New triterpenoid saponins from the leaves of <em>Cyclocarya paliurus</em>

doi:10.1016/j.cclet.2014.11.033

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[1]	Editor Committee for Flora of China of the Chinese Academy of Science, Flora of China, vol. 21, Science Publishing House, Beijing, 1979, pp. 18-19.
[2]	The Editorial Committee of the Administration Bureau of Traditional Chinese Medicine, Chinese Materia Medica, vol. 2, Shanghai Science and Technology Publishing House, Shanghai, 1999, pp. 370-371.
[3]	H. Kurihara, S. Asami, H. Shibata, H. Fukami, T. Tanaka, Hypolipemic effect of Cyclocarya paliurus (Batal) Iljinskaja in lipid-loaded mice, Biol. Pharm. Bull. 26 (2003) 383-385.
[4]	R.G. Shu, C.R. Xu, L.N. Li, Studies on the sweet principles from the leaves of Cyclocarya paliurus (Batal.) Iljinsk, Acta Pharm. Sin. 30 (1995) 757-761.
[5]	R.G. Shu, C.R. Xu, L.N. Li, Z.L. Yu, Cyclocariosides II and III: two secodammarane triterpenoid saponins from Cyclocarya paliurus, Planta Med. 61 (1995) 551-553.
[6]	E.J. Kennelly, L.N. Cai, L.N. Long, et al., Novel highly sweet secodammarane glycosides from Pterocarya puliurus, J. Agric. Food Chem. 43 (1995) 2602-2607.
[7]	Z.Y. Jiang, X.M. Zhang, J. Zhou, S.X. Qiu, J.J. Chen, Two new triterpenoid glycosides from Cyclocarya paliurus, J. Asian Nat. Prod. Res. 8 (2006) 93-98.
[8]	D.J. Yang, Z.C. Zhong, Z.M. Xie, Studies on the sweet principles from the leaves of Cyclocarya paliurus (Batal.) Iljinskaya, Acta Pharm. Sin. 27 (1992) 841-844.
[9]	R.J. Zhong, R.G. Shu, X.L. Ni, C.R. Xu, L.N. Li, Studies on the chemical structure of Cyclocaric acid A, Acta Pharm. Sin. 31 (1996) 398-400.
[10]	R.J. Zhong, Y.H. Gao, C.R. Xu, L.N. Li, Pentacyclic triterpenoids from Rounduingfruit Cyclocarya (Cyclocarya paliurus), Chin. Trad. Herbal Drugs 27 (1996) 387-388.
[11]	R.G. Shu, Z.R. Song, J.C. Shu, Study on the chemical constituents of the butanol extraction of Cyclocarya paliurus (Batal.) Iljinsk, J. Chin. Med. Mater. 29 (2006) 1304-1307.
[12]	R.G. Shu, J.C. Shu, Phenolic constituents of Cyclocarya paliurus, Chin. Trad. Herbal Drugs 38 (2007) 507-508.
[13]	J. Li, Y.Y. Lu, F. Li, et al., Study on chemical constituents of Cyclocarya paliurus, J. Chin. Med. Mater. 29 (2006) 441-442.
[14]	B.S. Cui, S. Li, Studies on chemical constituents from the leaves of Cyclocarya paliurus, Chin. Trad. Herbal Drugs 43 (2012) 2132-2136.
[15]	S. Li, B.S. Cui, Q. Liu, et al., New Triterpenoids from the leaves of Cyclocarya paliurus, Planta Med. 78 (2012) 290-296.
[16]	C. Seger, S. Pointinger, H. Greger, O. Hofer, Isoeichlerianic acid from Aglaia silvestris and revision of the stereochemistry of foveolin B, Tetrahedron Lett. 49 (2008) 4313-4315.
[17]	T. Aoki, S. Ohta, T. Suga, Six novel secodammarane-tape triterpenes from male flower of Alnus Japonica, Phytochemistry 27 (1988) 2915-2920.
[18]	T. Hirata, R. Ideo, T. Suga, Structure of Alnuselide, the first reported naturally occurring C31-secodammarane-type triterpene lactone from Alnus Serrulatoides, Chem. Lett. 6 (1977) 711-714.
[19]	A. Tadashi, O. Shinji, A. Satoshi, H. Toshifumi, S. Takayuki, The structures of four novel C31-secodammarane-type triterpenoid saponins from the female flowers of Alnus serrdatoides, J. Chem. Soc. Perkin Trans. 1 (1982) 1399-1403.
[20]	T. Suga, S. Ohta, E. Ohta, T. Aoki, A C31-secodammarane-type triterpenic acid, 12- deoxy alnustic acid, from the female flowers of Alnus pendula, Phytochemistry 25 (1986) 1243-1244.
[21]	T.R. Govindachari, G. Suresh, G.N. Krishna Kumari, Triterpenoids from Dysoxylum Malabaricum, Phytochemistry 37 (1994) 1127-1129.
[22]	L.K. Wah, F. Abas, G.A. Cordell, H. Ito, I.S. Ismail, Steroids from Dysoxylum grande (Meliaceae) leaves, Steroids 78 (2013) 210-219.
[23]	S. Yogendra, A. William, Dammarane triterpenoids from Dysoxylum richii, Phytochemistry 31 (1992) 4033-4035.
[24]	C.O. Esimone, G. Eck, T.N. Duong, et al., Potential anti-respiratory syncytial virus lead compounds from Aglaia species, Pharmazie 63 (2008) 768-773.
[25]	K. Mohamad, T. Sévenet,V. Dumontet, et al., Dammarane triterpenes and pregnane steroids from Aglaia lawii and A. tomentosa, Phytochemistry 51 (1999) 1031-1037.
[26]	H. Desi, T. Roekmiati, S. Agus, et al., Cytotoxic triterpenoids from the bark of Aglaia smithii (Meliaceae), Phytochem. Lett. 5 (2012) 496-499.
[27]	N. Joycharat, P. Plodpai, K. Panthong, Y. Boonek, P. Supayang, Terpenoid constituents and antifungal activity of Aglaia forbesii seed against phytopathogens, Can. J. Chem. 88 (2010) 937-944.
[28]	S. Pointinger, S. Promdang, S. Vajrodaya, et al., Silvaglins and related 2,3-secodammarane derivatives-unusual types of triterpenes from Aglaia silvestris, Phytochemistry 69 (2008) 2696-2703.
[29]	M.M. Rao, H. Meshulam, R. Zelnik, D. Lavie, Cabralea eichleriana DC. (Meliaceae) - I Structure and stereochemistry of wood extractives, Tetrahedron 31 (1975) 333- 339.
[30]	C.O. Esimone, G. Eck, C.S. Nworu, et al., Dammarenolic acid, a secodammarane triterpenoid from Aglaia sp. shows potent anti-retroviral activity in vitro, Phytomedicine 17 (2010) 540-547.