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MeODÈÜ£¬13C-NMR Êý¾ÝÈçÏ£º 7.76,16.16,16.20,16.63,18.51,20.34,28.06,29.37,29.90,30.75,31.13,31.45,31.85,31.89,36.61,37.20,38.14,44.15,44.43,50.06,52.53,61.37,
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 .     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
2 .     acodontasteroside D
    ÏàËÆ¶È:58.9%
Journal of Natural Products          1997          60          959-966
Isolation, Structure Elucidation, and Biological Activity of the Steroid Oligoglycosides and Polyhydroxysteroids from the Antarctic Starfish Acodontaster conspicuus
Simona De Marino, Maria Iorizzi, Franco Zollo, Luigi Minale, Charles D. Amsler, Bill J. Baker, and James B. McClintock
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     2,22-dideoxy-5¦Â-hydroxyecdysone25-O-¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside
C39H64O15     ÏàËÆ¶È:58.9%
Phytochemistry          2009          70          430-436
Ecdysteroids and a sucrose phenylpropanoid ester from Froelichia floridana
Ping Wang, Shiyou Li, Stacy Ownby, Zhizhen Zhang, Wei Yuan, Wanli Zhang, R. Scott Beasley
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     Borealoside A
    ÏàËÆ¶È:58.9%
Journal of Natural Products          1992          Vol 55          866
Starfish Saponins, 48. Isolation of Fifteen Sterol Constituents (Six Glycosides and Nine Polyhydroxysteroids) from the Starfish Solaster borealis
Maria Iorizzi, Luigi Minale, Raffaele Riccio, Takeshi Yasumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     Amoxanthoside A
C38H60O17     ÏàËÆ¶È:58.9%
Planta Medica          2010          76          461-464
Terpene Glycosides and Cytotoxic Constituents from the Seeds of Amomum xanthioides
Kim, Ki Hyun; Choi, Jung Wook; Choi, Sang Un; Lee, Kang Ro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     diosgenyl 2-deoxy-2-(3,5-dinitrobenzamido)-¦Â-D-glucopyranoside
C40H55N3O12     ÏàËÆ¶È:58.9%
Bioorganic & Medicinal Chemistry          2009          17          7670-7679
Structural analogues of diosgenyl saponins: Synthesis and anticancer activity
Matthew J. Kaskiw, Mary Lynn Tassotto, Mac Mok, Stacey L. Tokar, Roxanne Pycko, John Th¡¯ng, Zi-Hua Jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (25R)-5¦Â-spirostan-3¦Â-ol-12-one 3-O-¦Â-D-glucopyranosyl-(1¡ú2)-O-¦Â-D-galactopyranoside
C39H62O14     ÏàËÆ¶È:58.9%
Phytochemistry          2011          72          126-135
Steroidal saponins from Yucca gloriosa L. rhizomes: LC¨CMS profiling, isolation and quantitative determination
Alexandre Skhirtladze, Angela Perrone, Paola Montoro, Mariam Benidze, Ether Kemertelidze, Cosimo Pizza, Sonia Piacente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     acodontasteroside F
    ÏàËÆ¶È:57.5%
Journal of Natural Products          1997          60          959-966
Isolation, Structure Elucidation, and Biological Activity of the Steroid Oligoglycosides and Polyhydroxysteroids from the Antarctic Starfish Acodontaster conspicuus
Simona De Marino, Maria Iorizzi, Franco Zollo, Luigi Minale, Charles D. Amsler, Bill J. Baker, and James B. McClintock
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     1¦Â,3¦Â-dihydroxypregna-5,16-dien-20-one 1-O-{O-¦Á-L-rhamnopyranosyl-(1¡ú2)-O-[¦Â-D-xylopyranosyl-( 1¡ú3)]-¦Â-D-glucopyranoside}
C38H58O16     ÏàËÆ¶È:56.4%
Phytochemistry          1997          44          107-111
Pregnane glycosides from Sansevieria trifasciata
Yoshihiro Mimaki, Toshihiro Inoue, Minpei Kuroda, Yutaka Sashida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     6-epi-nodososide
    ÏàËÆ¶È:56.4%
Journal of Natural Products          1986          Vol 49          919
Starfish Saponins, 29. A Novel Steroidal Glycoside from the Starfish Pentaceraster alveolatus
Franco Zollo, Ester Finamore, Luigi Minale, Dominique Laurent, George Bargibant
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     pisasteroside F
    ÏàËÆ¶È:56.4%
Journal of Natural Products          1990          Vol 53          1000
Starfish Saponins, Part 44. Steroidal Glycosides from the Starfish Pisaster giganteus
Franco Zollo, Ester Finamore, Caterina Martuccio, Luigi Minale
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     compound 4a
    ÏàËÆ¶È:56.4%
Journal of Natural Products          1990          Vol 53          1000
Starfish Saponins, Part 44. Steroidal Glycosides from the Starfish Pisaster giganteus
Franco Zollo, Ester Finamore, Caterina Martuccio, Luigi Minale
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     culcitoside C8
    ÏàËÆ¶È:56.4%
Journal of Natural Products          1991          Vol 54          1254
Starfish Saponins, Part 46. Steroidal Glycosides and Polyhydroxysteroids from the Starfish Culcita novaeguineae
Maria Iorizzi, Luigi Minale, Raffaele Riccio, Tatsuo Higa, Junichi Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     oreasteroside B
    ÏàËÆ¶È:56.4%
Journal of Natural Products          1995          Vol 58          10-26
Starfish Saponins, Part 53. A Reinvestigation of the Polar Steroids from the Starfish Oreaster reticulatus: Isolation of Sixteen Steroidal Oligoglycosides and Six Polyhydroxysteroids
Maria Iorizzi, Giuseppe Bifulco, Francesco de Riccardis, Luigi Minale, Raffaele Riccio, Franco Zollo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     dioscoreanoside F
C39H62O15     ÏàËÆ¶È:56.4%
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 .     3¦Â-O-¦Â-D-glucopyranosyloxy-16¦Â,26,29-trihydroxy-5¦Á-stigmasta-7,9(11),24(28)Z-trien-6-one
C35H54O10     ÏàËÆ¶È:56.4%
Phytochemistry          2013          96          288-298
Steroids with anti-inflammatory activity from Vernonia nigritiana Oliv. & Hiern.
Antonio Vassallo, Nunziatina De Tommasi, Irmgard Merfort, Rokia Sanogo, Lorella Severino, Marco Pelin, Roberto Della Loggia, Aurelia Tubaro, Silvio Sosa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (25R)-5¦Â-spirostan-3¦Â,12¦Â-diol 3-O-¦Â-D-glucopyranosyl-(1¡ú2)-O-¦Â-D-glucopyranoside
C39H64O14     ÏàËÆ¶È:56.4%
Phytochemistry          2011          72          126-135
Steroidal saponins from Yucca gloriosa L. rhizomes: LC¨CMS profiling, isolation and quantitative determination
Alexandre Skhirtladze, Angela Perrone, Paola Montoro, Mariam Benidze, Ether Kemertelidze, Cosimo Pizza, Sonia Piacente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     3¦Â-O-¦Â-D-xylopyranosyl-(1¡ú2)-¦Â-D-glucuronopyranosyl-23-hydroxylup-20(29)-en-28-oic acid
C41H64O14     ÏàËÆ¶È:56.0%
Journal of Natural Products          1997          60          663-668
Triterpenoid Saponins from Schefflera divaricata
Nunziatina De Tommasi and Cosimo Pizza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     cariniferoside A
C41H72O14     ÏàËÆ¶È:56.0%
Steroids          2011          76          1280-1287
Cariniferosides A¨CF and other steroidal biglycosides from the starfish Asteropsis carinifera
Timofey V. Malyarenko, Alla A. Kicha, Natalia V. Ivanchina, Anatoly I. Kalinovsky, Pavel S. Dmitrenok, Svetlana P. Ermakova, Valentin A. Stonik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     (22S,24R)-3¦Â-O-(¦Á-D-xylopyranose)-29-O-(¦Â-D-xylopyranose)-cholest-5,16-dien-22¦Á-ol
C40H66O11     ÏàËÆ¶È:56.0%
New Journal of Chemistry          2013          37          3647-3661
Synthesis of analogues of linckoside B, a new neuritogenic steroid glycoside
Qingchao Liu, Yue Yu, Peng Wang and Yingxia Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     acodontasteroside B
    ÏàËÆ¶È:55%
Journal of Natural Products          1997          60          959-966
Isolation, Structure Elucidation, and Biological Activity of the Steroid Oligoglycosides and Polyhydroxysteroids from the Antarctic Starfish Acodontaster conspicuus
Simona De Marino, Maria Iorizzi, Franco Zollo, Luigi Minale, Charles D. Amsler, Bill J. Baker, and James B. McClintock
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     planciside B
C40H70O15     ÏàËÆ¶È:55%
Natural Product Communications          2014          9          1269-1274
Three New Steroid Biglycosides,Plancisides A,B,and C,from the Starfish Acanthaster planci
Alla A. Kicha, Thi H. Dinh, Natalia V. Ivanchina, Timofey V. Malyarenko, Anatoly I. Kalinovsky, Roman S. Popov, Svetlana P. Ermakova, Thi T. T. Tran and Lan P. Doan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     28-O-¦Â-D-Glucopyranosylbetulin 3¦Â-O-¦Á-L-rhamnopyranoside
C42H70O11     ÏàËÆ¶È:54.7%
Journal of Natural Products          2009          72          72-81
Synthesis and Cytotoxicity of Bidesmosidic Betulin and Betulinic Acid Saponins
Charles Gauthier,Jean Legault,Serge Lavoie, Simon Rondeau, Samuel Tremblay, and Andr¨¦ Pichette
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     solamargine
C45H73NO15     ÏàËÆ¶È:54.5%
Bioorganic & Medicinal Chemistry Letters          2011          21          2930-2933
Total synthesis of solamargine
Guohua Wei, Jing Wang, Yuguo Du
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     kurilensoside D
C38H66O14     ÏàËÆ¶È:53.8%
Journal of Natural Products          2008          71(5)          793-798
Steroidal Triglycosides, Kurilensosides A, B, and C, and Other Polar Steroids from the Far Eastern Starfish Hippasteria kurilensis
Alla A. Kicha, Natalia V. Ivanchina, Anatoly I. Kalinovsky,Pavel S. Dmitrenok, Irina G. Agafonova, and Valentin A. Stonik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     certonardoside C
    ÏàËÆ¶È:53.8%
Journal of Natural Products          2002          65          1649-1656
New Saponins from the Starfish Certonardoa semiregularis
Weihong Wang,Famei Li,Naseer Alam, Yonghong Liu,Jongki Hong,Chong-Kyo Lee,Kwang Sik Im,and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     certonardoside J
    ÏàËÆ¶È:53.8%
Journal of Natural Products          2002          65          1649-1656
New Saponins from the Starfish Certonardoa semiregularis
Weihong Wang,Famei Li,Naseer Alam, Yonghong Liu,Jongki Hong,Chong-Kyo Lee,Kwang Sik Im,and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     acodontasteroside G
    ÏàËÆ¶È:53.8%
Journal of Natural Products          1997          60          959-966
Isolation, Structure Elucidation, and Biological Activity of the Steroid Oligoglycosides and Polyhydroxysteroids from the Antarctic Starfish Acodontaster conspicuus
Simona De Marino, Maria Iorizzi, Franco Zollo, Luigi Minale, Charles D. Amsler, Bill J. Baker, and James B. McClintock
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     oreasteroside D
    ÏàËÆ¶È:53.8%
Journal of Natural Products          1995          Vol 58          10-26
Starfish Saponins, Part 53. A Reinvestigation of the Polar Steroids from the Starfish Oreaster reticulatus: Isolation of Sixteen Steroidal Oligoglycosides and Six Polyhydroxysteroids
Maria Iorizzi, Giuseppe Bifulco, Francesco de Riccardis, Luigi Minale, Raffaele Riccio, Franco Zollo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     3¦Â,6¦Â-dihydroxylup-20(29)-en-28-oic acid-¦Â-glucopyranosyl ester
C36H58O9     ÏàËÆ¶È:53.8%
Natural Product Research          2012          26          630-636
Two new lupene-type triterpenoids from the roots of Liquidambar formosana
Juan Yu, Shanshan Liu and Lijiang Xuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     Fuscaside A
C37H63O162S     ÏàËÆ¶È:53.8%
Russian Chemical Bulletin          2008          57          204-208
Polar steroidal compounds from the Far-Eastern starfish Lethasterias fusca
N. V. Ivanchina, T. V. Malyarenko, A. A. Kicha, A. I. Kalinovskii and P. S. Dmitrenok
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     (24R)-3¦Â-O-(¦Á-D-xylopyranose)-29-O-(¦Â-D-xylopyranose)-cholest-5,16-dien-22-one
C40H64O11     ÏàËÆ¶È:53.8%
New Journal of Chemistry          2013          37          3647-3661
Synthesis of analogues of linckoside B, a new neuritogenic steroid glycoside
Qingchao Liu, Yue Yu, Peng Wang and Yingxia Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     28-O-¦Â-D-Glucopyranosylbetulinic acid 3¦Â-O-¦Á-L-arabinopyranoside
C41H66O12     ÏàËÆ¶È:53.6%
Journal of Natural Products          2009          72          72-81
Synthesis and Cytotoxicity of Bidesmosidic Betulin and Betulinic Acid Saponins
Charles Gauthier,Jean Legault,Serge Lavoie, Simon Rondeau, Samuel Tremblay, and Andr¨¦ Pichette
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     oblonganoside D
C41H64O12     ÏàËÆ¶È:53.6%
Chemical & Pharmaceutical Bulletin          2007          55(3)          422-427
Six New Triterpenoid Saponins from the Leaves of Ilex oblonga and Their Inhibitory Activities against TMV Replication
Zu-Jian WU,Ming-An OUYANG,Cong-Zhou WANG,and Zheng-Kun ZHANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     lotoidoside C
C41H68O13     ÏàËÆ¶È:53.6%
Planta Medica          2005          71          554-560
Antiproliferative Hopane and Oleanane Glycosides from the Roots of Glinus lotoides
Arafa I. Hamed,Sonia Piacente, Giuseppina Autore,Stefania Marzocco,Cosimo Pizza,Wieslaw Oleszek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     cyclogalaginoside E
C35H58O9     ÏàËÆ¶È:53.6%
Chemistry of Natural Compounds          2003          39          373-378
STRUCTURE OF CYCLOGALEGINOSIDE E FROM Astragalus galegiformis
T. I. Gigoshvili, M. D. Alaniya, V. G. Tsitsishvili,R. Foure, L. Debrauver, and E. P. Kemertelidze
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     cariniferoside C
C41H72O15     ÏàËÆ¶È:53.6%
Steroids          2011          76          1280-1287
Cariniferosides A¨CF and other steroidal biglycosides from the starfish Asteropsis carinifera
Timofey V. Malyarenko, Alla A. Kicha, Natalia V. Ivanchina, Anatoly I. Kalinovsky, Pavel S. Dmitrenok, Svetlana P. Ermakova, Valentin A. Stonik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     Certonardoside 1
    ÏàËÆ¶È:53.6%
Archives of Pharmacal Research          2005          28          285-289
New cytotoxic sulfated saponins from the starfish Certonardoa semiregularis
Weihong Wang, Hyojin Jang, Jongki Hong, Chong-Ok Lee and Song-Ja Bae, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     yesanchinoside R2
C41H70O14     ÏàËÆ¶È:53.6%
Helvetica Chimica Acta          2011          94          2010-2019
New Dammarane-Type Saponins from the Rhizomes of Panax japonicus (pages 2010¨C2019)
Min Zhou, Min Xu, Dong Wang, Hong-Tao Zhu, Chong-Ren Yang and Ying-Jun Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     halityloside A 6-O-sulfate
    ÏàËÆ¶È:52.5%
Journal of Natural Products          1993          Vol 56          1057
Starfish Saponins, Part 50. Steroidal Glycosides from the Okinawan Starfish Nardoa tuberculata
I. Bruno, L. Minale, R. Riccio, L. Cariello, Tatsuo Higa, Junichi Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     caratuberside B
    ÏàËÆ¶È:52.5%
Pharmazie          1995          50          426-428
Structures of Caratuberside E and F
GHAZALA H.RIZWANI,K.USMANGHANI,MANSOOR AHMAD and VIOAR U.AHMED
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     Linckoside A
C40H68O14     ÏàËÆ¶È:52.5%
Bioorganic & Medicinal Chemistry          2002          10          1961-1966
linckosides A and B, two new neuritogenic steroid glycosides from the okinawan starfish linckia laevigata
Jianhua Qi, Makoto Ojika, Youji Sakagami
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     Linckoside B
C40H68O14     ÏàËÆ¶È:52.5%
Bioorganic & Medicinal Chemistry          2002          10          1961-1966
linckosides A and B, two new neuritogenic steroid glycosides from the okinawan starfish linckia laevigata
Jianhua Qi, Makoto Ojika, Youji Sakagami
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     milleporoside A
C41H72O15     ÏàËÆ¶È:52.5%
Russian Journal of Bioorganic Chemistry          2006          32          93-97
New Steroid Glycosides from the Starfish Fromia milleporella
E. V. Levina, A. I. Kalinovsky, and V. S. Levin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     28-O-¦Â-D-Glucopyranosylbetulinic acid 3¦Â-O-¦Á-L-rhamnopyranoside
C42H68O12     ÏàËÆ¶È:52.3%
Journal of Natural Products          2009          72          72-81
Synthesis and Cytotoxicity of Bidesmosidic Betulin and Betulinic Acid Saponins
Charles Gauthier,Jean Legault,Serge Lavoie, Simon Rondeau, Samuel Tremblay, and Andr¨¦ Pichette
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     28-O-¦Â-D-Glucopyranosylbetulinic acid 3¦Â-O-¦Â-D-glucopyranoside
C42H68O13     ÏàËÆ¶È:52.3%
Journal of Natural Products          2009          72          72-81
Synthesis and Cytotoxicity of Bidesmosidic Betulin and Betulinic Acid Saponins
Charles Gauthier,Jean Legault,Serge Lavoie, Simon Rondeau, Samuel Tremblay, and Andr¨¦ Pichette
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     urginin
C42H62O17     ÏàËÆ¶È:52.3%
Phytochemistry          2001          58          557-561
Bufadienolides from Drimia robusta and Urginea altissima (Hyacinthaceae)
Tracy Pohl, Chantal Koorbanally, Neil R. Crouch, Dulcie A. Mulholland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     3¦Â-O-¦Â-D-glucopyranosyl-(1¡ú3)-¦Â-D-glucuronopyranosyl-23-hydroxylup-20(29)-en-28-oic acid
C42H66O15     ÏàËÆ¶È:52.3%
Journal of Natural Products          1997          60          663-668
Triterpenoid Saponins from Schefflera divaricata
Nunziatina De Tommasi and Cosimo Pizza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     glykosid F       
    ÏàËÆ¶È:52.3%
Planta Medica          1988          54          227-232
Bufadienolides from Urginea hesperia
Liselotte Krenn, Martina Jambrits and Brigitte Kopp
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     ryobusaponin E
C42H66O14     ÏàËÆ¶È:52.3%
Chemical & Pharmaceutical Bulletin          2013          69          134-143
Triterpene Saponins from Clethra barbinervis and Their Hyaluronidase Inhibitory Activities
Toshihiro Murata, Atsushi Suzuki, Nagisa Mafune, Eriko Sato, Toshio Miyase, Fumihiko Yoshizaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     3-O-¦Â-D-glucopyranosyl-29-O-¦Â-D-glucopyranosyl-3¦Â,16¦Â,29-trihydroxyolean-12-ene
C42H70O13     ÏàËÆ¶È:52.3%
Phytochemistry          2014          97          70-80
Saponins with highly hydroxylated oleanane-type aglycones from Silphium asteriscus L.
Milena Masullo, Lalita Calabria, Dario Gallotta, Cosimo Pizza, Sonia Piacente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     11-hydroxy okadaic acid
C44H68O14     ÏàËÆ¶È:52.2%
Bioorganic & Medicinal Chemistry          2012          20          3742-3745
The structures of three metabolites of the algal hepatotoxin okadaic acid produced by oxidation with human cytochrome P450
Li Liu, Fujiang Guo, Sheila Crain, Michael A. Quilliam, Xiaotang Wang, Kathleen S. Rein
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     3'-O-¦Â-D-glucopyranosylcalactin
C35H50O14     ÏàËÆ¶È:51.2%
Journal of Natural Products          2006          69          1319-1322
Cardenolide Glycosides from Pergularia tomentosa and Their Proapoptotic Activity in Kaposi's Sarcoma Cells
Arafa I. Hamed, Alberto Plaza, Maria Luisa Balestrieri, Usama A. Mahalel,Irina V. Springuel, Wieslaw Oleszek, Cosimo Pizza, and Sonia Piacente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
54 .     certonardoside J2
C35H62O10     ÏàËÆ¶È:51.2%
Journal of Natural Products          2004          67          584-591
Cytotoxic Sterols and Saponins from the Starfish Certonardoa semiregularis
Weihong Wang, Jongki Hong, Chong-Ok Lee, Kwang Sik Im, Jae Sue Choi, and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
55 .     certonardoside H3
    ÏàËÆ¶È:51.2%
Journal of Natural Products          2004          67          1654-1660
Additional Cytotoxic Sterols and Saponins from the Starfish Certonardoa semiregularis
Weihong Wang, Hyojin Jang, Jongki Hong, Chong-Ok Lee, Kwang Sik Im, Song-Ja Bae, and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
56 .     boivinide D
C35H52O13     ÏàËÆ¶È:51.2%
Journal of Natural Products          2007          70          1766-1770
Cytotoxic Cardenolide Glycosides of Roupellina (Strophanthus) boiWinii from the Madagascar Rainforest1
Sampada Karkare, Eba Adou, Shugeng Cao, Peggy Brodie, James S. Miller, N. M. Andrianjafy, J. Razafitsalama, Rabodo Andriantsiferana,( Vincent E. Rasamison,( and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
57 .     certonardoside A derivative
39H65O14     ÏàËÆ¶È:51.2%
Journal of Natural Products          2002          65          1649-1656
New Saponins from the Starfish Certonardoa semiregularis
Weihong Wang,Famei Li,Naseer Alam, Yonghong Liu,Jongki Hong,Chong-Kyo Lee,Kwang Sik Im,and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
58 .     (5¦Á)-2,22-dideoxyecdysone 25-O-¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside
C39H64O14     ÏàËÆ¶È:51.2%
Phytochemistry          2009          70          430-436
Ecdysteroids and a sucrose phenylpropanoid ester from Froelichia floridana
Ping Wang, Shiyou Li, Stacy Ownby, Zhizhen Zhang, Wei Yuan, Wanli Zhang, R. Scott Beasley
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
59 .     obtusolactam-20(R)-O-[¦Â-thevetopyranosyl-(1¡ú4)-¦Â-cymaropyranoside]
C38H61O11N     ÏàËÆ¶È:51.2%
Phytochemistry          2000          53          417-422
Steroidal alkaloids from Cryptolepis obtusa
Alexandra Paulo, M. Luisa Jimeno, Elsa T. Gomes, Peter J. Houghton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
60 .     pisasteroside C
    ÏàËÆ¶È:51.2%
Journal of Natural Products          1989          Vol 52          693
Starfish Saponins, Part 37. Steroidal Glycoside Sulfates from Starfishes of the Genus Pisaster
Franco Zollo, Easter Finamore, Raffaele Riccio, Luigi Minale
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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