Reaction equation
[Na].[Na].[C@@H:3]1([N:41]2[C:50]3[N:49]=[CH:48][N:47]=[C:45]([NH2:46])[C:44]=3[N:43]=[CH:42]2)[O:40][C@H:12]([CH2:13][O:14][P:15]([O:18][P:19]([O:22][CH2:23][C:24]([C@H:27]([C:29]([NH:31][CH2:32][CH2:33][C:34]([NH:36][CH2:37][CH2:38][SH:39])=[O:35])=[O:30])[OH:28])([CH3:26])[CH3:25])([OH:21])=[O:20])([OH:17])=[O:16])[C@@H:6]([O:7][P:8]([OH:11])([OH:10])=[O:9])[C@H:4]1[OH:5].CCN(CC)CC>CN(C=O)C>[CH3:26][C:24]([C@@H:27]([OH:28])[C:29]([NH:31][CH2:32][CH2:33][C:34]([NH:36][CH2:37][CH2:38][SH:39])=[O:35])=[O:30])([CH2:23][O:22][P:19]([O:18][P:15]([O:14][CH2:13][C@H:12]1[O:40][C@@H:3]([N:41]2[C:50]3[N:49]=[CH:48][N:47]=[C:45]([NH2:46])[C:44]=3[N:43]=[CH:42]2)[C@H:4]([OH:5])[C@@H:6]1[O:7][P:8]([OH:11])([OH:10])=[O:9])([OH:17])=[O:16])([OH:21])=[O:20])[CH3:25]Participants
Reagents, catalysts & solvents 1
Procedure
To a solution of N-(ε-maleimidocaproic acid) hydrazide 2 (1 mg, 0.0044 mmol) in 50 μl DMF, a solution of coenzyme A disodium salt (3.6 mg, 0.0044 mmol, 1 eq.) in a DMF/buffer mixture (70 μl DMF/30 μl 50 mM Tris Cl, pH 7.5) is added. The reaction is followed by analytical HPLC (detection at 260 nm) to verify the completion of the reaction. Subsequently, a solution of 3-amino-3-deoxydigoxigenin hemisuccinamide succinimidyl ester (2.6 mg, 0.0044 mmol, 1 eq.) dissolved in 50 μl DMF and 10 μl Et3N is added, and the reaction mixture stirred for 4 hours at room temperature. The reaction is submitted to preparative HPLC and fractions containing the desired product are concentrated in vacuo, dissolved in DMSO, and analyzed by analytical HPLC for purity. Fractions containing pure product are combined. The concentration of CoA-Dg is determined using the extinction coefficient of adenine (ε(adenine, 260 nm)=15′300 [M−1 cm−1]). The yield of CoA-Dg is 2.37 mg (37%).
Workup
- customthe completion of the reaction
Sources & evidence
- ORD record
- ord-df53c23fcbed4461a3f88914925f5408
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08476031B2
Linked notes
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