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Gaoyumeng: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-10 15:44:18
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Gaoyumeng: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-10 15:44:18
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1 . 3-heptadecyl-5-methoxy-phenol C24H42O2 ÏàËÆ¶È:61.1% Journal of Ethnopharmacology 2003 88 241-247 Bioactive alkyl phenols and embelin from Oxalis erythrorhiza Gabriela Egly Feresin, Alejandro Tapia, Maximiliano Sortino, Susana Zacchino, Antonieta Rojas de Arias, Alba Inchausti, Gloria Yaluff, Jaime Rodriguez, Cristina Theoduloz, Guillermo Schmeda-Hirschmann Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . eleocharinol A ÏàËÆ¶È:61.1% Natural Product Research and Development 2013 25 1615-1620 Phenolic Constituents and Antioxidant Activity of Eleocharis tuberosa Peels LI Xing-ren, LUO Yang-he*, HE Juan, PENG Li-yan, WU Xing-de, DU Ru-nan, ZHAO Qin-shi Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 5-Pentyl-3-methoxy-N-butylaniline ÏàËÆ¶È:55.5% Phytochemistry 2009 70 1233-1238 Anti-mosquito and antimicrobial nor-halimanoids, isocoumarins and an anilinoid from Tessmannia densiflora Charles Kihampa, Mayunga H.H. Nkunya, Cosam C. Joseph, Stephen M. Magesa, Ahmed Hassanali, Matthias Heydenreich , Erich Kleinpeter Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3,4-dihydro-6,8-dimethoxxy-3-(2-hydroxypentyl)isocoumarin C16H22O5 ÏàËÆ¶È:55.5% Journal of Natural Products 2010 73 75-78 An Antimycobacterial Cyclodepsipeptide from the Entomopathogenic Fungus Ophiocordyceps communis BCC 16475 Rachada Haritakun, Malipan Sappan, Rapheephat Suvannakad, Kanoksri Tasanathai and Masahiko Isaka Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (+)-4-((1S,4S,4aS,8aR)-4-hydroxy-5,5,8a-trimethyl-2-methylenedecahydro-1-naphthalenyl)-2-butanone C18H30O2 ÏàËÆ¶È:55.5% Tetrahedron 2001 57 5663-5679 The synthesis of Ambrox®-like compounds starting from (+)-larixol Marjon G Bolster, Ben J.M Jansen, Aede de Groot Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (+)-4-((1S,4S,4aS,8aR)-4-hydroxy-5,5,8a-trimethyl-2-methylenedecahydro-1-naphthalenyl)-2-butanone C18H28O ÏàËÆ¶È:55.5% Tetrahedron 2001 57 8369-8379 The synthesis of Ambrox®-like compounds starting from (+)-larixol. Part 2 Marjon G Bolster, B¨¦atrice M.F Lagnel, Ben J.M Jansen, Christophe Morin, Aede de Groot Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 4c ÏàËÆ¶È:55.5% Magnetic Resonance in Chemistry 1997 35 821-828 Configurational and conformational study of new esters derived from 2-methyl-2-azabicyclo[2.2.2]octan-5-syn(anti)-ols by NMR spectroscopy and x-ray crystallography¡ªI M. J. Fern¨¢ndez, R. Huertas, M. S. Toledano, E. G¨¢lvez, J. Server and M. Mart¨ªnez-Ripoll Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (10'R)-5-(10-hydroxytridecyl)-1-O-methylresorcinol C20H34O3 ÏàËÆ¶È:55% Phytochemistry 1994 36 189-194 Resorcinol derivatives and other components from Ononis viscosa subsp. breviflora Alejandro.F. Barrero, Eduardo Cabrera, Ignacio Rodr¨ªguez, Eva M. Fern¨¢ndez-Gallego Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 1 C27H38O11 ÏàËÆ¶È:55% Journal of Shenyang Pharmaceutical University 2008 25 964-966 New diterpene from the seeds of Caesalpinia minax Hance WU Zhao-hua, WANG Li-bo, GAO Hui-yuan, SUN Bo-hang, HUANG Jian, WU Li-jun Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 11-hydroxytubotaiwine C20H24N2O3 ÏàËÆ¶È:55% Heterocycles 1994 38 2411-2414 Isolation of Two New Nitrogenous Metabolites from the Cultured Cells of Aspidosperma Quebracho-Blanco Norio Aimi, Naoki Uchida, Naoko Oya, Shin-ichiro Sakai, Luis A. Mendonza, Peter Obitz, and Joachim Stöckigt Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 27 ÏàËÆ¶È:52.6% Tetrahedron Letters 2000 41 6643-6647 An enantiospecific approach to thapsanes from R-carvone: synthesis of (− -thaps-8-en-5-olA. Srikrishna, K. Anebouselvy, T. Jagadeeshwar Reddy Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (1R,2R,6R,7R)-2-(tert-butyldimethylsilyloxy)-1,5,5,6,7-pentamethyl-8-methylenebicyclo[4.3.0]nonane C21H40OSi ÏàËÆ¶È:52.6% Indian Journal of Chemistry Section B 2008 47B 449-459 Enantiospecific synthesis of thaps-8-en-5-ol via stereospecific Srikrishna,A; Anebouselvy,K Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (1R*,3aS*,9bR*)-1-isopropyl-6-methoxy-3a,8-dimethyl-1,3,3a,4,5,9b-hexahydrocyclopenta[a]naphthalene-2-one C19H26O2 ÏàËÆ¶È:52.6% The Journal of Organic Chemistry 2004 69 2773-2784 Synthesis of ((+/-)-Hamigeran B, (-)-Hamigeran B, and ((+/-)-1-epi-Hamigeran B: Use of Bulky Silyl Groups to Protect a Benzylic Carbon-Oxygen Bond from Hydrogenolysis Derrick L. J. Clive and Jian Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . isodonhenrin C C21H30O7 ÏàËÆ¶È:52.3% Chemical & Pharmaceutical Bulletin 2011 59 1562-1566 Cytotoxic ent-Kaurane Diterpenoids from Isodon henryi Zhuo Hu, Rui Zhan, Xue Du, Jia Su, Xiao-Nian Li, Jian-Hong Yang, Hai-Bo Zhang, Yan Li, Han-Dong Sun, Gan-Peng Li and Jian-Xin Pu Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 11-(3-hydroxy-5-pentylphenoxy)-N0,N0-dimethylundecanehydrazide C24H42N2O3 ÏàËÆ¶È:52.1% Bioorganic & Medicinal Chemistry 2014 22 4770-4783 Structure¨Caffinity relationships and pharmacological characterization of new alkyl-resorcinol cannabinoid receptor ligands: Identification of a dual cannabinoid receptor/TRPA1 channel agonistOriginal Research Article Antonella Brizzi, Francesca Aiello, Pietro Marini, Maria Grazia Cascio, Federico Corelli, Vittorio Brizzi, Luciano De Petrocellis, Alessia Ligresti, Livio Luongo, Stefania Lamponi, Sabatino Maione, Roger G. Pertwee, Vincenzo Di Marzo Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . stilbostemin N C16H18O3 ÏàËÆ¶È:50% Phytochemistry 2008 69 457-463 Antibacterial stilbenoids from the roots of Stemona tuberosa Li-Gen Lin, Xin-Zhou Yang, Chun-Ping Tang, Chang-Qiang Ke, Ji-Bao Zhang, Yang Ye Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . stereumin C C16H22O4 ÏàËÆ¶È:50% Phytochemistry 2008 69 1439-1445 Stereumin A¨CE, sesquiterpenoids from the fungus Stereum sp. CCTCC AF 207024 Guo-Hong Li, Meng Duan, Ze-Fen Yu, Lei Li, Jin-Yan Dong, Xing-Biao Wang,Jian-Wei Guo, Rong Huang, Min Wang, Ke-Qin Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . ravidin A C20H24O5 ÏàËÆ¶È:50% Phytochemistry 2004 65 2533-2537 Clerodane-type diterpenoids from Nannoglottis ravida Hai-Lin Qin, Zhi-Hong Li Structure 13C NMR ̼Æ×Ä£Äâͼ |

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