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19.7,22.1,24.4,28.0,29.4,33.5,34.9,37.6,39.2,41.8,42.5,42.9,43.9,50.9,59.0,67.9,68.6,74.4,75.9,85.0,117.4,172.5,176.6
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PSA: ½ð±Ò+1, ÔٴθÐл 2012-12-14 17:06:36
ºÄ×Ó¹úÍõ: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2012-12-14 21:10:19
ÕâÊÇÄãÇóÖúµÄ»¯ºÏÎïÔÚÏàËÆ¶È60%ÒÔÉÏµÄÆ¥ÅäÐÅÏ¢
     1 .     17¦ÂH-gitoxigenin
    C23H34O5     ÏàËÆ¶È:78.2%
    Phytochemistry          1991          30          1503-1506
    Biotransformation of digitoxigenin by cell suspension cultures of Strophanthus divaricatus
    Kiichiro Kawaguchi, Masao Hirotani, Tsutomu Furuya
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    2 .     sarmentogenin
        ÏàËÆ¶È:73.9%
    Bulletin des Soci¨¦t¨¦s Chimiques Belges          1988          97          297-311
    New cardenolide glycosides from the defence glands of chrysolinina beetles (coleoptera: Chrysomelidae)
    S. van Oycke, T. Randoux, J. C. Braekman, D. Daloze and J. M. Pasteels
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    3 .     5¦Â-hydroxygitoxigenin
        ÏàËÆ¶È:69.5%
    Planta Medica          1981          42          160-166
    Biotransformation of Cardenolides by Plant Cell Cultures II. Metabolism of Gitoxigenin and its Derivatives by Suspension Cultures of Daucus carota
    A. Jones and I. A. Veliky
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    4 .     3-epi-17¦ÂH-gitoxiyenin
    C23H34O5     ÏàËÆ¶È:69.5%
    Phytochemistry          1991          30          1503-1506
    Biotransformation of digitoxigenin by cell suspension cultures of Strophanthus divaricatus
    Kiichiro Kawaguchi, Masao Hirotani, Tsutomu Furuya
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    5 .     19-(N,N-dimethylcarbamoxy)-2¦Â,8,13-trihydroxystemarane
    23H39NO5     ÏàËÆ¶È:65.2%
    Phytochemistry          2006          67          1088-1093
    Bioconversion of Stemodia maritima diterpenes and derivatives by Cunninghamella echinulata var. elegans and Phanerochaete chrysosporium
    Andrew S. Lamm, William F. Reynolds, Paul B. Reese
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    6 .     gitoxigenin
        ÏàËÆ¶È:65.2%
    Planta Medica          1981          42          160-166
    Biotransformation of Cardenolides by Plant Cell Cultures II. Metabolism of Gitoxigenin and its Derivatives by Suspension Cultures of Daucus carota
    A. Jones and I. A. Veliky
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    7 .     compound 1b
        ÏàËÆ¶È:65.2%
    Chemical & Pharmaceutical Bulletin          1998          46          12-16
    Study on the Bile Salts from Sunfish, Mola mola L. I. The Structures of Sodium Cyprinol Sulfates, the Sodium Salt of a New Bile Acid Conjugated with Taurine, and a New Bile Alcohol and Its New Sodium Sulfates
    Hitoshi ISHIDA,Hidetoshi NAKAYASU,Hidekazu MIYAMOTO,Haruo NUKAYA and Kuniro TSUJI
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    8 .     sarmentogenin
        ÏàËÆ¶È:65.2%
    Phytochemistry          1987          26          2351-2355
    Cardenolide glycosides of Strophanthus divaricatus
    Rong-Fu Chen,Fumiko Abe,Tatsuo Yamauchi,Masakatsu Taki
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    9 .     periplogenin
        ÏàËÆ¶È:65.2%
    Chinese Pharmaceutical Journal          2007          42          420-422
    Studies on Chemical Constituents of Streptocaulon griffithii
    ZHANG Lin, WANG Ye-fei, XU Li-zhen
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    10 .     2¦Â,3¦Á,14¦Â-Trihydroxy-5¦Â-card-20(22)-enolide
    C23H34O5     ÏàËÆ¶È:65.2%
    Bioorganic & Medicinal Chemistry          1998          6          1889-1894
    Synthesis and biological evaluation of 2-Hydroxy derivatives of digitoxigenin and 3-Epidigitoxigenin
    M Gobbini, G Marazzi, G Padoani, L Quadri, L Valentino, M.P Zappavigna, P Melloni
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    11 .     3¦Â,4¦Â,14¦Â-trihydroxy-5¦Â-card-20(22)-enolide
    C23H34O5     ÏàËÆ¶È:65.2%
    Bioorganic & Medicinal Chemistry          1998          6          1889-1894
    Synthesis and biological evaluation of 2-Hydroxy derivatives of digitoxigenin and 3-Epidigitoxigenin
    M Gobbini, G Marazzi, G Padoani, L Quadri, L Valentino, M.P Zappavigna, P Melloni
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    12 .     isodojaponin C
    C24H32O8     ÏàËÆ¶È:62.5%
    Journal of Natural Products          2008          71(6)          1055-1058
    ent-Kaurane Diterpenoids from Isodon japonicus
    Seong Su Hong, Seon A. Lee, Xiang Hua Han, Ji Sang Hwang, Chul Lee,Dongho Lee, Jin Tae Hong, Youngsoo Kim, Heesoon Lee, and Bang Yeon Hwang
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    13 .     tauroselocholic acid
    C26H45NO7S     ÏàËÆ¶È:61.5%
    Chemical & Pharmaceutical Bulletin          2009          57          528-531
    Novel Bile Acids from Bear Bile Powder and Bile of Geese
    Dan Bi, Xing-Yun Chai, Yue-Lin Song, Yu Lei and Peng-Fei Tu
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    14 .     tauroansocholic acid
    C26H45NO7S     ÏàËÆ¶È:61.5%
    Chemical & Pharmaceutical Bulletin          2009          57          528-531
    Novel Bile Acids from Bear Bile Powder and Bile of Geese
    Dan Bi, Xing-Yun Chai, Yue-Lin Song, Yu Lei and Peng-Fei Tu
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    15 .     macrodaphniphyllamine
        ÏàËÆ¶È:60.8%
    Journal of Natural Products          2006          69          1745-1748
    Yuzurimine-Type Alkaloids from Daphniphyllum yunnanense
    Ying-Tong Di, Hong-Ping He, Chun-Shun Li, Jun-Mian Tian,Shu-Zhen Mu, Shun-Lin Li, Suo Gao, and Xiao-Jiang Hao
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    16 .     yunnandaphnine A
    C23H33NO3     ÏàËÆ¶È:60.8%
    Journal of Natural Products          2006          69          1745-1748
    Yuzurimine-Type Alkaloids from Daphniphyllum yunnanense
    Ying-Tong Di, Hong-Ping He, Chun-Shun Li, Jun-Mian Tian,Shu-Zhen Mu, Shun-Lin Li, Suo Gao, and Xiao-Jiang Hao
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    17 .     yunnandaphnine D
    C23H33NO2     ÏàËÆ¶È:60.8%
    Journal of Natural Products          2006          69          1745-1748
    Yuzurimine-Type Alkaloids from Daphniphyllum yunnanense
    Ying-Tong Di, Hong-Ping He, Chun-Shun Li, Jun-Mian Tian,Shu-Zhen Mu, Shun-Lin Li, Suo Gao, and Xiao-Jiang Hao
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    18 .     gitoxigenin
        ÏàËÆ¶È:60.8%
    Planta Medica          1986          52          68-70
    Neue Cardenolide aus Adonis vernalis
    C. Winkler, M. Wichtl
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    19 .     spiramine C
    C21H31NO3     ÏàËÆ¶È:60.8%
    Chemical & Pharmaceutical Bulletin          1987          35          1670-1672
    THE STRUCTURES OF FOUR NEW DITERPENE ALKALOIDS, SPIRAMINES A, B, C, AND D
    Xiaojiang Hao,Manabu Node,Tooru Taga,Yoshihisa Miwa,Jun Zhou,Siying Chen and Kaoru Fuji
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    20 .     spiramilactams B
    C22H33NO5     ÏàËÆ¶È:60.8%
    Helvetica Chimica Acta          2009          92          1198-1202
    Two New Diterpenoid Lactams from Spiraea japonica var. ovalifolia
    Hai-Yang Liu, Wei Ni, Chang-Xiang Chen, Ying-Tong Di, Xiao-Jiang Hao
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    21 .     ibosol
        ÏàËÆ¶È:60.8%
    Phytochemistry          1998          49          1101-1105
    Diterpenes from pinus taeda
    M¨¢rio Geraldo de Carvalho, Victor M. Rumjanek, Maria de Jesus S. Lopes, Ac¨¢cio Geraldo de Carvalho
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    22 .     uzarigenin
        ÏàËÆ¶È:60.8%
    Phytochemistry          1992          31          2821-2824
    Proceragenin, an antibacterial cardenolide from Calotropis procera
    Nargis Akhtar, Abdul Malik, Samina Noor Ali, Shahana Urooj Kazmit
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    23 .     periplogenin
    C23H34O5     ÏàËÆ¶È:60.8%
    Phytochemistry          1988          27          3475-3479
    Biotransformation of digitoxigenin by cell suspension cultures of Strophanthus amboensis
    Kiichiro Kawaguchi,Masao Hirotani,Tsutomu Furuya
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    24 .     ajaconine
    C22H33NO3     ÏàËÆ¶È:60.8%
    Phytochemistry          1990          29          2381-2383
    A norditerpenoid alkaloid from Delphinium elatum
    S.William Pelletier,Samir A. Ross,Haridutt K. Desai
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    25 .     epimanoyl oxide acid methyl ester
        ÏàËÆ¶È:60.8%
    Phytochemistry          1985          24          1267-1271
    Resin acids of Pinus resinosa needles
    Duane F. Zinkel, Wilbur B. Clarke
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    26 .     13-Ethyl-1 7¦Â-hydroxyl1-methylene-18,19-dinor-5¦Â,17¦Á-pregnan-20-yn-3-one
    C22H30O2     ÏàËÆ¶È:60.8%
    Steroids          1997          62          437-443
    Preparation of 3-ketodesogestrel metabolites by microbial transformation and chemical synthesis
    Helmut Groh, Renate Schön, Michael Ritzau, Helmut Kasch, Katrin Undisz, Gerhard Hobe
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    27 .     13-ethyl-17¦Â-hydroxy-11-methylene-18,19-dinor-5¦Â,17¦Á-pregnan-20-yne-3¦Â,17¦Â-diol
    C22H32O2     ÏàËÆ¶È:60.8%
    Steroids          1997          62          437-443
    Preparation of 3-ketodesogestrel metabolites by microbial transformation and chemical synthesis
    Helmut Groh, Renate Schön, Michael Ritzau, Helmut Kasch, Katrin Undisz, Gerhard Hobe
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    28 .     Acovenosigenin A
    C23H34O5     ÏàËÆ¶È:60.8%
    Chinese Journal of Natural Medicines          2009          7          108-110
    Chemical Constituents from the Roots of Streptocaulon griffithii
    ZHOU Jin-Song; ZHANG Ting-Ting; CHEN Ji-Jun; WANG Qiang
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    29 .     2¦Á,3¦Á,14¦Â-Trihydroxy-5¦Â-card-20(22)-enolide
    C23H34O5     ÏàËÆ¶È:60.8%
    Bioorganic & Medicinal Chemistry          1998          6          1889-1894
    Synthesis and biological evaluation of 2-Hydroxy derivatives of digitoxigenin and 3-Epidigitoxigenin
    M Gobbini, G Marazzi, G Padoani, L Quadri, L Valentino, M.P Zappavigna, P Melloni
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    30 .     uzarigenin
        ÏàËÆ¶È:60.8%
    Natural Product Research and Development          2003          15          113-115
    CHEMICAL CONSTITUTES AND THE CYTOTOXIC ACTIVITY OF MYRIOPTERON EXTENSUM
    LI Yu yuan; ZHANG Guo lin
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    31 .     Calyciphylline L
    C23H35NO2     ÏàËÆ¶È:60.8%
    Tetrahedron          2008          64          1901-1908
    Calyciphyllines H¨CM, new Daphniphyllum alkaloids from Daphniphyllum calycinum
    Shizuka Saito, Hiroko Yahata, Takaaki Kubota, Yutaro Obara, Norimichi Nakahata, Jun'ichi Kobayashi
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    32 .     compound 31
        ÏàËÆ¶È:60.8%
    Tetrahedron          2005          61          4531-4544
    Novel cytotoxic kaurane-type diterpenoids from the New Zealand Liverwort Jungermannia species
    Fumihiro Nagashima, Masuo Kondoh, Makiko Fujii, Shigeru Takaoka, Yoshiteru Watanabe, Yoshinori Asakawa
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    33 .     ethyl ent-15¦Á-hydroxymethyl-16¦Â-hydroxybeyeran-19-oate
    C23H38O4     ÏàËÆ¶È:60.8%
    Bioorganic & Medicinal Chemistry          2009          17          1464-1473
    Stereoselective synthesis of bioactive isosteviol derivatives as ¦Á-glucosidase inhibitors
    Ya Wu, Jing-Hua Yang, Gui-Fu Dai, Cong-Jun Liu, Guo-Qiang Tian, Wen-Yan Ma, Jing-Chao Tao
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    34 .     hydroxyethyl ent-15¦Á-hydroxymethyl-16¦Â-hydroxybeyeran-19-oate
    C23H38O5     ÏàËÆ¶È:60.8%
    Bioorganic & Medicinal Chemistry          2009          17          1464-1473
    Stereoselective synthesis of bioactive isosteviol derivatives as ¦Á-glucosidase inhibitors
    Ya Wu, Jing-Hua Yang, Gui-Fu Dai, Cong-Jun Liu, Guo-Qiang Tian, Wen-Yan Ma, Jing-Chao Tao
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    35 .     ethyl ent-16-aminobeyeran-19-oate
    C22H37NO2     ÏàËÆ¶È:60.8%
    Bioorganic & Medicinal Chemistry          2009          17          1464-1473
    Stereoselective synthesis of bioactive isosteviol derivatives as ¦Á-glucosidase inhibitors
    Ya Wu, Jing-Hua Yang, Gui-Fu Dai, Cong-Jun Liu, Guo-Qiang Tian, Wen-Yan Ma, Jing-Chao Tao
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    36 .     3¦Â,20R-bis(acetoxy)-5¦Á-12¦Á-14¦Â-dihydroxy-pregnane
    C25H40O6     ÏàËÆ¶È:60.8%
    Steroids          2011          76          1166-1175
    Norrish¨CPrins reaction as a key step in the synthesis of 14¦Â-hydroxy-5¦Á (or 5¦Â or ¦¤5,6)-pregnane derivatives
    Philippe Geoffroy, Blandine Ressault, Eric Marchioni, Michel Miesch
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    37 .     17¦Â-(2',5'-Dihydro-5'-oxo-3'-furyl)-5¦Â,14¦Â-Sndrostane-3¦Â,14,16¦Â-triol
    C23H34O5     ÏàËÆ¶È:60.8%
    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

    38 .     16-O-acetylgitoxigenin
        ÏàËÆ¶È:60%
    Chinese Pharmaceutical Journal          2007          42          420-422
    Studies on Chemical Constituents of Streptocaulon griffithii
    ZHANG Lin, WANG Ye-fei, XU Li-zhen
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    39 .     2¦Â-Acetoxy-14¦Â-hydroxy-3-oxo-5¦Â-card-20(22)-enolide
    C25H34O6     ÏàËÆ¶È:60%
    Bioorganic & Medicinal Chemistry          1998          6          1889-1894
    Synthesis and biological evaluation of 2-Hydroxy derivatives of digitoxigenin and 3-Epidigitoxigenin
    M Gobbini, G Marazzi, G Padoani, L Quadri, L Valentino, M.P Zappavigna, P Melloni
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    40 .     daphniglaucin J
    C25H35NO5     ÏàËÆ¶È:60%
    Tetrahedron          2004          60          6279-6284
    Daphniglaucins D¨CH, J, and K, new alkaloids from Daphniphyllum glaucescens
    Hiroshi Takatsu, Hiroshi Morita, Ya-Ching Shen, Jun'ichi Kobayashi
    Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

    41 .     17¦Â-(2',5'-Dihydro-5'-oxo-3'-furyl)-5¦Â,14¦Â-androstane-3¦Â,14,16¦Â-triol 16-acetate
    C?5H38O6     ÏàËÆ¶È:60%
    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
2Â¥2012-12-14 16:55:22
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