Total synthesis and biological evaluation of oscillatoxins D, E, and F

被引:11
作者
Araki, Yusuke [1 ]
Hanaki, Yusuke [1 ,3 ]
Kita, Masaki [1 ]
Hayakawa, Koutaro [2 ]
Irie, Kazuhiro [2 ]
Nokura, Yoshihiko [1 ]
Nakazaki, Atsuo [1 ]
Nishikawa, Toshio [1 ]
机构
[1] Nagoya Univ, Grad Sch Bioagr Sci, Nagoya, Aichi, Japan
[2] Kyoto Univ, Grad Sch Agr, Kyoto, Japan
[3] Kagawa Univ, Fac Agr, Takamatsu, Kagawa, Japan
关键词
oscillatoxin; total synthesis; cytotoxicity; antileukemic; anticancer; PROTEIN-KINASE-C; PROMYELOCYTIC LEUKEMIA-CELLS; PHORBOL ESTERS; APLYSIATOXIN DERIVATIVES; STRUCTURAL BASIS; DEBROMOAPLYSIATOXIN; ACTIVATION; DIFFERENTIATION; INHIBITION; TELEOCIDIN;
D O I
10.1093/bbb/zbab042
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Oscillatoxins (OTXs) and aplysiatoxins are biosynthetically related polyketides produced by marine cyanobacteria. We previously developed a synthetic route to phenolic O-methyl analogs of OTX-D and 30-methyl-OTX-D during collective synthesis of these natural products. According to our synthetic strategy, we achieved total synthesis of OTX-D, 30-methyl-OTX-D, OTX-E, and OTX-F by deprotecting the O-methyl group in an earlier intermediate, and determined their biological activities. Although OTX-D and 30-methyl-OTX-D have been reported to show antileukemic activity against L1210 cell line, we found that their cytotoxicity in vitro against this cell line is relatively weak (IC50: 29-52 mu m). In contrast, OTX-F demonstrated cell line-selective antiproliferative activity against DMS-114 lung cancer cells, which implies that OTXs target as yet unknown target molecules as part of this unique activity.
引用
收藏
页码:1371 / 1382
页数:12
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