2. Academic Validation
  3. Cytotoxic components from the dried rhizomes of Zingiber officinale Roscoe

Cytotoxic components from the dried rhizomes of Zingiber officinale Roscoe

  • Arch Pharm Res. 2008 Apr;31(4):415-8. doi: 10.1007/s12272-001-1172-y.
Ju Sin Kim 1,  Sa Im Lee,  Hye Won Park,  Jae Heon Yang,  Tae-Yong Shin,  Youn-Chul Kim,  Nam-In Baek,  Sung-Hoon Kim,  Sang Un Choi,  Byoung-Mog Kwon,  Kang-Hyun Leem,  Mun Yhung Jung,  Dae Keun Kim
Affiliations

Affiliation

  • 1 College of Pharmacy, Woosuk University, Samrye, Korea.
PMID: 18449496 DOI: 10.1007/s12272-001-1172-y
Abstract

Five compounds were isolated from the chloroform-soluble fraction of the methanolic extract of the dried rhizomes of Zingiber officinale (Zingiberaceae) through repeated column chromatography. Their chemical structures were elucidated as 4-, 6-, 8-, and 10-gingerols, and 6-shogaol using spectroscopic analysis. Among the five isolated compounds, 6-shogaol exhibited the most potent cytotoxicity against human A549, SK-OV-3, SK-MEL-2, and HCT15 tumor cells. 6-shogaol inhibited proliferation of the transgenic mouse ovarian Cancer cell lines, C1 (genotype: p53(-/-), c-Myc, K-Ras) and C2 (genotype: p53(-/-), c-Myc, Akt), with ED(50) values of 0.58 microM (C1) and 10.7 microM (C2).

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