HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415662Generated: October 25, 2026
Sulphosuccinimidyl 4-(4-maleimidophenyl)butyrate → HCID 178502833, compound
https://huagongshe.com/reaction/1415662
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulphosuccinimidyl 4-(4-maleimidophenyl)butyrate | HCID 10274690 | — |
| Reactant | Ceftiofur Sodium | HCID 23671563 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178502833 | HCID 178502833 | — |
Reaction Steps
Ceftiofur sodium (82 mg)(The Upjohn Co., Kalamazoo, Mich.) was dissolved in 500 μL PBS-A, and 10 mg sulfosuccinimidyl 4-(p-maleimidophenyl)-butyrate (s-SMPB)(Pierce, Rockford, Ill.) in 20 μL DMF was added. The resulting mixture was stirred for 10-15 min, added dropwise to 30 mg BSA-SH (1.5 mL of a 20 mg/mL stock solution), stirred overnight at ambient temperature, and then dialyzed exhaustively against PBS-A. Similarly, 52 mg ceftiofur sodium in PBS-A and 5 mg s-SMPB in 20 μL N,N-dimethylformamide (DMF) were added dropwise to 20 mg of OVA-SH (1 mL of a 20 mg/mL stock solution), and the mixture was stirred overnight at ambient temperature and dialyzed exhaustively against PBS-B (0.05M sodium phosphate, 0.075M sodium chloride in deionized water, pH 7.2). These conjugates were abbreviated as BSA-S-SMPB-Cef and OVA-S-SMPB-Cef, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05908781 |
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| Source dataset | uspto-grants-1999_06 |
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| ORD ID | ord-10c91cd6bc1241bca5e43abef1a76624 |
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| Source note | uspto-grants-1999_06 |
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