dichloroacetate (DADCA) is a chemical that inhibits the metabolism of glucose. It has been shown to have a hypoglycemic effect in rats and is being investigated as a treatment for metabolic disorders such as diabetes and obesity. DADCA has also been shown to reduce liver lesions in animals with chronic viral hepatitis, and has been found to be effective in reducing tumor growth in mice. This drug can also be used to treat bowel disease by reducing the amount of ammonia released by bacteria. DADCA may also have physiological effects on humans, including an increase in blood pressure and fever, although these effects have not yet been studied.</p>

<p>Please enquire for more information about Methyl 4,5-dimethoxy-1-methyl-1H-indole-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(R,R)-1,2-Cyclohexanedicarboxylic acid is a cyclohexane carboxylic acid which has been used as a pharmaceutical intermediate. It is a chiral molecule with two stereogenic centers and can exist in enantiomeric forms. The (R,R) form of the compound is most commonly used in pharmaceuticals due to its higher solubility in water. The (S,S) form of the compound is more reactive than the (R,R) form and can be used for reactions that require a high reactivity. (S,S)-1,2-Cyclohexanedicarboxylic acid has been found to have clinical uses such as the treatment of amines and cyclohexane rings.</p>

<p>Methyl 2-pyridylacetate is a reactive compound that can be used as a reagent for trifluoromethylthiolation of terminal alkynes. This compound has been shown to react with anilines and form isomers, including the acid form. The reaction rate of the methyl 2-pyridylacetate with pyridine compounds is slow, but it reacts quickly with thionyl chloride and hydrochloric acid. Methyl 2-pyridylacetate also reacts with nucleophiles such as methyl anthranilate to form the corresponding quinolizine derivatives.</p>

<p>Methyl3-iodothiophene-2-carboxylate is a chemical compound that is involved in the biosynthesis of eicosanoids. It can be synthesized by the cyclization of the corresponding lactam to produce an intermediate, which is then converted to methyl3-iodothiophene-2-carboxylate by hydrolysis or reduction. This compound has been shown to inhibit malaria parasites such as Plasmodium falciparum and Plasmodium vivax. Methyl3-iodothiophene-2-carboxylate also inhibits the growth of bacteria such as Staphylococcus aureus and Bacillus subtilis. The mechanism of action is believed to be due to its ability to inhibit protein synthesis by binding with ribosomes in prokaryotic cells.END&gt;</p>

<p>Please enquire for more information about (2S,3S,5S)-5-[(N-Formyl-L-leucyl)oxy]-2-hexyl-3-hydroxyhexadecanoic acid 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 (2,7,8-Trimethyl-4-oxoquinazolin-3(4H)-yl)acetic acid 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 (3R)-1-Azabicyclo[2.2.2]oct-3-yl N-[2-(2-benzoylphenyl)ethyl]carbamate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Kisspeptin-54 is a mammalian peptide hormone that regulates the release of gonadotropin-releasing hormone (GnRH) from the hypothalamus. Kisspeptin-54 has been shown to be potently immunogenic in humans and can be used as an antigen for the production of monoclonal antibodies. It is also a candidate drug for the treatment of obesity and may have neuroprotective effects. Kisspeptin-54 has been shown to reduce body mass index, which may be due to its ability to stimulate the immune system and promote antibody production against tumors. This peptide also has potent on-line binding properties that are useful in polymerase chain reactions.</p>

<p>(3a,5b,6b,7a)-6-Ethyl-3,7-dihydroxycholan-24-oic acid is a synthetic cholestane derivative that has been shown to be useful in the treatment of biliary cirrhosis. The synthesis of this compound involves the reduction of an ethyl ester using a grignard reagent followed by UV irradiation. The reaction yield is high with a large excess of Grignard reagent used. This compound has been shown to be active against hepatic bile ducts and liver cells in vitro. It also has anti-inflammatory effects and can be used as an alternative treatment for patients who are intolerant to ursodeoxycholic acid or chenodeoxycholic acid.</p>

<p>4-(2-Oxopyrrolidin-1-yl)benzoic acid (4-OPBA) is a hydrogen bonding inhibitor that is used to study the interactions of cavity proteins. It has shown to interact with glutathione and prostaglandin D2, which are important for hematopoietic and inflammatory responses. 4-OPBA has been observed to bind with a water molecule in the cavity, which may explain its affinity for these molecular targets. The crystal structure of 4-OPBA shows that it forms an interaction with two water molecules and one other molecule in the cavity. This may be due to its ability to form hydrogen bonds with both water molecules as well as the molecule in the cavity.</p>

<p>Please enquire for more information about Bis(perfluorohexyl)phosphinic acid sodium salt 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 4-(tert-Butoxycarbonyl)thiomorpholine-3-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-(Bromomethyl)benzeneboronic acid pinacol ester (BBBA) is a hypochlorous acid derivative with a structural formula of C6H5BrOCH2. It is used as a fluorophore and has been shown to have anticancer activity. 4-Bromomethylbenzeneboronic acid pinacol ester reacts with hydrophobic molecules in the cell membrane, leading to disruption of the membrane and ultimately cell death. This compound can be used as an active oxygen source in biological assays, such as functional assays, because it generates reactive oxygen species and can act as a fluorescence probe for detection of biological samples.</p>

<p>2-Thiazoleacetic acid is a heterocyclic compound that can bind to iron and is an efficient ligand for the virus. It has been used as a linker in the synthesis of biologically active methylene compounds. 2-Thiazoleacetic acid also has anti-inflammatory properties and is used to treat inflammatory diseases. The compound reacts with hydrochloric acid, forming an acetic acid derivative. This reaction is catalyzed by metal ions such as Fe2+ or Hg2+. 2-Thiazoleacetic acid can be synthesized from two molecules of formaldehyde, two molecules of hydrogen cyanide, and two molecules of hydroxamic acids.</p>

<p>Please enquire for more information about (5-Chloropyridin-3-yl)boronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-(4-Fluorophenyl)-3-isoxazolecarboxylic acid is a high quality reagent with CAS No. 33282-24-5. It is a complex compound that is useful as an intermediate for the synthesis of various fine chemicals. 5-(4-Fluorophenyl)-3-isoxazolecarboxylic acid also has a number of uses in the synthesis of speciality chemicals, research chemicals, and versatile building blocks for organic chemistry. As a reaction component, it can be used to synthesize compounds with different functional groups on their molecules.</p>

<p>Methyl 1H-indazole-3-carboxylate is a synthetic cannabinoid that is structurally related to the natural cannabinoid, anandamide. It has been shown to be a potent activator of the CB2 receptor and to inhibit spontaneous activity in mice. Methyl 1H-indazole-3-carboxylate also binds to CB1 receptors and has potential use as a cancer therapy due to its ability to induce apoptosis. This compound is illegal in many countries, including the United States and Canada, where it is classified as a Schedule I drug.</p>

<p>Please enquire for more information about Glycochenodeoxycholic acid 3-sulfate disodium salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Phenoxybutyric acid is a molecule that is produced by filamentous fungi. It has been shown to inhibit the growth of many bacteria, including Staphylococcus aureus, Salmonella typhimurium, and Enterobacter aerogenes. 4-Phenoxybutyric acid binds to the receptor on the surface of the bacterial cell membrane and prevents it from functioning correctly. It also prevents the production of proteins necessary for growth and survival. This inhibition leads to a loss of energy in the cell, which eventually leads to death. The molecule has been shown to be effective in inhibiting bacteria even if they are resistant to antibiotics. 4-Phenoxybutyric acid has been shown to be more efficient than other methods for microbial biotransformation, such as dispersive solid-phase extraction or liquid-liquid extraction.</p>

<p>Please enquire for more information about Boc-(2R,5S)-5-phenylpyrrolidine-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-bromo-3-methylthiophene-2-carboxylic acid (5BmtCA) is a potential therapeutic that has been shown to have the same estrogenic activity as estradiol. It may be used for the treatment of osteoporosis and other conditions associated with estrogen deficiency, including resorption and bone loss. 5BmtCA is an amide with two phenyl groups at the C3 position, which are bioisosteres of the sulfur in estradiol. The substitutions on these phenyl groups can be changed to produce analogs with different properties. For example, 5BmtCA may be substituted with a ketone group at position C3 to produce the corresponding ketone analog 5BmtCK. This compound would be expected to have reduced bone resorption activity relative to 5BmtCA.</p>

<p>Please enquire for more information about Boc-D-glutamic acid-gamma-tert-butyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Isopropoxyphenylboronic acid is a boronic acid that can be used as a cross-coupling partner in palladium-catalyzed cross-coupling reactions. It is synthesized by reacting 4-hydroxyphenylacetic acid with 2 equivalents of naphthoquinone diazide. The addition of the 4-isopropoxy group to the phenyl substituent increases the reactivity of this boronic acid. This compound has been used in the synthesis of rofecoxib and cyclooxygenase inhibitors, such as aspirin and ibuprofen. The presence of an electron withdrawing group on one phenyl ring enhances the reactivity of this boronic acid towards nucleophiles, such as amines or alcohols.</p>

<p>Benzyl bromoacetate is a bicyclic heterocycle that is metabolized by the enzyme benzyl alcohol dehydrogenase. The resulting metabolites are then converted to methyl benzoate and benzyl alcohol. It has been shown to inhibit prostate cancer cells and basic fibroblasts, which may be due to its ability to inhibit enzymes involved in fatty acid synthesis. Benzyl bromoacetate also has therapeutic effects on autoimmune diseases such as bowel disease, which may be due to its ability to reduce inflammation and suppress the immune system.</p>

<p>Please enquire for more information about 1-Fluoro-5a-androst-2-en-17b-ol acetate 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 1-Methylindole-3-boronic acid pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Aminomethylphenylacetic acid is a nonsteroidal anti-inflammatory drug that is used to treat inflammation and pain. It belongs to the class of peptidomimetics, which are compounds that mimic the structure of a natural biological molecule. 4-Aminomethylphenylacetic acid has an analog with a lactam ring at position 3, which is not present in other NSAIDs. This structural difference may contribute to its high stability and low reactivity. 4-Aminomethylphenylacetic acid has been shown to exhibit antiviral activity against viruses such as HIV or Hepatitis C virus by inhibiting viral replication.</p>

<p>Please enquire for more information about 3-Chloro-4-cyanophenylboronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>7-Azaindole-5-carboxylic acid methyl ester is an ester derivative that can be synthesized from the reaction of acetyl chloride and diazotization. 7-Azaindole-5-carboxylic acid methyl ester has been used in research for its biological activity, specifically as a cytotoxic agent. It has also been shown to inhibit the growth of cancer cells by alkylation reactions and cyclization reactions. 7-Azaindole-5-carboxylic acid methyl ester has been shown to have antitumor properties with a mechanism that is not yet fully understood.</p>

<p>Tranexamic acid is a non-protein amino acid that is used to reduce the risk of blood loss in surgical procedures. It is an inhibitor of plasmin, which is an enzyme that breaks down clots and fibrin. Tranexamic acid binds to the active site of plasmin and blocks its activity, preventing the breakdown of fibrin clots. Tranexamic acid has been shown to be selective for plasmin, as other enzymes such as urokinase are not blocked by this drug. The picolyl group on tranexamic acid interacts with the benzyl group on plasmin and this interaction may be responsible for the selectivity of tranexamic acid for plasmin over other enzymes.</p>

<p>Please enquire for more information about 1-[2-(5-Fluoro-1H-indol-3-yl)ethyl]-5-oxopyrrolidine-3-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ethyl bromodifluoroacetate is a chemical substance that reacts with amines in the presence of copper to form a copper complex. It is used as an intermediate in the synthesis of organic compounds, such as pharmaceuticals. Ethyl bromodifluoroacetate is also used as a catalyst for cross-coupling reactions of organic molecules. This reaction requires low energy and can be performed under mild conditions. The asymmetric synthesis of ethyl bromodifluoroacetate requires few steps and only uses inexpensive starting materials. The carbonyl group is chemically stable, making it difficult to decompose or oxidize. However, hydrogen fluoride will react with ethyl bromodifluoroacetate and cause it to decompose into its elements, fluorine and carbon dioxide gas. In addition, nucleophilic attack by halides can lead to the formation of ethyl bromodifluoroacetate from other substances. Control agents are necessary</p>

<p>Please enquire for more information about [2-(4-Aminophenyl)ethyl]carbamic acid tert-butyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>