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1 .     4-hydroxy-17R-methylincisterol
     ÏàËÆ¶È:85.7%
Chinese Journal of Marine Drugs          2012          31          8-13
Secondary metabolites from a fungus Peniophora sp.isolated from a gorgonian Echinogorgia sp.
ZHOU Jing; CHEN Min; LI Yun; LIU Yun-zhang; WANG Chang-yun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     9¦Á-hydroxy-1,2,3,4,5,10,19-heptanorergosta-7,22-diene-6,9-lactone
C21H32O3     ÏàËÆ¶È:85%
Natural Medicines          1996          50          179-181
Sterol Constituents from the Sclerotium of Polyporus umbellatus Fries
OHTA KOJI,YAOITA YASUNORI,MATSUDA NORIKO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     (17R)-4-hydroxy-17-methylincisterol
     ÏàËÆ¶È:80.9%
Heterocycles          2006          69          253-258
Chaxine A, an Osteoclast-Forming Suppressing Substance, from the Mushroom Agrocybe chaxingu
Hirokazu Kawagishi,* Takuto Akachi, Tetsuhiro Ogawa, Kikuko Masuda, Kohji Yamaguchi, Kazunaga Yazawa, and Mamoru Takahashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     Demethylincisterol A3
C21H32O3     ÏàËÆ¶È:76.1%
Tetrahedron          2012          68          1729-1735
Synthesis of two osteoclast-forming suppressors, demethylincisterol A3 and chaxine A
Arata Yajima, Yuuma Kagohara, Keisuke Shikai, Ryo Katsuta, Tomoo Nukada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     demethylincisterol A2
C21H32O3     ÏàËÆ¶È:71.4%
Journal of Natural Products          2005          68          331-336
Cytotoxic Sterol Derivatives from a Marine Sponge Homaxinella sp.
Tayyab A. Mansoor, Jongki Hong, Chong-O. Lee, Song-Ja Bae, Kwang Sik Im, and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     volemolide
C22H36O3     ÏàËÆ¶È:68.1%
Natural Product Research and Development          2010          22          786-788
Chemical Constituents of Culture Broth of Hebeloma westraliense
SHAO Hong-jun;FANG Li-zhen; LIU Ji-kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     chaxine A
C21H34O3     ÏàËÆ¶È:66.6%
Heterocycles          2006          69          253-258
Chaxine A, an Osteoclast-Forming Suppressing Substance, from the Mushroom Agrocybe chaxingu
Hirokazu Kawagishi,* Takuto Akachi, Tetsuhiro Ogawa, Kikuko Masuda, Kohji Yamaguchi, Kazunaga Yazawa, and Mamoru Takahashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     Chaxine A
C21H34O3     ÏàËÆ¶È:66.6%
Tetrahedron          2012          68          1729-1735
Synthesis of two osteoclast-forming suppressors, demethylincisterol A3 and chaxine A
Arata Yajima, Yuuma Kagohara, Keisuke Shikai, Ryo Katsuta, Tomoo Nukada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     demethylincisterol A1
C20H30O3     ÏàËÆ¶È:65%
Journal of Natural Products          2005          68          331-336
Cytotoxic Sterol Derivatives from a Marine Sponge Homaxinella sp.
Tayyab A. Mansoor, Jongki Hong, Chong-O. Lee, Song-Ja Bae, Kwang Sik Im, and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     3¦Â,17¦Â-dihydroxyandrost-4-ene
     ÏàËÆ¶È:65%
Steroids          1999          64          770-779
Steroid transformations with Exophiala jeanselmei var. lecanii-corni and Ceratocystis paradoxa
Roy B. R. Porter, Winklet A. Gallimore, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     compound 12
C21H34O2     ÏàËÆ¶È:65%
Tetrahedron          2012          68          1729-1735
Synthesis of two osteoclast-forming suppressors, demethylincisterol A3 and chaxine A
Arata Yajima, Yuuma Kagohara, Keisuke Shikai, Ryo Katsuta, Tomoo Nukada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     sarcophytin
     ÏàËÆ¶È:65%
Tetrahedron Letters          2012          53          5759-5762
Pavidolides A¨CE, new cembranoids from the soft coral Sinularia pavida
Shi Shen, Huajie Zhu, Dawei Chen, Dong Liu, Leen van Ofwegen, Peter Proksch, Wenhan Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     volemolide
C22H34O3     ÏàËÆ¶È:63.6%
Bioscience, Biotechnology, and Biochemistry          1994          58          1542-1544
Volemolide, a Novel Norsterol from the Fungus Lactarius volemus
Kenji Kobata, Tomonari Wada, Yasuo Hayashi, Hisao Shisata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     incisterol
C21H32O3     ÏàËÆ¶È:61.9%
Journal of Natural Products          2005          68          331-336
Cytotoxic Sterol Derivatives from a Marine Sponge Homaxinella sp.
Tayyab A. Mansoor, Jongki Hong, Chong-O. Lee, Song-Ja Bae, Kwang Sik Im, and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     16-Methyl-17-acetoxy-5¦Á-androstan-3¦Â-ol 7c
C22H36O3     ÏàËÆ¶È:61.9%
Steroids          2001          66          833-843
Configurational analysis and relative binding affinities of 16-methyl-5¦Á-androstane derivatives
P¨¢l Tapolcs¨¢nyi, J¨¢nos Wölfling, Istv¨¢n T¨®th, Mih¨¢ly Sz¨¦csi, P¨¦ter Forg¨®, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     (1R,3aR,4Z,5R,7aR,10R,20E,40R)-5,6,7,7a-Tetrahydro-4-(2-hydroxyethylidene)-7a-methyl-1-(10,40,50-trimethyl-20-hexenyl)-3aHindan-5-ol
C21H36O2     ÏàËÆ¶È:61.9%
Tetrahedron          2012          68          1729-1735
Synthesis of two osteoclast-forming suppressors, demethylincisterol A3 and chaxine A
Arata Yajima, Yuuma Kagohara, Keisuke Shikai, Ryo Katsuta, Tomoo Nukada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     15-Azidoimbricatolic acid methyl ester
C21H35N3O2     ÏàËÆ¶È:61.9%
Molecules          2013          18          5936-5953
Dimeric Labdane Diterpenes: Synthesis and Antiproliferative Effects
Mariano Walter Pertino, Cristina Theoduloz, Marco Bast¨ªas and Guillermo Schmeda-Hirschmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     agallochin H
C20H30O3     ÏàËÆ¶È:60%
Journal of Natural Products          2002          65          382-385
ent-Kaurane and Beyerane Diterpenoids from Excoecaria agallocha1
Ammanamanchi S. R. Anjaneyulu, Vadali Lakshmana Rao, and Karanam Sreedhar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     compound 10
C18H30O4     ÏàËÆ¶È:60%
Journal of Natural Products          1997          60          1115-1120
Sesquiterpenoids of the Drimane Class from a Sponge of the Genus Dysidea
Valerie J. Paul, Youngwan Seo, Ki Woong Cho, Jung-Rae Rho, Jongheon Shin, and Patricia R. Bergquist
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     12-hydroxy-8,13e-labdadien-15-oic acid
     ÏàËÆ¶È:60%
Journal of Integrative Plant Biology          2006          48          478-482
Labdane doterpenoids from Coleus forskohlii Briq.
Ling-ling XU and Ling-yi KONG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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