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DOI: 10.1055/s-2008-1074546
© Georg Thieme Verlag KG Stuttgart · New York
Further Studies of the Norditerpene (+)-Harringtonolide Isolated from Cephalotaxus harringtonia var. drupacea: Absolute Configuration, Cytotoxic and Antifungal Activities
Publication History
Received: January 28, 2008
Revised: April 14, 2008
Accepted: April 19, 2008
Publication Date:
03 June 2008 (online)
Abstract
Harringtonolide (= hainanolide) is a complex polycyclic fused norditerpene isolated from Cephalotaxus harringtonia var. drupacea. In spite of its appealing biological properties – we measured an IC50 of 43 nM on KB cells and a significant antifungal activity – its absolute configuration has not yet been firmly established. This was done herein using X-ray anomalous scattering after bromination of the tropone ring, unambiguously giving the stereochemistry 5R,6R,7S,13S,14S,15R,16R. Detailed in vitro biological measurements are provided.
Key words
Cephalotaxus harringtonia var. drupacea - Cephalotaxaceae - norditerpenes - absolute configuration - X-ray diffraction - biological activities
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References
- 1 Buta J G, Flippen J L, Lusby W R. Harringtonolide, a plant growth inhibitory tropone from Cephalotaxus harringtonia (Forbes) K. Koch. J Org Chem. 1978; 43 1002-3
- 2 Sun N J, Xue Z, Liang X T, Wang L. Studies on the structure of a new antitumor agent, hainanolide. Yao Hsueh Hsueh Pao. 1979; 14 39-44. [Chem Abstr 1980 : 220590 g]
- 3 Sun N J, Zhao Z F, Chen R T, Lin W, Zhou Y Z. Isolation and identification of the antitumor component-hainanolide from Cephalotaxus fortunei. . Yao Hsueh Hsueh Pao. 1981; 16 233-4. [Chem Abstr 1981 : 156431p]
- 4 Ren L, Xue Z. Studies on the antitumor constituents of Cephalotaxus sinensis. . Zhongcaoyao. 1981; 12 1-4. [Chem Abstr 1982 : 3672p]
- 5 Sasse J M, Wardrop J J, Rowan K S, Aspinall D, Coombe B G, Paleg L G. et al . Some physiological effects of podolactone-type inhibitors. Physiol Plantarum. 1982; 55 51-9
- 6 Kang S, Cai S, Teng L. Antiviral effect of hainanolide. Yaoxue Xuebao. 1981; 16 867-8. [Chem Abstr 1982 : 82519v]
- 7 Xue Z, Sun N J, Chen D H, Xu L Z, Chen W M, Ren L J. et al .The studies of chemical constituents of Cephalotaxus hainanensis Li. Chem Nat Prod 1982: 195-9 [Chem Abstr 1983 : 194936b]
- 8 Xue Z, Sun N J, Liang X T. Studies on the structure of hainanolidol. Yao Hsueh Hsueh Pao. 1982; 17 236-7. [Chem Abstr 1982 : 177999r]
- 9 Du J, Chiu M H, Nie R L. Two new lactones from Cephalotaxus fortunei var. alpina. . J Nat Prod. 1999; 62 1664-5
- 10 Yoon K D, Jeong D G, Hwang Y H, Ryu J M, Kim J. Inhibitors of osteoclast differentiation from Cephalotaxus koreana. . J Nat Prod. 2007; 70 2029-32
- 11 Flippen-Anderson J L, Duesler E. Harringtonolide: a complex tropone. Acta Crystallogr B. 1979; 35 1253-4
- 12 Bao G, He C, Xu C. Crystal structure of hainanolide. Zhongguo Yixue Kexueyuan Xuebao. 1983; 5 89-93. [Chem Abstr 1984 : 59893e]
- 13 Frey B, Wells A P, Rogers D H, Mander L N. Synthesis of the unusual diterpenoid tropones hainanolidol and harringtonolide. J Am Chem Soc. 1998; 120 1914-5
- 14 Horeau A. Principe et applications d′une nouvelle méthode de détermination des configurations dite ”par dédoublement partiel”. Tetrahedron Lett. 1961; 15 506-12
- 15 Horeau A, Kagan H B. Détermination des configurations par ”dédoublement partiel” –III– Alcools stéroïdes. Tetrahedron. 1964; 20 2431-41
- 16 Fontana A, Albarella L, Scognamiglio G, Uriz M, Cimino G. Structural and stereochemical studies of C-21 terpenoids from Mediterranean Spongiidae sponges. J Nat Prod. 1996; 59 869-72
- 17 Kotowicz C, Hernández L R, Cerda-García-Rojas C M, Villecco M B, Catalán C AN, Joseph-Nathan P. Absolute configuration of trixanolides from Trixis pallida. . J Nat Prod. 2001; 64 1326-31
- 18 Fukuyama Y, Yokoyama R, Ohsaki A, Takahashi H, Minami H. An example of the co-occurrence of enantiomeric labdane-type diterpenes in the leaves of Mimosa hostilis. . Chem Pharm Bull. 1999; 47 454-5
- 19 Bijvoet J M, Peerdeman A F, Van Bammel A J. Determination of the absolute configuration of optically active compounds by means of X-rays. Nature. 1951; 168 271-2
- 20 Peerdeman A F, Bijvoet J M. The indexing of reflexions in investigations involving the use of the anomalous scattering effect. Acta Crystallogr. 1956; 9 1012-5
- 21 Flack H D. Acta Crystallogr A 1983 A39: 876-81
- 22 Evanno L, Deville A, Dubost L, Chiaroni A, Bodo B, Nay B. Utility of a chiral 1,3-dioxane template in stereoselective intramolecular Diels–Alder reactions. Tetrahedron Lett. 2007; 48 2893-6
Dr Bastien Nay
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