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12.01,16.24,17.57,19.61,19.92,21.06,22.95,28.27,31.92,33.04,38.32,39.02,
40.42,40.72,42.77,46.18,54.51,55.65,70.43,116.23,119.54,131.92,135.53

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1 .     ergosta-5,7,---triene-3¦Â-ol
    ÏàËÆ¶È:88.4%
Chinese Journal of Marine Drugs          2006          25(1)          6-10
Studies on the chemical constituents of the fermentation liquid from marine actinomyces Micromonos por a sp. and bacteria Ocea nos pi rillum sp.
SHI Ying, TIAN Li, WANG Jing, PEI Yue-hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

2 .     ergosta-5,7,22-t riene-3¦Â-ol
    ÏàËÆ¶È:88.4%
Chinese Journal of Marine Drugs          2004          23(1)          14-16
Study on the chemical constituents of the fermentation liquid from marine fungus Aspergillus versicolor
ZHANG Hai-long, MA Li, TIAN Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     ergosterol derived
    ÏàËÆ¶È:88.4%
Tetrahedron Letters          2000          41          2791-2795
Stereochemistry of hydrogen introduction at C-25 in ergosterol synthesized by the mevalonate-independent pathway
Wen-xu Zhou, W. David Nes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     Ergosterol
    ÏàËÆ¶È:88.4%
Archives of Pharmacal Research          2002          25          851-855
Cytotoxic ergosterols from paecilomyces sp. J300
Hak Cheol Kwon, Sang Deuk Zee, Sae Yun Cho, Sang Un Choi and Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     ergosterol
    ÏàËÆ¶È:88%
China Journal of Chinese Materia Medica          2002          27          674-676
Studies on the Chemical Constituents of Shiraia bambusicola
SHEN Yuxiu, RONG Xianguo, GAO Zonghua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     Ergosta-5,7,22-trien-3¦Â-ol
    ÏàËÆ¶È:85.1%
Helvetica Chimica Acta          2004          Vol. 87          1912
Vibratilicin: a Novel Compound from the Basidiomycete Cortinarius vibratilis
Fei Wang, Jian-Wen Tan, and Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

7 .     Âó½ÇçÞ´¼
C28H44O     ÏàËÆ¶È:84.6%
Chinese Traditional and Herbal Drugs          2004          35          493-495
È˹¤Ó¼³æ²Ý»¯Ñ§³É·ÖÑо¿
Íõ¸Õ,Âé±ø¼Ì,Áõ¼ª¿ª
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     ergosterol
    ÏàËÆ¶È:82.1%
Phytochemistry          1997          45          1669-1671
Ergosta-4, 6, 8, 22-tetraen-3-one from the edible fungus, Pleurotus ostreatus (oyster fungus)
Vladimir Chobot, Lubom¨ªr Opletal, Ludk J¨¢hod¨¢, Asmita V. Patel, Christopher G. Dacke, Gerald Blunden
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

9 .     ergosterol
C28H44O     ÏàËÆ¶È:82.1%
Natural Product Sciences          2009          15          173-179
Steroids and Triterpenoid from the Fruit Bodies of Ganoderma lucidum and Their Cytotoxic Activity
Lee, Joon-Seok; Lee, Mi-Kyoung; Hung, Tran-Manh; Lee, Ik-Soo; Min, Byung-Sun; Bae, Ki-Hwan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

10 .     ergosterol
    ÏàËÆ¶È:82.1%
Phytochemistry          1996          41          1301-1308
Sterol analysis of DMI-resistant and -sensitive strains of Venturia inaequalis
Noboru Shirane, Hideyuki Takenaka, Kazuo Ueda, Yutaka Hashimoto, Kenji Katoh, Hideo Ishii
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

11 .     (3¦Â,22E)-Ergosta-5,7,22-trien-3-ol
    ÏàËÆ¶È:82.1%
Chemistry of Natural Compounds          2011          Vol. 47, No. 4          541-544
BIOACTIVE METABOLITES FROM Penicillium sp. P-1,A FUNGAL ENDOPHYTE IN Huperzia serrata
You-Min Ying, Zha-Jun Zhan, Zhi-Shan Ding,and Wei-Guang Shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

12 .     ergosterol
    ÏàËÆ¶È:82.1%
Phytochemistry          1990          29          2513-2520
Effect on ergosterol biosynthesis of a fungicide,SSF-109,in Botrytis cinerea
Noboru Shirane,Akira Murabayashi,Michio Masuko,Atsuko Uomori,Yohko Yoshimura,Shujiro Seo,Kiyohisa Uchida,Ken'ichi Takeda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

13 .     (22E,24R)-ergosta-5,7,22-trien-3¦Â-ol
C28H44O     ÏàËÆ¶È:82.1%
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
--------------------------------------------------------------------------------

14 .     ¦Â-ergosterol
    ÏàËÆ¶È:82.1%
Chinese Traditional and Herbal Drugs          2000          31          328-330
ºÖÔ²¿×Å£¸Î¾ú»¯Ñ§³É·ÖµÄÑо¿
Íò»Ô
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

15 .     Ergosterol
    ÏàËÆ¶È:82.1%
Archives of Pharmacal Research          2009          32          1573-1579
Steroids and triterpenes from the fruit bodies of Ganoderma lucidum and their anti-complement activity
Hyo Won Seo, Tran Manh Hung, MinKyun Na, Hyun Ju Jung and Jin Cheol Kim, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

16 .     ergosta-5, 7, 22-trien-3¦Â-ol
C28H44O     ÏàËÆ¶È:82.1%
Acta Bot. Boreal. -Occident. Sin.          2010          30          601-603
Chemical Constituents in the Fruiting Bodies of Sarcodon scabrosus
MA Bing-ji, SHEN Jin-wen, YU Hai-you, ZHOU Hang, ZHAO Xu, RUAN Yuan, WU Ting-ting
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

17 .     ergosta-5,7,22-trien-3¦Â-ol
    ÏàËÆ¶È:82.1%
Chinese Pharmaceutical Journal          2009          44          418-421
Studies on Chemical Constituents in Forsythia suspensa (Thunb.) Vahl
FENG Wei-sheng, LI Ke-ke, ZHENG Xiao-ke
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

18 .     22 E-ergosta-5,7,22-trien-3¦Â-ol
    ÏàËÆ¶È:82.1%
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 .     (3¦Â,22E)-Âó½ÇçÞ-5,7,22-ÈýÏ©-3-´¼
C28H44O     ÏàËÆ¶È:82.1%
Chinese Journal of Medicinal Chemistry          2009          19          200-205
Chemical constituents from the endophytic fungus Acremonium sp. J1 of Antiaris toxicaria
QUE Dong-mei, DAI Hao-fu, ZENG Yan-bo, WU Jiao, MEI Wen-li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

20 .     ergosterol
    ÏàËÆ¶È:82.1%
Chemical Communications          1986                   1139-1140
Biosynthesis of Sitosterol in Tissue Cultures of Rabdosia japonica Hara and Ergosterol in Yeast from [2-13C, 2-2H3]Acetate
Shujiro Seo, * Ushio Sankawa, Haruo Seto, Atsuko Uomori, Yohko Yoshimura, Yutaka Ebizuka, Hiroshi Noguchi, and Ken'ichi Takeda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

21 .     Âó½ÇçÞ´¼
    ÏàËÆ¶È:82.1%
Journal of Shenyang Pharmaceutical University          2007          24          245-248
Fermentation products of endophyte HCCB00167
XIE Cui-hua, RUAN Li-jun, XIA Huan-zhang, CHEN Dai-jie, GE Mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

22 .     24(R)-methylcholesta-5,7,22-tiene-3-ol
    ÏàËÆ¶È:82.1%
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
--------------------------------------------------------------------------------

23 .     ergosterol
    ÏàËÆ¶È:82.1%
Bioscience, Biotechnology, and Biochemistry          1994          58          1542-1544
Volemolide, a Novel Norsterol from the Fungus Lactarius volemus
Kenji Kobata, Tomonari Wada, Yasuo Hayashi, Hisao Shisata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

24 .     ergosterol
C28H44O     ÏàËÆ¶È:82.1%
Natural Product Research and Development          2010          22          998-1000
Chemical Constituents and Identification of the Caules of Clematis armandii Franch. and Clematis montana Buch.-Ham.
LIU Jing-jing;CHEN Xing; WEI Zhi-qi; LI Bin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

25 .     (22E,24R)-ergosta-5,7,22-trien-3¦Â-ol
    ÏàËÆ¶È:82.1%
Natural Product Research and Development          2010          22          972-975
Chemical Constitutes of Termitomyces schimperi Collected from Africa
YANG Xiao-long;ZHU Ying-cheng; FANG Sheng-tao; JIANG Meng-yuan; LIU Ji-kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

26 .     ergosta-5,7,22-trien-3-ol
    ÏàËÆ¶È:82.1%
Natural Product Research and Development          2007          19          420-422
Isolation and Structures of Two Steroids from Mangrove Endophyte Penicillium sp.
LI Xiang;SUN Guang-zhi; ZHENG Yi-nan; LIN Wen-han; Isabel Sattler
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

27 .     (22E,24R)-ergosta-5,7,22-trine-3¦Â-ol
    ÏàËÆ¶È:82.1%
Natural Product Research and Development          2007          19          605-609
Study on the Chemical Constitutes of Hydnellum concrescens
YANG Xiao-long;WANG Fei; SHAO Hong-jun; DONG Ze-jun; DING Zhi-hui; YANG Wan-qiu; LIU Ji-kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

28 .     ergosta-5,7,22-trien-3¦Â-o-l
C28H44O     ÏàËÆ¶È:82.1%
Natural Product Research and Development          2004          16          204-206
THE CHEMICAL CONSTITUENTS OF BASIDIOMYCETE CALODON SUAVEOLENS
WANG Fei; LIU Ji-kai *
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

29 .     ¦Â-ergosterol
    ÏàËÆ¶È:82.1%
Natural Product Research and Development          1999          11(6)          18-21
THREE STEROLS FROM GYROPORUS CASTANEUS
Wan Hui; Sun Rongqi; Wu Dajun; Guo Beishu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

30 .     ergosterol
    ÏàËÆ¶È:82.1%
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
--------------------------------------------------------------------------------

31 .     ergosterol
    ÏàËÆ¶È:82.1%
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
--------------------------------------------------------------------------------

32 .     (22E,24R)-ergosta-5,7,22-trien-3¦Â-ol
    ÏàËÆ¶È:82.1%
Chinese Journal of Natural Medicines          2011          9          101-104
A New Biphenyl from the Fermentation Broth of Plant Endophytic Fungus Pestalotiopsis zonata isolated from Cyrtotachys lakka
YANG Xiao-Long, *, ZHANG Su, SONG Shao-Jun, ZHANG Yan, LUO Du-Qiang,, ZHANG Meng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

33 .     Ergosta-5,7,22-trien-3¦Â-ol ergosterol
C28H44O     ÏàËÆ¶È:82.1%
Organic Magnetic Resonance          1977          9          439-464
13C N.m.r. Spectra of steroids¡ªA Survey and Commentary
J.W.Blunt and J.B.Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

34 .     ergosterol
    ÏàËÆ¶È:82.1%
Chinese Journal of Natural Medicines          2012          10          72-76
Bioactive metabolites from Guignardia sp., an endophytic fungus residing in Undaria pinnatifida
Feng-Wu WANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

35 .     Ergosterol
C28H44O     ÏàËÆ¶È:78.5%
Chemistry of Natural Compounds          2009          45          759-761
STEROIDS AND OTHER CONSTITUENTS FROMTHE MUSHROOM Armillaria lueo-virens
Hui-Yan Xiong, Dong-Qing Fei, Jin-Song Zhou,Chun-Jiang Yang,and Guo-Liang Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

36 .     ergosterol
    ÏàËÆ¶È:78.5%
Acta Pharmaceutica Sinica          2000          Vol 35          367-369
THE STEROL CONSTITUENTS OF MYCENA DENDROBII
CHEN Xiao Mei; YANG Jun Shan; GUO Shun Xing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

37 .     ergosterol
    ÏàËÆ¶È:78.5%
Chinese Traditional and Herbal Drugs          2005          36          1601-1603
Chemical constituents from fruiting bodies of Ganoderma lucidum
ZHANG Xiao-qi; YIN Zhi-qi; YE Wen-cai; ZHAO Shou-xun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

38 .     ergosterol
    ÏàËÆ¶È:78.5%
Natural Product Research and Development          2010          22          422-424
Chemical Constituents from Fruiting Bodies of Phylloporia ribis(Lonicera japonica Thunb.)
LI Cong; ZHANG Yong-qing; LI Jia; QIU Li-li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

39 .     ergoaterol
    ÏàËÆ¶È:78.5%
Natural Product Research and Development          2010          22          1018-1020
Chemical Constituents from Fruiting Bodies of Ganoderma lucidum.(¢ò)
CHEN Man; ZHANG Mi; SUN Shi; XIA Bing; ZHANG Han-qing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

40 .     Ergosterol
C28H440     ÏàËÆ¶È:75%
Chemistry of Natural Compounds          2000          36          170-172
LOW-MOLECULAR-WEIGHT MUSHROOM METABOLITES.IV. SLIGHTLY POLAR COMPONENTS OF Stachybotrys alternans
L. S. Kamalov, M. A. Agzamova,S. F. Aripova, and M. I. Isaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

41 .     ergosterol
    ÏàËÆ¶È:75%
China Journal of Chinese Materia Medica          1997          22          485-486
Studies on Chemical Constituents of Bulgaria inquinans (Fries)
Cui Dongbin , Wang Shuqin and Ding Xiaokun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

42 .     24¦Â-methylcholesta-5,7,22,25-tetraen-3¦Â-ol
    ÏàËÆ¶È:75%
Journal of Natural Products          1993          Vol 56          2016
Biemnasterol, a New Cytotoxic Sterol with the Rare 22,25-Diene Side Chain, Isolated from the Marine Sponge Biemna sp.
Chun-min Zeng, Masami Ishibashi, Jun'ichi Kobayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

43 .     ergosterol(3¦Â-hydroxyergosta-5,7,22-triene)
C28H44O     ÏàËÆ¶È:75%
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
--------------------------------------------------------------------------------

44 .     Âó½ÇçÞ-5,7,2-ÈýÏ©-3¦Â-´¼
    ÏàËÆ¶È:75%
Chinese Traditional and Herbal Drugs          2007          38          337-339
Chemical constituents of fruiting bodies from basidiomycete Suillus granulatus and their anti-HIV-1 activity
DONG Ze-jun; WANG Fei; WANG Rui-rui; YANG Liu-meng; ZHENG Yong-tang; LIU Ji-kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

45 .     ergost-5,7,22-trien-3-ol
    ÏàËÆ¶È:75%
Chinese Traditional and Herbal Drugs          2006          37          1297-1300
Chemical constituents of basidiomycete Coltricium nitidum
DU Jian-chang; WANG Xing-na; TAN Ren-xiang; LIU Ji-kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

46 .     erogosterol
C28H46O     ÏàËÆ¶È:75%
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
--------------------------------------------------------------------------------

47 .     ergosta-5,7,22-trine-3-o-l
    ÏàËÆ¶È:75%
Natural Product Research and Development          2007          19          809-810
Study on the Chemical Constituents of Lasiosphaera fenzlii Reich.
WANG Xue-qin; SUN Long-ru*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

48 .     (22E,24R)-ergosta-5,7,22-triene-3¦Â-ol
C28H44O     ÏàËÆ¶È:75%
Natural Product Research and Development          2007          19          620-622
Chemical Constituents of Piper pedicellatum C. DC
LI Jun-zhu; LIU Hai-yang; DONG Qiu; CHEN Chang-xiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

49 .     compound 4
    ÏàËÆ¶È:73.9%
Bioscience, Biotechnology, and Biochemistry          1994          58          1542-1544
Volemolide, a Novel Norsterol from the Fungus Lactarius volemus
Kenji Kobata, Tomonari Wada, Yasuo Hayashi, Hisao Shisata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

50 .     ergosta-5,7-dien-3¦Â-ol
    ÏàËÆ¶È:71.4%
Phytochemistry          1996          41          1301-1308
Sterol analysis of DMI-resistant and -sensitive strains of Venturia inaequalis
Noboru Shirane, Hideyuki Takenaka, Kazuo Ueda, Yutaka Hashimoto, Kenji Katoh, Hideo Ishii
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

51 .     ×ØÍ©ËᵨçÞÏ©õ¥
    ÏàËÆ¶È:71.4%
Chinese Traditional and Herbal Drugs          1998          29          298-300
´óÂí²ªµÄ»¯Ñ§³É·ÖÑо¿
½ðÏòȺ,ÍõÁ¥Êé,³Ì¶«ÑÒ,ÒÁѧÁú,ÂÀ¾°É½
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
ûÓÐÍ´¿à---ûÓÐÊÕ»ñ
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