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17.3,17.3,17.5,17.6,17.8,18.8,22.3,23.2,25.8,26.7,27.8,30.8,31.0,32.2,36.1,39.4,39.7,40.0,41.2,46.0,49.1,49.6,51.4,51.7,60.9,62.9,63.1,69.5,70.2,71.7,72.3,72.4,72.6,74.2,74.6,75.2,78.2,78.3,78.4,78.7,79.2,79.4,83.3,101.9,126.0,130.9
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16.5,17.4,17.5,17.6,17.6,22.6,22.8,25.8,26.7,28.2,32.0,39.4,40.4,43.3,47.6,48.9,50.1,50.7,61.8,67.7,70.9,78.4,130.8
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1 .     ginsenoside-Re
    ÏàËÆ¶È:95.8%
Chemical & Pharmaceutical Bulletin          1986          34          4368-4372
Saponins of Plants of Panax Species Collected in Central Nepal and Their Chemotaxonomical Significance. II
TOSHINOBU MORITA,YUN-CHEUNG KONG,PAUL PUI-HAY BUT,KAM-HUNG NG,TAI-TUNG YIP,RYOJI KASAI and OSAMU TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     compound 5
    ÏàËÆ¶È:95.8%
Acta Pharmaceutica Sinica          1989          Vol 24          633-636
FURTHER STUDY ON DAMMARANE SAPONINS OF LEAVES OF PANAX JAPONICUS VAR.MAJOR COLLECTED IN QINLING M OUNTAINS CHINA
DQ Wang; BS Feng; XB Wang; CR Yang and J Zhou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     Ginsenoside Re
    ÏàËÆ¶È:95.8%
Natural Product Sciences          2008          14          171-176
Ginsenosides from the Roots of Korean Cultivated-Wild Ginseng
Yang, Min-Cheol; Seo, Dong-Sang; Hong, Jong-Ki; Hong, Sung-Hyun; Kim, Young-Choong; Lee, Kang-Ro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     ginsenoside-Re
    ÏàËÆ¶È:95.8%
Phytochemistry          1989          28          1855-1858
Dammarane and oleanane saponins from callus tissue of Panax japonicus
Naomi Fujioka,Hiroshi Kohda,Kazuo Yamasaki,Ryoji Kasai,Yukihiro Shoyama,Itsuo Nishioka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     ginsenoside-Re
    ÏàËÆ¶È:95.8%
Phytochemistry          1989          28          1855-1858
Dammarane and oleanane saponins from callus tissue of Panax japonicus
Naomi Fujioka,Hiroshi Kohda,Kazuo Yamasaki,Ryoji Kasai,Yukihiro Shoyama,Itsuo Nishioka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     ginsenoside-Re
    ÏàËÆ¶È:95.8%
Phytochemistry          1978          17          1353-1358
Dammarane saponins of leaves of Panax pseudo-ginseng subsp. himalaicus
Osamu Tanaka, Shoji Yahara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     ginsenoside Rg1
C42H72O14     ÏàËÆ¶È:95.8%
Chinese Traditional and Herbal Drugs          2010          41          1060-1065
Chemical components of active fractions from Qili Qiangxin Capsula
LIU Yi-xun; YU He-shui; KANG Li-ping; ZOU Peng; JIA Ji-ming; WANG Hong-tao ZHENG Ya-jie; TIAN Shu-yan; WU Yi-ling; MA Bai-ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     ginsenoside Re
    ÏàËÆ¶È:95.8%
Chinese Pharmaceutical Journal          2008          43          412-415
Study on Isolation and Structural Elucidation of Ginsenosides from Transgenic Crown Gall of Panax quinquefolium
ZHU Jian-hua YU Rong-min YAN Chun-yan SONG Li-yan ZHAO Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




9 .     ginsenoside Re
    ÏàËÆ¶È:95.8%
Natural Product Research and Development          2006          18          549-554
A Further Investigation on the Chemical Constituents from the Leaves of Panax notoginseng
LI Hai-zhou; ZHANG Ying-jun; YANG Chong-ren*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




10 .     ginsenoside-Re
    ÏàËÆ¶È:93.7%
China Journal of Chinese Materia Medica          1992          17          96-98
A sttudy on the Saponisns in Fruits Pedicels of Panax notoginseng (Burk.)F.H.Chen
Wei Junxian and Cao Shuming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




11 .     ginsenoside-Re
    ÏàËÆ¶È:93.7%
Magnetic Resonance in Chemistry          2002          40          483-488
Complete assignment of 1H and 13C NMR data for nine protopanaxatriol glycosides
Rongwei Teng, Haizhou Li, Jiangtao Chen, Dezu Wang, Yineng He and Chongren Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




12 .     compound 8a
    ÏàËÆ¶È:89.7%
Tetrahedron Letters          2003          44          5661-5664
Regioselective acylation of ginsenosides by Novozyme 435
Rongwei Teng, Chingseng Ang, David McManus, David Armstrong, Shaiolim Mau, Antony Bacic
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




13 .     notoginsenoside M
C48H82O19     ÏàËÆ¶È:89.5%
Chemical & Pharmaceutical Bulletin          2001          49(11)          1452-1456
Bioactive Saponins and Glycosides. XIX.1) Notoginseng (3):Immunological Adjuvant Activity of Notoginsenosides and Related Saponins: Structures of Notoginsenosides-L, -M, and -N from the Roots of Panax notoginseng (BURK.) F. H. CHEN.
Masayuki YOSHIKAWA,Toshio MORIKAWA, Kenichi YASHIRO, Toshiyuki MURAKAMI, and Hisashi MATSUDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




14 .     Ginsenoside Re1
C48H82O19     ÏàËÆ¶È:89.5%
Journal of Agricultural and Food Chemistry          2011          59          200-205
Protopanaxatriol-Type Ginsenosides from the Root of Panax ginseng
Guo-Yuan Zhu, Ying-Wei Li, Desmond Kwok-Po Hau, Zhi-Hong Jiang, Zhi-Ling Yu, and Wang-Fun Fong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




15 .     ginsenoside-Rg2
    ÏàËÆ¶È:89.1%
Planta Medica          1990          56          298-300
A New Minor Saponin from the Leaves of Panax ginseng
ShaolinZhang,Tadahiro Takeda, TinruZhu, Yingjie Chen, Xinsheng Yao, Osamu Tanaka, and Yukio Ogihara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




16 .     compound 8b
    ÏàËÆ¶È:89.1%
Tetrahedron Letters          2003          44          5661-5664
Regioselective acylation of ginsenosides by Novozyme 435
Rongwei Teng, Chingseng Ang, David McManus, David Armstrong, Shaiolim Mau, Antony Bacic
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




17 .     pseudoginsenoside-RS1
    ÏàËÆ¶È:88%
Chemical & Pharmaceutical Bulletin          1986          34          4368-4372
Saponins of Plants of Panax Species Collected in Central Nepal and Their Chemotaxonomical Significance. II
TOSHINOBU MORITA,YUN-CHEUNG KONG,PAUL PUI-HAY BUT,KAM-HUNG NG,TAI-TUNG YIP,RYOJI KASAI and OSAMU TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




18 .     floralginsenoside I
C48H82O20     ÏàËÆ¶È:87.5%
Heterocycles          2007          71          577-588
Structures of Dammarane-Type Triterpene Triglycosides from the Flower Buds of Panax ginseng
Seikou Nakamura, Sachiko Sugimoto, Hisashi Matsuda, and Masayuki Yoshikawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




19 .     floralginsenoside J
C48H82O20     ÏàËÆ¶È:87.5%
Heterocycles          2007          71          577-588
Structures of Dammarane-Type Triterpene Triglycosides from the Flower Buds of Panax ginseng
Seikou Nakamura, Sachiko Sugimoto, Hisashi Matsuda, and Masayuki Yoshikawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




20 .     Ginsenoside Re2
C48H82O19     ÏàËÆ¶È:87.5%
Journal of Agricultural and Food Chemistry          2011          59          200-205
Protopanaxatriol-Type Ginsenosides from the Root of Panax ginseng
Guo-Yuan Zhu, Ying-Wei Li, Desmond Kwok-Po Hau, Zhi-Hong Jiang, Zhi-Ling Yu, and Wang-Fun Fong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




21 .     notoginsenoside FP1
C47H80O18     ÏàËÆ¶È:87.2%
Helvetica Chimica Acta          2008          Vol. 91          60
Two New Dammarane-Type Bisdesmosides from the Fruit Pedicels of Panax notoginseng
Xian-You Wang, Dong Wang, Xiao-Xia Ma, Ying-Jun Zhang, and Chong-Ren Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




22 .     notoginsenoside-R1
    ÏàËÆ¶È:87.2%
China Journal of Chinese Materia Medica          1992          17          96-98
A sttudy on the Saponisns in Fruits Pedicels of Panax notoginseng (Burk.)F.H.Chen
Wei Junxian and Cao Shuming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




23 .     floralginsenoside La
C48H82O19     ÏàËÆ¶È:87.2%
Heterocycles          2007          71          577-588
Structures of Dammarane-Type Triterpene Triglycosides from the Flower Buds of Panax ginseng
Seikou Nakamura, Sachiko Sugimoto, Hisashi Matsuda, and Masayuki Yoshikawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ


»¯ºÏÎï2£º

1 .     (3S,4R,5S,9S,10S,11S)-3-S-(1,2-Dimercaptoethyl)morelian-1,7-dione 1-ethylenedithioketal
C19H30OS4     ÏàËÆ¶È:60.8%
Journal of Natural Products          2004          67          189-193
Preparation of Moreliane-Derived Volatile Sesquiterpenes
Carlos M. Cerda-Garca-Rojas, Mara A. Bucio, Luisa U. Romn, Juan D. Hernndez, and Pedro Joseph-Nathan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




2 .     3¦Â-hydroxyetio-17¦Â-dammaranic acid
C23H38O3     ÏàËÆ¶È:60.8%
Chinese Chemical Letters          2011          22          1461-1464
Two new dammarane-type sapogenins from Gynostemma pentaphyllum
Xia Li,Jia Qing Cao,Lin Shi,Yu Qing Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




3 .     compound 1a
    ÏàËÆ¶È:60.8%
Acta Chimica Sinica          1989          47          258-261
Studies on the Novel Diterpenoic Constituents of TU-JIN-PI IV. Isolation and Identification of Pseudolaric Acid D and Pseudolaric Acid E
Li Zhu-Lian; Chen Ke; Pan De-Ji; Xu Gnang-Yi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




4 .     3¦Â-hydroxy-4,4,14¦Á-trimethyl-5¦Á-pregna-7,9(11)-diene-20S-carboxylic acid
C25H38O3     ÏàËÆ¶È:57.6%
Journal of the Chemical Society, Perkin Transactions 1          1984                   1219-1221
New metabolic products of Verticillium lecanii. Part 2. 3¦Â,12¦Â,-Dihydroxy-4,4,14¦Á-trimethyl-5¦Á-pregna-7,9(11)-diene-20S-carboxylic acid and 4,4,14¦Á-trimethyl-3-oxo-5¦Á-pregna-7,9(11)-diene-20S-carboxylic acid
John Frederick Grove
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




5 .     3¦Â-hydroxy-20,20-(ethylenedioxy)-22,23,24,25,26,27-hexanordammarane
C29H48O3     ÏàËÆ¶È:57.6%
The Journal of Organic Chemistry          1999          64          9587-9595
The Fluorine Atom as a Cation-Stabilizing Auxiliary in Biomimetic Polyene Cyclizations:  Total Synthesis of dl-Dammarenediol1
William S. Johnson, William R. Bartlett, Boris A. Czeskis, Arnaud Gautier, Cheol H. Lee, R¨¦my Lemoine, Eric J. Leopold, Gregory R. Luedtke, and Katherine J. Bancroft
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




6 .     scutellaric acid
    ÏàËÆ¶È:57.6%
Lishizhen Medicine and Materia Medica Research          2005          16          620-621
Studies on the Chemical Constituents of Scutellaria barbata
TAO Shu-hong; WU Feng-e
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




7 .     Ocotillol-II
C30H52O3     ÏàËÆ¶È:57.1%
Phytochemistry          1993          32          472-474
Lup-20(29)-en-3¦Â,15¦Á-diol and ocotillol-II from the stem bark of Phyllanthus flexuosus
Reiko Tanaka, Kimiyo Masuda, Shunyo Matsunaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




8 .     19¦Á-Hydroxyasiatic acid
C30H50O4     ÏàËÆ¶È:57.1%
Natural Product Research and Development          2012          24          757-760
Chemical Constituents from Stems of Rhododendron delavayi Franch.
XU Jin-jin; WANG Yue-hu; WANG Hong-sheng; WANG Huan; HUANG Qiao-qin; LONG Chun-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     ent-(16S)-1¦Á,14¦Á-Diacetoxy-7¦Â-hydroxy-17-methoxykauran-15-one
C25H38O7     ÏàËÆ¶È:56.5%
Chemical & Pharmaceutical Bulletin          2005          53(3)          296-300
Cytotoxic Diterpenoids from Vietnamese Medicinal Plant Croton tonkinensis GAGNEP.
Phan Minh GIANG,Phan Tong SON,Yumi HAMADA,and Hideaki OTSUKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




10 .     caldaphnidine Q
C23H37NO3     ÏàËÆ¶È:56.5%
Journal of Natural Products          2008          71(10)          1663-1668
Alkaloids from the Twigs of Daphniphyllum calycinum
Chuan-Rui Zhang, Sheng-Ping Yang, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     (+)-17-oxocycloprotobuxine
C23H37NO     ÏàËÆ¶È:56.5%
Journal of Natural Products          1999          62          665-669
New Steroidal Alkaloids from the Roots of Buxus sempervirens
Atta-ur-Rahman, Athar Ata, Samina Naz, M. Iqbal Choudhary, Bilge Sener, and Songul Turkoz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     di-6-epi-3-anhydroophiobolin B
    ÏàËÆ¶È:56.5%
Journal of Natural Products          1999          62          895-897
Characterization of 6-epi-3-Anhydroophiobolin B from Cochliobolus heterostrophus
Xiaoyu Shen, Stuart B. Krasnoff, Shun-Wen Lu, Chuck D. Dunbar, James O¡¯Neal, B. Gillan Turgeon, Olen C. Yoder, Donna M. Gibson, and Mark T. Hamann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     16,17-dihydro-12b,16b-epoxyna-pelline
C22H33NO3     ÏàËÆ¶È:56.5%
Planta Medica          2005          71          1073-1076
Three New Diterpene Alkaloids from the Roots of Aconitum nagarum var.lasiandrum
Fan Zhang , Shu-Lin Peng , Xun Liao , Kai-Bai Yu , Li-Sheng Ding
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     isopropylidenkirenol
C23H38O4     ÏàËÆ¶È:56.5%
Planta Medica          1991          57          396-396
Diterpene aus Siegesbeckia glabrescens Diterpenes from Siegesbeckia glabrescens
K Liu and E. Roder
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     lepenine
C22H33NO     ÏàËÆ¶È:56.5%
Chemistry of Natural Compounds          1996          32          596-675
ALKALOIDS. PLANTS, STRUCTURES, PROPERTIES" Chapter 2, continued
R. Shakirov, M. V. Telezhenetskaya, I. A. Bessonova,S. F. Aripova, I. A. Israilov, M. N. Sultankhodzhaev,V. I. Vinogradova, V. I.Akhmedzhanova, T. S. Tulyaganov,B. T. Salimov, and V. A. Tel'nov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     Lepenine
C22H33N03     ÏàËÆ¶È:56.5%
Chemistry of Natural Compounds          1992          28          388-389
ALKALOIDS OF THE MONGOLIAN FLORA I. ALKALOIDS OF THE EPIGEAL PART OF Aconitum barbatum
N. Batbayar, D. Batsuren, and M. N. Sultankhodzhaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     ent-7¦Á-15¦Â,16¦Â-epoxykaurane
C22H32O2     ÏàËÆ¶È:56.5%
Natural Product Research          2002          16          33-37
Diterpenes from Sideritis Trojana
G¨¹laçti Topçu; Ahmet Gören; Turgut Kılİç; Y. Kemal YıLdız; G¨¹lendam T¨¹men
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




18 .     compound 1a
C22H34O3     ÏàËÆ¶È:56.5%
Natural Product Research          2007          21          135-140
New diterpenoids from Calceolaria polifolia
Juan A. Garbarino; Marisa Piovano; M. Cristina Chamy; Luis Espinoza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     strophanthidin
C23H32O6     ÏàËÆ¶È:56.5%
Journal of Natural Products          2010          73          338-345
Occurrence of Progesterone and Related Animal Steroids in Two Higher Plants'
Guido F. Pauli, J. Brent Friesen, Tanja Gödecke, Norman R. Farnsworth and Bernhard Glodny
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     GA14 dimethyl ester 16¦Á,17-epoxide
    ÏàËÆ¶È:56.5%
Phytochemistry          1992          31          1869-1877
Gibberellins A82 and A83 in seed of Lupinus albus
Paul Gaskin, Gordon V. Hoad, Jake Macmillan, Ian K. Makinson, Jo E. Readman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     ent-labdan-8¦Â,18¦Â-diol-15-al
    ÏàËÆ¶È:56.5%
Phytochemistry          1992          31          3274-3276
Diterpenoids from Baccharis neaei
Francesca Faini, Cecilia Labbe, M.In¨¦s Polanco
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     (10a'S)-2',3',5',6',7',10'-Hexahydro-10a'H-spiro[1,3-dithiolane-2,1'-pyrrolo[1,2-a]azocine]-10a'-carboxylic acid menthyl ester
C23H37NOS2     ÏàËÆ¶È:56.5%
Heterocycles          2006          68          47-58
Concise Highly Enantioselective Cascade Synthesis of Azacyclooctene Alkaloids with a Quaternary Stereocenter
Daniele Muroni, Antonio Saba,* and Nicola Culeddu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     mansumbinol
C22H36O     ÏàËÆ¶È:56.5%
Phytochemistry          1986          25          917-922
The mansumbinanes: Octanordammaranes from the resin of Commiphora incisa
Gordon J. Provan, Peter G. Waterman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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