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²éѯ½á¹û£º¹²²éµ½1356¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Trichocarpine B C41H56N2O6 ÏàËÆ¶È:63.4% Natural Product Communications 2009 4 897-901 Bis-Diterpenoid Alkaloids fromAconitum tanguticum var. trichocarpum Ling Lin, Dong-Lin Chen, Xiao-Yu Liu, Qiao-Hong Chen, Feng-Peng Wang andChong-Yi Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 12b-methoxy-tigogenyl 3,6-di-O-pivaloyl-¦Â-D-glucopyranoside C44H72O11 ÏàËÆ¶È:62.5% Bioorganic & Medicinal Chemistry 2012 20 4522-4531 Effect of C-ring modifications on the cytotoxicity of spirostan saponins and related glycosides Karell P¨¦rez-Labrada, Ignacio Brouard, Sara Est¨¦vez, Mar¨ªa Teresa Marrero, Francisco Est¨¦vez, Daniel G. Rivera Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 12a-methoxy-tigogenyl 3,6-di-O-pivaloyl-¦Â-D-glucopyranoside C44H72O11 ÏàËÆ¶È:62.5% Bioorganic & Medicinal Chemistry 2012 20 4522-4531 Effect of C-ring modifications on the cytotoxicity of spirostan saponins and related glycosides Karell P¨¦rez-Labrada, Ignacio Brouard, Sara Est¨¦vez, Mar¨ªa Teresa Marrero, Francisco Est¨¦vez, Daniel G. Rivera Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3,7,11,19,23,27-hexamethyl-15-hydroxymethylene-n-octacos-5,8,20-triene-10¦Â,18¦Á-diol-10¦Â-D-glucopyranoside C43H78O9 ÏàËÆ¶È:60.4% Bulletin of the Korean Chemical Society 2007 28 229-234 A New Chemical Constituent from the Hairy Root Cultures of Catharanthus roseus Ill-Min Chung, Han-Young Park, Mohd Ali, Ka Yiu San, Christie A. M. Peebles, Seung-Beom Hong, Ateeque Ahmad* Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Trichocarpine A C43H58N2O7 ÏàËÆ¶È:60.4% Natural Product Communications 2009 4 897-901 Bis-Diterpenoid Alkaloids fromAconitum tanguticum var. trichocarpum Ling Lin, Dong-Lin Chen, Xiao-Yu Liu, Qiao-Hong Chen, Feng-Peng Wang andChong-Yi Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . diosgenyl 2-deoxy-2-(3-nitrobenzamido)-¦Â-D-glucopyranoside C40H56N2O10 ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2009 17 7670-7679 Structural analogues of diosgenyl saponins: Synthesis and anticancer activity Matthew J. Kaskiw, Mary Lynn Tassotto, Mac Mok, Stacey L. Tokar, Roxanne Pycko, John Th¡¯ng, Zi-Hua Jiang Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . tigogenyl 3,6-di-O-pivaloyl-¦Â-D-glucopyranoside C43H70O10 ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2012 20 4522-4531 Effect of C-ring modifications on the cytotoxicity of spirostan saponins and related glycosides Karell P¨¦rez-Labrada, Ignacio Brouard, Sara Est¨¦vez, Mar¨ªa Teresa Marrero, Francisco Est¨¦vez, Daniel G. Rivera Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (3S,28S)3-O-acetyl-28-[3-morpholin-4-yl-prop-1-yn-1-yl]lup-20(29)-en-3,28-diol hydrochloride C39H62NO4Cl ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2013 21 425-435 Cytotoxic betulin-derived hydroxypropargylamines trigger apoptosis Ren¨¦ Csuk, Ronny Sczepek, Bianka Siewert, Christoph Nitsche Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (3¦Â,7¦Â,23E)-cucurbita-5,23-diene-3,7,19,25-tetrol 7-¦Â-D-glucopyranoside C36H60O9 ÏàËÆ¶È:60% Helvetica Chimica Acta 2013 96 1111-1120 Cucurbitane-Type Triterpenoids from Momordica charantia Bao-Hui Cheng, Jian-Chao Chen, Jie-Qing Liu, Lin Zhou and Ming-Hua Qiu Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 5 ÏàËÆ¶È:59.5% Chemical & Pharmaceutical Bulletin 1989 37 2229-2231 Study on the Constituents of Desmodium styracifolium Tomoko KUBO,Syuichi HAMADA,Toshihiro NOHARA,Zhi-rou WANG,Hideo HIRAYAMA,Keiichi IKEGAMI,Ken YASUKAWA and Michio TAKIDO Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ¦Â-sitosterol-3-O-¦Â-D-glucoside-6'-O-eicosanate ÏàËÆ¶È:59.5% Chinese Traditional and Herbal Drugs 2002 33 6-8 New steroid glycoside derivatives from Stelmatocrypton khasianum New steroid glycoside derivatives from Stelmatocrypton khasianum Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ilemaminoside B C41H66O13 ÏàËÆ¶È:58.5% Natural Product Research 2012 26 1991-1995 Triterpenoid saponins from Ilex mamillata C.Y. Wu ex C.J. Tseng Che Yan-Yun, Zhang Liang, Li Ning, Zeng Ke-Wu & Tu Peng-Fei Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Trichocarpidine C43H58N2O6 ÏàËÆ¶È:58.1% Helvetica Chimica Acta 2013 96 710-718 Bis-Diterpenoid Alkaloids from Aconitum tanguticum var. trichocarpum Zhong-Tang Zhang, Dong-Lin Chen, Qiao-Hong Chen and Feng-Peng Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Trichocarpinine C45H61N2O6 ÏàËÆ¶È:57.7% Helvetica Chimica Acta 2010 93 118-122 Trichocarpinine, a Novel Hetidine¨CHetisine Type Bisditerpenoid Alkaloid from Aconitum tanguticum var. trichocarpum Ling Lin, Dong-Lin Chen, Xiao-Yu Liu, Qiao-Hong Chen and Feng-Peng Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . trichocarpinine ÏàËÆ¶È:57.7% Helvetica Chimica Acta 2013 96 710-718 Bis-Diterpenoid Alkaloids from Aconitum tanguticum var. trichocarpum Zhong-Tang Zhang, Dong-Lin Chen, Qiao-Hong Chen and Feng-Peng Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 21¦Â, 22¦Á-O-diangeloyl prosapogenin C40H62O8 ÏàËÆ¶È:57.5% Phytochemistry 2002 59 825-832 Triterpenoid saponins and acylated prosapogenins from Harpullia austro-caledonica Laurence Voutquenne, C¨¦cile Kokougan, Catherine Lavaud,Isabelle Pouny, Marc Litaudon Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 4b ÏàËÆ¶È:57.5% Chemical & Pharmaceutical Bulletin 1994 42 1874-1878 Five New Triterpene Glycosides from Russell Lupine Junei KINJO,Fumiko KISHIDA,Kazutaka WATANABE,Fumio HASHIMOTO and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 1a C39H64O14 ÏàËÆ¶È:57.5% Chemical & Pharmaceutical Bulletin 1988 36 3226-3229 26-O-ACYLATED FUROSTANOL SAPONINS PARDARINOSIDE A AND B FROM THE BULBS OF LILIUM PARDARINUM Hiroko Shimomura,Yutaka Sashida and Yoshihiro Mimaki Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . Lilioglycoside C C39H60O13 ÏàËÆ¶È:57.5% Chemistry of Natural Compounds 1997 33 658-662 sTRuCTURES OF SOME LILIOGLYCOSIDES FROM THE BULBS OF Lilium regale P. K. Kintya, A. S. Gur'eva, N. E. Mashchenko,and A. S. Shashkov Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . compound 4 C40H68O13 ÏàËÆ¶È:57.5% Chemistry of Natural Compounds 1996 32 706-709 TRITERPENE GLYCOSIDES OF Astragalus AND THEIR GENINS. LIV. ASKENDOSIDE G FROM Astragalus taschkendicus M. I. Isaev Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . spirasine V/VI ÏàËÆ¶È:57.5% Journal of Integrative Plant Biology 2005 47 120-123 Two New Diterpenoid from Spiraea japonica L.F. var. fortunei (Planchon)Rehd Li-Ming FAN, Hong-Ping HE, Yue-Mao SHENand Xiao-Jiang HAO Structure 13C NMR ̼Æ×Ä£Äâͼ |

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