Chee Chin-Fei, Lee Hong Boon, Ong Hean Chooi, Ho Anthony Siong-Hock
Cancer Research Initiatives Foundation, Level 2 Subang Jaya Medical Centre, 47500 Subang Jaya, Selangor Darul Ehsan, Malaysia.
Chem Biodivers. 2005 Dec;2(12):1648-55. doi: 10.1002/cbdv.200590134.
In our screening program for new photosensitizers from the Malaysian biodiversity, we found five pheophorbide-related compounds from the leaves and stems of Aglaonema simplex. Detailed spectroscopic analyses showed that compounds 1-3 and 5 are pheophorbide and hydroxy pheophorbide derivatives of chlorophyll a and b. Compound 4, identified as 15(1)-hydroxypurpurin-7-lactone ethyl methyl diester, was isolated for the first time from the Araceae family. An MTT-based short-term survival assay showed that all five compounds exhibit moderate-to-strong photocytotoxic activities towards human leukemia (HL60) and two oral squamous carcinoma cell lines (HSC-2 and HSC-3). Compounds 4 and 5 showed the strongest photocytotoxicities, with IC(50) values of 0.30-0.41 muM (Table 2). Compounds 1-3 with Et chains at C(17(3)) were less photocytotoxic than the parent pheophorbide a (5).
在我们从马来西亚生物多样性中筛选新型光敏剂的项目中,我们从粗肋草的叶和茎中发现了5种脱镁叶绿酸相关化合物。详细的光谱分析表明,化合物1 - 3和5是叶绿素a和b的脱镁叶绿酸及羟基脱镁叶绿酸衍生物。化合物4被鉴定为15(1)-羟基紫红素-7-内酯乙基甲基二酯,首次从天南星科植物中分离得到。基于MTT的短期存活试验表明,所有5种化合物对人白血病细胞(HL60)和两种口腔鳞状癌细胞系(HSC - 2和HSC - 3)均表现出中度至强烈的光细胞毒性活性。化合物4和5表现出最强的光细胞毒性,IC(50)值为0.30 - 0.41 μM(表2)。在C(17(3))位带有乙基链的化合物1 - 3的光细胞毒性低于母体脱镁叶绿酸a(5)。