Carboxylic Acids

<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>Please enquire for more information about Methyl 3-amino-5-fluoro-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>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>Please enquire for more information about N-Nitroso-N-methyl-4-aminobutyric acid methyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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

<p>Please enquire for more information about tert-Butyl-n-(6-methoxy-3-pyridyl)carbamate 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-(1,3-Dimethyl-1H-pyrazol-4-yl)isoxazole-5-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5,6-Epoxy retinoic acid is a synthetic retinoid that has been shown to have biological properties in tissue culture and rat liver microsomes. It is an agonist of the retinoic acid receptor (RAR) and binds to DNA at the same site as all-trans retinoic acid. 5,6-Epoxyretinoic acid also has effects on gene expression in human serum and inhibits the proliferation of cancer cells by inducing apoptosis. The synthetic retinoid can be used as a novel chemotherapeutic agent for breast cancer or leukemia.</p>

<p>2-Methyl-4-(2-methylbenzamido)benzoic acid is a synthetic drug that has oxidizing properties. It is used as an intermediate in the synthesis of medicines, and can also be used as an intermediate in the synthesis of dyes and pesticides. The structure of this molecule consists of two methyl groups on a benzene ring with two aminobenzoic acid molecules attached to it. This molecule has hydrogen bonds with both aminobenzoic acid groups, one of which has an alkyl group attached to it. 2-Methyl-4-(2-methylbenzamido)benzoic acid crystallizes in the monoclinic system and its molecular weight is 256.24 g/mol.</p>

<p>Please enquire for more information about (R)-3-Amino-butyric acid methyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Trestolone acetate is a synthetic anti-cancer compound that has been shown to inhibit the growth of cancer cells in animal models. It is an estrogen receptor modulator that binds to the estrogen receptor and inhibits its activation by estradiol. Trestolone acetate has also been shown to inhibit the production of inflammatory cytokines, such as tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β), which may be due to its ability to act as a growth factor for immune cells. Trestolone acetate can be used for the treatment of degenerative diseases or bowel disease, such as Crohn's disease. This drug also has a beneficial effect in inflammatory diseases, such as IBD, and autoimmune diseases, such as rheumatoid arthritis. The effective dose is 10 mg/kg body weight per day given orally.</p>

<p>Mercuric trifluoroacetate is an organic compound that contains mercury and a carboxylic acid. It is an acid that is formed when mercury reacts with hydrochloric acid. Mercuric trifluoroacetate has been shown to be effective in the synthesis of a number of organic compounds, including the nonsteroidal anti-inflammatory drug (NSAID) 3-hydroxyanthranilic acid. This compound also inhibits the production of prostaglandin E2 in human leukocytes, which may be related to its inhibitory properties on congestive heart failure. Mercuric trifluoroacetate can also cause autoimmune diseases in mice by suppressing the production of interleukin-4 and interleukin-10, which are cytokines involved in immune responses.</p>

<p>4-Bromo-pyridine-2-carboxylic acid is a metabotropic glutamate receptor antagonist that inhibits the neurotransmitter glutamate. It has been shown to have antibacterial activity against Staphylococcus aureus and anti-inflammatory properties against the fungus Candida albicans. The drug is orally bioavailable, which means it can be taken by mouth, and has a pharmacokinetic profile that increases its bioavailability. This means that 4-Bromo-pyridine-2-carboxylic acid is an inhibitor of deoxycytidine kinase and may be used as an antifungal agent.</p>

<p>Tolfenamic acid is a non-steroidal anti-inflammatory drug that has been shown to inhibit the MCL-1 protein, which is involved in the regulation of programmed cell death. It has been used for the treatment of bowel disease and can be given orally or rectally. Tolfenamic acid may be effective against inflammatory bowel diseases such as ulcerative colitis and Crohn's disease. Tolfenamic acid binds to anionic sites on the matrix of cartilage and inhibits the production of prostaglandin E2 by inhibiting cyclooxygenase activity. Tolfenamic acid has also been shown to reduce pain by inhibiting the enzyme COX-2, which is associated with inflammation. The drug also has a strong effect on human polymorphonuclear leukocytes (PMN).</p>

<p>4-Methylcyclohex-3-ene-1-carboxylic acid is an anionic compound that is used in the preparation of perfumes. This substance has been shown to have a cycloaddition reaction with nonionic detergents and isoprene, catalyzing the oxidation of terephthalic acid to ethylene. 4-Methylcyclohex-3-ene-1-carboxylic acid can also be used as a medicinal agent for aromatization or as a catalyst for the production of aldehydes.</p>

<p>5-Chlorofuran-2-carboxylic acid is an unlabeled compound that has been found in the chloroacetate fraction of a crude extract of leaves from the plant Garcinia hombroniana. The compound was evaluated for its potential as a bioactive molecule using acetylation, which led to the formation of 5-chlorofuran-2-carboxylic acid methyl ester. This compound was then analysed for its chemical properties, including sequences and parameters. 5-Chlorofuran-2-carboxylic acid methyl ester had no effects on the growth rate of Escherichia coli, but did inhibit the activity of some enzymes involved in DNA replication and repair. Furan, an anion found in 5-chlorofuran-2-carboxylic acid methyl ester, is also present in many other compounds such as 2,4,6 trichlorophenol and 2,5 dichlorophenol</p>

9,10-Anthracenediyl-bis(methylene)dimalonic acid (ADMA) is a fluorescent probe that is used to measure the levels of ADMA in cells. This compound is able to bind to cell nuclei, which can then be detected by fluorescence microscopy. ADMA has been shown to be useful as a marker for cancer and other diseases such as diabetes or Alzheimer's disease. The detection sensitivity of ADMA can be increased by combining it with heparin, which binds strongly to this molecule and increases its solubility in water. The use of ADMA as an imaging agent has been reported in several clinical studies.

Thiocyanic acidpiperidine is a substrate for film hydroxide solution. It reacts with hydrochloric acid to form hydrogen chloride and thiocyanate ion. Thiocyanic acidpiperidine is a reactive compound that can be used as a radiation-sensitive reagent in the synthesis of β-unsaturated ketones. The reaction is carried out in an immiscible solvent such as dichloromethane or chloroform and sodium hydroxide solution. This efficient method has been shown to be useful for the preparation of β-unsaturated ketones.

<p>Please enquire for more information about 21-Hydroxy-pregna-1,4,16-triene-3,11,20-trione 21-acetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl 6-chloro-2-pyridinecarboxylate is a reactive, organic compound that belongs to the class of monomers. It is a white crystalline solid with a melting point of approximately 130 degrees Celsius. This chemical can be synthesized by reacting 2-chlorobenzothiazole with sodium carbonate in water at temperatures between 100 and 140 degrees Celsius. The reaction yields methyl 6-chloro-2-pyridinecarboxylate as well as chloride and picolinic acid as side products. This compound has been shown to have neurotoxic effects when administered to rats at high doses.</p>

<p>Native Melan-A (26-35) decapeptide derives from the melanocyte lineage-specific protein Melan-A/MART-1, which is expressed in almost 75-100% of primary and metastatic melanomas.<br>The region 26-35 of Melan-A protein acts as an antigenic peptide that is recognized by CD8+ tumor-reactive cytolytic T lymphocytes (CTLs) for designing antigen-specific cancer vaccines1. It has been shown that CD8+ Melan-A-specific CTLs isolated from melanoma patients efficiently lyse the Melan-A-expressing HLA-A*0201+ melanoma cell line. However, CTLs preferentially recognize the Melan-A (26-35) peptide as compared with the Melan-A (27-35) peptide. Moreover, the Melan-A (26-35) A27L analog (ELAGIGILTV) has a higher binding affinity to HLA-A*0201 than the native Melan-A (26-35) peptide (EAAGIGILTV), and consequently displays more potent antigenicity and immunogenicity.<br>It has been reported that the concentration of Melan-A (26-35) A27L analog required to obtain 50% of maximal antigenic activity (EC50) is 0.01nM, whereas that of the native Melan-A (26-35) peptide is 0.25nM1. Therefore, the relative activity of Melan-A (26-35) A27L analog is 25 fold higher than that of the native Melan-A (26-35) peptide.<br>Furthermore, functional competition assay has shown that the concentration of Melan-A (26-35) A27L analog required to achieve 50% inhibition (IC50) of tumor lysis is 2nM, which is 10 fold lower than that of the native Melan-A (26-35) peptide. Regarding peptide stability in human serum, the half-lifes (t1/2) of the native Melan-A (26-35) peptide and the A27L analog are quite similar (45 and 40min, respectively) as measured by HPLC-ESI-MS, but much higher than that of the Melan-A (27-35) nonapeptide (5min).</p>

Please enquire for more information about 3-(2-Oxo-imidazolidin-1-yl)benzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>N-Hexylboronic acid is an organometallic compound that has been used as a model system to study the catalytic mechanism of the Suzuki coupling reaction. It has also been shown to be a substrate film for use in the suzuki coupling reaction when combined with Raney nickel, which can be used to synthesize organic compounds. N-Hexylboronic acid has been shown to inhibit the activity of pancreatic lipase, but not cholesterol esterase or cholesterol ester hydrolase. The skeleton of this molecule is made up of six carbon atoms and one boron atom. Hydrogen chloride and aliphatic hydrocarbons are inhibitors of N-hexylboronic acid.</p>

<p>Please enquire for more information about N,N'-bis-Fmoc-diaminoacetic 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 Spiro[2.3]hexane-1-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]acetic acid is a potent antimicrobial agent that inhibits the growth of bacteria by binding to the 50S ribosomal subunit. It has shown antiinflammatory properties in animal models of bowel disease, skin cancer, and autoimmune diseases. This drug has also been shown to have no observable toxicity in humans at doses up to 5000 mg/day for 28 days. The drug binds to a number of enzymes including reactive oxygen species (ROS) scavengers and metabolic enzymes. There are no known drug interactions with this drug and it can be used safely with other nonsteroidal antiinflammatory drugs (NSAIDs).</p>

<p>3,5-Di-(tert-butyl)benzoic acid (3,5-DTBA) is a polynuclear organic solvent that is used as an additive in polymers, plastics, and rubbers. 3,5-DTBA has potent antiproliferative effects on cells and can be used to inhibit the growth of cancer cells. This compound also stabilizes terephthalic acid from oxidation and prevents the formation of amide products. 3,5-DTBA is synthesized from benzoic acid by reacting with methylene chloride in the presence of a catalyst such as aluminum chloride or zinc chloride.</p>

Please enquire for more information about Ac-Lys(Ac)-D-Ala-D-lactic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>2-(Chloromethyl)benzoic acid (CMBA) is a reactive chemical that can be used as an oxidant or a carbanion. CMBA is activated by sulfinyl, alicyclic, and sulfoxides, which are organic compounds with one or more sulfur atoms. These reactions may be either alkylation or condensation reactions. The activated CMBA can then react with chlorine to form chlorinated products. This reaction can be catalyzed by low energy sources, such as light or heat.</p>

<p>Piperidinium acetate is a photochemical agent that has been used in the photochemical oxidation of organic compounds. It is also used as a catalyst for the oxidative coupling of piperidinium salts with sodium salts to form piperidine. Piperidinium acetate can be used for the treatment of metabolic disorders, such as lactic acidosis and hyperglycemia, and autoimmune diseases such as rheumatoid arthritis and systemic lupus erythematosus. This compound is also known to cause allergic symptoms and anhydrous sodium may be generated in the process.</p>

<p>Tert-butyl(8-anti)-3-azabicyclo[3.2.1]oct-8-ylcarbamate (tBAA) is a heterocycle that has been modified to enhance its pharmacokinetic properties. Tert-butyl(8-anti)-3-azabicyclo[3.2.1]oct-8-ylcarbamate was designed to be metabolically stable and have a high bioavailability and isosteric properties with phosphatidylinositol, which it uses as a substrate in the catalytic cycle. This modification also increased tBAA's stability in vivo, leading to an increase in efficacy. The covalent attachment of the phenyl ring on the tertiary amine nitrogen of tBAA provides additional protection against hepatic metabolism by CYP450 enzymes, making it more potent than other compounds with similar structures that are not covalently attached to the amine group.</p>

<p>2-Bromo-5-methylbenzoic acid is an organic compound that can be synthesized in the laboratory. It is used as a starting material for synthesis of various quinazolinones, which are ionic liquid catalysts. 2-Bromo-5-methylbenzoic acid has also been shown to inhibit ethylene production from glycols and to act as a potential catalyst for the conversion of trifluoromethane into ionic liquids. The synthesis of 2-bromo-5-methylbenzoic acid is not well documented, but it can be made by reacting methyl bromide with benzaldehyde or acetone in the presence of sodium hydroxide or potassium hydroxide. This reaction produces bromobenzene, which reacts with phosphorus pentachloride to produce 2-bromo-5-methylbenzoic acid.</p>

<p>Please enquire for more information about 4-(2-Hydroxyethyl)-1H-pyrrole-3-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>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>3,4-Dihydro-1H-isochromene-1-carboxylic acid is a pyridine derivative that has been used as an intermediate in the synthesis of other compounds. 3,4-Dihydro-1H-isochromene-1-carboxylic acid is a weak acid that can be prepared by the reaction of 3,4-dihydroisoquinoline with chloroform and hydrochloric acid. It is also synthesized from 1,4 benzodioxane and phenylacetic acid. This compound has been used to prepare amides, amidines, and ureas. 3,4-Dihydroisoquinoline is also used as a precursor for the synthesis of pyridinium salts.</p>

<p>Please enquire for more information about 2-Amino-4,6-difluorobenzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ethyl 6-methylpyridine-2-carboxylate is a pyridine derivative that has a nitrogen at the 6 position. It is an anionic compound, which is soluble in methanol and dichloromethane. The compound can be used to synthesize pharmaceuticals or as a precursor for polymers. It has been shown to inhibit the growth of tumor cells by binding to type 1 receptor sites on the surface of cancer cells. It also binds to quinine and enolate groups, which are found in many drugs. These binding sites may be exploited for drug design purposes.</p>

2-Amino-3-(4-hydroxy-3-methoxyphenyl)propanoic acid is a metabolite of levodopa in the body. It is formed by oxidation of levodopa via the enzyme catechol-O-methyltransferase (COMT). This compound is used as an analytical reagent to measure levels of levodopa and its metabolites in biological samples. 2-Amino-3-(4-hydroxy-3-methoxyphenyl)propanoic acid can also be used to diagnose Parkinson’s disease, since it is produced in excess when dopamine production decreases due to the degeneration of dopaminergic neurons. The concentration–time curve for this compound can be used to calculate the clearance rate of levodopa from the blood plasma.

<p>Alpha-amino-2H-tetrazole-5-acetic acid (AAT) is a neurotoxin that inhibits glutamate receptors and causes neuronal cell death. It also decreases heart function in rats by inhibiting the cardiac sodium channel. AAT has been shown to be effective for inducing neuronal death in Xenopus oocytes, as well as decreasing the expression of certain receptor protein, such as NMDA and AMPA receptor subtypes. AAT is also known to cause apoptosis, which may be due to its inhibition of receptor function.</p>

<p>Fluperolone acetate is a synthetic steroid that has been used as an anti-inflammatory agent. It is a potent corticosteroid and has been shown to inhibit the growth of microorganisms, such as bacteria and fungi. Fluperolone acetate does not cross the blood-brain barrier into the central nervous system, so it can be used for the treatment of inflammatory diseases in the eye without affecting vision. This drug also has been shown to reduce choroidal neovascularization in patients with age-related macular degeneration. Some biodegradable implants have been made from fluoropolymers, which are biocompatible polymers that are degraded by hydrolysis or enzymatic action in vivo. These implants may provide a sealant for use in surgical procedures and for treating cavities.</p>

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

<p>3-Cyanopropionic acid methyl ester is a compound that belongs to the class of aliphatic carboxylic acids. It is an intermediate in the production of adiponitrile and acrylonitrile. This compound is used as a feedstock for the manufacture of vinylene, which can be used to produce c1-6 alkyl. 3-Cyanopropionic acid methyl ester can be produced from propylene and hydrogen cyanide in a high salt, activated reaction system. It has been shown that this compound may have metabolic disorders due to its ability to inhibit fatty acid oxidation and increase viscosity. 3-Cyanopropionic acid methyl ester is a colorless liquid at room temperature with a boiling point of 154°C and a molecular weight of 98.14 g/mol.</p>

<p>Morpholin-4-yl-acetic acid is a water-soluble drug that has been used for the treatment of infectious diseases, such as hepatitis and malaria. It can be detected using a number of analytical methods, including gas chromatography, mass spectroscopy, and nuclear magnetic resonance. Morpholin-4-yl-acetic acid has also been used in the treatment of autoimmune diseases and cancer. It is a pharmacological agent with a variety of biological effects, including antiinflammatory activities. Morpholin-4-yl-acetic acid binds to protein kinase C (PKC) receptors and inhibits the activity of PKC enzymes by interfering with their ability to bind to phospholipids on the outside of cells. This binding prevents the formation of an enzyme complex with the cell membrane that is required for signal transduction pathways. Morpholin-4-yl-acetic acid also has hydroxyl group that can react with inorganic acids to form salts or esters.</p>

<p>Ethyl 1,2-dimethyl-5-hydroxyindole-3-carboxylate (EDMC) is an implantable drug that is used to treat hypertension. It is a diuretic that can be taken orally or injected. EDMC works by reducing the amount of urea nitrogen in the blood and increasing the amount of chlorine atom in the urine. This leads to an increase in active substances such as malonic acid and a decrease in arthropoda. EDMC has been shown to have antihypertensive activity due to its ability to lower diastolic and systolic pressure. The molecule also contains hydroxyl group and aldehyde groups that are analyzed by analytical chemistry.</p>

<p>1-Benzylindole-3-carboxylic acid is a bioactive molecule that has been shown to inhibit the activity of histamine, which is a neurotransmitter involved in inflammatory reactions. 1-Benzylindole-3-carboxylic acid has an affinity ligand for binding to the H1 receptor and can be used as an antihistaminic agent. It also has antihistaminic effects by inhibiting the release of histamine from mast cells and basophils, which are two types of white blood cells that are involved in allergic reactions. The pharmacophore model for 1-benzylindole-3-carboxylic acid suggests that it could be used as an antihistamine or anticholinergic.</p>

<p>3-Aminopicolinic acid is a carboxylate that can be found in the cytosol, mitochondria, and nucleus of cells. It is an efficient method for the synthesis of picolinic acid from 3-aminopyridine-2-carboxylic acid. The synthesis of picolinic acid has been shown to have structural analogs to molecules involved in nucleotide metabolism such as single-stranded DNA, mitochondrial DNA, and mitochondrial RNA. 3-Aminopicolinic acid has been shown to increase renal blood flow by stabilizing complexes with chloride and phosphoenolpyruvate. This compound also enhances the renal excretion of picolinic acid. 3-Desacetylcefotaxime potassium Tilmicosin Gatifloxacin 3-Aminopicolinic acid</p>

<p>(S)-(+)-2,2-Dimethylcyclopropanecarboxylic acid is an organic compound with a chiral center. It can be isolated from natural sources or synthesized in the laboratory. This compound has been used as a solvent and reaction system for organic reactions. (S)-(+)-2,2-Dimethylcyclopropanecarboxylic acid is also a carboxylate that can be hydrolyzed by esterases to form the corresponding alcohol and carboxylic acid. It is hydrophobic and lipophilic, which makes it useful in isolating compounds from reaction solution. (S)-(+)-2,2-Dimethylcyclopropanecarboxylic acid has been shown to have enzyme specificity for lipases and cilastatin.br&gt; br&gt;</p>

Please enquire for more information about 4-(4-Bromophenyl)piperazine-1-carboxylic acid tert-butyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>Please enquire for more information about Methyl 1,5-dimethyl-1H-indole-2-carboxylate 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 1-N-Boc-pyrrolidine-3-(S)-methylcarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>E-Hexen-1-ylboronic acid is a reactive, boron-containing compound that can be used for Suzuki coupling reactions and metathesis reactions. It is also useful in the analysis of organic compounds, due to its ability to form brightly coloured complexes with metal ions. E-Hexen-1-ylboronic acid has been shown to react with chloride, reoxidant and hexane. This compound can be used as an analytical reagent for the detection of stereoselectively in a stepwise reaction. E-Hexen-1-ylboronic acid forms crystals x-ray diffraction patterns that are characteristic of a chair conformation.</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>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>(±)-3-Methyl-2-oxovaleric acid is a fatty acid that is found in the mitochondria of liver cells and other tissues. It is an intermediate in the citric acid cycle and can be converted into acetyl-CoA, which is used for energy production. (±)-3-Methyl-2-oxovaleric acid has been shown to cause necrotic cell death when it binds to the mitochondrial membrane potential and causes a loss of ATP production. This results in a lack of energy for the cell, leading to cell death. (±)-3-Methyl-2-oxovaleric acid has also been shown to inhibit protein synthesis by decreasing uptake and increasing creatine kinase activity. This inhibition leads to decreased body formation and tissue culture growth in vitro. In vivo, (±)-3-Methyl-2-oxovaleric acid causes primary sclerosing cholangitis, a disease characterized by inflammation of bile ducts that</p>

<p>Please enquire for more information about (3a,5b,7a,12a)-3-Amino-7,12-dihydroxycholan-24-oic acidmethylester 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>Please enquire for more information about 2-Methyl-3-(2-methyl-1H-imidazol-1-yl)propanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-(Aminomethyl)-2-furoic acid hydrochloride is a molecule that belongs to the group of carboxylates. It has a molecular weight of 191.2 g/mol and a chemical formula of CHNO. The structure of 5-(aminomethyl)-2-furoic acid hydrochloride is similar to that of hexamethylenetetramine, a common organic compound with the formula (CH)N(H)CH. 5-(Aminomethyl)-2-furoic acid hydrochloride can be used as an acceptor in hydrogen chloride gas generation reactions, which are used in the synthesis of some pharmaceutical drugs and other organic compounds. The molecule also has potential use in telomerase research because it is structurally similar to natural telomeres. In addition, this molecule has been shown to have anti-inflammatory properties due to its ability to inhibit prostaglandin synthesis.</p>

<p>7-Phenylacetamide-3-chloromethyl-3-cephem-4-carboxylic acid diphenylmethyl ester is an organic solution that is used in the detoxification of chemical substances. It has a hydroxyl group and is soluble in nonpolar solvents. 7PAMC has been shown to be effective against bone lesions caused by acylation reactions. This drug also binds to the enzyme called cytochrome P450, which is involved in the metabolism of many drugs. It also inhibits bacterial growth by binding to DNA gyrase and topoisomerase IV, enzymes that maintain bacterial DNA integrity. The particle size of this drug is small, with a diameter of less than 10 microns. 7PAMC has a viscosity of 1 cps at 25°C and a melting point of 129°C.</p>

<p>Please enquire for more information about 6-Chloro-1-methyl-1H-indole-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Alisol B is a natural compound that has been shown to have significant cytotoxicity in vitro. Alisol B also inhibits the mitochondrial membrane potential, which is vital for cell survival. Alisol B is found to be active against several human cancer cell lines, including leukemia and breast cancer cells. It has also been shown to inhibit autophagy, the process by which cells degrade their own components and organelles in response to starvation or other stresses. This inhibition of autophagy leads to increased cell death. The anti-cancer effects of Alisol B are mediated through a number of different mechanisms, including the inhibition of protein synthesis and the induction of apoptosis. Alisol B has also been shown to have hepatoprotective properties in animal models.</p>

<p>Please enquire for more information about tert-Butyl 4-hydroxy-1-oxa-9-azaspiro[5.5]undecane-9-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ethyl 5-acetoxy-6-bromo-2-(bromomethyl)-1-methyl-1H-indole-3-carboxylate is a chemical compound that has been shown to have anti viral activity in vitro. The structure of the compound suggests that it may inhibit the production of inflammatory cytokines. This drug inhibits the activity of enzymes such as hydroxylases and lipases, which are important for the inflammatory process. Ethyl 5-acetoxy-6-bromo-2-(bromomethyl)-1-methyl-1H-indole-3 carboxylate may be an effective treatment for bowel disease and other inflammatory conditions.</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 (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>3,3-Difluoropentanedioic Acid is a reagent that is used in organic chemistry. It can be hydrolyzed to give 3,3-difluoro-1,2-propanediol. This chemical reacts with dithianes to give 1,2-dithiane and quantitatively produces 3-fluoro-1,2-propanediol. It is an ester of 3,3-difluoropentanedioic acid and has been shown to have antiinflammatory properties in rats.</p>

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

<p>Methyl chlorooxoacetate is an oxalyl ester that has been used for the synthesis of glycol esters. Methyl chlorooxoacetate has been shown to have a high solubility in water and organic solvents, which is desirable for industrial processes. This molecule also has the ability to be acylated with various organic groups and can act as a process-optimization agent in plant physiology. Methyl chlorooxoacetate binds as a receptor to growth factors and HIV infection, which leads to amide formation and carbonyl group formation.</p>

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

<p>2-Phenylisobutyric acid is a colorless to white crystalline solid with a molecular weight of 218.29 g/mol and a melting point of 120-122 °C. It is soluble in water, but not in alcohol or ether. 2-Phenylisobutyric acid is used as an intermediate for pharmaceutical preparations and as a reagent for organic synthesis. It is also used to produce thiomorpholine, which has been shown to have anti-inflammatory properties and can be used in the treatment of bowel disease. Thiomorpholine reacts with acylation agents such as phosphorus pentachloride to form esters that are useful pharmaceuticals, including corticosteroids. 2-Phenylisobutyric acid has been shown to inhibit insulin resistance by reacting with reactive sites on the insulin receptor, thus preventing the binding of insulin molecules to their receptors on cells.</p>

A labelled form of the oxalacetic acid (FO12113).

<p>(R)-(-)-a-[[(4-Ethyl-2,3-dioxo-1-piperazinyl)carbonyl]amino]benzeneacetic Acid is an inhibitor of the enzyme histamine N-methyltransferase (HNMT), which is responsible for the synthesis of histamine. The inhibition of HNMT leads to a decrease in histamine levels and therefore has been used as a treatment for chronic prostatitis, lacrimal gland, and energy efficiency. Histamine N-methyltransferase also participates in the regulation of apoptosis by methylating proapoptotic proteins like Bax, so inhibition can lead to an increase in apoptosis. This chemical is also able to bind with chloride ions and form diphenyl ethers through a reaction solution, which are known to have anticancer properties.</p>

<p>Cyclobutanecarboxylic acid chloride is an acyl halide that is a reactive chemical intermediate. Cyclobutanecarboxylic acid chloride reacts with naphthalene to produce cyclobutane, which can undergo a Friedel-Crafts reaction to form a benzene ring. The compound also has been shown to inhibit the growth of human cervical carcinoma cells by inhibiting the production of growth factors and interferon, as well as by inducing apoptosis. Cyclobutanecarboxylic acid chloride has been used in the treatment of infectious diseases such as tuberculosis, leprosy, and malaria. This drug was originally synthesized for use as a protein inhibitor, but it has not been found to be active in this application.</p>

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<p>(R)-2-Chloromandelic acid is an organic compound with the formula CHClCOH. It is a mandelonitrile, which is a benzene ring fused to a nitrile. It has an optimal reaction at acidic pH and in organic solvents and is enantiopure. The cell lysis of Escherichia coli can be achieved by this compound, as seen through the use of acid dehydrogenase. (R)-2-Chloromandelic acid has been shown to inhibit platelet aggregation, making it an antiplatelet agent. This product can be synthesized using methods such as the enantioselective synthesis of clopidogrel or the asymmetric synthesis of D-mandelic acid methyl ester. The isolated yield for (R)-2-Chloromandelic acid is about 45%.</p>

<p>Fmoc-trans-4-(aminomethyl)cyclohexane-1-carboxylic acid is a synthetic amino acid that has been shown in vitro to inhibit the growth of prostate cancer cells. It is an analog of butyric acid, a naturally occurring fatty acid. Fmoc-trans-4-(aminomethyl)cyclohexane-1-carboxylic acid has been synthesized by solid phase methods and labeled with radiotracers such as indium 111 or technetium 99m. The use of Fmoc-trans-4-(aminomethyl)cyclohexane-1-carboxylic acid in vivo is limited by its short circulating half life, rapid metabolism, and high toxicity.</p>

<p>Methyl 4-methylthiazole-5-carboxylate (MTMC) is a compound with high chemical and biological activity. MTMC has been shown to inhibit the growth of S. aureus, and also exhibits cytotoxic effects on human cancer A549 cells in vitro. MTMC has been shown to be active against HIV in cell culture and also inhibits the replication of influenza virus. MTMC has significant activity against cancer, and is also effective against immunodeficiencies that are due to viral infection. It can be synthesized by a high-yielding process involving the reaction of methyl 4-nitrobenzoate with thiourea in an organic solvent under reflux conditions. The crystal structure of MTMC was determined by X-ray diffraction methods, revealing that it is centrosymmetric with four molecules present in the asymmetric unit.</p>

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<p>4-(Trifluoromethoxy)phenylboronic acid is a boron-containing compound that has been shown to be a potent inhibitor of the histone deacetylase (HDAC) enzyme. It also has surfactant properties and can be used as a photochemical reagent. 4-(Trifluoromethoxy)phenylboronic acid is orally bioavailable and may have therapeutic potential for neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease, and Huntington's disease. It also has the ability to inhibit cancer cell growth by inhibiting HDAC activity. This drug has been found to cross-couple with organosilicon compounds in order to form new compounds with potent inhibitory activity against HDAC enzymes.</p>

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Butyl acetate is a reactive solvent that has been used in wastewater treatment. It has also been proposed as an analytical method for the determination of the concentration of butyl ester in mixtures. In this technique, a constant pressure is maintained until the butyl ester is released from the sample matrix and enters into a gas phase. The gas phase is then drawn into a solid-phase microextraction (SPME) fiber and analyzed by gas chromatography/mass spectrometry. Butyl acetate has limited solubility in water, which limits its practical use as a solvent. However, it can be mixed with other solvents such as ethanoate or n-butyl acetate to produce solutions that are more easily soluble in water. The structural analysis of butyl acetate was carried out using infrared spectroscopy and nuclear magnetic resonance (NMR).

<p>9-Bromononanoic acid is a conjugate of a brominated fatty acid. It is used in the chemical ionization process to produce ions for mass spectrometry analysis. 9-Bromononanoic acid has an inhibitory effect on the growth of bacteria and was shown to be effective against bacterial cell division by inhibiting the synthesis of proteins vital for cell division. 9-Bromononanoic acid also inhibits the production of fatty acids, which may be due to its ability to bind to fatty acids and form esters with them.</p>

Fmoc-2,2,6,6-tetramethylpiperidine-N-oxyl-4-amino-4-carboxylic acid (FMOC) is a highly reactive nitroxide that reacts with oxygen to form superoxide radicals. FMOC has been used to study the effects of radiation on proteins and peptides. It can be synthesized by reacting an amino acid with the reagent N-(3-(dimethylamino)propyl)-N'-methylcarbodiimide hydrochloride (EDC). The product then reacts with 4-(2,2,6,6,-tetramethylpyridinium) perchlorate in acetonitrile to create a fluorescent compound. When FMOC is labeled with a heavy metal such as gadolinium or manganese it becomes paramagnetic and can be detected using magnetic resonance imaging (MRI). FMOC also binds to the sarcoplasmic reticulum