Bode C W, Hänsel W
Institute of Pharmacy, Department of Pharmaceutical Chemistry, Christian-Albrechts-University Kiel, Germany.
Pharmazie. 2005 Mar;60(3):225-8.
5-(3-Phenylpropoxy)psoralen and 5-(4-phenylbutoxy)psoralen are blockers of the lymphocyte potassium channel Kv1.3 with EC50 values < 10 nM and may be used as new potential immunosuppressive drugs. As reported for many furocoumarins, these compounds show phototoxic properties and react under UV radiation with different targets in the cell, e.g. DNA or proteins and lipids in membranes. The photoreactions with these targets were investigated and compared to the well-known derivatives psoralen, 5-methoxypsoralen, 8-methoxypsoralen and 4,5',8-trimethylpsoralen. Moreover, absorption properties and the capability to photoproduce singlet oxygen (1O2) and reactive oxygen species (ROS) were studied. It was found that 5-(3-phenylpropoxy)psoralen and 5-(4-phenylbutoxy)psoralen are similar or less phototoxic in vitro as 5-methoxypsoralen which is the furocoumarin with the weakest phototoxicity in vivo compared to psoralen, 8-methoxypsoralen and 4,5',8-trimethylpsoralen.
5-(3-苯丙氧基)补骨脂素和5-(4-苯丁氧基)补骨脂素是淋巴细胞钾通道Kv1.3的阻滞剂,其半数有效浓度(EC50)值<10 nM,可用作新型潜在免疫抑制药物。正如许多呋喃香豆素所报道的那样,这些化合物具有光毒性,在紫外线辐射下会与细胞中的不同靶点发生反应,例如DNA或膜中的蛋白质和脂质。研究了与这些靶点的光反应,并与著名的衍生物补骨脂素、5-甲氧基补骨脂素、8-甲氧基补骨脂素和4,5',8-三甲基补骨脂素进行了比较。此外,还研究了它们的吸收特性以及光产生单线态氧(1O2)和活性氧(ROS)的能力。结果发现,5-(3-苯丙氧基)补骨脂素和5-(4-苯丁氧基)补骨脂素在体外的光毒性与5-甲氧基补骨脂素相似或更低,而5-甲氧基补骨脂素是与补骨脂素、8-甲氧基补骨脂素和4,5',8-三甲基补骨脂素相比体内光毒性最弱的呋喃香豆素。