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1 1 . ¦Â-sitosterol ÏàËÆ¶È:84.3% Phytochemistry 2004 65 2463-2470 Biosynthesis of the irregular monoterpene artemisia ketone, the sesquiterpene germacrene D and other isoprenoids in Tanacetum vulgare L. (Asteraceae) Dirk Umlauf, Josef Zapp, Hans Becker, Klaus Peter Adam Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ¦Â-sitosterol ÏàËÆ¶È:84.3% Planta Medica 1988 54 33-36 In vitro Fibrinolytic Phytosterols Isolated from the Roots of Spatholobus suberetus Yoshiyasu Fukuyama, Yoshinori Nakano, Geng Pei-Wu, Wang Rui, Junko Sumitomo, Bao Jinxian,and Kazuyuki Nakagawa Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . sitosterol ÏàËÆ¶È:84.3% Chemical & Pharmaceutical Bulletin 1979 27 38-42 Carbon-13 Nuclear Magnetic Resonance of 24-Substituted Steroids NAOYUKI KOIZUMI,YOSHINORI FUJIMOTO,TORU TAKESHITA and NOBUO IKEKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . clionasterol ÏàËÆ¶È:84.3% Chemical & Pharmaceutical Bulletin 1979 27 38-42 Carbon-13 Nuclear Magnetic Resonance of 24-Substituted Steroids NAOYUKI KOIZUMI,YOSHINORI FUJIMOTO,TORU TAKESHITA and NOBUO IKEKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:84.3% Acta Botanica Sinica 2003 45 1003-1007 Two New Triterpenes from Neonauclea sessilifolia KANG Wen-Yi, LI Guo-Hong, HAO Xiao-Jiang Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ¦Â-Sitosterol ÏàËÆ¶È:84.3% Journal of Asian Natural Products Research 2008 10 281-283 Artemisterol, a new steryl ester from the whole plant of Artemisia apiacea Sung-Jin Lee Hye Min Kim, Jeong Min Lee, Hee Seung Park and Sanghyun Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . stigmasterol ÏàËÆ¶È:84.3% Chemical & Pharmaceutical Bulletin 1998 46 1408-1411 New Sterols and Triterpenoids of Ficus pumila Fruit Junichi KITAJIMA,Kaoru KIMIZUKA and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . ¦Â-sitosterol ÏàËÆ¶È:84.3% Korean Journal of Pharmacognosy 1981 12(1) 12-24 Revision of 13C NMR Assignments of ¦Â-sitosterol and ¦Â-sitosteryl-3-O-¦Â-D-glucopyranoside Isolated from Plantago asiatica Seed Chang, Il-Moo; YunChoi, Hye-Sook; Yamasaki, Kazuo Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . ¦Â-¹ÈçÞ´¼ ÏàËÆ¶È:84.3% Chinese Traditional and Herbal Drugs 2010 41 704-707 Âúɽºì»¯Ñ§³É·ÖµÄÑо¿ ¸¶ÏþÀö;ÕÅÁ¢Î°;ÁÖÎĺ²;ÀîÇàɽ Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ¦Â-rosasterol ÏàËÆ¶È:84.3% Chinese Traditional and Herbal Drugs 2009 40 1704-1707 Chemical constituents of mangrove plant Excoecaria agallocha in Hainan Province XU Jie; DENG Zhi-wei; LIN Wen-han; LI Qing-shan Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ¦Â-rosasterol C29H50O ÏàËÆ¶È:84.3% Chinese Traditional and Herbal Drugs 2006 37 666-668 Å·ÑÇÐý¸²»¨ÖÐÈýÝÆºÍçÞÌ廯ºÏÎïµÄ·ÖÀëºÍ½á¹¹¼ø¶¨ ÎâÒ»±ø;ÍõÔÆÖ¾;²é½¨Åî;ÑîË«¸ï;ʯÏþΰ;ÕŵÕȺ Structure 13C NMR ̼Æ×Ä£Äâͼ 2 1 . plantamajoside ÏàËÆ¶È:68.9% Phytochemistry 1988 27 3433-3437 Structure and antibacterial activity of plantamajoside,a caffeic acid sugar ester from Plantago major subs major Helle Ravn,Leon Brimer Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Scroside D C30H38O16 ÏàËÆ¶È:66.6% Helvetica Chimica Acta 2004 Vol. 87 598 Phenyl and Phenylethyl Glycosides from Picrorhiza scrophulariiflora Sheng-Xiong Huang, Xun Liao, Quan-Jiang Nie, Li-Sheng Ding, and Shu-Lin Peng Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . scroside E C30H38O16 ÏàËÆ¶È:66.6% Helvetica Chimica Acta 2004 Vol. 87 598 Phenyl and Phenylethyl Glycosides from Picrorhiza scrophulariiflora Sheng-Xiong Huang, Xun Liao, Quan-Jiang Nie, Li-Sheng Ding, and Shu-Lin Peng Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Plantamajoside ÏàËÆ¶È:65.5% Molecules 2008 13 2049-2057 New secoiridoid Glycosides from the Roots of Picrorhiza Scrophulariiflora Lian-Chun Zou, Tong-Fei Zhu, Hua Xiang, Lu Yu, Zhi-Hui Yan, Shu-Cai Gan, Da-Cheng Wang, Sheng Zeng and Xu-Ming Deng Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Plantainoside D ÏàËÆ¶È:65.5% Molecules 2008 13 2049-2057 New secoiridoid Glycosides from the Roots of Picrorhiza Scrophulariiflora Lian-Chun Zou, Tong-Fei Zhu, Hua Xiang, Lu Yu, Zhi-Hui Yan, Shu-Cai Gan, Da-Cheng Wang, Sheng Zeng and Xu-Ming Deng Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . lagotiside A ÏàËÆ¶È:65.5% China Journal of Chinese Materia Medica 2009 34 2054-2056 A new phenylethanoid glucoside from Lagotis brevituba CHI Feng, DENG Jun, WANG Yanhan Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . lugrandoside C29H36O16 ÏàËÆ¶È:65.5% Chemical & Pharmaceutical Bulletin 1999 47 1305-1307 Phenylethanoid Glycosides from Digitalis ferruginea subsp. ferruginea (=D. aurea LINDLEY) (Scrophulariacear) Ihsan CALIS,Deniz TASDEMIR,Otto STICHER and Sansei NISHIBE Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . ferruginoside A ÏàËÆ¶È:65.5% China Journal of Chinese Materia Medica 2010 35 992-996 Phenolic and phenylethanoidal glycosides from branch of Fraxinus sieboldiana LIN Sheng; LIU Mingtao; WANG Sujuan; LI Shuai; YANG Yongchun; SHI Jiangong Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . isolugrandoside ÏàËÆ¶È:65.5% China Journal of Chinese Materia Medica 2010 35 992-996 Phenolic and phenylethanoidal glycosides from branch of Fraxinus sieboldiana LIN Sheng; LIU Mingtao; WANG Sujuan; LI Shuai; YANG Yongchun; SHI Jiangong Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . hemiphroside A ÏàËÆ¶È:64.5% Helvetica Chimica Acta 2004 Vol. 87 598 Phenyl and Phenylethyl Glycosides from Picrorhiza scrophulariiflora Sheng-Xiong Huang, Xun Liao, Quan-Jiang Nie, Li-Sheng Ding, and Shu-Lin Peng Structure 13C NMR ̼Æ×Ä£Äâͼ 3 1 . 2-arachidonylglycerol ÏàËÆ¶È:78.2% Tetrahedron Letters 2000 41 3589-3592 Facile synthesis and stabilization of 2-arachidonylglycerol via its 1,3-phenylboronate ester Herbert H. Seltzman, Denise N. Fleming, Gregory D. Hawkins, F. Ivy Carroll Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 2-arachidonyl-cis-1,3-O-benzylideneglycerol ÏàËÆ¶È:73.9% Tetrahedron Letters 2000 41 3589-3592 Facile synthesis and stabilization of 2-arachidonylglycerol via its 1,3-phenylboronate ester Herbert H. Seltzman, Denise N. Fleming, Gregory D. Hawkins, F. Ivy Carroll Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (¡À)-glycidyl arachidonate C23H36O3 ÏàËÆ¶È:73.9% Tetrahedron Letters 2002 43 1759-1761 Novel, regioselective transformation of an oxirane system. An efficient approach to the synthesis of endocannabinoid 2-arachidonoylglycerol Stephan D. Stamatov, Jacek Stawinski Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 1,3-bis(trifluoroacetyl)-2-arachidonoylglycerol C27H36O6F6 ÏàËÆ¶È:73.9% Tetrahedron Letters 2002 43 1759-1761 Novel, regioselective transformation of an oxirane system. An efficient approach to the synthesis of endocannabinoid 2-arachidonoylglycerol Stephan D. Stamatov, Jacek Stawinski Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . PX27 ÏàËÆ¶È:73.9% Journal of the Chemical Society, Perkin Transactions 1 1996 2651-2656 Preparative transformation of natural phospholipids catalysed by phospholipase D from Streptomyces Paola D'Arrigo, Lorenzo de Ferra, Valentino Piergianni, Antonio Selva, Stefano Servi and Alberto Strini Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . GV-V ÏàËÆ¶È:73.9% Bulletin of the Korean Chemical Society 1988 9 264-266 Glycolipid from the Korean Marine Red Alga Gracilaria verrucosa Byeng Wha Son Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . PX10 ÏàËÆ¶È:72% Journal of the Chemical Society, Perkin Transactions 1 1996 2651-2656 Preparative transformation of natural phospholipids catalysed by phospholipase D from Streptomyces Paola D'Arrigo, Lorenzo de Ferra, Valentino Piergianni, Antonio Selva, Stefano Servi and Alberto Strini Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . PX19 ÏàËÆ¶È:71.4% Journal of the Chemical Society, Perkin Transactions 1 1996 2651-2656 Preparative transformation of natural phospholipids catalysed by phospholipase D from Streptomyces Paola D'Arrigo, Lorenzo de Ferra, Valentino Piergianni, Antonio Selva, Stefano Servi and Alberto Strini Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (+)-(12R,4Z,7Z,10Z,12E,16Z)-14-hydroxy-4,7,10,12,16-docosapentaenoic acid ÏàËÆ¶È:69.5% Journal of Natural Products 1990 Vol 53 57 Hydroxyicosatetraenoic, Hydroxyicosapentaenoic, Hydroxydocosapentaenoic, and Hydroxydocosahexaenoic Acids from the Sponge Echinochalina mollis of the Coral Sea Antonio Guerriero, Michele D'Ambrosio, Francesco Pietra, Olivier Ribes, Daniel Duhet Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 11b ÏàËÆ¶È:69.5% Journal of Natural Products 1990 Vol 53 1430 Stigmasterols from Typha latifolia Marina Della Greca, Pietro Monaco, Lucio Previtera Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Arachidonic acid C20H32O2 ÏàËÆ¶È:69.5% Marine drugs 2010 8 2142-2152 Cytotoxic Cembranes from Indonesian Specimens of the Soft Coral Nephthea sp. Hedi Indra Januar,Ekowati Chasanah,Cherie A. Motti,Dianne M. Tapiolas,Catherine H. Liptrot and Anthony D. Wright Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 2-hydroxymethyl-tricosa-8(Z),11(Z),14(Z),17(Z)-tetraene-1,4-diol C24H42O3 ÏàËÆ¶È:69.5% Bioorganic & Medicinal Chemistry Letters 2001 11 1985-1988 Synthesis and biological activities of novel structural analogues of 2-arachidonoylglycerol, an endogenous cannabinoid receptor ligand Yoshitomo Suhara, Shinji Nakane, Shunsuke Arai, Hiroaki Takayama, Keizo Waku, Yoshio Ishima, Takayuki Sugiura Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-06-20 20:11:30
luky001
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3Â¥2013-06-20 21:18:25
mzp-0
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4 1 . 2-(3,4-dihydroxyphenyl)ethyl ¦Â-D-glucopyranoside ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2010 35 992-996 Phenolic and phenylethanoidal glycosides from branch of Fraxinus sieboldiana LIN Sheng; LIU Mingtao; WANG Sujuan; LI Shuai; YANG Yongchun; SHI Jiangong Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3,4-¶þôÇ»ù±½ÒÒ´¼ÆÏÌÑÌÇÜÕ C14H20O8 ÏàËÆ¶È:100% Chinese Traditional and Herbal Drugs 2010 41 867-870 ´óѪÌٵĻ¯Ñ§³É·ÖÑо¿(¢ò) ³ÂÖÇÏÉ;¸ßÎÄÔ¶;Áõá·ÁÕ;ÕÅÌú¾ü Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 2-(3,4-dihydroxyphenyl)-ethyl-O-¦Â-D-glucopyranoside ÏàËÆ¶È:100% Chinese Pharmaceutical Journal 2011 46 745-747 Chemical Constituents of Water Soluble Fraction of Trollius ledebouri Reichb WU Li-zhen, XU Xu-dong, YANG Jun-shan Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3',4'-¶þôÇ»ù±½ÒÒ´¼ÆÏÌÑÌÇÜÕ ÏàËÆ¶È:100% Journal of Chinese Medicinal Materials 2007 30 291-294 Chemical Constituents from Cirsium pendulum Fisch. ex DC. CHEN Guo-liang, LI Xin-li, SHI Ling-gang, ZHANG Shu-jun Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3,4-¶þôÇ»ù-±½ÒÒ´¼-¦Â-D-ÆÏÌÑÌÇÜÕ ÏàËÆ¶È:92.8% China Journal of Chinese Materia Medica 2012 37 1245-1248 Chemical constituents of Aconitum tanguticum LUO Ming; LIN Limei; LI Chun; WANG Zhimin; GUO Wubao Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 3',4'-dihydroxyphenethyl alcohol 1-O-¦Â-D-glucopyranoside C14H20O8 ÏàËÆ¶È:85.7% Chemical & Pharmaceutical Bulletin 1985 33 527-531 Isolation and Characterization of Phenolic Compounds from Coptidis Rhizoma SHOJI YAHARA,MAYUMI SATOSHIRO,ITSUO NISHIOKA,TETSURO NAGASAWA and HIKOKICHI OURA Structure 13C NMR ̼Æ×Ä£Äâͼ |
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