HuagongsheHuagongshe Chemistry Print Report · For research reference only
5'-Atp → HCID 178518213, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5'-Atp | HCID 5957 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Monobasic potassium phosphate | HCID 516951 | — |
| Reactant | (2R,3S,4R,5R)-2-(hydroxymethyl)-5-(6-hydroxypurin-9-yl)oxolane-3,4-diol | HCID 178521066 | — |
| Product | HCID 178518213 | HCID 178518213 | — |
| Product | (2R,3S,4R,5R)-2-(hydroxymethyl)-5-(6-hydroxypurin-9-yl)oxolane-3,4-diol | HCID 178521066 | — |
Reaction Steps
After completion of fermentation, about 30 g/l of inosine was accumulated in the medium obained in (8) above. As indicated in Table 9, 20 ml of a reaction mixture containing this medium was prepared. In a manner similar to (9), while keeping at 32° C. with vigorously stirring and also keeping pH at 7.2 with 4N NaOH, a reaction was carried out for 13 hours. During the course of reaction, monopotassium phosphate was added as in (9). From 23.5 g/l of initial inosine, 46 g/l of 5'-IMP was produced and accumulated. Also in this case, its molar conversion rate was 90% or more, as in (9).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05874272 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-c7ee8822f04e4e4f8a298542ae390a4c |
| Source note | uspto-grants-1999_02 |