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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 13.2,17.1,17.6,18.7,18.9,19.5,19.6,21.3,25.7,26.4,27.1,27.4,28.3, 31.8,35.5,35.9,36.1,37.2,39.9, .2,46.6,49.4,50.0,51.3,60.4,61.5,62.4,70.7,72.9,73.1,74.3,75.4,75.5,76.6,76.7,77.2,77.3,77.5, 78.5,81.4,89.4,103.0,105.1,107.0,129.1,135.7,135.9,143.4,171.1 ÈܼÁÑ¡Ï È«²¿ CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O (CH3)4Si C4D8O2 CD3COOD C4D8O2 H2O D2O CF3COOD CD3OD ND3 CD3COCD3 C6D6 CD3CN ²éѯ¿ÕÖµ Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½3320¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . scillascilloside D-1 ÏàËÆ¶È:71.1% Chemical & Pharmaceutical Bulletin 1994 42 327-332 Lanosterol Oligosaccharides from the Plants of the Subfamily Scilloideae and Their Antitumor-Promoter Activity Yoshihiro MIMAKI,Hoyoku NISHINO,Kazutomo ORI,Minpei KURODA,Tomoko MATSUI and Yutaka SASHIDA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 3¦Â-O-[¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-glucopyranosyl]-22S-hydroxycycloart-24E-en-26-oic acid C48H78O19 ÏàËÆ¶È:69.3% Phytochemistry 1994 37 515-519 Cycloartane glucosides from juncus effusus Maria Michela Corsaro, Marina della Greca, Antonio Fiorentino, Pietro Monaco, Lucio Previtera Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . peruvianoside A C49H78O20 ÏàËÆ¶È:69.3% Bulletin of the Chemical Society of Japan 1993 66 1182-1186 Peruvianosides A and B, Novel Triterpene Glycosides from the Bulbs of Scilla peruviana Yoshihiro Mimaki, Kazutomo Ori, Yutaka Sashida, Tamotsu Nikaido, Lian-Gang Song, Taichi Ohmoto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 23-epi-15-deoxoeucosterol 3-O-{O-¦Á-L-rhamnopyranosyl-(1¡ú2)-O-¦Â-D-glucopyranosyl-(1¡ú2)-O-¦Á-L-arabinopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside } C52H84O22 ÏàËÆ¶È:69.2% Chemical & Pharmaceutical Bulletin 1994 42 327-332 Lanosterol Oligosaccharides from the Plants of the Subfamily Scilloideae and Their Antitumor-Promoter Activity Yoshihiro MIMAKI,Hoyoku NISHINO,Kazutomo ORI,Minpei KURODA,Tomoko MATSUI and Yutaka SASHIDA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 3¦Â,20S,21-trihydroxydamma¦Á-24-ene 3-O-{[¦Á-L-rhamnopyranosyl(1¡ú2)][¦Â-D-glucopyranosyl(1¡ú3)]-¦Â-D-glucopyranosyl}-21-O-¦Â-D-glucopyranoside C54H92O22 ÏàËÆ¶È:68.5% Journal of Natural Products 2004 67 942-952 Dammarane-Type Glycosides from Gynostemma pentaphyllum Feng Yin, Lihong Hu, Fengchang Lou, and Ruixiang Pan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 3¦Â,-20S,21-trihydroxydammar-24-ene 3-O-{[¦Á-L-rhamnopyranosyl-(1¡ú2)][¦Â-D-glucopyranosyl (1¡ú3)]-¦Á-L-arabinopyranosyl}-21-O-¦Â-D-glucopyranoside C53H90O21 ÏàËÆ¶È:67.9% Journal of Natural Products 2006 69 1394-1398 Triterpene Saponins from Gynostemma cardiospermum Feng Yin, Yinan Zhang, Zhengyi Yang, Qiuqun Cheng, and Lihong Hu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 3¦Â,20S,21-trihydroxydamma¦Á-24-ene 3-O-{[¦Á-L-rhamnopyranosyl(1¡ú2)][¦Â-D-xylopyranosyl(1¡ú3)]-¦Â-D-glucopyranosyl}-21-O-¦Â-D-glucopyranoside C53H90O21 ÏàËÆ¶È:67.9% Journal of Natural Products 2004 67 942-952 Dammarane-Type Glycosides from Gynostemma pentaphyllum Feng Yin, Lihong Hu, Fengchang Lou, and Ruixiang Pan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . scillascilloside D-1 ÏàËÆ¶È:67.9% Chemical & Pharmaceutical Bulletin 1994 42 327-332 Lanosterol Oligosaccharides from the Plants of the Subfamily Scilloideae and Their Antitumor-Promoter Activity Yoshihiro MIMAKI,Hoyoku NISHINO,Kazutomo ORI,Minpei KURODA,Tomoko MATSUI and Yutaka SASHIDA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (23S,25R)-3¦Â,30,31-trihydroxy-17¦Á,23-epoxy-5¦Á-lanost-5-en-23,26-olactone 3-O-{O-¦Á-L-rhamopyranosyl-(1¡ú2)-O-¦Â-D-glucopyranosyl-(1¡ú2)-O-¦Á-L-arabinopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside } C53H84O24 ÏàËÆ¶È:67.9% Chemical & Pharmaceutical Bulletin 1994 42 327-332 Lanosterol Oligosaccharides from the Plants of the Subfamily Scilloideae and Their Antitumor-Promoter Activity Yoshihiro MIMAKI,Hoyoku NISHINO,Kazutomo ORI,Minpei KURODA,Tomoko MATSUI and Yutaka SASHIDA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (20S)-3¦Â,20,21-Trihydroxydammara-23,25-diene 3-O-[¦Á-L-Rhamnopyranosyl-(1¡ú2)][¦Â-D-xylopyranosyl-(1¡ú3)]-¦Â-D-glucopyranosyl-21-O-¦Â-D-glucopyranoside ÏàËÆ¶È:67.9% Helvetica Chimica Acta 2010 93 1785-1794 Three New Triterpene Saponins from Gynostemma pentaphyllum Lin Shi, Jia-Qing Cao, Wei Li and Yu-Qing Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . Khekadaengoside M C48H82O18 ÏàËÆ¶È:67.3% Phytochemistry 2002 59 215-228 Cucurbitane, hexanorcucurbitane and octanorcucurbitane glycosides from fruits of Trichosanthes tricuspidata Tripetch Kanchanapoom, Ryoji Kasai, Kazuo Yamasaki Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . (25S)-5¦Á-spirostan-3¦Â-ol-3-O-¦Â-D-galactopyranosyl(1¡ú2)-¦Â-D-glucopyranosyl(1¡ú4)-¦Â-D-galactopyranoside ÏàËÆ¶È:67.3% Chemical Research in Chinese Universities 2010 26 915-921 Separation and Bio-activities of Spirostanol Saponin from Tribulus terrestris ZHANG Shuang, YANG Rui-jie, LI Hong, YIN Zong-yuan, ZHOU Hong-yu,LI Xu-wen, JIN Yong-ri and YANG Shi-jie Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . peruvianoside B C49H78O21 ÏàËÆ¶È:67.3% Bulletin of the Chemical Society of Japan 1993 66 1182-1186 Peruvianosides A and B, Novel Triterpene Glycosides from the Bulbs of Scilla peruviana Yoshihiro Mimaki, Kazutomo Ori, Yutaka Sashida, Tamotsu Nikaido, Lian-Gang Song, Taichi Ohmoto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 3¦Â,-19,20S,21-tetrahydroxydamma¦Á-24-ene 3-O-{[¦Á-L-rhamnopyranosyl(1¡ú2)][¦Â-D-xylopyranosyl(1¡ú3)]-¦Á-L-arabinopyranosyl}-21-O-¦Â-D-glucopyranoside C52H88O21 ÏàËÆ¶È:67.3% Journal of Natural Products 2004 67 942-952 Dammarane-Type Glycosides from Gynostemma pentaphyllum Feng Yin, Lihong Hu, Fengchang Lou, and Ruixiang Pan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . muscaroside C ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1994 42 327-332 Lanosterol Oligosaccharides from the Plants of the Subfamily Scilloideae and Their Antitumor-Promoter Activity Yoshihiro MIMAKI,Hoyoku NISHINO,Kazutomo ORI,Minpei KURODA,Tomoko MATSUI and Yutaka SASHIDA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . scillasaponin D C53H84O24 ÏàËÆ¶È:66.0% Phytochemistry 1993 34 791-797 Lanosterol and 27-norlanosterol oligosaccharides from the bulbs of Chionodoxa gigantea Yoshihiro Mimaki, Satoshi Kubo, Youji Kinoshita, Yutaka Sashida, Lian-Gang Song, Tamotsu Nikaido, Taichi Ohmoto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . (23S,25R)-3¦Â,30,31-trihydroxy-17¦Á,23-epoxy-5¦Á-lanost-5-en-23,26-olactone 3-O-{O-¦Â-apio-D-furanosyl-(1¡ú2)-O-¦Â-D-glucopyranosyl-(1¡ú2)-O-¦Á-L-arabinopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside } C52H86O24 ÏàËÆ¶È:65.3% Chemical & Pharmaceutical Bulletin 1994 42 327-332 Lanosterol Oligosaccharides from the Plants of the Subfamily Scilloideae and Their Antitumor-Promoter Activity Yoshihiro MIMAKI,Hoyoku NISHINO,Kazutomo ORI,Minpei KURODA,Tomoko MATSUI and Yutaka SASHIDA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . sapinmusaponin R C49H80O17 ÏàËÆ¶È:65.3% Chemical & Pharmaceutical Bulletin 2007 55(9) 1412-1415 Anti-platelet Aggregation Triterpene Saponins from the Galls of Sapindus mukorossi Hui-Chi HUANG,Wei-Jern TSAI,Chia-Ching LIAW,Shih-Hsiung WU,Yang-Chang WU,and Yao-Haur KUO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . Acanjaposide F C48H76O20 ÏàËÆ¶È:65.3% Chemical & Pharmaceutical Bulletin 2005 53(9) 1147-1151 New Oleanene Glycosides from the Leaves of Acanthopanax japonicus Sang-Yong PARK,Chang-Soo YOOK,and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . Rotundifolioside E C47H76O17 ÏàËÆ¶È:65.3% Chemical & Pharmaceutical Bulletin 2003 51(4) 365-37 Antiproliferative Constituents from Umbelliferae Plants VI.1,2) New Ursane-Type Saikosaponin Analogs from the Fruits of Bupleurum rotundifolium Toshihiro FUJIOKA,Keisuke YOSHIDA, Hiroko FUJII, Tsuneatsu NAGAO, Hikaru OKABE, and Kunihide MIHASHI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . abutiloside H ÏàËÆ¶È:65.3% Chemical & Pharmaceutical Bulletin 2002 50(2) 284-286 Four New 26-Aminocholestane-Type Glycosides from Solanum abutiloides Hitoshi YOSHIMITSU,Makiko NISHIDA, Mitsuko YOSHIDA,and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . abutiloside J C48H81NO17 ÏàËÆ¶È:65.3% Chemical & Pharmaceutical Bulletin 2002 50(2) 284-286 Four New 26-Aminocholestane-Type Glycosides from Solanum abutiloides Hitoshi YOSHIMITSU,Makiko NISHIDA, Mitsuko YOSHIDA,and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . lucilianoside A C48H76O23 ÏàËÆ¶È:65.3% Phytochemistry 2003 1351-1359 Lanosterol and tetranorlanosterol glycosides from the bulbs of Muscari paradoxum Kazutomo Ori, Minpei Koroda, Yoshihiro Mimaki,Hiroshi Sakagami, Yutaka Sashida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . 11¦Á,12¦Á-epoxy-3¦Â-[(O-¦Â-D-galactopyrano-syl-(1¡ú3)-O-[¦Â-D-glucopyranosyl-(1¡ú2)]-¦Â-D-glucuronopyranosyl)-oxy]olean-28,13-olide C48H74O20 ÏàËÆ¶È:65.3% Journal of Natural Products 2006 69 1606-1610 Oleanane and Taraxerane Glycosides from the Roots of Gomphrena macrocephala Minpei Kuroda, Taku Aoshima, Mitsue Haraguchi, Maria Cludia Marx Young, Hiroshi Sakagami, and Yoshihiro Mimaki Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . eryloside V C48H80C17 ÏàËÆ¶È:65.3% Journal of Natural Products 2007 70 1871-1877 Isolation and Structures of Erylosides from the Carribean Sponge Erylus goffrilleri Shamil Sh. Afiyatullov,Anatoly I. Kalinovsky, Alexandr S. Antonov, Ludmila P. Ponomarenko, Pavel S. Dmitrenok,Dmitry L. Aminin, Vladimir B. Krasokhin, Valentina M. Nosova, and Alexandr V. Kisin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . 6-O-¦Á-L-rhamnopyranosyl-16,24-di-O-¦Â-D-glucopyranosyl-3¦Â,6¦Á,16¦Â,24(S),25-pentahydroxy-cycloartane C48H82O19 ÏàËÆ¶È:65.3% Phytochemistry 2009 70 628-634 Cycloartane-type glycosides from Astragalus amblolepis Emre Polat, Ozgen Caliskan-Alankus, Angela Perrone, Sonia Piacente, Erdal Bedir Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . abutiloside A ÏàËÆ¶È:65.3% Chemical & Pharmaceutical Bulletin 1996 44 1119-1121 Cholestane Glycosides from Solanum abutiloides Rui-Hua TIAN,Emi OHMURA,Hitoshi YOSHIMITSU,Toshihiro NOHARA and Masaharu MATSUI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . anagallosaponin III C48H78O18 ÏàËÆ¶È:65.3% Chemical & Pharmaceutical Bulletin 1994 42 1750-1755 Structures of Anagallosaponins I-V and Their Companion Substances from Anagallis arvensis L. Noboru SHOJI,Akemi UMEYAMA,Kazuko YOSHIKAWA and Shigenobu ARIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . kaikasaponin III methyl ester ÏàËÆ¶È:65.3% Chemical & Pharmaceutical Bulletin 1992 40 2995-2999 Triterpene Glycosides from the Bark of Robinia pseudo-acacia L. I Baoliang CUI,Junei KINJO and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . compound 2 ÏàËÆ¶È:65.3% Chemical & Pharmaceutical Bulletin 1986 34 1158-1167 Chemical Evaluation of Bupleurum Species Collected in Yunnan, China JING-KAI DING,HIROKO FUJINO(nee KIMATA),RYOJI KASAI,NAOKO FUJIMOTO,OSAMU TANAKA,JUN ZHOU,HIROMICHI MATSUURA and TOHRU FUWA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . Glycoside L-I1 ÏàËÆ¶È:65.3% Chemistry of Natural Compounds 2000 36 506-509 TRITERPENOID GLYCOSIDES OF Scheffleropsis angkae.III. STRUCTURE OF GLYCOSIDE L-I1 V. V. Kachala, A. S. Stolyarenko, V. I. Grishkovets,A. S. Shashkov, and V. Ya. Chirva Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . abutiloside A C49H83NOI7 ÏàËÆ¶È:65.3% Phytochemistry 1997 44 723-726 Abutiloside A, A 26-acylamino-3¦Â, 16¦Á-dihydroxy-5¦Á-cholesta-22-one glycoside from Solanum abutiloides Rui-Hua Tian, Emi Ohmura, Masaharu Matsui, Toshihiro Noharas Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . anagallosaponin III ÏàËÆ¶È:65.3% Phytochemistry 1994 37 1397-1402 Triterpenoid glycosides from Anagallis arvensis Noboru Shoji, Akemi Umeyama, Kazuko Yoshikawa, Shigenobu Arihara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . 3¦Â,20S,21-trihydroxydammar-24-ene 3-O-[¦Á-L-rhamnopyranosyl(1¡ú2)][¦Â-D-glucopyranosyl(1¡ú3)]¦Â-D-glucopyranoside C48H82O17 ÏàËÆ¶È:65.3% Planta Medica 2012 78 597-605 New Dammarane-type Glycosides from the Roots of Gynostemma pentaphyllum Lei Ma,Wen-Juan Xiang, Pham Van Khang, Yang Liang, Yaping Xiao, Li-Hong Hu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . carnosiflosideVI C48H80O18 ÏàËÆ¶È:65.3% Phytochemistry 1987 26 1371-1376 Sweet and bitter cucurbitane glycosides from hemsleya carnosiflora Ryoji Kasai,Kazuhiro Matsumoto,Rui-Lin Nie,Toshinobu Morita,Akimi Awazu,Jun Zhou,Osamu Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 36 . Compound 7 C48H80O15 ÏàËÆ¶È:65.3% Bioorganic & Medicinal Chemistry Letters 2009 19 2310-2314 Synthesis, cytotoxicity, and haemolytic activity of chacotrioside lupane-type neosaponins and their germanicane-type rearrangement products Charles Gauthier, Jean Legault, Marianne Piochon, Serge Lavoie, Samuel Tremblay, Andr¨¦ Pichette Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 37 . saikosaponin c ÏàËÆ¶È:65.3% Journal of China Pharmaceutical University 2003 34 305-308 Study on the Constituents of the Roots of Bupleurum marginatum LIANG Zhi-Tao; QIN Min-Jian; TANG Li; WANG Zheng-Tao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 38 . 3-O-[¦Á-L-Rhamnopyranosyl (1¡ú2)-¦Â-D-galactopyranosyl (1¡ú2)-¦Â-D-glucuronopyranosyl]-complogenin C48H76O19 ÏàËÆ¶È:65.3% Zeitschrift f¨¹r Naturforschung C 2005 60 813-820 Bioactive Saponins from Astragalus suberi L. Growing in Yemen F. Abbas and R. Zayed Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 39 . anagallosaponin V C54H88O23 ÏàËÆ¶È:64.8% Chemical & Pharmaceutical Bulletin 1994 42 1750-1755 Structures of Anagallosaponins I-V and Their Companion Substances from Anagallis arvensis L. Noboru SHOJI,Akemi UMEYAMA,Kazuko YOSHIKAWA and Shigenobu ARIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 40 . Thalictoside C ÏàËÆ¶È:64.8% Chemistry of Natural Compounds 2005 41 117-140 STRUCTURAL STUDIES AND BIOLOGICAL ACTIVITY OF PLANT TRITERPENOIDS FROM THE Thalictrum GENUS V. I. Lutskii, A. S. Gromova,E. A. Khamidullina, and N. L. Owen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 41 . Glycoside A C54H88O22 ÏàËÆ¶È:64.8% Chemical Research in Chinese Universities 1994 10 185-192 Studies on the Glycosides in the Leaves of Oplopanax elatus NAKAI(I) WANG Guang-shu,ZHAO Chun-fang and XU Jing-da Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 42 . Pavioside A ÏàËÆ¶È:64.8% Bioorganic & Medicinal Chemistry 2012 20 3280-3286 Paviosides A¨CH, eight new oleane type saponins from Aesculus pavia with cytotoxic activity Original Research Article Virginia Lanzotti, Pasquale Termolino, Marcello Dolci, Paolo Curir Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 43 . Pavioside B ÏàËÆ¶È:64.8% Bioorganic & Medicinal Chemistry 2012 20 3280-3286 Paviosides A¨CH, eight new oleane type saponins from Aesculus pavia with cytotoxic activity Original Research Article Virginia Lanzotti, Pasquale Termolino, Marcello Dolci, Paolo Curir Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 44 . glycoside 3 C53H90O21 ÏàËÆ¶È:64.1% Chemical & Pharmaceutical Bulletin 2004 52(12) 1440-1444 Novel Dammarane-Type Glycosides from Gynostemma pentaphyllum Feng YIN, Lihong HU,and Ruixiang PAN Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 45 . 3¦Â,19,20S,21-tetrahydroxydamma¦Á-24-ene 3-O-{[¦Á-Lrhamnopyranosyl(1¡ú2)][¦Â-D-xylopyranosyl(1¡ú3)]-¦Â-D-glucopyranosyl}-21-O-¦Â-D-glucopyranoside C53H90O22 ÏàËÆ¶È:64.1% Journal of Natural Products 2004 67 942-952 Dammarane-Type Glycosides from Gynostemma pentaphyllum Feng Yin, Lihong Hu, Fengchang Lou, and Ruixiang Pan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 46 . 3¦Â-O-{¦Â-D-xylopyranosyl-(1¡ú2)-O-¦Â-D-glucopyranosyl-(1¡ú4)-[O-¦Â-D-glucopyranosyl-(1¡ú2)]-¦Á-L-arabinopyranosyl}-16¦Á-hydroxy-13¦Â,28-epoxy oleanane ÏàËÆ¶È:64.1% Journal of Natural Products 1994 Vol 57 1354 Cytotoxic Saponins from New Zealand Myrsine Species Stephen J. Bloor, Lu Qi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 47 . 3¦Â-O-{¦Â-D-xylopyranosyl-(1¡ú2)-O-¦Â-D-glucopyranosyl-(1¡ú4)-[O-¦Â-D-glucopyranosyl-(1¡ú2)]-¦Á-L-arabinopyranosyl}-16¦Á,28-dihydroxy-13¦Â,28-epoxy oleanane ÏàËÆ¶È:64.1% Journal of Natural Products 1994 Vol 57 1354 Cytotoxic Saponins from New Zealand Myrsine Species Stephen J. Bloor, Lu Qi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 48 . ÏàËÆ¶È:64% Chemical & Pharmaceutical Bulletin 1992 40 2995-2999 Triterpene Glycosides from the Bark of Robinia pseudo-acacia L. I Baoliang CUI,Junei KINJO and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 49 . compound 1b ÏàËÆ¶È:64% Chemistry of Natural Compounds 2005 41 436-441 TRITERPENE GLYCOSIDES FROM Cussonia paniculata.II. ACETYLATED GLYCOSIDES FROM LEAVES V. I. Grishkovets, I. I. Dovgii, V. V. Kachala,and A. S. Shashkov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 50 . phyteumoside A C50H84O20 ÏàËÆ¶È:64% Organic Letters 2011 Vol.13,No.6 1354-1357 Phyteumosides A and B: New Saponins with Unique Triterpenoid Aglycons from Phyteuma orbiculare L. Christian Abbet, Markus Neuburger, Trixie Wagner, Melanie Quitschau,Matthias Hamburger, and Olivier Potterat Structure 13C NMR ̼Æ×Ä£Äâͼ |
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