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1 .     (24S)-24-ethyl-5¦Á-cholestane-3¦Â,5-diol
     ÏàËÆ¶È:75.8%
Planta Medica          1993          59          572-573
Two New Sterols from the Marine Red Alga Gracilaria edulis
B. Das and K. V. N. S. Srinivas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     (24R)-3¦Â-hydroxy-ethylcholest-5-en-6-one
     ÏàËÆ¶È:75.8%
Phytochemistry          1998          48          471-474
Chemical constituents of aquatic fern Azolla nilotica
Yôko Arai, Tomomi Nakagawa, Mari Hitosugi, Kenji Shiojima, Hiroyuki Ageta, Osama Basher, Abdel-Halim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     6¦Á-hydroxystigmast-4-en-3-one
     ÏàËÆ¶È:75.8%
Archives of Pharmacal Research          2005          28          1147-1151
Antimicrobial constituents from fruits of Ailanthus altissima SWINGLE
Chun-Chao Zhao, Jian-Hua Shao, Xian Li, Jing Xu and Peng Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     blattellastanoside-A
C35H59ClO7     ÏàËÆ¶È:75.8%
Journal of Chemical Ecology          1993          19          2521-2541
Aggregation arrestant pheromone of the German cockroach,Blattella germanica (L.) (Dictyoptera: Blattellidae): Isolation and structure elucidation of blattellastanoside-A and -B
Masayuki Sakuma, Hiroshi Fukami
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     3,3-dimethoxy-24-ethyl-cholestan
C31H56O2     ÏàËÆ¶È:73.3%
Journal of the Chinese Chemical Society          2009          56          600-605
Palaeophytochemical Components from the Miocene-Fossil Wood of Pinus griffithii
Jian-Rong Luo, Qing-Yun Ma, You-Xing Zhao,Tie-Mei Yi, Cheng-Sen Li and Jun Zhou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     ¦Â-sitosterol
     ÏàËÆ¶È:72.4%
Phytochemistry          2004          65          2463-2470
Biosynthesis of the irregular monoterpene artemisia ketone, the sesquiterpene germacrene D and other isoprenoids in Tanacetum vulgare L. (Asteraceae)
Dirk Umlauf, Josef Zapp, Hans Becker, Klaus Peter Adam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     stigmast-4-ene-3,6-dione
     ÏàËÆ¶È:72.4%
Journal of Natural Products          2002          65          1857-1862
Antimicrobial Activities of Naphthazarins from Arnebia euchroma
Chien-Chang Shen,Wan-Jr Syu,Shyh-Yuan Li, Chia-Hung Lin, Gum-Hee Lee, and Chang-Ming Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     (24R)-24-ethylcholest-4-en-3,6-dione
     ÏàËÆ¶È:72.4%
Chemistry of Natural Compounds          2001          37          351-355
13C NMR SPECTRA OF 6-HYDROXIMINOSTEROIDS OF THE STIGMASTANE SERIES
N. V. Kovganko and Yu. G. Chernov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     compound 8
     ÏàËÆ¶È:72.4%
Chemistry of Natural Compounds          1999          35          646-649
13C NMR SPECTRA OF II-SITOSTEROL DERIVATIVES WITH OXIDIZED RINGS A AND B
N. V. Kovganko, Zh. N. Kashkan,E. V. Borisov, and E. V. Batura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     compound
     ÏàËÆ¶È:72.4%
Biochemical Systematics and Ecology          2000          28          911-913
Stigmast-4-ene-3,6-dione an unusual phytotoxic sterone from the roots of Echium vulgare L.
Fernando Pardo, Fernando Perich, Ren¨¦ Torres, Franco Delle Monache
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     5¦Á-Cholestan-3¦Á-yl chloroethanoate
     ÏàËÆ¶È:72.4%
Steroids          2007          72          615-626
Synthesis and antimicrobial evaluation of water-soluble, dendritic derivatives of epimeric 5¦Á-cholestan-3-amines and 5¦Á-cholestan-3-yl aminoethanoates
Eko W. Sugandhi, Carla Slebodnick, Joseph O. Falkinham III, Richard D. Gandour
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     (24R) 24-ethyl-6¦Â-hydroperoxy-cholest-4-en-3-one
     ÏàËÆ¶È:72.4%
Natural Product Research          1994          5          7-14
Hydroperoxysterols in Arum italicum
Marina Della Greca; Antonio Fiorentino; Antonio Molinaro; Pietro Monaco; Lucio Previtera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     (24R)24-ethyl-6¦Á-hydroperoxy-cholest-4-en-3-one
     ÏàËÆ¶È:72.4%
Natural Product Research          1994          5          7-14
Hydroperoxysterols in Arum italicum
Marina Della Greca; Antonio Fiorentino; Antonio Molinaro; Pietro Monaco; Lucio Previtera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     ¦Â-sitostenone
C29H48O     ÏàËÆ¶È:72.4%
Natural Product Research          2008          22          1085-1093
Isolation of antibacterial diterpenoids from Cryptomeria japonica bark
Wen-Hsin Li; Shang-Tzen Chang; Shan-Chwen Chang; Hui-Ting Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     stigmast-4-en-3-one
     ÏàËÆ¶È:72.4%
China Journal of Chinese Materia Medica          2009          34          1809-1811
Steroids from Monascus purpureus metabolite
SHANG Xiaoya, WANG Ruolan, YI N Suqin, LI Jinjie, JIN Zonglian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     ¦Â-sitostenone
     ÏàËÆ¶È:72.4%
China Journal of Chinese Materia Medica          2008          33          405-408
Studies on phenolic compounds from Stellera chamaejasme
FENG Bao, GONG Xiaojie, SHI Liying, JIAN Ge, PEI Yue-hu, WANG Yong-qi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     stigmast-4-en-3¦Â,6¦Â-diol
     ÏàËÆ¶È:72.4%
China Journal of Chinese Materia Medica          2008          33          1035-1038
Study on Steroids of Cacalia tangutica
LIU Qing, LIU Zhenling, TIAN Xuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     sitgmast-4-en-3-one
     ÏàËÆ¶È:72.4%
China Journal of Chinese Materia Medica          2006          31          1953-1955
Chemical constitutents of Bauhinia aurea
SHANG Xiaoya, LI Shuai, WANG Yinghong, WANG Sujuan, YANG Yongchun, SHI Jiangong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     stigmasta-4-ene-3,6-dione
     ÏàËÆ¶È:72.4%
China Journal of Chinese Materia Medica          2005          30          124-126
Studies on the chemical constituents in herb of Ranunculus sceleratus
GAO Xiaozhong, ZHOU Changxin, ZHANG Shuili, YAO Wei, ZHAO YU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     stigmast-4-en-3-one
     ÏàËÆ¶È:72.4%
China Journal of Chinese Materia Medica          2005          30          671-674
Study on chemical constituents in rhizome of Pinellia ternata
HE Ping, LI Shuai, WANG Su-juan, YANG Yong-chun, SHI Jian-gong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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