[(2R,3R,4R,5R)-5-(2-Amino-6-oxo-3H-purin-9-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-[hydroxy-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydr oxymethyl)oxan-2-yl]oxy-phosphoryl]oxy-phosphinic acid
CAS: 5750-57-2
Ref. 3D-FA166225
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- GDP-<span class="text-smallcaps">D</span>-glucose
- GDP-glucose
- GDP-α-<span class="text-smallcaps">D</span>-glucose
- Guanosine 5′-(trihydrogen diphosphate), P′-<span class="text-smallcaps">D</span>-glucopyranosyl ester
- Guanosine 5′-(trihydrogen diphosphate), P′-α-<span class="text-smallcaps">D</span>-glucopyranosyl ester
- Guanosine 5′-(trihydrogen pyrophosphate), mono-<span class="text-smallcaps">D</span>-glucopyranosyl ester
- Guanosine 5′-(trihydrogen pyrophosphate), mono-<span class="text-smallcaps">D</span>-glucosyl ester
- Guanosine 5′-(trihydrogen pyrophosphate), mono-α-<span class="text-smallcaps">D</span>-glucopyranosyl ester
- Guanosine 5′-(trihydrogen pyrophosphate), monoglucopyranosyl ester
- Guanosine 5′-diphosphate glucose
- See more synonyms
- Guanosine 5′-diphosphate-<span class="text-smallcaps">D</span>-glucose
- Guanosine 5′-pyrophosphate, <span class="text-smallcaps">D</span>-glucosyl ester
- Guanosine 5′-pyrophosphate, glucosyl ester
- Guanosine 5′-pyrophosphate, α-<span class="text-smallcaps">D</span>-glucopyranosyl ester
- Guanosine 5′-pyrophosphate, α-<span class="text-smallcaps">D</span>-glucosyl ester
- Guanosine diphosphate <span class="text-smallcaps">D</span>-glucose
- Guanosine diphosphate glucose
- Guanosine diphosphoglucose
- Guanosine pyrophosphates, α-<span class="text-smallcaps">D</span>-glucopyranosyl ester
- [(2R,3S,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl (2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl dihydrogen diphosphate (non-preferred name)
Galacturonic acid is a dicarboxylic acid that is produced in plants by the enzyme L-galactono-1,4-lactone oxidase. The compound inhibits the synthesis of galacturonate, which is a precursor for the biosynthesis of pectin, a major component of plant cell walls. Galacturonic acid also has anti-inflammatory properties and may be useful in treatment of inflammatory disorders such as arthritis. The compound has significant interactions with enzymes involved in protein synthesis and chemical biology. In vitro assays show that galacturonic acid inhibits the activity of synthetase, an enzyme that catalyzes the transfer of amino acids to a growing peptide chain during protein synthesis. It also inhibits hydrogen bonding between phosphate groups and hydroxyl groups on proteins. Moreover, it has been shown to have an optimum pH of 3.2 and can inhibit energy metabolism in plants at high concentrations. This effect may be due to inhibition of mitochondrial resp
Chemical properties
Technical inquiry about: 3D-FA166225 [(2R,3R,4R,5R)-5-(2-Amino-6-oxo-3H-purin-9-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-[hydroxy-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydr oxymethyl)oxan-2-yl]oxy-phosphoryl]oxy-phosphinic acid
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