References
- Akihisa T, Yamamoto K, Tamura T, Kimura Y, Iida T, Nambara T, Chang FC. 1992. Triterpenoid ketones from Lingnania chungii mcclure: arborinone, friedelin and glutinone. Chem Pharm Bull. 40:789–791. doi:10.1248/cpb.40.789.
- Atun S, Aznam N, Arianingrum R, Takaya Y, Masatake N. 2008. Resveratrol derivatives from stem bark of Hopea and their biological activity test. J Phys Sci. 19:7–21.
- Joshi K. 2003. Leaf flavonoid patterns in Dipterocarpus and Hopea (dipterocarpaceae). Bot J Linn Soc. 143:43–46. doi:10.1046/j.1095-8339.2003.00196.x.
- Kennedy EM, P'pool SJ, Jiang J, Sliva D, Minto RE. 2011. Semisynthesis and biological evaluation of ganodermanontriol and its stereoisomeric triols. J Nat Prod. 74:2332–2337. doi:10.1021/np200205n.
- Mahato SB, Kundu AP. 1994. 13C NMR spectra of pentacyclic triterpenoids—a compilation and some salient features. Phytochemistry. 37:1517–1575. doi:10.1016/S0031-9422(00)89569-2.
- Nguyen QH, Phan TN, Ngo Van Q, Phan VK. 2007. [Oligostilbenes from stem bark of Hopea odorata Roxb]. Tap Chi Duoc Hoc. 47:37–39. Vietnamese.
- Nuanyai T, Sappapan R, Teerawatananond T, Muangsin N, Pudhom K. 2009. Cytotoxic 3,4-seco-cycloartane triterpenes from gardenia sootepensis. J Nat Prod. 72:1161–1164. doi:10.1021/np900156k.
- Nuanyai T, Sappapan R, Vilaivan T, Pudhom K. 2011. Gardenoins E–H, cycloartane triterpenes from the apical buds of Gardenia obtusifolia. Chem Pharm Bull. 59:385–387. doi:10.1248/cpb.59.385.
- Row LC, Ho JC, Chen CM. 2007. Cerebrosides and tocopherol trimers from the seeds of Euryale ferox. J Nat Prod. 70:1214–1217. doi:10.1021/np070095j.
- Salazar GC, Silva GD, Duarte LP, Vieira Filho SA, Lula IS. 2000. Two epimeric friedelane triterpenes isolated frommaytenus truncata Reiss: 1H and13C chemical shift assignments. Magn Reson Chem. 38:977–980. 10.1002/1097-458X(200011)38:11 < 977:AID-MRC757>3.0.CO;2-9.
- Satiraphan M, Pamonsinlapatham P, Sotanaphun U, Sittisombut C, Raynaud F, Garbay C, Michel S, Cachet X. 2012. Lupane triterpenes from the leaves of the tropical rain forest tree Hopea odorata Roxb. and their cytotoxic activities. Biochem Syst Ecol. 44:407–412. doi:10.1016/j.bse.2012.05.014.
- Shiva MP, Jantan I. 1998. Non-timber forest products from dipterocarps. In: Appanah S, Turnbull JM, editors. A review of dipterocarps: taxonomy, ecology and silviculture. Bogor: Center for International Forestry Research; p. 194–196.
- Sy LK, Brown GD. 1999. Novel seco-cycloartanes from kadsura coccinea and the assisted autoxidation of a tri-substituted alkene. Tetrahedron. 55:119–132. doi:10.1016/S0040-4020(98)01021-7.
- Yang XW, Li SM, Wu L, Li YL, Feng L, Shen YH, Tian JJ, Tang J, Wang N, Liu Y, Zhang WD. 2010. Abiesatrines A–J: anti-inflammatory and antitumor triterpenoids from abies georgei orr. Org Biomol Chem. 8:2609–2616. doi:10.1039/c001885f.
- Yang Y, Yu T, Lee YG, Yang WS, Oh J, Jeong D, Lee S, Kim TW, Park YC, Sung G, Cho JY. 2013. Methanol extract of Hopea odorata suppresses inflammatory responses via the direct inhibition of multiple kinases. J Ethnopharmacol. 145:598–607. doi:10.1016/j.jep.2012.11.041.
- Zhang HJ, Tan GT, Hoang VD, Hung NV, Cuong NM, Soejarto DD, Pezzuto JM, Fong HH. 2003. Natural anti-hiv agents. Part IV. Anti-HIV constituents from Vatica cinerea. J Nat Prod. 66:263–268. doi:10.1021/np020379y.
- Zhao Z, Matsunami K, Otsuka H, Shinzato T, Takeda Y. 2008. Tareciliosides A–G: cycloartane glycosides from leaves of Tarenna gracilipes (Hay.) Ohwi. Chem Pharm Bull. 56:1153–1158. doi:10.1248/cpb.56.1153.