Carboxylic Acids

<p>Please enquire for more information about 17-Hydroxy-19-nor-17alpha-pregna-4,6-dien-20-yn-3-one acetate 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>Please enquire for more information about H-Gly-Phe-Gly-aldehyde semicarbazone acetate salt 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>Please enquire for more information about 3-Methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazole-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</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 3-(4-Chlorophenyl)-1-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>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>[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>L-Menthyl 2,2-dihydroxyacetate is a synthetic compound that belongs to the group of salicylic acid derivatives. It is an intermediate in the synthesis of other compounds and can be recycled. L-Menthyl 2,2-dihydroxyacetate reacts with primary amines to form iminoacetic esters and glyoxylates by acidic hydrolysis. The reaction time depends on the type of amine and the acidity of the solution. This compound has been used as a reagent to synthesize maleic anhydride from maleic acid. L-Menthyl 2,2-dihydroxyacetate is also used in methodologies for oxidizing aromatic compounds to produce benzoic acids or phenols.</p>

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

<p>Fluorometholone acetate is a fluorinated corticosteroid that is used in ophthalmology to treat eye disorders. It has been shown to reduce intraocular pressure in patients with glaucoma and other eye diseases. Fluorometholone acetate inhibits the activity of the glucocorticoid receptor, which prevents it from binding to DNA and altering gene expression. This leads to a decrease in inflammatory responses by decreasing the production of cytokines and chemokines that are involved in inflammation. Fluorometholone acetate also binds to other receptors, such as the mineralocorticoid receptor, which may lead to its use as a potential biomarker for infectious diseases.</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>Please enquire for more information about 4-Chloro-3,5-difluorobenzoic acid 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>Tetrahydro-1-naphthoic acid is a toxic chemical that is used in the synthesis of various organic compounds. It is an organic acid that has a pungent odor and can cause irritation of the nose and throat. When heated, it evolves toxic fumes of hydrogen chloride gas and phosgene. Tetrahydro-1-naphthoic acid reacts with metal hydroxides to form metal tetrahydro-1-naphthoates, which have useful properties as catalysts in organic reactions. Tetrahydro-1-naphthoic acid has been used as a growth regulator in plants and animals. It binds to DNA at the C–H site, preventing protein synthesis and cell division by inhibiting RNA synthesis.</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>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>Please enquire for more information about N-alpha-Trityl-Nbeta-Fmoc-L-2,3-diaminopropionic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>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>Please enquire for more information about 3,3-Difluoro-1-methylcyclobutanecarboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>L-Azetidine-2-carboxylic acid is a natural product that has been shown to have anticancer effects. It has been shown to induce apoptosis in cancer cells by binding to response elements on the DNA, which causes DNA damage and cell death. L-Azetidine-2-carboxylic acid also inhibits protein synthesis by interfering with the uptake of amino acids, which are essential for protein production. This compound is not toxic to healthy cells because it cannot cross the lipid bilayer of the cell membrane. L-Azetidine-2-carboxylic acid also induces autophagy in cancer cells, causing them to destroy their own cellular components. There is evidence that this compound may be effective for other diseases such as diabetes and neurodegenerative disorders due to its ability to regulate intracellular calcium levels and its cytosolic function as a substrate molecule.</p>

<p>Ribonucleic acid free acid (ribo-FAA) is a derivative of the immunosuppressive drug rapamycin. It is an immunosuppressant that inhibits the immune system by binding to a protein called FKBP12, which is involved in the activation of T cells and other immune system cells. Ribo-FAA has been shown to be effective in treating HIV patients undergoing active antiretroviral therapy, as well as for treatment of other infectious diseases such as tuberculosis or leishmaniasis. Ribo-FAA binds to FKBP12 and prevents it from activating T cells or other immune system cells, which leads to suppression of the immune response.</p>

<p>Please enquire for more information about Methyl 1,5-diphenyl-1H-pyrazole-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-(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>Please enquire for more information about 3-{[(3,4-Dichlorophenyl)amino]carbonyl}bicyclo[2.2.1]hept-5-ene-2-carboxylic 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>Please enquire for more information about 5a-Dihydrocortisol 21-acetate 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 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 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>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>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>N10-Methyl pteroic acid is a novel immunosuppressant that inhibits T-cell proliferation and promotes regression of inflammatory bowel disease. It has been shown to be effective in treating cancer patients, with the terminal half-life being approximately 20 hours. N10-Methyl pteroic acid is a potent inhibitor of human acute lymphoblastic leukemia cells. It can also be used as an immunosuppressant for organ transplantation, with desorption from gels using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI TOF MS) and bioanalytical methods such as high performance liquid chromatography (HPLC).</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>Hemokinin 1 is a protein that is encoded by the NK1R gene. It has been shown to be associated with insulin resistance, inflammatory diseases, and pain control. Hemokinin 1 is also a potential treatment for viral infections such as HIV and hepatitis C. Hemokinin 1 interacts with nicotinic acetylcholine receptors (nAChRs) in the brain and blood vessels, which leads to an increase in blood pressure. This protein also interacts with hematopoietic cells, which may be responsible for its function as an antinociceptive agent. Hemokinin 1 has been implicated in autoimmune diseases such as arthritis and atrial fibrillation. This protein is expressed mainly in the brain, liver, heart, kidneys and spleen.</p>

<p>Please enquire for more information about [(5-Methyl-4-phenyl-4H-1,2,4-triazol-3-yl)thio]acetic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>The 4-chloro-benzenesulfinic acid sodium salt is a type of sulfinic acid. It can be used to control experiments involving methides, halides, and human macrophages. Sodium salts of this compound have been shown to inhibit the growth of Candida glabrata and Galleria mellonella in vitro. The 4-chloro-benzenesulfinic acid sodium salt reacts with chloride ion to form a nucleophilic trifluoroacetate anion, which reacts with thiosulfonates to produce type strain. Trifluoroacetic acid is used as a solvent in the reaction.</p>

<p>Cyclopiazonic acid is a sesquiterpene lactone that inhibits the transcription activator-binding site in the promoter region of c-myc and c-jun. Cyclopiazonic acid also inhibits protein synthesis by preventing phosphorylation of dinucleotide phosphate, which leads to an increase in intracellular calcium levels. This compound also has a cytotoxic effect on HL60 cells, which may be due to its ability to inhibit the production of secretases. Cyclopiazonic acid's effects on pluripotent cells have not been well studied, but it is known to have pharmacological properties that are similar to other compounds that are being studied for their potential anti-cancer effects.</p>

<p>Please enquire for more information about 5-Chloro-2-(ethylsulfonyl)pyrimidine-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-(2,5-Dioxoimidazolidin-4-yl)propanoic acid (3DAP) is a histidine analog that belongs to the group of fatty acid derivatives. It has been shown to be effective in the diagnosis of obesity and provides a new approach for the treatment of obesity. 3DAP binds to organic anion transporters, which are proteins that transport organic anions across cell membranes. This binding inhibits the transport of organic anion substrates and leads to increased concentrations of these substrates in blood plasma. 3DAP is a competitive inhibitor against estrone sulfate, which is one of its major metabolites. 3DAP has shown efficacy in animal models for obesity, diabetes, and hepatic steatosis.</p>

<p>4b-Hydoxy cholesterol 4-acetate is a pleiotropic drug with a wide range of pharmacological activities. It is an inhibitor of the sirtuin family of proteins and may have anti-cancer effects. It has also been shown to be effective in the treatment of depression and myelodysplastic syndrome. The mechanism of action for this agent is not well understood, but it may be due to its ability to inhibit DNA methyltransferases, which would lead to a change in DNA methylation patterns. 4b-Hydroxy cholesterol 4-acetate has also been shown to decrease lipid levels in the blood and increase the activity of liver enzymes that metabolize fatty acids. This drug can also modify lamellar bodies and short-chain fatty acids by inhibiting the enzyme ATP citrate lyase, which catalyzes citrate cleavage into acetyl CoA and oxaloacetate.</p>

<p>3-(Methylsulfonyl)propanoic acid is a polynucleotide that is used in sequencing reactions. It has been shown to bind to the protein Smegmatis and increase the rate of the polymer composition. 3-(Methylsulfonyl)propanoic acid has also been shown to have a structural similarity with porins, which are proteins that form pores in cell membranes for ion transport. 3-methylsulfanylpropanoic acid binds to porins by coordinating geometry, allowing it to be transported into cells. The 6-Fluoro-3-indoxyl-beta-D-galactopyranoside is an antituberculosis drug that belongs to the class of rifamycins. Rifapentine inhibits bacterial growth by binding to DNA-dependent RNA polymerase, thereby preventing transcription and replication. The high frequency of human activity has been shown using a patch-clamp technique on human ery</p>

<p>(S)-1,2,3,4,5,6,7,8-Octahydro-1-[(4-methoxyphenyl)methyl]isoquinoline (acetate salt ) is a diphosphine that can be used as a catalyst to produce formic acid from methanol and carbon monoxide. This product is an enantiomer of picric acid and has been shown to be an effective additive in the crystallization of picric acid. The acetate salt is also optically pure.</p>

<p>N-Cbz-L-aspartic acid 1-benzyl ester is a synthetic stereoselective allyl group that can be used for biochemical studies. It has been shown to have a role in the repair of damaged DNA and cellular growth. N-Cbz-L-aspartic acid 1-benzyl ester is an adenosine diphosphate (ADP) analog, which acts as an acceptor of ADP and inhibits phosphatases.</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>Chloranilic acid is a thermally unstable compound that undergoes a number of reactions with the addition of heat. It reacts with nitrogen atoms to form amides, nitriles, and nitro compounds. Chloranilic acid also reacts with polymerases to form stable complexes. The proton at the center of the chloranilic acid molecule is lost when it forms an acid complex. This reaction occurs in aqueous solution as well as in biological systems, where it is used for hydrogen bonding interactions. The stable complexes that are formed by chloranilic acid have been shown to have biological properties such as antimicrobial activity, antiviral activity, and antifungal activity.</p>

<p>Phosphonooxy acetic acid is a product of the reaction between phosphoglycolate and oxygen. It is involved in photosynthesis and has been shown to have a physiological function in plants. Phosphonooxy acetic acid also has enzyme activities, including hydroxylase and phosphatase activities. The bacterial strain can affect the production of this compound, as well as the plant's physiological conditions. Epidermal growth factor (EGF) is an important protein that regulates cell proliferation and differentiation that has been found to be regulated by phosphonooxy acetic acid in vitro. In addition, structural analysis of this compound has revealed that it binds to transcriptional regulators such as activator protein 1 and nuclear factor-kappa B, which are important for autoimmune diseases. This chemical also has biochemical properties, including its optimum pH of 7.0 and x-ray diffraction data.</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 Ethyl5-acetyloxy-1,2-dimethylindole-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>All-cis-6,9,12,15-octadecatetraenoic acid is a polyunsaturated fatty acid that has been shown to have anti-inflammatory properties. It is found in the form of stearidonic acid and can be derived from plants such as flaxseed or soybeans. All-cis-6,9,12,15-octadecatetraenoic acid has been shown to inhibit the production of chemoattractant protein (MCP) in 3T3L1 preadipocytes by blocking the synthesis of arachidonic acid. This compound also inhibits the proliferation of MDA-MB 231 breast cancer cells and induces cell death via apoptosis.</p>

<p>2-Diethylaminoethyl 1-cyclohexylcyclohexane-1-carboxylate hydrochloride is a methyltransferase inhibitor that blocks the synthesis of monoethyl ether, which is used to synthesize dicyclomine. It has been shown to be effective in vitro against biological samples such as rat liver and blood cells. 2-Diethylaminoethyl 1-cyclohexylcyclohexane-1-carboxylate hydrochloride also has been shown to have a pharmacological effect on rats with bowel disease, congestive heart failure, and crystalline cellulose. The chemical structure of 2-Diethylaminoethyl 1-cyclohexylcyclohexane-1-carboxylate hydrochloride is similar to that of phosphorus pentoxide, which makes it difficult for this drug to cross the blood brain barrier.</p>

<p>Please enquire for more information about 6-(Methoxycarbonyl)spiro[3.3]heptane-2-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 6-Formylpyridine-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 2,4-dichloropyrimidine-6-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>Please enquire for more information about Methyl 6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>a functionalised glucoside</p>

<p>4-(Butylamino)benzoic acid is a non-steroidal anti-inflammatory drug (NSAID) that has been used to treat pain. It is a prodrug, which is metabolized in the liver to 4-(butylamino)-phenylacetic acid, its active form. The 4-(butylamino)benzoic acid molecule has a hydrophobic effect and binds to chloride ions. This binding inhibits the production of prostaglandins, which are mediators of pain. 4-(Butylamino)benzoic acid also reduces the activity of plasma cells that produce antibodies and increases the activity of lymphocytes and platelets, leading to an increase in immunoglobulin levels.</p>

<p>4,6-Diaminobenzene-1,3-dicarboxylic acid is an inorganic copper compound that is used as a copper salt. It has been shown to be effective as a chelating agent for the treatment of copper toxicity. 4,6-Diaminobenzene-1,3-dicarboxylic acid binds to metal ions and forms a complex with them. This complex can then be excreted from the body through urine or bile.</p>

<p>Sodium acetate trihydrate is a salt that is used in the production of sodium salts and surface methodology, as well as in analytical methods. It is also used to prepare anhydrous sodium. Sodium acetate trihydrate can be used as a cell lysis agent for water vapor.</p>

<p>Ganoderic acid S is a triterpenoid compound that has been shown to inhibit the growth of human cancer cells in vitro. It contains a carbonyl group and an hydroxyl group, which are reactive molecules that can form covalent bonds with proteins and other molecules. Ganoderic acid S also has anti-inflammatory properties and can inhibit the release of growth factors, such as monoclonal antibodies, from immune cells. In addition, it inhibits the production of mitochondrial enzymes, such as hydroxylases and oxidases, by binding to the heme moiety in their active site.<br>Ganoderic acid S is found in rhizoma gastrodiae (a type of mushroom), which has been used for centuries in traditional Chinese medicine to treat various conditions. The populations of mice given ganoderic acid S orally for three months showed increased life span and reduced tumor incidence.</p>

<p>4-Bromobenzenesulfonic acid is a chemical used in the synthesis of organic molecules. It is an intermediate in the production of cyclopropylboronic acid, which is used as a building block in various organic syntheses. 4-Bromobenzenesulfonic acid can be prepared by reacting pyridine with acetic anhydride and then adding sodium carbonate to remove water. This reaction produces a molecule with two acid groups that are nucleophilic and can react with carboxylic acids to form esters. The yield for this reaction is high and it does not require any special equipment or conditions. This chemical is also used as a linker for other compounds during synthesis reactions, such as diazonium salts or dioxane. 4-Bromobenzenesulfonic acid reacts with triethylphosphite to give disulfides, which are important for protein structure.</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 methyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Cyclopropylpropanoic acid is a synthetic derivative of oxalyl chloride. It has been shown to inhibit the growth of viruses, notably influenza A virus and human immunodeficiency virus (HIV), in cell culture. 3-Cyclopropylpropanoic acid also inhibits the g1 phase of the cell cycle. In addition, it has been shown to inhibit skin cancer and cardiovascular diseases in humans.</p>

<p>Please enquire for more information about tert-Butyl 3-(cyclopropylamino)azetidine-1-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>Tetrahydro-a-(1-naphthalenylmethyl)-2-furanpropanoic Acid 2-(Diethylamino)ethyl Ester is a fatty acid analog that has antimicrobial properties. It is used in the treatment of bone cancer, and can be used to diagnose and treat other diseases such as glomerular filtration rate, receptor binding, and malonic acid. Tetrahydro-a-(1-naphthalenylmethyl)-2-furanpropanoic Acid 2-(Diethylamino)ethyl Ester binds to receptors on cells, which leads to an increase in the amount of monoamine neurotransmitters released by the cells.</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>Trifluoroacetic acid is an organic acid that is used in the synthesis of esters, ethers, and amides. It can be used to produce 3,4,5-triacetoxybenzoic acid (TABA), which inhibits the proliferation of leukemia cells. TABA binds to the active site of the protein runx2, which is involved in development and differentiation. It also inhibits vibrational spectra and chemical profiles that are related to cancer cell growth. TABA has been shown to induce autophagy through activation of AMPK signaling pathways in leukemia cells. TABA also inhibits lipid accumulation by inhibiting the expression of genes such as SREBP1c and ACC2.</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 ACTH (2-24) (human, bovine, rat) trifluoroacetate salt 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>Boc-1-amino-1-cyclobutane carboxylic acid is a synthetic and potent agonist of the androgen receptor. It is an analog of apalutamide, which is a selective antagonist of the androgen receptor. Boc-1-amino-1-cyclobutane carboxylic acid has been shown to have high oral bioavailability, which makes it suitable for oral administration. Boc-1-amino-1-cyclobutane carboxylic acid has been shown to have increased functional activity in cancer cells, which may be due to its ability to inhibit the growth of tumor cells by binding to their androgen receptors. Boc-1-amino-1-cyclobutane carboxylic acid has also been found to have good affinity for the androgen receptor when tested on cultured cells.</p>

<p>Taraxeryl acetate is a fatty acid that is found in the extract of Curcuma aromatica (turmeric). It has been shown to inhibit cervical cancer cells in tissue culture. Taraxeryl acetate inhibits the growth of Streptococcus faecalis by binding to its ribosomal RNA and inhibiting protein synthesis. Toxicological studies on rats have shown that this compound does not have any harmful effects on physiological functions. This molecule has also been shown to be an inhibitor for protocatechuic acid, which is a chemical structure involved in the cycle analysis of curcuminoids. In addition, taraxeryl acetate has been used as an active ingredient in Chinese medicine preparations for the treatment of symptoms related to herpes simplex virus infections.</p>

<p>Fmoc-1-amino-4,7,10-trioxa-13-tridecanamine succinimic acid is a synthetic amide that is used as an intermediate in the synthesis of peptides. It has a conformational structure and can be labeled with dyes to study the structures of proteins or peptides. Fmoc-1-amino-4,7,10-trioxa-13-tridecanamine succinimic acid has been used as an immunogen in the preparation of monoclonal antibodies. It also can be conjugated to drugs or other compounds for use as bioconjugates. This compound has been shown to have enzymatic activity and can be used as a substrate for enzyme linked immunosorbent assays (ELISA). Trifluoroacetic acid is commonly used in the synthesis of this compound.</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>

<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>

<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>(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>2,3-Dibromopropanoic acid is a carcinogenic chemical that has been shown to cause liver tumors in rats. It is a nucleophile that reacts with amide groups to form an amide bond. The analytical method for 2,3-dibromopropanoic acid is gas chromatography with flame ionization detection. Its structural formula is CHBrCHBrCOH. It has a carbonyl group and acidic properties, as well as a chloride ion present on the molecule. 2,3-Dibromopropanoic acid is an anxiolytic drug that has been shown to have health effects such as drowsiness and headache.</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>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>Octyl 3-octyloxiraneoctanoic acid is a chloride compound that is used as a surfactant in the formulation of paints, lacquers, and coatings. Octyl 3-octyloxiraneoctanoic acid has been shown to be an effective emulsifier for water and oil based systems. It can also be used as a solvent for polyvinyl chloride. This compound reacts with water to form hydrogen chloride gas. The octadecyl group on the molecule is responsible for this property. Octyl 3-octyloxiraneoctanoic acid has been shown to react with boron nitride and cationic polymerization products, such as polylactic acid or polyethyleneimine. This reactive functional group allows it to be used in reactive coating applications, including powder coating and flame retardants.</p>

<p>3-Bromo-4-pyridinecarboxylic acid is a naphthyridine derivative that is used in drug development. It is a crystalline solid that can be dissolved in organic solvents. 3-Bromo-4-pyridinecarboxylic acid has been shown to have antiinflammatory properties and can be used as an oxidant. 3-Bromo-4-pyridinecarboxylic acid is being investigated as a receptor subtype for inflammatory diseases, and it has also been used to study the mechanism of chronic inflammatory diseases.</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>Polyoxyethylated 12-hydroxystearic acid is a surface active agent that is used as an adjuvant in pharmaceutical preparations. Polyoxyethylated 12-hydoxystearic acid has been shown to have antimicrobial properties, which are due to its ability to disrupt the lipid membrane of bacteria and fungi. This agent also has a protective effect against the cytotoxicity of trifluoroacetic acid, which is often used in cell culture studies. Polyoxyethylated 12-hydoxystearic acid also has potential applications in cancer therapy because it can be conjugated with anticancer drugs to form liposome nanoparticles, which may allow for more efficient delivery of these drugs into cancer cells.</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>2-Fluoro-3-(trifluoromethyl)benzoic acid is an amide that has been shown to inhibit the growth of Huh-7 human hepatoma cells, which express ABCA1. This compound has been shown to bind to and inhibit the activity of the enzyme acid hydrazide. It has also been shown to be active against methoxy functional assays and macrophage cell lines.</p>

<p>Please enquire for more information about 5-Oxo-1-(pyridin-3-ylmethyl)pyrrolidine-3-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ethoxyphenylboronic acid is a triazine compound which inhibits inflammation by inhibiting the kinase that catalyzes the phosphorylation of arachidonic acid. It also inhibits lipid kinase, which is involved in the metabolism of lipids, and it has been shown to inhibit cancer cell growth through hydrogen bond interactions with DNA. Ethoxyphenylboronic acid has been shown to have anti-inflammatory properties and may be useful for the treatment of inflammatory diseases such as arthritis. The compound can also inhibit hydrogen peroxide-induced oxidative damage in cells, due to its ability to release intracellular glutathione.</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>