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199.15,171.62,125.73,125.69,55.92,55.87,53.83,46.80,42.36,39.61,38.66,36.08,35.68,35.60,33.96,33.86,32.92,32.04,29.41,28.17,26.06,24.16,23.05,21.01,19.79,19.02,18.68,17.35,11.96,11.95
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leecius: ½ð±Ò+1, лл²ÎÓ룡 2012-06-17 20:39:21
zhaocaigui: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2012-06-19 23:21:51
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21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2
11.95,11.96,17.35,18.68,19.02,19.79,21.01,23.05,24.16,26.06,28.17,29.41,32.04,32.92,33.86,33.96,35.6,35.68,36.08,38.66,39.61,42.36,46.8,53.83,55.87,55.92,125.69,125.73,171.62,199.15  
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1 .     ¦Â-sitostenone
C29H48O     ÏàËÆ¶È:93.3%
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
--------------------------------------------------------------------------------

2 .     stigmast-4-en-3-one
    ÏàËÆ¶È:93.3%
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
--------------------------------------------------------------------------------

3 .     ¦Â-sitostenone
    ÏàËÆ¶È:93.3%
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
--------------------------------------------------------------------------------

4 .     sitgmast-4-en-3-one
    ÏàËÆ¶È:93.3%
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
--------------------------------------------------------------------------------

5 .     stigmast-4-en-3-one
    ÏàËÆ¶È:93.3%
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
--------------------------------------------------------------------------------

6 .     stigmastan-4-en-3-one
    ÏàËÆ¶È:93.3%
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
--------------------------------------------------------------------------------

7 .     Stigmast-4-en-3-one
    ÏàËÆ¶È:93.3%
Natural Product Sciences          2008          14          100-106
Phytochemical Constituents of Schizonepeta tenuifolia Briquet
Lee, Il-Kyun; Kim, Min-Ah; Lee, Seung-Young; Hong, Jong-Ki; Lee, Jei-Hyun; Lee, Kang-Ro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     (24R)-Stigmast-4-ene-3-one
C29H46O2     ÏàËÆ¶È:93.3%
Phytochemistry          1993          34          523-527
Steroidal constituents from mature wheat straw
Elvira M.M. Gaspar, Higuinaldo J.C. das Neves
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

9 .     stigmast-4-en-3-one
    ÏàËÆ¶È:93.3%
Korean Journal of Pharmacognosy          2000          31(1)          109-111
A Study on the Constituents from the roots of Astragalus membranaceus(Bunge) (III)
Kim, Chung-Sook; Kim, Jin-Sook
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

10 .     ¦Â-sitost-4-en-3-one
    ÏàËÆ¶È:93.3%
Korean Journal of Pharmacognosy          1996          27(1)          75-79
Phytochemical Constituents from Aconitum pseudolaeve Var. erectum
Kim, Dae-Keun; Kwak, Jong-Hwan; Song, Ki-Won; Kwon, Hack-Cheol; Zee, Ok-Pyo; Lee, Kang-Ro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

11 .     stigmasta-4-en-3-one
    ÏàËÆ¶È:93.3%
Chinese Journal of Marine Drugs          2009          28(3)          23-28
Sterols from the mangrove plant Acanthus ilicifolius
HAI Fang, T ANG Xu-li, LI Guo-qiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

12 .     ¦Â-sitostenone
    ÏàËÆ¶È:93.3%
Chinese Journal of Marine Drugs          2008          27(1)          40-42
Studies on the chemical constituents of Nypa fruticans
NAN Hai-han, YIN Hao, ZHANG Si
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

13 .     stigmasta-4-en-3-one
C29H48O     ÏàËÆ¶È:93.3%
Chinese Journal of Marine Drugs          2007          26(6)          5-9
Studies on chemical constituents in ethanol ic extract from A-ca nt hus ilici f olius as a pharmaceutic mangrove
ZHANG Liang-liang, WANG Zhan-chang, CHEN Jun-de, LIN Peng, YANG Zhi-wei, LIN Yi-ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

14 .     ¦Â-Sitostenone
C29H48O     ÏàËÆ¶È:93.3%
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
--------------------------------------------------------------------------------

15 .     stigmasta-4-en-3-one
    ÏàËÆ¶È:93.3%
China Journal of Chinese Materia Medica          2010          35          1137-1141
Ethyl acetate-soluble chemical constituents from whole plants of Senecio chrysanthemoides
LIN Sheng; ZHANF Zhongxiao; SHEN Yunheng; LI Huiliang; SHAN Lei; LIU Runhui; XU Xike; ZHANF Weidong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

16 .     ¶¹çÞ-4-Ï©-3-ͪ
    ÏàËÆ¶È:93.3%
Chinese Traditional and Herbal Drugs          2009          40          536-538
ÂæÍÕÌã°ê¾¥µÄ»¯Ñ§³É·ÖÑо¿
·ëÓýÁÖ;ÎâÝí;ÀîÔÆÇï;ÐìÀöÕä;ÑîÊÀÁÖ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

17 .     stigmast-4-en-3-one
    ÏàËÆ¶È:93.3%
Chinese Traditional and Herbal Drugs          2008          39          1296-1298
¿íÒ¶Ý¡Â黯ѧ³É·ÖµÄÑо¿
ÖÜÔ¨;¼½±£È«;Íõì¿;ãÆÐ˹ú;Ê·ÀöÓ±;ÍõÓÀÆæ;·ë±¦Ãñ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

18 .     stigmast-4-en-3-one
C29H48O     ÏàËÆ¶È:93.3%
Chinese Traditional and Herbal Drugs          2002          33          205-206
Studies on chemical constituents of Uvaria tonkinensis var. subglabra
LIU An; TIAN Jing kui; ZOU Zhong mei; XU Li zhen; MU Hong mei; YANG Shi lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

19 .     sitosterone
C29H48O     ÏàËÆ¶È:93.3%
Chinese Journal of Natural Medicines          2005          3          181-183
Chemical Constituents of Nauclea officinalis
XUAN Wei-Dong; CHEN Hai-Sheng); YUAN Zhi-Xian; ZHU Ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

20 .     stigmast-4-en-3-one
C29H48O     ÏàËÆ¶È:93.3%
Chinese Journal of Natural Medicines          2008          6          268-270
Chemical Constituents from the Seeds of Ziziphus jujuba var.spinosa
WANG Jian-Rong; ZHANG Jian; YIN Zhi-Qi; LIANG Jing-Yu; YE Wen-Cai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

21 .     Enone (Stigmast-4-en-3-one)
    ÏàËÆ¶È:93.3%
Pharmazie          2004          59          885-888
Terpenoids and steroids from Lappula anocarpa
Yuan-Peng Jin, and Yan-Ping Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

22 .     Stigmast-4-en-3-one
    ÏàËÆ¶È:93.3%
Archives of Pharmacal Research          2010          33          1317-1323
Scopoletin from the flower buds of Magnolia fargesii inhibits protein glycation, aldose reductase, and cataractogenesis Ex Vivo
Jun Lee, Nan Hee Kim, Joo Won Nam, Yun Mi Lee and Dae Sik Jang, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

23 .     sitosterone
    ÏàËÆ¶È:93.3%
Chinese Pharmaceutical Journal          2009          44          576-580
Studies on Antitumor Steroids and Flavonoids from Tamarix chinensis Lour.
WANG Bin, REN Shu-wen, LI Guo-qiang, GUAN Hua-shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

24 .     stigmast-4-en-3-one
C29H48O     ÏàËÆ¶È:93.3%
Journal of Shenyang Pharmaceutical University          2008          25          711-713
Chemical constituents of the root of Urtica mairei Levl.
WANG Wei, ZHOU Yuan, TAN GLing, YAN Xing-guo, WANG Yong-qi, FENG Bao-min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

25 .     (24R)-stigmast-4-ene-3-one
    ÏàËÆ¶È:93.3%
Natural Product Research and Development          2007          19          240-243
Chemical Constituents of Cibotium barometz
WU Qi; YANG Xiu-wei; YANG Shi-hai; ZOU Lei; YAN Jing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

26 .     stigmast-4-en-3-one
C29H48O     ÏàËÆ¶È:93.3%
Chinese Journal of Natural Medicines          2011          9          190-192
Triterpenes and Steroids from Semi-mangrove Plant Hibiscus tiliaceus
WANG Zhong-Zhao, LI Jun, TANG Xv-Li, LI Guo-Qiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

27 .     [24S]¶¹çÞ-4-Ï©-3-ͪ
    ÏàËÆ¶È:90%
Acta Botanica Yunnanica          1993          15(3)          306-308
THE CHEMICAL CONSTITUENTS OF ARISTOLOCHIA KUNMINGENSIS
WANG Xi-Hong, HAN Gui-Qiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

28 .     Stigmast-4-en-3-one
    ÏàËÆ¶È:90%
Phytochemical Analysis          2000          11          345-350
Chemical composition of the light petroleum extract of Hibiscus cannabinus bark and core
Ana M. L. Seca, Artur M. S. Silva, Armando J. D. Silvestre, Jos¨¦ A. S. Cavaleiro, Fernando M. J. Domingues and Carlos P. Neto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

29 .     ergosta-4-en-3-one
C28H46O     ÏàËÆ¶È:90%
Chinese Traditional and Herbal Drugs          2005          36          510-511+548
Å£¶ú¶ä»¯Ñ§³É·ÖµÄÑо¿
²ÌÏ麣,µËµÂɽ,ÂíÔÆ±£,ÂÞÏþ¶«
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

30 .     stigmast-4-en-3-one
    ÏàËÆ¶È:90%
Chinese Traditional and Herbal Drugs          2003          34          392-394
Stigmasterols from pericarp of Sphaerophysa salsula
LI Guo-yu; WANG Jin-hui; LI Xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

31 .     stigmasta-4-en-3-one
C29H46O     ÏàËÆ¶È:90%
Chinese Journal of Natural Medicines          2008          6          271-274
Chemical Constituents from the Roots and Stems of Ervatamia hainanensis
JIN Li; LU Jia; JIN Yong-Sheng; YANG Xiang-Nan; CHEN Hai-Sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

32 .     12¦Á-Hydroxystigmast-4-en-3-one
C29H48O2     ÏàËÆ¶È:90%
Pharmazie          2003          58          272-273
12?-Hydroxystigmast-4-en-3-one: a new bioactive steroid from Toona ciliata (Meliaceae)
R. Chowdhury - R. B. Rashid - M. H. Sohrab - C. M. Hasan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

33 .     (24S)-stigmasterol-4-en-3-one
    ÏàËÆ¶È:90%
Chinese Journal of Medicinal Chemistry          2008          18          449-451
Isolation and identification of the chemical constituents from Blumea riparia DC. (II)
CAO Jia-qing, WANG Ya-nan, ZHOU Yu-zhi, QIAO Li, CHEN Huan, PEI Yue-hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

34 .     stigmast-4-en-3-one
    ÏàËÆ¶È:90%
Journal of Shenyang Pharmaceutical University          2009          26          444-446
Isolation and identification of the chemical constituents from the whole plant of Siegesbeckia pubescens Makino
JIANG Lin, DING Huai-wei, SONG Shao-jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

35 .     ¦Â-Sitostenone
    ÏàËÆ¶È:86.6%
Molecules          2009          14          850-867
Bioactive Metabolites from Spilanthes acmella Murr.
Supaluk Prachayasittikul, Saowapa Suphapong, Apilak Worachartcheewan, Ratana Lawung, Somsak Ruchirawat and Virapong Prachayasittikul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

36 .     4-sitosten-3-one
    ÏàËÆ¶È:86.6%
Journal of Chinese Pharmaceutical Sciences          1996          5          37
Two New Coumarins from the Roots of Aegle marmelos
Xiu Wei Yang , Masao Hattori and Tsuneo Namba
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

37 .     (24R)24-ethyl-6¦Á-hydroperoxy-cholest-4-en-3-one
    ÏàËÆ¶È:86.6%
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
--------------------------------------------------------------------------------

38 .     eupha-7,24-diene
    ÏàËÆ¶È:86.6%
Chemical & Pharmaceutical Bulletin          1998          46          1408-1411
New Sterols and Triterpenoids of Ficus pumila Fruit
Junichi KITAJIMA,Kaoru KIMIZUKA and Yasuko TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

39 .     (24R)-3¦Â-hydroxy-ethylcholest-5-en-6-one
    ÏàËÆ¶È:86.6%
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
--------------------------------------------------------------------------------

40 .     3-oxo-¦¤(4.5)-sitosterone
    ÏàËÆ¶È:86.6%
Phytochemistry          1995          40          1183-1189
Monoterpene diol, iridoid glucoside and dibenzo-¦Á-pyrone from Anthocleista djalonensis
Patricia A. Onocha, Dominic A. Okorie, Joseph D. Connolly, David S. Roycroft
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

41 .     stigmasta-4,22-dien-3-one
    ÏàËÆ¶È:86.6%
Chinese Journal of Marine Drugs          2008          27(1)          40-42
Studies on the chemical constituents of Nypa fruticans
NAN Hai-han, YIN Hao, ZHANG Si
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

42 .     4-sitost-4-en-3-one
    ÏàËÆ¶È:86.6%
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
--------------------------------------------------------------------------------

43 .     stigmast-4-en-3-one
    ÏàËÆ¶È:86.6%
Chinese Traditional and Herbal Drugs          2007          38          342-344
Chemical constituents in Ficus tikoua of Miao nationality
GUAN Yong-xia; YANG Xiao-sheng; TONG Li-hua; YANG Bo; HAO Xiao-jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

44 .     stigmast-4-ene-3,6-dione
    ÏàËÆ¶È:83.3%
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
--------------------------------------------------------------------------------

45 .     (24R)-24-ethylcholest-4-en-3,6-dione
    ÏàËÆ¶È:83.3%
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
--------------------------------------------------------------------------------

46 .     compound 8
    ÏàËÆ¶È:83.3%
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
--------------------------------------------------------------------------------

47 .     compound
    ÏàËÆ¶È:83.3%
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
--------------------------------------------------------------------------------

48 .     24-ethylcholest-4-en-3-one
C29H48O     ÏàËÆ¶È:83.3%
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
--------------------------------------------------------------------------------

49 .     (3E)-Hydroximino-24-ethylcholest-4-en
    ÏàËÆ¶È:83.3%
Steroids          2009          74          62-72
Synthesis and evaluation of some steroidal oximes as cytotoxic agents: Structure/activity studies (I)
Jian-Guo Cui, Lei Fan, Li-Liang Huang, Hong-Li Liu, Ai-Min Zhou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

50 .     ¶¹çÞ-4-Ï©-3,6-¶þͪ
    ÏàËÆ¶È:83.3%
China Journal of Chinese Materia Medica          2003          28          278-279
¼Ô¹ûÞ§¹áÖÚ»¯Ñ§³É·ÖµÄÑо¿
Ñî á°, ÕÔÓñÓ¢, ÍÀßÏßÏ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

51 .     stigmastan-4-en-3,6-dione
    ÏàËÆ¶È:83.3%
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
--------------------------------------------------------------------------------

52 .     compound 3
    ÏàËÆ¶È:83.3%
Acta Pharmaceutica Sinica          1999          Vol 34          682-685
STUDIES ON THE CHEMICAL CONSTITUENTS FROM DESMOS DUMOSUS (ROXB.) SAFF
Wu Jiuhong (Wu JH); Liao Shixuan (Liao SX); Mao Shilong (Mao SL); Yi Yanghua (Yi YH); Takeya K; Su Zhongwu (Su ZW) and Lan Chuanqing (Lan CQ)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

53 .     22-dihydro-stigmast-4-en-3,6-dione
    ÏàËÆ¶È:83.3%
Korean Journal of Pharmacognosy          1996          27(1)          75-79
Phytochemical Constituents from Aconitum pseudolaeve Var. erectum
Kim, Dae-Keun; Kwak, Jong-Hwan; Song, Ki-Won; Kwon, Hack-Cheol; Zee, Ok-Pyo; Lee, Kang-Ro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

54 .     Stigmast-4-ene-3,6-dione
    ÏàËÆ¶È:83.3%
Magnetic Resonance in Chmesitry          2004          42          355-359
Complete 1H and 13C NMR assignments of two phytosterols from roots of Piper nigrum
Kun Wei, Wei Li, Kazuo Koike, Yuping Pei, Yingjie Chen and Tamotsu Nikaido
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

55 .     stigmast-4-en-3-one
C29H48O     ÏàËÆ¶È:83.3%
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   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

56 .     ¶¹çÞ-4-Ï©-3,6-¶þͪ
C29H48O2     ÏàËÆ¶È:83.3%
Chinese Traditional and Herbal Drugs          2008          39          671-672
ºúÍÇ×ÓÒ¶»¯Ñ§³É·ÖÑо¿
¸¶Òå³É;ÍõÏþ¾²;¼ÖÏ×»Û;Àî¿¡æ¼
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

57 .     stigmast-4-en-3,6-dione
    ÏàËÆ¶È:83.3%
Chinese Traditional and Herbal Drugs          2002          33          205-206
Studies on chemical constituents of Uvaria tonkinensis var. subglabra
LIU An; TIAN Jing kui; ZOU Zhong mei; XU Li zhen; MU Hong mei; YANG Shi lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

58 .     6¦Á-hydroxystigmast-4-en-3-one
    ÏàËÆ¶È:83.3%
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
--------------------------------------------------------------------------------

59 .     stigmast-4-ene-3,6-dione
    ÏàËÆ¶È:83.3%
Chinese Pharmaceutical Journal          2009          44          576-580
Studies on Antitumor Steroids and Flavonoids from Tamarix chinensis Lour.
WANG Bin, REN Shu-wen, LI Guo-qiang, GUAN Hua-shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

60 .     stigmast-4-ene-3,6-dione
    ÏàËÆ¶È:83.3%
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
--------------------------------------------------------------------------------

61 .     ¶¹çÞÍé-4-Ï©-3-ͪ
    ÏàËÆ¶È:83.3%
Chinese Journal of Medicinal Chemistry          2004          14          294-297
Isolation, identification of the chemical constituents from Bauhinia variegata L.
ZHAO Yan-yan, CUI Cheng-bin, CAI Bing, SUN Qi-shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

62 .     stigmast-4-en-3,6-dione
    ÏàËÆ¶È:83.3%
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
--------------------------------------------------------------------------------

63 .     stigmast-4-en-3,6-dione
    ÏàËÆ¶È:83.3%
Journal of Shenyang Pharmaceutical University          2009          26          434-437
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
--------------------------------------------------------------------------------

64 .     stigmast-4-ene-3,6-dione
    ÏàËÆ¶È:83.3%
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
--------------------------------------------------------------------------------

65 .     stigmast-4-ene-6¦Á-ol-3-one
    ÏàËÆ¶È:83.3%
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
--------------------------------------------------------------------------------

66 .     enedione
    ÏàËÆ¶È:83.3%
Natural Product Research and Development          2000          12(5)          14-16
STEROID CONSTITUENTS FROM EUONYMUS MUPINENSIS
Mao Shilong; Sang Shengmin; Lao Aina and Chen Zhongliang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

67 .     stigma-4-en-3,6-dione
    ÏàËÆ¶È:83.3%
Zeitschrift f¨¹r Naturforschung C          2003          58          521-526
Cytotoxic Benzophenanthridine and Benzylisoquinoline Alkaloids from Argemone mexicana
Y.-C. Chang, F.-R. Chang, A. T. Khalil, P.-W. Hsieh, and Y.-C. Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

68 .     campest-5-en-3-one
    ÏàËÆ¶È:80%
Steroids          2000          65          443-449
Synthesis of 6-oxy functionalized campest-4-en-3-ones: efficient hydroperoxidation at C-6 of campest-5-en-3-one with molecular oxygen and silica gel
Hideharu Seto, Shozo Fujioka, Suguru Takatsuto, Hiroyuki Koshino, Takeshi Shimizu, Shigeo Yoshida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

69 .     (24R) 24-ethyl-6¦Â-hydroperoxy-cholest-4-en-3-one
    ÏàËÆ¶È:80%
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
--------------------------------------------------------------------------------

70 .     stigmast-4-en-6¦Á-ol-3-one
    ÏàËÆ¶È:80%
China Journal of Chinese Materia Medica          2008          33          1566-1569
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
--------------------------------------------------------------------------------

71 .     stigmasta-4-ene-3,6-dione
    ÏàËÆ¶È:80%
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
--------------------------------------------------------------------------------

72 .     stigmastan-4-en-6¦Â-ol-3-one
C29H4802     ÏàËÆ¶È:80%
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
--------------------------------------------------------------------------------

73 .     6¦Á-hydroxy enone
    ÏàËÆ¶È:80%
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
--------------------------------------------------------------------------------

74 .     (24R)-stigmast-4-ene-3,6-dione
C29H48O2     ÏàËÆ¶È:80%
Phytochemistry          1993          34          523-527
Steroidal constituents from mature wheat straw
Elvira M.M. Gaspar, Higuinaldo J.C. das Neves
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

75 .     tigmasta-4-en-3,6-dione
    ÏàËÆ¶È:80%
Chinese Journal of Marine Drugs          2009          28(3)          23-28
Sterols from the mangrove plant Acanthus ilicifolius
HAI Fang, T ANG Xu-li, LI Guo-qiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

76 .     Stigmast-4-en-3,6-dione
    ÏàËÆ¶È:80%
Phytochemical Analysis          2000          11          345-350
Chemical composition of the light petroleum extract of Hibiscus cannabinus bark and core
Ana M. L. Seca, Artur M. S. Silva, Armando J. D. Silvestre, Jos¨¦ A. S. Cavaleiro, Fernando M. J. Domingues and Carlos P. Neto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

77 .     ¶¹çÞÍé-4-Ï©-3-ͪ
C29H48O     ÏàËÆ¶È:80%
Chinese Traditional and Herbal Drugs          2007          38          1788-1790
Chemical constituents of Houttuynia cordata
WANG Li-qin; ZHAO You-xing; ZHOU Lu; ZHOU Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

78 .     ¶¹çÞ-4-Ï©-3,6-¶þͪ
    ÏàËÆ¶È:80%
Chinese Traditional and Herbal Drugs          2006          37          1780-1781
Á¬Ç®²ÝÖÐÈýÝÆÀ໯ѧ³É·Ö
ÕÅǰ¾ü;ÑîСÉú;Ö캣Ñà;Ò¦ÔÆ;ºÂС½­;Ëα¦°²
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

79 .     stigmast-4,2 2-dien-3-one
    ÏàËÆ¶È:80%
Chinese Traditional and Herbal Drugs          2002          33          205-206
Studies on chemical constituents of Uvaria tonkinensis var. subglabra
LIU An; TIAN Jing kui; ZOU Zhong mei; XU Li zhen; MU Hong mei; YANG Shi lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

80 .     3¦Â,5¦Á,6¦Â-ÈýôÇ»ù¶¹çÞÍé
    ÏàËÆ¶È:80%
Chinese Traditional and Herbal Drugs          2010          41          1782-1785
¹óÖÝ´ó·½ÁÖÏÂÔÔÅàÌìÂéµÄ»¯Ñ§³É·ÖÑо¿
ÕÅΰ;ËÎÆôʾ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

81 .     Stignast-4-en-6¦Á-3-one
    ÏàËÆ¶È:80%
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
--------------------------------------------------------------------------------

82 .     stigmastane-3¦Â,6¦Á-diol
    ÏàËÆ¶È:80%
Journal of Shenyang Pharmaceutical University          2009          26          434-437
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
--------------------------------------------------------------------------------

83 .     stigma-4-en-3,6-dione
C29H46O2     ÏàËÆ¶È:80%
Natural Product Research and Development          2004          16          210-212
STUDY ON THE CHEMICAL CONSTITUENTS OF OSTODES PANICULATA
QI Shu-hua; GUO Jian-wei; WU Da-gang; LUO Xiao-dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

84 .     stigmsat-4-en-3,6-dione
    ÏàËÆ¶È:80%
Natural Product Research and Development          2003          15          24-26
CHEMICAL CONSTITUENTS OF BUCKWHEAT
BAO Ta-na; PENG Shu lin; ZHOU Zheng zhi; LI Bo gang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

85 .     stigmastane-3¦Â,6¦Á-diol
    ÏàËÆ¶È:80%
Natural Product Research and Development          2000          12(5)          14-16
STEROID CONSTITUENTS FROM EUONYMUS MUPINENSIS
Mao Shilong; Sang Shengmin; Lao Aina and Chen Zhongliang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

86 .     stigmast-4-en-3,6-dione
    ÏàËÆ¶È:80%
Natural Product Research and Development          2000          12(3)          38-41
CHEMICAL CONSTITUENTS FROM CLEMATOCLETHRA SCANDENS
Zhang Xiaorong; Ding Lisheng; Peng Shulin; Wang Mingkui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

87 .     24¦Á-ethyl-cholestan-3¦Á-ol
    ÏàËÆ¶È:80%
Chinese Journal of Organic Chemistry          2005          25          1100-1102
Steroids from Pliocene Fossil Pinus armandii
ZHAO, You-Xing LI, Cheng-Sen LUO, Xiao-Dong YI, Tie-Mei ZHOU, Jun*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

88 .     24-ethylcholesta-4,24(28)-dien-3-one
C29H46O     ÏàËÆ¶È:76.6%
Journal of Natural Products          1999          62          224-227
New Cytotoxic Oxygenated Fucosterols from the Brown Alga Turbinaria conoides
Jyh-Horng Sheu, Guey-Horng Wang, Ping-Jyun Sung, and Chang-Yih Duh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

89 .     stigmastane-3¦Â,6¦Á-diol
C29H52O2     ÏàËÆ¶È:76.6%
Chemical & Pharmaceutical Bulletin          1995          43          1813-1817
Structures of Five Hydroxylated Sterols from the Seeds of Trichosanthes kirilowii MAXIM.
Yumiro KIMURA,Toshihiko AKIHISA,Ken YASUKAWA,Michio TAKIDO and Toshitake TAMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

90 .     poriferastane-3¦Â,6¦Á-diol
C29H52O2     ÏàËÆ¶È:76.6%
Chemical & Pharmaceutical Bulletin          1995          43          1813-1817
Structures of Five Hydroxylated Sterols from the Seeds of Trichosanthes kirilowii MAXIM.
Yumiro KIMURA,Toshihiko AKIHISA,Ken YASUKAWA,Michio TAKIDO and Toshitake TAMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

91 .     cholesta-4,24-dien-3-one
    ÏàËÆ¶È:76.6%
Chemistry of Natural Compounds          2007          43          86-89
KETOSTEROIDS FROM THE FAR-EAST MARINE PROSOBRANCH MOLLUSK Onchidiopsis variegata
E. A. Santalova, V. A. Denisenko, A. V. Chernyshev,M. Gavagnin, and K. E. Sanamyan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

92 .     (24R,6E)-24-ethylcholest-6-hydroximino-4-en-3-one
    ÏàËÆ¶È:76.6%
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
--------------------------------------------------------------------------------

93 .     (24R,6E)-24-ethylcholest-6-hydroximino-4-en-3-one
    ÏàËÆ¶È:76.6%
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
--------------------------------------------------------------------------------

94 .     stigmastan-3-one
C29H50O     ÏàËÆ¶È:76.6%
Acta Bot. Boreal. -Occident. Sin.          2006          26          0188-0192
Chemical Constituents of Dracocephalum tanguticum
LI J i-xin, JIA Zhong-jian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

95 .     24R-ethyl-5¦Á-cholestane-3¦Â,6¦Á-diol
    ÏàËÆ¶È:76.6%
Chinese Chemical Letters          2004          15          659-660
A New Phytosterone from Passiflora wilsonii
Gan Peng LI, Jing Feng ZHAO, Yong Qiang TU, Xiao Dong YANG, Hong Bin ZHANG,Liang LI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

96 .     Campest-4-ene-3,6-dione
C28H45O2     ÏàËÆ¶È:76.6%
Steroids          2000          65          443-449
Synthesis of 6-oxy functionalized campest-4-en-3-ones: efficient hydroperoxidation at C-6 of campest-5-en-3-one with molecular oxygen and silica gel
Hideharu Seto, Shozo Fujioka, Suguru Takatsuto, Hiroyuki Koshino, Takeshi Shimizu, Shigeo Yoshida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

97 .     6¦Á-Hydroperoxycampest-4-en-3-one
C28H47O3     ÏàËÆ¶È:76.6%
Steroids          2000          65          443-449
Synthesis of 6-oxy functionalized campest-4-en-3-ones: efficient hydroperoxidation at C-6 of campest-5-en-3-one with molecular oxygen and silica gel
Hideharu Seto, Shozo Fujioka, Suguru Takatsuto, Hiroyuki Koshino, Takeshi Shimizu, Shigeo Yoshida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

98 .     6¦Á-Hydroxycampest-4-en-3-one
C28H47O2     ÏàËÆ¶È:76.6%
Steroids          2000          65          443-449
Synthesis of 6-oxy functionalized campest-4-en-3-ones: efficient hydroperoxidation at C-6 of campest-5-en-3-one with molecular oxygen and silica gel
Hideharu Seto, Shozo Fujioka, Suguru Takatsuto, Hiroyuki Koshino, Takeshi Shimizu, Shigeo Yoshida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

99 .     Stigmastane-3¦Â,6¦Á-diol
    ÏàËÆ¶È:76.6%
Steroids          2006          71          700-705
Steryl esters and phenylethanol esters from Syringa komarowii
Yinggang Luo, Yan Liu, Huayi Qi, Zhijun Wu, Guolin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

100 .     compound 28
    ÏàËÆ¶È:76.6%
Steroids          2006          71          700-705
Steryl esters and phenylethanol esters from Syringa komarowii
Yinggang Luo, Yan Liu, Huayi Qi, Zhijun Wu, Guolin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2012-06-17 18:00:16
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