Phenylphthalimide 衍生物合成及生物活性之研究

Synthesis and Bioactive Studies on phenylphthalimide analogues

張嘉富(Jia-Fu Chang)

指導教授 ： 林本元

臺北醫學大學/藥學院/藥學研究所/碩士(2001年)

摘要

Thalidomide [N(a)-phthalimidoglutarimide] 是一個鎮靜劑，但是它會引起嬰孩出生肢幹嚴重畸形。因此，被撤出市場。最近研究顯示它可以用於治療發炎、愛滋病病患體欉虛耗、口瘡潰瘍、眼睛斑狀退化、乳癌,攝護腺癌、腦癌、愛滋病病患常見的Kaposi's腫瘤，和其他的相關疾病等。這些疾病治療可能是thalidomide能夠調節，由monocyctes或是macrophages所分泌的腫瘤壞死因子 (tumor necrotic factor, TNF-a)，然而，thalidomide的光學結構容易消旋 (racemize) 和水解 (hydrolysis)。因此，本實驗嘗試簡化thalidomide的glutarimide的部份，獲得 phthalimide 衍生物，包括四個系列phenyl-phthalimide、pyridyl-phthalimide 、aminobenzyl-phtalimide及diphenylazo-phtalimide analogues；本實驗亦嘗試採用數個anhydrides修飾phthalimide中1H-isoindole的部分，以進行結構與活性關係之探討。本實驗利用phthalic anhydride及anhydrides 與amino substrates 於高溫鹼性條件下，以封管加熱反應，製備一系列化合物。並進行HL-60、HEP-2、HEP G2、HONE-1、NUGC五種癌細胞的體外細胞毒性試驗，結果大部分不具細胞毒性。另外本實驗利用thalidomide及thalidomide analogues合成物來探討對NO之抑制作用機制。研究數據顯示，thalidomide和所合成的thalidomide analogues合成物具有抑制NO的作用。此結果將有助於研究此類化合物抑制iNOS形成NO的相關免疫性疾病、癌症生長與血管增生。

關鍵字

一氧化氮 ； 腫瘤壞死因子 ； 沙利多邁 ； 血管新生 ； 鼠巨噬細胞

並列摘要

Thalidomide [N(a)-phthalimidoglutarimide] is a sedative agent, but withdraw from the market, because it caused infants born with a severe deformity of the limbs. At present, this drug is useful to treat inflammation common to a host of diseases, and combat weight loss and aphthous ulcers in AIDS patients, on the eye disease macular degeneration, on breast, prostate and brain cancer, on Kaposi's sarcoma (a form of cancer common in AIDS patients), and other related diseases. The treatment for these diseases may result from thalidomide can regulate tumor necrotic factor (TNF-a), which secreted mainly by activated monocyctes or macrophages. Because optically pure forms of thalidomide readily racemize and undergo hydrolysis, we tried to simplify the part of glutarimide of thalidomide to obtain four series of phthalimide derivatives, including phenyl-phthalimide, pyridyl-phthalimide, aminobezyl- phthalimide, and diphenylazo-phthalimide analogues. In order to further structural studies and bioactivities, we used anhydrides to replace the 1H-isoindole moiety of phthalimide derivatives to obtain related compounds. We used anhydrides and amino substrates to prepare all the above compounds and to evaluate the bioactivities. The compounds were evaluated in vitro cytotoxicity against five human tumor cell growth (HL-60﹐Hep-2﹐Hep G2﹐HONE-1 and NUGC). The data indicated that almost compounds are non-cytotoxicity. On the other hand, we evaluated the effects of thalidomide and the thalidomide-like compounds on the synthesis of nitric oxide (NO). The data suggest that thalidomide and the thalidomide-like compounds potent inhibiting activities on NO. The results are helpful to further studies on immunological diseases, tumor growth and angiogenesis.

並列關鍵字

nitric oxide ； tumor necrosis factor-alpha ； thalidomide ； angiogenesis ； RAW264.7

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