HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → CS-045 succinimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Troglitazone | HCID 5591 | — |
| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | CS-045 succinimide | HCID 86749100 | — |
Reaction Steps
To make the succinyl CS-045 conjugate of β-phycoerythrin, first 44 mg of CS-045 was reacted for 5 hours at room temperature with 20 mg succinic anhydride in pyridine. Then 4 mg of the resulting succinyl CS-045 was reacted overnight at 4° C. with 2 mg EDC and 1.2 mg N-hydroxysuccinimide to produce CS-045 succinimide. Forty micrograms of this CS-045 succinimide was reacted for 4 hours at room temperature with 500 μg β-phycoerythrin. The final succinyl CS-045 conjugate of β-phycoerythrin was precipitated with 60% final (w/v) saturated ammonium sulfate and resuspended in phosphate buffered saline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05466610 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-6192c1e9fdbe40cba892f641eff308c6 |
| Source note | uspto-grants-1995_11 |