| Project/Area Number |
12557202
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 展開研究 |
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| Research Field |
Chemical pharmacy
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| Research Institution | The University of Tokushima |
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Principal Investigator |
SHIBUYA Masayuki The University of Tokushima, Faculty of Pharmaceutical Sciences, Professor, 薬学部, 教授 (40027066)
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| Co-Investigator(Kenkyū-buntansha) |
YAMADA Yuji Taiho Pharmaceutical Co., Chief Manager, 第1がん研究所, 所長
SUZUKI Ichiro The University of Tokushima, Faculty of Pharmaceutical Sciences, Assis. Professor, 薬学研究科, 助手 (40294714)
NEMOTO Hisao The University of Tokushima, Faculty of Pharmaceutical Sciences, Assoc. Professor, 薬学部, 助教授 (30208293)
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| Project Period (FY) |
2000 – 2002
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| Project Status |
Completed (Fiscal Year 2002)
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| Budget Amount *help |
¥13,200,000 (Direct Cost: ¥13,200,000)
Fiscal Year 2002: ¥3,200,000 (Direct Cost: ¥3,200,000)
Fiscal Year 2001: ¥3,800,000 (Direct Cost: ¥3,800,000)
Fiscal Year 2000: ¥6,200,000 (Direct Cost: ¥6,200,000)
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| Keywords | enediyne / enyne-allene / synthesis / lexitropsin / radical / optically-active / DNA / cleavage / ハロゲン |
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| Research Abstract |
Various acyclic (Z)-1, 2, 4-heptatrien-6-ynes, which undergo cycloaromatization to produce reactive dehydrotoluene biradicals, have been investigated as chemical models for a class of potent antitumor antibiotics, neocarzinostatin (NCS). The preparation of enyne-allene models possessing characteristic triggering devices which initiate the generation of dehydrotoluene biradicals is a challenging current problem. For the development of this class of molecules, we designed various models which produce carbon-biradicals via Myers-Saito-type cyclization. For typical examples, we synthesized the naphthoate esters having the α-hydroxy naphthoate moiety in NCS and demonstrated the biradical formation reactions in acidic media.
For the elucidation of these cascade reaction mechanisms and development of biologically active substances, the preparation of thermally stable carboxylic acid derivatives, which cycloaromatize under mild conditions, is essential. For this purpose, we designed novelα-alkynylacetic acid derivatives. A series of decarboxylative cycloaromatization reactions under various conditions were carried out. The reaction rates in MeOH were relatively slow and the reactions in the absence or presence of a radical scavenger (O_2 or 1, 4-cyclohexadiene) produced the products in similar yields, respectively. These results suggest that the cycloaromatization proceeded via an ionic cyclization pathway but not via the biradical intermediate.
In order to prevent the ionic pathway during the cyclization reaction, the molecules possessing electron-withdrawing groups which destabilize the cationic carbon center were synthesized. The reactions of these compounds in acidic media produced predominantly or exclusively the products via biradical intermediates. Some of them showed relatively potent DNA-damaging activity. Studies on the analogues of this class of compounds and development of bio-active enediynes are continuing.
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