Glycoscience

Carprofen acyl-glucuronide is an acidic drug that is used for the treatment of inflammation, pain and fever. It has been shown to be active in humans at a dosage of 10 mg/kg. Carprofen acyl-glucuronide binds to nicotinic acetylcholine receptors (nAChR) and has been shown to have a high affinity for ligands containing lysine residues. The molecule can also bind to fatty acids, which may lead to its reactivity with human serum and plasma proteins, as well as the matrix effect seen in acidic pH. This drug is also selective for glutamate stereospecificity. Carprofen acyl-glucuronide has been shown to produce a dose-dependent inhibition of diazepam binding to its specific ligand, alpha 1 beta 2 gamma 2 subunit.

Ethyl a-D-thioglucopyranoside is an organic compound that is used as a precursor in the synthesis of complex sugars. Ethyl a-D-thioglucopyranoside is an oligosaccharide that contains a methylated and glycosylated sugar. The glycosidic bond in this product can be modified by fluorination to give ethyl 2,3,4,5-tetrafluorothioglucopyranoside.

D-myo-inositol-1,3,5-triphosphate is a carbohydrate that is modified with fluorine. It is a custom synthesis and can be synthesized in high purity. D-myo-inositol-1,3,5-triphosphate has several glycosylations and methylations. The modification of this compound includes click chemistry for the synthesis of oligosaccharides and saccharides. D-myo-inositol-1,3,5-triphosphate can be used as a sugar or an oligosaccharide in the modification of proteins or carbohydrates.

1,2:4,5-Di-O-isopropylidene-b-L-erythro-2,3-hexodiulo-2,6-pyranose is a sugar that can be found in the human body. It has been shown to have a high level of hydrogen bonding and can be used as an energy source by replicon cells. It is also an enantiomer of 1,2:4,5:8,9-di-O-isopropylidene-b-(D)-threo--2,3--hexodiulo--2,6--pyranose. This molecule has been shown to inhibit the growth of herpes simplex virus in vitro and in vivo and has been investigated for its potential use as an antiherpes agent. 1,2:4,5:8,9 Di--O--isopropylidene--b-(D)--threo--2

3',4'-Di-O-(β-D-glucopyranosyl)-L-DOPA is a methylated form of L-DOPA that is used as a precursor in the synthesis of dopamine. It is available on custom synthesis, and can be modified with fluorination or click chemistry. This product is a synthetic monosaccharide sugar that is used in the production of polysaccharides and saccharides. It has a CAS number and is sold with high purity, which makes it an excellent candidate for modification.

Losartan N1-glucuronide is a glucuronidated metabolite of losartan that is produced naturally in the human body. It is converted from losartan by the enzyme UDP-glucuronosyltransferase, which is found in humans and other animals. The rate of glucuronidation varies between individuals and is determined by genetic factors. Losartan N1-glucuronide has shown to be an effective inhibitor of angiotensin II, with an IC50 value of 1.4 μM. This inhibition can be reversed by dobutamine or recombinant human UGT2B7 enzyme, which are both competitive inhibitors of the enzyme UGT2B7. Magnetic resonance spectroscopy has been used to study the kinetic properties of this inhibitor and its effect on dobutamine-induced changes in cardiac function.

4-Deoxy-4-fluoro-a-D-glucopyranose is a carbohydrate that belongs to the group of carbohydrates. It has enthalpy and entropy values of -1,865.2 kJ/mol and -3,363.6 J/(mol·K) at 298 K, respectively. This compound has been shown to interact with water molecules in solution phase. 4-Deoxy-4-fluoro-a-D-glucopyranose is soluble in water and interacts with other carbohydrate molecules at an intermolecular level. 4DFA has an extrapolated melting point of about 216 degrees Celsius.