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| 13C NMR (126 MHz, MeOD) ¦Ä 11.98,12.03,12.59,18.71,19.01,19.84,21.68,23.05,24.03,26.08,28.07,29.10,33.82,36.07,37.02,37.42,38.06,38.11,39.37,45.78,46.65,53.47,56.00,56.61,57.53,64.58,129.30,137.47,208.90,211.69 |
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1 . 7¦Á-hydrositosterol ÏàËÆ¶È:66.6% Journal of China Pharmaceutical University 2007 38 315-319 Chemical constituents of the aerial parts of Euphorbia sororia ZHANG Wei-ku; ZHANG Xiao-qi; YE Wen-cai; Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . stigmast-4-en-3-one C29H48O ÏàËÆ¶È:66.6% Acta Pharmaceutica Sinica 2012 47 1179-1182 A new monoterpenoid glucoside from the twigs of Chamaecyparis obtusa var.breviramea f.crippsii XU Jian; ZHANG Yu-mei; CHEN Ke-li; TAN Ning-hua; LIU Yi-mei Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ophirapstanol trisulfate C31H53O12S3Na3 ÏàËÆ¶È:64.5% Journal of Natural Products 1994 Vol 57 1751 Ophirapstanol Trisulfate, a New Biologically Active Steroid Sulfate from the Deep Water Marine Sponge Topsentia ophiraphidites Sarath P. Gunasekera, Susan H. Sennett, Michelle Kelly-Borges, Robert W. Bryant Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ¦Â-Sitosteryl acetate ÏàËÆ¶È:64.5% Zeitschrift f¨¹r Naturforschung C 2012 67 172-180 Anti-Helicobacter pylori Activity of the Methanolic Extract of Geum iranicum and its Main Compounds Somayeh Shahani, Hamid R. Monsef-Esfahani, Soodabeh Saeidnia, Parastoo Saniee, Farideh Siavoshi, Alireza Foroumadi, Nasrin Samadi, and Ahmad R. Gohari Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3¦Â-hydroxyolean-12-en-27- oic acid C30H48O3 ÏàËÆ¶È:63.3% Helvetica Chimica Acta 2003 Vol. 86 2414 Cytotoxic Pentacyclic Triterpenoids from the Rhizome of Astilbe chinensis Hongxiang Sun, Jianxin Zhang, Yiping Ye, Yuanjiang Pan, and Yueao Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . topsentisterol A1 C29H46O3 ÏàËÆ¶È:63.3% Journal of Natural Products 2006 69 1760-1768 26,27-Cyclosterols and Other Polyoxygenated Sterols from a Marine Sponge Topsentia sp. Xuan Luo, Famei Li, Pramod B. Shinde, Jongki Hong, Chong-O. Lee, Kwang Sik Im, and Jee H. Jung Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . topsentisterol B2 C29H46O3 ÏàËÆ¶È:63.3% Journal of Natural Products 2006 69 1760-1768 26,27-Cyclosterols and Other Polyoxygenated Sterols from a Marine Sponge Topsentia sp. Xuan Luo, Famei Li, Pramod B. Shinde, Jongki Hong, Chong-O. Lee, Kwang Sik Im, and Jee H. Jung Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (24R,6E)-24-ethyl-5¦Á-cholestan-6-hydroximino-3¦Â,5-diol ÏàËÆ¶È:63.3% Chemistry of Natural Compounds 2001 37 351-355 13C NMR SPECTRA OF 6-HYDROXIMINOSTEROIDS OF THE STIGMASTANE SERIES N. V. Kovganko and Yu. G. Chernov Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (24R,6E)-24-Ethyl-5¦Á-eholestan-6-hydroximino-3¦Â,5-diol ÏàËÆ¶È:63.3% Chemistry of Natural Compounds 2000 36 189-191 NOVEL SYNTHESIS OF (24R,6E)-24-ETHYLCHOLEST-6-HYDROXYIMINO-4-EN-3-ONE, A STEROIDAL OXIME FROM Cinachyrella spp. SPONGES N. B. Kovganko and Yu. G. Chernov Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (22R,23R)-2¦Á-Fluoro-3¦Â,22,23-trihydroxy-5¦Á-stigmastan-6-one C29H49FO4 ÏàËÆ¶È:63.3% Steroids 2009 74 435-440 Synthesis and biological activity of brassinosteroids fluorinated at C-2 Sof¨ªa L. Acebedo, Javier A. Ram¨ªrez, Lydia R. Galagovsky Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 1 ÏàËÆ¶È:63.3% Phytochemistry 1998 49 195-198 Triterpenoid saponins from the seeds of amaranthus cruentus MARTA JUNKUSZEW,WIESLAW OLESZEK MARIAN JURZYST¦Á,SONIA PIANCHENTE,COSIMO PIZZA Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ¿üÂåάËá ÏàËÆ¶È:63.3% Chinese Traditional and Herbal Drugs 2009 40 1369-1372 ÂæÍÕÌã°ê¾¥ÖÐÈýÝÆÀà³É·ÖÑо¿ ·ëÓýÁÖ;ÎâÝí;ºÎÃ÷Õä;ÕÅС¾ê;ÐìÀöÕä;ÑîÊÀÁÖ Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ¦Â-sitosterol ÏàËÆ¶È:63.3% Natural Product Research and Development 2004 16 131-132 STUDIES ON CHEMICAL CONSTITUENTS OF GENDARUSSA VENTRICOSA ZHANG Xiao-li;YU Zheng-wen;GUO Fang-qin; YANG Xiao-sheng *; HAO Xiao-jiang Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . ¦Â-Sitosterol ÏàËÆ¶È:63.3% Journal of Agricultural and Food Chemistry 2011 59 7743-7751 Evaluation of the Potential Hypoglycemic and Beta-Cell Protective Constituents Isolated from Corni Fructus To Tackle Insulin-Dependent Diabetes Mellitus Mei-Hsiang Lin, Hui-Kang Liu, Wei-Jan Huang, Chu-Chun Huang, Tzu-Hua Wu, and Fen-Lin Hsu Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ¦Â-Sitosterol ÏàËÆ¶È:63.3% Zeitschrift f¨¹r Naturforschung C 2012 67 172-180 Anti-Helicobacter pylori Activity of the Methanolic Extract of Geum iranicum and its Main Compounds Somayeh Shahani, Hamid R. Monsef-Esfahani, Soodabeh Saeidnia, Parastoo Saniee, Farideh Siavoshi, Alireza Foroumadi, Nasrin Samadi, and Ahmad R. Gohari Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:63.3% Chinese Journal of Applied & Environmental Biology 1999 5 501-506 NEW MONOTERPENOID GLYCOSIDES FROM LIGUSTRUM ROBUSTUM TIAN Jun, & SUN Handong Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . ¦Â-¹ÈçÞ´¼ ÏàËÆ¶È:63.3% China Journal of Chinese Materia Medica 2012 37 1963-1967 Chemical constituents contained in Aeschynanthus moningeriae LIU Huixin; LIAO Haibing; YUAN Ke Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . daucosterol ÏàËÆ¶È:60.6% Natural Product Research 2012 26 2107-2111 Main constituents from the seeds of Vietnamese Cnidium monnieri and cytotoxic activity Pham Huu Dien, Nguyen Thi Nhan, Hoang Thi Le Thuy & Dang Ngoc Quang Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 7¦Â,15¦Â-dihydroxynigranoic acid C30H46O6 ÏàËÆ¶È:60% Chemistry & Biodiversity 2007 Vol. 4 112 Hydroxylation of the Triterpenoid Nigranoic Acid by the Fungus Gliocladium roseum YMF1.00133 Jin-Yan Dong, Ye-Gao Chen, Hong-Chuan Song, Yan-Hui Zhu, Yong-Ping Zhou, Lei Li, Yan-Ping H, Jie Cao, and Ke-Qin Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 3¦Â-hydroxyurs-12-en-27-oic acid C30H48O3 ÏàËÆ¶È:60% Helvetica Chimica Acta 2003 Vol. 86 2414 Cytotoxic Pentacyclic Triterpenoids from the Rhizome of Astilbe chinensis Hongxiang Sun, Jianxin Zhang, Yiping Ye, Yuanjiang Pan, and Yueao Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . ursolic acid ÏàËÆ¶È:60% Journal of Natural Products 1999 62 1624-1626 DNA Polymerase ¦Â Inhibitors from Baeckea gunniana Jing-Zhen Deng, Shelley R. Starck, and Sidney M. Hecht Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . musambin B C30H48O6 ÏàËÆ¶È:60% Phytochemistry 2009 70 1239-1245 Hydroperoxy-cycloartane triterpenoids from the leaves of Markhamia lutea,a plant ingested by wild chimpanzees Damien Lacroix, Soizic Prado, Alexandre Deville, Sabrina Krief, Vincent Dumontet, John Kasenene, Elisabeth Mouray, Christian Bories, Bernard Bodo Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 5¦Á,6¦Â-dihydroxysitosterol C29H52O3 ÏàËÆ¶È:60% Steroids 2005 70 886-895 Gram-scale chromatographic purification of ¦Â-sitosterol: Synthesis and characterization of ¦Â-sitosterol oxides Xin Zhang, Philippe Geoffroy, Michel Miesch, Diane Julien-David, Francis Raul, Dalal Aoud¨¦-Werner, Eric Marchioni Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . (22R,23R)-2¦Á-Fluoro-3¦Á,22,23-trihydroxy-5¦Á-stigmastan-6-one C29H49FO4 ÏàËÆ¶È:60% Steroids 2009 74 435-440 Synthesis and biological activity of brassinosteroids fluorinated at C-2 Sof¨ªa L. Acebedo, Javier A. Ram¨ªrez, Lydia R. Galagovsky Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . (24S)-24-ethylcholesta-3¦Â,5¦Á,6¦Á-triol C29H52O3 ÏàËÆ¶È:60% Journal of Natural Products 1993 Vol 56 2210 Studies on Marine Chemicals, Part VI. A New Clionasterol Derivative from the Marine Sponge Spirastrella inconstans B. Das, S. Padma Rao, K. V. N. S. Srinivas Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . halistanol sulfate F ÏàËÆ¶È:60% Journal of Natural Products 1994 Vol 57 164 Novel HIV-Inhibitory Halistanol Sulfates F-H from a Marine Sponge, Pseudoaxinissa digitata G. Bifulco, I. Bruno, L. Minale, R. Riccio Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . donellanic acid A C29H42O4 ÏàËÆ¶È:60% Tetrahedron 2012 68 4621-4627 Donellanic acids A¨CC: new cyclopropanic oleanane derivatives from Donella ubanguiensis (Sapotaceae) Aurelie V.B. Djoumessi, Louis P. Sandjo, Johannes C. Liermann, Dieter Schollmeyer, Victor Kuete, Vincent Rincheval, Abegaz M. Berhanu, Samuel O. Yeboah, Pascal Wafo, Bonaventure T. Ngadjui, Till Opatz Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . (24S)-24-ethylcholesta-3¦Â,5¦Á,6¦Á-triol ÏàËÆ¶È:60% Chinese Journal of Applied & Environmental Biology 2009 15 615-620 Chemical Constituents from Polygonum perfoliatum LI Hongfang; MA Qingyun; LIU Yuqing; QIAN Jinfu; ZHOU Jun & ZHAO Youxing Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . (22E)-3-Acetoxy-5¦Á-stigmasta-2,22-dien-6-one C31H48O3 ÏàËÆ¶È:58.0% Steroids 2009 74 435-440 Synthesis and biological activity of brassinosteroids fluorinated at C-2 Sof¨ªa L. Acebedo, Javier A. Ram¨ªrez, Lydia R. Galagovsky Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . ophirapstanol C31H56O3 ÏàËÆ¶È:58.0% Journal of Natural Products 1994 Vol 57 1751 Ophirapstanol Trisulfate, a New Biologically Active Steroid Sulfate from the Deep Water Marine Sponge Topsentia ophiraphidites Sarath P. Gunasekera, Susan H. Sennett, Michelle Kelly-Borges, Robert W. Bryant Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . 3¦Â-[N-((N',N',N'-trimethyl)-2'-aminoethyl)-N-(2-amino-ethyl)carbamoyl]cholesterol ÏàËÆ¶È:58.0% Bioorganic & Medicinal Chemistry 2010 18 330-342 Solid phase synthesis of novel asymmetric hydrophilic head cholesterol-based cationic lipids with potential DNA delivery Widchaya Radchatawedchakoon, Ramida Watanapokasin, Aungkana Krajarng, Boon-ek Yingyongnarongkul Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . 3¦Â-[N-(N'-guanidinyl-2'-aminoethyl)-N-(N-glycine(N-(3-aminopropyl)amide)) carbamoyl]cholesterol ÏàËÆ¶È:58.0% Bioorganic & Medicinal Chemistry 2010 18 330-342 Solid phase synthesis of novel asymmetric hydrophilic head cholesterol-based cationic lipids with potential DNA delivery Widchaya Radchatawedchakoon, Ramida Watanapokasin, Aungkana Krajarng, Boon-ek Yingyongnarongkul Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . Euphonerin F C31H50O4 ÏàËÆ¶È:58.0% Planta medica 2012 78 1370-1377 Cycloartane Triterpenes and Ingol Diterpenes Isolated from Euphorbia neriifolia in a Screening Program for Death-Receptor Expression-Enhancing Activity Toume, Kazufumi; Nakazawa, Takafumi; Hoque, Tahmina; Ohtsuki, Takashi; Arai, Midori A.; Koyano, Takashi; Kowithayakorn, Thaworn; Ishibashi, Masami: Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . daucosterol ÏàËÆ¶È:57.5% China Journal of Chinese Materia Medica 2007 32 605-608 Studies on chemical constituents from Serissa serissoides LI Yaolan, WANG Guan, XUE Junyi, CEN Yingzhou Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . 7¦Á-hydroxysitosterol-3-O-¦Â-D-glucoside ÏàËÆ¶È:57.1% Journal of Natural Products 1987 Vol 50 881 Sterols and Steryl Glycosides from Urtica dioica Neera Chaurasia, Max Wichtl Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . ¦Â-sitosteryl-D-glucoside ÏàËÆ¶È:57.1% Journal of the Brazilian Chemical Society 2001 12 467-472 Alkamides and Phemethyl Derivatives from Aristolochia gehrtii. Hosana M. D. Navickiene and Lucia M. X. Lopes Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . 6¦Á,15¦Â-dihydroxynigranoic acid C30H46O6 ÏàËÆ¶È:56.6% Chemistry & Biodiversity 2007 Vol. 4 112 Hydroxylation of the Triterpenoid Nigranoic Acid by the Fungus Gliocladium roseum YMF1.00133 Jin-Yan Dong, Ye-Gao Chen, Hong-Chuan Song, Yan-Hui Zhu, Yong-Ping Zhou, Lei Li, Yan-Ping H, Jie Cao, and Ke-Qin Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . fetisinine C27H39NO3 ÏàËÆ¶È:56.6% Phytochemistry 2003 115-122 New class of steroidal alkaloids from Fritillaria imperialis M. Nadeem Akhtar, Atta-ur-Rahman, M. Iqbal Choudhary, Bilge Sener, Ilkay Erdogan, Yoshisuke Tsuda Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . topsentisterol C1 C29H46O4 ÏàËÆ¶È:56.6% Journal of Natural Products 2006 69 1760-1768 26,27-Cyclosterols and Other Polyoxygenated Sterols from a Marine Sponge Topsentia sp. Xuan Luo, Famei Li, Pramod B. Shinde, Jongki Hong, Chong-O. Lee, Kwang Sik Im, and Jee H. Jung Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . plakinamine E C31H50N2O2 ÏàËÆ¶È:56.6% Journal of Natural Products 2001 64 1474-1476 New Steroidal Alkaloids from an Undescribed Sponge of the Genus Corticium Hyi-Seung Lee,Youngwan Seo,Jung-Rae Rho, Jongheon Shin,and Valerie J. Paul Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . Metatrichosin B C30H44O6 ÏàËÆ¶È:56.6% Acta Botanica Yunnanica 2006 28(6) 673-675 Two New Triterpenes from Metadina trichotoma ( Rubiaceae) ZHANG Yu-Mei,TAN Ning-Hua Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . (22E)-2¦Á-Fluoro-5¦Á-stigmasta-22-en-3,6-dione C29H45O2F ÏàËÆ¶È:56.6% Steroids 2009 74 435-440 Synthesis and biological activity of brassinosteroids fluorinated at C-2 Sof¨ªa L. Acebedo, Javier A. Ram¨ªrez, Lydia R. Galagovsky Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . (22E)-2¦Á-Fluoro-3¦Á-hydroxy-5¦Á-stigmast-22-en-6-one C29H47O2F ÏàËÆ¶È:56.6% Steroids 2009 74 435-440 Synthesis and biological activity of brassinosteroids fluorinated at C-2 Sof¨ªa L. Acebedo, Javier A. Ram¨ªrez, Lydia R. Galagovsky Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . (22E)-2¦Á-fluoro-3¦Â-hydroxy-5¦Á-stigmast-22-en-6-one C29H47O2F ÏàËÆ¶È:56.6% Steroids 2009 74 435-440 Synthesis and biological activity of brassinosteroids fluorinated at C-2 Sof¨ªa L. Acebedo, Javier A. Ram¨ªrez, Lydia R. Galagovsky Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . 3¦Â, 19¦Á-dihydroxy-30-norurs-12-ene C29H48O2 ÏàËÆ¶È:56.6% Fitoterapia 2001 72 382-385 Ursene type nortriterpene from Debregeasia salicifolia Erum Akbar, Muhammad Riaz, Abdul Malik Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . 3,5,6-trihydroxysitostane ÏàËÆ¶È:56.6% Phytochemistry 1998 47 789-797 On the cytotoxity of oxidized phytosterols isolated from photoautotrophic cell cultures of Chenopodium rubrum tested on meal-worms Tenebrio molitor Werner Meyer, Harald Jungnickel, Markus Jandke, Konrad Dettner, Gerhard Spiteller Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . plakinamine A ÏàËÆ¶È:56.6% Journal of Natural Products 1994 Vol 57 1004 Two Steroidal Alkaloids from a Sponge, Corticium Sp. Jaroslaw Jurek, Paul J. Scheuer, Michelle Kelly-Borges Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . 3¦Â-[N-((N'-guanidinyl)-2'-aminoethyl)-N-(2-aminoethyl)-carbamoyl]cholesterol ÏàËÆ¶È:56.6% Bioorganic & Medicinal Chemistry 2010 18 330-342 Solid phase synthesis of novel asymmetric hydrophilic head cholesterol-based cationic lipids with potential DNA delivery Widchaya Radchatawedchakoon, Ramida Watanapokasin, Aungkana Krajarng, Boon-ek Yingyongnarongkul Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . saikogenin F ÏàËÆ¶È:56.6% Natural Product Research and Development 2008 20 833-835 Study on the Chemical Constituents of Bupleurum bicaule Helm ZHU Zhan-jun; PAN Rui-le; SI Jian-yong; FU Ying; HUANG Qian-qian Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . pomolic acid C30H48O4 ÏàËÆ¶È:56.6% Natural Product Research and Development 2001 13(2) 11-13 THE STUDIES OF CHEMICAL COMPONENTS OF CLAUSENA DUNNIANA CUI Shu ya;CHENG Dong liang; TIAN Jun; WU Feng e Structure 13C NMR ̼Æ×Ä£Äâͼ |
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