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4.32,6.91,8.28,8.49,9.34,14.49,14.58,15.04,16.97,17.1,19.35,22.12,23.93,24.08,24.34,25.41,28.15,30.21,31.04,33.26,33.5,34.49,37.76,38.15,38.69,55.11,55.67,55.94,59.19,60.15,60.7,60.88,62.28,63.14,63.51,64.74,66.87,71.24,72.8,92.06,94.73,95.15,114.14,135.75,172.37
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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
17 .     Å£Ï¥ÔíÜÕ ¢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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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