Planta Med 2010; 76(10): 1011-1014
DOI: 10.1055/s-0029-1240863
Natural Product Chemistry
Letters
© Georg Thieme Verlag KG Stuttgart · New York

SIRT1 Inhibitory Diterpenoids from the Vietnamese Medicinal Plant Croton tonkinensis

Trong Tuan Dao1 [*] , Thi Van Thu Le1 [*] , Phi Hung Nguyen1 , Phuong Thien Thuong1 , Pham Thi Hong Minh2 , Eun-Rhan Woo1 , Kwang Youl Lee3 , Won Keun Oh1
  • 1BK21 Project Team, College of Pharmacy, Chosun University, Gwangju, Republic of Korea
  • 2Institute of Chemistry, Vietnam Academy of Science and Technology, Caugiay, Hanoi, Vietnam
  • 3College of Pharmacy, Chonnam National University, Yongbong-dong, Gwangju, Republic of Korea
Further Information

Publication History

received August 17, 2009 revised December 30, 2009

accepted January 10, 2010

Publication Date:
22 February 2010 (online)

Abstract

Silent information regulator two ortholog 1 (SIRT1) is a member of the sirtuin deacetylase family of enzymes that removes acetyl groups from the lysine residues in histones and other proteins. It has been suggested that SIRT1 inhibitors might be beneficial in the treatment of cancer and neurodegenerative diseases. Bioassay-guided fractionation of the MeOH extract of the leaves of Croton tonkinensis resulted in the isolation of a new ent-kaurane diterpenoid (1) along with 11 known compounds (212). The structure of the new compound 1 was determined to be ent-11α-acetoxy-7β-hydroxykaur-16-en-15-one based on spectroscopic analyses. Compounds 3, 4, 69, 11, and 12 exhibited SIRT1 inhibitory activity in an in vitro assay, with IC50 values ranging from 16.08 ± 0.11 to 44.34 ± 2.32 µM. This is the first report showing the potential of ent-kaurane diterpenoids as a new class of natural SIRT1 inhibitors.

References

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1 These authors contributed equally to this work.

Won Keun Oh

College of Pharmacy
Chosun University

375 Seosuk-dong, Dong-gu

Gwangju 501–759

Republic of Korea

Phone: + 82 62 2 30 63 70

Fax: + 82 6 22 30 63 70

Email: wkoh@chosun.ac.kr

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