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1 .     cerevisterol
C28H46O3     ÏàËÆ¶È:92.8%
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
2 .     ergosta-7,22-diene-3,5,6-triol
C28H46O3     ÏàËÆ¶È:92.8%
Chemistry of Natural Compounds          2009          45          124-125
COMPONENTS OF THE SCLEROTIAOF Polyporus umbellatus
Weiwei Zhou, Shunxing Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol (=cerevisterol)
    ÏàËÆ¶È:92.8%
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
4 .     ergosta-7,22E-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:92.8%
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
5 .     stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol
C28H46O3     ÏàËÆ¶È:92.8%
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
6 .     6,9-epidioxyergosta-7,22-dien-3¦Â-ol
    ÏàËÆ¶È:92.8%
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
7 .     (22E,24R)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol
    ÏàËÆ¶È:92.8%
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
8 .     cerevisterol(3¦Â,5¦Á,6¦Â-trihydroxyergosta-7,22-diene)
C28H46O3     ÏàËÆ¶È:92.8%
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
9 .     ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
C28H46O3     ÏàËÆ¶È:92.8%
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
10 .     (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:92.8%
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
11 .     (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
C28H46O3     ÏàËÆ¶È:92.8%
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
12 .     stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:92.8%
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
13 .     (22E,24S)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol
C28H46O3     ÏàËÆ¶È:92.8%
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
14 .     cerevisterol
    ÏàËÆ¶È:92.8%
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
15 .     (22E,24R)-ergosta-7,22E-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:92.8%
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
16 .     ergosta-7,22-diene-3,5,6-triol
C28H46O3     ÏàËÆ¶È:92.8%
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   Ì¼Æ×Ä£Äâͼ
17 .     ergosta-7,22-dien-2¦Â,3¦Á,9¦Á-triol
    ÏàËÆ¶È:92.8%
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   Ì¼Æ×Ä£Äâͼ
18 .     22 E-ergosta-7,22-dien-3¦Â,5¦Â,6¦Â-triol
    ÏàËÆ¶È:92.8%
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   Ì¼Æ×Ä£Äâͼ
19 .     (22E,24R)-ergos-ta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:92.8%
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   Ì¼Æ×Ä£Äâͼ
20 .     (22E,24R)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol
    ÏàËÆ¶È:92.8%
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   Ì¼Æ×Ä£Äâͼ
21 .     (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
C28H46O3     ÏàËÆ¶È:92.8%
Natural Product Research and Development          2007          19          436-438
Chemical Constituents of Basidiomycetes Russula subnigricans
GONG Qing-fang; ZHANG Yu-mei; TAN Ning-hua; CHEN Zuo-hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:92.8%
Chinese Traditional and Herbal Drugs          2011          42          251-254
Chemical constituents of Omphalia lapidescens
XU Ming-feng, SHEN Lian-qing, WANG Kui-wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     6,9-epidioxyergosta-7,22-dien-3¦Â-ol
C28H44O2     ÏàËÆ¶È:92.8%
Mycosystema          2009          28          407-409
Chemical components from the fruiting bodies of Ganoderma duropora
ZHAO Fen LI Ye LIU Chao LI Bao-Ming CHEN Ruo-Yun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:92.8%
Chinese Traditional and Herbal Drugs          2012          43          2365-2368
Study on chemical constituents in Cryptotaenia japonica
LI Sheng-hua; NIU You-ya Key
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     8,9-epoxyergosta-5,22-dien-3¦Â,15-diol
C28H44O3     ÏàËÆ¶È:89.6%
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
26 .     (24R)-ergosta-7,22-diene-3,5,6-triol
    ÏàËÆ¶È:89.2%
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
27 .     24-Ethylcholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:89.2%
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   Ì¼Æ×Ä£Äâͼ
28 .     24-Methylcholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:89.2%
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   Ì¼Æ×Ä£Äâͼ
29 .     (20S,22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
C28H46O3     ÏàËÆ¶È:89.2%
Natural Product Research and Development          2004          16          277-280
METABOLITES OF RHIZOPUS ARRHIZUS 3078
LI Guo-you; LI Bo-gang; LIU Guang-ye; ZHANG Guo-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     (22E,24R)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
C28H46O3     ÏàËÆ¶È:89.2%
Biological and Pharmaceutical Bulletin          2002          25          1040-1044
Stimulative Effects of (22E,24R)-Ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol from Fruiting Bodies of Tricholoma auratum, on a Mouse Osteoblastic Cell Line, MC3T3-E1
Keishi Hata, Fuyuki Sugawara, Naganori Ohisa, Saori Takahashi, Kazuyuki Hori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     (22E,24R)-Ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:89.2%
Chemistry of Natural Compounds          2012          48          913-913
Chemical constituents of basidiomycetes Cortinarius longipes
Xiang-Dong Qin, Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     (24R)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
C10H13N5O4     ÏàËÆ¶È:89.2%
Chinese Journal of Marine Drugs          2012          31          7-10
Secondary metabolites of marine fungus zp6 and their antifungal bioactivities
GAO Chang-song; ZHONG Hui-min; CAO Jun-wei; CHEN Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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