Chemistry of Ecteinascidins. Part 5: An Additional Proof of Cytotoxicity Evaluation of Ecteinascidin 770 Derivatives
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- Toyoshima Ryoko
- Graduate School of Pharmaceutical Sciences, Meiji Pharmaceutical University
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- Mori Nanae
- Graduate School of Pharmaceutical Sciences, Meiji Pharmaceutical University
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- Suzuki Toshihiro
- Graduate School of Pharmaceutical Sciences, Meiji Pharmaceutical University
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- Lowtangkitcharoen Witaya
- Center for Bioactive Natural Products from Marine Organisms and Endophytic Fungi (BNPME), Department of Pharmacognosy and Pharmaceutical Botany, Faculty of Pharmaceutical Sciences, Chulalongkorn University
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- Suwanborirux Khanit
- Center for Bioactive Natural Products from Marine Organisms and Endophytic Fungi (BNPME), Department of Pharmacognosy and Pharmaceutical Botany, Faculty of Pharmaceutical Sciences, Chulalongkorn University
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- Saito Naoki
- Graduate School of Pharmaceutical Sciences, Meiji Pharmaceutical University
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Eleven 2′-N-acyl derivatives (5a–k) were prepared from ecteinascidin 770 (Et 770: 1b) via known 18,6′-O-bisallyl-protected compound (3) in three steps. Their in vitro cytotoxicities were determined by measuring IC50 values against human cell lines HCT116 and DU145. 5-Isoxazolecarboylamide derivative (5i) and 4-methoxybenzoylamide derivative (5k) were found to be promising leads for further optimization.
収録刊行物
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- CHEMICAL & PHARMACEUTICAL BULLETIN
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CHEMICAL & PHARMACEUTICAL BULLETIN 64 (7), 966-969, 2016
公益社団法人 日本薬学会
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詳細情報
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- CRID
- 1390282679155515136
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- NII論文ID
- 130005160038
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- NII書誌ID
- AA00602100
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- ISSN
- 13475223
- 00092363
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- NDL書誌ID
- 027451781
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- PubMed
- 27373655
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
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- PubMed
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- 使用不可