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Some C-benzylated flavonoids based on gericudranin A were synthesized and evaluated their cytotoxic activities for the elucidation of structure-activity relationship. 2,4,6-Trihydroxyacetophenone was converted to target molecules in 6~7 steps via sequential protection, aldol condensation, cyclization, regioselective C-benzylation, and deprotection. The cellular growth inhibition of the synthetic C-benzylated flavonoids was investigated against sixteen human cancer cell lines. Among these compounds, 5b showed the most potent cytotoxicities against several cell lines, especially as potent as adriamycin against SNB19 cell lines with an IC50 value of 0.7 μM.

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참고문헌 (12건) : 자료제공( 네이버학술정보 )

참고문헌 목록에 대한 테이블로 번호, 참고문헌, 국회도서관 소장유무로 구성되어 있습니다.
번호 참고문헌 국회도서관 소장유무
1 Total Synthesis of (±)-Gericudranin A 네이버 미소장
2 Uvaretin, a new antitumor agent from Uvaria acuminata (Annonaceae). 네이버 미소장
3 Harborne, J. B., The Flavonoids: Advance in Research since 1980, Chapman and Hall, London (1988). 미소장
4 Uvaretin and isouvaretin. Two novel cytotoxic c-benzylflavanones from uvaria chamae L. 네이버 미소장
5 Uvarinol: a novel cytotoxic tribenzylated flavanone from Uvaria chamae 네이버 미소장
6 New Dihydrochalcones and Flavanones From Uvaria Angolensis 네이버 미소장
7 Cytotoxic C-Benzylated Dihydrochalcones from Uvaria acuminata 네이버 미소장
8 Two Benzylated Dihydroflavonols from Cudrania Tricuspidata 네이버 미소장
9 Cytotoxic benzyl dihydroflavonols from Cudrania tricuspidata 네이버 미소장
10 Induction of Apoptosis in Human Promyelocytic Leukemia Cell Line HL-60 by C-Benzylated Dihydrochalcones, Uvaretin, Isouvaretin and Diuvaretin(Medicinal Chemistry) 네이버 미소장
11 Skehan, P., Storeng, R., Scudiero, D., Monks, A., MaMahon, J., Vistica, D., Warren, J. T., Bokesch, H., Kenny, S., and Boyd, M. R., New colorimetric cytotoxicity assay for anticancer- drug screening. J. Natl. Cancer Inst., 82, 1107-1112 (1990). 미소장
12 Wirasathien, L., Pengsuparp, T., Moriyasu, M., Kawanish, K., and Suttisri, R., Cytotoxic C-benzylated chalcone and other constituents of Ellipeiopsis cherrevensis. Arch. Pharm. Res., 29, 497-502 (2006). 미소장