HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glutaric anhydride → HCID 178455886, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glutaric anhydride | HCID 7940 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | HCID 178455884 | HCID 178455884 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178455886 | HCID 178455886 | — |
Reaction Steps
3.0 mg (3.3 μmol) of α-amanitin, dried in vacuo over P4O10 was dissolved in 0.25 ml of dry pyridine and reacted with 0.9 mg (79 μmol) glutaric anhydride in 0.1 ml pyridine for 24 h at RT in the dark. The peptide was precipitated by addition of 7 ml of dry diethylether, centrifuged, and the solid washed a second time with diethylether and centrifuged. By way of this reaction an α-amanitin derivative is obtained wherein R1=—OH (in FIG. 1) is replaced by R1=—O—C(O)—(CH2)3—COOH.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09233173B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-b48fb12dcc6a41bf835f68c33aaec932 |
| Source note | uspto-grants-2016_01 |