Carboxylic Acids

<p>Please enquire for more information about Ethyl 3-(difluoromethyl)-1H-pyrazole-5-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Aminoguanidine is a selective inhibitor of the enzyme succinic dehydrogenase, which catalyzes the conversion of succinic acid to fumarate. Aminoguanidine is used in the treatment of diabetic complications and other conditions that result from high levels of blood glucose in order to lower the levels of blood sugar. The drug is administered orally or intravenously as aminoguanidine hydrochloride, which is converted to aminoguanidine in the body. Aminoguanidine can also be synthesized by reacting succinic anhydride with guanidine hydrochloride in a regioselective reaction. This synthesis yields quantitatively aminoguanidine, with little or no formation of guanidine. The product can be purified by washing with alkali and recrystallizing it from water. X-ray diffraction studies have shown that aminoguanidine hydrochloride exists as zwitterions in solution at physiological pH values.</p>

<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>Please enquire for more information about tert-Butyl azetidine-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Dehydrotumulosic acid is a natural product that has been shown to inhibit the activity of P-glycoprotein (P-gp) in vitro. It also inhibits tumor growth and metastasis by inducing apoptosis in HL60 cells, as well as inhibiting the proliferation of human leukemia cells. Dehydrotumulosic acid is not toxic to normal cells because it does not induce apoptosis in these cells. The effect on tumor cell proliferation was found with an acetate extract of dehydrotumulosic acid and matrix effects were observed by use of poria, which may lead to a more accurate analytical method. Pharmacokinetic studies have been done with dehydrotumulosic acid, but no toxicity or adverse effects have been reported for this drug. This compound is being investigated for its potential use in cancer therapy and treatment.</p>

<p>Please enquire for more information about 6-Deschloro-4-chloro cyproterone acetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ethyl 4-chloroacetoacetate is a chiral organic compound that is synthesized by the asymmetric synthesis of ethyl chloroacetate. This reaction is performed in an organic solution, using sodium salts as the solvent. The expression plasmid and logarithmic growth phase are needed for the enzyme catalysis and stereoselective reactions. The reaction solution is recombined with hydrochloric acid and chiral compound to produce high yields of ethyl 4-chloroacetoacetate.</p>

<p>Please enquire for more information about Ethyl 1-benzyl-3-(4-bromophenyl)-1H-pyrazole-5-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Methylnicotinic acid methyl ester is a synthetic chemical compound that belongs to the isomer family. It has been used in the synthesis of cocaine and isomers, as well as in the modification of drugs. 2-Methylnicotinic acid methyl ester can be synthesised from 2-methylpyridine and formaldehyde via the method of methylmagnesium iodide. 2-Methylnicotinic acid methyl ester has been shown to be a potent inhibitor of human platelet aggregation, which may be due to its structural similarity to nicotine.</p>

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

<p>2-Ketobutyric acid is a chemical compound that is an intermediate in the metabolism of amino acids. It can be synthesized from malic acid and glutamic acid by asymmetric synthesis. 2-Ketobutyric acid inhibits the production of ATP, leading to metabolic inhibition. Sprague-Dawley rats were used to prove this theory. 2-Ketobutyric acid has also been shown to inhibit insulin resistance and cell culture. Hydrogen bonds between 2-ketobutyric acid and the enzyme glutamate dehydrogenase are thought to be responsible for this effect on glucose uptake and conversion into energy.</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>

<p>Z-alpha-aminoisobutyric acid is an amide with a conformational pattern that resembles the alpha-helix. It has been shown to inhibit the formation of oligomers, which are aggregates of peptides and proteins, in the gas phase. Z-alpha-aminoisobutyric acid also stabilizes peptides and proteins in aqueous solution by preventing them from forming intramolecular hydrogen bonds. The infrared spectroscopy shows that z-alpha-aminoisobutyric acid is a conformer with a dihedral angle of about 120 degrees.</p>

<p>Please enquire for more information about (2S)-2-(1H-Tetrazol-1-yl)propanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

Ziconotide acetate is a polymer conjugate of ziconotide and goserelin acetate. It is used to treat severe chronic pain in patients who have not responded to other treatments, such as opioids or local anesthetics. Ziconotide acetate is administered by injection into the intrathecal space, where it acts on nerve cells in the dorsal horn of the spinal cord. The drug is slowly released from the polymer conjugate over time, which effectively reduces its irritant effects. It also has low solubility in water, which helps reduce its rate of clearance from the body. The active substances in this drug are ziconotide and goserelin acetate, both of which have been shown to be effective for treating chronic pain. Ziconotide acetate has also been shown to cause a decrease in blood levels of cholesterol and lipoproteins, although this effect may be due to goserelin acetate rather than ziconotide itself.

<p>1-Methyl-1H-benzimidazole-2-carboxylic acid is a synthetic compound that can be used as an antiprotozoal. It has been shown to have good activity against intestinalis, vaginalis, and intestinalis species. 1-Methyl-1H-benzimidazole-2-carboxylic acid binds to the acetyl groups of the parasite's cell membrane and inhibits the formation of the cytoplasmic membrane. This prevents the parasite from synthesizing ATP, which causes them to die. 1-Methyl-1H-benzimidazole-2-carboxylic acid also has strong activity against Giardia lamblia, which is caused by its ability to inhibit protein synthesis in this organism.</p>

<p>Methyl 2-cyclohexyl-2-hydroxyphenylacetate is a c6 alkyl and diode. It is an orally active hormone with potential use in catalysis of additives, as well as in the treatment of metabolic disorders. Methyl 2-cyclohexyl-2-hydroxyphenylacetate has been shown to have anticholinergic properties, which may be due to its ability to inhibit acetylcholine release from nerve endings. Lectins are proteins found on the surface of cells that bind to specific sugars and play a role in many biological processes. A lectin that binds to erythrocytes can be used as a marker for damaged red blood cells. Methyl 2-cyclohexyl-2-hydroxyphenylacetate has been shown to react with this lectin in plasma samples from humans, indicating that it is metabolized by enzymes present in red blood cells.</p>

<p>Please enquire for more information about Dimethyl 1-[2-(1H-indol-3-yl)ethyl]-2,5-dimethyl-1H-pyrrole-3,4-dicarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Gamma-oxo-3-pyridinebutyric acid (GOBA) is a non-protein amino acid that has been shown to be involved in the development of cancer. GOBA was found to be present in urine samples from patients with liver cancer and breast cancer, as well as in healthy individuals. GOBA is also present in rat liver microsomes and human liver, where it is converted into gamma-aminobutyric acid (GABA). This conversion may be due to GOBA's hydroxy group that can be oxidized by cytochrome P450 enzymes. The biological activity of GOBA appears to depend on its carboxyl group, which can form a complex with molybdenum. This complex inhibits the activity of the protein polymerase chain reaction, leading to a decrease in transcriptional regulation. In animal experiments, GOBA has been shown to inhibit tumor growth and induce cell cycle arrest by inhibiting the expression of cyclin D1 at the</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>Please enquire for more information about 4-[(4-Acetylphenyl)amino]-4-oxobutanoic 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 Boc-4-(4-fluorophenyl)-piperidine-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>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>

<p>3,4-Dimethylbenzoic acid is a benzoate compound that is produced by bacteria. It has been shown to have a viscosity of 0.05 cP at 25°C and a melting point of 181°C. It also has the molecular formula C9H11O2, which consists of two carbons, 11 hydrogens, and one oxygen atom. 3,4-Dimethylbenzoic acid is found in urine samples as a metabolite of p-hydroxybenzoic acid (p-OHBA). This compound also has photochemical properties and can be used for analytical determination of urinary p-OHBA levels. 3,4-Dimethylbenzoic acid is not active against bacterial pathogens such as Staphylococcus aureus or Salmonella enterica serovar Typhimurium. However, it does show some activity against Pseudomonas aeruginosa and Escherichia coli.</p>

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

<p>Methyl (1R,2S,3S)-8-(3-Fluoropropyl)-3-(4-Iodophenyl)-8-Azabicyclo[3.2.1]Octane-2-Carboxylate is a potent dopamine receptor agonist with a high affinity for the D2 and D3 receptors in the brain. It has been shown to have antiparkinsonian effects in animal models of Parkinson's disease by increasing dopamine levels in the prefrontal cortex and striatum. This drug has also been shown to be effective in clinical studies for the diagnosis of Parkinson's disease. Methyl (1R,2S,3S)-8-(3-Fluoropropyl)-3-(4-Iodophenyl)-8-Azabicyclo[3.2.1]Octane-2-Carboxylate binds to both dopamine and serotonin receptors, which may account for its therapeutic effects on Parkinson</p>

<p>Please enquire for more information about 2-(1-(tert-Butoxycarbonyl)azetidin-3-yl)acetic acid 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>Please enquire for more information about 1-(4-Bromophenyl)-3-phenyl-1H-pyrazole-5-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 (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>Phenylphosphonic acid is an inorganic compound that belongs to the group of phosphonic acids. It is used as a model system for reactions involving zirconium oxide, pyrazole ring, and p-nitrophenyl phosphate. Phenylphosphonic acid has been shown to be able to efficiently react with metal hydroxides under acidic conditions. The rate of this reaction increases with increasing concentration of the metal hydroxide and decreasing pH. This reaction also produces picolinic acid, which can be detected by its yellow color. Phenylphosphonic acid has been shown to have covalent linkages between nitrogen atoms and phosphorus atoms. X-ray crystal structures have revealed that the molecule has a linear structure with the nitrogen atom located on one side of the molecule and the phosphorus atom on the other side. It also contains two electron pairs at its center, which are responsible for its electrochemical properties.</p>

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

<p>Piperazine-2-carboxylic acid methyl ester (PPCM) is a chemical compound that is used as an intermediate in the production of ethylenediamine and piperazine-2-carboxylic acid dihydrochloride. It is a white crystalline solid that can be synthesized by reacting ethylene diamine with piperazine-2-carboxylic acid. PPCM has been shown to inhibit the growth of bacteria, yeast, and fungi by inhibiting protein synthesis. This chemical also inhibits the production of proteins essential for respiration and cell wall formation.</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>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>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>2-Bromoisonicotinic acid is a phenylpyridine molecule that has been shown to have inhibitory activity against the NF-κB pathway, which regulates inflammatory responses. This compound inhibits the production of TNF-α triggered by lipopolysaccharide (LPS) in vitro and in vivo. 2-Bromoisonicotinic acid may be synthesized from commercially available starting materials and can be easily scaled up for large-scale synthesis. The properties of this molecule make it an excellent candidate for further investigation as a potential therapeutic or prophylactic agent for diseases involving inflammation.</p>

<p>Please enquire for more information about 1-Cyclohexyl-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 7,7-Azo-3-a,12-a-dihydroxytaurocholanic acid sodium salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Trifluoro acetic anhydride is a chemical compound that is used in the laboratory as a model system to study antimicrobial agents and the reaction mechanism of these compounds. It has been shown to have receptor activity against infectious diseases and enzyme activities against bacterial growth. Trifluoroacetic anhydride has also been shown to inhibit plasma mass spectrometry, which may be due to its ability to react with water vapor. The chemical inhibitor can be recovered and reused for other experiments.</p>

<p>Please enquire for more information about Methyl 3-bromoindole-6-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 1-aminocyclohexanecarboxylate hydrochloride 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 4-(4-Oxopiperidine-1-carbonyl)phenylboronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>5-Octanoylsalicylic acid is an anti-inflammatory and antioxidant agent that has been shown to have skin-conditioning properties. It has been found to be effective in the treatment of skin diseases, such as erythema, scaling, and itching, due to its ability to inhibit tyrosinase activity. 5-Octanoylsalicylic acid has also been shown to increase cellular proliferation and lymphocyte transformation in vitro. This compound is a precursor of all-trans-retinoic acid (a form of vitamin A), which is used for the treatment of acne. 5-Octanoylsalicylic acid can be synthesized from methyl ethyl ketone and potassium dichromate by a Friedel-Crafts reaction. It is also found in fruits such as apples, bananas, peaches, and oranges. Animal studies have shown that chronic oral administration may lead to a decrease in dehydroascorbic acid levels and an increased risk</p>

<p>AG 1-X2 ion exchange resin 200-400 acetate is a resin for strong anion exchange.   Use this chloride-form resin for gravity or low-pressure chromatography.MW limit: ca 2700Wet density : ≤ 0.74 g/mL</p>

<p>Please enquire for more information about Methyl 4-methoxy-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>DL-3-Aminobutyric acid is a natural compound that belongs to the group of amino acids. It is found in human immunoglobulin, enzymes, and proteins. DL-3-Aminobutyric acid has been shown to have an effect on iron homeostasis, signal pathways, and water permeability. It has also been shown to have anti-fungal activity in vitro and can be used as a model system for plant physiology.</p>

<p>2,1,3-Benzoxadiazole-5-carboxylic acid is a functional theory that is an agonist of the opioid receptors. It is also a quaternary ammonium salt that has been shown to cause respiratory depression and death in mice. This drug is used as an anion in pentobarbital sodium, which has been linked to overdoses. 2,1,3-Benzoxadiazole-5-carboxylic acid can be activated by membrane proteins and other agents to increase its energy efficiency. It can also enhance the effect of molecules such as coulombic forces and depression.</p>

<p>Please enquire for more information about 2-(4-Bromophenyl)succinic 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 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 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>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>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 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>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>4-(Benzyloxy)butanoic acid, also known as 4-BABA, is an organic compound that is a white solid. It has a molecular weight of 128.11 and it can be found in the form of its chloride salt. The compound is used in analytical chemistry and has been shown to have potential use in analytical methods. 4-BABA can be synthesized from 2-hydroxyphenylacetic acid which is obtained through alkylation with benzyl bromide. This reaction yields a molecule with one more carbon atom than the starting material, which is called an epoxide. The epoxide reacts with chloride to produce the desired product along with a molecule of hydrogen chloride gas. The process requires catalysts such as palladium(II) acetate and triethylamine or platinum(IV) oxide and triethylamine. 4-(Benzyloxy)butanoic acid has two functional groups: an alcohol group (-OH) and an ether</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>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>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>

<p>Please enquire for more information about Fmoc-(4-aminomethyl) benzoic acid 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>

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Please enquire for more information about Dimethylaminoacetic acid hydrazide dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>4-(Hydroxymethyl)phenylboronic acid is an organic compound that has been identified as a reactive, fatty acid. It has shown antibacterial efficacy against gram-positive and gram-negative bacteria in the presence of nanogels. 4-(Hydroxymethyl)phenylboronic acid is also a cross-linking agent that can be used to form hydrogels for tissue engineering applications. This chemical is being studied as a potential treatment for inflammatory bowel disease and diabetes mellitus. 4-(Hydroxymethyl)phenylboronic acid has been shown to have anti-cancer properties by inhibiting the proliferation of cancer cells and inducing apoptosis. The molecule also undergoes structural analysis using confocal microscopy.</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 4-(2-Chlorophenyl)-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-2-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 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>(S)-2-Acetoxy-propionic acid is a hexyl, enantiopure, and biologically active chemical. It is a pheromone that is secreted by the streptomycetaceae bacterium as part of its mating process. It has been shown to have an inhibitory effect on stingless bees, which are native to Central America and South America. (S)-2-Acetoxy-propionic acid has been found in the mandibular glands of these bees and is believed to play a role in their behavior. This chemical can be synthesized from propionic acid and acetaldehyde or from lactic acid and acetaldehyde. It is also possible to produce it from 2-bromopropanoic acid through the tripropionate pathway. The chemical was first isolated in 1957 by Takaichi Yamashita, who named it for its ability to inhibit bee stings when applied externally. (S)-2-Acetoxy</p>

<p>Please enquire for more information about 1-(4-Fluorophenyl)-5-methyl-1H-pyrazole-4-carboxylic acid 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)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>

<p>Cobalt(II) acetate tetrahydrate is a model system that can be used to study the structures of coordination complexes. The cobalt ion has a coordination geometry with two water molecules, two oxygen atoms from the acetate anion, and one proton from the hydroxide anion. The crystal structure is composed of six-membered rings of alternating metal ions and oxygen atoms. The reaction solution contains excess sodium hydroxide and water vapor. It was determined that cobalt(II) acetate tetrahydrate reacts electrochemically at low frequencies as well as with 5-hmf, an oxidizing agent, in the presence of sodium citrate as an oxidation catalyst.</p>

<p>Methyl trichloroacetate (MTCA) is a reactive chemical that is used as an intermediate in the synthesis of various organic compounds. It has been shown to react with nucleophiles, such as hydroxyl groups, to form a copper complex. MTCA has also been found to produce light emission when exposed to air and aryl halides. The synthesis of MTCA involves treating 1-chloro-2-propanol with hydrogen fluoride in the presence of an acid catalyst. The chemical can be detected by gas chromatography or liquid chromatography, but it is not readily available on the market.</p>

<p>Ferroceneacetic acid is a compound that has been shown to have chemiluminescent properties. It is a potent reductant and oxidant, which means that it can reduce or oxidize other compounds. Ferroceneacetic acid is also an active enzyme, and its redox potential changes depending on the concentration of ferrocene in the solution. Ferroceneacetic acid can be used as a model system for analytical chemistry and electrochemistry.</p>

<p>Please enquire for more information about 2-Methyl-3-(4-methyl-1H-pyrazol-1-yl)propanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(-)-trans-1,2-Cyclohexanedicarboxylic Anhydride is a macrocyclic molecule that can be used to synthesize glutaric anhydride. This compound is an analogue of the succinic anhydride and 1,2-cyclohexanedicarboxylic anhydride. (-)-trans-1,2-Cyclohexanedicarboxylic Anhydride has been shown to catalyze the hydrogenation of epoxides. It also has been shown to be a potential precursor for the synthesis of pyrrolizidine alkaloids.</p>

<p>Betamethasone 21-acetate is a potent corticosteroid that is effective in the treatment of inflammatory conditions, such as asthma and arthritis. It also helps to reduce the symptoms of inflammatory skin diseases, including atopic dermatitis, contact dermatitis, and psoriasis. Betamethasone 21-acetate is used to treat perinatal complications such as preterm labor and neonatal respiratory distress syndrome. This drug has been shown to have a low cardiac effect when administered at a low dose (1 mg/kg). The stability of betamethasone 21-acetate in blood samples is increased by adding benzalkonium chloride or trifluoroacetic acid. Betamethasone 21-acetate has been shown to be absorbed rapidly from the gastrointestinal tract and distributed widely throughout the body. It binds to plasma proteins and has a short elimination half-life of 1.5 hours.</p>

<p>3,6-Dichlorobenzo[b]thiophene-2-carboxylic acid is an extracellular metabolite that is involved in the metabolism of muscle. It is produced as a byproduct of the reaction catalyzed by dehydrogenase, which converts 3,6-dichlorobenzo[b]thiophene to 2-carboxybenzothiophene. This compound has been shown to inhibit the enzyme histidine carboxylate synthetase, which is involved in branched-chain amino acid synthesis. The enzyme can be inhibited by either a wild type or an analog of 3,6-dichlorobenzo[b]thiophene-2-carboxylic acid.</p>

<p>Valeric acid hydrazide (VAH) is a monoclonal antibody that binds to the receptor molecule. The binding of VAH to the receptor molecule leads to a change in the reaction mechanism and prevents the initiation of an immune response. This drug has been shown to have therapeutic properties in a number of autoimmune diseases, such as rheumatoid arthritis and multiple sclerosis, by blocking the production of TNF-α and other inflammatory cytokines. Valeric acid hydrazide also shows biological properties against cancerous cells. It inhibits the growth factor activity, which is believed to be responsible for tumor formation and growth. This agent may also inhibit angiogenesis by preventing endothelial cell proliferation and migration.</p>

<p>(E)-8-Methyl-6-nonenoic acid is a fatty acid that is found in the acetate extract of Capsicum annuum. It is an analog of the natural compound (E)-8-methyl-6-nonenal, which has been shown to have anticancer properties. The synthesis of this compound has been achieved using a novel approach based on enzymatic reactions and chemical transformations. This compound has been shown to have potential anticancer activity against human prostate cancer cells in vitro and to inhibit the growth of triticum aestivum seeds.</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>Please enquire for more information about Tetrakis[N-phthaloyl-(S)-phenylalaninato]dirhodium Ethyl Acetate Adduct 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 6-Bromo-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>Des-Gly10,D-Ala6,Pro-NHEt 9)-LHRH acetate salt Pyr-His-Trp-Ser-Tyr-D-Ala-Leu-Arg-Pro-NHEt acetate (DGPRP) is a drug that is used to treat endometriosis. It is an agonist of the LHRH receptor and inhibits body formation by preventing the release of gonadotropin hormones. DGPRP has been shown to inhibit cell proliferation in cancer tissues and may be useful for the treatment of leukemia. This drug has also been shown to be biocompatible with polymer scaffolds and can be synthesized using methods such as solid phase peptide synthesis.</p>

<p>D-Aspartic acid b tert-butyl ester (DATB) is an antimicrobial agent that has been shown to inhibit the growth of drug-resistant bacteria. DATB has been shown to be active against both gram-positive and gram-negative bacteria, with a selectivity for those with a peptidoglycan cell wall. DATB inhibits the synthesis of amide and peptide bonds and has been shown to have a wide range of uses in the production of antibiotics, such as carbamates and natural products.</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>Please enquire for more information about 1-[2-(Methoxycarbonyl)phenyl]-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>(5-Fluoro-2-methyl-1H-inden-3-yl)acetic acid (FMIAA) is a phase transfer catalyst that catalyses the condensation of alkyl esters. It can be used in the condensation of aromatic and aliphatic aldehydes in liquid phase with potassium as a reagent and organic solvent. The FMIAA is then removed by dehydrating the product, leaving it in solid form. FMIAA has been shown to be effective for the synthesis of a wide range of compounds, including pharmaceuticals such as cyclopentanone, aminomethylpiperidine, and 4-aminoquinoline.</p>

<p>Isoamyl acetate is a volatile, colorless liquid with the smell of bananas. Isoamyl acetate is found in many foods and drinks, such as banana, apple, pear, pineapple, and strawberry flavors. It has been shown that isoamyl acetate can inhibit the growth of resistant mutants of Escherichia coli by inhibiting their ability to synthesize proteins for locomotor activity. This inhibition may be due to the reaction mechanism that involves methyl ethyl alcohol (MEA). Methyl ethyl alcohol is involved in the production of isoamyl acetate. MEA reacts with 3-methyl-2-oxobutanoic acid (3M2B) to form 2-methyl-3-oxopropanoic acid (MOPA) and then reacts with ATP to form AMP and MOPP. The reaction between MOPP and ATP results in the conversion of MEA into isoamyl acetate.</p>

<p>Please enquire for more information about 3-(4-Methyl-1,4-diazepan-1-yl)propanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>12-Aminododecanoic acid is a fatty acid that is used in the manufacture of magnetic particles. It is synthesized by cationic polymerization of 4-tert-butylbenzoic acid and dodecanedioic acid. The process involves the use of water vapor to remove hydrochloric acid from the solution and form a salt, which then reacts with dodecanedioic acid to produce 12-aminododecanoic acid. This compound has been shown to have transport properties for nitrogen atoms and can be used in exfoliated materials such as nanometals. 12-Aminododecanoic acid has also been shown to exhibit redox activity due to its ability to react with hydrogen peroxide.</p>

<p>Please enquire for more information about 2,2,4-Trimethyl-1,2-dihydroquinolin-6-yl phenylacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl 2-methylpropanimidic acid hydrochloride is a neutralizing agent that can be used to react with water, acids, and bases. It has been shown to react with gaseous compounds at temperatures as high as 200°C. Methyl 2-methylpropanimidic acid hydrochloride is soluble in organic solvents such as alcohols, ethers, and acetone and can be used to prepare esters by reacting with the corresponding alcohol or phenol. In addition, it has been shown to interact with haloalkyl groups and oxazinones. This compound also has nod-like receptor binding properties that have been shown to play a role in mediating the transport of organic solutions into cells. A receptor protein that reacts with methyl 2-methylpropanimidic acid hydrochloride has been identified in some organisms. The stereostructure of this compound resembles that of triazines and other organometallic compounds.</p>

<p>Tricosafluorododecanoic Acid (TCDA) is a potent cytotoxic agent that has been shown to be effective in killing cancer cells. TCDA is a strong inducer of apoptosis and necrosis, which are processes that cause the death of cells. TCDA also induces cell cycle arrest by binding to mitochondrial membranes and inhibiting the flow of ions across the membrane, leading to a loss of mitochondrial membrane potential. This leads to an accumulation of intracellular calcium and activates signal pathways that activate the cell's death program. TCDA has been shown to have significant cytotoxicity against human breast cancer cells, with little toxicity against healthy human erythrocytes. TCDA is not active against bacteria or fungi, but it is highly toxic to certain protozoans such as Plasmodium falciparum. TCDA can be used as an effective treatment for cancer in combination with radiation therapy because it enhances the therapeutic effects of radiation on tum</p>

<p>2-[4-(2-Methylpropenyl)phenyl]propionic acid is an analgesic and antipyretic agent. It has been shown to have antiinflammatory properties, which are mediated through inhibition of prostaglandin synthesis. This agent binds to the enzyme cyclooxygenase and inhibits the biosynthesis of prostaglandins that are responsible for inflammation. 2-[4-(2-Methylpropenyl)phenyl]propionic acid also has optical antipyretic activity, which may be due to its ability to inhibit the release of prostaglandins from arachidonic acid in the hypothalamus. The optical antipyretic activity is most likely due to the enantiomers that this drug contains. 2-[4-(2-Methylpropenyl)phenyl]propionic acid has a pharmacologic profile that includes analgesic and antipyretic activities.END&gt;&gt;</p>

<p>Please enquire for more information about (S)-alpha-Ethyl-2-oxo-1-pyrrolidineacetic acid(R)-alpha-methylbenzenemethanaminesalt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Isopentylboronic acid is a boron-containing organic compound that is used for the catalysis of cross-coupling reactions, such as the Suzuki reaction. It reacts with aryl halides to form an alkylboronic ester and a metal salt. Isopentylboronic acid is also used to produce trimers in the presence of formyl or nitro groups. Isopentylboronic acid may also be used as a reagent to convert alcohols into chlorides or bromides. This compound has been shown to react with alkali metal ions on one side and alkyl substituents on the other side, leading to deuterium incorporation at the carbon atom adjacent to the carboxylic acid group. Isopentylboronic acid can also be used for dehydrating alcohols and converting alkynes into alkenes when heated in the presence of an alkali metal chloride.</p>