• Title/Summary/Keyword: (-)-hinokinin

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Neuroprotective Lignans from Biota orientalis leaves

  • Yoon, Jeong-Seon;Koo, Kyung-Ah;Ma, Choong-Je;Sung, Sang-Hyun;Kim, Young-Choong
    • Natural Product Sciences
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    • v.14 no.3
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    • pp.167-170
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    • 2008
  • We previously reported that 90% MeOH fraction of Biota orientalis leaves (L.) ENDL. had significant neuroprotective activity against glutamate-induced neurotoxicity in primary cultures of rat cortical cells. In the present study, (-)-savinin (1), (-)-hinokinin (2), dehydroheliobuphthalmin (3) were isolated by bioactivity-guided fractionation from the 90% MeOH fraction. All three lignans had significant neuroprotective activities against glutamate-induced neurotoxicity at the concentrations ranging from 0.1 to 10.0 ${\mu}M$.

Inhibitory Lignans against NFAT Transcription Factor from Acanthopanax koreanum

  • Cai, Xing-Fu;Lee, Im-Seon;Dat, Nguyen-Tien;Guanghai-Shen;Kang, Jong-Seong;Kim, Dong-Hyun;Kim, Young-Ho
    • Archives of Pharmacal Research
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    • v.27 no.7
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    • pp.738-741
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    • 2004
  • Three lignans isolated from the roots of A. koreanum (Araliaceae), namely eleutheroside E(1), tortoside A(2), and hemiariensin(4), were evaluated for their ability to inhibit NFAT transcription factor. Of these compounds, compound 4, possessing a diarylbutane skeleton, exhibited potent inhibitory activity against NFAT transcription factor (($IC_{50}$ : 36.3${\pm}2.5{\mu}\textrm{M}$). However, the activities of 1 (($IC_{50}$:>500 11M) and 2 (($IC_{50}$: 136.1 ${\pm}9.4\mu\textrm{M}$), which possess bisaryldioxabicy-clooctane skeletons, were lower. As the lignan derivatives of the same skeletons, hinokinin (5) and (-)-yatein (6) with diarylbutane skeletons and(+)-syringaresinol (3) with a bisaryldioxabicy-clooctane skeleton were also studied for their inhibitory effects on NFAT transcription factor.