HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-2-deoxy-6-O-phosphono-alpha-D-glucopyranose → 102029-88-9
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-2-deoxy-6-O-phosphono-alpha-D-glucopyranose | HCID 439217 | — |
| Reactant | N-acetylsuccinimide | HCID 11457741 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | 102029-88-9 | HCID 898 | — |
Reaction Steps
In one process, GlcN-6-P was acetylated in THF/water using N-acetylsuccinimide (NAS) to form GlcNAc-6-P. Acetic anhydride can also be used. That N-acetyl compound was treated with an enzyme preparation from Candida utilis containing N-acetylglucosamine phosphomutase (EC 2.7.5.2) and UDP-GlcNAc pyrophosphorylase (EC 2.7.7.23) to first form GlcNAc-1-P and then UDP-GlcNAc in the presence of UTP and inorganic pyrophosphatase (EC 3.6.1.1) to destroy the inorganic pyrophosphate formed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05516665 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-c6489ca1bef64d9c964dd3c83a9517d9 |
| Source note | uspto-grants-1996_05 |