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Hemslepenside A
C36H56O8 ÏàËÆ¶È:80.5%
Bioorganic & Medicinal Chemistry Letters 2014 24 2159-2162
Three new cucurbitane triterpenoids from Hemsleya penxianensis and their cytotoxic activities
Xiaoting Xu, Hong Bai, Ling Zhou, Zhipeng Deng, Hao Zhong, Zhongyu Wu, Qingqiang Yao
Structure 13C NMR ̼Æ×Ä£Äâͼ
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2 . stemodiosides B3
C36H58O10 ÏàËÆ¶È:75%
Phytochemical Analysis 2006 17 226-235
The bioactivity-guided isolation and structural identification of toxic cucurbitacin steroidal glucosides from stemodia kingii
Jeremy G. Allen, Steven M. Colegate, Andrew A. Mitchell, Roger J. Mulder and Merl F. Raisbeck
Structure 13C NMR ̼Æ×Ä£Äâͼ
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3 . delavanoside D
C36H58O8 ÏàËÆ¶È:75%
Acta Chimica Sinica 2007 65 1679-1684
Chemical Constituents from the Tubers of Hemsleya delavayi
CHEN, Jian-Chao ZHANG, Zhong-Quan QIU, Ming-Hua*
Structure 13C NMR ̼Æ×Ä£Äâͼ
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4 . scandenoside R1
C36H58O9 ÏàËÆ¶È:72.2%
Chemical & Pharmaceutical Bulletin 1988 36 234-243
Glycosides from Chinese Medicinal Plant, Hemsleya panacis-scandens, and Structure-Taste Relationship of Cucurbitane Glycosides
RYOJI KASAI,KAZUHIRO MATSUMOTO,RUI-LIN NIE,JUN ZHOU and OSAMU TANAKA
Structure 13C NMR ̼Æ×Ä£Äâͼ
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5 . bryonioside A
C36H60O9 ÏàËÆ¶È:69.4%
Journal of Natural Products 2002 65 179-183
Anti-Inflammatory and Anti-Tumor-Promoting Effects of Cucurbitane Glycosides from the Roots of Bryonia dioica
Motohiko Ukiya,Toshihiro Akihisa, Ken Yasukawa, Harukuni Tokuda, Masakazu Toriumi, Kazuo Koike,Yumiko Kimura, Tamotsu Nikaido, Wataru Aoi, Hoyoku Nishino, and Michio Takido
Structure 13C NMR ̼Æ×Ä£Äâͼ
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6 . 16¦Á,23¦Á-epoxy-20¦Â,25-dihydroxy-10¦ÁH,23¦ÂH-cucurbit-5-ene-11-one 3-O-¦Â-D-glucopyranoside
C36H58O10 ÏàËÆ¶È:69.4%
Planta Medica 2008 74 1741-1744
Cytotoxic Cucurbitane-Type Triterpenoids from Elaeocarpus hainanensis
Dahai Meng, Shigao Qiang, Liguang Lou1,Weimin Zhao
Structure 13C NMR ̼Æ×Ä£Äâͼ
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7 . scandenoside R2
C36H58O9 ÏàËÆ¶È:69.4%
Chemical & Pharmaceutical Bulletin 1988 36 234-243
Glycosides from Chinese Medicinal Plant, Hemsleya panacis-scandens, and Structure-Taste Relationship of Cucurbitane Glycosides
RYOJI KASAI,KAZUHIRO MATSUMOTO,RUI-LIN NIE,JUN ZHOU and OSAMU TANAKA
Structure 13C NMR ̼Æ×Ä£Äâͼ
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8 . cabenoside D
ÏàËÆ¶È:69.4%
Phytochemistry 1995 39 209-211
Cucurbitacin glycosides from Cabeça-de-negro
Kimiko Nakano, Yuu Kanai, K¨taro Murakami, Yoshihisa Takaishi
Structure 13C NMR ̼Æ×Ä£Äâͼ
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9 . 11-oxomogroside IA1
ÏàËÆ¶È:69.4%
Chinese Journal of Magnetic Resonance 2007 24 249-260
NMR Structural Elucidation of Mogrol and Its Glycosides
YANG Xiu-wei, ZHANG Jian-ye
Structure 13C NMR ̼Æ×Ä£Äâͼ
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10 . 11-Oxomogroside I A1
C36H60O9 ÏàËÆ¶È:69.4%
Journal of Agricultural and Food Chemistry 2002 50 6710-6713
Inhibitory Effects of Cucurbitane Glycosides and Other Triterpenoids from the Fruit of Momordica grosvenori on Epstein−Barr Virus Early Antigen Induced by Tumor Promoter 12-O-Tetradecanoylphorbol-13-acetate
Motohiko Ukiya, Toshihiro Akihisa, Harukuni Tokuda, Masakazu Toriumi, Teruo Mukainaka, Norihiro Banno, Yumiko Kimura, Jun-ichi Hasegawa, and Hoyoku Nishino
Structure 13C NMR ̼Æ×Ä£Äâͼ
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11 . Jinfushanencin E
C42H66O12 ÏàËÆ¶È:69.4%
Natural Products and Bioprospecting 2012 2 138-144
Cucurbitane triterpenoids from Hemsleya penxianensis
Jian-Chao Chen, Lin Zhou, Yun-Hua Wang, Ren-Rong Tian, Yun-Xin Yan, Yin Nian, Yun Sun, Yong-Tang Zheng, Ming-Hua Qiu
Structure 13C NMR ̼Æ×Ä£Äâͼ
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12 . Jinfushanencin G
C36H60O8 ÏàËÆ¶È:69.4%
Natural Products and Bioprospecting 2012 2 138-144
Cucurbitane triterpenoids from Hemsleya penxianensis
Jian-Chao Chen, Lin Zhou, Yun-Hua Wang, Ren-Rong Tian, Yun-Xin Yan, Yin Nian, Yun Sun, Yong-Tang Zheng, Ming-Hua Qiu
Structure 13C NMR ̼Æ×Ä£Äâͼ
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13 . 3-O-¦Â-D-glucopyranosyl-16¦Â-hydroxy-gratiogenine
ÏàËÆ¶È:69.4%
Monatshefte f¨¹r Chemie 1995 126 1331-1339
New Cucurbitacine Glycosides from Gratiola offcinalis L.
J. Rothenburger I and E. Haslinger
Structure 13C NMR ̼Æ×Ä£Äâͼ
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14 . saponin K7C
C42H72O13 ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin 1985 33 1400-1406
Studies on the Constituents of Hedera rhombea BEAN. II. On the Dammarane Triterpene Glycosides. (1)
HARUHISA KIZU,MICHIYO KOSHIJIMA,MASATOMI HAYASHI and TSUYOSHI TOMIMORI
Structure 13C NMR ̼Æ×Ä£Äâͼ
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15 . momordicine II
ÏàËÆ¶È:66.6%
Zeitschrift f¨¹r Naturforschung C 2007 62 603-607
A New Oviposition Deterrent to the Leafminer, Liriomyza trifolii: Cucurbitane Glucoside from ß1{Momordica charantia}
T. Kashiwagi, D. B. Mekuria, A. Dekebo, K. Sato, S.-i. Tebayashi, and C.-S. Kim
Structure 13C NMR ̼Æ×Ä£Äâͼ
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16 . charantoside VIII
C38H62O9 ÏàËÆ¶È:65.7%
Journal of Natural Products 2007 70 1233-1239
Cucurbitane-Type Triterpenoids from the Fruits of Momordica charantia and Their Cancer Chemopreventive Effects
Toshihiro Akihisa,Naoki Higo,Harukuni Tokuda,Motohiko Ukiya, Hiroyuki Akazawa, Yuichi Tochigi,Yumiko Kimura, Takashi Suzuki, and Hoyoku Nishino
Structure 13C NMR ̼Æ×Ä£Äâͼ
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17 . cimifoetidanoside H
C37H58O11 ÏàËÆ¶È:64.8%
Journal of Natural Products 2014 77 1997-2005
Cycloartane Triterpenoids and Their Glycosides from the Rhizomes of Cimicifuga foetida
Ji-Yong Chen, Ping-Lin Li, Xu-Li Tang, Shu-Jiang Wang, Yong-Tao Jiang, Li Shen, Ben-Ming Xu, Yong-Liang Shao, and Guo-Qiang Li
Structure 13C NMR ̼Æ×Ä£Äâͼ
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18 . 11-oxomogroside IA1
ÏàËÆ¶È:63.8%
Chemical & Pharmaceutical Bulletin 2006 54(10) 1425-1428
Cucurbitane Glycosides from Unripe Fruits of Lo Han Kuo (Siraitia grosvenori)
Dianpeng LI,Tsuyoshi IKEDA,Nanae MATSUOKA,Toshihiro NOHARA,Hourui ZHANG,Tatsunori SAKAMOTO,and Gen-Ichiro NONAKAd
Structure 13C NMR ̼Æ×Ä£Äâͼ
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19 . sutherlandioside D
C36H58O9 ÏàËÆ¶È:63.8%
Journal of Natural Products 2008 71(10) 1749-1753
Cycloartane Glycosides from Sutherlandia frutescens
Xiang Fu, Xing-Cong Li, Troy J. Smillie, Paulo Carvalho, Wilfred Mabusela, James Syce, Quinton Johnson, William Folk, Mitchell A. Avery, and Ikhlas A. Khan
Structure 13C NMR ̼Æ×Ä£Äâͼ
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20 . bryonioside D
C36H60O10 ÏàËÆ¶È:63.8%
Journal of Natural Products 2002 65 179-183
Anti-Inflammatory and Anti-Tumor-Promoting Effects of Cucurbitane Glycosides from the Roots of Bryonia dioica
Motohiko Ukiya,Toshihiro Akihisa, Ken Yasukawa, Harukuni Tokuda, Masakazu Toriumi, Kazuo Koike,Yumiko Kimura, Tamotsu Nikaido, Wataru Aoi, Hoyoku Nishino, and Michio Takido
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
21 . bryonioside F
C36H58O9 ÏàËÆ¶È:63.8%
Journal of Natural Products 2002 65 179-183
Anti-Inflammatory and Anti-Tumor-Promoting Effects of Cucurbitane Glycosides from the Roots of Bryonia dioica
Motohiko Ukiya,Toshihiro Akihisa, Ken Yasukawa, Harukuni Tokuda, Masakazu Toriumi, Kazuo Koike,Yumiko Kimura, Tamotsu Nikaido, Wataru Aoi, Hoyoku Nishino, and Michio Takido
Structure 13C NMR ̼Æ×Ä£Äâͼ
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22 . jinfushanoside B
C36H56O9 ÏàËÆ¶È:63.8%
Planta Medica 2005 71 983-986
Four New Cucurbitane Glycosides from Hemsleya jinfushanensis
Jian-Chao Chen, Xue-Mei Niu , Zhong-Rong Li , Ming-Hua Qiu
Structure 13C NMR ̼Æ×Ä£Äâͼ
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23 . stemodiosides B4
C36H58O11 ÏàËÆ¶È:63.8%
Phytochemical Analysis 2006 17 226-235
The bioactivity-guided isolation and structural identification of toxic cucurbitacin steroidal glucosides from stemodia kingii
Jeremy G. Allen, Steven M. Colegate, Andrew A. Mitchell, Roger J. Mulder and Merl F. Raisbeck
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
24 . momordicine II
C36H58O9 ÏàËÆ¶È:63.8%
Zeitschrift f¨¹r Naturforschung C 2006 61 81-86
Cucurbitane Glucosides from Momordica charantia Leaves as Oviposition Deterrents to the Leafminer, Liriomyza trifolii
D. B. Mekuria, T. Kashiwagi, S.-i. Tebayashi, and C.-S. Kim
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
25 . mogroside IE1
ÏàËÆ¶È:63.8%
Chinese Journal of Magnetic Resonance 2007 24 249-260
NMR Structural Elucidation of Mogrol and Its Glycosides
YANG Xiu-wei, ZHANG Jian-ye
Structure 13C NMR ̼Æ×Ä£Äâͼ
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26 . ¦Â-sitosterol-3-O-¦Â-D-glucopyranoside
ÏàËÆ¶È:63.8%
Planta Medica 2012 78 79-81
Bioenhancing and Antimycobacterial Agents from Ammannia multiflora
Upadhyay, Harish C.; Dwivedi, Gaurav R.; Darokar, Mahendra P.; Chaturvedi, Vinita; Srivastava, Santosh K.:
Structure 13C NMR ̼Æ×Ä£Äâͼ
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27 . Mogroside I E1
ÏàËÆ¶È:63.8%
Journal of Agricultural and Food Chemistry 2002 50 6710-6713
Inhibitory Effects of Cucurbitane Glycosides and Other Triterpenoids from the Fruit of Momordica grosvenori on Epstein−Barr Virus Early Antigen Induced by Tumor Promoter 12-O-Tetradecanoylphorbol-13-acetate
Motohiko Ukiya, Toshihiro Akihisa, Harukuni Tokuda, Masakazu Toriumi, Teruo Mukainaka, Norihiro Banno, Yumiko Kimura, Jun-ichi Hasegawa, and Hoyoku Nishino
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
28 . Jinfushanencin F
C42H66O13 ÏàËÆ¶È:63.8%
Natural Products and Bioprospecting 2012 2 138-144
Cucurbitane triterpenoids from Hemsleya penxianensis
Jian-Chao Chen, Lin Zhou, Yun-Hua Wang, Ren-Rong Tian, Yun-Xin Yan, Yin Nian, Yun Sun, Yong-Tang Zheng, Ming-Hua Qiu
Structure 13C NMR ̼Æ×Ä£Äâͼ
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29 . Jinfushanencin H
C42H68O12 ÏàËÆ¶È:63.8%
Natural Products and Bioprospecting 2012 2 138-144
Cucurbitane triterpenoids from Hemsleya penxianensis
Jian-Chao Chen, Lin Zhou, Yun-Hua Wang, Ren-Rong Tian, Yun-Xin Yan, Yin Nian, Yun Sun, Yong-Tang Zheng, Ming-Hua Qiu
Structure 13C NMR ̼Æ×Ä£Äâͼ
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30 . momordicin IV
ÏàËÆ¶È:63.8%
Chinese Traditional and Herbal Drugs 2012 43 1712-1715
Chemical constituents from leaves of Momordica charantia
LI Wen; CHEN Yan-fen; WU Nan; CHI Mo-yao; FEI Jia
Structure 13C NMR ̼Æ×Ä£Äâͼ
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31 . Kuguaoside C
C36H58O9 ÏàËÆ¶È:63.8%
Journal of Agricultural and Food Chemistry 2013 61 2979-2986
Antiproliferative and Hypoglycemic Cucurbitane-Type Glycosides from the Fruits of Momordica charantia
Ping-Chun Hsiao, Chia-Ching Liaw, Syh-Yuan Hwang, Hui-Ling Cheng, Li-Jie Zhang, Chien-Chang Shen, Feng-Lin Hsu, and Yao-Haur Kuo
Structure 13C NMR ̼Æ×Ä£Äâͼ
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32 . Kaguasaponin C
C38H62O9 ÏàËÆ¶È:63.1%
Journal of Functional Foods 2014 6 564−574
Cucurbitane-type glycosides from the fruits of Momordica charantia and their hypoglycaemic and cytotoxic activities
Li-Jie Zhang, Chia-Ching Liaw, Ping-Chun Hsiao, Hui-Chi Huang, Ming-Jen Lin, Zhi-Hu Lin, Feng-Lin Hsu, Yao-Haur Kuo
Structure 13C NMR ̼Æ×Ä£Äâͼ
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33 . (3¦Â,7¦Â,23E)-3,7-dihydroxy-25-methoxy-cucurbita-5,23-dien-19-al 3-¦Â-D-allopyranoside
C37H60O9 ÏàËÆ¶È:62.1%
Helvetica Chimica Acta 2013 96 1111-1120
Cucurbitane-Type Triterpenoids from Momordica charantia
Bao-Hui Cheng, Jian-Chao Chen, Jie-Qing Liu, Lin Zhou and Ming-Hua Qiu
Structure 13C NMR ̼Æ×Ä£Äâͼ
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34 . 3¦Â,16¦Á-dihydroxy-12-acetoxy-16,22-cyclo-23-ketone-24R,25-epoxy-cycloartane-7-ene-3-O-¦Â-D-xylopyranoside
C37H54O11 ÏàËÆ¶È:62.1%
Bioorganic & Medicinal Chemistry Letters 2014 24 5688-5691
New 9,19-cycloartenol glycosides isolated from the roots of Cimicifuga simplex and their anti-inflammatory effects
Yang Su, Lun Wu, Qiuhong Wang, Bingyou Yang, Haixue Kuang
Structure 13C NMR ̼Æ×Ä£Äâͼ
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35 . kuguaglycoside C
C36H56O8 ÏàËÆ¶È:61.1%
Helvetica Chimica Acta 2008 Vol. 91 920
Eight New Cucurbitane Glycosides, Kuguaglycosides A¨C H, from the Root of Momordica charantia L.
Jian-Chao Chen, Lu Lu, Xian-Ming Zhang, Lin Zhou, Zhong-Rong Li, and Ming-Hua Qiu
Structure 13C NMR ̼Æ×Ä£Äâͼ
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36 . 20-hydroxy-11-oxomogroside IA1
C36H62O10 ÏàËÆ¶È:61.1%
Chemical & Pharmaceutical Bulletin 2006 54(10) 1425-1428
Cucurbitane Glycosides from Unripe Fruits of Lo Han Kuo (Siraitia grosvenori)
Dianpeng LI,Tsuyoshi IKEDA,Nanae MATSUOKA,Toshihiro NOHARA,Hourui ZHANG,Tatsunori SAKAMOTO,and Gen-Ichiro NONAKAd
Structure 13C NMR ̼Æ×Ä£Äâͼ
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37 . kahiricoside II
C36H60O9 ÏàËÆ¶È:61.1%
Phytochemistry 2004 65 2909-2913
Kahiricosides II¨CV, cycloartane glycosides from an Egyptian collection of Astragalus kahiricus
Mohamed M. Radwan, Nadia A. El-Sebakhy, Aya M. Asaad, Soad M. Toaima,David G.I. Kingston
Structure 13C NMR ̼Æ×Ä£Äâͼ
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38 . charantoside VII
C36H54O8 ÏàËÆ¶È:61.1%
Journal of Natural Products 2007 70 1233-1239
Cucurbitane-Type Triterpenoids from the Fruits of Momordica charantia and Their Cancer Chemopreventive Effects
Toshihiro Akihisa,Naoki Higo,Harukuni Tokuda,Motohiko Ukiya, Hiroyuki Akazawa, Yuichi Tochigi,Yumiko Kimura, Takashi Suzuki, and Hoyoku Nishino
Structure 13C NMR ̼Æ×Ä£Äâͼ
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39 . cyclocantogenin
ÏàËÆ¶È:61.1%
Chemistry of Natural Compounds 2002 38 447-449
TRITERPENE GLYCOSIDES FROM PLANTS OF THE Astragalus GENUS. III. STRUCTURE OF CYCLOUNIFOLIOSIDE C FROM Astragalus unifoliolatus
K. Dzh. Kucherbaev,K. K. Uteniyazov,V. V. Kachala,Z. Saatov, and A. S. Shashko
Structure 13C NMR ̼Æ×Ä£Äâͼ
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40 . cyclounifolioside C
ÏàËÆ¶È:61.1%
Chemistry of Natural Compounds 2002 38 574-576
TRITERPENE GLYCOSIDES OF PLANTS OF THE Astragalus GENUS. IV. STRUCTURE OF CYCLOUNIFOLIOSIDE D FROM Astragalus unifoliolatus
K. Dzh. Kucherbaev,K. K. Uteniyazov,V. V. Kachala,Z. Saatov, and A. S. Shashkov
Structure 13C NMR ̼Æ×Ä£Äâͼ
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41 . Sphaerophysone C
C36H58O9 ÏàËÆ¶È:61.1%
Journal of Asian Natural Products Research 2004 6 259-264
CYCLOARTANE-TYPE TRITERPENOIDS FROM SPHAEROPHYSA SALSULA
ZHONG-JUN MA, XIAN LI, JIN-HUIWANG, YANG LU, WEI LI, QI-TAI ZHENG,CHENG WANG, YU-XIAWANG, ISAO FUJII and YUTAKA EBIZUKA
Structure 13C NMR ̼Æ×Ä£Äâͼ
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42 . (2¦Â,3¦Â,9¦Â,10¦Á,16¦Á,20¦Â,24Z)-2-(¦Â-D-glucopyranosyloxy)-16,20,26-tetrahydroxy-9-methyl-19-norlanost-5,24-diene-11-one
C36H56O11 ÏàËÆ¶È:61.1%
Phytochemistry 1993 33 1139-1145
Cucurbitacins with unusual side chains from Picrorhiza kurroa
H. Stuppner, E.P. Moller
Structure 13C NMR ̼Æ×Ä£Äâͼ
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43 . (2¦Â,3¦Â,9¦Â,10¦Á,16¦Á,20¦Â,24Z)-2-(¦Â-D-glucopyranosyloxy)-3,16,20,26-tetrahydroxy-9-methyl-19-norlanost-5,24-diene-11-one
C36H58O11 ÏàËÆ¶È:61.1%
Phytochemistry 1993 33 1139-1145
Cucurbitacins with unusual side chains from Picrorhiza kurroa
H. Stuppner, E.P. Moller
Structure 13C NMR ̼Æ×Ä£Äâͼ
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44 . Schefflerin D
C36H62O9 ÏàËÆ¶È:61.1%
Chemical & Pharmaceutical Bulletin 2010 58 1343-1348
Schefflerins A¡ªG, New Triterpene Glucosides from the Leaves of Schefflera arboricola
Zhimin Zhao, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Yoshio Takeda, Masatoshi Kawahata, Kentaro Yamaguchi
Structure 13C NMR ̼Æ×Ä£Äâͼ
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45 . Schefflerin G
C36H62O9 ÏàËÆ¶È:61.1%
Chemical & Pharmaceutical Bulletin 2010 58 1343-1348
Schefflerins A¡ªG, New Triterpene Glucosides from the Leaves of Schefflera arboricola
Zhimin Zhao, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Yoshio Takeda, Masatoshi Kawahata, Kentaro Yamaguchi
Structure 13C NMR ̼Æ×Ä£Äâͼ |
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