4.7 Article

Antiproliferative Compounds from Cleistanthus boivinianus from the Madagascar Dry Forest

期刊

JOURNAL OF NATURAL PRODUCTS
卷 78, 期 7, 页码 1543-1547

出版社

AMER CHEMICAL SOC
DOI: 10.1021/np501020m

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资金

  1. Fogarty International Center
  2. National Cancer Institute
  3. National Institute of Allergy and Infectious Diseases
  4. National Institute of Mental Health
  5. National Institute on Drug Abuse
  6. National Heart Lung and Blood Institute
  7. National Center for Complementary and Alternative Medicine
  8. Office of Dietary Supplements
  9. National Institute of General Medical Sciences
  10. Biological Sciences Directorate of the National Science Foundation
  11. Office of Biological and Environmental Research of the U.S. Department of Energy [U01 TW00313]
  12. International Cooperative Biodiversity Groups
  13. National Research Initiative of the Cooperative State Research, Education and Extension Service, USDA [2008-35621-04732]
  14. NSF S-STEM award [DUE-0850198]
  15. National Science Foundation [CHE-0722638]

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The two new lignans 3 alpha-O-(beta-D-glucopyranosyl)desoxypodophyllotoxin) (1) and 4-O-(beta-D-glucopyranosyl)dehydropodophyllotoxin (2) were isolated from Cleistanthus boivinianus, together with the known lignans deoxypicropodophyllotoxin (3), (+/-)-beta-apopicropodophyllin (4), (-)-desoxypodophyllotoxin (5), (-)-yatein (6), and beta-peltatin-5-O-beta-D-glucopyranoside (7). The structures of all compounds were characterized by spectroscopic techniques. Compounds 1, 4, and 5 showed potent antiproliferative activities against the A2780 ovarian cancer cell line, with IC50 values of 33.0 +/- 3.6, 63.1 +/- 6.7, and 230 +/- 1 nM, respectively. Compounds 2 and 7 showed only modest A2780 activities, with IC50 values of 2.1 +/- 0.3 and 4.9 +/- 0.1 mu M, respectively, while compounds 3 and 6 had IC50 values of >10 mu M. Compound 1 also had potent antiproliferative activity against the HCT-116 human colon carcinoma cell line, with an IC50 value of 20.5 nM, and compound 4 exhibited modest antiproliferative activity against the A2058 human caucasian metastatic melanoma and MES-SA human uterine sarcoma cell lines, with IC50 values of 4.6 and 4.0 mu M, respectively.

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