Planta Med 2010; 76(15): 1742-1745
DOI: 10.1055/s-0030-1249833
Natural Product Chemistry
Letters
© Georg Thieme Verlag KG Stuttgart · New York

Two New Sesquiterpenes from Acorus calamus

Weiwei Dong2 , 4 , Minjie Li3 , Dajian Yang2 , Runhua Lu1
  • 1Department of Applied Chemistry, College of Sciences, China Agricultural University, Beijing, P. R. China
  • 2State Key Laboratory of Chinese Medicine and Molecular Pharmacology, Shenzhen, P. R. China
  • 3Department of Chemistry, Shanghai University, Shanghai, P. R. China
  • 4Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu, P. R. China
Further Information

Publication History

received September 26, 2009 revised March 20, 2010

accepted March 23, 2010

Publication Date:
23 April 2010 (online)

Abstract

A novel cadinane sesquiterpene with a propan-2-ylidene, named (1R,4R,6S,10R)-1-hydroxy-7(11)-cadinen-5,8-dione (1), and a new sesquiterpene, named (2R,6R,7S,9S)-1(10),4-cadinadiene-2,9-diol (2), were isolated from the ethanol extract of the rhizome of Acorus calamus L. Their structures were elucidated on the basis of spectroscopic data including NMR spectroscopy and X-ray crystallography. The absolute configurations of compounds 1 and 2 were confirmed by comparison of their experimental optical rotations with those obtained from theoretical calculations at the B3LYP/6–311+G (d) level of theory.

References

  • 1 Nawamaki K, Kuroyanagi M. Sesquiterpenoids from Acorus calamus as germination inhibitors.  Phytochemistry. 1996;  43 1175-1182
  • 2 Iguchi M, Niwa M, Nishiyama A, Yamamura S. Isolation and structure of acoragermacrone.  Tetrahedron Lett. 1973;  29 2759-2762
  • 3 Patra A, Mitra A K. Constituents of Acorus calamus Linn.  Indian J Chem. 1979;  17 B 412-414
  • 4 Rai R, Siddiqui I R, Singh J. Triterpenoid saponins from Acorus calamus.  Indian J Chem. 1998;  37 B 473-476
  • 5 Robert B, Henrey T. Medicinal plants. London; Churchill 1983
  • 6 Frisch M J, Trucks G W, Schlegel H B, Scuseria G E, Robb M A, Cheeseman J R, Montgomery J A, Vreven Jr T, Kudin K N, Burant J C, Millam J M, Iyengar S S, Tomasi J, Barone V, Mennucci B, Cossi M, Scalmani G, Rega N, Petersson G A, Nakatsuji H, Hada M, Ehara M, Toyota K, Fukuda R, Hasegawa J, Ishida M, Nakajima T, Honda Y, Kitao O, Nakai H, Klene M, Li X, Knox J E, Hratchian H P, Cross J B, Adamo C, Jaramillo J, Gomperts R, Stratmann R E, Yazyev O, Austin A J, Cammi R, Pomelli C, Ochterski J W, Ayala P Y, Morokuma K, Voth G A, Salvador P, Dannenberg J J, Zakrzewski V G, Dapprich S, Daniels A D, Strain M C, Farkas O, Malick D K, Rabuck A D, Raghavachari K, Foresman J B, Ortiz J V, Cui Q, Baboul A G, Clifford S, Cioslowski J, Stefanov B B, Liu G, Liashenko A, Piskorz P, Komaromi I, Martin R L, Fox D J, Keith T, Al-Laham M A, Peng C Y, Nanayakkara A, Challacombe M, Gill P M W, Johnson B, Chen W, Wong M W, Gonzalez C, Pople J A. Gaussian 03, Revision B.04. Pittsburgh; Gaussian, Inc. 2003
  • 7 Kondru R K, Peter W, Beratan D N. Theory-assisted determination of absolute stereochemistry for complex natural products via computation of molar rotation angles.  J Am Chem Soc. 1998;  120 2204-2205
  • 8 Rice J E, Handy N C. The calculation of frequency-dependent polarizabilities as pseudo-energy derivatives.  J Chem Phys. 1991;  94 4959-4971
  • 9 Liu D Z, Wang F, Liao T G, Tang J G, Steglich W, Zhu H J, Liu J K. Vibralactone: a lipase inhibitor with an unusual fused β-lactone produced by cultures of the basidiomycete Boreostereum vibrans.  Org Lett. 2006;  8 5749-5752
  • 10 Sheldrick G M. SHELXS-97: Program for the solution of crystal structures. Göttingen; University of Göttingen 1997
  • 11 Sheldrick G M. SHELXL-97: Program for the refinement of crystal structures. Göttingen; University of Göttingen 1997

Prof. Dr. Runhua Lu

Department of Applied Chemistry
College of Sciences
China Agricultural University

17# Qinghua East Road

100094 Beijing

People's Republic of China

Phone: + 861062736957

Fax: + 861062736777

Email: rhlu@cau.edu.cn