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frp-11 氘代甲醇 10.01,12.65,13.00,18.86,20.45,22.63,23.55,28.74,30.22,30.32,34.17,38.78,43.05,46.45,46.65,62.77,65.26,67.70,78.66,99.52,101.37,128.22,128.47,129.16,129.78,130.95,131.01,132.96,166.25,167.94,211.04 |
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查询模式：模糊查询 碳谱数据输入： 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97个化合物(查询结果仅供参考) 1 . 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 碳谱模拟图 2 . 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 碳谱模拟图 3 . 2,3-dihydro-3-hydroxywithacnistine 相似度:54.8% Phytochemistry 1993 34 517-521 Withanolides from Iochroma coccineum Dorothée Alfonso, Gérald Bernardinelli, Ilias Kapetanidis Structure 13C NMR 碳谱模拟图 4 . 2-(2-ethylhexyl)-4-(2-ethyl hexyloxy)-6-phenyl-3-(2-thienyl)pyrrolo[3,4-c]pyrrol-1(2H)-one 相似度:54.8% Tetrahedron Letters 2011 52 5769-5773 O- and N-alkylated diketopyrrolopyrrole derivatives Štĕpán Frebort, Zdenĕk Eliáš , Antonín Lyčk,Stanislav Luňák Jr., Jan Vyňuchal,Lubomír Kubáč, Radim Hrdina , Ladislav Burgert Structure 13C NMR 碳谱模拟图 5 . compound 2 C28H38O6 相似度:54.8% Tetrahedron 2007 63 8174-8180 Musanahol: a new aureonitol-related metabolite from a Chaetomium sp. Ruchi G. Marwah, Majekodunmi O. Fatope, Mike L. Deadman, Yousif Mohammed Al-Maqbali, John Husband Structure 13C NMR 碳谱模拟图 6 . 5-(n-butyl)-10-(tert-butyl)porphyrin C28H30N4 相似度:54.8% European Journal of Organic Chemistry 2010 237-258 Synthesis of meso-Substituted ABCD-Type Porphyrins by Functionalization Reactions Mathias O. Senge, Yasser M. Shaker, Monica Pintea, Claudia Ryppa, Sabine S. Hatscher, Aoife Ryan and Yulia Sergeeva Structure 13C NMR 碳谱模拟图 7 . benzyl 3α-hydroxy-6-ethyliden-7-keto-5β-cholan-24-oate C33H46O4 相似度:54.8% 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 碳谱模拟图 8 . euphoractin F C27H36O6 相似度:54.8% Journal of Natural Products 2013 76 1039-1046 Diterpenoids with Diverse Skeletons from the Roots of Euphorbia micractina Ye Tian, Wendong Xu, Chenggen Zhu, Sheng Lin, Ying Guo, and Jiangong Shi Structure 13C NMR 碳谱模拟图 9 . scutebata Q C34H38O8 相似度:54.8% Journal of Asian Natural Products Research 2013 15 941-949 Bioassay-guided isolation of neo-clerodane diterpenoids from Scutellaria barbata Yuan-Yuan Li, Xu-Li Tang, Tao Jiang, Pei-Fen Li, Ping-Lin Li & Guo-Qiang Li Structure 13C NMR 碳谱模拟图 10 . (+)-(3aS,5aR,8E,10aR)-8-(tert-butyldiphenylsilyloxymethyl)-2,3,3a,4,5,5a,6,7,10,10a-decahydro-1-isopropyl-5a-methyl-6-oxocyclohepta[e]indene-3a-carbaldehyde C36H46O3Si 相似度:54.8% Angewandte Chemie International Edition 2013 52 7569-7573 Total Syntheses of (−  -Scabronines G and A, and (−-Episcabronine AYu Kobayakawa and Prof. Masahisa Nakada Structure 13C NMR 碳谱模拟图 11 . compound 34 C40H48O8 相似度:54.2% 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 碳谱模拟图 12 . 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 碳谱模拟图 |
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