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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulphosuccinimidyl 4-(4-maleimidophenyl)butyrateHCID 10274690—
ReactantCeftiofur SodiumHCID 23671563—
SolventDimethylformamideHCID 6228—
ProductHCID 178502833HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05908781
Source datasetuspto-grants-1999_06
ORD IDord-10c91cd6bc1241bca5e43abef1a76624
Source noteuspto-grants-1999_06