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13C NMR (126 MHz, MeOD) ¦Ä  20.74, 23.88, 27.32, 31.71, 34.79, 35.91, 36.33, 41.74, 50.47, 57.03, 57.20, 66.84, 67.48, 74.59, 79.63, 101.22, 118.67, 152.12, 172.74,174.12, 202.26.
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1 .     nodosin
    ÏàËÆ¶È:71.4%
China Journal of Chinese Materia Medica          2009          34          1523-1526
Two en-kaurene diterpenoids from Tibetan medicine Caryopteris toroetii
QUE Sheng, ZHAO Yuying, ZHOU Yong, ZHANG Qingying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     carpalasionin
    ÏàËÆ¶È:68.1%
Journal of Natural Products          1994          Vol 57          650
Longirabdolide C, a New Diterpenoid from Rabdosia longituba
Yoshio Takeda, Takashi Matsumoto, Hideaki Otsuka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     nodosin
    ÏàËÆ¶È:57.1%
Journal of Natural Products          1994          Vol 57          650
Longirabdolide C, a New Diterpenoid from Rabdosia longituba
Yoshio Takeda, Takashi Matsumoto, Hideaki Otsuka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     nodosin
C20H26O6     ÏàËÆ¶È:57.1%
Journal of the Chinese Chemical Society          2008          55          933-936
Two New Diterpenoids and other Constituents from Isodon nervosus
Fu-Lin Yan*, Lan-Qing Guo,Su-Ping Bai and Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     compound B
    ÏàËÆ¶È:57.1%
The Journal of Antibiotics          1996          49          682-688
Mechanism of Multiple Aminoglycoside Resistance of Kasugamycin-producing Streptomyces kasugaensis MB273: Involvement of Two Types of Acetyltransferases in Resistance to Astromicin Group Antibiotics
KUNIMOTO HOTTA, TETSU OGATA, JUN ISHIKAWA, MASANORI OKANISHI, SATOSHI MIZUNO, MOTO MORIOKA, HIROSHI NAGANAWA, YOSHIRO OKAMI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     3¦Â,14¦Â,15-trihydroxy-14,15-seco-5¦Â-card-20(22)-enolide
    ÏàËÆ¶È:56.5%
Steroids          1996          61          572-582
Digitalis-like compounds: Synthesis and biological evaluation of seco-D and D-homo derivatives
Mauro Gobbini, Alessandra Benicchio, Giuseppe Marazzi, Gloria Padoani, Marco Torri, Piero Melloni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     3¦Â-Hydroxy-14-oxo-14,15-seco-5¦Â-card-20( 22)-enolide
C23H34O4     ÏàËÆ¶È:56.5%
Steroids          1996          61          572-582
Digitalis-like compounds: Synthesis and biological evaluation of seco-D and D-homo derivatives
Mauro Gobbini, Alessandra Benicchio, Giuseppe Marazzi, Gloria Padoani, Marco Torri, Piero Melloni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     19-(N,N-dimethylcarbamoxy)-2¦Â,8,13-trihydroxystemarane
23H39NO5     ÏàËÆ¶È:54.5%
Phytochemistry          2006          67          1088-1093
Bioconversion of Stemodia maritima diterpenes and derivatives by Cunninghamella echinulata var. elegans and Phanerochaete chrysosporium
Andrew S. Lamm, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     2¦Á-methoxy-populifolic acid methyl ester
    ÏàËÆ¶È:54.5%
Tetrahedron          1994          50          10791-10802
Ring a functionalized Neo-clerodane diterpenoids from Cistus populifolius
Julio G. Urones, Pilar Basabe, Isidro S. Marcos, Alicia Jim¨¦nez, Anna M. Lithgow, Margarita L¨®pez, Rosalina F. Moro, Antonio G¨®mez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     5¦Â-3¦Â,16¦Â-dihydroxybufa-20,22-dienolide
C24H34O4     ÏàËÆ¶È:54.1%
Phytochemistry          2007          68          1731-1734
Bufadienolides from the southern African Drimia depressa (Hyacinthaceae: Urgineoideae)
Neil R. Crouch, Angela Langlois, Dulcie A. Mulholland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     sculponeatin G
C24H34O8     ÏàËÆ¶È:54.1%
Planta Medica          2002          68          921-925
Cytotoxic ent-Kaurane Diterpenoids from Isodon sculponeata
Bei Jiang,Ai-Jun Hou,Ma-Lin Li,Sheng-Hong Li,Quan-Bin Han,Su-Jun Wang,Zhong-Wen Lin,Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     5-epipisiferol
    ÏàËÆ¶È:52.3%
Phytochemistry          2007          68          210-217
Antibacterials and modulators of bacterial resistance from the immature cones of Chamaecyparis lawsoniana
Eileen C.J. Smith, Elizabeth M. Williamson, Neale Wareham,Glenn W. Kaatz, Simon Gibbons
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     (13S,17R)-17-Acetoxy-6¦Â-methoxy-3¦Á,5-cyclo-13,14-seco-5¦Á-androst-14(E)-ene
    ÏàËÆ¶È:52.3%
Steroids          2004          69          501-509
Synthesis of 13,14-secotestosterone derivatives
Vladimir A. Khripach, Vladimir N. Zhabinskii, Anna I. Kuchto, Yuliya Y. Zhiburtovich, Galina P. Fando, Alexander S. Lyakhov, Alla A. Govorova, Marinus B. Groen, Jaap van der Louw, Aede de Groot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     nodosin
    ÏàËÆ¶È:52.3%
China Journal of Chinese Materia Medica          2009          34          1523-1526
Two en-kaurene diterpenoids from Tibetan medicine Caryopteris toroetii
QUE Sheng, ZHAO Yuying, ZHOU Yong, ZHANG Qingying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     exsertifolin G
C20H28O2     ÏàËÆ¶È:52.3%
Phytochemistry          1996          41          1129-1141
Ent-kaurane-type diterpenoids from the liverwort Jungermannia exsertifolia ssp. Cordifolia
Fumihiro Nagashima, Hironao Tanaka, Shigeru Takaoka, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     Methyl 2¦Á,3¦Â-dihydroxy-4(18)-neo-cleroden-15-oate
C21H36O4     ÏàËÆ¶È:52.3%
Phytochemistry          1995          38          443-445
2¦Á, 3¦Â-dihydroxy-4(18)-neo-cleroden-15-oic acid from cistus populifolius
Julio G. Urones, Isidro S. Marcos, Pilar Basabe, Alicia Jimenez, Antonio Gomez, Anna M. Lithgow
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     nodosin
C20H26O6     ÏàËÆ¶È:52.3%
Phytochemistry          1994          37          1367-1370
Nervosanin a and b and ent-kauranoids from Isodon nervosus
Wang Xian-Rong, Hu Hui-Ping, Wang Hong-Ping, Wang Su-Qing, Shinichi Ueda, Tetsuro Fujita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     pisiferanol
    ÏàËÆ¶È:52.3%
Phytochemistry          1991          30          2339-2343
Abietane diterpenoids from Lepechinia meyeni and Lepechinia hastata
Maurizio Bruno, Giuseppe Savona, Franco Piozzi, Maria C. de la Torre, Benjamin Rodriguez, Michel Marlier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     compound 9a
    ÏàËÆ¶È:52.3%
Phytochemistry          1991          30          2991-3000
Diterpenes and norditerpenes from the Aristeguetia group
C. Zdero, F. Bohlmann, R.M. King
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     20-hydroxyferruginol
    ÏàËÆ¶È:52.3%
Bioorganic & Medicinal Chemistry Letters          2005          15          2019-2021
Anti-tumor abietane diterpenes from the cones of Sequoia sempervirens
Kwang-Hee Son, Hyun-Mi Oh, Sung-Kyu Choi, Dong Cho Han, Byoung-Mog Kwon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-08-29 19:31:57
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