Fan X N, Zi J C, Zhu C G, et al. Chemical constituents of Heteroplexis micocephala [J]. J Nat Prod, 2009, 72(6): 1184.
[3]
Maldonado E, Apan M T R, P rez-Castorena A L. Anti-inflammatory activity of phenyl propanoids from Coreopsis mutica var. mutica[J]. Planta Med, 1998, 64: 660.
[4]
Okada N, Shirata K, Niwano M, et al. Immunosuppressive activity of a monoterpene from Eucommia ulmoides[J]. Phytochemistry, 1994, 37: 281.
[5]
Sanz J F, Marco J A. Sesquiterpene lactones from Artemisia caerulescens subsp. Gargantae [J]. Phytochemistry, 1990, 29(9): 2913.
[6]
Hikino H, Aota K, Kuwano D, et al. Structure and absolute configuration of α-totunol and β-rotunol, sesquiterpenoids of Cyperus rotundus[J]. Tetrahedron, 1971, 27: 4831.
[7]
Iijima T, Yaoita Y, Kikuchi M. Five new sesquiterpenoids and a new diterpenoid from Erigeron annuus(L.) Pers., Erigeron philadelphicus L. and Erigeron sumatrensis Retz [J]. Chem Pharm Bull, 2003, 51(5): 545.
[8]
Wu C L, Chien S C, Wang S Y, et al. Structure-activity relationships of cadinane-type sesquiterpene derivatives against wood-decay fungi [J]. Holzforschung, 2005, 59: 620.
[9]
Jakupovic J, Castro V, Bohlmann F. Further sesquiterpene lactones from costa rican eupatorieae [J]. Phytochemistry, 1987, 26: 451.
[10]
Piet D P, Schrijvers R, Franssen M C R, et al. Biotransformation of germacrane epoxides by Cichorium intybus[J]. Tetrahedron, 1995, 51: 6303.
[11]
Nyasse B, Ghogomu-Tih R, Sondengam B L, et al. Mandassidione and other sesquiterpenic ketones from Cyperus articulatus[J]. Phytochemistry, 1988, 27: 3319.
[12]
Simirgiotis M J, Favier L S, Rossomando P C, et al. Diterpenes from Laennecia sophiifolia[J]. Phytochemistry, 2000, 55: 721.
[13]
Dahmy E I, Sameeh I. A new furoclerodane from erigeron canadensis[J]. Zagazig J Pharmace Sci, 1993, 2: 111.
[14]
Raha P, Das A K, Adityachaudhuri N, et al. Cleroinermin, a neo-clerodane diterpenoid from Clerodendron inermi[J]. Phytochemistry, 1991, 30: 3812.
[15]
Faini F, Rivera P, Mah M, et al. Neo-clerodane diterpenoids and other constituents from Baccharis species[J]. Phytochemistry, 1987, 26: 3281.
[16]
Pinhey J T, Simpson R F, Batey I L. The constituents of Olearia heterocarpa. The structure of olearin, a diterpene dilactone of the cascarillin group[J]. Aust J Chem, 1972, 25: 2621.
Kuo Y H, Li Y C. Constituents of the bark of Ficus microcarpa L.f[J]. J Chin Chem Soc, 1997, 44: 321.
[20]
Siddiqui-S S S B, Naeed A, Begum S. Pentacyclic triterpenoids from the leaves of Plumeria obtuse[J]. Phytochemistry, 1989, 28: 3143.
[21]
Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays[J]. J Immunol Method, 1983, 65: 55.
[22]
Carmichael J, DeGraff W G., Gazdar A F, et al. Evaluation of a tetrazolium-based semiautomated colorimetric assay: Assessment of chemosensitivity testing[J]. Cancer Res, 1987, 47: 936.
[23]
Mo S Y, Wang S J, Shi J G. Phelligridins C(F: cytotoxic pyrano
[24]
benzo- pyran-1,6-dione and furo pyran-4-one derivatives from the fungus Phellinus igniarius[J]. J Nat Prod, 2004, 67, 823.
[25]
Zhang Y L, Gan M L, Shi J G, et al. Glycosides from the bark of Adina polycephala [J]. J Nat Prod, 2008, 71(5): 905.
[26]
Song W X, Li S, Shi J G, et al. Pyridinium alkaloid-coupled secoiridoids from the flower buds of Lonicera japonica[J]. J Nat Prod, 2008, 71(5), 922.
