| Project/Area Number |
09672282
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
医薬分子機能学
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| Research Institution | Osaka University |
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Principal Investigator |
MIYASHITA Kazuyuki Graduate School of Pharmaceutical Sciences, Osaka University Associate Professor, 薬学研究科, 助教授 (10166168)
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| Co-Investigator(Kenkyū-buntansha) |
宮下 和之 大阪大学, 薬学研究科, 助教授 (10166168)
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| Project Period (FY) |
1997 – 1999
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| Project Status |
Completed (Fiscal Year 1999)
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| Budget Amount *help |
¥2,900,000 (Direct Cost: ¥2,900,000)
Fiscal Year 1999: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 1998: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1997: ¥1,800,000 (Direct Cost: ¥1,800,000)
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| Keywords | Unnatural amino acids / Unnatural peptides / pyridoxal / Stereoselective synthesis / Regioselective synthesis |
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| Research Abstract |
In order to establish the synthetic method for unnatural amino acids and peptides containing such amino acids by employing pyridoxal derivatives, we studied α-alkylation and β-replacement reaction of Ser derivatives and the following results were obtained.
1) Asymmetric α-alkylation of amino esters were successfully achieved by employing pyridoxal derivatives having a chiral ionophore side chain at C-3 and/or a chiral ansa-structure, giving rise to optically active α, α-dialkyl amino esters. The stereoselectivity of the reaction was found to depend on the kind of metal ion : the chiral environment is specifically constructed by coordination of the metal ion with the ionophore side chain. On application of this reaction to peptides, stereoselective and N-terminal selective α-alkylation of peptides was accomplished, being a novel method for the synthesis of unnatural peptides by direct modification.
2) Pyridoxal derivatives having an ethoxyethoxy group at C-3 and an imidazole side chain at C-5 was found to catalyze β-replacement reaction of Ser O-carbonate with thiols to give various S-substituted Cys derivatives in the presence of LiィイD1+ィエD1. Peptides having Ser O-carbonate at the N-terminal position were also successfully converted to the peptides having S-substituted Cys at the N-terminal position by the same reaction. The β-replacement reaction with a carbon nucleophile such as nitroacetate also took place in the presence of LiィイD1+ィエD1 and ZnィイD12+ィエD1 by using pyridoxal derivatives having a methylthio group at C-2.
We are studying the application of these reactions to solid-phase reactions, which would be of great use and versatile particularly on application to construction of peptides library.
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