Purine nucleotide sugars
Purine Nucleotide Sugars are a class of compounds that consist of purines, such as adenine and guanine, linked to sugar molecules via a nitrogen atom. These unique structures play critical roles in various biological processes within the body. For instance, they serve as essential substrates for biosynthesis pathways, including glycosylation reactions where these sugars attach to proteins or lipids to form glycans. This process is crucial for protein maturation, cell signaling, and immune function. Additionally, purine nucleotide sugars are involved in the metabolism of nucleic acids and can modulate cellular responses by influencing glycan composition on the cell surface. In pharmaceutical research, these compounds are of significant interest due to their potential applications as therapeutic agents or tools for probing cellular mechanisms.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Guanosine5'-(trihydrogen diphosphate), P'-a-D-glucopyranosyl ester | 5750-57-2 | C16H25N5O16P2 |
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GDP-L-fucose | 15839-70-0 | C16H25N5O15P2 |
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6-deoxy-beta-L-galactopyranosylguanosine-5'-diphosphate | 16597-51-6 | C16H25N5O15P2 |
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Adenosine 5'-(trihydrogen diphosphate), P'-L-glycero-β-D-manno-heptopyranosyl ester | 322640-23-3 | C17H27N5O16P2 |
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Guanosine 5'-Pyrophosphate Ester 6-Deoxytalose | 18657-20-0 | C16H25N5O15P2 |
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Adenosine 5'-(trihydrogen diphosphate), P'-α-D-glucopyranosyl ester | 2140-58-1 | C16H25N5O15P2 |
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Guanosine5'-(trihydrogen diphosphate), P'-a-D-mannopyranosyl ester | 3123-67-9 | C16H25N5O16P2 |
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GDP-D-glucose Disodium Salt | 103301-72-0 | C16H24N5NaO16P2 |
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Guanosine 5'-(trihydrogen diphosphate), P'-b-L-galactopyranosyl ester | 6815-91-4 | C16H25N5O16P2 |
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O5'-(2-D-mannopyranosyloxy-1,2-dihydroxy-diphosphoryl)-guanosine | 755712-80-2 | C16H25N5O16P2 |
Related Literature
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Abdelaziz Houmam,Emad M. Hamed Chem. Commun., 2012,48, 11328-11330
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