| Project/Area Number |
10557204
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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 | HOKKAIDO UNIVERSITY |
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Principal Investigator |
KOBAYASHI Jun'ichi Hokkaido Univ., Grad. School of Pharm. Sci., Professor, 大学院・薬学研究科, 教授 (90221241)
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| Co-Investigator(Kenkyū-buntansha) |
TSUDA Masashi Hokkaido Univ., Grad. School of Pharm. Sci., Instructor, 大学院・薬学研究科, 助手 (10261322)
SHIGEMORI Hideyuki Hokkaido Univ., Grad. School of Pharm. Sci., Associate Professor, 大学院・薬学研究科, 助教授 (70202108)
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| Project Period (FY) |
1998 – 1999
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| Project Status |
Completed (Fiscal Year 1999)
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| Budget Amount *help |
¥11,500,000 (Direct Cost: ¥11,500,000)
Fiscal Year 1999: ¥4,500,000 (Direct Cost: ¥4,500,000)
Fiscal Year 1998: ¥7,000,000 (Direct Cost: ¥7,000,000)
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| Keywords | Japanese yew / multidrug-resistance / glycoprotein / tubulin / MDR modifier / antitumor / taxoids / inhibition of microtubule depolymerization / P-糖蛋白質 / タキシニン / 構造活性相関 |
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| Research Abstract |
In this research project, search for and molecular design of bioactive taxoids were carried out.
From the Japanese yew Taxus cuspidata Sieb. Et Zucc. collected at Sapporo, ten new taxoids and related diterpenoids, taxezopidines B 〜 H and J 〜 L, were isolated and the structures were elucidated on the basis of spectroscopic data and chemical means. Taxezopidines G and H increased accumulation of vincristine in multidrug-resistant cells, while taxol did not show such activity and taxezopidines G and H exhibited no cytotoxicity. Taxuspine C, a known taxoid from the yew, enhanced the chemotherapeutic effect of vincristine (VCR) in P388/VCR-bearing mice. These results suggest that some taxoids may become useful lead compounds to overcome multidrug resistance in tumor cells. On the other hand, taxezopidines K and L markedly inhibited 2+ Ca -induced depolymerization of microtubules and the potency corresponded to half to one third of that of taxol, although taxezopidines K and L lack both the oxetane ring and N-acylphenylisoserine moiety which are associated with this unique activity in taxol. Taxuspine D, a known taxoid from the yew, induced unusual shape change of mitotic spindles like taxol. More powerful and specific MDR modifiers may be found through further studies of structure-activity relationships on the new compounds obtained in this study.
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