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13C NMR  (cdcl3)

12.65,13.39,16.57,20.18,21.69,23.42,26.33,29.32,29.95,33.91,38.51,38.89,45.08,52.16,58.19,63.99,78.77,92.11,134.58,143.90,169.76,195.30

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1 .     (-)-(12E,2S,3S,4R,5R,6R,9S,11S,15R)-15-Acetoxy-5,6-epoxylathyr-12-en-3-ol-14-one
C22H32O5     ÏàËÆ¶È:100%
Journal of Natural Products          2011          74          1221-1229
Lathyrane Diterpenoids from the Roots of Euphorbia micractina and Their Biological Activities
Ye Tian, Wendong Xu, Chenggen Zhu, Sheng Lin, Yanru Li, Liang Xiong, Sujuan Wang, Ling Wang, Yongchun Yang, Ying Guo, Hua Sun, Xiaoliang Wang, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (-)-(12E,2S,3S,4R,5R,6R,9S,11S,15R)-3,15-Diacetoxy-5,6-epoxylathyr-12-en-14-one
C24H34O6     ÏàËÆ¶È:87.5%
Journal of Natural Products          2011          74          1221-1229
Lathyrane Diterpenoids from the Roots of Euphorbia micractina and Their Biological Activities
Ye Tian, Wendong Xu, Chenggen Zhu, Sheng Lin, Yanru Li, Liang Xiong, Sujuan Wang, Ling Wang, Yongchun Yang, Ying Guo, Hua Sun, Xiaoliang Wang, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     15-O-acetyl-3-O-iso-butyryljolkinol-5¦Â,6¦Â-oxide
    ÏàËÆ¶È:80.7%
Phytochemistry          1983          22          1791-1795
Lathyrane type diterpenoid esters from Euphorbia characias
Edgar H. Seip, Erich Hecker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (-)-(12E,2S,3S,4R,5R,6R,9S,11S,15R)-3-Acetoxy-5,6-epoxylathyr-12-en-15-ol-14-one
C22H32O5     ÏàËÆ¶È:72.7%
Journal of Natural Products          2011          74          1221-1229
Lathyrane Diterpenoids from the Roots of Euphorbia micractina and Their Biological Activities
Ye Tian, Wendong Xu, Chenggen Zhu, Sheng Lin, Yanru Li, Liang Xiong, Sujuan Wang, Ling Wang, Yongchun Yang, Ying Guo, Hua Sun, Xiaoliang Wang, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     latilagascene B
C29H36O6     ÏàËÆ¶È:66.6%
Planta Medica          2006          72          162-168
New Macrocyclic Lathyrane Diterpenes, from Euphorbia lagascae, as Inhibitors of Multidrug Resistance of Tumour Cells
No¨¦lia Duarte,Nora Gy¨¦m¨¢nt,Pedro M. Abreu,Joseph Moln¨¢r,Maria-Jos¨¦ U. Ferreira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (-)-(12E,2S,3S,4R,5R,6R,9S,11S,15R)-3-Acetoxy-15-benzoyloxy-5,6-epoxylathyr-12-en-14-one
C29H36O6     ÏàËÆ¶È:66.6%
Journal of Natural Products          2011          74          1221-1229
Lathyrane Diterpenoids from the Roots of Euphorbia micractina and Their Biological Activities
Ye Tian, Wendong Xu, Chenggen Zhu, Sheng Lin, Yanru Li, Liang Xiong, Sujuan Wang, Ling Wang, Yongchun Yang, Ying Guo, Hua Sun, Xiaoliang Wang, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (+)-(12E,2S,3S,4R,5R,6R,9S,11S,15R)-3-Benzoyloxy-5,6-epoxylathyr-12-en-15-ol-14-one
C27H34O5     ÏàËÆ¶È:60%
Journal of Natural Products          2011          74          1221-1229
Lathyrane Diterpenoids from the Roots of Euphorbia micractina and Their Biological Activities
Ye Tian, Wendong Xu, Chenggen Zhu, Sheng Lin, Yanru Li, Liang Xiong, Sujuan Wang, Ling Wang, Yongchun Yang, Ying Guo, Hua Sun, Xiaoliang Wang, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 4
C29H36O6     ÏàËÆ¶È:59.2%
Tetrahedron          2004          60          5025-5030
New tri- and tetracyclic diterpenes from Euphorbia villosa
Andrea Vasas, Judit Hohmann, Peter Forgo, P¨¢l Szab¨®
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     compound 4
C29H36O6     ÏàËÆ¶È:59.2%
Tetrahedron          2004          60          5025-5030
New tri- and tetracyclic diterpenes from Euphorbia villosa
Andrea Vasas, Judit Hohmann, Peter Forgo, P¨¢l Szab¨®
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     compound 14
    ÏàËÆ¶È:59.0%
European Journal of Organic Chemistry          1993          1993          491-495
Studies on the Constituents of the Stems of Tinospora tuberculata, IV. Isolation and Structure Elucidation of the Five New Furanoid Diterpene Glycosides Borapetoside C¨CG
Naomichi Fukuda, Michiko Yonemitsu and Takeatsu Kimura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     (-)-(5E,12E,2S,3S,4S,9S,11S,15R)-3,15-Diacetoxylathyra-5,12-dien-14-one
C24H34O5     ÏàËÆ¶È:58.3%
Journal of Natural Products          2011          74          1221-1229
Lathyrane Diterpenoids from the Roots of Euphorbia micractina and Their Biological Activities
Ye Tian, Wendong Xu, Chenggen Zhu, Sheng Lin, Yanru Li, Liang Xiong, Sujuan Wang, Ling Wang, Yongchun Yang, Ying Guo, Hua Sun, Xiaoliang Wang, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     rel-(3'R)-3',8'-dihydrotokinolide B
C24H30O4     ÏàËÆ¶È:56.5%
Natural Product Research          2011          Vol. 25, No. 13          1234-1242
Phthalides and other constituents from Ligusticum porteri; sedative and spasmolytic activities of some natural products and derivatives
Alejandra Le¨®n, Rub¨¦n A. Toscano, Jaime Tortoriello and Guillermo Delgado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     methyl 15-acetoxy(10),13E-ent-halimadien-18-oate
    ÏàËÆ¶È:56.5%
Phytochemistry          1987          26          1077-1079
Diterpenoids from halimium viscosum
L.G. Urones,J. De Pascual Teresa,L.S¨¢nchez Marcos,D. D¨ªez Mart¨ªn,N. Mart¨ªn Garrido,R.Alfayate Guerra
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     methyl-(13S,14S)-epoxy-15-acetoxy-1(10)-ent-halimen-18-oate
    ÏàËÆ¶È:56.5%
Phytochemistry          1990          29          1247-1251
ent-Halimane diterpenes from Halimium viscosum
Julio G. Urones,Isidro S¨¢nchez Marcos,MJos¨¦ Sexmero Cuadrado,Pilar Basabe,Anna M. Lithgow Bertelloni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     methyl-(13R,14R)-epoxy-15-acetoxy-1(10)-ent-halimen-18-oate
    ÏàËÆ¶È:56.5%
Phytochemistry          1990          29          1247-1251
ent-Halimane diterpenes from Halimium viscosum
Julio G. Urones,Isidro S¨¢nchez Marcos,MJos¨¦ Sexmero Cuadrado,Pilar Basabe,Anna M. Lithgow Bertelloni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     20-acetoxy-pinusolide
C23H32O6     ÏàËÆ¶È:56.5%
Phytochemistry          1985          24          2041-2046
Diterpenes from the seed of Sciadopitys verticillata
Shinichi Hasegawa, Yoshiyuki Hirose
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (22E)-24¦Á-methyl-ergost-6,22(23)-diene-5¦Á,8¦Á-epidioxy-3¦Â-ol
C28H44O3     ÏàËÆ¶È:55.5%
Indian Journal of Chemistry          1996          35B          806-809
Lipid constituents of marine sponge Suberites carnosus
Prabhu D Mishra, Solimabi Wahidulla, L D Souza & S Y Kamat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     (+)-(12E,2S,3S,4R,5R,6R,9S,11S,15R)-3-Cinnamoyloxy-5,6-epoxylathyr-12-en-15-ol-14-one
C29H36O5     ÏàËÆ¶È:55.5%
Journal of Natural Products          2011          74          1221-1229
Lathyrane Diterpenoids from the Roots of Euphorbia micractina and Their Biological Activities
Ye Tian, Wendong Xu, Chenggen Zhu, Sheng Lin, Yanru Li, Liang Xiong, Sujuan Wang, Ling Wang, Yongchun Yang, Ying Guo, Hua Sun, Xiaoliang Wang, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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2Â¥2013-07-22 19:38:57
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