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1 . cerevisterol
ÏàËƶÈ:96.5%
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 ̼Æ×Ä£Äâͼ
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2 . 6,9-epoxyergosta-7,22-dien-3-ol
ÏàËƶÈ:96.5%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
3 . 6,9-Epoxy-ergosta-7,22-dien-3¦Â-ol
ÏàËƶÈ:96.5%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
4 . 5¦Á,6¦Á-epoxy-24(R)-methylcholesta-7,22-dien-3¦Â-ol
C28H44O2 ÏàËƶÈ:96.5%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
5 . ergosta-7,22-diene-2¦Â,3¦Á,9¦Á-triol
C28H46O3 ÏàËƶÈ:96.5%
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 ̼Æ×Ä£Äâͼ
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6 . 6,9-epoxy-ergosta-7,22-dien-3-ol
C28H44O2 ÏàËƶÈ:96.5%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
7 . 5,6-Epoxy-22-en-3-ol-ergosterol
C28H44O2 ÏàËƶÈ:96.5%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
8 . cerevisterol (3¦Â,5¦Á,6¦Â-trihydroxyergosta-7,22-diene)
ÏàËƶÈ:96.5%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
9 . ergosta-6,22-dien-3¦Â,5¦Â,8¦Â-triol
ÏàËƶÈ:96.5%
Chinese Traditional and Herbal Drugs 2000 31 328-330
ºÖÔ²¿×Å£¸Î¾ú»¯Ñ§³É·ÖµÄÑо¿
Íò»Ô
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
10 . ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
ÏàËƶÈ:96.5%
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 ̼Æ×Ä£Äâͼ
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11 . 5¦Á,6¦Á-epoxy-24(R)-methylcholesta-7,22-dien-3¦Â-ol
ÏàËƶÈ:96.5%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
12 . (22E,24S)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
ÏàËƶÈ:96.5%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
13 . (22E,24S)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
ÏàËƶÈ:96.5%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
14 . ergosta-6,22-dien-3¦Â,5¦Â,8¦Â-triol
ÏàËƶÈ:96.5%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
15 . ergosta-7,22-diene-2¦Â,3¦Á,9¦Á-triol
ÏàËƶÈ:96.5%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
16 . cerevisterol
ÏàËƶÈ:96.5%
Journal of Guangdong Phamaceutical University 2011 27 256-259
Chemical constituents of the mycelia of Guignardia mangiferae,an endophyte from Smilax glabra
LIANG Fa-liang, LI Dong-li, TAO Mei-hua, ZHANG De-zhi, ZHANG Wei-min
Structure 13C NMR ̼Æ×Ä£Äâͼ
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17 . ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
C28H44O2 ÏàËƶÈ:96.5%
Natural Medicines 1996 50 179-181
Sterol Constituents from the Sclerotium of Polyporus umbellatus Fries
OHTA KOJI,YAOITA YASUNORI,MATSUDA NORIKO
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
18 . (22E)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
ÏàËƶÈ:96.5%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
19 . cerevisterol
ÏàËƶÈ:96.5%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
20 . ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
ÏàËƶÈ:96.5%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
21 . 22E-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
C28H46O3 ÏàËƶÈ:96.5%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
22 . (22E,24S)-cerevisterol
ÏàËƶÈ:96.5%
Journal of Chinese Medicinal Materials 2005 28 998-999
²èË‘×ÓÒ¶¿×¾ú»¯Ñ§³É·ÖµÄÑо¿
ÁõÓñºì, ÐìÁè´¨, Íõ½¨Æ½, Ìï¾°Õñ
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
23 . ergost-7,22-diene-3¦Â,5¦Á,6¦Â-triol
ÏàËƶÈ:96.5%
Journal of Chinese Medicinal Materials 2010 33 1262-1265
Studies on the Chemical Constituents from Petroleum Ether Portion of Abelmoschus esculentus
JIA Lu, LI Dong, JING Lin-lin, GUO Ming-ming
Structure 13C NMR ̼Æ×Ä£Äâͼ
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24 . cerevisterol
ÏàËƶÈ:96.5%
Journal of Chinese Medicinal Materials 2011 34 549-551
Studies on the Secondary Metabolites of Coriolopsis sp.G066
SANG Zhi-gao, LI Dong-li, TAO Mei-hua, ZHANG Wei-min, TU Guo-quan
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
25 . 3¦Â,5¦Á,6¦Â-ÈýôÇ»ù-(22E,24R)-Âó½ÇçÞ-7,22-¶þÏ©
ÏàËƶÈ:96.5%
Journal of Tropical and Subtropical Botany 2011 19 75-78
Steroidal Metabolites of Fimetariella rabenhorstii,Endophytic Fungus from Aquilaria sinensis
TAO, Meihua, YAN, Jian, WEI, Xiaoyi, LI, Dongli, ZHANG, Weimin, TAN, Jianwen
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
26 . cerevisterol
ÏàËƶÈ:93.1%
Phytochemistry 1997 44 1443-1448
Cytochalasins and phytotoxins from the fungus Xylaria obovata
Dawit Abate, Wolf-Rainer Abraham, Holger Meyer
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
27 . 22E,24R)-ergost-7,22-dien-3¦Â,5¦Á,6¦Â-triol
ÏàËƶÈ:93.1%
Academic Journal of Second Military Medical University 2010 31 421-424
Studies on chemical constituents of Anthogorgia sp.
XU Yuan-yuan, LI Ling, YI Yang-hua, ZHANG Wen
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
28 . ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
ÏàËƶÈ:93.1%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
29 . Ergosta-7,22-dien-3¦Â,5¦Á,6¦Á-triol
C28H46O3 ÏàËƶÈ:93.1%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
30 . (3¦Â,5¦Á,6¦Â,22E)-Âó½ÇçÞ-7,22-¶þÏ©-3,5,6-Èý´¼
C28H46O3 ÏàËƶÈ:93.1%
Chinese Journal of Antibiotics 2011 36 576-580
Antibacterial metabolites from the endophytic fungus R7 of Aquilaria sinensis
Wei, Jing, Dai, Hao-Fu, Yu, Lei, Wang, Hui, and, Mei, Wen-Li
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
31 . 3¦Â,16¦Â,30-trihydroxycycloart-20,24-diene
C30H52O3 ÏàËƶÈ:90%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
32 . (3¦Â,5¦Á,6¦Â,22E)-6-methoxyergosta-7,22-diene-3,5-diol
ÏàËƶÈ:89.6%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
33 . (22E,24R)-23-methylergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
C29H48O3 ÏàËƶÈ:89.6%
Chemical & Pharmaceutical Bulletin 1999 47 847-851
Sterol Constituents from Seven Mushrooms
Yasunori YAOITA,Makiko ENDO,Yoshino TANI,Kaori MACHIDA,Keiko AMEMIYA,Katsuyuki FURUMURA and Masao KIKUCHI
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
34 . biemnasterol
C28H44O3 ÏàËƶÈ:89.6%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
35 . 3¦Â,5¦Á-dihydroxy-6¦Â-methoxyergosta-7,22-diene
C29H48O3 ÏàËƶÈ:89.6%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
36 . (24R)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
ÏàËƶÈ:89.6%
Chinese Pharmaceutical Journal 2006 41 1131-1133
Chemical Constituents of Monascus anka
LI Li-li, CHEN Jie-peng, KONG Ling-yi
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
37 . (22E,24R)-rgosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
ÏàËƶÈ:89.6%
Natural Product Research and Development 2007 19 610-613
Chemical Constituents from Schizophyllum commune
MAO Shao-chun; LI Zhu-ying; LI Cong
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
38 . 6-methoxy-cerevisterol
ÏàËƶÈ:89.6%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
39 . ergosta-7,22-dien-3,5,6-triol
C28H46O3 ÏàËƶÈ:89.6%
Academic Journal of Second Military Medical University 2007 28 266-271
Isolation,identification,and biological characterization of 6 secondary metabolites extracted from Myxococcus xanthus 095B06
SHI Xiao-qiong, XU Qiang-zhi, LIU Xiao-yu, HAN Wen-ju, LIU Xin-li, JIAO Bing-hua, LI Yue-zhong
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
40 . 22E-6¦Â-methoxyergosta-7,22-diene-3¦Â,5¦Á-diol
C29H48O3 ÏàËƶÈ:89.6%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
41 . (22E,24R)-6-Acetoxy-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
ÏàËƶÈ:86.6%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
42 . (22E,24R)-6-Acetoxy-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
ÏàËƶÈ:86.6%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
43 . ergost-5,22-dien-3¦Â,7¦Â-diol
C28H46O2 ÏàËƶÈ:86.2%
Chinese Traditional and Herbal Drugs 2005 36 510-511+550
Å£¶ú¶ä»¯Ñ§³É·ÖµÄÑо¿
²ÌÏ麣,µËµÂɽ,ÂíÔƱ£,ÂÞÏþ¶«
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
44 . 8,9-epoxyergosta-5,22-dien-3¦Â,15-diol
C28H44O3 ÏàËƶÈ:86.2%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
45 . cholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
ÏàËƶÈ:86.2%
Journal of Chinese Medicinal Materials 2006 29 555-557
Chemical Constituents from the South China Sea Gorgonian Coral Subergorgia reticulata
YANG Jin, QI Shu-hua, ZHANG Si, LI Qing-xin
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
46 . (22E,24R)-6¦Â-¼×Ñõ»ùÂó½ÇçÞ-7,22-¶þÏ©-3¦Â,5¦Á-¶þ´¼
ÏàËƶÈ:86.2%
Journal of Chinese Medicinal Materials 2008 31 1343-1347
Studies on the Anti-tumor Activity Principles of a Marine-derived Fungus BZYT-21
GAO Zong-hua, MA Li-ying, SHEN Yun-xiu
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
47 . 5¦Á,6¦Á-epoxy-24(R)-methylcholesta-7,22-dien-3¦Â-ol
C28H44O2 ÏàËƶÈ:86.2%
Guihaia 2011 31 699-701
Chemical constituents of endophyte Talaromyces sp.T1BF from Taxus yunnanensis
LI, Liang-Qun, YANG, Yan-Guang, ZENG, Ying, ZOU, Cheng, ZHAO, Pei-Ji
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
48 . 3¦Â-acteoxy-(22E, 24R)-24-methyl-5¦Á-cholest-7, 22-diene-5, 6¦Â-diol
C30H48O4 ÏàËƶÈ:83.3%
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 ̼Æ×Ä£Äâͼ
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49 . 5,6¦Â-Dihydroxy-5¦Á-ergosta-7,22-dien-3¦Â-ylacetate
C30H48O4 ÏàËƶÈ:83.3%
Steroids 2006 71 565-577
Regio and stereoselective oxidations of unsaturated steroidal compounds with H2O2 mediated by CH3ReO3
Francesco P. Ballistreri, Rosa Chillemi, Sebastiano Sciuto, Gaetano A. Tomaselli, Rosa M. Toscano
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
50 . cerevisterol
C28H46O3 ÏàËƶÈ:82.7%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
51 . (22E)-27-nor-24-methyl-5(-cholesta-7, 22-diene-3¦Â, 5, 6¦Â-triol
C27H44O3 ÏàËƶÈ:82.7%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
52 . ergosta-7,22-diene-3,5,6-triol
C28H46O3 ÏàËƶÈ:82.7%
Chemistry of Natural Compounds 2009 45 124-125
COMPONENTS OF THE SCLEROTIAOF Polyporus umbellatus
Weiwei Zhou, Shunxing Guo
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
53 . stigmasta-7,22-diene-3¦Â,5¦Á,6¦Á-triol,respectively
C28H46O3 ÏàËƶÈ:82.7%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
54 . (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol (=cerevisterol)
ÏàËƶÈ:82.7%
Steroids 2001 66 771-775
A novel sterol from Chinese truffles Tuber indicum
Gao Jinming, Hu Lin, Liu Jikai
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
55 . 5¦Á,6¦Á-Epoxy-26,27-dinorergosta-7,22-en-3¦Â-ol
C26H40O2 ÏàËƶÈ:82.7%
Steroids 2008 73 568-573
A series of new 5,6-epoxysterols from a Chinese sponge Ircinia aruensis
Shihai Xu, Xiaojian Liao, Bin Du, Xulong Zhou, Qichang Huang, Chumei Wu
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
56 . 5¦Á,6¦Á-Epoxyergosta-7-en-3¦Â-ol
C28H46O2 ÏàËƶÈ:82.7%
Steroids 2008 73 568-573
A series of new 5,6-epoxysterols from a Chinese sponge Ircinia aruensis
Shihai Xu, Xiaojian Liao, Bin Du, Xulong Zhou, Qichang Huang, Chumei Wu
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
57 . 5¦Á,6¦Á-Epoxystigmasta-7-en-3¦Â-ol
C29H48O2 ÏàËƶÈ:82.7%
Steroids 2008 73 568-573
A series of new 5,6-epoxysterols from a Chinese sponge Ircinia aruensis
Shihai Xu, Xiaojian Liao, Bin Du, Xulong Zhou, Qichang Huang, Chumei Wu
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
58 . ergosta-7,22E-diene-3¦Â,5¦Á,6¦Â-triol
ÏàËƶÈ:82.7%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
59 . stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol
C28H46O3 ÏàËƶÈ:82.7%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
60 . 6,9-epidioxyergosta-7,22-dien-3¦Â-ol
ÏàËƶÈ:82.7%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
61 . (22E,24R)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol
ÏàËƶÈ:82.7%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
62 . cerevisterol(3¦Â,5¦Á,6¦Â-trihydroxyergosta-7,22-diene)
C28H46O3 ÏàËƶÈ:82.7%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
63 . 5¦Á,6¦Á-epoxys-tigmasta-7-en-3¦Â-ol
ÏàËƶÈ:82.7%
Chinese Journal of Marine Drugs 2009 28(4) 21-25
Studies on chemical constituents of marine sponge Aplysinopsis sp.
LI Xue, SONG Shao-jiang, PIAO Shu-juan, DONG Tao, LIN Hou-wen
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
64 . ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
C28H46O3 ÏàËƶÈ:82.7%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
65 . (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
ÏàËƶÈ:82.7%
Chinese Traditional and Herbal Drugs 2010 41 1065-1068
СҶÈ̶¬ÌٵĻ¯Ñ§³É·ÖÑо¿
Áõΰ;°×ËØƽ;Áº»á¾ê;Ô¬ÓÀÁÁ
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
66 . stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol
ÏàËƶÈ:82.7%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
67 . (22E,24S)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol
C28H46O3 ÏàËƶÈ:82.7%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
68 . (24R)-ergosta-7,22-diene-3,5,6-triol
ÏàËƶÈ:82.7%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
69 . 3¦Â,5¦Á-Dihydroxy-6¦Â-methoxyergosta-7,22-diene
ÏàËƶÈ:82.7%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
70 . cerevisterol
ÏàËƶÈ:82.7%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
71 . 3¦Â,5¦Á-dihydroxy-6¦Â-methoxyergosta-7,22-diene
ÏàËƶÈ:82.7%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
72 . Cerevisterol
ÏàËƶÈ:82.7%
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 ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
73 . ergosta-7,22-diene-3,5,6-triol
C28H46O3 ÏàËƶÈ:82.7%
Chinese Pharmaceutical Journal 2003 38 499-5001
Studies on chemical constituents of Cordyceps sinensis(Berk) Sacc
LI Jie-xiu, LI Jin, XU Li-zhen, YANG Shi-lin, ZOU Zhong-mei
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
74 . ergosta-7,22-dien-2¦Â,3¦Á,9¦Á-triol
ÏàËƶÈ:82.7%
Chinese Pharmaceutical Journal 2010 45 413-415
A New Sterol from the Fruiting Bodies of Ganoderma sinense Zhao, Xu et Zhang
LIU Chao, CHEN Ruo-yun
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
75 . 22 E-ergosta-7,22-dien-3¦Â,5¦Â,6¦Â-triol
ÏàËƶÈ:82.7%
Chinese Journal of Medicinal Chemistry 2006 16 98-101
The constituents of marine fungus 97F49
ZHANG Qing-hua, WANG Nai-li, GAO Hao, LIU Hong-wei, SONG Shan-shan, MICHIO Namikoshi, YAO Xin-sheng
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
76 . (22E,24R)-ergos-ta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
ÏàËƶÈ:82.7%
Journal of Shenyang Pharmaceutical University 2009 26 796-799
Isolation and identification of steroids from the leaves of theMagnolia sieboldii K. Koch
WANG Ru-ping, WU Di, GAO Hui-yuan, SUN Bo-hang, HUANG Jian, WU Li-jun
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
77 . (22E,24R)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol
ÏàËƶÈ:82.7%
Journal of China Pharmaceutical University 2007 38 315-319
Chemical constituents of the aerial parts of Euphorbia sororia
ZHANG Wei-ku; ZHANG Xiao-qi; YE Wen-cai;
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
78 . 24-Ethylcholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
ÏàËƶÈ:82.7%
Bulletin of the Korean Chemical Society 2011 32 697-700
Isolation of Protein Tyrosine Phosphatase 1B Inhibitory Constituents from the Sclerotia of Polyporus umbellatus Fries
Hee Sang Lee, In Hyun Hwang, Jeong Ah Kim, Ji Young Choi, Tae Su Jang, Hiruyuki Osada, Jong Seog Ahn*, MinKyun Na*, Seung Ho Lee*
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
79 . 24-Methylcholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
ÏàËƶÈ:82.7%
Bulletin of the Korean Chemical Society 2011 32 697-700
Isolation of Protein Tyrosine Phosphatase 1B Inhibitory Constituents from the Sclerotia of Polyporus umbellatus Fries
Hee Sang Lee, In Hyun Hwang, Jeong Ah Kim, Ji Young Choi, Tae Su Jang, Hiruyuki Osada, Jong Seog Ahn*, MinKyun Na*, Seung Ho Lee*
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
80 . ergosta-7,11-dien-3¦Â,5¦Á,6¦Â-triol
C28H46O3 ÏàËƶÈ:82.7%
Natural Product Research and Development 2010 22 235-237
Studies on the Chemical Constituents of Rhodobryum giganteum (schwaegr.) Par.
JIAO Wei; LU Gai-li; SHAO Hua-wu; LU Run-hua;
Structure 13C NMR ̼Æ×Ä£Äâͼ |
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