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²éѯ½á¹û£º¹²²éµ½756¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (+)-10(R)-isothiocyanatoalloaromadendrane ÏàËÆ¶È:70.5% Natural Product Research and Development 2003 15 199-202 STUDIES ON THE CHEMICAL CONSTITUENTS OF MARINE SPONGE ACANTHELLASP.FROM THE SOUTH CHINA SEA YAN Xiao-hong; SONG Guo-qiang; ZHOU Xiu-hong; LIU Song-bai; GUO Yue-wei Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (+)-10(R)-isothiocyanatoalloaromadendrane ÏàËÆ¶È:70.5% Tetrahedron 1996 52 2359-2368 Terpenoids with antifouling activity against barnacle larvae from the marine sponge Acanthella cavernosa Hiroshi Hirota, Yasuhiko Tomono, Nobuhiro Fusetani Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (+)-muurolan-4,7-peroxide C15H26O2 ÏàËÆ¶È:64.7% Phytochemistry 2005 66 599-609 Sesquiterpene constituents from the essential oil of the liverwort Plagiochila asplenioides Adewale Martins Adio, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 2 ÏàËÆ¶È:64.7% Tetrahedron Letters 1995 36 6347-6350 Junicedranol, a sesquiterpene with a novel carbon skeleton from Juniperus oxycedrus ssp. macrocarpa Alejandro F. Barrero, Enrique Alvarez-Manzaneda, Armando Lara Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (+)-viridiflorol C15H26O ÏàËÆ¶È:64.7% Journal of the Brazilian Chemical Society 1990 1 105-109 Composition of the Essential Oil of Vassoura. Carmen Lucia Queiroga, Alberto Fukai and Anita J. Marsaioli Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 9b N-carbomethoxy derivative C12H25NO3 ÏàËÆ¶È:64.7% Canadian Journal of Chemistry 1996 74 2434-2443 A revised structure for the piperidine alkaloid andrachamine Sibel Mill, Claude Hootel¨¦ Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 5-methyl-8-hexadecyn-1-ol C17H32O ÏàËÆ¶È:64.7% Journal of Chemical Ecology 2000 26 987-1000 Synthesis and Biological Characterization of (Z)-9-Heptadecenoic and (Z)-6-Methyl-9-Heptadecenoic Acids: Fatty Acids with Antibiotic Activity Produced by Pseudozyma flocculosa T. J. Avis, R. R. Boulanger, R. R. B¨¦langer Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . phellinuin F C17H28O4 ÏàËÆ¶È:64.7% Natural Products and Bioprospecting 2014 4 21-25 Seven New Drimane-Type Sesquiterpenoids from Cultures of Fungus Phellinus tuberculosus Jiang-Bo He, Tao Feng, Shen Zhang, Ze-Jun Dong, Zheng-Hui Li, Hua-Jie Zhu and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . N-3',7'-dimethyloctyl-7-oxabicyclo[2.2.1]heptane-2,3-dicarboximide C18H29NO3 ÏàËÆ¶È:64.7% Molecules 2014 19 6911-6928 Synthesis of Novel Lipophilic N-Substituted Norcantharimide Derivatives and Evaluation of Their Anticancer Activities Jin-Yi Wu, Cheng-Deng Kuo, Chien-Yu Chu, Min-Shin Chen, Jia-Hua Lin, Yu-Jen Chen and Hui-Fen Liao Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . hinokiol ÏàËÆ¶È:63.1% Bioorganic & Medicinal Chemistry 2010 18 7940-7947 Biflavonoids from Torreya nucifera displaying SARS-CoV 3CLpro inhibition Young Bae Ryu, Hyung Jae Jeong, Jang Hoon Kim, Young Min Kim, Ji-Young Park, Doman Kim, Thi Thanh Hanh Naguyen, Su-Jin Park, Jong Sun Chang, Ki Hun Park, Mun-Chual Rho, Woo Song Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . N-3',7',11'-trimethyldodecyl-7-oxabicyclo[2.2.1]heptane-2,3-dicarboximide C23H39NO3 ÏàËÆ¶È:63.1% Molecules 2014 19 6911-6928 Synthesis of Novel Lipophilic N-Substituted Norcantharimide Derivatives and Evaluation of Their Anticancer Activities Jin-Yi Wu, Cheng-Deng Kuo, Chien-Yu Chu, Min-Shin Chen, Jia-Hua Lin, Yu-Jen Chen and Hui-Fen Liao Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (3S,4aR,6aR,7R,10aR,10bS)-3,10b-ethano-4,4,6a-trimethyl-3,4,4a,5,6,6a,7,8,9,10,10a,10b-dodecahydro-1H-naphto[1,2-c]pyran-3,7-diol C18H30O3 ÏàËÆ¶È:61.1% Tetrahedron 2012 68 9029-9034 First synthesis of decaturin C, an antiinsectant diterpenoid isolated from Penicillium thiersii Kimiharu Nakazaki, Kojiro Hayashi, Shintaro Hosoe, Takuya Tashiro, Masaki Kuse, Hirosato Takikawa Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ent-trachyloban-3¦Â-ol ÏàËÆ¶È:60% Planta Medica 2002 68 647-649 ent-Trachyloban-3¦Â-ol,a New Cytotoxic Diterpene from Croton zambesicus S.Block1,C.St¨¦vigny,M.-C.De Pauw-Gillet,E.de Hoffmann, G.Llabr¨¨s,V.Adjakidj¨¦,J.Quetin-Leclercq Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . ent-3-hydroxytrachylobane C20H32O ÏàËÆ¶È:60% 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 ̼Æ×Ä£Äâͼ 15 . Hinokiol ÏàËÆ¶È:60% Phytochemistry 1994 35 1279-1284 Abietanes and kauranes from leaves of Cryptomeria japonica Wen-Chiung Su, Jim-Min Fang, Yu-Shia Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Sapinsignoid F C20H36O2 ÏàËÆ¶È:60% Journal of Natural Products 2012 75 722-727 Cytotoxic Diterpenoids from Sapium insigne Hong-Bing Liu, Hua Zhang, Jin-Hai Yu, Cheng-Hui Xu, Jian Ding, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Blumeaene B C20H30O5 ÏàËÆ¶È:60% Planta Medica 2010 76 897-902 Blumeaenes A¨CJ, Sesquiterpenoid Esters from Blumea balsamifera with NO Inhibitory Activity Chen, Ming; Qin, Jiang-Jiang; Fu, Jian-Jun; Hu, Xiao-Jia; Liu, Xiao-Hua; Zhang, Wei-Dong; Jin, Hui-Zi Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (4R)-4-hydroxyisophytol ÏàËÆ¶È:60% Phytochemistry 1984 23 194-195 A linear diterpene diol from Lemna minor Lucio Previtera, Pietro Monaco Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 16¦Á-hydroxy-ent-kauran-19-oic acid ÏàËÆ¶È:60% 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 ̼Æ×Ä£Äâͼ 20 . comopound 2 ÏàËÆ¶È:60% 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 ̼Æ×Ä£Äâͼ 21 . conicumol ÏàËÆ¶È:58.8% Chemical & Pharmaceutical Bulletin 2000 48(8) 1190-1195 Ichthyotoxic Phloroglucinol Derivatives from Dryopteris fragrans and Their Anti-tumor Promoting Activity Hideyuki ITO,Takashi MURANAKA,Kazuko MORI,Zhe-Xiong JIN,Harukuni TOKUDA,Hoyoku NISHINO and Takashi YOSHIDA Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . ambreinolide-18-oic acid C17H26O4 ÏàËÆ¶È:58.8% Phytochemistry 2008 69 1005-1012 Secondary metabolites from the aerial parts of Salvia palaestina Bentham Giuseppina Cioffi, Ammar Bader, Anna Malafronte,Fabrizio Dal Piaz, Nunziatina De Tommasi Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 7-epi-eudesm-4(15)-ene-1¦Â,6¦Â-diol C15H26O2 ÏàËÆ¶È:58.8% Journal of Natural Products 2003 66 609-615 New Sesquiterpenes from Litsea verticillata Hong-Jie Zhang, Ghee Teng Tan, Bernard D. Santarsiero, Andrew D. Mesecar, Nguyen Van Hung, Nguyen Manh Cuong, D. Doel Soejarto, John M. Pezzuto, and Harry H. S. Fong Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 3-acetoxyspathulenol C17H26O3 ÏàËÆ¶È:58.8% Journal of Natural Products 2001 64 370-372 3-Acetoxyspathulenol, a New Aromadendrane-Type Natural Product from the Soft Coral Parerythropodium fulvum Matthias Wessels, Gabriele M. König, and Anthony D. Wright Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . pentacyclo[10,2,2,2 5,8 0 1,9,0 2.8]octadecane C18H28 ÏàËÆ¶È:58.8% Helvetica Chimica Acta 1980 63 1812-1822 Synthesis of 1-Bicyclo [3.2.2]nonene and 1 (7)-Bicyclo [3.2.2]nonene by Intramolecular Wittig Reaction Konrad B. Becker, Jacques L. Chappuis Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . 2,2,8,9,9-Pentadeuterio-3¦Á-hydroxy-d-homo-17a-oxa-5¦Á-androstan-17-one C19H25D5O3 ÏàËÆ¶È:58.8% Steroids 2003 68 85-96 A facile and high yielding synthesis of 2,2,3,4,4-d5-androsterone-¦Â--glucuronide¡ªan internal standard in dope analysis Peter Gärtner, Clemens Novak, Christian Einzinger, Wolfgang Felzmann, Max Knollm¨¹ller, G¨¹nter Gmeiner, Wilhelm Schänzer Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . compound 2a ÏàËÆ¶È:58.8% Natural Product Research 2000 14 447-452 (-)-Ledol from Calophyllum teysmanii: Structure and Stereochemistry Shu-Geng Cao; Keng-Yeow Sim; S. H. Goh Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . compound 2b ÏàËÆ¶È:58.8% Natural Product Research 2000 14 447-452 (-)-Ledol from Calophyllum teysmanii: Structure and Stereochemistry Shu-Geng Cao; Keng-Yeow Sim; S. H. Goh Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . 7-epi-eudesm-4(15)-ene-1',6¦Â-diol ÏàËÆ¶È:58.8% China Journal of Chinese Materia Medica 2009 34 1101-1103 Chemical constituents from air-dried Piper longum LIU Wenfeng, JIANG Zhiyong, CHEN Jijun, ZHANG Xuemei, MA Yunbao Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . (+)-ledol ÏàËÆ¶È:58.8% Phytochemistry 1997 44 1393-1395 Terpenoids from Salvia tchihatcheffii G¨¹laçti Topçu, Murat Kartal, Ayhan Ulubelen Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . compound 10b ÏàËÆ¶È:58.8% Phytochemistry 1996 42 159-162 Sesquiterpene alcohols from Chamaecyparis obtusa leaf oil Toshihiko Hieda, Masato Tazaki, Yukari Morishita, Takashi Aoki, Shizuo Nagahama Structure 13C NMR ̼Æ×Ä£Äâͼ |

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