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jessiegao07金虫 (小有名气)
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[求助]
微谱数据求助，非常感谢
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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 非常非常感谢！ |
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wangkaibo123
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jessiegao07: 金币+10, ★★★★★最佳答案, 非常非常感谢！ 2013-07-22 19:55:30
感谢参与，应助指数 +1
jessiegao07: 金币+10, ★★★★★最佳答案, 非常非常感谢！ 2013-07-22 19:55:30
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按从小到大顺序输入，数字间用英文半角逗号(,)分隔例如： 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 溶剂选项： 匹配容差： (数字格式，可自行设定) 相似度： %(相似度>=50%) 查询结果：共查到380个化合物(查询结果仅供参考) 1 . (-)-(12E,2S,3S,4R,5R,6R,9S,11S,15R)-15-Acetoxy-5,6-epoxylathyr-12-en-3-ol-14-one C22H32O5 相似度: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 碳谱模拟图 2 . (-)-(12E,2S,3S,4R,5R,6R,9S,11S,15R)-3,15-Diacetoxy-5,6-epoxylathyr-12-en-14-one C24H34O6 相似度: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 碳谱模拟图 3 . 15-O-acetyl-3-O-iso-butyryljolkinol-5β,6β-oxide 相似度:80.7% Phytochemistry 1983 22 1791-1795 Lathyrane type diterpenoid esters from Euphorbia characias Edgar H. Seip, Erich Hecker Structure 13C NMR 碳谱模拟图 4 . (-)-(12E,2S,3S,4R,5R,6R,9S,11S,15R)-3-Acetoxy-5,6-epoxylathyr-12-en-15-ol-14-one C22H32O5 相似度: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 碳谱模拟图 5 . latilagascene B C29H36O6 相似度:66.6% Planta Medica 2006 72 162-168 New Macrocyclic Lathyrane Diterpenes, from Euphorbia lagascae, as Inhibitors of Multidrug Resistance of Tumour Cells Noélia Duarte,Nora Gyémánt,Pedro M. Abreu,Joseph Molnár,Maria-José U. Ferreira Structure 13C NMR 碳谱模拟图 6 . (-)-(12E,2S,3S,4R,5R,6R,9S,11S,15R)-3-Acetoxy-15-benzoyloxy-5,6-epoxylathyr-12-en-14-one C29H36O6 相似度: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 碳谱模拟图 7 . (+)-(12E,2S,3S,4R,5R,6R,9S,11S,15R)-3-Benzoyloxy-5,6-epoxylathyr-12-en-15-ol-14-one C27H34O5 相似度: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 碳谱模拟图 8 . compound 4 C29H36O6 相似度:59.2% Tetrahedron 2004 60 5025-5030 New tri- and tetracyclic diterpenes from Euphorbia villosa Andrea Vasas, Judit Hohmann, Peter Forgo, Pál Szabó Structure 13C NMR 碳谱模拟图 9 . compound 4 C29H36O6 相似度:59.2% Tetrahedron 2004 60 5025-5030 New tri- and tetracyclic diterpenes from Euphorbia villosa Andrea Vasas, Judit Hohmann, Peter Forgo, Pál Szabó Structure 13C NMR 碳谱模拟图 10 . compound 14 相似度: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–G Naomichi Fukuda, Michiko Yonemitsu and Takeatsu Kimura Structure 13C NMR 碳谱模拟图 11 . (-)-(5E,12E,2S,3S,4S,9S,11S,15R)-3,15-Diacetoxylathyra-5,12-dien-14-one C24H34O5 相似度: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 碳谱模拟图 12 . rel-(3'R)-3',8'-dihydrotokinolide B C24H30O4 相似度: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 León, Rubén A. Toscano, Jaime Tortoriello and Guillermo Delgado Structure 13C NMR 碳谱模拟图 13 . methyl 15-acetoxy(10),13E-ent-halimadien-18-oate 相似度:56.5% Phytochemistry 1987 26 1077-1079 Diterpenoids from halimium viscosum L.G. Urones,J. De Pascual Teresa,L.Sánchez Marcos,D. Díez Martín,N. Martín Garrido,R.Alfayate Guerra Structure 13C NMR 碳谱模拟图 14 . methyl-(13S,14S)-epoxy-15-acetoxy-1(10)-ent-halimen-18-oate 相似度:56.5% Phytochemistry 1990 29 1247-1251 ent-Halimane diterpenes from Halimium viscosum Julio G. Urones,Isidro Sánchez Marcos,MJosé Sexmero Cuadrado,Pilar Basabe,Anna M. Lithgow Bertelloni Structure 13C NMR 碳谱模拟图 15 . methyl-(13R,14R)-epoxy-15-acetoxy-1(10)-ent-halimen-18-oate 相似度:56.5% Phytochemistry 1990 29 1247-1251 ent-Halimane diterpenes from Halimium viscosum Julio G. Urones,Isidro Sánchez Marcos,MJosé Sexmero Cuadrado,Pilar Basabe,Anna M. Lithgow Bertelloni Structure 13C NMR 碳谱模拟图 16 . 20-acetoxy-pinusolide C23H32O6 相似度:56.5% Phytochemistry 1985 24 2041-2046 Diterpenes from the seed of Sciadopitys verticillata Shinichi Hasegawa, Yoshiyuki Hirose Structure 13C NMR 碳谱模拟图 17 . (22E)-24α-methyl-ergost-6,22(23)-diene-5α,8α-epidioxy-3β-ol C28H44O3 相似度: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 碳谱模拟图 18 . (+)-(12E,2S,3S,4R,5R,6R,9S,11S,15R)-3-Cinnamoyloxy-5,6-epoxylathyr-12-en-15-ol-14-one C29H36O5 相似度: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 碳谱模拟图 |
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