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S40:
12.6,12.7,19.5,19.5,21.6,21.8,21.9,22.3,26.5,27.4,30.4,32.3,33.2,37.6,38.2,40.9,41.2,41.9,42.5,43.9,50.1,52.8,56.9,57.8,72.1,73.8,127.4,130.6,139.8,144.1

S41:
12.4,12.4,19.4,19.4,20.2,22.3,24.2,27.2,27.4,29.7,30.4,32.3,35.2,37.4,37.6,38.2,41.0,41.2,42.5,44.0,47.3,50.1,56.9,57.8,72.1,73.8,127.4,144.1
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yangyinhe

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SunHaoli: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2015-03-16 23:10:13
1 .     ¶¹çÞ´¼-5,22-¶þÏ©-¶þÏ©-3¦Â,7¦Â-¶þ´¼
C29H48O2     ÏàËÆ¶È:86.6%
Chinese Traditional and Herbal Drugs          2005          36          982-983
ÄϰåÀ¶¸ùµÄ»¯Ñ§³É·ÖÑо¿
ÎâìÏÇï,Ç®±ó,ÕÅÈÙÆ½,×Þ³Î,Áõ¹â
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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2 .     st igmasterol
    ÏàËÆ¶È:80%
Natural Product Research and Development          2003          15          502-503
STUDYS ON THE CHEMICAL CONSTITUENTS OF ORTHOSIPHON WULFENIOIDES(DIES)HAND.-MAZZ
LUO Yu; TIAN Jun; WU Feng-e
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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3 .     stigmasterol
    ÏàËÆ¶È:76.6%
Chinese Traditional and Herbal Drugs          2010          41          36-39
É¡»¨Ä¾»¯Ñ§³É·ÖÑо¿
ºÎéó; ÕÔÃ÷; ×ÚÓñÓ¢; ²ÌÈýЭ; ³µÕòÌÎ
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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4 .     stigmasterol
    ÏàËÆ¶È:76.6%
Food Chemistry          2013          136          563-568
Identification of a novel phenolic compound in litchi (Litchi chinensis Sonn.) pericarp and bioactivity evaluation
Guoxiang Jiang, Sen Lin, Lingrong Wen, Yueming Jiang, Mouming Zhao, Feng Chen, K. Nagendra Prasad, Xuewu Duan, Bao Yang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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5 .     stigmasterol
    ÏàËÆ¶È:76.6%
Journal of Chinese Medicinal Materials          2012          35          404-406
Study on the Chemical Constituent from the Dichloromethane Extract.
of the Pine Needles of Cedrus deodara
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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6 .     stigmasterol
    ÏàËÆ¶È:76.6%
Acta Academiae Medicinae Neimongol          2011          33          548-550
THE STUDIE OF CHEMICAL CONSTITUENTS OF SONCHUS OLERACEUS L
ZHOU Yan, BO Yu£­kun, ZHANG Shuo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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7 .     stigmasterol
C29H48O     ÏàËÆ¶È:76.6%
Journal of the Chemical Society of Pakistan          2013          35          130−134
Phytochemical Studies on Sorbus cashmiriana
SADIA KHAN, MEHDI HASSAN KAZMI*, EJAZ AHMED** ABDUL MALIK AND AHSAN SHARIF
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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8 .     stigmastcrol
    ÏàËÆ¶È:73.3%
Chemistry of Natural Compounds          1999          35          642-645
I3C NMR SPECTRA OF STEROL DERIVATIVES,INTERMEDIATES IN THE SYNTHESIS OF ECDY- AND BRASSINOSTEROIDS
N. V. Kovganko, Zh. N. Kashkan,and E. V. Borisov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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9 .     24-isopropyl-5¦Á-cholest-22Z-en-3¦Â-ol acetate
    ÏàËÆ¶È:73.3%
Chemistry of Natural Compounds          1990          26          172-174
STEROID COMPOUNDS OF MARINE SPONGES. Xl. STEROIDS OF THE AUSTRALIAN SPONGE Trachyopsis sp.
T. N. Makar'eva, V. V. Isakov, and V. A. Stonik
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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10 .     Stellasteryl
C30H48O2     ÏàËÆ¶È:73.3%
Phytochemistry          1983          22          1300-1301
(22E,24S)-5¦Á-Ergosta-7, 22-dien-3¦Â-ol from the seeds of Cucumis sativus
T. Matsumoto, T. Shigemoto, T. Itoh
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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11 .     stigmasterol
C29H48O     ÏàËÆ¶È:73.3%
Chemistry and Industry of Forest Products          2011          31          77-80
Study on Chemical Constituents of Root-bark of Ficus tsiangii
WANG Xue-gui, SHEN Li-tao, TIAN Yong-qing, XU Han-hong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-03-16 15:14:20
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yangyinhe

ÖÁ×ðľ³æ (ÖøÃûдÊÖ)

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SunHaoli: ½ð±Ò+5, ¡ïÓаïÖú 2015-03-16 23:10:25
1 .     ¶¹çÞ´¼-5,22-¶þÏ©-¶þÏ©-3¦Â,7¦Â-¶þ´¼
C29H48O2     ÏàËÆ¶È:86.2%
Chinese Traditional and Herbal Drugs          2005          36          982-983
ÄϰåÀ¶¸ùµÄ»¯Ñ§³É·ÖÑо¿
ÎâìÏÇï,Ç®±ó,ÕÅÈÙÆ½,×Þ³Î,Áõ¹â
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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2 .     schleicheol 2
C30H52O2     ÏàËÆ¶È:82.7%
Journal of Asian Natural Products Research          2001          3          299-311
CONSTITUENTS FROM LIMONIA CRENULATA
XUE-ME1 NIU, SHENG-HONG LI, LI-YAN PENG,and HAN-DONG SUN,ZHONG-WEN LIN, GAO-XIONG RAO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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3 .     cholest-5-ene-3¦Â,7¦Â-diol
    ÏàËÆ¶È:82.1%
Shoyakugaku Zasshi          1993          47          200-206
Chemotaxonomy of Ferns 4. : Cheilanthes chusana and Aleuritopteris Species
KAMAYA RUMIKO, NAKAMURA MASAKO, TAMARU KAYO, TAKAHATA CHIHARU,AGETA HIROYUKI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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4 .     ¦Â-Sitosterol
    ÏàËÆ¶È:79.3%
Natural Product Sciences          2007          13          394-397
Chemical Constituents of the Moss Hylocomium splendens
Kang, Shin-Jung; Jovel, Eduardo; Hong, Seong-Su; Hwang, Bang-Yeon; Liu, Patty; Lee, Meng-Hsin; Lee, Meng-Chun; Lee, Kyung-Soon; Towers, George Hugh Neil
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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5 .     ¦Â-sitosterol
    ÏàËÆ¶È:79.3%
Chinese Journal of Medicinal Chemistry          2006          16          303-305
The constituents of Veratrum japonicum Loes. f.
ZHOU Jian-xia, KANG Lu, SHEN Zheng-wu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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6 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:79.3%
Journal of Beijing University of Chemical Technology (Natural Science Edition)          2012          39          40-45
Isolation of the triterpenes from Eriobotrya japonica leaves
CHEN Huan CHEN Guang REN HongMei YANG QuanHua YU ChangYuan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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7 .     5-ene-3¦Â,7¦Â-diol
    ÏàËÆ¶È:78.5%
Chemical & Pharmaceutical Bulletin          1990          38          2400-2403
Marine Sterols. XVII. : Polyhydroxysterols of the Soft Corals of the Andaman and Nicobar Coasts. : (2). Isolation and Structures of Three 16¦Â-Hydroxy Steroidal Glycosides from an Alcyonium sp. Soft Coral
Masaru KOBAYASHI,Fuyuko KANDA,Srinivasa Rao DAMARLA,Desaraju Venkata RAO and Chaganti Bheemasankara RAO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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8 .     7¦Á-hydroxysitosterol
C29H5O2     ÏàËÆ¶È:75.8%
Chinese Traditional and Herbal Drugs          2010          41          1052-1056
Chemical constituents from stems of Melicope pteleifolia
LI Shuo-guo; YANG Yin; YE Wen-cai; JIANG Ren-wang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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9 .     stigmastane-3¦Â,6¦Á-diol
    ÏàËÆ¶È:75.8%
Journal of China Pharmaceutical University          2003          34          216-219
Steroids and Anthraquinones from Astragalus hoantchy
ZHAO Ming; DUAN Jin-Ao; HUANG Wen-Zhe; ZHOU Rong-Han; CHE Chun-Tao
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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10 .     7¦Â-[(triethylsilyl)oxy]cholesterol
C33H60O2Si     ÏàËÆ¶È:75.8%
Journal of Medicinal Chemistry          1990          33          2264-2270
Monophosphoric acid diesters of 7.beta.-hydroxycholesterol and of pyrimidine nucleosides as potential antitumor agents: synthesis and preliminary evaluation of antitumor activity
Yu Hua Ji, Christiane Moog, Gaby Schmitt, Pierre Bischoff, Bang Luu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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11 .     7¦Á-hydroxysitosterol
    ÏàËÆ¶È:75.8%
Chemistry and Industry of Forest Products          2008          28          1-5
Antitumor Constituents from the Leaves of Aquilaria sinensis (Lour.) Gilg
WANG Hong-gang, ZHOU Min-hua, LU Jing-jing, YU Bo-yang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3Â¥2015-03-16 15:17:28
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