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12.12,15.209,15.429,18.065,18.878,20.792,22.46,24.016,26.174,26.318,27.173,27.642,30.672,30.751,32.766,35.467,36.804,38.113,38.667,44.787,47.703,50.242,76.593,77.73,78.497,81.042,133.952,134.446
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xianlu: ½ð±Ò+25, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ÕæµÄÊǸøÁËÎҺܴóµÄ°ïÖú£¬Ð»Ð»Ð»Ä㣡 2013-01-19 14:01:23
PSA: ½ð±Ò+1, ÐÁ¿à 2013-01-21 16:30:39
1 .     24-methylenelanost-8-ene-3¦Â, 22-diol
    ÏàËÆ¶È:77.4%
Phytochemistry          2009          70          558-563
Lanostane-triterpenoids from the fungus Phellinus gilvus
Hui-Kang Liu, Tung-Hu Tsai, Tun-Tschu Chang, Cheng-Jen Chou, Lie-Chwen Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     compound 3a
    ÏàËÆ¶È:77.4%
Chemical & Pharmaceutical Bulletin          1994          42          694-697
Isolation and Characterization of Immunosuppressive Components of Three Mushrooms, Pisolithus tinctorius, Microporus flabelliformis and Lenzites betulina
Haruhiro FUJIMOTO,Megumi NAKAYAMA,Yuji NAKAYAMA and Mikio YAMAZAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     neoabieslactone B
C30H48O4     ÏàËÆ¶È:76.6%
Journal of Natural Products          2009          72          1065-1068
Terpenoid Constituents of Abies chensiensis with Potential Anti-inflammatory Activity
Yong-Li Li, Xian-Wen Yang, Su-Mei Li, Yun-Heng Shen, Hua-Wu Zeng, Xiao-Hua Liu, Jian Tang,and Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     inonotsutriol D
C30H50O3     ÏàËÆ¶È:76.6%
Phytochemistry Letters          2011          4          328-332
New lanostane-type triterpenoids, inonotsutriols D, and E, from Inonotus obliquus
Reiko Tanaka, Misaki Toyoshima, Takeshi Yamada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




5 .     inonotsutriol E
C30H50O3     ÏàËÆ¶È:76.6%
Phytochemistry Letters          2011          4          328-332
New lanostane-type triterpenoids, inonotsutriols D, and E, from Inonotus obliquus
Reiko Tanaka, Misaki Toyoshima, Takeshi Yamada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     astrahygrol
C30H48O     ÏàËÆ¶È:76.6%
Phytochemistry          1987          26          2341-2344
Three triterpenes from Astraeus hygrometricus
Yoshihisa Takaishi,Yoshito Murakami,Takashi Ohashi,Kimiko Nakano,Ko¯tarou Murakami,Toshiaki Tomimatsu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     3-epi-astrahygrol
C30H48O     ÏàËÆ¶È:76.6%
Phytochemistry          1987          26          2341-2344
Three triterpenes from Astraeus hygrometricus
Yoshihisa Takaishi,Yoshito Murakami,Takashi Ohashi,Kimiko Nakano,Ko¯tarou Murakami,Toshiaki Tomimatsu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




8 .     compound 10
    ÏàËÆ¶È:76.6%
Phytochemistry          1990          29          923-928
Malonate half-esters of homolanostanoid from an asian Ganoderma fungus
Chairul,Takashi Tokuyama,Mugio Nishizawa,Motoo Shiro,Harukuni Tokuda,Yuji Hayashiji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     24-hydroperoxy-4¦Á,14¦Á-dimethylcholesta-8,25-dien-3¦Â-ol
    ÏàËÆ¶È:75.8%
Phytochemistry          1996          41          1191-1195
Antibacterial hydroperoxysterols from Xanthosoma robustum
Takeshi Kato, Barbara Frei, Michael Heinrich, Otto Sticher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     4¦Á,14¦Á-Dimethylcholesta-8,25-dien-3¦Â,24-diol
    ÏàËÆ¶È:75.8%
Phytochemistry          1996          41          1191-1195
Antibacterial hydroperoxysterols from Xanthosoma robustum
Takeshi Kato, Barbara Frei, Michael Heinrich, Otto Sticher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     23,24,25,26,27-pentanorlanost-8-ene-3¦Â,22,diol
    ÏàËÆ¶È:75%
Chemical & Pharmaceutical Bulletin          2000          48(10)          1422-1426
A New Pentanorlanostane Derivative, Cladosporide A, as a Characteristic Antifungal Agent against Aspergillus fumigatus, Isolated form Cladosporium sp.
Tomoo HOSOE,Hideaki OKADA,Takeshi ITABASHI,Koohei NOZAWA,Kaoru OKADA,Galba Maria de CAMPOS TAKAKI,Kazutaka FUKUSHIMA,Makoto MIYAJI and Ken-ichi KAWAI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




12 .     23,24,25,26,27-pentanorlanost-8-en-3¦Â,22-diol
C25H42O2     ÏàËÆ¶È:75%
Phytochemistry          1984          23          1721-1723
23,24,25,26,27-Pentanorlanost-8-en-3¦Â,22-diol from Verticillium lecanii
John Frederick Grove
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     igniaren D
C31H52O2     ÏàËÆ¶È:74.1%
Planta Medica          2009          75          1602-1607
Lanostanes from Phellinus igniarius and Their iNOS Inhibitory Activities
Guei-JaneWang, Tung-Hu Tsai, Tun-Tschu Chang, Cheng-Jen Chou, Lie-Chwen Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




14 .     compound 3b
    ÏàËÆ¶È:74.1%
Chemical & Pharmaceutical Bulletin          1994          42          694-697
Isolation and Characterization of Immunosuppressive Components of Three Mushrooms, Pisolithus tinctorius, Microporus flabelliformis and Lenzites betulina
Haruhiro FUJIMOTO,Megumi NAKAYAMA,Yuji NAKAYAMA and Mikio YAMAZAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




15 .     24-methyllanosta-8,24(24')-diene-3¦Â,22¦Î-diol
    ÏàËÆ¶È:74.1%
Phytochemistry          1997          45          499-504
Triterpenoids from Pisolithus tinctorius isolates and ectomycorrhizas
Alfred Baumert, Brigitte Schumann, Andrea Porzel, J¨¹rgen Schmidt, Dieter Strack
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     pisolactone
    ÏàËÆ¶È:74.1%
Phytochemistry          1997          45          499-504
Triterpenoids from Pisolithus tinctorius isolates and ectomycorrhizas
Alfred Baumert, Brigitte Schumann, Andrea Porzel, J¨¹rgen Schmidt, Dieter Strack
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




17 .     compound 1
C31H50O3     ÏàËÆ¶È:74.1%
Chinese Journal of Chemistry          2001          19          702-704
A Novel Lanostanoid Lactone From the Alga Hypnea cerricornis
Xiao-Hua Xu, Xiao Chen, Jian-Hua Lu, Guang-Min Yao, Yan-Ming Li and Long-Mei Zeng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     inonotsutriol B
C30H50O3     ÏàËÆ¶È:73.3%
Helvetica Chimica Acta          2008          Vol. 91          1513
Three New Lanostane Triterpenoids, Inonotsutriols A, B, and C, from Inonotus obliquus
Sayaka Taji, Takeshi Yamada, and Reiko Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     inotodiol
    ÏàËÆ¶È:73.3%
Planta Medica          1986          52          495-496
3¦Â,22-Dihydroxylanosta-7,9(11),24-triene: A New, Minor Compound from Inonotus obliquus
Kirsti Kahlos and R. Hiltunen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     inotodiol
    ÏàËÆ¶È:73.3%
Planta Medica          1984          50          197-198
3¦Â-Hydroxy-lanosra-8,24-dien-21-al, a New Triterpene from Inonotus obliquus
Kirsti Kahlos, R. Hiltunen and M. v. Schantz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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