4-马来酰亚胺基丁酸-N-羟基琥珀酰亚胺酯

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: The EDTA-benzylthiocarbazide prepared in step 1 (20 mg; 34 μmol) and N-(gamma-maleimidobutyryloxy)succinimide (8 mg, 29 μmol=0.9 equiv.) were stirred in anhydrous dimethylformamide for 1 h. The mixture was then evaporated to dryness, and the residue was dried under high vacuum. The mixture was then evaporated to dryness the residue was dried under high vacuum

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: The EDTA-benzylthiocarbazide prepared in step 1 (20 mg; 34 μmol) and N-(gamma-maleimidobutyryloxy)succinimide (8 mg, 29 μmol=0.9 equiv.) were stirred in anhydrous dimethylformamide for 1 h. The mixture was then evaporated to dryness, and the residue was dried under high vacuum. The mixture was then evaporated to dryness the residue was dried under high vacuum

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: The EDTA-benzylthiocarbazide prepared in step 1 (20 mg; 34 μmol) and N-(gamma-maleimidobutyryloxy)succinimide (8 mg, 29 μmol=0.9 equiv.) were stirred in anhydrous dimethylformamide for 1 h. The mixture was then evaporated to dryness, and the residue was dried under high vacuum. The mixture was then evaporated to dryness the residue was dried under high vacuum