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wangali526: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-07-08 15:18:54
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½1053¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . wanpeinine A ÏàËÆ¶È:66.6% Chinese Chemical Letters 1992 3 979-980 SIECHUANSINE,A NEW STEROIDAL ALKALOID FROM FRITILLARIA SIECHUANICA X.S.CHEN FENG PENG WANG,RONG ZHANG,XIN YUE TANG AND JIAN ZHONG WANG Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 6 ÏàËÆ¶È:66.6% Phytochemistry 1988 27 1665-1668 Three ecdysteroid glycosides from Pfaffia iresinoides Nobushige Nishimoto,Yoshinori Shiobara,Shun-suke Inoue,Masumi Fujino,Tsunematsu Takemoto,Cheow Lin Yeoh,Fernando de Oliveira,Gokithi Akisue,Maria Kubota Akisue,Goro Hashimoto Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . tuboanosigenin p-Bromobenzoate ÏàËÆ¶È:65.6% Chemical & Pharmaceutical Bulletin 2008 56(7) 1038-1040 New C28 Steroidal Glycosides from Tubocapsicum anomalum Naoko KIYOTA,Kazushi SHINGU,Koki YAMAGUCHI,Yasuyuki YOSHITAKE,Kazunobu HARANO,Hitoshi YOSHIMITSU,Hiroyuki MIYASHITA,Tsuyoshi IKEDA,Chie TAGAWA,and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . spinogenin D3 ÏàËÆ¶È:63.3% Phytochemistry 1993 33 891-895 3-epi-Oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus Masazumi Miyakoshi, Yoshiteru Ida, Susumu Isoda, Junzo Shoji Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-O-[¦Á-L-rhamnopyranosyl(1¡ú2)-¦Â-D-glucopyranosyl(1¡ú4)-¦Â-D-glucuronopyranosyl]-soyasapogenol B ÏàËÆ¶È:63.3% Acta Chimica Sinica 1987 45 145-149 Studies on the Chemical Components of Oxtropis ochrocephala Bunge II. The Structures of Two Triterpenoid Saponins Sun Rong-Qi Cheng Dong-Liang Jia Zhong-JianZhu Zi-Qing Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . etioline ÏàËÆ¶È:62.9% Phytochemistry 1996 43 705-707 Steroidal alkaloids from roots of Solanum spirale Helmut Ripperger Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . verticine ÏàËÆ¶È:62.9% Acta Pharmaceutica Sinica 1988 Vol 23 34-37 CHEMICAL STUDIES OF EPIMEDIUM WUSHANENSE T. S. YING HR Liang; WM Yan; JS Li and CS Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . verticinone C27H43N3O ÏàËÆ¶È:62.9% Acta Pharmaceutica Sinica 1988 Vol 23 415-421 ISOLATION AND IDENTIFICATION OF ALKALOIDS FROM FRITILLARIA NINGGUOENSIS S.C.CHEN ET S. F. YIN QH Li; ZH Wu; LL Zhang and L Shao Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Solafloridine C27H43NO ÏàËÆ¶È:62.9% Phytochemistry 1996 41 1629-1631 22, 26-epiminocholestane alkaloids with unusual (20R)-configurations from Solanum species Helmut Ripperger Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ent-15¦Â-Senecioyloxy-16-en-kaur-19-oic acid ÏàËÆ¶È:62.9% Phytochemistry 1993 32 1611-1613 An ent-kaurenolide from Stevia lucida J.Manuel Amaro-Luis Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . peiminine ÏàËÆ¶È:62.9% Phytochemistry 1986 25 2008-2009 Two steroidal alkaloids from fritillaria harelinii Min Zhi-da, Qian Jing-fang, Munekazu Iinuma, Toshiyuki Tanaka, Mizuo Mizuno Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (22E)-5 ¦Á-cholest-22-ene-3¦Â,6¦Á,8,15¦Á,24-pentol C27H46O5 ÏàËÆ¶È:62.9% Russian Chemical Bulletin 1997 46 186-191 New polyhydroxysteroids and steroid glycosides from the far east starfishCeramaster patagonicus A. A. Kicha, A. I. Kalinovsky and V. A. Stonik |

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²éѯ½á¹û£º¹²²éµ½4294¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . wanpeinine A ÏàËÆ¶È:66.6% Chinese Chemical Letters 1992 3 979-980 SIECHUANSINE,A NEW STEROIDAL ALKALOID FROM FRITILLARIA SIECHUANICA X.S.CHEN FENG PENG WANG,RONG ZHANG,XIN YUE TANG AND JIAN ZHONG WANG Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 6 ÏàËÆ¶È:66.6% Phytochemistry 1988 27 1665-1668 Three ecdysteroid glycosides from Pfaffia iresinoides Nobushige Nishimoto,Yoshinori Shiobara,Shun-suke Inoue,Masumi Fujino,Tsunematsu Takemoto,Cheow Lin Yeoh,Fernando de Oliveira,Gokithi Akisue,Maria Kubota Akisue,Goro Hashimoto Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . podecdysone B ÏàËÆ¶È:66.6% Russian Journal of Organic Chemistry 2003 39 952-956 Transformation of 20-Hydroxyecdysone Acetonides into Podecdysone B V. N. Odinokov, I. V. Galyautdinov, D. V. Nedopekin, N. A. Ves'kina and L. M. Khalilov Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . tuboanosigenin p-Bromobenzoate ÏàËÆ¶È:65.6% Chemical & Pharmaceutical Bulletin 2008 56(7) 1038-1040 New C28 Steroidal Glycosides from Tubocapsicum anomalum Naoko KIYOTA,Kazushi SHINGU,Koki YAMAGUCHI,Yasuyuki YOSHITAKE,Kazunobu HARANO,Hitoshi YOSHIMITSU,Hiroyuki MIYASHITA,Tsuyoshi IKEDA,Chie TAGAWA,and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (3¦Â,5¦Á)-20-hydroxy-6-oxocevan-3-yl acetate C29H45NO4 ÏàËÆ¶È:65.5% Chemistry & Biodiversity 2008 Vol. 5 259 Cytotoxic Alkaloids from the Bulbs of Fritillaria hupehensis Yong-Hui Zhang, Xi-Liang Yang, Peng Zhang, Xue-Feng Zhou, Han-Li Ruan, Hui-Fang Pi, Ji-Zhou Wu, and Han-Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (2¦Â,3¦Â,4¦Á,5¦Á,8¦Â,11¦Â)-4-methylergosta-22,24(28)-diene- 2,3,8,11-tetrol ÏàËÆ¶È:65.5% Helvetica Chimica Acta 2006 Vol. 89 1330 Two New Polyhydroxylated Steroids from the Hainan Soft Coral Sinularia sp. Rui Jia, Yue-Wei Guo, Ernesto Mollo, Margherita Gavagnin, and Guido Cimino Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . hyrtiosterol C29H48O4 ÏàËÆ¶È:65.5% Journal of Natural Products 2004 67 1736-1739 Hyrtiosenolides A and B, Two New Sesquiterpene ¦Ã-Methoxybutenolidesand a New Sterol from a Red Sea Sponge Hyrtios Species Diaa T. A. Youssef, Abdel Nasser B. Singab, Rob W. M. van Soest, and Nobuhiro Fusetani Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Philadelphicalactone C C28H40O8 ÏàËÆ¶È:64.2% Steroids 2011 76 724-728 Philadelphicalactones C and D and other cytotoxic compounds from Physalis philadelphica Emma Maldonado, Ana L. P¨¦rez-Castorena, Consuelo Garc¨¦s, Mahinda Mart¨ªnez Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (24S)-24-ethyl-4¦Â-methyl-5¦Á-cholestan-3¦Â-ol C30H52O ÏàËÆ¶È:64.2% Marine Drugs 2012 10 2448-2466 Preliminary Structure-Activity Relationship on Theonellasterol, a New Chemotype of FXR Antagonist, from the Marine Sponge Theonella swinhoei Valentina Sepe, Raffaella Ummarino, Maria Valeria D'Auria, Orazio Taglialatela-Scafati, Simona De Marino, Claudio D'Amore, Barbara Renga, Maria Giovanna Chini, Giuseppe Bifulco, Yoichi Nakao, Nobuhiro Fusetani, Stefano Fiorucci and Angela Zampella Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 1¦Â,3¦Â-dihydroxyurs-12-en-27-oic acid C30H48O4 ÏàËÆ¶È:63.3% Journal of Natural Products 2003 66 1628-1631 A Novel Antibacterial Iridoid and Triterpene from Caiophora coronata Smriti Khera,Girma M. Woldemichael, Maya P. Singh,Enrique Suarez, and Barbara N. Timmermann Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . spinogenin D3 ÏàËÆ¶È:63.3% Phytochemistry 1993 33 891-895 3-epi-Oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus Masazumi Miyakoshi, Yoshiteru Ida, Susumu Isoda, Junzo Shoji Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . maytenfolic acid C30H48O4 ÏàËÆ¶È:63.3% Phytochemistry 1986 25 479-485 Antitumour triterpenes of Maytenus diversifolia Hiroshi Nozaki, Hideyo Suzuki, Teruhisa Hirayama, Ryoji Kasai, Rong-Yang Wu, Kuo-Hsiung Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 3-O-[¦Á-L-rhamnopyranosyl(1¡ú2)-¦Â-D-glucopyranosyl(1¡ú4)-¦Â-D-glucuronopyranosyl]-soyasapogenol B ÏàËÆ¶È:63.3% Acta Chimica Sinica 1987 45 145-149 Studies on the Chemical Components of Oxtropis ochrocephala Bunge II. The Structures of Two Triterpenoid Saponins Sun Rong-Qi Cheng Dong-Liang Jia Zhong-JianZhu Zi-Qing Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 9¦Á,11-Epoxy-5¦Á-ergosta-7,22-dien-3¦Â-yl acetate C30H46O3 ÏàËÆ¶È:63.3% Organic Magnetic Resonance 1977 9 439-464 13C N.m.r. Spectra of steroids¡ªA Survey and Commentary J.W.Blunt and J.B.Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ebeiedine ÏàËÆ¶È:62.9% Chemical & Pharmaceutical Bulletin 2002 50(8) 1013-1016 New Steroidal Alkaloids from Fritillaria imperialis and Their Cholinesterase Inhibiting Activities ATTA-UR-RAHMAN,Muhammad Nadeem AKHTAR, Muhammad Iqbal CHOUDHARY, Yoshisuke TSUDA,Bilge SENER,Assad KHALID, and Masood PARVEZ Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . certonardoside G C27H46O4 ÏàËÆ¶È:62.9% Journal of Natural Products 2003 66 384-391 Bioactive Sterols from the Starfish Certonardoa semiregularis Weihong Wang, Famei Li, Yujin Park, Jongki Hong, Chong-Ok Lee, Jae Yang Kong, Sook Shin, Kwang Sik Im, and Jee H. Jung Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . ebeiedine ÏàËÆ¶È:62.9% Chemical & Pharmaceutical Bulletin 1988 36 4316-4329 The Structural Elucidation of Fritillaria Alkaloids from Fritillaria ebeiensis var. purpurea. I. : The Structures of Ebeienine, Ebeiedine and Ebeiedinone PING LEE,YUKIE KITAMURA,KOH KANEKO,MOTOO SHIRO,GUO-JUN XU,YUH-PAN CHEN and HONG-YEN HSU Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . peimine ÏàËÆ¶È:62.9% Acta Pharmaceutica Sinica 1991 26 829-835 STUDIES ON CHEMICAL CONSTITUENTS OF FRITILLARIA IN HUBEI. ¢ü¢ñ ISOLATION AND STRUCTURE ELUCIDATION OF HUPEHEMONOSIDE JZ Wu; M Tang and R Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . wanpemine ÏàËÆ¶È:62.9% Acta Pharmaceutica Sinica 1991 26 829-835 STUDIES ON CHEMICAL CONSTITUENTS OF FRITILLARIA IN HUBEI. ¢ü¢ñ ISOLATION AND STRUCTURE ELUCIDATION OF HUPEHEMONOSIDE JZ Wu; M Tang and R Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . etioline ÏàËÆ¶È:62.9% Phytochemistry 1996 43 705-707 Steroidal alkaloids from roots of Solanum spirale Helmut Ripperger Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . cholest-5-ene-3¦Â,7¦Â,19-triol C27H46O3 ÏàËÆ¶È:62.9% Journal of Natural Products 1992 Vol 55 321 Four New Bioactive Polyhydroxylated Sterols from the Black Coral Antipathes subpinnata Anna Aiello, Ernesto Fattorusso, Marialuisa Menna Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . verticine ÏàËÆ¶È:62.9% Acta Pharmaceutica Sinica 1988 Vol 23 34-37 CHEMICAL STUDIES OF EPIMEDIUM WUSHANENSE T. S. YING HR Liang; WM Yan; JS Li and CS Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . verticinone C27H43N3O ÏàËÆ¶È:62.9% Acta Pharmaceutica Sinica 1988 Vol 23 415-421 ISOLATION AND IDENTIFICATION OF ALKALOIDS FROM FRITILLARIA NINGGUOENSIS S.C.CHEN ET S. F. YIN QH Li; ZH Wu; LL Zhang and L Shao Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . Solafloridine C27H43NO ÏàËÆ¶È:62.9% Phytochemistry 1996 41 1629-1631 22, 26-epiminocholestane alkaloids with unusual (20R)-configurations from Solanum species Helmut Ripperger Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . ent-15¦Â-Senecioyloxy-16-en-kaur-19-oic acid ÏàËÆ¶È:62.9% Phytochemistry 1993 32 1611-1613 An ent-kaurenolide from Stevia lucida J.Manuel Amaro-Luis Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . 16,17-epoxy-15-[(2-methyl-1-oxo-2-butenyl)oxy]-4¦Á,15¦Â(E),kauran-18-oic acid ÏàËÆ¶È:62.9% Planta Medica 2010 76 1870-1873 Antimalarial Activity of Aspilia pruliseta, a Medicinal Plant from Uganda Sebisubi, Fred Musoke; Odyek, Olwa; Anokbonggo, William Wilberforce; Ogwal-Okeng, Jasper; Carcache-Blanco, Esperanza J.; Ma, Cuiying; Orjala, Jimmy; Tan, Ghee T. Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 15¦Á-hydroxy-kaur-16-en-19-oic acid C20H30O3 ÏàËÆ¶È:62.9% Phytochemistry 1979 18 1681-1685 New diterpenes from Porella perrottetiana Yoshinori Asakawa, Masao Toyota, Tsunematsu Takemoto Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . peiminine ÏàËÆ¶È:62.9% Phytochemistry 1986 25 2008-2009 Two steroidal alkaloids from fritillaria harelinii Min Zhi-da, Qian Jing-fang, Munekazu Iinuma, Toshiyuki Tanaka, Mizuo Mizuno Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . peimine ÏàËÆ¶È:62.9% Chinese Traditional and Herbal Drugs 2009 40 15-17 Alkaloid constituents of Fritillaria cirrhosa CAO Xin-wei; ZHANG Meng; LI Jun; XIAO Pei-gen; CHEN Si-bao; CHEN Shi-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . verticine ÏàËÆ¶È:62.9% Chinese Traditional and Herbal Drugs 1994 25 344-346+390 Studies on the Chemical Constituents of the Stems and Leaves of Thunberg Fritillary (Fritillaria thunbergii) Yan Mingming; Jin Xiangqun; Xu Dongming(Jilin provincial Institute of Trad itional Chinese Medicine and Materia Medica; Changchun); Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . lepidiumterpeniod C27H48O2 ÏàËÆ¶È:62.9% Pharmazie 1999 54 851-853 Three new phytoconstituents from Lepidium sativum S.D. Pande - M. Ali - M. Iqbal - S.D. Pande Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . verticine ÏàËÆ¶È:62.9% Tetrahedron letters 1979 20 3737-3740 13C-NMR studies on the cevanine alkaloids : the application of 13C-NMR spectrum for structure elucidation of new alkaloids, baimonidine and isoverticine Kô Kaneko, Mikako Tanaka, Kimiaki Haruki, Nobuaki Naruse, Hiroshi Mitsuhashi Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . (22E,24S)-2¦Á,3¦Á-dihydroxy-5¦Á-stigmast-22-en-6-one C29H48O3 ÏàËÆ¶È:62.9% Steroids 2012 77 91-99 Brassinosteroids and analogs as neuroprotectors: Synthesis and structure¨Cactivity relationships Jihane Ismaili, Martin Boisvert, Fanny Longpr¨¦, Julie Carange, C¨¦line Le Gall, Maria-Grazia Martinoli, Benoit Daoust Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . (24S)-3¦Â-hydroxy-5¦Á-stigmastan-6-one C29H50O2 ÏàËÆ¶È:62.9% Steroids 2012 77 91-99 Brassinosteroids and analogs as neuroprotectors: Synthesis and structure¨Cactivity relationships Jihane Ismaili, Martin Boisvert, Fanny Longpr¨¦, Julie Carange, C¨¦line Le Gall, Maria-Grazia Martinoli, Benoit Daoust Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . (22E)-5 ¦Á-cholest-22-ene-3¦Â,6¦Á,8,15¦Á,24-pentol C27H46O5 ÏàËÆ¶È:62.9% Russian Chemical Bulletin 1997 46 186-191 New polyhydroxysteroids and steroid glycosides from the far east starfishCeramaster patagonicus A. A. Kicha, A. I. Kalinovsky and V. A. Stonik Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . (20R,24S)-5¦Á-cholestane-3¦Â,6¦Â,15¦Â,24-tetraol C27H48O4 ÏàËÆ¶È:62.9% Russian Chemical Bulletin 2002 51 2295-2298 Steroid polyols from the Far-Eastern starfish Henricia sanguinolenta E. V. Levina, A. I. Kalinovskii, P. V. Andriyashchenko, V. A. Stonik and P. S. Dmitrenok Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . Iwayoside A C26H42O8 ÏàËÆ¶È:62.9% Bulletin of the Korean Chemical Society 2010 31 2422-2423 Iwayoside A, a New Diterpene Glycoside from Artemisia iwayomogi Kitamura that Enhances IL-2 Secretion Yan Ding, Chun Liang, Seo Young Yang, Jun Ho Kim, Young Mi Lee, Young Ho Kim* Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . compound 2 ÏàËÆ¶È:62.9% Phytotherapy Research 1995 9 460-462 Active constituents of the bulbs of Fritillaria ebeiensis and their antitumour activity in mice Li Ping, Xu Guojun, Xu Luoshan and Wang Yixian Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . ebeiedine ÏàËÆ¶È:62.9% Phytotherapy Research 1995 9 460-462 Active constituents of the bulbs of Fritillaria ebeiensis and their antitumour activity in mice Li Ping, Xu Guojun, Xu Luoshan and Wang Yixian Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . cholesta-5-en-3,7,19-triol ÏàËÆ¶È:62.9% Academic Journal of Second Military Medical University 2010 31 421-424 Studies on chemical constituents of Anthogorgia sp. 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