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schaduwÎÞ³æ (СÓÐÃûÆø)
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| 21.55, 22.70, 29.23, 29.71, 31.93, 36.01, 38.13, 39.32, 40.41, 43.64, 55.47, 56.70, 58.03, 59.18, 74.54, 78.70, 113.82, 122.33, 131.68, 163.51, 165.84, 170.00 |
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²éѯ½á¹û£º¹²²éµ½287¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . N-deethyldehydrobicoloridine ÏàËÆ¶È:60.8% Phytochemistry 1995 39 1459-1465 Norditerpenoid alkaloids from Delphinium peregrinum var. elongatum Gabriel de la Fuente, Lastenia Ruiz-Mes¨ªa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 4 ÏàËÆ¶È:59.0% Steroids 2002 67 621-626 13C-NMR study of 4-azasteroids in solution and solid state Jacek W. Morzycki, Iwona Wawer, Agnieszka Gryszkiewicz, Jadwiga Maj, Leszek Siergiejczyk, Alicja Zaworska Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 13-ethyl-17¦Â-hydroxy-11-methylene-18,19-dinor-17¦Á-pregna-4,15-dien-20-yn-3-one ÏàËÆ¶È:59.0% Magnetic Resonance in Chemistry 1990 28 656-658 Substituent effects in the 13C NMR spectra of 17¦Á-ethinyl-19-nortestosterone derivatives Peter E. Hammann, Elke Wöbbecke and Hans-Otto Hoppen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 7 ÏàËÆ¶È:59.0% Australian Journal of Chemistry 1981 34 1073-1078 Chemistry of the Podocarpaceae. LVI. Resin acids from Phyllocladus trichomanoides RC Cambie, BA Grigor and T Mee-Ing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . Caesalpinolide G C22H32O7 ÏàËÆ¶È:59.0% Natural Product Research 2013 27 818-823 Two new diterpenes from Caesalpinia minax Hance Guo-Xu Ma, Jing-Quan Yuan, Li Cao, Jun-Shan Yang & Xu-Dong Xu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 5¦Â-cholest-1-ene-20-hydroxy-7,11-dione ÏàËÆ¶È:57.6% Phytochemistry 1990 29 2029-2031 An hydroxy diketosteroid from the marine red alga Hypnea musciformis J. Moses Babu,Hari H. Mathur,Girish K. Trivedi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . gelomulide S C24H34O8 ÏàËÆ¶È:56.5% Phytochemistry 2008 69 276-287 Cytotoxic ent-abietane diterpenes from Gelonium aequoreum Chia-Lin Lee,Fang-Rong Chang,Pei-Wen Hsieh,Michael-Y. Chiang,Chin-Chung Wu,Zih-You Huang,Yu-Hsuan Lan,Mei Chen,Kuo-Hsiung Lee,Hsin-Fu Yen,Wen-Chun Hung,Yang-Chang Wu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . yantuine III C23H28O7 ÏàËÆ¶È:56.5% Indian Journal of Chemistry Section B 2002 41B 228-231 Studied on the new diterpene lactone from Rodgersia sambucifolia H. Shangzhen Zheng*,Hongang An, Tong Shen, Xuwei Shen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . epoxyvesceritenol C25H34O8 ÏàËÆ¶È:56% Phytochemistry 2008 69 1933-1938 Sesquiterpenes from aerial parts of Ferula vesceritensis Karima Oughlissi-Dehak, Philippe Lawton, Serge Michalet, Christine Bayet, Nicole Darbour,Mahfoud Hadj-Mahammed, Yacine A. Badjah-Hadj-Ahmed,Marie-Genevi¨¨ve Dijoux-Franca, David Guilet Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . (13S,21R/S)-21-hydroxy-23,21-olide-18-nor-20(22)en-limonoid C25H36O5 ÏàËÆ¶È:56% Tetrahedron 2007 63 8939-8948 Nor-limonoid and homoisoanticopalane lactones from methyl isoanticopalate Pilar Basabe, Sergio Delgado, Isidro S. Marcos, David Diez, Alberto Diego, M¨®nica de Rom¨¢n, Francisca Sanz, J.G. Urones Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . Dulcinodiol C27H38O4 ÏàËÆ¶È:56% Phytochemistry Letters 2012 5 609-612 New labdane diterpenes from the aerial parts of Scoparia dulcis L. Monira Ahsan, Mohammad R. Haque, S.K.N. Islam, Alexander I. Gray, Choudhury M. Hasan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 2¦Á,3¦Â,13(S),16¦Á-tetrahydroxystemodane C20H34O2 ÏàËÆ¶È:54.5% Phytochemistry 2004 65 701-710 Investigation of the importance of the C-2 oxygen function in the transformation of stemodin analogues by Rhizopus oryzae ATCC 11145 Glenroy D.A. Martin, William F. Reynolds, Paul B. Reese Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . O-Methylaureol C22H32O2 ÏàËÆ¶È:54.5% Journal of Natural Products 2002 65 476-480 New Antiinfective and Human 5-HT2 Receptor Binding Natural and Semisynthetic Compounds from the Jamaican Sponge Smenospongia aurea Jin-Feng Hu, John A. Schetz, Michelle Kelly, iang-Nan Peng,Kenny K. H. Ang, Horst Flotow,Chung Yan Leong, Siew Bee Ng, Antony D. Buss, Scott P. Wilkins, and Mark T. Hamann Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . ent-11¦Â-acetoxy-3¦Â,16¦Á,17-trihydroxyatis-13-ene C22H34O5 ÏàËÆ¶È:54.5% Journal of Natural Products 1997 60 86-92 Biotransformation of ent-Atisenes and ent-Beyerenes by Rhizopus nigricans and Fusarium moniliforme Cultures Andr¨¦s Garc¨ªa-Granados, Andr¨¦s Parra, and Jos¨¦Mar¨ªa Arias Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . ent-17-acetoxy-3¦Â,16¦Á-dihydroxyatis-13-en-11-one C22H32O5 ÏàËÆ¶È:54.5% Journal of Natural Products 1997 60 86-92 Biotransformation of ent-Atisenes and ent-Beyerenes by Rhizopus nigricans and Fusarium moniliforme Cultures Andr¨¦s Garc¨ªa-Granados, Andr¨¦s Parra, and Jos¨¦Mar¨ªa Arias Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 3¦Â-Acetoxy-5¦Á,6¦Á-epoxy-20-hydroxyiminopregnan-20-one ÏàËÆ¶È:54.5% Molecules 2009 14 4655-4668 Synthesis of Pregnane Derivatives, Their Cytotoxicity on LNCap and PC-3 Cells, and Screening on 5¦Á-Reductase Inhibitory Activity Sujeong Kim and Eunsook Ma Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 5'-O-methyl-aureol C22H32O2 ÏàËÆ¶È:54.5% Natural Product Research 2006 20 578-585 Isolation of aureol from Smenospongia sp. and cytotoxic activity of some aureol derivatives Ya-Ching Shen; Chia-Ching Liaw; Jing-Ren Ho; Ashraf Taha Khalil; Yau-Haur Kuo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . kalihinol J C22H35N2SO3Cl ÏàËÆ¶È:54.5% Journal of Natural Products 1991 Vol 54 71 Anthelmintic Polyfunctional Nitrogen-Containing Terpenoids from Marine Sponges K. A. Alvi, Laura Tenenbaum, Phillip Crews Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . lasidiol p-methoxybenzoate ÏàËÆ¶È:54.5% Journal of Natural Products 1991 Vol 54 460 New Sesquiterpenes from Xanthium catharticum Jativa Cumanda, Giulio Marinoni, Maria De Bernardi, Giovanni Vidari, Paola Vita Finzi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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