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1 .     emindole SB beta-mannoside
C34H49NO6     ÏàËÆ¶È:70.5%
Journal of Natural Products          2014          77          673-677
Indoloditerpenes from a Marine-Derived Fungal Strain of Dichotomomyces cejpii with Antagonistic Activity at GPR18 and Cannabinoid Receptors
Henrik Harms, Viktor Rempel, Stefan Kehraus, Marcel Kaiser, Peter Hufendiek, Christa E. M¨¹ller, and Gabriele M. König
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Entinclole SB
    ÏàËÆ¶È:68.9%
Chemistry of Natural Compounds          2007          43          655-658
A NEW ISOCOUMARIN FROM MANGROVE ENDOPHYTIC FUNGUS (No. dz17) ON THE SOUTH CHINA SEA COAST
Zhongjing Huang, Changlun Shao, Yiguang Chen,Zhigang She Yongcheng Lin, and Shining Zhou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     paspaline
C28H39NO2     ÏàËÆ¶È:68.9%
Phytochemistry          1996          41          327-332
Isolation of paspaline B, an indole-diterpenoid from Penicilium paxilli
Sarah C. Munday-Finch, Alistair L. Wilkins, Christopher O. Miles
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     27-O-methylasporyzin C
C29H41NO2     ÏàËÆ¶È:68.9%
Journal of Natural Products          2014          77          673-677
Indoloditerpenes from a Marine-Derived Fungal Strain of Dichotomomyces cejpii with Antagonistic Activity at GPR18 and Cannabinoid Receptors
Henrik Harms, Viktor Rempel, Stefan Kehraus, Marcel Kaiser, Peter Hufendiek, Christa E. M¨¹ller, and Gabriele M. König
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     optically active paspaline
    ÏàËÆ¶È:65.5%
Journal of the Chemical Society, Perkin Transactions 1          1988                   1689-1694
Studies on fungal products. Part 17. Isolation and structures of novel indoloditerpenes, emindoles DA and DB, from Emericella desertorum: X-ray molecular structure of emindole DA acetate
Koohei Nozawa, Shoichi Nakajima, Ken-ichi Kawai and Shun-ichi Udagawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     paspaline
    ÏàËÆ¶È:65.5%
Journal of the Chemical Society, Perkin Transactions 1          1988                   2607-2610
Isolation and structures of indoloditerpenes, possible biosynthetic intermediates to the tremorgenic mycotoxin, paxilline, from Emericella striata
Koohei Nozawa, Shoichi Nakajima, Ken-ichi Kawai and Shun-ichi Udagawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     JBIR-03
C28H37NO     ÏàËÆ¶È:65.5%
The Journal of Antibiotics          2007          60          645-648
A Novel Indole-diterpenoid, JBIR-03 with Anti-MRSA Activity from Dichotomomyces cejpii var. cejpii NBRC 103559 FREE
Masahiro Ogata, Jun-ya Ueda, Midori Hoshi, Junko Hashimoto, Takuji Nakashima, Kozue Anzai, Motoki Takagi and Kazuo Shin-ya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     cimigenol
    ÏàËÆ¶È:63.3%
China Journal of Chinese Materia Medica          2003          28          118-121
Studies on New Trierpenoid Constituents from the Rhizoma of Cimicifuga fortida
ZHAO Xiaohong, CHEN Dihua, SI Jianyong, PAN Ruile, SHEN Liangang, CHEN Duo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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