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1 .     (+)-(4R,5S,7R)-11,12-Dihydroxynootkatone
    ÏàËÆ¶È:60%
Bioorganic & Medicinal Chemistry          2011          19          2464-2469
Microbial transformation of (+)-nootkatone and the antiproliferative activity of its metabolites
Anna Gliszczy¨½ska, Agnieszka Łysek, Tomasz Janeczko, Marta Świtalska,Joanna Wietrzyk, Czesław Wawrze¨½czyk
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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2 .     rishitinone
C15H24O2     ÏàËÆ¶È:60%
Bulletin of the Chemical Society of Japan          1982          55          2428-2433
Structure of Rishitinone, a Valencane Stress Metabolite in Diseased Potato
Nobukatsu Katsui, Fujio Yagihashi, Akio Murai, Tadashi Masamune
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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3 .     3¦Á,8¦Á-Dihydroxypathoulol
C15H26O3     ÏàËÆ¶È:60%
Helvetica Chimica Acta          2011          94          218-223
New Patchoulol-Type Sesquiterpenoids from Pogostemon cablin
Lei Zhou, Min Xu, Chong-Ren Yang, Yi-Fei Wang and Ying-Jun Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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4 .     1-naphthalene acetic-7-oxo-1,2,3,4,4a,7,8,8a-octahydro-1,2,4a,5-tetramethyl acid
C16H24O3     ÏàËÆ¶È:56.2%
Phytochemistry          1992          31          1823-1825
Tetranorditerpenes from Detarium microcarpum
Rita Aquino, Maria Letizia Ciavatta, Nunziatina De Tommasi, Eszter G¨¤cs-Baitz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     tessaric acid
C15H20O3     ÏàËÆ¶È:53.3%
Journal of Natural Products          2003          66          1078-1081
Eudesmane Derivatives and Other Sesquiterpenes from Laggera alata
Qun Xiong Zheng,Zhao Jun Xu,Xian Feng Sun,Françoise Gu¨¦ritte,Michele Cesario, Han Dong Sun,Christopher H. K. Cheng,Xiao-Jiang Hao,and Yu Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     8¦Â-hydroxyprespatane
C15H24O     ÏàËÆ¶È:53.3%
Journal of Natural Products          2007          70          1449-1453
Sesquiterpenoids and Artificial 19-Oxygenated Steroids from the Formosan Soft Coral Nephthea erecta
Shi-Yie Cheng,Chang-Feng Dai, and Chang-Yih Duh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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7 .     (4R*,5R*,7S*,10R*)-4-formamidoeudesm-11-ene
C16H27NO     ÏàËÆ¶È:53.3%
Journal of Natural Products          2002          65          851-855
New Nitrogenous Eudesmane-Type Compounds Isolated from the Caribbean Sponge Axinyssa ambrosia
Natalia V. Petrichtcheva,Carmenza Duque, Adriana Dueñas, Sven Zea, Noriyuki Hara,and Yoshinori Fujimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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8 .     oxyphyllol B
C15H22O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          2002          65          1468-1474
Absolute Stereostructures of Three New Sesquiterpenes from the Fruit of Alpinia oxyphylla with Inhibitory Effects on Nitric Oxide Production and Degranulation in RBL-2H3 Cells1
Toshio Morikawa, Hisashi Matsuda, Iwao Toguchida, Kazuho Ueda, and Masayuki Yoshikawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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9 .     (8R)-8-hydroxypatchoulol
C15H26O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          1999          62          437-440
Biotransformation of the Fungistatic Sesquiterpenoid Patchoulol by Botrytis cinerea
Josefina Aleu, James R. Hanson, Rosario Hern¨¢ndez Gal¨¢n, and Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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10 .     compound 18
C15H26O     ÏàËÆ¶È:53.3%
Journal of Natural Products          1998          61          22-28
Enantioselective Total Syntheses of (-)-7¦ÂH-Eudesmane-4¦Á, 11-diol and (+)-ent-7¦ÂH-Eudesmane-4¦Á, 11-diol
Fumito Shimoma, Hisao Kondo, Saori Yuuya, Toshio Suzuki, Hisahiro Hagiwara, and Masayoshi Ando
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

11 .     chiloscypha-2,7,9-trione
C15H18O3     ÏàËÆ¶È:53.3%
Journal of Natural Products          1997          60          1281-1286
Bioactive and Other Sesquiterpenes from Chiloscyphus rivularis
Chongming Wu, A. A. Leslie Gunatilaka, Francis L. McCabe, Randall K. Johnson, Richard W. Spjut, and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

12 .     eremophilanoid
C15H20O3     ÏàËÆ¶È:53.3%
Chinese Chemical Letters          2003          14          393-396
New Eudesmane and Eremophilane Derivatives from Laggera Alata
Qun Xiong ZHENG, Zhao Jun XU, Xian Feng SUN, Françoise GUÉRITTE,Michele CESARIO, Christopher H.K. CHENG, Han Dong SUN, Yu ZHAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

13 .     ent-kauran-16¦Â-ol
C20H34O     ÏàËÆ¶È:53.3%
Journal of Asian Natural Products Research          2004          6          29-34
STRUCTURAL ELUCIDATION OF FRITILLAHUPEHIN FROM BULBS OF FRITILLARIA HUPEHENSIS HSIAO ET K.C. HSIA
YONG-HUI ZHANG, HAN-LI RUAN, HUI-FANG PI, JI-ZHOU WU,HAN-DONG SUNb and TETSURO FUJITA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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14 .     3¦Â,4¦Á-dihydroxy-7-epi-eudesm-11(13)-ene
C15H26O2     ÏàËÆ¶È:53.3%
Phytochemistry          1998          49          2421-2424
Eudesmane derivatives from Laggera crispata and Pluchea carolonesis
Ahmed A. Ahmed, Hesham R. El-Seedi, Ahmed A. Mahmoud, Abd El-Aziz A. El-Douski, Ibrahim F. Zeid, Lars Bohlin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

15 .     8¦Á,11-dihydroxy-5-epi-eremophil-1(10)-en-2-one
    ÏàËÆ¶È:53.3%
Phytochemistry          1992          31          863-880
Sesquiterpene lactones and other constituents from Ursinia species
J. Jakupovic, U. Ganzer, P. Pritschow, L. Lehmann, F. Bohlmann, R.M. King
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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16 .     (+)-nootkatone
    ÏàËÆ¶È:53.3%
Bioorganic & Medicinal Chemistry          2011          19          2464-2469
Microbial transformation of (+)-nootkatone and the antiproliferative activity of its metabolites
Anna Gliszczy¨½ska, Agnieszka Łysek, Tomasz Janeczko, Marta Świtalska,Joanna Wietrzyk, Czesław Wawrze¨½czyk
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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17 .     (+)-(4R,5S,7R,11S)-11,12-epoksynootkatone
    ÏàËÆ¶È:53.3%
Bioorganic & Medicinal Chemistry          2011          19          2464-2469
Microbial transformation of (+)-nootkatone and the antiproliferative activity of its metabolites
Anna Gliszczy¨½ska, Agnieszka Łysek, Tomasz Janeczko, Marta Świtalska,Joanna Wietrzyk, Czesław Wawrze¨½czyk
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

18 .     nootkatone
    ÏàËÆ¶È:53.3%
Phytochemistry          1987          26          571-572
A valencane sesquiterpenoid from Teucrium carolipaui
Giuseppe Savona,Franco Piozzi,Mar¨ªa C. De La Torre,Orietta Servettaz,Benjam¨ªn Rodr¨ªguez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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19 .     compound 2a
    ÏàËÆ¶È:53.3%
Phytochemistry          1987          26          1755-1757
Sesquiterpene lactols from Laserpitium halleri
Giovanni Appendino,Maria Grazia Valle,Pierluigi Gariboldi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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20 .     (4R,5S,7R,10S)-eudesm-11-en-4-ol
    ÏàËÆ¶È:53.3%
Phytochemistry          1990          29          3207-3211
Eudesmane glycosides from Carthamus lanatus
Arturo San Feliciano,Manuel Medarde,Benedicto Del Rey,Jose M. Miguel Del Corral,Alejandro F. Barrero
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

21 .     (-)-solavetivone
C15H22O2     ÏàËÆ¶È:53.3%
Chemical Communications          1977                   27-28
Vetispirane sesquiterpene glucosides from flue-cured virginia tobacco: structure, absolute stereochemistry, and synthesis. X-Ray structure of the p-bromobenzenesulphonate of one of the derived aglycones
Robert C. Anderson, Donald M. Gunn, Judith Murray-Rust, Peter Murray-Rust and James S. Roberts
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

22 .     oleodaphnone
C15H18O2     ÏàËÆ¶È:53.3%
Natural Product Research and Development          2009          21          733-736
Chemical Constituents from the Aerial Parts of Daphne bholua
CHEN Hu-hai;ZHANG Wei-dong;SU Juan; CHEN Yu-qi; SHEN Yun-heng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

23 .     Halichonadin D
C15H27N     ÏàËÆ¶È:53.3%
Tetrahedron          2005          61          1101-1105
Halichonadins A¨CD, new sesquiterpenoids from a sponge Halichondria sp.
Haruaki Ishiyama, Amane Hashimoto, Jane Fromont, Yasutaka Hoshino, Yuzuru Mikami, Jun'ichi Kobayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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24 .     epi-rosulantol
C15H24O2     ÏàËÆ¶È:53.3%
Tetrahedron          1999          55          9117-9132
New acorane- and cuparane-type sesqui- and new labdane- and seco-labdanne-type diterpenoids from the Japanese liverwort Jungermannia infusca (Mitt.) Steph.
Fumihiro Nagashima, Makoto Suzuki, Shigeru Takaoka, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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25 .     acanthene C
C16H27NO     ÏàËÆ¶È:53.3%
Tetrahedron          1993          49          4503-4510
Acanthenes A to C: a chloro, isothiocyanate, formamide sesquiterpene triad isolated from the Northeastern Pacific marine sponge Acanthella sp. and the dorid nudibranch Cadlina luteomarginata
David L. Burgoyne, Eric J. Dumdei, Raymond J. Andersen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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26 .     (1R*,3R*)-3-[4-(1,1-dimethylbutyl)phenyl]cyclohexanol
C18H28O     ÏàËÆ¶È:53.3%
Bioorganic & Medicinal Chemistry          2008          16          322-335
Synthesis and pharmacology of 1-deoxy analogs of CP-47,497 and CP-55,940
John W. Huffman, Alicia L.S. Thompson, Jenny L. Wiley, Billy R. Martin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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27 .     (6S*,7S*)-3-norhimachal-1-en-3-one
    ÏàËÆ¶È:53.3%
Natural Product Communications          2008          3          1755-1758
21,28-Epoxy-18¦Â,21¦Â-dihydroxbaccharan-3-one and OtherTerpenoids from the Liverwort Lepidozia chordulifera T. Taylor
Hildegard Zapp, Kerstin Orth, Josef Zapp, Joseph D. Connolly, and Hans Becker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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28 .     Androst-4-ene-3,6-dione
    ÏàËÆ¶È:52.6%
Steroids          2006          71          30-33
An efficient one-pot synthesis generating 4-ene-3,6-dione functionalised steroids from steroidal 5-en-3¦Â-ols using a modified Jones oxidation methodology
A. Christy Hunter, Shelley-Marie Priest
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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29 .     2-oxoclerod-3-en-15-oic acid
    ÏàËÆ¶È:50%
Helvetica Chimica Acta          2003          Vol. 86          3187
Dinorditerpene, Diterpenes, Alkaloids, and Coumarins from Clausena dunniana
Hong-Ping He, Yue-Mao Shen, Guo-Ying Zuo, Xiao-Sheng Yang, and Xiao-Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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30 .     methyl 3-oxoartemisinate structure
C16H22O3     ÏàËÆ¶È:50%
Planta Medica          1996          62          359-360
Production of Methyl 3-Oxoartemisinate from Methyl Artemisinate by Suspension Cell Culture of Mentha piperita
Soo-Un Kim and Hyung-Jin Kwon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

31 .     compound 24a
    ÏàËÆ¶È:50%
Organic & Biomolecular Chemistry          2011          9          2156-2165
Substrate specificity of Rv3378c, an enzyme from Mycobacterium tuberculosis, and the inhibitory activity of the bicyclic diterpenoids against macrophage phagocytosis
Tsutomu Hoshino, Chiaki Nakano, Takahiro Ootsuka, Yosuke Shinohara and Takashi Hara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

32 .     compound 24b
    ÏàËÆ¶È:50%
Organic & Biomolecular Chemistry          2011          9          2156-2165
Substrate specificity of Rv3378c, an enzyme from Mycobacterium tuberculosis, and the inhibitory activity of the bicyclic diterpenoids against macrophage phagocytosis
Tsutomu Hoshino, Chiaki Nakano, Takahiro Ootsuka, Yosuke Shinohara and Takashi Hara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

33 .     compound 26a+b
    ÏàËÆ¶È:50%
Organic & Biomolecular Chemistry          2011          9          2156-2165
Substrate specificity of Rv3378c, an enzyme from Mycobacterium tuberculosis, and the inhibitory activity of the bicyclic diterpenoids against macrophage phagocytosis
Tsutomu Hoshino, Chiaki Nakano, Takahiro Ootsuka, Yosuke Shinohara and Takashi Hara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

34 .     Tricalysione A
C18H26O3     ÏàËÆ¶È:50%
Tetrahedron          2007          63          4558-4562
Three new diterpenoids, tricalysiolide H and tricalysiones A and B, from Tricalysia dubia
Koichi Nishimura, Yukio Hitotsuyanagi, Kei-ichi Sakakura, Kazuya Fujita, Shigeki Tachihara, Haruhiko Fukaya, Yutaka Aoyagi, Tomoyo Hasuda, Takeshi Kinoshita, Koichi Takeya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

35 .     Halichonadin A
C31H52N2O     ÏàËÆ¶È:50%
Tetrahedron          2005          61          1101-1105
Halichonadins A¨CD, new sesquiterpenoids from a sponge Halichondria sp.
Haruaki Ishiyama, Amane Hashimoto, Jane Fromont, Yasutaka Hoshino, Yuzuru Mikami, Jun'ichi Kobayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

36 .     4-phenyl-N-propyl-2-(propylamino)cyclopent-1-enecarboxamide
C18H26N2O     ÏàËÆ¶È:50%
Tetrahedron          2012          68          2496-2508
Efficient one-pot synthesis of cyclic ¦Â-enaminoamides by thermal Wolff rearrangement of cyclic 2-diazo-1,3-dicarbonyls and conversion to uracil derivatives
Pratik Neupane, Xin Li, Jae Hak Jung, Yong Rok Lee, Sung Hong Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

37 .     (1R,3E,7E,11S,12S)-3,7,18-Dolabellatriene
C20H32     ÏàËÆ¶È:50%
Journal of Natural Products          2011          74          213-222
Dolabellanes with Antibacterial Activity from the Brown Alga Dilophus spiralis
Efstathia Ioannou, Antonio Quesada, M. Mukhlesur Rahman, Simon Gibbons, Constantinos Vagias, and Vassilios Roussis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2012-06-16 12:01:39
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