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16.26,18.00,18.13,18.71,19.89,21.97,27.27,30.90,31.69,
32.79,33.42,36.15,38.24,38.64,39.69,47.46,52.32,58.00,
62.07,69.24,69.94,70.60,72.30,72.53,72.57,73.07,73.10,
74.00,74.09,76.84,78.13,79.43,79.64,81.00,100.64,102.51,
102.78,103.34,22.60,125.74,142.46,156.53,199.55
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huadong1227: ½ð±Ò+5, ¡ïÓаïÖú 2014-11-10 15:33:58
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1 .     pregna-5,16-diene-3b-ol-20-one 3-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-[¦Á-L-rhamnopyranosyl-(1¡ú4)]-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside
C45H70O19     ÏàËÆ¶È:91.1%
Magnetic Resonance in Chemistry          2012          50          813-817
Steroidal saponins and pregnane glycosides from Smilax microphylla
Tao Lin, Hui-Lian Huang, Rong-Hua Liu, Ji-Cheng Shu, Gang Ren, Feng Shao and Li-sha Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     hypoglaucin H
    ÏàËÆ¶È:86.0%
China Journal of Chinese Materia Medica          2014          39          2034-2038
Chemical constituents from Solanum rostratum
HAO Li-juan, WANG Shan, ZHU Jing-jing, WANG Zhi-min, WEI Shou-hui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (3¦Â-dihydroxy pregn-5,16-dien-20-one 3-O-¦Â-chacotrioside
    ÏàËÆ¶È:83.7%
Phytochemistry          1999          50          481-484
Steroidal saponins from Asparagus dumosus
Viqar Uddin Ahmad, Syed Muhammad Khaliq-uz-Zaman, Simin Shameel, Shaista Perveen, Zulfiqar Ali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     1-O-¦Â-D-glucopyranosyl-22-O-methyl-(25R)-furost-5(6)-en-1¦Â,3¦Â,22¦Î,26-tetraol-26-O-¦Á-L-rhamnopyranosyl-(1'''¡ú6'')-O-¦Â-D-galactopyranoside
    ÏàËÆ¶È:82.6%
Food Chemistry          2005          93          205-214
Furostanol saponins in Allium caepa L. Var. tropeana seeds
Irene Dini, Gian Carlo Tenore, Elena Trimarco, Antonio Dini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     3-O-[bis-¦Á-L-rhamnopyranosyl-(1¡ú4 and 1¡ú2)¦Â-D-glucopyranosyl]-(25R)-furosta-5,2O-dien-3¦Â,26-diol
    ÏàËÆ¶È:82.2%
Planta Medica          1988          54          344-346
Oligofurostanosides from Asparagus cochinchinensis
Zhou Zhong Liang, Rita Aquino, Francesco De Simone, Antonio Dini, Oreste Schettino, and Cosimo Pizza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     1-O-¦Â-D-glucopyranosyl-(25R)-fur-ost-5(6)-en-1¦Â,3¦Â,22¦Â,26-tetraol-26-O-¦Á-L-rhamnopyranosyl-(1'''¡ú6'')-O-¦Â-D-galactopyranoside
    ÏàËÆ¶È:82.2%
Food Chemistry          2005          93          205-214
Furostanol saponins in Allium caepa L. Var. tropeana seeds
Irene Dini, Gian Carlo Tenore, Elena Trimarco, Antonio Dini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     solamargine
C45H73NO15     ÏàËÆ¶È:81.8%
Bioorganic & Medicinal Chemistry Letters          2011          21          2930-2933
Total synthesis of solamargine
Guohua Wei, Jing Wang, Yuguo Du
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (25R)-26-O-¦Â-D-glucopyranosyl-22¦Á-methoxy-furost-5-ene-1¦Â,3¦Â,26-triol 1-O-[¦Á-L-rhamnopyranosyl-(1¡ú2)-6-O-acetyl¦Â-D-glucopyranoside and
    ÏàËÆ¶È:80.4%
Phytochemistry          2011          72          651-661
Steroidal glycosides from Ruscus ponticus
Assunta Napolitano, Tamar Muzashvili, Angela Perrone, Cosimo Pizza, Ether Kemertelidze, Sonia Piacente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     ¦Â-solamarine
    ÏàËÆ¶È:80%
Phytochemistry          2002          59          79-84
Bioactive steroidal alkaloid glycosides from Solanum aculeastrum
Alphonse W. Wanyonyi, Sumesh C. Chhabra, Gerald Mkoji, Udo Eilert,Wilson M. Njue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     solamargine
    ÏàËÆ¶È:80%
Phytochemistry          2002          59          79-84
Bioactive steroidal alkaloid glycosides from Solanum aculeastrum
Alphonse W. Wanyonyi, Sumesh C. Chhabra, Gerald Mkoji, Udo Eilert,Wilson M. Njue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     dioscin
    ÏàËÆ¶È:80%
Natural Product Research          2003          17          287-292
A New Steroidal Saponin from Dioscorea Zingiberensis Wright
Wenji Sun; Guangzhong Tu; Yongmin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     dioscin
    ÏàËÆ¶È:80%
Natural Product Research          2003          17          287-292
A New Steroidal Saponin from Dioscorea Zingiberensis Wright
Wenji Sun; Guangzhong Tu; Yongmin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     tribol
    ÏàËÆ¶È:80%
Fitoterapia          2004          75          117-122
Anovel furostanol saponin from Tribulus terrestris of Bulgarian origin
J. Conrad , D. Dinchev , I. Klaiber , S. Mika , I. Kostova,W. Kraus
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     dioscoreanoside C
C45H72O19     ÏàËÆ¶È:80%
Phytochemistry          2013          95          341-350
Steroidal saponins from the flowers of Dioscorea bulbifera var. sativa
L¨¦on Azefack Tapondjou, Kristina Jenett-Siems, Stefan Böttger, Matthias F. Melzig
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     dioscoreanoside E
C45H72O19     ÏàËÆ¶È:80%
Phytochemistry          2013          95          341-350
Steroidal saponins from the flowers of Dioscorea bulbifera var. sativa
L¨¦on Azefack Tapondjou, Kristina Jenett-Siems, Stefan Böttger, Matthias F. Melzig
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     1-O-¦Â-D-glucopyranosyl-(25R)-furost-5(6)-en-1¦Â,3¦Â,22¦Á,26-tetraol-26-O-¦Á-L-rhamnopyranosyl-(1'''¡ú2'')-O-¦Á-L-arabinopyranoside
    ÏàËÆ¶È:79.5%
Food Chemistry          2005          93          205-214
Furostanol saponins in Allium caepa L. Var. tropeana seeds
Irene Dini, Gian Carlo Tenore, Elena Trimarco, Antonio Dini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     1-O-¦Â-D-glucopyranosyl-(25R)-furost-5(6)-en-1¦Â,3¦Â,22¦Â,26-tetraol-26-O-¦Á-L-rhamnopyranosyl-(1'''¡ú2'')-O-¦Á-L-arabinopyranoside
    ÏàËÆ¶È:79.5%
Food Chemistry          2005          93          205-214
Furostanol saponins in Allium caepa L. Var. tropeana seeds
Irene Dini, Gian Carlo Tenore, Elena Trimarco, Antonio Dini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     (25R)-26-O-¦Â-D-glucopyranosyl-furost-5-ene-3¦Â,22¦Á,26-triol 3-O-[¦Á-L-arabinopyranosyl-(1¡ú4)-O-¦Â-D-glucopyranoside]
    ÏàËÆ¶È:79.5%
Phytochemistry          2011          72          651-661
Steroidal glycosides from Ruscus ponticus
Assunta Napolitano, Tamar Muzashvili, Angela Perrone, Cosimo Pizza, Ether Kemertelidze, Sonia Piacente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     ÊíÝ÷ÔíÜÕ
    ÏàËÆ¶È:79.0%
Chinese Traditional and Herbal Drugs          2001          32          18,38
ÊÖÕÆ²ÎµÄ»¯Ñ§³É·ÖÑо¿
Àî˧,Íõ¶°,¿ïº£Ñ§,¸ÔÌï¼ÎÈÊ,°Âɽ?Ø
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     1-O-[¦Á-L-rhamnopyranosyl-(1)-6-O-acetyl-¦Â-D-galactopyranosyl]-1¦Â,3¦Â,22¦Î-26-tetrahydroxyfurost-5(6)-ene-26-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:78.7%
Chemistry of Natural Compounds          2009          45          756-758
Analysis and isolation of saponins from Limoniastrum feei by LC-UV
N. Belboukhari, A. Cheriti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     (25R,26R)-3¦Â,17¦Á-dihydroxy-26-methoxyspirostan-5-ene-3¦Â-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-[¦Â-D-glucopyranosyl-(1¡ú6)]-¦Â-D-glucopyranoside
C47H76O18     ÏàËÆ¶È:78.2%
Chinese Traditional and Herbal Drugs          2011          42          21-24
Steroidal saponins and phenylic constituents from Lilium lancifolium and their anti-oxidant activities
ZHOU Zhong-liu, SHI Ren-bing, LIU Bin, ZOU Jie-ming, YIN Wen-qing, XIA Jing-min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     (23S,25R)-23-hydroxyspirost-5-en-3¦Â-yl O-¦Á-L-rhamnopyranosyl-(1¡ú2)-O-[¦Â-D-glucopyranosyl-(1¡ú6)]-¦Â-D-glucopyranoside
C45H72O18     ÏàËÆ¶È:77.7%
Phytochemistry          1999          51          567-573
Steroidal saponins from the bulbs of Lilium candidum
Yoshihiro Mimaki, Tadaaki Satou, Minpei Kuroda, Yutaka Sashida, Yoshio Hatakeyama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     asparasaponin II
    ÏàËÆ¶È:77.7%
Chinese Traditional and Herbal Drugs          1999          30(12)          888-890
Studies on the Chemical Constituents of Commmon Asparagus Bark (Asparagus officinalis)
Sun Jianhua; Zuo Chunxu; Yang Shangjun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     compound 5
C45H72O     ÏàËÆ¶È:77.7%
Zeitschrift f¨¹r Naturforschung C          2002          57          33-38
Two New Sulfated Furostanol Saponins from Tribulus terrestris
I. Kostova, D. Dinchev, G. Hopp Rentsch, V. Dimitrov, and A. Ivanova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     1-O-¦Â-D-glucopyranosyl-22-O-methyl-(25R)-furost-5(6)-en-1¦Â,3¦Â,22¦Î,26-tetraol-26-O-¦Á-L-rhamnopyranosyl-(1'''¡ú2'')-O-¦Á-L-arabinopyranoside
    ÏàËÆ¶È:77.7%
Food Chemistry          2005          93          205-214
Furostanol saponins in Allium caepa L. Var. tropeana seeds
Irene Dini, Gian Carlo Tenore, Elena Trimarco, Antonio Dini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     hauptsaponine S2
    ÏàËÆ¶È:77.7%
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
27 .     ascalonicoside A1
C45H74O19     ÏàËÆ¶È:77.7%
Journal of Agricultural and Food Chemistry          2002          50          5686-5690
Chemical Composition of Shallot (Allium ascalonicum Hort.)
Ernesto Fattorusso, Maria Iorizzi, Virginia Lanzotti, and Orazio Taglialatela-Scafati
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     ascalonicoside A2
C45H74O19     ÏàËÆ¶È:77.7%
Journal of Agricultural and Food Chemistry          2002          50          5686-5690
Chemical Composition of Shallot (Allium ascalonicum Hort.)
Ernesto Fattorusso, Maria Iorizzi, Virginia Lanzotti, and Orazio Taglialatela-Scafati
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     (3¦Â,5¦Á,6¦Â)-5,6-dihydroxysolanidan-3-yl 6-deoxy-¦Á-l-mannopyranosyl-(1¡ú2)-[6-deoxy-¦Á-l-mannopyranosyl-(1¡ú4)]-¦Â-D-glucopyranoside
C45H75NO16     ÏàËÆ¶È:77.7%
Helvetica Chimica Acta          2013          96          931-940
Five New Steroidal Alkaloid Glycosides from Solanum tuberosum
Zhi-Qiang Zhang, Jian-Guang Luo, Jun-Song Wang and Ling-Yi Kong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     dioscin
    ÏàËÆ¶È:77.7%
China Journal of Chinese Materia Medica          2014          39          2034-2038
Chemical constituents from Solanum rostratum
HAO Li-juan, WANG Shan, ZHU Jing-jing, WANG Zhi-min, WEI Shou-hui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     (23S,25R)-spirost-5-en-3,23-diol 3-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-O-[¦Á-L-rhamnopyranosyl-(1¡ú4)]-¦Â-D-glucopyranoside
C45H72O17     ÏàËÆ¶È:77.7%
Records of Natural Products          2015          9          94-104
Chemical Constituents from Solanum glabratum Dunal var. sepicula
Essam Abdel-Sattar, Mohamed A Farag and Engy A Mahrous
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     (6S,13S)-13-O[¦Á-L-rhamnopyranosyl-(1¡ú4)-¦Â-D-fucopyranosyl]-6-O-[¦Â-D-glucopyranosyl-(1¡ú4)-¦Á-L-rhamnopyranosyl]cleroda-3,14-diene-6,13-diol
    ÏàËÆ¶È:77.2%
Phytochemistry          1997          46          839-844
Biologically active clerodane-type diterpene glycosides from the root-stalks of Dicranopteris pedata
Tadashi Aoki, Tadashi Ohro, Yoshikazu Hiraga, Takayuki Suga, Mihoko Uno, Shinji Ohta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     Solamargine
C45H73NO15     ÏàËÆ¶È:77.2%
Fitoterapia          2010          81          767-771
Evaluation of the biological activity of the molluscicidal fraction of Solanum sisymbriifolium against non target organisms
Jean-Jacques M. Bagalwa, Laurence Voutquenne-Nazabadioko, Charlotte Sayagh, Augustin S. Bashwira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     ¦Â-solamarine
C45H73NO15     ÏàËÆ¶È:77.2%
Fitoterapia          2010          81          767-771
Evaluation of the biological activity of the molluscicidal fraction of Solanum sisymbriifolium against non target organisms
Jean-Jacques M. Bagalwa, Laurence Voutquenne-Nazabadioko, Charlotte Sayagh, Augustin S. Bashwira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     (25S)-26-O-¦Â-D-glucopyranoyl-20(22)-en-furost-1¦Â,3¦Â,5¦Â,26-tetraol-1-O-¦Â-D-arabinopyranoside-3-O-¦Á-L-rhamnopyranoside
C44H72O19     ÏàËÆ¶È:77.2%
Natural Product Research          2013          27          85-92
Three new steroidal glycosides from roots of Reineckia carnea
Qian Wang, Qune Hou, Zhiyong Guo, Kun Zou, Yanhong Xue, Nianyu Huang, Fan Cheng & Yuan Zhou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     26-O-¦Â-D-glucopyranosyl-furost¦Á-5,25(27)-diene-3¦Â,22¦Á,26-triol 3-O-[¦Á-L-arabinopyranosyl-(1¡ú4)-O-¦Â-D-glucopyranoside]
    ÏàËÆ¶È:77.2%
Phytochemistry          2011          72          651-661
Steroidal glycosides from Ruscus ponticus
Assunta Napolitano, Tamar Muzashvili, Angela Perrone, Cosimo Pizza, Ether Kemertelidze, Sonia Piacente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     (25R)-26-O-¦Â-D-glucopyranosyl-furost¦Á-5,20(22)-diene-3¦Â,26-diol 3-O-[¦Á-L-arabinopyranosyl-(1¡ú4)-O-¦Â-D-glucopyranoside]
    ÏàËÆ¶È:77.2%
Phytochemistry          2011          72          651-661
Steroidal glycosides from Ruscus ponticus
Assunta Napolitano, Tamar Muzashvili, Angela Perrone, Cosimo Pizza, Ether Kemertelidze, Sonia Piacente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     Ceposide A
C44H72O18     ÏàËÆ¶È:77.2%
Phytochemistry          2012          74          133-139
Antifungal saponins from bulbs of white onion, Allium cepa L.
Virginia Lanzotti, Adriana Romano, Stefania Lanzuise, Giuliano Bonanomi, Felice Scala
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     digitoxigenin 3-O-[O-¦Â-D-glucopyranosyl-(1¡ú6)-O-¦Â-D-glucopyranosyl-(1¡ú4)-2-O-acetyl-¦Â-D-digitalopyranoside]
C44H69O19     ÏàËÆ¶È:77.2%
Phytochemistry          2013          88          105-111
Cardenolide glycosides from root of Streptocaulon juventas
Rui Xue, Na Han, Chun Ye, Hai-bo Wang, Jun Yin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     3-O-[¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-Dgalactopyranosyl-(1¡ú2)-¦Â-D-glucuronopyranosyl]-3¦Â,16¦Â,22¦Á-trihydroxy-olean-12-ene
C48H78O18     ÏàËÆ¶È:77.0%
Journal of Natural Products          2007          70          979-983
Oleanane Saponins from Stylosanthes erecta
Marinella De Leo,Rokia Sanogo, Nunziatina De Tommasi, and Alessandra Braca
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     incanumine
C49H79NO19     ÏàËÆ¶È:77.0%
Journal of Natural Products          1990          Vol 53          513
The Cytotoxic Principles of Solanum incanum
Chun-Nan Lin, Chai-Ming Lu, Ming-Kung Cheng, Kim-Hong Gan, Shen-Jeu Won
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     ent-14-labden-8¦Â-ol 13¦Á-O-[¦Â-D-quinovopyranosyl-(1¡ú2)-3'-O-acetyl-¦Á-L-rhamnopyranosyl]-19-O-¦Á-L-rhamnopyranoside
C40H68O16     ÏàËÆ¶È:76.7%
Journal of Natural Products          2007          70          1837-1845
Diterpenoid Glycosides from the Bitter Fern Gleichenia quadripartita
Cecilia Socolsky,Yoshinori Asakawa,and Alicia Bard¨®n
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     macrophyllosaponin C
C42H72O14     ÏàËÆ¶È:76.7%
Journal of Natural Products          1996          59          1019-1023
Four Novel Cycloartane Glycosides from Astragalus oleifolius
I¨²hsan Çalış, Murat Zor, İclal Saracoğlu, Aşkın Işımer, and Heinz R¨¹egger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     26-O-¦Â-D-glucopyranosyl-22-O-methylfurosta-5,25(27)-diene-1¦Â,3¦Â,22¦Î,26-tetrol 1-O-{O-¦Á-L-rhamnopyranosyl-(1¡ú2)-3-O-acetyl-4-O-sulfo-¦Á-L-arabinipyranoside}
    ÏàËÆ¶È:76.5%
Chemical & Pharmaceutical Bulletin          1998          46          298-303
New Steroidal Constituents of the Underground Parts of Ruscus aculeatus and Their Cytostatic Activity on HL-60 Cells
Yoshihiro MIMAKI,Minpei KURODA,Aiko KAMEYAMA,Akihito YOKOSUKA and Yutaka SASHIDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     Acankoreoside J
C47H73O20     ÏàËÆ¶È:76.5%
Planta Medica          2010          76          189-194
Lupane-Type Triterpene Glycosides from the Leaves of Acanthopanax koreanum and Their In Vitro Cytotoxicity
Nhiem, Nguyen Xuan; Kiem, Phan Van; Minh, Chau Van; Ha, Do Thi; Tai, Buu Huu; Yen, Pham Hai; Tung, Nguyen Huu; Hyun, Jae-Hee; Kang, Hee-Kyoung; Kim, Young Ho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     Acanthifolioside G
C47H80O17     ÏàËÆ¶È:76.5%
Journal of Natural Products          2012          75          2094-2100
Isolation of Steroidal Glycosides from the Caribbean Sponge Pandaros acanthifolium
Fabrice Berru¨¦, Malcolm W. B. McCulloch, Patricia Boland, Saskia Hart, Mary Kay Harper, James Johnston, and Russell Kerr
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     compound 19
C46H76O22     ÏàËÆ¶È:76.0%
Tetrahedron          2002          58          5837-5848
New pregnane glycosides from Caralluma negevensis
Alessandra Braca, Ammar Bader, Ivano Morelli, Roberto Scarpato, Gino Turchi, Cosimo Pizza, Nunziatina De Tommasi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     26-O-¦Â-D-glucopyranosyl-furost-3¦Â,26-diol-22-methoxy-3-O-¦Á-L-rhamnopyranosy(1¡ú4)-O-¦Â-D-glucopyranoside
C46H78O18     ÏàËÆ¶È:76.0%
Academic Journal of Second Military Medical University          2007          28          1241-1244
Studies on chemical constituents of Asparagus cochinchinensis
SHEN Yang, CHEN Hai-sheng, WANG Qiong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     solamargine
    ÏàËÆ¶È:75.5%
Planta Medica          1993          59          483-484
Solamargine: The Main Glycoalkaloid from the Fruits of Solanum paludosum
Mich¨¨le Valverde, CatherineLavaud, Joel Boustie,Houriya El Badaoui, BrunoMuguet, and Max Henr
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     3-O-[¦Á-L- rhamnopyranosyl-(1¡ú4)-¦Â-D-glucopyranosyl]-26-O-(¦Â-D-glucopyranosyl)-(25R)-furosta-5,20-dien-3¦Â,26-diol
    ÏàËÆ¶È:75.5%
Planta Medica          1988          54          344-346
Oligofurostanosides from Asparagus cochinchinensis
Zhou Zhong Liang, Rita Aquino, Francesco De Simone, Antonio Dini, Oreste Schettino, and Cosimo Pizza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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