学術雑誌論文 Total synthesis of natural derivatives and artificial analogs of 13-oxyingenol and their biological evaluation

Ohyoshi, Takayuki  ,  Tamura, Yuki  ,  Hayakawa, Ichiro  ,  Hirai, Go  ,  Miyazawa, Yamato  ,  Funakubo, Shota  ,  Sodeoka, Mikiko  ,  Kigoshi, Hideo

14 ( 48 )  , pp.11426 - 11437 , 2016-12 , Royal Society of Chemistry
ISSN:1477-0520
NII書誌ID(NCID):AA1168650X
内容記述
We have established an efficient synthetic methodology for the 13-oxyingenol natural derivative (13-oxyingenol-13-dodecanoate-20-hexanoate), featuring a ring-closing olefin metathesis reaction for the “direct” construction of a highly strained inside–outside framework and a Mislow–Evans-type [2,3]-sigmatropic rearrangement for the stereoselective introduction of the hydroxy group at C5. We also synthesized artificial analogs of 13-oxyingenol and ingenol by using our synthetic strategy. In vitro activation assays of protein kinase C (PKC) α and δ revealed that the dodecanoyl group at O13 on 13-oxyingenol analogs had a significant role in PKCδ activation. The PKCα- or PKCδ-activating 13-oxyingenol and ingenol analogs induced both distinct morphological changes and increases of CD11b expression in HL-60 cells, which would be typical signs of HL-60 cell differentiation to macrophage-like cells, as expected by previous reports. Intriguingly, however, similar differentiation phenotypes were observed with the use of 13-oxyingenol natural derivatives and 13-oxyingenol-13-dodecanoate showing a remarkably less potent PKCα or PKCδ activation ability, which the PKC inhibitor Gö6983 diminished. This indicated the involvement of other PKC isozymes or related kinase activities. 13-Oxyingenol analogs, which induced HL-60 cell differentiation, also induced HL-60 cell death, similar to the action of a phorbol ester, a strong PKC activator.
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