Di Stefano A, Mosciatti B, Cingolani G M, Giorgioni G, Ricciutelli M, Cacciatore I, Sozio P, Claudi F
Dipartimento di Scienze del Farmaco, Università G. D'Annunzio, Chieti, Italy.
Bioorg Med Chem Lett. 2001 Apr 23;11(8):1085-8. doi: 10.1016/s0960-894x(01)00140-8.
A series of dimeric derivatives (+)-1, and (+)-2, and (+)-3a-d of L-Dopa diacetyl esters was synthesized and evaluated as potential L-Dopa prodrugs with improved physicochemical properties. All the new compounds showed chemical stability in aqueous buffer solutions (pH 1.3 and 7.4). A relatively slow release of L-Dopa in human plasma was observed.
合成了一系列L-多巴二乙酰酯的二聚体衍生物(+)-1、(+)-2和(+)-3a - d,并将其作为具有改善理化性质的潜在L-多巴前药进行评估。所有新化合物在水性缓冲溶液(pH 1.3和7.4)中均表现出化学稳定性。在人血浆中观察到L-多巴的释放相对缓慢。