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²éѯ½á¹û£º¹²²éµ½61¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . dihypoestoxide C44H64O10 ÏàËÆ¶È:54.5% Journal of Natural Products 1984 Vol 47 308-311 Roseatoxide and Dihypoestoxide: Additional New Diterpenoids from Hypoestes rosea Akinbo A. Adesomoju, Joseph I. Okogun Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3-O-¦Â-D-glucopyranosyl-3-¦Â-hydroxyolean-12-en-28-oic acid 28-O-[¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-galactopyranosyl] ester C48H78O18 ÏàËÆ¶È:54.1% Journal of Natural Products 2010 73 247-251 Sesquiterpene Lactones from Anthemis melanolepis and Their Antibacterial and Cytotoxic Activities. Prediction of Their Pharmacokinetic Profile Vasiliki Saroglou, Anastasia Karioti, Ana Rancic, Kostas Dimas, Catherine Koukoulitsa, Maria Zervou and Helen Skaltsa Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3-O-(6'-butyl ester)-¦Â-D-glucuropyranosyl-oleanolic acid-28-O-¦Á-L-arabinopyranoside C45H72O13 ÏàËÆ¶È:53.3% Acta Botanica Yunnanica 2003 25(5) 613-619 A New Cucurbitacin and A New Oleanolic Acid Glycosides from Hemsleya gigantha CHEN Ya,QIU Ming-Hua, GU Kun, CHEN Jian-Chao Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3-O-¦Â-D-glucopyranosyl-3-¦Â-hydroxyolean-12-en-28-oic acid 28-O-[¦Â-Dapiofuranosyl-(1¡ú2)-¦Â-D-glucopyranosyl] ester C47H76O17 ÏàËÆ¶È:53.1% Journal of Natural Products 2010 73 247-251 Sesquiterpene Lactones from Anthemis melanolepis and Their Antibacterial and Cytotoxic Activities. Prediction of Their Pharmacokinetic Profile Vasiliki Saroglou, Anastasia Karioti, Ana Rancic, Kostas Dimas, Catherine Koukoulitsa, Maria Zervou and Helen Skaltsa Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3¦Â-(2-O-sulfo-¦Á-L-arabinopyranosyl)-27-dihydroxyurs-12-en-28-oic acid 28-O-¦Â-D-glucopyranoside C41H66O16S ÏàËÆ¶È:52.2% Journal of Natural Products 2007 70 584-588 Sulfated Triterpene Derivatives from Fagonia arabica Angela Perrone,Milena Masullo, Carla Bassarello, Arafa I. Hamed, Maria Antonietta Belisario, Cosimo Pizza, and Sonia Piacente Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 21 ÏàËÆ¶È:52.2% Planta Medica 1984 50 322-327 Saponins from Chinese Medicinal Plants. (I). Isolation and Structures of Hemsiosides Rui-Lin Nie, Toshinobu Morita, Ryoji Kasai, Jun Zhou, Cheng-Yih Wu and Osamu Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 7 ÏàËÆ¶È:52.2% Chinese Pharmaceutical Journal 2007 42 178-180 Studies on Triterpenoid Saponins from Achyranthese bidentata Bl LI Juan, BI Zhi-ming, XIAO Ya-jie, LI Ping Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 7g ÏàËÆ¶È:52.2% Bioorganic & Medicinal Chemistry 1998 6 2029-2039 New 1¦Á,25-dihydroxy vitamin D3 analogues with side chains attached to C-18: synthesis and biological activity Gunnar Grue-Sørensen, Christina Mørk Hansen Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . apratoxin A C45H69N5O8S ÏàËÆ¶È:52.2% Journal of the American Chemical Society 2001 123 5418-5423 Total Structure Determination of Apratoxin A, a Potent Novel Cytotoxin from the Marine Cyanobacterium Lyngbya majuscula Hendrik Luesch, Wesley Y. Yoshida, Richard E. Moore, Valerie J. Paul, and Thomas H. Corbett Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . chikusetsusaponin IVa methyl ester ÏàËÆ¶È:52.2% 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 ̼Æ×Ä£Äâͼ 11 . Cyclo[D-Val-Ser-D-Phe-Ser-Phe-Pro-allo-Thr] ÏàËÆ¶È:52.2% Journal of the American Chemical Society 1996 118 12358-12367 Total Synthesis and Assignment of Configuration of Lissoclinamide 7 Peter Wipf and Paul C. Fritch Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 3-O-(6'-butyl ester)-¦Â-D-glucur opyranosyl-oleanolic acid-28-O-¦Â-D-glucopyranoside C46H74O14 ÏàËÆ¶È:52.1% China Journal of Chinese Materia Medica 2008 33 1770-1773 Studies on the Chemical Constituents of Triterpenoid Saponins in Hemsleya chensnsis Cogn XU Jinzhong, WANG Xianqin, HUANG Kexin, YANG Xinyu, MA Xiyan, ZHANG Hongye, DONG Jianyong Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . taibaienoside IV C46H74O14 ÏàËÆ¶È:52.1% Chinese Pharmaceutical Journal 1997 32 78-80 Two new oleanolic acid saponins from the root bark of Aralia taibaiensis Tang Haifeng(Tang HF), Yi Yanghua(Yi YH), Wang Zhongzhuang(Wang ZZ), et al Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Peracetylated dumosasaponin 6 ÏàËÆ¶È:52.1% 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 ̼Æ×Ä£Äâͼ 15 . 3-O-¦Â-D-glucopyranosyl-3-¦Â-hydroxyolean-12-en-28-oic acid 28-O-[¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-glucopyranosyl] ester C48H78O17 ÏàËÆ¶È:52.0% Journal of Natural Products 2010 73 247-251 Sesquiterpene Lactones from Anthemis melanolepis and Their Antibacterial and Cytotoxic Activities. Prediction of Their Pharmacokinetic Profile Vasiliki Saroglou, Anastasia Karioti, Ana Rancic, Kostas Dimas, Catherine Koukoulitsa, Maria Zervou and Helen Skaltsa Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . funingenoside L C38H58O14 ÏàËÆ¶È:51.0% Helvetica Chimica Acta 2004 Vol. 87 516 Six Novel 5¦Á-Adynerin-Type Cardenolides from Parepigynum funingense Yan Hua, Li Da Han, and Chang Xiang Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . ţϥÔíÜÕ ¢ó C47H70O20 ÏàËÆ¶È:51.0% Chinese Journal of Medicinal Chemistry 2005 15 224-226 The triterpenoid saponins in Achyra nt hes bientata Bl WANG Guang-shu, CONG Deng-li, YANGJin-zhu, YANG Xiao-hong Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . syringostatin B ÏàËÆ¶È:51.0% Journal of the Chemical Society, Perkin Transactions 1 1992 875-880 Isolation and structural elucidation of syringostatins, phytotoxins produced by Pseudomonas syringae pv. syringae lilac isolate Naoyuki Fukuchi, Akira Isogai, Jiro Nakayama, Seiji Takayama, Shuichi Yamashita, Kazuo Suyama and Akinori Suzuki Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . micropeptin HU909 C41H64ClN9NaO12 ÏàËÆ¶È:50% Journal of Natural Products 2009 72 1429-1436 Protease Inhibitors from a Water Bloom of the Cyanobacterium Microcystis aeruginosa Shiri Gesner-Apter and Shmuel Carmeli Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . apratoxin D C48H75N5O8S ÏàËÆ¶È:50% Journal of Natural Products 2008 71(6) 1099-1103 Apratoxin D, a Potent Cytotoxic Cyclodepsipeptide from Papua New Guinea Collections of the Marine Cyanobacteria Lyngbya majuscula and Lyngbya sordida Marcelino Gutie#rrez, Takashi L. Suyama, Niclas Engene,Joshua S. Wingerd, Teatulohi Matainaho, and William H. Gerwick Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . actinomycin G4 C61H84N12O17 ÏàËÆ¶È:50% Journal of Natural Products 2006 69 1153-1157 Actinomycins with Altered Threonine Units in the ¦Â-Peptidolactone Jens Bitzer, Victoria Gesheva, and Axel Zeeck Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . certonardoside H ÏàËÆ¶È:50% Journal of Natural Products 2002 65 1649-1656 New Saponins from the Starfish Certonardoa semiregularis Weihong Wang,Famei Li,Naseer Alam, Yonghong Liu,Jongki Hong,Chong-Kyo Lee,Kwang Sik Im,and Jee H. Jung Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . lotoidoside E C44H71NO13 ÏàËÆ¶È:50% Planta Medica 2005 71 554-560 Antiproliferative Hopane and Oleanane Glycosides from the Roots of Glinus lotoides Arafa I. Hamed,Sonia Piacente, Giuseppina Autore,Stefania Marzocco,Cosimo Pizza,Wieslaw Oleszek Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . chikusetsusaponin-IVa ÏàËÆ¶È:50% Planta Medica 1984 50 322-327 Saponins from Chinese Medicinal Plants. (I). Isolation and Structures of Hemsiosides Rui-Lin Nie, Toshinobu Morita, Ryoji Kasai, Jun Zhou, Cheng-Yih Wu and Osamu Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . betavulgaroside I 1'''-methyl ester C48H72O20 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1996 44 1212-1217 Medicinal Foodstuffs. III. Sugar Beet. (1) : Hypoglycemic Oleanolic Acid Oligoglycosides, Betavulgarosides, I, II, III, and IV, from the Root of Beta vulgaris L. (Chenopodiaceae) Masayuki YOSHIKAWA,Toshiyuki MURAKAMI,Masashi KADOYA,Hisashi MATSUDA,Osamu MURAOKA,Johji YAMAHARA and Nobutoshi MURAKAMI Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . betavulgaroside II C41H60O15 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1996 44 1212-1217 Medicinal Foodstuffs. III. Sugar Beet. (1) : Hypoglycemic Oleanolic Acid Oligoglycosides, Betavulgarosides, I, II, III, and IV, from the Root of Beta vulgaris L. (Chenopodiaceae) Masayuki YOSHIKAWA,Toshiyuki MURAKAMI,Masashi KADOYA,Hisashi MATSUDA,Osamu MURAOKA,Johji YAMAHARA and Nobutoshi MURAKAMI Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . chikusetsusaponin Iva C42H66O15 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1990 38 375-377 Saponins from Bran of Quinoa, Chenopodium quinoa WILLD. II Fumie MIZUI,Ryoji KASAI,Kazuhiro OHTANI and Osamu TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . 20S-(2',3',4',6'-Tetra-O-acetyl-¦Â-D-glucopyransoyloxy)dammar-24-en-3,12-dione C44H66O12 ÏàËÆ¶È:50% Chemistry of Natural Compounds 2006 42 452-458 SYNTHESIS OF 20S-PROTOPANAXADIOL 20-O-b-D-GLUCOPYRANOSIDE, A METABOLITE OF Panax ginseng GLYCOSIDES, AND COMPOUNDS RELATED TO IT L. N. Atopkina and V. A. Denisenko Structure 13C NMR ̼Æ×Ä£Äâͼ |

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