Monossacáridos

2-Methylphenyl 4-O-benzyl-a-L-thiorhamnopyranoside is a custom synthesis that can be modified to suit the needs of the customer. It is a fluorinated oligosaccharide with a complex carbohydrate structure. The product has been shown to have high purity and will be synthesized according to customer specifications. 2-Methylphenyl 4-O-benzyl-a-L-thiorhamnopyranoside is an oligosaccharide that contains a saccharide and monosaccharide unit, which are linked together by glycosidic bonds. This product is also known as methylated thioretinamide or MTT.

Please enquire for more information about Allyl 2,3,4,-tri-O-benzyl-b-L-fucopyranoside including the price, delivery time and more detailed product information at the technical inquiry form on this page

Sennoside C is a bioactive phytochemical extracted from the leaves of Eclipta prostrata. It has been shown to have anti-tumor and anti-inflammatory properties. Sennoside C has also been found to be effective in treating autoimmune diseases, including psoriasis and rheumatoid arthritis. Sennoside C is a low-energy compound that binds with fatty acids to form a bound form. This bound form can be hydrolyzed by sodium hydroxide solution to release free sennosides, which are anthraquinone glycosides that can be used for the treatment of skin conditions such as eczema and dermatitis.

Mogroside II A2 is a fructan that is found in the fruit of the plant Glycosmis erythrorhiza, which is a member of the family Rutaceae. This compound has been shown to have immune-modulating properties and is used as an ingredient in some pharmaceutical drugs. Mogroside II A2 has also been demonstrated to have antiviral activity and may be helpful for cancer treatment. The effects of this compound on kidney fibrosis are unclear; however, it does have anti-inflammatory properties.

1,5-Dideoxy-1,5-imino-D-xylitol is a synthetic molecule that inhibits the enzyme glycinamide ribonucleotide transformylase (GART) and blocks the synthesis of purines. 1,5-Dideoxy-1,5-imino-D-xylitol has been shown to be potent in inhibiting GART with an IC50 of 0.3 μM. This inhibitory effect was observed in Sprague Dawley rats after oral administration of 1,5-dideoxy-1,5 imino D xylitol at a dose of 10 mg/kg. The inhibition was found to be specific for amination reactions that are catalyzed by GART and not by other enzymes such as glycine amidinotransferase or adenylate kinase. It can be used to study the structure and function of tissue cells.

Naproxen is a non-steroidal anti-inflammatory drug (NSAID) that is used to relieve pain and reduce inflammation. The NSAIDs are metabolized in the liver by oxidation, reduction, hydrolysis, or conjugation with glucuronic acid. Naproxen undergoes a number of metabolic transformations including fragmentation, which can be detected using an MS/MS analyzer. Naproxen acyl-b-D-glucuronide is an oxidative metabolite of naproxen that has been shown to have high uptake into mammalian cells and bioconcentrates in fish. This metabolite has also been shown to be metabolized in the liver by conjugation with glucuronic acid.

α-D-Maltotetraose is a natural carbohydrate that has been shown to have potential as an anticancer agent. It is an inhibitor of tumor-associated kinases and has been found to induce apoptosis in cancer cells. α-D-Maltotetraose has also been shown to inhibit streptokinase, an enzyme involved in the breakdown of blood clots. This carbohydrate analog has been detected in human urine and may play a role in regulating gastrin secretion. Studies have shown that α-D-Maltotetraose can inhibit the growth of Chinese hamster ovary cells, suggesting its potential as a novel anticancer therapy.