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12.32, 15.74, 17.61, 18.42, 19.65, 19.96, 21.11, 22.16, 22.88, 27.94, 30.89, 32.77, 33.07, 37.20, 39.37, 39.46, 40.41, 42.81, 43.84, 43.88, 54.91, 55.96, 65.65, 67.92, 76.36, 80.30, 115.90, 132.04, 135.45, 142.97

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1 .     (3¦Â,5¦Á,6¦Â,22E)-6-methoxyergosta-7,22-diene-3,5-diol
    ÏàËÆ¶È:90%
Helvetica Chimica Acta          2007          Vol. 90          1165
New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori
Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     3¦Â,5¦Á-dihydroxy-6¦Â-methoxyergosta-7,22-diene
C29H48O3     ÏàËÆ¶È:90%
Phytochemistry          1988          27          2777-2779
Cytotoxic steroids from the mushroom Agaricus blazei
Hirokazu Kawagishi,Ryosuke Katsumi,Toshimi Sazawa,Takashi Mizuno,Toshihiko Hagiwara,Takuji Nakamura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     6-methoxy-cerevisterol
    ÏàËÆ¶È:90%
Natural Product Research and Development          2007          19          605-609
Study on the Chemical Constitutes of Hydnellum concrescens
YANG Xiao-long;WANG Fei; SHAO Hong-jun; DONG Ze-jun; DING Zhi-hui; YANG Wan-qiu; LIU Ji-kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     22E-6¦Â-methoxyergosta-7,22-diene-3¦Â,5¦Á-diol
C29H48O3     ÏàËÆ¶È:90%
Journal of Shenyang Pharmaceutical University          2012          29          678-684
A new disecosteroid from an endolichenic fungal stain Sporormiella irregularis(No.71-11-4-1)
LI Yan-jun; LI Xiao-xia; CHEN Guo-dong; GAO Hao; GUO Liang-dong; YAO Xin-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     5¦Á,6¦Á-epoxy-24(R)-methylcholesta-7,22-dien-3¦Â-ol
C28H44O2     ÏàËÆ¶È:86.6%
Phytochemistry          1999          51          891-898
Antitumor sterols from the mycelia of Cordyceps sinensis
Jin Woo Bok, Leonard Lermer, Jeff Chilton, Hans G. Klingeman, G.H. Neil Towers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     ergosta-7,22-diene-2¦Â,3¦Á,9¦Á-triol
C28H46O3     ÏàËÆ¶È:86.6%
Journal of Natural Products          1991          Vol 54          998
Novel Cytotoxic Principles of Formosan Ganoderma lucidum
Chun-Nan Lin, Whey-Pim Tome, Shen-Jeu Won
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     5,6-Epoxy-22-en-3-ol-ergosterol
C28H44O2     ÏàËÆ¶È:86.6%
Chemical Research in Chinese Universities          1998          14          270-272
Chemical Constituent of Natural Body of Armillaria mellea and Structure of 5, 6-Epoxy-22-en-3-ol-ergosterol
SHI Lei, CAO Rui-min, LU Shi-xiang and WU Guang-xuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     cerevisterol (3¦Â,5¦Á,6¦Â-trihydroxyergosta-7,22-diene)
    ÏàËÆ¶È:86.6%
Phytochemistry          1988          27          2777-2779
Cytotoxic steroids from the mushroom Agaricus blazei
Hirokazu Kawagishi,Ryosuke Katsumi,Toshimi Sazawa,Takashi Mizuno,Toshihiko Hagiwara,Takuji Nakamura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     ergosta-6,22-dien-3¦Â,5¦Â,8¦Â-triol
    ÏàËÆ¶È:86.6%
Chinese Traditional and Herbal Drugs          2000          31          328-330
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Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     3¦Â,5¦Á-Dihydroxy-6¦Â-methoxyergosta-7,22-diene
    ÏàËÆ¶È:86.6%
Archives of Pharmacal Research          2002          25          851-855
Cytotoxic ergosterols from paecilomyces sp. J300
Hak Cheol Kwon, Sang Deuk Zee, Sae Yun Cho, Sang Un Choi and Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     5¦Á,6¦Á-epoxy-24(R)-methylcholesta-7,22-dien-3¦Â-ol
    ÏàËÆ¶È:86.6%
Chinese Journal of Medicinal Chemistry          2008          18          452-456
Secondary metabolites produced by Fusarium sp. 2TnP1-2, an endophytic fungus from Trewia nudif lora
DU Zhi-zhi, SONG Cheng-zhi, YU Bu-zhu, LUO Xiao-dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     ergosta-6,22-dien-3¦Â,5¦Â,8¦Â-triol
    ÏàËÆ¶È:86.6%
Natural Product Research and Development          1999          11(6)          18-21
THREE STEROLS FROM GYROPORUS CASTANEUS
Wan Hui; Sun Rongqi; Wu Dajun; Guo Beishu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     ergosta-7,22-diene-2¦Â,3¦Á,9¦Á-triol
    ÏàËÆ¶È:86.6%
Phytotherapy Research          2011          25          1579-1585
Ergosta-7,22-diene-2¦Â,3¦Á,9¦Á-triol from the Fruit Bodies of Ganoderma lucidum Induces Apoptosis in Human Myelocytic HL-60 Cells
Mi Kyoung Lee, Tran Manh Hung, To Dao Cuong, MinKyun Na, Jin Cheol Kim, Eun-Jung Kim, Hee-Sung Park, Jae Sue Choi, IkSoo Lee, KiHwan Bae, Masao Hattori and Byung Sun Min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     cerevisterol
    ÏàËÆ¶È:86.6%
Mycosystema          2010          29          249-253
Steroids from fruiting bodies of Coprinus comatus and their inhibition to tumor cell proliferation
FENG Na; ZHANG Jing-Song TANG Qing-Jiu HAO Rui-Xia LIU Yan-Fang YANG Yan JIA Wei ZHOU Shuai TANG Chuan-Hong ZHONG Jian-Jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     cerevisterol
    ÏàËÆ¶È:83.3%
Helvetica Chimica Acta          2007          Vol. 90          1165
New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori
Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     6,9-epoxyergosta-7,22-dien-3-ol
    ÏàËÆ¶È:83.3%
Acta Botanica Sinica          2002          44          1239-1242
Chemical Constituents of One Species of Endophytic Fungus in Taxus chinensis
ZHANGJi-Hui, GUO Shun-Xing YANGJun-Shan, XIAO Pei-Gen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     6,9-Epoxy-ergosta-7,22-dien-3¦Â-ol
    ÏàËÆ¶È:83.3%
Biochemical Systematics and Ecology          2007          35          790-793
Triterpenes and steroids from Armillaria mellea Vahl. ex Fr.
Wen-Juan Guo, Shun-Xing Guo, Jun-Shan Yang, Xiao-Mei Chen, Pei-Gen Xiao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     cerevisterol
    ÏàËÆ¶È:83.3%
Phytochemistry          1997          44          1443-1448
Cytochalasins and phytotoxins from the fungus Xylaria obovata
Dawit Abate, Wolf-Rainer Abraham, Holger Meyer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:83.3%
Chinese Journal of Medicinal Chemistry          2005          15          221-223
The chemical constituents from the mycel ia of marine fungus Rhizopus sp.
SHI Ying, TIAN Li, PEI Yue-hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     (22E,24S)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:83.3%
Natural Product Research and Development          2006          18          238-242
Chemical Study on Porandra scandens
HE Zhi-heng; LUO Ying-gang; LI Hong-juan£¨; ZHANG Guo-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     (22E,24S)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:83.3%
Natural Product Research and Development          2006          18          411-414
Phytochemical Study on Zehneria maysorensis
LI Hong-juan;LUO Ying-gang; HE Zhi-heng; ZHANG Guo-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     ergosta-7,22-diene-3¦Â,5¦Á,6¦Á-triol
C28H46O3     ÏàËÆ¶È:83.3%
Natural product sciences          2011          17          85-89
Cytotoxicity of Ergosterol Derivatives from the Fruiting Bodies of Hygrophorus russula
Lee, Ik-Soo; Kim, Jin-Pyo; Na, Min-Kyun; Jung, Hyun-Ju; Min, Byung-Sun; Bae, Ki-Hwan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:83.3%
Chinese Traditional and Herbal Drugs          2011          42          31-33
Chemical constituents of Dendrobium crystallinum
WANG Lei, ZHANG Chao-feng, WANG Zheng-tao, ZHANG Mian, XU Luo-shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     (22E,24R)-ergosta-7,22-dien-2¦Á,3¦Á,9¦Á-triol
C28H46O3     ÏàËÆ¶È:83.3%
The Journal of Antibiotics          2012          65          437-440
Inhibition of human neutrophil elastase by ergosterol derivatives from the mycelium of Phellinus linteus
Ik-Soo Lee, KiHwan Bae, Jae Kuk Yoo, In-Ja Ryoo, Bo Yeon Kim, Jong Seog Ahn and Ick-Dong Yoo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
C28H44O2     ÏàËÆ¶È:83.3%
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
26 .     (22E)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:83.3%
Chinese Journal of Marine Drugs          2012          31          5-10
Studies on chemical constituents of the South China Sea Gorgonian Rumphella aggregata
LIU Cai-xia; LI Ping-lin; TANG Xu-li; LI Guo-qiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:83.3%
Chinese Traditional and Herbal Drugs          2012          43          664-666
Studies on chemical constituents of Lasiosphaera fenzlii
SU Ming-zhi; LUO Zhou; YAN Ming; ZHAO Qing-chun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     22E-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
C28H46O3     ÏàËÆ¶È:83.3%
Journal of Shenyang Pharmaceutical University          2012          29          678-684
A new disecosteroid from an endolichenic fungal stain Sporormiella irregularis(No.71-11-4-1)
LI Yan-jun; LI Xiao-xia; CHEN Guo-dong; GAO Hao; GUO Liang-dong; YAO Xin-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     stigmasta-7,22-diene-3¦Â,5¦Á,6¦Á-triol,respectively
C28H46O3     ÏàËÆ¶È:80%
Chinese Chemical Letters          2006          17          481-484
An Abietane Diterpene and a Sterol from Fungus Phellinus igniarius
Ying WANG, Su Juan WANG, Shun Yan MO, Shuai LI, Yong Chun YANG, Jian Gong SHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     biemnasterol
C28H44O3     ÏàËÆ¶È:80%
Journal of Natural Products          1993          Vol 56          2016
Biemnasterol, a New Cytotoxic Sterol with the Rare 22,25-Diene Side Chain, Isolated from the Marine Sponge Biemna sp.
Chun-min Zeng, Masami Ishibashi, Jun'ichi Kobayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     6,9-epoxy-ergosta-7,22-dien-3-ol
C28H44O2     ÏàËÆ¶È:80%
Acta Pharmaceutica Sinica          2000          Vol 35          367-369
THE STEROL CONSTITUENTS OF MYCENA DENDROBII
CHEN Xiao Mei; YANG Jun Shan; GUO Shun Xing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     9(11)-dehydroergosterol peroxide
C28H44O3     ÏàËÆ¶È:80%
Natural Product Sciences          2009          15          173-179
Steroids and Triterpenoid from the Fruit Bodies of Ganoderma lucidum and Their Cytotoxic Activity
Lee, Joon-Seok; Lee, Mi-Kyoung; Hung, Tran-Manh; Lee, Ik-Soo; Min, Byung-Sun; Bae, Ki-Hwan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
C28H46O3     ÏàËÆ¶È:80%
Chinese Traditional and Herbal Drugs          2008          39          1776-1778
Chemical constituents of Russula virescens
TANG Jian-guo; SHAO Hong-jun; LIU Ji-kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     8,9-epoxyergosta-5,22-dien-3¦Â,15-diol
C28H44O3     ÏàËÆ¶È:80%
Journal of the Chinese Chemical Society          1991          38          71-76
Studies on the Constituents of Ganoderma lucidum
½ªºêÕÜ(Hung-Cheh Chiang);ÖìÊÀ²ý(Shih-Chang Chu)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     3¦Â,16¦Â,30-trihydroxycycloart-20,24-diene
C30H52O3     ÏàËÆ¶È:80%
Zeitschrift f¨¹r Naturforschung C          2002          57          489-495
Microbial Transformation of a Mixture of Argentatin A and Incanilin
Key words: Argentatin A, Incanilin, Biotransformation
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     (22E,24R)-6-Acetoxy-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:80%
Natural Product Communications          2009          4          1449-1454
Ring B Aromatic Steroids from an Endophytic Fungus, Colletotrichum sp.
Wen Zhang , Siegfried Draeger, Barbara Schulz and Karsten Krohn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     (22E,24R)-3¦Â,5¦Á,6¦Á-trihydroxyergosta-7,22-diene
    ÏàËÆ¶È:80%
Journal of Natural Medicines          2011          65          307-312
Constituents of cultivated Agaricus blazei
Yumi Ueguchi ,Katsuyoshi Matsunami ,Hideaki Otsuka ,Kazunari Kondo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     Ergosta-7,22-dien-3¦Â,5¦Á,6¦Á-triol
C28H46O3     ÏàËÆ¶È:80%
Journal of Anhui Agricultural Sciences          2010          38          2356-2357
Research on the Chemical Componen ts of the Fruit Bodies ofBoletus calopus
ZUOW ei et al
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     24-methyl-7¦Á,8¦Á-epoxy-3¦Â,5¦Á,6¦Á-trihydroxycholest-22-ene
C28H46O4     ÏàËÆ¶È:76.6%
Journal of Natural Products          1996          59          679-682
Isolation of Polyhydroxysteroids from the Gorgonian Acabaria undulata
Jongheon Shin, Youngwan Seo, Jung-Rae Rho, and Ki Woong Cho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     cerevisterol
C28H46O3     ÏàËÆ¶È:76.6%
Acta Botanica Yunnanica          2006          28(3)          315-318
A New Steroidal Glycoside from the Fruiting Bodies of Tylopilus virens (Boletaceae)
WANG Fei,ZHANGLing, DONG Ze-Jun,LIU Ji-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     3¦Â-acteoxy-(22E, 24R)-24-methyl-5¦Á-cholest-7, 22-diene-5, 6¦Â-diol
C30H48O4     ÏàËÆ¶È:76.6%
Acta Botanica Yunnanica          2002          24(4)          125-128
The Chemical Constituents from Basidiocarps of Sarcodon aspratum
HUANG Yue,DONG Ze-Jun,LIU Ji-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     ergosta-7,22-diene-3,5,6-triol
C28H46O3     ÏàËÆ¶È:76.6%
Chemistry of Natural Compounds          2009          45          124-125
COMPONENTS OF THE SCLEROTIAOF Polyporus umbellatus
Weiwei Zhou, Shunxing Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol (=cerevisterol)
    ÏàËÆ¶È:76.6%
Steroids          2001          66          771-775
A novel sterol from Chinese truffles Tuber indicum
Gao Jinming, Hu Lin, Liu Jikai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     Globosterol
C29H47O3     ÏàËÆ¶È:76.6%
Steroids          2009          74          786-790
Polyhydroxylated steroids from an endophytic fungus, Chaetomium globosum ZY-22 isolated from Ginkgo biloba
Jian-Chun Qin, Jin-Ming Gao, Ya-Mei Zhang, Sheng-Xiang Yang, Ming-Sheng Bai, Ya-Tuan Ma, Hartmut Laatsch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     ergosta-7,22E-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:76.6%
Journal of Asian Natural Products Research          2005          7          165-169
Sterols from the pericarp of Sphaerophysa salsula DC
GUO-YU LI, JIN-HUI WANG and XIAN LI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol
C28H46O3     ÏàËÆ¶È:76.6%
Natural Product Research          2008          22          154-166
Antifouling and antibacterial compounds from the gorgonians Subergorgia suberosa and Scripearia gracillis
S. H. Qi; S. Zhang; L. H. Yang; P. Y. Qian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     6,9-epidioxyergosta-7,22-dien-3¦Â-ol
    ÏàËÆ¶È:76.6%
China Journal of Chinese Materia Medica          2007          32          235-237
Studies on chemical constituents from the fruiting bodies of Ganoderma sinense Zhao,Xu et Zhang
LIU Chao , WANG Hongqing, LI Baoming, CHEN Ruoyun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     (22E,24R)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol
    ÏàËÆ¶È:76.6%
Journal of Natural Products          1987          Vol 50          915
Four New Trihydroxylated Sterols from the Sponge Spongionella gracilis Four New Trihydroxylated Sterols from the Sponge Spongionella gracilis
Vincenzo Piccialli, Donato Sica
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     cerevisterol(3¦Â,5¦Á,6¦Â-trihydroxyergosta-7,22-diene)
C28H46O3     ÏàËÆ¶È:76.6%
Phytochemistry          1991          30          4117-4120
Glycosides of ergosterol derivatives from Hericum erinacens
Yoshihisa Takaishi, Minoru Uda, Takashi Ohashi, Kimiko Nakano, Koutarou Murakami, Toshiaki Tomimatsu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     24-methyl-cholesta-7,22E-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:76.6%
Chinese Journal of Marine Drugs          2011          30(1)          31-36
Studies on Chemical Constituents of Subergorgia ret iculata
LI Jun, LI Yong-ai, XU Jing, TANG Xu-li, LI Ping-lin, LI Guo-qiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     (3¦Â,5¦Á,6¦Á,7¦Â,22E)-ergosta-7,22-diene-3,5,6-triol
C28H46O3     ÏàËÆ¶È:76.6%
Chinese Journal of Marine Drugs          2008          27(4)          9-13
Studies on the chemical constituents from the endophytic fungus Penicillium sp.091402 of managrove plant Brugurera sexangula
HAN Zhuang, MEI Wen-li, CUI Hai-bin, LIN Hai-peng, HONG Kui, DAI Hao-fu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
C28H46O3     ÏàËÆ¶È:76.6%
Indian Journal of Chemistry          2005          44B          1291-1294
Sterols and flavonol glycosides from Melothria purpusila
Langoljam,Reena D; Kongbrailatpam,Brajeshwari D; Laitonjam,Warjeet S
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     ( 22 E)-3¦Â-Acetoxv-5 ¦Á-hydroxyergosta-7,22-dien-6-one
    ÏàËÆ¶È:76.6%
Steroids          1996          61          540-543
New synthetic strategy for the synthesis of 24-epibrassinolide
Carme Brosa, Rita Puig, Xavier Comas, Cristina Fern¨¢ndez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
54 .     (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:76.6%
Chinese Traditional and Herbal Drugs          2010          41          1065-1068
СҶÈ̶¬ÌٵĻ¯Ñ§³É·ÖÑо¿
Áõΰ;°×ËØÆ½;Áº»á¾ê;Ô¬ÓÀÁÁ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
55 .     stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:76.6%
Chinese Traditional and Herbal Drugs          2008          39          1606-1609
Chemical constituents of Amtipathes dichotoma
SU Guo-chen; ZHANG Si; QI Shu-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
56 .     (22E,24S)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol
C28H46O3     ÏàËÆ¶È:76.6%
Chinese Traditional and Herbal Drugs          1994          25          342-343+390
Studies on the Chemical Constituents of Kuhonggu (Russula rosacea)(¢ò)
Wang Huaibin; Xu Weishen; et al(Institute of Materia Medica; Chinese Academy of Medica Sciences; Beijing);
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
57 .     (24R)-ergosta-7,22-diene-3,5,6-triol
    ÏàËÆ¶È:76.6%
Chinese Journal of Natural Medicines          2008          6          348-353
Chemical Constituents of Marine Sponge Biemna fortis Topsent
HUANG Xiao-Chun; LIU Hai-Li; GUO Yue-Wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
58 .     cerevisterol
    ÏàËÆ¶È:76.6%
Archives of Pharmacal Research          2005          28          889-891
Antibacterial constituents from fruit bodies of Ascomyce Bulgaria inquinans
Peng Zhang, Xian Li, Ning Li, Jing Xu and Zhan-Lin Li, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
59 .     3¦Â,5¦Á-dihydroxy-6¦Â-methoxyergosta-7,22-diene
    ÏàËÆ¶È:76.6%
Archives of Pharmacal Research          2006          29          548-555
Cytotoxic and COX-2 inhibitory constituents from the aerial parts ofAralia cordata
Ik Soo Lee, Wen Yi Jin, Xinfeng Zhang, Tran Manh Hung and Kyung Sik Song, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
60 .     Cerevisterol
    ÏàËÆ¶È:76.6%
Archives of Pharmacal Research          2006          29          479-483
Constituents from the fruiting bodies of Ganoderma applanatum and their aldose reductase inhibitory activity
Sang Hyun Lee, Sang Hee Shim, Ju Sun Kim and Sam Sik Kang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
61 .     (22E,24R)-ergosta-7,22E-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:76.6%
Archives of Pharmacal Research          2007          30          28-33
Cytotoxic constituents isolated from the fruit bodies of Hypsizigus marmoreus
Ming-Lu Xu, Jae-Young Choi, Byeong-Seon Jeong, Gao Li and Kap-Rang Lee, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
62 .     (24R)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:76.6%
Chinese Pharmaceutical Journal          2006          41          1131-1133
Chemical Constituents of Monascus anka
LI Li-li, CHEN Jie-peng, KONG Ling-yi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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