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1 .     artesteversin
C30H36O5     ÏàËÆ¶È:60%
Phytochemistry          1985          24          1009-1015
Dimeric guaianolides from Artemisia sieversiana
Ferdinand Bohlmann, Widayati Ang, Carola Trinks, Jasmin Jakupovic, Siegfried Huneck
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     Allosxde A
     ÏàËÆ¶È:54.5%
Chemistry of Natural Compounds          1991          27          198-207
STEROIDS OF THE SPIROSTAN AND FUROSTAN SERIES FROM PLANTS OF THE GENUS Allium. XXVII. ALLIOSTEROL AND ALLOSIDES A AND B FROM Allium suvorovii AND Allium stipitatum - STRUCTURAL ANALOGS OF FUROSTANOLS
Yu. S. Vollerner, S. D Kravets,A. S. Shashkov, B. Tashkhodzhaev,M. B. Gorovits, M. R. Yagudaev,and N. K. Abubakirov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     (1S,5S,7R,9R,13S,15S,16R)-15-(benzyloxy)-5-(hydroxymethyl)-7-[(p-methoxybenzyl)oxy]-6,6,9,16-tetramethyl-11-(phenylsulfonyl)-4,-17-dioxabicyclo[11.3.1]heptadecane-3,10-dione
     ÏàËÆ¶È:54.5%
Journal of the American Chemical Society          2000          122          619-631
Stereocontrolled Elaboration of Natural (−-Polycavernoside A, a Powerfully Toxic Metabolite of the Red Alga Polycavernosa tsudai
Leo A. Paquette, Louis Barriault, Dmitri Pissarnitski, and Jeffrey N. Johnston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     Antifungalmycin
C35H60O14     ÏàËÆ¶È:54.2%
Natural Products and Bioprospecting          2012          2          41-45
Antifungalmycin, an antifungal macrolide from Streptomyces padanus 702
Yi-Fen Wang, Sai-Jin Wei, Zhi-Ping Zhang, Tong-He Zhan, Guo-Quan Tu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     Pseudolarolide O
C30H42O5     ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2003          Vol. 86          787
Pseudolarolides O and P, Two Novel Triterpene Dilactones from Pseudolarix kaempferi
Guo-Fu Chen, Chang-Heng Tan, Zhu-Lian Li, Shan-Hao Jiang, and Da-Yuan Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     neviotine b
C30H50O6     ÏàËÆ¶È:53.3%
Journal of Natural Products          2001          64          175-180
New Triterpenoids from the Red Sea Sponge Siphonochalina siphonella
Yoel Kashman, Tesfamariam Yosief, and Shmuel Carmeli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     3¦Á,5¦Á,19¦Â,28-diepoxy-A-neo-18¦Á-oleane
C30H48O2     ÏàËÆ¶È:53.3%
Chemistry of Natural Compounds          2006          42          618-619
STRUCTURE OF THE MINOR OZONOLYSIS PRODUCT OF 19b,28-EPOXY-A-neo-18a-OLEAN-3(5)-ENE
N. I. Medvedeva, O. B. Flekhter,A. Gzella, and L. Zaprutko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     19¦Â,28-Epoxy-18¦Á-olean-3(5)-ene
C30H48O     ÏàËÆ¶È:53.3%
Chemistry of Natural Compounds          2004          40          247-249
SYNTHESIS OF 4,5-SECO-DERIVATIVES OF ALLOBETULIN
N. I. Medvedeva, O. B. Flekhter, L. A. Baltina,F. Z. Galin, and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     compound 11
     ÏàËÆ¶È:53.3%
Chemistry of Natural Compounds          1984          20          170-173
GLYCOSYLATION OF BETULIN AND ITS ACETATES IN THE PRESENCE OF CADMIUM CARBONATE
L. E. Odinokova, G. I. Oshitok, V. A. Denisenko, V. F. Anufriev, A. M, Tolkach, and N. I. Uvarova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     pseudolarohde K
C30H44O7     ÏàËÆ¶È:53.3%
Journal of Asian Natural Products Research          1999          2          207-214
Structures and Stereochemistry of Pseudolarolides K and L, Novel Triterpene Dilactones from Pseudolarix Kaempferi
KE CHEN, QIAN SHI, ZHU-LIAN LI, CHI-DUEN POONC, REN-JIU TANG and KUO-HSIUNG LEE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     herniaria saponin A
C65H102O32     ÏàËÆ¶È:53.3%
Natural Product Research          1995          6          233-240
Herniaria Saponin A, A Novel Saponin from Herniaria Fontanesii
Addi Nait Mbark; Zoubida Charrouf; Jean Michel Wieruszeski; Yves Leroy; Ossarath Kol
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     acnistin E
     ÏàËÆ¶È:53.3%
Phytochemistry          1994          36          1297-1301
Acnistins C and D, withanolides from Dunalia solanacea
Javier G. Luis, Fernando Echeverri, Antonio G. Gonz¨¢lez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     compound 93
     ÏàËÆ¶È:53.3%
Phytochemistry          1994          37          1517-1575
13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features
Shashi B. Mahato, Asish P. Kundu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     Ainsliadimer C
C30H36O7     ÏàËÆ¶È:53.3%
Planta Medica          2011          77          1545-1550
New Sesquiterpenoids from Ainsliaea macrocephala and Their Nitric Oxide Inhibitory Activity
Zhi-JunWu, Xi-Ke Xu, Hua-Wu Zeng, Yun-Heng Shen, Jun-Mian Tian, Juan Su, Hui-Liang Li, Lei Shan, Run-Hui Liu, Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     19¦Â,28-Epoxy-A-neo-18¦Á-olean-3(5)-ene
C30H48O     ÏàËÆ¶È:53.3%
Chemistry of Natural Compounds          2011          Vol. 47, No. 4          579-582
ALLYLIC OXIDATION OF 19¦Â,28-EPOXY-A-NEO-5 -METHYL-25-NOR-18¦Á-OLEAN-9-ENE
O. B. Kazakova, E. F. Khusnutdinova, A. N. Lobov,N. I. Medvedeva, and L. V. Spirikhin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     Anthogorgsteroid D
C26H44O4     ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2012          95          522-527
Polyhydroxylated Steroids from the South China Sea Gorgonian Anthogorgia
Peng Sun,Yuanyuan Xu,Taofang Liu,Hua Tang,Yanghua Yi, Karsten Krohn,Ling Li, and Wen Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     (24S)-stigmast-3¦Â,5¦Á,6¦Â-triol
     ÏàËÆ¶È:53.3%
Chinese Traditional and Herbal Drugs          2010          41          1065-1068
СҶÈ̶¬ÌٵĻ¯Ñ§³É·ÖÑо¿
Áõΰ;°×ËØÆ½;Áº»á¾ê;Ô¬ÓÀÁÁ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     A-Nor-5¦ÁH-19¦Â,28-epoxy-18¦Á-olean-3(5)-ene
C30H48O     ÏàËÆ¶È:53.3%
Russian Journal of Organic Chemistry          2004          40          1092-1097
Synthetic Transformations of Higher Terpenoids: XI. Synthesis of A-Nor-5bH-19b,28-epoxy-18a-olean-3-one Derivatives
N. I. Medvedeva, O. B. Flekhter, E. V. Tretyakova, F. Z. Galin and L. A. Baltina, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-11-28 17:43:09
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