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²éѯ½á¹û£º¹²²éµ½116¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
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