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1 .     6-hydroxystigmast-4-en-3-one
C29H48O2     ÏàËÆ¶È:96.6%
Steroids          2006          71          647-652
Ketosteroids and hydroxyketosteroids, minor metabolites of sugarcane wax
Patricia Georges, Muriel Sylvestre, Heinz Ruegger, Paul Bourgeois
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     stigmast-4-en-6¦Â-ol-3-one
C29H48O2     ÏàËÆ¶È:96.6%
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   Ì¼Æ×Ä£Äâͼ

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3 .     stigmast-4-en-6¦Â-ol-3-one
    ÏàËÆ¶È:96.6%
China Journal of Chinese Materia Medica          2008          33          1566-1568
Studies on chemical constituents from stem bark of Trwia nudiflora
WU Shaohua, SHENG Yuemao, CHEN Youwei, YANG Liyuan, LI Shaolan, LI Zhiying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     (24R)-6¦Â-hydroxy-24-ethylcholest-4-en-3-one
C29H48O2     ÏàËÆ¶È:96.6%
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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5 .     stigmastan-4-en-6¦Â-ol-3-one
C29H4802     ÏàËÆ¶È:96.6%
Journal of Natural Products          1990          Vol 53          1430
Stigmasterols from Typha latifolia
Marina Della Greca, Pietro Monaco, Lucio Previtera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     6¦Â-Hydroxy-4-stigmasten-3-one
    ÏàËÆ¶È:96.6%
Natural Product Sciences          2007          13          332-336
Norsesquiterpene and Steroid Constituents of Humulus japonicus
Yu, Byung-Chul; Yang, Min-Cheol; Lee, Kyu-Ha; Kim, Ki-Hyun; Lee, Kang-Ro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     (24R)-6¦Â-hydroxy-24-ethylcholest-4-en-3-one
    ÏàËÆ¶È:96.6%
Korean Journal of Pharmacognosy          2007          38(4)          376-381
Isolation of Melanin Biosynthesis Inhibitory Compounds from the Seeds of Plantago asiatica L.
Oh, Joon-Seok; Lee, Jong-Gu; Jung, Hee-Wook; Choi, Ji-Young; Choi, Eun-Hyang; Kim, Dong-Chun; Kim, Jeong-Ah; Son, Jong-Keun; Lee, Seung-Ho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     6¦Â-hydroxy-stigmasta-4-en-3-one
    ÏàËÆ¶È:96.6%
China Journal of Chinese Materia Medica          2011          Vol 36,Issue 7          891-895
Chemical constituents from petroleum ether portion of Abelmoschus esculentus
JIA Lu, GUO M ingm ing, LI Dong, JING Lin lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     Stigmast-4-en-6¦Â-ol-3-one
C29H48O2     ÏàËÆ¶È:96.6%
Natural Product Research          2011          Vol. 25, No. 13          1243-1249
Chemical constituents from the roots of Xanthium sibiricum
Suqin Kan, Guangying Chen, Changri Han, Zhong Chen, Xinming Song, Ming Ren and Hong Jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     6¦Â-hydroxy-stigmast-4-en-3-one
    ÏàËÆ¶È:96.6%
Chinese Traditional and Herbal Drugs          2007          38          14-17
Chemical constituents of whole herb of Dicliptera chinensis
GAO Yu-tao; YANG Xiu-wei; AI Tie-min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

11 .     stigmast-4-en-6¦Â-ol-3-one
    ÏàËÆ¶È:96.6%
Chinese Traditional and Herbal Drugs          2007          38          348-350
Æ¿»¨Ä¾»¯Ñ§³É·ÖµÄÑо¿
ÌÕÊïºì;Å˽£Óî;ÆáÊ绪;ÀîÇìÐÀ;ÕÅ‚Æ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

12 .     stigmast-4-en-6¦Â-ol-3-one
C29H48O2     ÏàËÆ¶È:96.6%
Chinese Traditional and Herbal Drugs          2005          36          510-511+545
Å£¶ú¶ä»¯Ñ§³É·ÖµÄÑо¿
²ÌÏ麣,µËµÂɽ,ÂíÔÆ±£,ÂÞÏþ¶«
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     stigmast-4-en-6¦Â-ol-3-one
C29H48O2     ÏàËÆ¶È:96.6%
Chinese Traditional and Herbal Drugs          2001          32          778-780
Studies on chemical constituents of Cipadessa baccifera
LUO Xiao dong; WU Shao hua; MA Yun bao; WU Da gang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     stigmast-4-en-6¦Â-ol-3-one
    ÏàËÆ¶È:96.6%
Chinese Journal of Natural Medicines          2009          7          425-427
Chemical Constituents from Houttuynia cordata
QU Wei; LIANG Jing-Yu; LI Meng-Ran
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

15 .     Stignast-4-en-6¦Â-3-one
    ÏàËÆ¶È:96.6%
Chinese Journal of Natural Medicines          2010          8          16-20
Chemical Constituents from Helwingia japonica
XIA Li-Zi; ZHOU Min; XIAO Yan-Hua; LI Guo-You; CHEN Xiao-Zhen; ZHANG Guo-Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     6¦Â-Hydroxyenone (Stigmast-4-en-6¦Â-ol-3-one)
    ÏàËÆ¶È:96.6%
Pharmazie          2004          59          885-888
Terpenoids and steroids from Lappula anocarpa
Yuan-Peng Jin, and Yan-Ping Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

17 .     stigmast-4-en-6¦Â-ol-3-one
    ÏàËÆ¶È:96.6%
Pharmazie          2005          60          464-467
Steroids from Saussurea ussuriensis
Jia-Tao Feng and Yan-Ping Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

18 .     (24R)-6¦Â-hydroxy-24-ethyl-cholest-4-en-3-one
    ÏàËÆ¶È:96.6%
Chinese Pharmaceutical Journal          2005          40          255-258
Study on phenolic constituents of Pholidota yunnanensis
BI Zhi ming, WANG Zheng tao *, XU Luo shan, XU Guo jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

19 .     stigmast-4-en-6¦Â-ol-3-one
    ÏàËÆ¶È:96.6%
Chinese Pharmaceutical Journal          2010          45          1615-1617
Chemical Constituents of Tetrastigma planicaule(Hook.) Gagnep.
SHAO Jia-chun, HE Cui-hong, LEI Ting, HONGi-hua, CEN Ying-zhou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     6¦Â-hydroxystigmast-4-en-3-one
    ÏàËÆ¶È:96.6%
Modern Chinese Medicine          2010          12(1)          23-24
Study on the Chemical Constituents of from the Roots of Tripterygium wilfordii
Yan Zhen, Tian Yang, Ma Yueping, Fu Xiaochun, Zhang Zhenxue, Wang Jinhui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

21 .     6¦Â-hydroxystigmast-4-en-3-one
    ÏàËÆ¶È:96.6%
Chinese Journal of Medicinal Chemistry          2003          13          211-214
Studies on the chemical constituents of Fructus Ailanthi altissimae
ZHAO Chun-chao, WANG Jin-hui, LI Wen, SHA Yi, LI Xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

22 .     stigmast-4-en-6¦Â-ol-3-one
    ÏàËÆ¶È:96.6%
Journal of Shenyang Pharmaceutical University          2009          26          874-877
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

--------------------------------------------------------------------------------

23 .     stigmast-4-en-6¦Â-ol-3-one
    ÏàËÆ¶È:96.6%
Journal of Shenyang Pharmaceutical University          2009          26          23-26
Chemical constituents from the involucre of Castanea mollissima Blume
JIAO Qi-yang, WU Li-jun, HUANG Jian, SUN Bo-hang, GAO Hui-yuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

24 .     stigmast-4-en-6¦Â-ol-3-one
    ÏàËÆ¶È:96.6%
Journal of Shenyang Pharmaceutical University          2009          26          357-360
Isolation and identification of chemical constituents from testa of Castanea mollissima Blume
LU Chuan, WU Zhao-hua, GAO Hui-yuan, SUN Bo-hang, HUANG Jian, WU Li-jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     (24R)-6¦Â-ôÇ»ù-24-ÒÒ»ù-µ¨çÞ-4-Ï©-3-ͪ
    ÏàËÆ¶È:96.6%
Journal of Shenyang Pharmaceutical University          2007          24          611-614
Chemical constituents of Duchesnea indica Focke
XU Wen-dong, LIN Hou-wen, QIU Feng, CHEN Wan-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     tigmast-4-en-6¦Â-ol-3-one
    ÏàËÆ¶È:96.6%
Natural Product Research and Development          2010          22          995-997
Chemical Constituent of Active Fraction from Radix Aerio Fici microcarpae L.
YA Qi-kang; LU Wen-jie; CHEN Jia-yuan; TAN Xiao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

27 .     stigmast-4-ene-6¦Â-ol-3-one
    ÏàËÆ¶È:96.6%
Natural Product Research and Development          2009          21          960-962
Study on the Chemical constituents of Callipteris esculenta(Athyriaceae)
WANG Zi-juan;ZHAO Qin-shi; PENG Li-yan; CHENG Xiao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

28 .     stigmast-4-en-6¦Â-ol-3-one
    ÏàËÆ¶È:96.6%
Natural Product Research and Development          1999          11(1)          44-47
THE CONSTITUNETS OF PIPER BOEHMERIAEFOLIUM VAR. TONKINENSE
Zhang Ke; Ni Wei; Chen Changxiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     stigmast-4-ene-6¦Â-ol-3-one
    ÏàËÆ¶È:96.6%
Guihaia          2012          32          548-550
Study on chemical constituents of Abies yuanbaoshanensis
HE Rui-Jie; FANG Hong; WU Ying-Rui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     stigmast-4-en-6¦Â-ol-3-one
C29H48O2     ÏàËÆ¶È:96.6%
Lishizhen Medicine and Materia Medica Research          2007          18          2121-2122
Studies on the Chemical Constituents of Juncus effusus L.
TIAN Xue-jun; LI Hong-xia; CHEN Yu; WANG Xiao-qiong; YANG Guang-zhong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

31 .     stigmast-4-en-6¦Â-ol-3-one
    ÏàËÆ¶È:96.6%
Chinese Traditional and Herbal Drugs          2012          43          2346-2350
Chemical constituents from fruits of Vitex negundo
ZHAO Xiang-xiang; ZHENG Cheng-jian; QIN Lu-ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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32 .     6-Hydroxystigmast-4-en-3-one
C29H48O2     ÏàËÆ¶È:93.3%
Chemistry of Natural Compounds          2007          43          563-566
CHEMICAL CONSTITUENTS FROM THE ROOTS OF Polygonum bistorta
Xiao-Bai Sun, Pei-Hua Zhao, Yang-Jun Xu,Li-Mei Sun, Mei-Ai Cao, and Cheng-Shan Yuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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33 .     6¦Â-hydroxy stigmast-4-en-3-one
    ÏàËÆ¶È:93.3%
Phytochemistry          1999          50          1229-1236
Triterpenoids from Mangifera indica
V. Anjaneyulu , P. Satyanarayan¦Á, K.N. Viswanadham, V.G. Jyothi, K. Nageswara Rao, P. Radhika
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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34 .     Procesterol
C29H48O     ÏàËÆ¶È:93.3%
Chemistry of Natural Compounds          2012          48          155-157
CHARACTERIZATION OF CHEMICAL CONSTITUENTS OF Calotropis procera
Arun Kakkar,D. R. Verma,Sanjay Suryavanshi,and Pradeep Dubey
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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35 .     procesterol
C29H48O2     ÏàËÆ¶È:93.3%
Phytochemistry          1989          28          2859-2861
A steroid from Calotropis procera
Abdul Qasim Khan,Abdul Malik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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36 .     7-O-¦Â-sitosterol
    ÏàËÆ¶È:93.3%
Chinese Traditional and Herbal Drugs          2008          39          497-499
Chemical constituents from roots of Euphorbia songarica
LIN Jia AN Ning LIU Chun-yu XU Li-zhen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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37 .     (24R)-ethylcholest-5-en-3-ol-7-one
    ÏàËÆ¶È:93.3%
Bulletin of the Korean Chemical Society          2008          29          615-619
Human Acyl-CoA: Cholesterol Acyltransferase (hACAT) Inhibitory Activities of Triterpenoids from Roots of Glycine max (L.) Merr.
Jin Hwan Lee, Young Bae Ryu, Byong Won Lee, Jin Hyo Kim, Woo Song Lee, Yong-Dae Park, Tae-Sook Jeong, Ki Hun Park*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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38 .     6¦Â-hydroxystigmast-4-en-3-one
    ÏàËÆ¶È:93.3%
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

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39 .     7¦Â-hydroxystigmast-4-en-3-one
C29H48O2     ÏàËÆ¶È:93.3%
Phytotherapy Research          2011          25          522-529
Antioxidant and anticholinesterase constituents from the petroleum ether and chloroform extracts of Iris suaveolens
Işıl Hacıbekiroğlu and Ufuk Kolak
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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40 .     6¦Â-hidroxi-estigmast-4-en-3-ona
    ÏàËÆ¶È:93.3%
Qu¨ªmica Nova          2007          30          41-44
Chemical constituents of Philodendrom imbe Schott
Feitosa, Chistiane Mendes; Bezerra, Maria Zeneide Barbosa; Cit¨®, Antônia Maria das Graças Lopes; Costa J¨²nior, Joaquim Soares da; Lopes, Jos¨¦ Arimat¨¦ia Dantas; Moita Neto, Jos¨¦ Machado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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41 .     (24R)-¦Á-ethylcholest-6¦Â-hydroxy-4-en-3-one
C29H48O2     ÏàËÆ¶È:93.3%
Chinese Traditional and Herbal Drugs          2012          43          873-876
Studies on chemical constituents in stems of Kadsura coccinea
JI Gai; YU Shu; HU Wen; OU Ying-bao; LI He-ran; YANG Shi-lin;
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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42 .     stigmastan-4-en-6¦Â-ol-3-one
    ÏàËÆ¶È:93.3%
Natural Product Research and Development          2012          24          179-181
Studies on Chemical Constituents from the Leaves of Actephila merrilliana
TANG Bei; CHEN Guang-ying; SONG Xiao-ping; HAN Chang-ri; SONG Xin-Ming; ZHONG Qiong-xin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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43 .     3¦Â-Acetoxysitost-5-ene-7¦Â-ol
C31H52O3     ÏàËÆ¶È:90.3%
Steroids          2005          70          886-895
Gram-scale chromatographic purification of ¦Â-sitosterol: Synthesis and characterization of ¦Â-sitosterol oxides
Xin Zhang, Philippe Geoffroy, Michel Miesch, Diane Julien-David, Francis Raul, Dalal Aoud¨¦-Werner, Eric Marchioni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

44 .     24-isopropyl-5¦Á-cholest-22Z-en-3¦Â-ol acetate
    ÏàËÆ¶È:90%
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   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

45 .     5,6¦Â-epoxy-5¦Â-sitostan-3¦Â-ol acetate
C31H52O3     ÏàËÆ¶È:90%
Steroids          2005          70          886-895
Gram-scale chromatographic purification of ¦Â-sitosterol: Synthesis and characterization of ¦Â-sitosterol oxides
Xin Zhang, Philippe Geoffroy, Michel Miesch, Diane Julien-David, Francis Raul, Dalal Aoud¨¦-Werner, Eric Marchioni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

46 .     6-hydroxystigmasta-4,22-dien-3-one
    ÏàËÆ¶È:90%
China Journal of Chinese Materia Medica          2009          34          712-714
Chemical constituents from Hedyotis diffusa
HUANGWeihua , LI Youbin , JIANG Jianqin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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47 .     ethylpavlovol
    ÏàËÆ¶È:90%
Fitoterapia          2005          76          433-438
A new dihydroxysterol from the marine phytoplankton Diacronema sp.
Am¨¦lia P. Rauter, Manuela M. Filipe, Carla Prata,João P. Noronha, Maria A.M. Sampayo,Jorge Justino,Jaime Bermejo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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48 .     compound 1a
C31H32O2     ÏàËÆ¶È:90%
Phytochemistry          1987          26          753-754
Iridoid glycosides from Penstemon richardsonii
Birgit Gering,Peter Junior,Max Wichtl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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49 .     ethylpavlovol
    ÏàËÆ¶È:90%
Lipids          1993          28          771-773
Identification of two novel dihydroxysterols fromPavlova
Gleen W. Patterson, Patricia K. Gladu, Gary H. Wikfors, Edward J. Parish and Peter D. Livant, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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50 .     estigmast-4-en-6¦Â-ol-3-ona
    ÏàËÆ¶È:90%
Qu¨ªmica Nova          2003          26          36-38
Constituents of the bark of Tapirira guianensis (Anacardiaceae)
Correia, Suzimone de J.; David, Juceni P.; David, Jorge M.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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