Carboxylic Acids

Please enquire for more information about 2-Methoxy-4-amino-5-ethylthiobenzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

[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).

Please enquire for more information about (4-Chloro-3-(methoxycarbonyl)phenyl)boronic 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 2-(2-Nitrobenzylidene)-3-oxobutanoic acid, methyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page

Murideoxycholic acid is a bile acid that is used in combination with other antibiotics to treat infections caused by bacteria. Murideoxycholic acid inhibits the bacterial transport of bile acids, which are important for the digestion of fats and proteins. Murideoxycholic acid binds to the cytochrome P450 enzyme in humans and rats, inhibiting its activity. This binding prevents the production of bile acids from cholesterol in the liver, which prevents their normal excretion into the intestine and leads to an increased risk for gallstones. Murideoxycholic acid also has been shown to inhibit human CYP3A4 enzyme activity. The hydroxyl group on this molecule reacts with ferrous ions to produce hydroxyl radicals, which can lead to oxidative stress and lipid peroxidation.

3,4’-O-dimethylellagic acid is a phenolic compound, which is a type of ellagic acid derivative. It is derived from natural sources, typically found in various fruits, nuts, and vegetables, particularly in certain berries and pomegranates. The compound is formed through the methylation of ellagic acid, which amplifies its lipophilicity and enhances its bioavailability.

(R)-(-)-3-Hydroxybutyric acid methyl ester is a monocarboxylic acid that is metabolized by phosphofructokinase and other enzymes to produce the corresponding 3-hydroxybutyrate. This compound is synthesized from tiglic acid, which can be obtained from corynebacterium. The production of (R)-(-)-3-Hydroxybutyric acid methyl ester can be optimized by using a biotransformation process. This process includes enzymatic reactions and chemical transformations, such as hydroxylation, carbonylation, and stereoselective synthesis. The metabolic pathway for this compound has been studied using a DNA microarray analysis.