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FRP-11 C谱图数据如下:10.01,12.65,13.00,18.86,20.45,22.63,23.55,28.74,30.22,30.32,34.17,38.78,43.05,46.45,46.69,47.17,47.60,62.77,65.26,67.70,78.66,99.52,101.37,128.22,128.47,129.16,129.78,130.95,131.01,132.96,166.26,167.94,211.04 试剂氘代甲醇 版主我尽力改了,每次都扣分桑心 |
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lifeliuyan
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bababa416: 金币+8, ★★★★★最佳答案 2014-04-10 12:16:10
感谢参与,应助指数 +1
bababa416: 金币+8, ★★★★★最佳答案 2014-04-10 12:16:10
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查询结果:共查到79个化合物(查询结果仅供参考) 1 . compound 34 C40H48O8 相似度:60% Bioorganic & Medicinal Chemistry 2012 20 3016-3030 Synthesis and cytotoxic activity evaluation of dihydrocucurbitacin B and cucurbitacin B derivatives Karen Luise Lang, Izabella Thaís Silva, Lara Almida Zimmermann, Vanessa Rocha Machado, Marina Rodrigues Teixeira, María Ivana Lapuh, Mariana Alejandra Galetti, Jorge Alejandro Palermo, Gabriela Myriam Cabrera, Lílian Sibelle Campos Bernardes, Cláudia Mari Structure 13C NMR Structure & 13C NMR 碳谱模拟图 2 . Orthoarisin F C38H46O11 相似度:58.8% Phytochemistry Letters 2013 6 412-417 Diterpenoids from the aerial parts of Orthosiphon aristatus var. aristatus Xia-Xia Di, Shu-Qi Wang, Xue-Liang Zhang, Bo Wang, Hong-Xiang Lou, Xiao-Ning Wang Structure 13C NMR Structure & 13C NMR 碳谱模拟图 3 . 17-benzoyloxy-3-O-(2,3-dimethylbutanoyl)-13-(2,3-dimethylbutanoyloxy)-20-deoxyingenol C39H52O9 相似度:56.7% Phytochemistry 2008 69 812-819 Ingenane diterpenoids from Euphorbia esula Zhi-Qiang Lu, Min Yang, Jin-Qiang Zhang, Guang-Tong Chen, Hui-Lian Huang,Shu-Hong Guan, Chao Ma, Xuan Liu, De-An Guo Structure 13C NMR Structure & 13C NMR 碳谱模拟图 4 . compound 30 C38H42O7 相似度:55.8% Bioorganic & Medicinal Chemistry 2012 20 3016-3030 Synthesis and cytotoxic activity evaluation of dihydrocucurbitacin B and cucurbitacin B derivatives Karen Luise Lang, Izabella Thaís Silva, Lara Almida Zimmermann, Vanessa Rocha Machado, Marina Rodrigues Teixeira, María Ivana Lapuh, Mariana Alejandra Galetti, Jorge Alejandro Palermo, Gabriela Myriam Cabrera, Lílian Sibelle Campos Bernardes, Cláudia Mari Structure 13C NMR Structure & 13C NMR 碳谱模拟图 5 . Orthoarisin G C38H44O11 相似度:55.8% Phytochemistry Letters 2013 6 412-417 Diterpenoids from the aerial parts of Orthosiphon aristatus var. aristatus Xia-Xia Di, Shu-Qi Wang, Xue-Liang Zhang, Bo Wang, Hong-Xiang Lou, Xiao-Ning Wang Structure 13C NMR Structure & 13C NMR 碳谱模拟图 6 . orthosiphol X C36H42O10 相似度:54.5% Journal of Natural Products 2003 66 255-258 Nitric Oxide Inhibitory Isopimarane-type Diterpenes from Orthosiphon stamineus of Indonesia Suresh Awale, Yasuhiro Tezuka, Arjun H. Banskota, I Ketut Adnyana, and Shigetoshi Kadota Structure 13C NMR Structure & 13C NMR 碳谱模拟图 7 . orthosiphol N C36H40O10 相似度:54.5% Journal of Natural Products 2001 64 592-596 Five Novel Highly Oxygenated Diterpenes of Orthosiphon stamineus from Myanmar Suresh Awale,Yasuhiro Tezuka,Arjun H. Banskota, Kyoji Kouda, Kyaw Myint Tun, and Shigetoshi Kadota Structure 13C NMR Structure & 13C NMR 碳谱模拟图 8 . 3β-hydroxy-5α,14β-cholest-16-en-15-one 3β-benzoate 相似度:54.5% Bioorganic & Medicinal Chemistry 1995 3 367-374 Chemical synthesis of 15-ketosterols and their inhibitions of cholesteryl ester transfer protein Hong-Seok Kim, Sang Ho Oh, Dong-Il Kim, In-Chul Kim, Kyung-Hyun Cho, Yong Bok Park Structure 13C NMR Structure & 13C NMR 碳谱模拟图 9 . 3-benzoateerythralosamine 相似度:54.5% Bioorganic & Medicinal Chemistry 1995 3 587-604 Conformational change due to esterification of hydroxy groups in erythromycin A and its major metabolite: Analysis of these derivatives with different biological properties using NMR and Molecular Dynamics (MD) data Patrick Ladam, Josyane Gharbi-Benarous, Marcel Delaforge, Marie-Rose Van Calsteren, Christophe K. Jankowski, Jean-Pierre Girault Structure 13C NMR Structure & 13C NMR 碳谱模拟图 10 . orthosipol T C38H44O12 相似度:54.5% Tetrahedron 2002 58 5503-5512 Norstaminane- and isopimarane-type diterpenes of Orthosiphon stamineus from Okinawa Suresh Awale, Yasuhiro Tezuka, Arjun H Banskota, Seikichi Shimoji, Kazuhiko Taira, Shigetoshi Kadota Structure 13C NMR Structure & 13C NMR 碳谱模拟图 11 . benzyl 3α-hydroxy-6-ethyliden-7-keto-5β-cholan-24-oate C33H46O4 相似度:54.5% Journal of Medicinal Chemistry 2012 55 84-93 Conicasterol E, a Small Heterodimer Partner Sparing Farnesoid X Receptor Modulator Endowed with a Pregnane X Receptor Agonistic Activity, from the Marine Sponge Theonella swinhoei Valentina Sepe, Raffaella Ummarino, Maria Valeria D’Auria, Maria Giovanna Chini, Giuseppe Bifulco, Barbara Renga, Claudio D’Amore, Cécile Debitus, Stefano Fiorucci, and Angela Zampella Structure 13C NMR Structure & 13C NMR 碳谱模拟图 12 . (22S,25R)-3β-hydroxy-16β-acetoxy-22,26-N-Cbz-epimino-cholestan-5,6-oxido-4-one 相似度:54.2% Journal of Natural Products 1992 Vol 55 1178 On the Synthesis of 4-Keto-Steroidal Alkaloids Elizabeth Viloria, Gina Meccia, Alfredo N. Usubillaga Structure 13C NMR Structure & 13C NMR 碳谱模拟图 13 . methyl 3a-benzoyloxy-4β,7α-dibenzyloxymethoxy-5α-cholan-24-oate 相似度:54.2% Tetrahedron 2004 60 6971-6980 Synthesis and identification of an endogenous sperm activating and attracting factor isolated from eggs of the ascidian Ciona intestinalis; an example of nanomolar-level structure elucidation of novel natural compound Tohru Oishi, Hiroshi Tsuchikawa, Michio Murata, Manabu Yoshida, Masaaki Morisawa Structure 13C NMR Structure & 13C NMR 碳谱模拟图 14 . marinisporolide C C38H58O10 相似度:54.2% The Journal of Organic Chemistry 2009 74 675-684 Marinisporolides, Polyene-Polyol Macrolides from a Marine Actinomycete of the New Genus Marinispora Hak Cheol Kwon, Christopher A. Kauffman, Paul R. Jensen and William Fenical Structure 13C NMR Structure & 13C NMR 碳谱模拟图 |
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