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1 .     Hypotrachynic acid
C18H16O7     ÏàËÆ¶È:52.6%
Molecules          2007          12          997-1005
¦Â-Orcinol Metabolites from the Lichen Hypotrachyna revoluta
Panagiota Papadopoulou, Olga Tzakou, Constantinos Vagias, Panagiotis Kefalas and Vassilios Roussis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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2 .     3-formyl-2,4-dihydroxy-6-methylbenzoic acid 3-hydroxy-4-(methoxycarbonyl)-2,5-di-methylphenyl ether
    ÏàËÆ¶È: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   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     cladonioidesin
    ÏàËÆ¶È: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   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     3-hydroxy-2,4,5-trimethylphenyl 2,4-dihydroxy-3,6-dimethylbenzoate
C18H20O5     ÏàËÆ¶È:52.6%
Helvetica Chimica Acta          2011          94          1077-1084
Antimicrobial Depsides Produced by Cladosporium uredinicola, an Endophytic Fungus Isolated from Psidium guajava Fruits
L¨ªvia Soman de Medeiros, Michael Murgu, Antônia Q. L. de Souza, and Edson Rodrigues-Fo.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     atranorin
    ÏàËÆ¶È: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   Ì¼Æ×Ä£Äâͼ
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6 .     atranorin
    ÏàËÆ¶È:52.6%
Chemical & Pharmaceutical Bulletin          2013          69          176-183
Cytotoxic Evaluation of Phenolic Compounds from Lichens against Melanoma Cells
Luiz Fabr¨ªcio Gardini Brandão, Glaucia Braz Alcantara, Maria de F¨¢tima Cepa Matos, Danielle Bogo, Deisy dos Santos Freitas, Nath¨¢lia Mitsuko Oyama, Neli Kika Honda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

7 .     atranorin
    ÏàËÆ¶È: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. Garc¨ªa Castellano, F. Est¨¦vez Rosas, J. Quintana Aguiar, J. Bermejo Barrera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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8 .     pseudocalanolide C
C22H26O5     ÏàËÆ¶È: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   Ì¼Æ×Ä£Äâͼ
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9 .     3-[2'-(5'-hydroxymethyl)furyl]-1(2H)-isoquinolinone-7-O-¦Â-D-glucosdie
C20H21NO9     ÏàËÆ¶È: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¦a Wen-zheng; WANG Kang-cai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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10 .     calanolide C
C22H26O5     ÏàËÆ¶È: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   Ì¼Æ×Ä£Äâͼ
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