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[求助]
微谱求助化合物结构
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| 6.53,8.37,11.75,17.20,23.53,78.05,102.15,108.93,110.85,115.48,116.00,120.07,137.01,140.05,150.64,158.02,160.96,163.74,169.99 |
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查询结果：共查到10个化合物(查询结果仅供参考) -------------------------------------------------------------------------------- 1 . Hypotrachynic acid C18H16O7 相似度:52.6% Molecules 2007 12 997-1005 β-Orcinol Metabolites from the Lichen Hypotrachyna revoluta Panagiota Papadopoulou, Olga Tzakou, Constantinos Vagias, Panagiotis Kefalas and Vassilios Roussis Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 2 . 3-formyl-2,4-dihydroxy-6-methylbenzoic acid 3-hydroxy-4-(methoxycarbonyl)-2,5-di-methylphenyl ether 相似度:52.6% Fitoterapia 2001 72 565-567 Antifungal constituent from Gordonia dassanayakei P.S. Athukoralage, H.M.T.B. Herath,S.A. Deraniyagala, R.L.C ijesundera,P.A. Weerasinghe Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 3 . cladonioidesin 相似度:52.6% Fitoterapia 2001 72 832-833 Constituents from Lethariella cladonioides Bei Jiang, Qin-Shi Zhao, Hui Yang, Ai-Jun Hou,Zhong-Wen Lin, Han-Dong Sun Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 4 . 3-hydroxy-2,4,5-trimethylphenyl 2,4-dihydroxy-3,6-dimethylbenzoate C18H20O5 相似度:52.6% Helvetica Chimica Acta 2011 94 1077-1084 Antimicrobial Depsides Produced by Cladosporium uredinicola, an Endophytic Fungus Isolated from Psidium guajava Fruits Lívia Soman de Medeiros, Michael Murgu, Antônia Q. L. de Souza, and Edson Rodrigues-Fo. Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 5 . atranorin 相似度:52.6% Phytochemical Analysis 1999 10 279-284 1H and 13C-NMR and biological activity investigations of four lichen-derived compounds Gabriele M. König and Anthony D. Wright Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 6 . atranorin 相似度:52.6% Chemical & Pharmaceutical Bulletin 2013 69 176-183 Cytotoxic Evaluation of Phenolic Compounds from Lichens against Melanoma Cells Luiz Fabrício Gardini Brandão, Glaucia Braz Alcantara, Maria de Fátima Cepa Matos, Danielle Bogo, Deisy dos Santos Freitas, Nathália Mitsuko Oyama, Neli Kika Honda Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 7 . atranorin 相似度:52.6% Journal of Chemical Ecology 2003 29 2049-2071 Identification and Quantitation of Allelochemicals from the Lichen Lethariella canariensis: Phytotoxicity and Antioxidative Activity F. J. Toledo Marante, A. García Castellano, F. Estévez Rosas, J. Quintana Aguiar, J. Bermejo Barrera Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 8 . pseudocalanolide C C22H26O5 相似度:50% Journal of Natural Products 1995 Vol 58 916-920 The Pseudocalanolides: Structure Revision of Calanolides C and D Tawnya C. McKee, John H. Cardellina II, Geoffrey B. Dreyer, Michael R. Boyd Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 9 . 3-[2'-(5'-hydroxymethyl)furyl]-1(2H)-isoquinolinone-7-O-β-D-glucosdie C20H21NO9 相似度:50% Acta Pharmaceutica Sinica 2006 Vol 41 1193-1196 Chemical constituents from water extract of Radix isatidis HE Li-wei; LI Xiang; CHEN Jian-wei; SUN Dong-dong; J Wen-zheng; WANG Kang-cai Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 10 . calanolide C C22H26O5 相似度:50% Journal of Medicinal Chemistry 1992 35 2735-2743 HIV inhibitory natural products. Part 7. The calanolides, a novel HIV-inhibitory class of coumarin derivatives from the tropical rainforest tree, Calophyllum lanigerum Yoel Kashman, Kirk R. Gustafson, Richard W. Fuller, John H. Cardellina II, James B. McMahon, Michael J. Currens, Robert W. Buckheit Jr., Stephen H. Hughes, Gordon M. Cragg, Michael R. Boyd Structure 13C NMR 碳谱模拟图 |
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