HuagongsheHuagongshe Chemistry Print Report · For research reference only
Paclitaxel → Baccatin Iii
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Paclitaxel | HCID 36314 | — |
| Reactant | 7-Epi-Taxol | HCID 184492 | — |
| Product | Baccatin Iii | HCID 65366 | — |
Reaction Steps
Degradation products were formed in the same proportions as in the experiments conducted under room temperature but in significantly lower quantities. Again, 7-epi-taxol was the main degradation product of paclitaxel. Its amounts formed during 32 h increased from about 3% at pH 7.0 to about 10% at pH 8.0 (see Table 11). Baccatin III and 10-deacethyltaxol were formed for about 5 to 6% at pH 8.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238021B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-3853dc7c11d2490489bb61f620740aa9 |
| Source note | uspto-grants-2016_01 |