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xiewan: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-08-16 11:40:29
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xiewan: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-08-16 11:40:29
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²éѯ½á¹û£º¹²²éµ½2215¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 8(9),15-Isopimaradien-3¦Â-ol C20H32O ÏàËÆ¶È:65% Journal of Natural Products 2004 67 631-637 Labdanes and Isopimaranes from Platycladus orientalis and Their Effects on Erythrocyte Membrane and on Plasmodium falciparum Growth in the Erythrocyte Host Cells Javad Asili, Maja Lambert, Hanne L. Ziegler, , Majid Sairafianpour, Matthias Witt, Gholamreza Asghari, Ismaiel S. Ibrahimi, and Jerzy W. Jaroszewski Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 13,17-Epoxy-3,4-seco-cleistantha-4(18),15-dien-3-oic acid C20H30O3 ÏàËÆ¶È:65% Chemistry of Natural Compounds 2009 45 641-646 NEW CLEISTANTHANE DITERPENOIDSAND 3,4-seco-CLEISTANTHANE DITERPENOIDSFROM Croton oblongifolius S. Roengsumran, P. Pata, N. Ruengraweewat,J. Tummatorn, S. Pornpakakul, P. Sangvanich,S. Puthong, and A. Petsom1, Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . ent-3¦Â-hydroxy-17-trachylobanoic acid C20H30O3 ÏàËÆ¶È:65% Journal of Natural Products 2010 73 656-663 Structure and Anti-TB Activity of Trachylobanes from the Liverwort Jungermannia exsertifolia ssp. Cordifolia Jochen M. Scher, Andreas Schinkovitz, Josef Zapp, Yuehong Wang, Scott G. Franzblau, Hans Becker, David C. Lankin and Guido F. Pauli Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . ent-7¦Á-acetoxy-16¦Â,17-epoxykaurane C22H34O3 ÏàËÆ¶È:65% Phytochemistry 1994 37 717-721 The microbiological transformation of two ent-16¦Â, 17-epoxykaurane derivatives by Gibberella fujikuroi Braulio M. Fraga, Pedro Gonz¨¢lez, Ricardo Guillermo, James R. Hanson, Melchor G. Hern¨¢ndez, Jacqueline A. Takahashi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 18-oxo-3-virgene C20H32O ÏàËÆ¶È:65% Phytochemistry 1987 26 3029-3031 Cembrane-derived diterpenoid having a carbotricyclic skeleton Reiko Uegaki,Takane Fujimori,Nasuo Ueda,Akio Ohnishi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . serratezomine E C18H32N2O ÏàËÆ¶È:65% Bioorganic & Medicinal Chemistry Letters 2009 19 3577-3580 Serratezomines D and E, new Lycopodium alkaloids from Lycopodium serratum var. serratum Takaaki Kubota, Hiroko Yahata, Sunao Yamamoto, Shigeki Hayashi, Toshiro Shibata, Jun¡¯ichi Kobayashi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 16¦Á-hydroxy-ent-kauran-19-oic acid ÏàËÆ¶È:65% Archives of Pharmacal Research 2006 29 548-555 Cytotoxic and COX-2 inhibitory constituents from the aerial parts ofAralia cordata Ik Soo Lee, Wen Yi Jin, Xinfeng Zhang, Tran Manh Hung and Kyung Sik Song, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . (1S,2E,4S,6E,8S,11S,12S)-2,6-cembradiene-4,8,11,12-tetrol ÏàËÆ¶È:65% Acta Chemica Scandinavica 1986 40 123-134 Tobacco Chemistry. 69. Five New Labdanic Compounds from Tobacco. Wahlberg, Inger; Eklund, Ann-Marie; Nordfors, Kerstin; Vogt, Carmen; Enzell, Curt R.; Berg, Jan-Eric Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . (2R/S,3S,7S)-3,7-dimethyl-2-heptacosanol C29H60O ÏàËÆ¶È:65% European Journal of Organic Chemistry 2000 2000 1307-1312 Synthesis of (3S,7S)- and (3S,7S,15S)- Stereoisomers of 3,7-Dimethyl-2-heptacosanone and 3,7,15-Trimethyl-2-heptacosanone, the Ketones Identified from the Locust Schistocerca gregaria Yoshihide Nakamura and Kenji Mori Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 3¦Á-hydroxy-17a-oxa-D-homo-5¦Á-androstan-17-one C19H30O3 ÏàËÆ¶È:65% Molecules 2013 18 13812-13822 Baeyer-Villiger Oxidation of Some C19 Steroids by Penicillium lanosocoeruleum Alina Świzdor Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . comopound 2 ÏàËÆ¶È:65% Chemistry of Natural Compounds 2014 50 165-168 Abietane, Labdane, and Pimarane Diterpenoids from the Pulp of Torreya nucifera Hong-feng Zhang, Xian-ling Zheng, Le Wang, Bao-yuan Xu, Gen-dong Yao, Rui-Xia Guo, Qing-Wen Shi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 21,24-cyclopentalanosta-3¦Â,21,25-triol-8-ene C30H50O3 ÏàËÆ¶È:65% Journal of Wood Science 2001 47 313-316 Chemical constituents of Inonotus obliquus Ih a new triterpene, 21, 24-cyclopentalanosta-3¦Â, 21, 25-triol-8-ene from sclerotium Yusoo Shin, Yutaka Tamai, Minoru Terazawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . komaroviquinone C21H28O5 ÏàËÆ¶È:61.9% Journal of Natural Products 2003 66 128-131 New Icetexane and 20-Norabietane Diterpenes with Trypanocidal Activity from Dracocephalum komarovi Nahoko Uchiyama, Fumiyuki Kiuchi, Michiho Ito, Gisho Honda, Yoshio Takeda, Olimjon K. Khodzhimatov, and Ozodbek A. Ashurmetov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . Methyl 17¦Á-hydroxyandrostane-16¦Á-carboxylate ÏàËÆ¶È:61.9% Steroids 2004 69 271-277 Selective ring-opening carbonylation of epoxy-steroids Attila Bal¨¢zs, Csilla Benedek, G¨¢bor Szalontai, Szil¨¢rd Tőrös Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . ent-clerod-3-en-15-oic acid-18,19-olide methyl ester C21H32O4 ÏàËÆ¶È:61.9% Phytochemistry 1992 31 1703-1711 Clerodane and labdane derivatives from Olearia teretifolia C. Zdero, F. Bohlmann, R.M. King Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . methyl 15-hydroxy-7-labden-17-oate C21H36O3 ÏàËÆ¶È:61.9% Phytochemistry 1987 26 3037-3040 Labdane diterpenoids from Halimium viscosum and H. verticilatum Julio G. Urones,Isidro S¨¢nchez Marcos,David Diez Martin,F.M.S.Brito Palma,Jes¨²s M. Rodilla Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . methyl ent-7¦Á,13,16-trihydroxykauran-19-oate C21H34O5 ÏàËÆ¶È:61.9% Phytochemistry 1990 29 3805-3807 The microbiological transformation of steviol derivatives by Rhizopus stolinifer and Gibberella fujikuroi James R. Hanson,Bras H. De Oliveira Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 10 ÏàËÆ¶È:61.9% Phytochemistry 1977 16 1583-1586 Ein neues clerodan-derivat sowie weitere inhaltsstoffe aus der gattung Macowania ag Ferdinand Bohlmann, Christa Zdero Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . ent-16¦Á-hydroxy-kauran-19-oic acid methyl ester ÏàËÆ¶È:61.9% Natural Product Communications 2011 6 935-938 On the Isomerization of ent-Kaurenic Acid Julio Rojas, Rosa Aparicio, Thayded Villasmil, Alexis Peña and Alfredo Usubillaga Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . (4S,4aS,5R,6aS,8S,9S,11aS,11bS)-4-cyano-8-(methoxymethyl)oxy-9,11b-dimethyl-1,2,3,4,4a,5,6,6a,7,8,9,10,11,11b-tetradecahydro-9,11amethano-11aH-cyclohepta[a]naphthalen-5-ol C21H33NO3 ÏàËÆ¶È:61.9% Journal of the American Chemical Society 1999 121 5467-5480 Enantiodivergent Total Syntheses of (+)- and (− -Scopadulcic Acid AMartin E. Fox, Chi Li, Joseph P. Marino, Jr., and Larry E. Overman Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . 3-acetoxy-16-aldehyde-17-aminoandrosta-5,16-diene C22H31NO3 ÏàËÆ¶È:61.9% Steroids 2013 78 1200-1208 Design and synthesis of novel D-ring fused steroidal heterocycles Bao-Le Zhang, En Zhang, Lu-Ping Pang, Li-Xing Song, Ya-Fei Li, Bin Yu, Hong-Min Liu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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