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66.33,68.34,70.42,70.81,71.00,72.54,76.30,77.64,77.81,77.96,89.19,89.89,99.14,100.76,109.56,121.22,104.50
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1 .     pennogenin-3-O-¦Á-L-rhamnopyranosyl-(1¡ú2)]¦Â-D-glucopyranoside
    ÏàËÆ¶È:92.3%
Chinese Joumal of Experimental Traditional Medical Fomulae          2014          20          99-102
Studies on Chemical Constituents of Trillium tschonoskii
JIA Lan-ting, YANG Shang-jun, BAI Shao-yan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     compound 13
C39H62O13     ÏàËÆ¶È:79.4%
Steroids          2013          78          670-682
Steroidal glycosides from the bulbs of Fritillaria meleagris and their cytotoxic activities
Yukiko Matsuo, Daisuke Shinoda, Aina Nakamaru, Yoshihiro Mimaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     pennogenin3-O-[¦Â-D-xylopyranosyl-(1¡ú5)-¦Á-L-arabinofuranosyl-(1¡ú4)]-[¦Á-L-rhamnopyranosyl-(1¡ú2)]-¦Â-D-glucopyranoside
    ÏàËÆ¶È:78.9%
West China Journal of Pharmaceutical Sciences          2010          25          508-511
Isolation and identification of steroidal saponins of Paris polyphylla Smith var. pseudothibetica
LIU Xian-bo, ZHANG Hao, YONG Zheng-ping, XUE Dan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     3-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:76.9%
Chemical & Pharmaceutical Bulletin          2007          55(4)          551-556
Two New Steroid Glycosides and a New Sesquiterpenoid Glycoside from the Underground Parts of Trillium kamtschaticum
Masateru ONO,Chika TAKAMURA,Fumie SUGITA,Chikako MASUOKA,Hitoshi YOSHIMITSU,Tsuyoshi IKEDA,and Toshihiro NOHARAc
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     25(R)-pennogenin-3-O-¦Á-L-rhamnopyranosyl(1¡ú2)-¦Â-D-glucopyranoside
    ÏàËÆ¶È:76.9%
Chemistry of Natural Compounds          2008          44          821-823
STEROIDAL SAPONINS FROM Paris mairei
Xiao-xiao Liu, Lei Wang,Jie Yang, and Qiang Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     pennogenin-3-O-¦Á-L-rhamnopyranosyl(1¡ú2)-¦Â-D-glucopyranoside
    ÏàËÆ¶È:76.9%
Chemistry of Natural Compounds          2007          43          672-677
SEPARATION AND IDENTIFICATION OF STEROIDAL COMPOUNDS WITH CYTOTOXIC ACTIVITY AGAINST HUMAN GASTRIC CANCER CELL LINES IN VITRO FROM THE RHIZOMES OF Paris polyphylla VAR. chinensis
Huang Yun, Cui Lijian, Zhan Wenhong Dou Yuhong,Wang Yongli, Wang Qiang, and Zhao Ding
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     pennogenin diglycoside
C39H60O12     ÏàËÆ¶È:76.9%
Chinese Journal of Medicinal Chemistry          2005          15          25-30
Isolation and identif iciation of steroidal saponins from Paris polyphylla Smith
KANG Li-ping, MA Bai-ping, ZHANG Jie, XIONG Cheng-qi, TAN Da-wei, CONG Yu-wen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Tb
    ÏàËÆ¶È:76.9%
Chinese Jouranl of Magnetic Resonance          2012          29          101-111
An NMR Study on Two Glucosylated Steroidal Saponins of Tb
KANG Li-ping, WANG Yong-ze, FENG Bing, ZHOU Wen-bin, XIONG Cheng-qi, ZHAO Yang, TAN Da-wei, LIU Chao, MA Bai-ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     pallidifloside C
C39H62O14     ÏàËÆ¶È:76.9%
Journal of Asian Natural Products Research          2011          13          1014-1022
Three new steroidal saponins from Fritillaria pallidiflora
Shuo Shen, Chao-Jun Chen, Ren Bu, Lu Ga, Guo-Yu Li, Yong Tan, Xian Li and Jin-Hui Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     pennogenin-3-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside
C39H62O13     ÏàËÆ¶È:76.9%
Acta Botanica Yunnanica          1983          5          91-97
STUDLES ON THE SAPONIN COMPONENTS OF PLANTS IN YUNNAN VI. STESOID GLYCOSIDES OF PARIS POLYPHYLLA SM. VAR. YUNNANENSIS (FR.) H-M. (2 )
Chen Changxiang, Zhang Yutong and Zhou Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     pennogenin 3-O-¦Â-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside
C39H62O13     ÏàËÆ¶È:76.3%
West China Journal of Pharmaceutical Sciences          2009          24          007-009
Chemical constituents of Paris polyphylla var. pseudothibetica
XIAO Cao-mao, HUANG Jing, TAN Xiao-yan, TANG Min, ZHANG Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     pennogenin-3-O-¦Á-L-rhamnopyranosyl(1¡ú2)-[¦Á-L-arabinofuranosyl(1¡ú4)]-¦Â-D-glucopyranoside
    ÏàËÆ¶È:74.3%
Chemistry of Natural Compounds          2007          43          672-677
SEPARATION AND IDENTIFICATION OF STEROIDAL COMPOUNDS WITH CYTOTOXIC ACTIVITY AGAINST HUMAN GASTRIC CANCER CELL LINES IN VITRO FROM THE RHIZOMES OF Paris polyphylla VAR. chinensis
Huang Yun, Cui Lijian, Zhan Wenhong Dou Yuhong,Wang Yongli, Wang Qiang, and Zhao Ding
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     hauptsaponine S1
    ÏàËÆ¶È:74.3%
Pharmazie          1987          42          143-143
Steroidsaponine aus Dioscorea hispida L.
Ng. X. Cuong, D. Zeigan, Gabriele Voigt, und K. Hiller
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     Paris Saponins VII
    ÏàËÆ¶È:74.3%
Natural Product Research and Development          2011          23          1017-1020
Chemical Constituents of Phyllanthus niruri L.
ZHU, Hong-lin, WEI, Wan-xing, ZHOU, Min, YANG, Dan, FAN, Xi-wang, LIU, Jian-xiong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     26-O-¦Â-D-glucopyranosyl-(25R)-furost-5-en-3¦Â,17¦Á,22¦Á,26-tetraol-3-O-[2''-OAc-¦Á-L-rhamnopyranosyl-(1¡ú2)]-¦Â-D-xylopyranosyl-(1¡ú3)-¦Â-D-glucopyranoside
C52H84O24     ÏàËÆ¶È:74.3%
Chemistry of Natural Compounds          2014          50          489-493
Steroidal Saponins from Polygonatum glaberrimum Rhizomes
L. N. Gvazava, V. S. Kikoladze
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     (25R)-17¦Á-hydroxyspirost-5-en-3¦Â-yl O-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-xylopyranoside
C38H60O12     ÏàËÆ¶È:73.6%
Steroids          2013          78          670-682
Steroidal glycosides from the bulbs of Fritillaria meleagris and their cytotoxic activities
Yukiko Matsuo, Daisuke Shinoda, Aina Nakamaru, Yoshihiro Mimaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (25R)-spirost-5-en-3¦Â,17¦Á-diol 3-O-[¦Á-L-rhamnopyranosyl-(1¡ú2)]-¦Â-D-glucopyranosyl-(1¡ú4)-¦Â-D-xylopyranoside
C44H70O17     ÏàËÆ¶È:72.5%
Chemistry of Natural Compounds          2014          50          489-493
Steroidal Saponins from Polygonatum glaberrimum Rhizomes
L. N. Gvazava, V. S. Kikoladze
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     Diosgenyl ¦Â-L-fucopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside
C39H62O12     ÏàËÆ¶È:71.7%
Bioorganic & Medicinal Chemistry          2008          16          2063-2076
Synthesis of novel spirostanic saponins and their cytotoxic activity
Juan C. Hern¨¢ndez, Francisco Le¨®n, Ignacio Brouard, Fernando Torres, Sara Rubio, Jos¨¦ Quintana, Francisco Est¨¦vez, Jaime Bermejo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     pennogenin 3-O-¦Á-L-arabinofuranosyl(1¡ú4)-[¦Á-L-rhamnopyranosyl(1¡ú2)]-¦Â-D-glucopyranoside
    ÏàËÆ¶È:71.7%
Acta Botanica Yunnanica          1983          5          219-223
STUDIES ON THE SAPONIN COMPONENTS OF PLANTS IN YUNNAN VIII STEROIDAL SAPONINS IN PARIS LUQUANENSIS
Chen Changxiang, Zhou Jun, Zhang Yutong, Gao Chongkun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     (25S)spirost-5-en-3¦Â,17¦Á,27-triol-3-O-[¦Â-D-glucopyranosy(1-4)[¦Á-L-arabinopyranpsy](1-6)]-¦Â-D-glucopyranoside
    ÏàËÆ¶È:71.0%
Chinese Chemical Letters          1992          3          431-432
NEW MINOR STEROIDAL SAPONINS FROM SMILAXLEBRUNII
ZHONG JIAN JIA,YONG JU AND MEI DU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     Aspafilioside F
C38H62O13     ÏàËÆ¶È:71.0%
Steroids          2008          73          83-87
Steroidal saponins from the roots of Asparagus filicinus
Li-Bo Zhou, Dao-Feng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     compound 7
    ÏàËÆ¶È:71.0%
Phytochemistry          1994          36          1005-1008
Steroidal prosapogenins from Dioscorea olfersiana
Mitsue Haraguchi, Ana Paula Zaccarias Dos Santos, Maria Claudia Marx Young, Edison Paulo Chui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     (25S)-spirost-5-en-3¦Â,17¦Á,27-triol-3-O-[¦Á-L-arabinopyranosyl(1¡ú6)]-¦Â-D-glucopyranoside
    ÏàËÆ¶È:71.0%
Phytochemistry          1993          33          1193-1195
Minor steroidal glycosides from the roots of Smilax lebrunii
Ju Zhong-Jian Jia Yong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     pennogenin-3-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:71.0%
Chinese Traditional and Herbal Drugs          2005          36          978-982
Biotransformation of polyphyllins by Curvularia lunata fermentation
FENG Bing; MA Bai-ping; KANG Li-ping; XIONG Cheng-qi; WANG Sheng-qi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     pennogenin-3-O-¦Â-D-glucopyrano-side
    ÏàËÆ¶È:71.0%
Tetrahedron          2007          63          6796-6812
The substrate specificity of a glucoamylase with steroidal saponin-rhamnosidase activity from Curvularia lunata
Bing Feng, Li-ping Kang, Bai-ping Ma, Bo Quan, Wen-bin Zhou, Yong-ze Wang, Yu Zhao, Yi-xun Liu, Sheng-qi Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     pennogenin-3-O-¦Á-L-arabinofuranosyl-(1¡ú4)-¦Â-D-glucopyranoside
    ÏàËÆ¶È:71.0%
Tetrahedron          2007          63          6796-6812
The substrate specificity of a glucoamylase with steroidal saponin-rhamnosidase activity from Curvularia lunata
Bing Feng, Li-ping Kang, Bai-ping Ma, Bo Quan, Wen-bin Zhou, Yong-ze Wang, Yu Zhao, Yi-xun Liu, Sheng-qi Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     compound A1
    ÏàËÆ¶È:71.0%
Acta Botanica Yunnanica          1990          12          323-329
STEROID SAPONINS OF AERIAL PARTS OF PARIS POLYPHYLLA VAR. YUNNANENSIS
Chen Changxiang, Zhou Jun, Zhang Yutong, Zhao Yongyan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     (25S)-17¦Á,27-dihydroxyspirost-5-en-3¦Â-yl O-(4-O-acetyl-¦Á-L-rhamnopyranosyl)-(1¡ú2)-¦Â-D-glucopyranoside
C41H64O15     ÏàËÆ¶È:70.7%
Phytochemistry          2008          69          2724-2730
Steroidal glycosides from the underground parts of Trillium erectum and their cytotoxic activity
Akihito Yokosuka , Yoshihiro Mimaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     diosgenin 3-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-glucuroniduronic acid methyl ester
    ÏàËÆ¶È:70%
Zeitschrift f¨¹r Naturforschung C          2006          61          171-176
Diosgenin Glucuronides from Solanum lyratum and their Cytotoxicity against Tumor Cell Lines
L.-X. Sun, W.-W. Fu, W. Li, K.-S. Bi, and M.-W. Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     (3¦Â,17¦Á,25R)-spirost-5-ene-3,17-diol-3-O-¦Â-D-xylopyranosyl-(1¡ú5)-¦Á-L-arabinofuranosyl-(1¡ú4)-¦Â-D-glucopyranoside
C43H68O17     ÏàËÆ¶È:69.7%
Phytochemistry          2012          81          133-143
Steroidal saponins from Paris polyphylla var. yunnanensis
Xia Wu, Lei Wang, Hui Wang, Yi Dai, Wen-Cai Ye, Yao-Lan Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     trikamsteroside A
C39H62O14     ÏàËÆ¶È:69.2%
Chemical & Pharmaceutical Bulletin          2007          55(4)          551-556
Two New Steroid Glycosides and a New Sesquiterpenoid Glycoside from the Underground Parts of Trillium kamtschaticum
Masateru ONO,Chika TAKAMURA,Fumie SUGITA,Chikako MASUOKA,Hitoshi YOSHIMITSU,Tsuyoshi IKEDA,and Toshihiro NOHARAc
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     (25S)spirost-5-en-3¦Â,17¦Á,27-triol-3-O-(¦Á-L-rhamnopyranosyl(1-4))-¦Â-D-glucopyranoside
    ÏàËÆ¶È:69.2%
Chinese Chemical Letters          1993          4          137-138
TWO MINOR SPIROSTANOL GLYCOSIDES FROM
YONG JU,ZHONG JIAN JIA,HAI RUO PENG AND XUE JUN SUN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     (25S)spirost-5-en-3¦Â,17¦Á,27-triol-3-O-[¦Á-1-rhamnopyranosyl(1¡ú4)]-¦Â-D-galactopyranoside
    ÏàËÆ¶È:69.2%
Phytochemistry          1994          37          1433-1436
Steroidal saponins from Smilax menispermoidea and S. Lebrunii
Ju Yong, Jia Zhongjian, Sun Xuejun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     Pennogenin-3-O-¦Á-L-rhamnopyranosyl-(1¡ú3)-¦Â-D-glucopyranoside
    ÏàËÆ¶È:69.2%
Archives of Pharmacal Research          2008          31          653-658
In vivo anti-inflammatory effect of a new steroidal saponin, mannioside A, and its derivatives isolated from Dracaena mannii
Leon Azefack Tapondjou, Kemvoufo Beaudelaire Ponou, Remy Bertrand Teponno, Marius Mbiantcha and Jules D¨¦sir¨¦ Djoukeng, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     penogenin 3-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:68.4%
Chemical & Pharmaceutical Bulletin          2007          55(4)          551-556
Two New Steroid Glycosides and a New Sesquiterpenoid Glycoside from the Underground Parts of Trillium kamtschaticum
Masateru ONO,Chika TAKAMURA,Fumie SUGITA,Chikako MASUOKA,Hitoshi YOSHIMITSU,Tsuyoshi IKEDA,and Toshihiro NOHARAc
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     compound 7
    ÏàËÆ¶È:68.4%
Chemical & Pharmaceutical Bulletin          1989          37          116-118
Studies on the Constituents of Heloniopsis orientalis (THUNB.) C. TANAKA
Kimiko NAKANO,Kotaro MURAKAMI,Yoshihisa TAKAISHI,Toshiaki TOMIMATSU and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     Diosgenyl ¦Â-D-xylopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside
C38H60O12     ÏàËÆ¶È:68.4%
Bioorganic & Medicinal Chemistry          2008          16          2063-2076
Synthesis of novel spirostanic saponins and their cytotoxic activity
Juan C. Hern¨¢ndez, Francisco Le¨®n, Ignacio Brouard, Fernando Torres, Sara Rubio, Jos¨¦ Quintana, Francisco Est¨¦vez, Jaime Bermejo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     Æ«ÅµÔíÜÕÔª-3-O-¦Â-D-ÆÏÌÑÌÇÜÕ
    ÏàËÆ¶È:68.4%
Chinese Traditional and Herbal Drugs          2005          36          978-982
Biotransformation of polyphyllins by Curvularia lunata fermentation
FENG Bing; MA Bai-ping; KANG Li-ping; XIONG Cheng-qi; WANG Sheng-qi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     ruscogenin 1-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:68.4%
Natural Product Research and Development          2013          25          1017-1021
Study on the Biotransformation of Pennogenin by Gliocladium deliquescens NRRL 1086
DU Chen-Hui, ZHANG Jian*, YU Bo-Yang*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     diosbulbiside A
C39H62O14     ÏàËÆ¶È:66.6%
Journal of Natural Products          2009          72          1964-1968
Steroidal Sapogenins and Glycosides from the Rhizomes of Dioscorea bulbifera
Hai Liu, Gui-Xin Chou,Tao Wu,Yin-Long Guo, Shun-Chun Wang, Chang-Hong Wang, and Zheng-Tao Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     (25S)-27-hydroxypenogenin 3- O-¦Á-L-rhamnopyranosyl-(1¡ú2)-O-¦Â-D-glucopyranoside
C39H62O14     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          2007          55(4)          551-556
Two New Steroid Glycosides and a New Sesquiterpenoid Glycoside from the Underground Parts of Trillium kamtschaticum
Masateru ONO,Chika TAKAMURA,Fumie SUGITA,Chikako MASUOKA,Hitoshi YOSHIMITSU,Tsuyoshi IKEDA,and Toshihiro NOHARAc
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     compound 2a
C39H64O13     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1988          36          3226-3229
26-O-ACYLATED FUROSTANOL SAPONINS PARDARINOSIDE A AND B FROM THE BULBS OF LILIUM PARDARINUM
Hiroko Shimomura,Yutaka Sashida and Yoshihiro Mimaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     Diosgenyl ¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside
C39H62O12     ÏàËÆ¶È:66.6%
Bioorganic & Medicinal Chemistry          2008          16          2063-2076
Synthesis of novel spirostanic saponins and their cytotoxic activity
Juan C. Hern¨¢ndez, Francisco Le¨®n, Ignacio Brouard, Fernando Torres, Sara Rubio, Jos¨¦ Quintana, Francisco Est¨¦vez, Jaime Bermejo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     solanoside A
    ÏàËÆ¶È:66.6%
Chemistry of Natural Compounds          2014          49          1091-1094
Two New Steroidal Glycosides from Solanum surattense
Haq Nawaz, Ejaz Ahmed, Ahsan Sharif, Muhammad Arshad, Nayab Batool, Muhammad Azam Rasool, Mukhtar-Ul-Hassan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     Diosgenin 3-O-[¦Á-L-rhamnopyranosyl(1¡ú2)]-[¦Â-D-glucopyranosyl(1¡ú3)-¦Â-D-glucopyranosyl(1¡ú4)]-¦Â-D-glucopyranoside
    ÏàËÆ¶È:66.6%
Journal of Separation Science          2008          31          2486-2491
Preparative separation of dioscin derivatives from Dioscorea villosa by centrifugal partition chromatography coupled with evaporative light scattering detection
Kee Dong Yoon and Jinwoong Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     paris saponin V
    ÏàËÆ¶È:66.6%
Chinese Traditional and Herbal Drugs          2013          44          2808-2811
Studies on chemical constituents in roots and rhizomes of Trillium tschonoskii (II)
ZHANG Zhong-li, ZUO Yue-ming, CAI Miao-ting, WANG Yan-yan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     diosgenin3-O-¦Â-D-glucopyranosyl-(1¡ú3)-[¦Á-L-rhamnopyranosyl-(1¡ú2)]-¦Â-D-glucopyranoside
    ÏàËÆ¶È:65.8%
West China Journal of Pharmaceutical Sciences          2010          25          508-511
Isolation and identification of steroidal saponins of Paris polyphylla Smith var. pseudothibetica
LIU Xian-bo, ZHANG Hao, YONG Zheng-ping, XUE Dan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     diosgenin 3-O-[¦Á-L-pyranrhamnose(1¡ú2)][¦Â-D-pyranxylose(1¡ú3)]-¦Â-D-pyranglycoside
C44H70O16     ÏàËÆ¶È:65.8%
Northwest Pharmaceutical Journal          2013          28          562-565
Studies on the chemical constituents of the flowers of Ophiopogon japonicus
ZHANG Jinghua, REN Lu, MA Yufang, BAO He, ZHAO Guilan, JING Hang, WANG Junxian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     compopund 15
    ÏàËÆ¶È:65.7%
Chemical & Pharmaceutical Bulletin          1982          30          712-718
Steroid Saponins from Paris polyphylla SM.-Supplement
MITSUHIKO MIYAMURA,KIMIKO NAKANO,TOSHIHIRO NOHARA,TOSHIAKI TOMIMATSU and TOSHIO KAWASAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     (25S)spirost-5-en-3¦Â,17¦Á,27-triol-3-O-[¦Â-D-glucopyranosy(1-4)[¦Á-L-arabinopyranpsy](1-6)]-¦Â-D-glucopyranoside
    ÏàËÆ¶È:65.7%
Chinese Chemical Letters          1991          2          853-854
A NEW STEROIDAL SAPONIN FROM SMILAX LEBRUNII
YONG JU ZHONG JIAN JJA AND YI NAN WU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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