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Slotus5389ľ³æ (ÕýʽдÊÖ)
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[ÇóÖú]
1 C лл ÒÑÓÐ1È˲ÎÓë
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| 13C NMR (101 MHz, MeOD) ¦Ä 176.43, 143.85, 133.99, 103.80, 102.92, 100.56, 88.01, 85.18, 76.58, 73.81, 73.62, 72.79, 72.37, 71.05, 70.68, 69.72, 68.83, 67.20, 63.36, 60.95, 55.62, 49.62, 45.67, 44.89, 42.35, 38.99, 38.83, 36.72, 34.63, 32.29, 31.58, 28.40, 28.27, 27.11, 25.89, 25.11, 20.51, 18.68, 17.85, 16.60, 16.17, 15.88, 15.70. |
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Slotus5389: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-01-30 10:53:03
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²éѯ½á¹û£º¹²²éµ½3031¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ilekudinoside S C42H64O14 ÏàËÆ¶È:72.0% Journal of Natural Products 2005 68 1169-1174 Triterpene Saponins from the Leaves of Ilex kudingcha Li Tang, Yong Jiang, Hai-Tao Chang, Ming-Bo Zhao, Peng-Fei Tu, Jing-Rong Cui, and Rui-Qing Wang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . tuberoside D C45H74O17 ÏàËÆ¶È:71.1% Chemical & Pharmaceutical Bulletin 2000 48(3) 362-365 Steroidal Oligoglycosides from the Seeds of Allium tuberosum Tsuyoshi IKEDA,Hidetsugu TSUMAGARI,and Toshihiro NOHARA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . gypenoside VN5 C47H80O18 ÏàËÆ¶È:70.2% Phytochemistry 2010 71 994-1001 Dammarane-type saponins from Gynostemma pentaphyllum Pham Thanh Ky, Pham Thanh Huong, Than Kieu My, Pham Tuan Anh, Phan Van Kiem, Chau Van Minh, Nguyen Xuan Cuong, Nguyen Phuong Thao, Nguyen Xuan Nhiem, Jae-Hee Hyun, Hee-Kyoung Kang, Young Ho Kim Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . oleanolic acid-3-O-¦Â-D-glucopyranosyl(1¡ú3)-¦Á-L-rhamnopyranosyl(1¡ú2)-¦Á-L-arabinopyranoside ÏàËÆ¶È:70.2% Chinese Pharmaceutical Journal 1997 32 271-273 Chemical constituents of Patrinia heterophylla Lei Haimin (Lei HM), Zhu Rong (Zhu R), Wei Luxue (Wei LX) Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . Glycoside B1 ÏàËÆ¶È:67.4% Chemistry of Natural Compounds 1999 35 547-551 TRITERPENE GLYCOSIDES FROM Tupidanthus calyptratus.I. STRUCTURE OF GLYCOSIDES B l, B2, F i, AND F 2 FROM LEAVES OF HOODED TUPIDANTHUS V. I. Grishkovets Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 3-O-rhamnopyranosyl-(1¡ú2)-arabinopyranosyl oleanolic acid ÏàËÆ¶È:67.4% Journal of Shenyang Pharmaceutical University 2005 22 183-186 Chemical constituents of the seeds of Acanthopanax senticosus(Rupr. et Maxim) Harms ZHANG Jie, LI Wen, GAO Hui-Yuan, WU Bin, WU Li-jun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . stellatoside E C42H66O14 ÏàËÆ¶È:67.4% Heterocycles 2012 85 1377-1392 New Triterpenoid Saponins from Stenocereus eruca Kazutaka Kakuta, Takeshi Koike, Kaoru Kinoshita, Satoru Ito, Kiyotaka Koyama, and Kunio Takahashi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . ¦Â-chacotriosyl lilagenin C45H72O17 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 2000 48(3) 362-365 Steroidal Oligoglycosides from the Seeds of Allium tuberosum Tsuyoshi IKEDA,Hidetsugu TSUMAGARI,and Toshihiro NOHARA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . tuberoside C45H74O18 ÏàËÆ¶È:66.6% Phytochemistry 2001 57 1219-1222 A steroidal saponin from the seeds of Allium tuberosum Zhong-Mei Zou, De-Quan Yu, Pu-Zhu Cong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . tuberoside D C45H74O17 ÏàËÆ¶È:66.6% Journal of Natural Products 1999 62 1028-1029 Two New Spirostanol Saponins from Allium tuberosum Shengmin Sang, Aina Lao, Hongcheng Wang, and Zhongliang Chen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . (25R)-spirost-5-en-2¦Á,3¦Â-diol 3-O-¦Á‑L-rhamnopyranosyl-(1¡ú2)-[¦Á‑L-rhamnopyranosyl-(1¡ú4)]-¦Â‑D-glucopyranoside C45H72O17 ÏàËÆ¶È:66.6% Planta Medica 2012 78 276¨C285 Spirostanol Saponins Derivated from the Seeds of Trigonella foenum-graecum by ¦Â-Glucosidase Hydrolysis and Their Inhibitory Effects on Rat Platelet Aggregation Xu Pang, Yue Cong, He-Shui Yu, Li-Ping Kang, Bing Feng, Bing-Xing Han, Yang Zhao, Cheng-Qi Xiong,Da-Wei Tan,Wei Song, Bin Liu, Yu-Wen Cong, Bai-Ping Ma Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 3-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-[(4-sulfo)-¦Â-D-glucopyranosyl-(1¡ú3)]-¦Á-L-arabinopyranosyljujubogenin C47H76O20S ÏàËÆ¶È:65.9% Journal of Natural Products 2004 67 1639-1643 Four New Dammarane Saponins from Zizyphus lotus Alexandre Maciuk, Catherine Lavaud, Philippe Thpenier,Marie-Jos Jacquier, Kamel Ghdira, and Monique Zches-Hanrot Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . kudinoside LZ2 C47H72O18 ÏàËÆ¶È:65.9% Chinese Chemical Letters 2009 20 1331-1334 A new triterpene saponin from the leaves of Ilex kudincha Wen Jian Zuo , Yi Mei Zeng , Yue Hu , He Meng , Zhen Hui Wang, Jin Hui Wang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . dudinoside F C47H74O18 ÏàËÆ¶È:65.9% Chinese Pharmaceutical Journal 2010 45 1228-1232 Triterpenoid Saponins from the Leaves of Ilex latifolia FAN Chun-lin, FAN Long, ZHANG Xiao-qi, WANG Ying, ZHANG Jun-qing, YE Wen-cai, Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . ilekudinchoside A C47H74O18 ÏàËÆ¶È:65.9% Planta Medica 2011 77 1835-1840 Triterpenes and Triterpenoid Saponins from the Leaves of Ilex kudincha Zuo, Wen-Jian; Dai, Hao-Fu; Chen, Jing; Chen, Hui-Qin; Zhao, You-Xing; Mei, Wen-Li; Li, Xian; Wang, Jin-Hui: Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . (3¦Â,20S)-3,20,21-trihydroxydammar-24-ene 3-O-[¦Á-L-rhamno-pyranosyl-(1¡ú2)]-[¦Â-D-xylopyranosyl-(1¡ú3)]-¦Á-L-arabinopyrano-side C46H78O15 ÏàËÆ¶È:65.2% Journal of Natural Products 2012 75 1373-1382 Dammarane Glycosides from the Root of Machilus yaoshansis Maoluo Gan, Mingtao Liu, Lishe Gan, Sheng Lin, Bo Liu, Yanling Zhang, Jiachen Zi, Weixia Song, and Jiangong Shi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . Peracetylated dumosasaponin 6 ÏàËÆ¶È:65.2% Journal of Agricultural and Food Chemistry 1997 45 1027-1031 Saponins from Ilex dumosa, an Erva-mat¨¦ (Ilex paraguariensis) Adulterating Plant Viviane S. Pires, Dominique Guillaume, Grace Gosmann, and Eloir P. Schenkel Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 28-O-¦Á-L-Rhamnopyranosylbetulin 3¦Â-O-¦Á-L-rhamnopyranoside C42H70O10 ÏàËÆ¶È:65.1% Journal of Natural Products 2009 72 72-81 Synthesis and Cytotoxicity of Bidesmosidic Betulin and Betulinic Acid Saponins Charles Gauthier,Jean Legault,Serge Lavoie, Simon Rondeau, Samuel Tremblay, and Andr¨¦ Pichette Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . St-C2 ÏàËÆ¶È:65.1% Chemistry of Natural Compounds 2001 37 462-465 TRITERPENE GLYCOSIDES FROM Tetrapanax papyriferum.III. MINOR MONODESMOSIDE GLYCOSIDES FROM STEM BARK V. S. Strigunov,1 V. I. Grishkovets,A. S. Shashkov, and V. Ya. Chirva Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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