Synthesis of New Peptidic Glycoclusters Derived from β-Alanine Part 2 : Optionally Modulated Distance between Side-Chain Branched Points
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概要
- 論文の詳細を見る
The synthesis of an asymmetric glycocluster 1 has been achieved using two glycocluster units 12 and 13, prepared by coupling the cluster chain unit 4 with each ω-amino acid (β-alanine and 6-aminocapronic acid) trichloroethyl ester, and peptidic C-terminal block glycocluster 16, prepared by coupling the bifunctional linker 14 with sugar unit 9. This method facilitated the synthesis of the cluster optionally modulated the distance between the side-chain branched points by using various ω-amino acids. We also synthesized glycodendron 2 using the same intermediate.
- 公益社団法人日本薬学会の論文
- 2005-09-01
著者
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TAKEDA Tadahiro
Kyoritsu University of Pharmacy
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竹田 忠紘
Kyoritsu College Of Pharmacy
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Sato K
Division Of Pharmacology National Institute Of Health Sciences
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Sato K
National Inst. Health Sci. Tokyo Jpn
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Taguchi Tomiko
Laboratory Of Plant Pathology And Genetic Engineering Faculty Of Agriculture Okayama University
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HADA Noriyasu
Kyoritsu College of Pharmacy
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Hada N
Kyoritsu University Of Pharmacy
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SATO Koji
Kyoritsu University of Pharmacy
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JIN Yuhua
Kyoritsu University of Pharmacy
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Takeda T
Kyoritsu University Of Pharmacy
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Takeda Tadahiro
Kyoritsu College Of Pharmacy
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Sato K
Kyoritsu University Of Pharmacy
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Takeda Tadahiro
Kyoritsu College Of Pharmac
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Hada Noriyasu
Kyoritsu University of Pharmacy
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