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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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