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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 176.21, 145.81, 137.09, 103.82, 102.93, 100.55, 88.19, 85.56, 80.95, 76.58, 76.55, 73.82, 73.62, 73.59, 72.38, 70.69, 70.67, 69.71, 68.84, 67.23, 66.16, 63.38, 60.95, 55.89, 44.25, 43.73, 43.31, 41.33, 39.03, 38.67, 36.49, 34.88, 31.80, 28.17, 27.32, 27.22, 25.88, 25.24, 23.79, 22.19, 18.00, 17.84, 17.09, 16.64, 15.87, 15.68. |
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²éѯ½á¹û£º¹²²éµ½2588¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ilekudinoside Q C42H66O14 ÏàËÆ¶È:73.9% 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 . oleanolic acid-3-O-¦Â-D-glucopyranosyl(1¡ú3)-¦Á-L-rhamnopyranosyl(1¡ú2)-¦Á-L-arabinopyranoside ÏàËÆ¶È:72.3% 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 3 . 3-O-¦Â-D-glucopyranosyl (1¡ú3)-¦Á-L-rhamnopyranosyl( 1¡ú2)-¦Á-L-arabinopyranosyloleanolic acid ÏàËÆ¶È:70.2% Planta Medica 1987 53 62-65 Triterpenoid Glycosides from the Roots of Patrinia scab iosaefolia Jae Sue Choi and Won Sick Woo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 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 5 . tuberoside D C45H74O17 ÏàËÆ¶È:69.5% 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 6 . tuberoside D C45H74O17 ÏàËÆ¶È:69.5% 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 7 . stellatoside D C48H76O19 ÏàËÆ¶È:68.7% 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 . 3-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-[(4-sulfo)-¦Â-D-glucopyranosyl-(1¡ú3)]-¦Á-L-arabinopyranosyljujubogenin C47H76O20S ÏàËÆ¶È:68.0% 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 9 . scoposide E C46H73O15 ÏàËÆ¶È:67.3% Journal of Natural Products 2010 73 825-830 Antimicrobial Triterpenoid Glycosides from Cephalaria scoparia Nazlı Böke Sarıkahya and S¨¹heyla Kırmızıg¨¹l Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . (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:67.3% 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 11 . 3-O-[¦Á-L-rhamnopyranosyl(1¡ú3)-¦Á-L-arabinopyranosyl(1¡ú3)-¦Â-D-xylopyranosy1(1¡ú3)-¦Â-D-glucopyranosyl]-25R,5¦Á-spirostan-2¦Á,3¦Â-diol ÏàËÆ¶È:65.3% Journal of Natural Products 1990 Vol 53 1557 A New Molluscicidal Spirostanol Glycoside of Yucca aloifolia Navin Kishor, O. P. Sati Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . tuberoside C45H74O18 ÏàËÆ¶È:65.2% 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 13 . ilekudinoside I ÏàËÆ¶È:65.2% Journal of Natural Products 1999 62 1128-1133 Triterpenoid Saponins from Ilex kudincha Keiichi Nishimura, Toshio Miyase, and Hiroshi Noguchi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . gyloniposide I C46H76O16 ÏàËÆ¶È:65.2% Acta Pharmaceutica Sinica 1997 32 524-529 STUDIES ON THE CHEMICAL CONSTITUENTS OF GYNOSTEMMA LONGIPES C.Y.WU XL Guo ; TJ Wang and BL Bian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . Indioside I C45H74O16 ÏàËÆ¶È:65.2% Journal of Natural Products 2012 75 636-643 Indiosides G-K: Steroidal Glycosides with Cytotoxic and Antiinflammatory Activities from Solanum violaceum Chiao-Ting Yen, Chia-Lin Lee, Fang-Rong Chang, Tsong-Long Hwang, Hsin-Fu Yen, Chao-Jung Chen, Shu-Li Chen, and Yang-Chang Wu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . (3¦Â,20S,23S)-3,20,23-trihydroxydammar-24-en-21-oic acid-21,23-lactone 3-O-[¦Á-L-rhamnopyranosyl-(1¡ú2)]-[¦Â-D-xylopyranosyl(1¡ú3)]-¦Á-L-arabinopyranoside C46H74O16 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 . kudzusaponin B1 ÏàËÆ¶È:64.5% Chemical & Pharmaceutical Bulletin 1996 44 1970-1972 Oleanene-Type Triterpene Glycosides from Puerariae Radix. III.Three New Saponins from Pueraria thomsonii Tomonori ARAO,Tomoko IDZU,Junei KINJO,Toshihiro NOHARA and Ryuichi ISOBE Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 3¦Â-O-[¦Â-D-xylopyranosyl-(1¡ú3)-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-gluco-pyranosyl]-12-oleanene-3¦Â,28-diol C47H78O15 ÏàËÆ¶È:63.8% Biochemical Systematics and Ecology 2012 40 49-52 Triterpenoid saponins from Clematis argentilucida Mei Zhao, Hai-Feng Tang, Feng Qiu, Xiang-Rong Tian, Yu Ding, Xiao-Yang Wang, Xiao-Ming Zhou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . Melilotoside C1 C47H78O16 ÏàËÆ¶È:63.8% Chemistry of Natural Compounds 2010 46 572-575 Triterpene and steroidal glycosides from the genus Melilotus and their genins.V. melilotosides A1, B1, and C1 from Melilotus officinalis roots G. V. Khodakov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . 3¦Â-O-[¦Â-D-xylopyranosyl-(1¡ú3)-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-glucopyranosyl]-12-oleanene-3¦Â,28-diol C47H78O15 ÏàËÆ¶È:63.8% Biochemical Systematics and Ecology 2012 40 49-52 Triterpenoid saponins from Clematis argentilucida Mei Zhao, Hai-Feng Tang, Feng Qiu, Xiang-Rong Tian, Yu Ding, Xiao-Yang Wang, Xiao-Ming Zhou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . kudzusaponin A3 ÏàËÆ¶È:63.2% Chemical & Pharmaceutical Bulletin 1992 40 139-142 Triterpenoid Glycosides from Sophorae Subprostratae Radix Yi DING,Takashi TAKESHITA,Kei YOKOYAMA,Junei KINJO and Toshihiro NOHARA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . Compound 1a C49H78O18 ÏàËÆ¶È:63.2% Journal of Natural Medicines 2006 60 49-53 Triterpenoid saponins from cultural plants of Stenocereus stellatus (Cactaceae) Takeo Imai, Sachie Okazaki, Kaoru Kinoshita, Kiyotaka Koyama and Kunio Takahashi, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . compound 7 C46H74O17 ÏàËÆ¶È:63.0% Chemistry & Biodiversity 2006 Vol. 3 771 Nine New Dammarane Saponins from Gynostemma pentaphyllum Feng Yin, Yi-Nan Zhang, Zheng-Yi Yang, and Li-Hong Hu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 24 . ¦Â-chacotriosyl lilagenin C45H72O17 ÏàËÆ¶È:63.0% 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 25 . ilekudinoside L C41H64O14 ÏàËÆ¶È:63.0% 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 26 . ilekudinoside S C42H64O14 ÏàËÆ¶È:63.0% 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 |
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