Acides carboxyliques

Please enquire for more information about 2-Methylpyridine-4-boronic acid pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page

(3R,5R)-6-Cyano-3,5-dihydroxy-hexanoic acid tert-butyl ester is a building block for organic synthesis. It is a versatile intermediate that can be used in the preparation of pharmaceuticals and other organic compounds. The compound is also used as a reagent to study the biological activity of other compounds. CAS No. 125971-93-9 is a fine chemical that has been shown to have high quality and purity.

Please enquire for more information about 4-(4-Ethoxyphenyl)-2-indol-3-yl-4-oxobutanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Ethylbenzoic acid is a fatty acid that is found in plants, animals and microorganisms. It dissolves in water to form an amorphous drug with a molecular weight of about 170. 2-Ethylbenzoic acid has been shown to inhibit the activity of several enzymes, such as protein kinases and phospholipases. It also inhibits the activity of liver enzymes involved in the metabolism of drugs and other xenobiotics, such as phenylpropionic acid and malic acid. This drug has been shown to have an inhibitory effect on glucose uptake by cells and may be used as an anti-diabetic agent.

2-Amino-4-bromobenzoic acid is a molecule that has an acidic carboxylic group and two aromatic amino groups. It has a hydroxyl group and a fluorescence that can be activated or deactivated by ultraviolet light. 2-Amino-4-bromobenzoic acid is used in the synthesis of certain organic compounds. This molecule can be synthesized from other molecules, such as phenol, aminobenzene, and nitrobenzene. The reaction time for this chemical species is dependent on the catalytic agent used during the reaction process. A variety of chemical species are produced when 2-Amino-4-bromobenzoic acid is synthesized, including hydrogen bromide, ammonia, nitrogen gas, and water vapor. The population of 2-Amino-4-bromobenzoic acid is unknown because it is not abundant in nature.

Please enquire for more information about 4-(4-Ethoxyphenyl)-2-(3-methyl-5-oxo-1-phenyl(2-pyrazolin-4-yl))-4-oxobutanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Amino-3-chlorobenzoic acid is a white solid with a molecular weight of 170.1 g/mol, melting point of 158.5°C and boiling point of 267°C. It has the molecular formula C6H5ClNO2 and the IUPAC name 4-(aminomethyl)-3-chlorobenzoic acid. The chemical structure of this compound is shown in Figure 1.

3-(2-Carboxyphenyl)propionic acid is a chemical compound that belongs to the group of phytoalexins. It is a synthetic compound that is used as a raw material for the synthesis of various pharmaceuticals and other organic compounds. 3-(2-Carboxyphenyl)propionic acid has shown luminescence properties, which may be due to its oxidation products. The isoquinoline alkaloids present in this compound are responsible for its anti-inflammatory effects. 3-(2-Carboxyphenyl)propionic acid can also be found in conjugates with chloride or other organic acids, such as diazide, which inhibit bacterial growth and increase the solubility of this substance.

Tungstosilicic acid hydrate is an alkanoic acid that has a chemical formula of ZrO(OH)(SO)2. It is insoluble in water and reacts with hydrogen fluoride to form tungsten hexafluoride. Tungstosilicic acid hydrate is used as a catalyst in wastewater treatment, and also has biological properties that can be used for the synthesis of esters. The chemical stability of tungstosilicic acid hydrate is high, and it has been shown to be an excellent catalyst for the hydrogenation of alkenes. Tungstosilicic acid hydrate does not react with protonated amines or amides, which makes it a good candidate for catalyzing reactions involving these functional groups.

DL-3-Aminoisobutyric acid (LAA) is a metabolite of the amino acid L-arginine. It is produced in the liver by the enzyme arginase and can be used to diagnose hepatic steatosis. It is also found in urine and human serum, as well as in microbial metabolism. LAA has been shown to regulate gene transcription and metabolism through its ability to inhibit the activity of gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter that regulates energy metabolism and metabolic disorders. In addition, LAA has been shown to have antioxidant properties, which may be related to its role in caproic acid biosynthesis.

5-Azido-pentanoic acid is a cyclic peptide that is synthesized in the presence of a polymer drug. The polymer drug is used to control the molecular weight and purity of the product. 5-Azido-pentanoic acid has been shown to induce apoptosis in cancer cells by interacting with calcium, which leads to an increase in cytosolic calcium concentrations. This chemical also interacts with hydrogen bonds and intramolecular hydrogen bonds, which may affect its pharmacokinetic properties.

cis-5-Aza-4-oxo-oct-2-en-dioic acid is a chemical that belongs to the group of reagents and is used as a reaction component. cis-5-Aza-4-oxo-oct-2-en-dioic acid has been shown to react with aniline in a one pot reaction to produce 4,6 diaminohexanoic acid. cis -5 Aza -4 oxo oct 2 en dioic acid also reacts with methyl acetoacetate in a one pot reaction to produce 3,4,5 triamino pentanoic acid. cis -5 Aza -4 oxo oct 2 en dioic acid is versatile and can be used as a building block or an intermediate for complex compounds. It has been shown to be useful in the synthesis of fine chemicals, such as benzofuran derivatives.

Glutamic acid is a non-essential amino acid that has been shown to play an important role in the pathogenesis of many diseases. Glutamic acid has been shown to be involved in the production of glutamate, which is a neurotransmitter that can lead to neuronal death. Glutamic acid also plays an important role in the maintenance of mitochondrial membrane potential and energy metabolism. Glutamate is an inhibitory neurotransmitter, and it regulates the release of other neurotransmitters, such as dopamine and serotonin. This amino acid may also be involved in brain functions and neurotrophic factors.

Di-O-benzoyl L-tartaric acid is a chiral compound that is used in the synthesis of enantiopure compounds. It is a racemic mixture of two diastereoisomers, which means it has an asymmetric carbon atom. The two diastereoisomers can be separated using high performance liquid chromatography (HPLC). Di-O-benzoyl L-tartaric acid is used to produce β-amino acids from α-amino acids, and also as a chiral auxiliary for organic synthesis. Di-O-benzoyl L-tartaric acid can also be obtained by hydrolysis of malonic acid with hydrochloric acid or sodium hydroxide.

5-Methylindole-2-carboxylic acid (5MICA) is a synthetic compound that has been shown to be cytotoxic in vitro. It has been shown to inhibit the growth of multiple cancer cell lines, including hepatoma cells, and is currently being studied as a potential anticancer drug. 5MICA inhibits the synthesis of protein and RNA by binding to the ribosome. This inhibition leads to cell death by apoptosis. 5MICA also exhibits an antimicrobial effect against opportunistic fungal pathogens such as Candida albicans, Aspergillus fumigatus, and Cryptococcus neoformans. The mechanism for this inhibition is unknown but may involve inhibition of protein synthesis or other cellular processes.

Please enquire for more information about 3-((2-Fluorophenyl)piperazinylcarbamoyl)prop-2-enoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Ethyl 3-((4-chlorophenyl)amino)-5-methyl-2,4-thiazolecarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Beta-(3-aminophenyl)propionic acid (BAPA) is a β-amino acid that inhibits the formation of nitric oxide and other reactive oxygen species by binding to a receptor on the surface of cells. BAPA also has inhibitory properties against certain enzymes, such as aminopyrine N-demethylase and carbonic anhydrase. It is used in analytical methods for amines, malonic acid, and hydrochloride salts. Carbon sources that are metabolized by fungi can be converted into BAPA through the process of asymmetric synthesis. This compound is also used as a precursor for gamma-aminobutyric acid (GABA), which is a neurotransmitter in the central nervous system.

4-Morpholinylacetic acid hydrochloride is a fluorescent probe that is used to study the interaction between extracellular proteins and cells. It can be detected in tissues by fluorescence microscopy and has been tested on animal tissues. The linker group allows for the encapsulation of the probe into mesoporous silica particles that can be recovered from biological fluids and analyzed using analytical methods. 4-Morpholinylacetic acid hydrochloride is not acidic, which means it does not interact with DNA or RNA. The fluorescent properties of this compound allow for easy detection in tissues and microenvironments where other probes may not be detectable.

3,4,5-Trimethoxyphenylacetic acid is a synthetic compound that is used as an anticancer drug. It has been shown to inhibit the growth of cancer cells in vitro and in vivo by binding to the DNA. 3,4,5-Trimethoxyphenylacetic acid has been shown to be stereoselective with respect to the anticancer activity of the two isomers. The hydroxyl group present on one side of the molecule may be responsible for this effect. 3,4,5-Trimethoxyphenylacetic acid also inhibits enzymes called oxidases that are involved in the production of prostaglandins from arachidonic acid (prostaglandins play a role in inflammation). This property may account for its anti-inflammatory effects.

Dibenzoyl-L-tartaric acid monohydrate is a chiral molecule that can be found in nature. It is soluble in organic solvents, but insoluble in water. Dibenzoyl-L-tartaric acid monohydrate has an affinity for carboxylate ligands and absorbs at 360 nm. The optical rotation of this compound is +20° to -50°, depending on the concentration and pH of the solution. This molecule is a potential pollutant because it can be degraded by oxidation or photolysis, yielding environmentally hazardous compounds. Its conformation may be changed by light or heat and, as a result, its properties may also change.

3,5-Dihydroxyphenylacetic acid is a versatile building block that can be used to synthesize complex molecules. 3,5-Dihydroxyphenylacetic acid is a reagent in organic chemistry and has been used in the synthesis of novel drugs, among other applications. This chemical has been shown to be useful as a building block for the synthesis of high-quality compounds. 3,5-Dihydroxyphenylacetic acid can be used as an intermediate for the synthesis of pharmaceuticals or other chemicals. It is also a useful scaffold for the production of new molecules with desired properties.

5-Amino-2-methoxybenzoic acid (5AMBA) is a hydrogen bond acceptor that binds to peptides and rna. It also has enzymatic activity, which can be used in the treatment of diseases such as Alzheimer's disease. 5AMBA is a small molecule that contains two methoxy groups and one hydrogen. It has been shown to bind to an intramolecular hydrogen bond within a peptide or rna sequence and inhibit enzymatic activity. This inhibition occurs by removing the nucleophile from the enzyme's active site or by sterically hindering access to the enzyme's active site. The luminescent properties of 5AMBA make it an ideal candidate for fluorescent labeling, with applications in biomolecular research.

Bis-Boc-amino-oxyacetic acid is an analog of goserelin acetate. It binds to the androgen receptor in prostate cancer cells, which leads to cytostatic effects. This drug has shown a low potency in human serum and does not bind to human serum proteins.
The uptake of Bis-Boc-amino-oxyacetic acid by prostate cancer cells was found to be significantly greater than that of goserelin acetate. The binding affinity of this drug for the androgen receptor is also lower than that of goserelin acetate, making it more selective for prostate cancer cells over other tissues.