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14.2, 14.5, 19.4, 20.9, 21.1, 21.7, 24.5, 29.7, 38.2, 38.8, 39.8, 42.0, 51.5, 55.5, 60.9, 61.1, 62.8, 65.6, 106.7, 121.1, 149.3, 156.5, 193.1
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1 .     11-(5'-epxoy-4'-hydroxy-3'-hydroxymethylcyclo-2'-hexenone)-¡÷8(12)-drimene
C22H32O4     ÏàËÆ¶È:78.2%
Phytochemistry          1990          29          1661-1665
Three piperazinediones and a drimane diterpenoid from Penicillium brevi-compactum  
William A. Ayer,Ian Van Altena,Lois M. Browne
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     macrophorin A
     ÏàËÆ¶È:76.9%
Bioscience, Biotechnology, and Biochemistry          1998          62          2260-2262
Isolation and Identification of New Antifungal Macrophorins E, F and G as Malonyl Meroterpenes from Botryosphaeria berengeriana
Takeshi SASSA, Atsuko ISHIZAKI, Manabu NUKINA, Michimasa IKEDA, Takeyoshi SUGIYAMA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     macrophorin G
     ÏàËÆ¶È:69.5%
Bioscience, Biotechnology, and Biochemistry          1998          62          2260-2262
Isolation and Identification of New Antifungal Macrophorins E, F and G as Malonyl Meroterpenes from Botryosphaeria berengeriana
Takeshi SASSA, Atsuko ISHIZAKI, Manabu NUKINA, Michimasa IKEDA, Takeyoshi SUGIYAMA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     compound 10
     ÏàËÆ¶È:68%
Phytochemistry          1990          29          1661-1665
Three piperazinediones and a drimane diterpenoid from Penicillium brevi-compactum  
William A. Ayer,Ian Van Altena,Lois M. Browne
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     macrophorin E
C26H36O7     ÏàËÆ¶È:65.3%
Bioscience, Biotechnology, and Biochemistry          1998          62          2260-2262
Isolation and Identification of New Antifungal Macrophorins E, F and G as Malonyl Meroterpenes from Botryosphaeria berengeriana
Takeshi SASSA, Atsuko ISHIZAKI, Manabu NUKINA, Michimasa IKEDA, Takeyoshi SUGIYAMA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     4'-oxomacrophorin A
C22H30O4     ÏàËÆ¶È:65.2%
Journal of Natural Products          2001          64          1234-1237
Immunomodulatory Constituents from an Ascomycete, Eupenicillium crustaceum, and Revised Absolute Structure of Macrophorin D
Haruhiro Fujimoto,Etsuko Nakamura, Yong-Pil Kim, Emi Okuyama, Masami Ishibashi,and Takeshi Sassa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     16-acetoxy-ent-labda-8(17),13Z-dien-15-oic acid methyl ester
C23H36O4     ÏàËÆ¶È:65.2%
Phytochemistry          1992          31          1631-1638
Ent-labdanes, manoyloxide and helipterol derivatives from Chrysocephalum ambiguum
C. Zdero, F. Bohlmann, R.M. King
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     Labd-8(17)-en-15-ol
     ÏàËÆ¶È:65.2%
Flavour and Fragrance Journal          1998          13          295-318
Constituents of commercial Labdanum oil
Peter Weyerstahl, Helga Marschall, Marlies Weirauch, Katrin Thefeld and Horst Surburg
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     (+)-copalyl acetate
C22H36O2     ÏàËÆ¶È:60.8%
Journal of Natural Products          2006          69(3)          381-386
(+)-Agelasine D: Improved Synthesis and Evaluation of Antibacterial and Cytotoxic Activities
Anders Vik, Erik Hedner, Colin Charnock, rjan Samuelsen,Rolf Larsson, Lise-Lotte Gundersen, and Lars Bohlin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     15,16-epoxy-12-hydroxy-labda-8(17),13(16),14-triene(a)
     ÏàËÆ¶È:60.8%
Journal of Natural Products          1998          61          1394-1396
A Concise Conversion of (-)-Sclareol into (+)-Coronarin E and (-)-7-epi-Coronarin A
Mankil Jung, Imju Ko, and Seokjoon Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     15-acetoxy-12-hydroxy-16-methyl-labda-8(17),13E-diene
C22H36O3     ÏàËÆ¶È:60.8%
Planta Medica          2007          73          491-495
Diterpenoids from Turraeanthus mannii
Juliette Catherine Vardamides,Valerie Tedjon Sielinou,Brigitte Ndemangou, Augustin Ephrem Nkengfack,Zacharias Tanee Fomum,Herve Martial Poumale Poumale,Hartmut Laatsch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     compound 2
     ÏàËÆ¶È:60.8%
Phytochemistry          1998          49          1741-1744
Determination of the absolute stereochemistry of the epoxide group in alpinia epoxide by NMR
Lai-King Sy, Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     labda-8(17),12-diene-15,16-diol
     ÏàËÆ¶È:60.8%
Phytochemistry          1988          27          435-438
Diterpenes from the rhizomes of Alpinia formosana
Hideji Itokawa,Shinji Yoshimoto,Hiroshi Morita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     15-acetoxylabd-8(17)-en-19-ol
C22H38O3     ÏàËÆ¶È:60.8%
Zeitschrift f¨¹r Naturforschung C          2005          60          511-522
Gastroprotective Effect and Cytotoxicity of Natural and Semisynthetic Labdane Diterpenes from Araucaria araucana Resin
G. Schmeda-Hirschmann, L. Astudillo, B. Sep¨²lveda, J. A. Rodr¨ªguez, C. Theoduloz, T. Y¨¢ñez, and J. A. Palenzuela
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     13-Methyl-labda-8(17)-en-15-oic acid
C20H35O2     ÏàËÆ¶È:60.8%
Natural Product Communications          2010          5          1535 - 1538
Terpenoids from Turraeanthus species
Juliette Catherine Vardamides,*, Valerie Tedjon Sielinou, Sergi Herve Akone,Augustin Ephrem Nkengfack and Berhanu M. Abegaz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     16,19-diacetoxy-ent-labda-8(17),13Z-dien-15-oic acid methyl ester
C25H38O6     ÏàËÆ¶È:60%
Phytochemistry          1992          31          1631-1638
Ent-labdanes, manoyloxide and helipterol derivatives from Chrysocephalum ambiguum
C. Zdero, F. Bohlmann, R.M. King
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     7-dehydro-nor-erythrosuamide
C24H35NO6     ÏàËÆ¶È:58.3%
Planta Medica          2006          72          442-449
New Cassaine Diterpenoid Amides with Cytotoxic Activities from the Bark of Ery throphleum fordii
Jing Qu,You-Cai Hu,Shi-Shan Yu,Xiao-Guang Chen,Yan Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     Isorosthin F
C24H32O8     ÏàËÆ¶È:58.3%
Journal of Natural Products          2013          76          1267-1277
Bioactive ent-Kaurane Diterpenoids from Isodon rosthornii
Rui Zhan, Xiao-Nian Li, Xue Du, Wei-Guang Wang, Ke Dong, Jia Su, Yan Li, Jian-Xin Pu, and Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     Franganine
     ÏàËÆ¶È:57.6%
Journal of Natural Products          2012          75          1220-1222
Absolute Configuration of Franganine
Miguel S. B. Caro, Leonardo H. de Oliveira, Vinicius Ilha, Robert A. Burrow, Ionara I. Dalcol, and Ademir F. Morel
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     16-acetoxy-12(R),15-epoxy-15b-hydroxylabda-8(17),13(16)-diene
C22H34O4     ÏàËÆ¶È:56.5%
Phytochemistry          2004          65          3083-3087
Two labdane diterpenoids and a seco-tetranortriterpenoid from Turreanthus africanus
Pierre Tane, Mac Thomas Akam, Apollinaire Tsopmo, Chi P. Ndi, Olov Sterner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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