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Ly-10
13C NMR (126 MHz, cd3od) ¦Ä15.98,16.88, 17.74, 19.32, 23.96, 24.01, 24.56, 26.30, 27.07, 28.43, 28.91, 31.53, 33.49, 37.87, 40.39, 40.72, 42.61, 42.94, 48.03, 49.28, 49.46, 50.38, 52.81, 56.97, 62.42, 63.11, 68.74, 71.12, 71.92, 73.01, 73.93, 76.27, 76.52, 77.69, 77.86, 78.31, 78.35, 78.69, 80.46, 91.81, 95.71, 104.45, 105.58, 123.81, 130.56, 144.83, 171.13, 178.06.

Ly-9
13C NMR (126 MHz, cd3od) ¦Ä16.11, 17.12, 17.64, 17.82, 17.96, 22.83, 24.23, 25.87, 27.24, 27.58, 30.95, 31.38, 31.53, 36.63, 40.18, 40.36, 40.48, 41.86, 45.28, 49.41, 50.59, 52.43, 53.12, 61.77, 62.52, 62.90, 71.19, 71.69, 71.86, 75.37, 75.48, 77.64, 77.91, 78.21, 79.05, 79.85, 80.93, 84.92, 98.28, 105.54, 125.83, 132.29.

Ly-7
13C NMR (126 MHz, cd3od) ¦Ä16.28,16.76, 17.30, 17.97, 19.24, 22.86, 24.21, 25.89, 27.19, 27.23, 28.43, 30.99, 31.63, 35.88, 36.63, 37.89, 40.57, 40.96, 49.73, 51.03, 52.47, 53.08, 57.53, 62.48, 62.77, 63.07, 71.15, 71.47, 71.87, 75.31, 76.26, 77.63, 77.85, 78.18, 78.26, 78.42, 81.03, 84.90, 91.31, 98.22, 104.43, 105.36, 125.81, 132.27.

Ly-4
13C NMR (126 MHz, cd3od) ¦Ä15.92,16.12, 16.86, 17.05, 17.64, 17.82, 23.88, 24.08, 26.26, 26.46, 27.00, 31.53, 37.88, 40.16, 40.71, 42.92, 48.01, 49.00, 52.73, 52.90, 56.91, 57.08, 62.40, 73.07, 76.52, 76.68, 91.09, 91.15, 95.61, 95.76, 106.92, 107.12, 123.62, 123.95, 144.82, 171.38, 178.04.
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libinoook: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-12-25 17:28:21
ly-7
²éѯ½á¹û£º¹²²éµ½823¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     ginsenoside Rd
    ÏàËÆ¶È:91.4%
Journal of Industrial Microbiology & Biotechnology          2009          36          721-726
Highly selective biotransformation of ginsenoside Rb1 to Rd by the phytopathogenic fungus Cladosporium fulvum (syn.Fulvia fulva)
Xuesong Zhao, Juan Wang, Jie Li, Ling Fu, Juan Gao, Xiuli Du, Hongtao Bi, Yifa Zhou, Guihua Tai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     gypenosideXLVI
C48H82O19     ÏàËÆ¶È:87.5%
Bioorganic & Medicinal Chemistry Letters          2014          24          186-191
Cytotoxic activity of gypenosides and gynogenin against non-small cell lung carcinoma A549 cells
Dao-Jin Chen, Hui-Min Liu, Shao-Fang Xing, Xiang-Lan Piao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     gypenoside XLVI
C48H82O19     ÏàËÆ¶È:87.5%
Chinese Joumal of Experimental Traditional Medical Fomulae          2013          19          106-111
Saponins from Zhuang-medicine Gocaekmbaw before and after Heat-processing
LIU Hui-min, CHEN Dao-jin, PIAO Xiang-lan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     gypenoside XVII
    ÏàËÆ¶È:83.3%
China Journal of Chinese Materia Medica          1992          17          611-613
Studies on the Saponins in the Fruit Pedicels of Panax notoginseng(Burk.)F.H.Chen(continue)
Wei Junxian, Chen Yegao and Cao Shuming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     vina-ginsenoside-R9
C48H82O19     ÏàËÆ¶È:81.2%
Chemical & Pharmaceutical Bulletin          1994          42          115-122
Saponins from Vietnamese Ginseng, Panax vietnamensis HA et GRUSHV. Collected in Central Vietnam. II
Nguyen MINH DUC,Ryoji KASAI,Kazuhiro OHTANI,Aiko ITO,Nguyen THOI NHAM,Kazuo YAMASAKI and Osamu TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     ginsenoside Rg1
    ÏàËÆ¶È:79.5%
Chinese Traditional and Herbal Drugs          1996          27          647-649
Isolation and Identification of Ginsenoside from the Leaves of Wild Ginseng(Panax ginseng)
Li Jing; Wei Yongdi(Berhune Medical University; Changchun);
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     gypenoside L
C42H72O14     ÏàËÆ¶È:79.5%
Bioorganic & Medicinal Chemistry Letters          2014          24          186-191
Cytotoxic activity of gypenosides and gynogenin against non-small cell lung carcinoma A549 cells
Dao-Jin Chen, Hui-Min Liu, Shao-Fang Xing, Xiang-Lan Piao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Gypenoside L
C42H72O14     ÏàËÆ¶È:79.5%
Archives of Pharmacal Research          2013          36          874-879
Dammarane-type saponins from heat-processed Gynostemma pentaphyllum show fortified activity against A549 cells
Xiang-Lan Piao, Qian Wu, Jing Yang, Seo Young Park, Dao-Jin Chen, Hui-Min Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     gypenoside L
C42H72O14     ÏàËÆ¶È:79.5%
Chinese Joumal of Experimental Traditional Medical Fomulae          2013          19          106-111
Saponins from Zhuang-medicine Gocaekmbaw before and after Heat-processing
LIU Hui-min, CHEN Dao-jin, PIAO Xiang-lan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     gypenoside LI
    ÏàËÆ¶È:77.2%
Bioorganic & Medicinal Chemistry Letters          2014          24          186-191
Cytotoxic activity of gypenosides and gynogenin against non-small cell lung carcinoma A549 cells
Dao-Jin Chen, Hui-Min Liu, Shao-Fang Xing, Xiang-Lan Piao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     ginsenoside-Rg1
C42H72O14     ÏàËÆ¶È:77.2%
Chinese Traditional and Herbal Drugs          2012          43          1462-1470
Studies on chemical constituents from Aidi Injection
ZHANG Miao-miao; LIU Yan-li; CHEN Zhong; LI Xiao-ran; XU Qiong-ming; YANG Shi-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     Gypenoside LI
C42H72O14     ÏàËÆ¶È:77.2%
Archives of Pharmacal Research          2013          36          874-879
Dammarane-type saponins from heat-processed Gynostemma pentaphyllum show fortified activity against A549 cells
Xiang-Lan Piao, Qian Wu, Jing Yang, Seo Young Park, Dao-Jin Chen, Hui-Min Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     gypenoside LI
C42H72O14     ÏàËÆ¶È:77.2%
Chinese Joumal of Experimental Traditional Medical Fomulae          2013          19          106-111
Saponins from Zhuang-medicine Gocaekmbaw before and after Heat-processing
LIU Hui-min, CHEN Dao-jin, PIAO Xiang-lan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     lanost-5,24-dien-3¦Â-ol-3-O-¦Â-D-glucopyranosyl-(6'¡ú1'')-¦Â-D-glucopyranosyl-(6''¡ú1''')-¦Â-D-glucopyranoside
C48H80O16     ÏàËÆ¶È:72.9%
Bioorganic & Medicinal Chemistry Letters          2014          24          4203-4208
Triterpene glycosides from red ginseng marc and their anti-inflammatory activities
Ill-Min Chung, Young-Ock Kim, Mohammed Ali, Seung-Hyun Kim, Inmyoung Park, Eun-Hye Kim, Ye-Sul Yang, Hye-Ran Park, Eun-Suk Son, Ateeque Ahmad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     ginsenoside Rg5
    ÏàËÆ¶È:72.7%
Archives of Pharmacal Research          1996          19          551-553
High performance liquid chromatographic assay of a new fluoroquinolone, LB20304, in the plasma of rats and dogs
Mi-Kyeong Seo, Yi-Na Jeong, Hoon-Joo Kim, In-Chull Kim and Yong-Hee Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     ginsenoside Rf
    ÏàËÆ¶È:72.7%
Chinese Joumal of Experimental Traditional Medical Fomulae          2012          18          78-81
Study of Chemical Components from Qili Qiangxin Capsule (¢ò)
QIAO Li, WANG Zong-quan, MENG Zuo-huan, JIANG Xin-gang, JIA Ji-ming, SONG Jian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (25R)-26-O-¦Â-D-glucopyranosyl-5¦Â-furostan-3¦Â,22¦Á,26-triol 3-O-[¦Â-D-glucopyranosyl-(1¡ú2)-O-¦Â-D-glucopyranoside]
C45H76O19     ÏàËÆ¶È:71.1%
Biochemical Systematics and Ecology          2006          34          809-814
Furostanol saponins from Yucca gloriosa L. rhizomes
Alexandre Skhirtladze, Alberto Plaza, Paola Montoro, Mariam Benidze, Ether Kemertelidze, Cosimo Pizza, Sonia Piacente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     ecliptasaponin B
C48H47O19     ÏàËÆ¶È:70.8%
Journal of Chinese Pharmaceutical Sciences          1996          5          177-181
Isolation and Identification of Ecliptasaponin A and Ecliptasaponin B from Eclipta alba (L.) Hasssk
Mei Zhang and Ya-Yan Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     ecliptasaponin B
    ÏàËÆ¶È:70.8%
Acta Pharmaceutica Sinica          1996          31          196-199
ISOLATION AND IDENTIFICATION OF ECLIPTASAPONIN A AND ECLIPTASAPONIN B FROM ECLIPTA ALBA(L.)HASSK
M Zhang and YY Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     ginsenoside Re
    ÏàËÆ¶È:70.8%
Chinese Joumal of Experimental Traditional Medical Fomulae          2012          18          78-81
Study of Chemical Components from Qili Qiangxin Capsule (¢ò)
QIAO Li, WANG Zong-quan, MENG Zuo-huan, JIANG Xin-gang, JIA Ji-ming, SONG Jian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     damulin B
C42H70O13     ÏàËÆ¶È:70.4%
Bioorganic & Medicinal Chemistry          2011          19          6254-6260
New dammarane-type glucosides as potential activators of AMP-activated protein kinase (AMPK) from Gynostemma pentaphyllum
Phi Hung Nguyen, Rehman Gauhar, Seung Lark Hwang, Trong Tuan Dao, Dong Chan Park, Ji Eun Kim, Hebok Song, Tae Lin Huh, Won Keun Oh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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libinoook: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-12-25 17:28:00
ly-10
²éѯ½á¹û£º¹²²éµ½790¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     ¦Â-D-Glucopyranosyl 3-(O-¦Â-D-glactopyranosyl (1¡ú2)(O-¦Â-D-glucopyranosyloxy))-oleanolate
C48H76O19     ÏàËÆ¶È:87.5%
Monatshefte f¨¹r Chemie          2000          131          195-204
Three Saponins, a Steroid, and a Flavanol Glycoside from Achyrantes aspera
Olaf Kunert, Ernst Haslinger, Martin G. Schmid, Josef Reiner, Franz Bucar, Efrem Mulatu, Dawit Abebe, and Asfaw Debella
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     3-O-¦Â-D-glucopyranosyl(1¡ú3)-¦Â-D-glucuronopyranoside-28-O-¦Â-D-glucopyranosyl oleanolic acid methyl ester
    ÏàËÆ¶È:83.6%
Bioorganic & Medicinal Chemistry Letters          2010          20          7110-7115
Oleanane-type triterpenoids from Panax stipuleanatus and their anticancer activities
Chun Liang, Yan Ding, Huu Tung Nguyen, Jeong-Ah Kim, Hye-Jin Boo, Hee-Kyoung Kang, Mahn Cuong Nguyen, Young Ho Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     Sandrosaponin X
    ÏàËÆ¶È:83.3%
Journal of Natural Products          2000          63          1479-1482
Four New Triterpenoid Saponins from the Roots of Bupleurum rigidum
Sandra Svnchez-Contreras, Ana Mar¨ªa Dvaz-Lanza, and Manuel Bernab¨¦
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     spinasaponin A 28-O-glucoside
    ÏàËÆ¶È:83.3%
Bioorganic & Medicinal Chemistry Letters          2010          20          7110-7115
Oleanane-type triterpenoids from Panax stipuleanatus and their anticancer activities
Chun Liang, Yan Ding, Huu Tung Nguyen, Jeong-Ah Kim, Hye-Jin Boo, Hee-Kyoung Kang, Mahn Cuong Nguyen, Young Ho Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     pseudoginsenoside RT1 methyl ester
    ÏàËÆ¶È:83.3%
Bioorganic & Medicinal Chemistry Letters          2010          20          7110-7115
Oleanane-type triterpenoids from Panax stipuleanatus and their anticancer activities
Chun Liang, Yan Ding, Huu Tung Nguyen, Jeong-Ah Kim, Hye-Jin Boo, Hee-Kyoung Kang, Mahn Cuong Nguyen, Young Ho Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     ¦Â-D-glucopyranosyl 3¦Â-[O-¦Â-D-galactopyranosyl-(1¡ú2)-O-¦Á-D-glucopyranuronosyloxy]machaerinate
C40H75O20     ÏàËÆ¶È:81.2%
Helvetica Chimica Acta          2000          Vol. 83          359
New Triterpenoid Saponins from Achyrantes aspera Linn.
G¨¹nter Michl,Dawit Abebe,Franz Bucar,Asfaw Debella), Olaf Kunert, Martin G. Schmid, Efrem Mulatu, and Ernst Haslinger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     ecliptasaponin B
C48H47O19     ÏàËÆ¶È:81.2%
Journal of Chinese Pharmaceutical Sciences          1996          5          177-181
Isolation and Identification of Ecliptasaponin A and Ecliptasaponin B from Eclipta alba (L.) Hasssk
Mei Zhang and Ya-Yan Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     ecliptasaponin B
    ÏàËÆ¶È:81.2%
Acta Pharmaceutica Sinica          1996          31          196-199
ISOLATION AND IDENTIFICATION OF ECLIPTASAPONIN A AND ECLIPTASAPONIN B FROM ECLIPTA ALBA(L.)HASSK
M Zhang and YY Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     pseudoginsenoside RT1
    ÏàËÆ¶È:81.2%
Bioorganic & Medicinal Chemistry Letters          2010          20          7110-7115
Oleanane-type triterpenoids from Panax stipuleanatus and their anticancer activities
Chun Liang, Yan Ding, Huu Tung Nguyen, Jeong-Ah Kim, Hye-Jin Boo, Hee-Kyoung Kang, Mahn Cuong Nguyen, Young Ho Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     3-O-¦Â-D-xylopyranosyl(1¡ú2)-¦Â-D-glucopyranosyl-28-O-¦Â-D-glucopyranosyl oleanolic acid
    ÏàËÆ¶È:81.2%
Bioorganic & Medicinal Chemistry Letters          2010          20          7110-7115
Oleanane-type triterpenoids from Panax stipuleanatus and their anticancer activities
Chun Liang, Yan Ding, Huu Tung Nguyen, Jeong-Ah Kim, Hye-Jin Boo, Hee-Kyoung Kang, Mahn Cuong Nguyen, Young Ho Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     Bifinoside C
C53H85O22     ÏàËÆ¶È:79.2%
Chemical & Pharmaceutical Bulletin          2011          59          1417-1420
Oleanolic Triterpene Saponins from the Roots of Panax bipinnatifidus
Nguyen Huu TUNG, Tran Hong QUANG, Nguyen Thi Thanh NGAN, Chau Van MINH, Bui Kim ANH, Pham Quoc LONG, Nguyen Manh CUONG, and Young Ho KIM
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     guaiacin A
C46H72O19     ÏàËÆ¶È:79.1%
Planta Medica          1989          55          307-308
Guaiacin A and B from the Leaves of Guaiacum officinale
Viqar Uddin Ahmad, Shaista Perveen, and Shaheen Bano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     tauroside I
    ÏàËÆ¶È:79.1%
Chemistry of Natural Compounds          1992          28          593-596
TRITERPENE GLYCOSIDES OF Hedera taurica X. STRUCTURES OF COMPOUNDS F 4, I, AND J FROM THE LEAVES OF CRIMEAN IVY
V. I. Grishkovets, N. V. Tolkacheva,A. S. Shashkov, and V. Ya. Chirva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     guaiacin B
    ÏàËÆ¶È:79.1%
Phytochemistry          1999          51          1049-1053
Triterpenoid saponins from Fagonia indica
Kamel H. Shaker, Mirko Bernhardt, M. Hani A. Elgamal, Karlheinz Seifert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     oleanolic acid-3-O-[¦Â-D-galactopyranosyl-(1¡ú3)-¦Â-D-glucuronopyranosyl]-28-O-¦Â-D-glucopyranoside
C48H76O19     ÏàËÆ¶È:79.1%
Food Chemistry          2009          113          411-419
Saponins in Ipomoea batatas tubers: Isolation, characterization, quantification and antioxidant properties
Irene Dini, Gian Carlo Tenore, Antonio Dini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     oleanolic acid 3-O-[2'-4'-di-O-(¦Â-D-glucopyranosyl)-¦Â-D-glucopyranosyl]-28-O-¦Â-D-glucopyranoside
C54H88O23     ÏàËÆ¶È:79.1%
Journal of Agricultural and Food Chemistry          1996          44          3528-3533
Constituents of Chenopodium pallidicaule (Cañihua) Seeds:  Isolation and Characterization of New Triterpene Saponins
Luca Rastrelli, Francesco De Simone, Oreste Schettino, and Antonio Dini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     Tuberoside A
C48H76O19     ÏàËÆ¶È:79.1%
European Journal of Organic Chemistry          1996          1996          781-784
Tuberosides A, B, and C, Novel Triterpenoid Saponins from the Hypoglucaemic Fraction of Ullucus tuberosus
Alfonso Espada, Carlos Jim¨¦nez, Jose Dopeso and Ricardo Riguera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     3-O-{[¦Â-D-glucopyranosyl-(1¡ú2)-O]-¦Â-D-galactopyranoside}-16-O-¦Â-D-glucopyranosyl-3¦Â,6¦Â,16¦Â-trihydroxyolean-12-ene
C48H80O18     ÏàËÆ¶È:79.1%
Phytochemistry          2014          97          70-80
Saponins with highly hydroxylated oleanane-type aglycones from Silphium asteriscus L.
Milena Masullo, Lalita Calabria, Dario Gallotta, Cosimo Pizza, Sonia Piacente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     phytolaccagenic acid 3-O-[¦Â-D-glucopyranosyl-(1¡ú4)-¦Â-D-glucopyranosyl]-28-O-¦Â-D-glucopyranoside
C49H78O21     ÏàËÆ¶È:77.5%
Journal of Agricultural and Food Chemistry          1996          44          3528-3533
Constituents of Chenopodium pallidicaule (Cañihua) Seeds:  Isolation and Characterization of New Triterpene Saponins
Luca Rastrelli, Francesco De Simone, Oreste Schettino, and Antonio Dini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     phytolaccagenic acid 3-O-[¦Â-D-glucopyranosyl-(1¡ú4)-¦Â-D-glucopyranosyl-(1¡ú4)-¦Â-D-glucopyranosyl]-28-O-¦Â-D-glucopyranoside
C55H88O26     ÏàËÆ¶È:77.5%
Journal of Agricultural and Food Chemistry          1996          44          3528-3533
Constituents of Chenopodium pallidicaule (Cañihua) Seeds:  Isolation and Characterization of New Triterpene Saponins
Luca Rastrelli, Francesco De Simone, Oreste Schettino, and Antonio Dini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     3‑O-2-(acetylamino)-2-deoxy-¦Â-D-glucopyranosylentagenicacid-28-O-¦Â-D-xylopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside
C49H79NO19     ÏàËÆ¶È:77.5%
Planta Medica          2014          80          710-718
Triterpene Saponins from the Stems of Entada phaseoloides
Xiong, Hui; Ding, Xin; Yang, Xin-zhou; Yang, Guang-zhong; Mei, Zhi-nan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     3-O-(¦Â-D-glucopyranosyl-(1-2)-¦Â-D-glucopyranosyl)-28-O-(¦Â-D-xylopyranosyl(1-6)-¦Â-D-glucopyranosyl)-oleanolic acid
C53H86O22     ÏàËÆ¶È:77.3%
Phytochemistry Letters          2012          5          188-193
Saponins and alkaloids from Abuta grandifolia
Charlotte Sayagh,Christophe Long,Christian Moretti,Catherine Lavaud
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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1 .     ginsenoside Rg1
    ÏàËÆ¶È:97.6%
Chinese Traditional and Herbal Drugs          1996          27          647-649
Isolation and Identification of Ginsenoside from the Leaves of Wild Ginseng(Panax ginseng)
Li Jing; Wei Yongdi(Berhune Medical University; Changchun);
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     ginsenoside-Rg1
C42H72O14     ÏàËÆ¶È:92.8%
Chinese Traditional and Herbal Drugs          2012          43          1462-1470
Studies on chemical constituents from Aidi Injection
ZHANG Miao-miao; LIU Yan-li; CHEN Zhong; LI Xiao-ran; XU Qiong-ming; YANG Shi-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     ginsenoside Rf
    ÏàËÆ¶È:88.0%
Chinese Joumal of Experimental Traditional Medical Fomulae          2012          18          78-81
Study of Chemical Components from Qili Qiangxin Capsule (¢ò)
QIAO Li, WANG Zong-quan, MENG Zuo-huan, JIANG Xin-gang, JIA Ji-ming, SONG Jian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     ginsenoside Rd
    ÏàËÆ¶È:76.5%
Journal of Industrial Microbiology & Biotechnology          2009          36          721-726
Highly selective biotransformation of ginsenoside Rb1 to Rd by the phytopathogenic fungus Cladosporium fulvum (syn.Fulvia fulva)
Xuesong Zhao, Juan Wang, Jie Li, Ling Fu, Juan Gao, Xiuli Du, Hongtao Bi, Yifa Zhou, Guihua Tai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     20S-sanchirhinoside A1
C40H66O10     ÏàËÆ¶È:76.1%
Molecules          2013          18          10352-10366
Bioactive Protopanaxatriol Type Saponins Isolated from the Roots of Panax Notoginseng (Burk.) F. H. Chen
Yi Zhang, Li-Feng Han, Kaunda Joseph Sakah, Zhi-Zhen Wu, Li-Li Liu, Kojo Agyemang, Xiu-Mei Gao and Tao Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     gypenoside L
C42H72O14     ÏàËÆ¶È:73.8%
Bioorganic & Medicinal Chemistry Letters          2014          24          186-191
Cytotoxic activity of gypenosides and gynogenin against non-small cell lung carcinoma A549 cells
Dao-Jin Chen, Hui-Min Liu, Shao-Fang Xing, Xiang-Lan Piao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     gypenoside LI
    ÏàËÆ¶È:73.8%
Bioorganic & Medicinal Chemistry Letters          2014          24          186-191
Cytotoxic activity of gypenosides and gynogenin against non-small cell lung carcinoma A549 cells
Dao-Jin Chen, Hui-Min Liu, Shao-Fang Xing, Xiang-Lan Piao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Gypenoside L
C42H72O14     ÏàËÆ¶È:73.8%
Archives of Pharmacal Research          2013          36          874-879
Dammarane-type saponins from heat-processed Gynostemma pentaphyllum show fortified activity against A549 cells
Xiang-Lan Piao, Qian Wu, Jing Yang, Seo Young Park, Dao-Jin Chen, Hui-Min Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     Gypenoside LI
C42H72O14     ÏàËÆ¶È:73.8%
Archives of Pharmacal Research          2013          36          874-879
Dammarane-type saponins from heat-processed Gynostemma pentaphyllum show fortified activity against A549 cells
Xiang-Lan Piao, Qian Wu, Jing Yang, Seo Young Park, Dao-Jin Chen, Hui-Min Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     gypenoside L
C42H72O14     ÏàËÆ¶È:73.8%
Chinese Joumal of Experimental Traditional Medical Fomulae          2013          19          106-111
Saponins from Zhuang-medicine Gocaekmbaw before and after Heat-processing
LIU Hui-min, CHEN Dao-jin, PIAO Xiang-lan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     gypenoside LI
C42H72O14     ÏàËÆ¶È:73.8%
Chinese Joumal of Experimental Traditional Medical Fomulae          2013          19          106-111
Saponins from Zhuang-medicine Gocaekmbaw before and after Heat-processing
LIU Hui-min, CHEN Dao-jin, PIAO Xiang-lan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     ginsenoside Rg2
    ÏàËÆ¶È:71.4%
Chinese Traditional and Herbal Drugs          1996          27          647-649
Isolation and Identification of Ginsenoside from the Leaves of Wild Ginseng(Panax ginseng)
Li Jing; Wei Yongdi(Berhune Medical University; Changchun);
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     yesanchinoside R2
C41H70O14     ÏàËÆ¶È:71.4%
Helvetica Chimica Acta          2011          94          2010-2019
New Dammarane-Type Saponins from the Rhizomes of Panax japonicus (pages 2010¨C2019)
Min Zhou, Min Xu, Dong Wang, Hong-Tao Zhu, Chong-Ren Yang and Ying-Jun Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     sapinmusaponin O
C42H72O12     ÏàËÆ¶È:69.0%
Phytochemistry          2008          69          1609-1616
Triterpenoid saponins from the fruits and galls of Sapindus mukorossi
Hui-Chi Huang,Ming-Der Wub,Wei-Jern Tsai,Sin-Chung Liao,Chia-Ching Liaw,Li-Chuan Hsu,Yang-Chang Wua,Yao-Haur Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     ginsenoside Rg5
    ÏàËÆ¶È:69.0%
Archives of Pharmacal Research          1996          19          551-553
High performance liquid chromatographic assay of a new fluoroquinolone, LB20304, in the plasma of rats and dogs
Mi-Kyeong Seo, Yi-Na Jeong, Hoon-Joo Kim, In-Chull Kim and Yong-Hee Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     3-O-¦Â-D-glucopyranosyl-29-O-¦Â-D-glucopyranosyl-3¦Â,6¦Â,16¦Â,29-tetrahydroxyolean-12-en-23-oic
C42H68O16     ÏàËÆ¶È:69.0%
Phytochemistry          2014          97          70-80
Saponins with highly hydroxylated oleanane-type aglycones from Silphium asteriscus L.
Milena Masullo, Lalita Calabria, Dario Gallotta, Cosimo Pizza, Sonia Piacente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     ursan-3¦Â,19¦Á,22¦Â-triol-3-O-¦Â-D-glucopyranosyl (2'¡ú1'')-¦Â-D-glucopyranoside
C42H72O13     ÏàËÆ¶È:69.0%
Bioorganic & Medicinal Chemistry Letters          2014          24          4203-4208
Triterpene glycosides from red ginseng marc and their anti-inflammatory activities
Ill-Min Chung, Young-Ock Kim, Mohammed Ali, Seung-Hyun Kim, Inmyoung Park, Eun-Hye Kim, Ye-Sul Yang, Hye-Ran Park, Eun-Suk Son, Ateeque Ahmad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     glinuside F
C45H76O16     ÏàËÆ¶È:68.8%
Journal of Natural Products          2005          68          443-446
Hopane-Type Saponins from the Seeds of Glinus lotoides
Abebe Endale, Victor Wray, Renato Murillo, Peter C. Schmidt, and Irmgard Merfort
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     3¦Â,6¦Â,16¦Â-trihydroxyolean-12-en-23-oic acid-3-O-¦Â-glucopyranosyl-16-O-¦Â-glucopyranoside
C42H68O15     ÏàËÆ¶È:66.6%
Phytochemistry          2008          69          961-972
Triterpene saponins from Silphium radula
Lalita M. Calabria, Sonia Piacente, Ireneusz Kapusta,Suranganie F. Dharmawardhane, Frances M. Segarra, Peter J. Pessiki f, Tom J. Mabry
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     16-O-¦Á-L-arabinopyranosyl-20-O-¦Â-D-glucopyranosyl-6¦Á,16¦Á,20¦Â,21¦Á-tetrahydroxytetrahymanol
C41H70O14     ÏàËÆ¶È:66.6%
Journal of Natural Products          2014          77          657-662
Unusual Fernane and Gammacerane Glycosides from the Aerial Parts of Spergula fallax
Arafa I. Hamed, Milena Masullo, Lukasz Pecio, Dario Gallotta, Usama A. Mahalel, Sylwia Pawelec, Anna Stochmal, and Sonia Piacente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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libinoook: ½ð±Ò+10 2014-12-25 17:28:30
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1 .     ginsenoside Rd
    ÏàËÆ¶È:91.4%
Journal of Industrial Microbiology & Biotechnology          2009          36          721-726
Highly selective biotransformation of ginsenoside Rb1 to Rd by the phytopathogenic fungus Cladosporium fulvum (syn.Fulvia fulva)
Xuesong Zhao, Juan Wang, Jie Li, Ling Fu, Juan Gao, Xiuli Du, Hongtao Bi, Yifa Zhou, Guihua Tai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     gypenosideXLVI
C48H82O19     ÏàËÆ¶È:87.5%
Bioorganic & Medicinal Chemistry Letters          2014          24          186-191
Cytotoxic activity of gypenosides and gynogenin against non-small cell lung carcinoma A549 cells
Dao-Jin Chen, Hui-Min Liu, Shao-Fang Xing, Xiang-Lan Piao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     gypenoside XLVI
C48H82O19     ÏàËÆ¶È:87.5%
Chinese Joumal of Experimental Traditional Medical Fomulae          2013          19          106-111
Saponins from Zhuang-medicine Gocaekmbaw before and after Heat-processing
LIU Hui-min, CHEN Dao-jin, PIAO Xiang-lan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     gypenoside XVII
    ÏàËÆ¶È:83.3%
China Journal of Chinese Materia Medica          1992          17          611-613
Studies on the Saponins in the Fruit Pedicels of Panax notoginseng(Burk.)F.H.Chen(continue)
Wei Junxian, Chen Yegao and Cao Shuming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     vina-ginsenoside-R9
C48H82O19     ÏàËÆ¶È:81.2%
Chemical & Pharmaceutical Bulletin          1994          42          115-122
Saponins from Vietnamese Ginseng, Panax vietnamensis HA et GRUSHV. Collected in Central Vietnam. II
Nguyen MINH DUC,Ryoji KASAI,Kazuhiro OHTANI,Aiko ITO,Nguyen THOI NHAM,Kazuo YAMASAKI and Osamu TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     ginsenoside Rg1
    ÏàËÆ¶È:79.5%
Chinese Traditional and Herbal Drugs          1996          27          647-649
Isolation and Identification of Ginsenoside from the Leaves of Wild Ginseng(Panax ginseng)
Li Jing; Wei Yongdi(Berhune Medical University; Changchun);
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     gypenoside L
C42H72O14     ÏàËÆ¶È:79.5%
Bioorganic & Medicinal Chemistry Letters          2014          24          186-191
Cytotoxic activity of gypenosides and gynogenin against non-small cell lung carcinoma A549 cells
Dao-Jin Chen, Hui-Min Liu, Shao-Fang Xing, Xiang-Lan Piao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Gypenoside L
C42H72O14     ÏàËÆ¶È:79.5%
Archives of Pharmacal Research          2013          36          874-879
Dammarane-type saponins from heat-processed Gynostemma pentaphyllum show fortified activity against A549 cells
Xiang-Lan Piao, Qian Wu, Jing Yang, Seo Young Park, Dao-Jin Chen, Hui-Min Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     gypenoside L
C42H72O14     ÏàËÆ¶È:79.5%
Chinese Joumal of Experimental Traditional Medical Fomulae          2013          19          106-111
Saponins from Zhuang-medicine Gocaekmbaw before and after Heat-processing
LIU Hui-min, CHEN Dao-jin, PIAO Xiang-lan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     gypenoside LI
    ÏàËÆ¶È:77.2%
Bioorganic & Medicinal Chemistry Letters          2014          24          186-191
Cytotoxic activity of gypenosides and gynogenin against non-small cell lung carcinoma A549 cells
Dao-Jin Chen, Hui-Min Liu, Shao-Fang Xing, Xiang-Lan Piao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     ginsenoside-Rg1
C42H72O14     ÏàËÆ¶È:77.2%
Chinese Traditional and Herbal Drugs          2012          43          1462-1470
Studies on chemical constituents from Aidi Injection
ZHANG Miao-miao; LIU Yan-li; CHEN Zhong; LI Xiao-ran; XU Qiong-ming; YANG Shi-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     Gypenoside LI
C42H72O14     ÏàËÆ¶È:77.2%
Archives of Pharmacal Research          2013          36          874-879
Dammarane-type saponins from heat-processed Gynostemma pentaphyllum show fortified activity against A549 cells
Xiang-Lan Piao, Qian Wu, Jing Yang, Seo Young Park, Dao-Jin Chen, Hui-Min Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     gypenoside LI
C42H72O14     ÏàËÆ¶È:77.2%
Chinese Joumal of Experimental Traditional Medical Fomulae          2013          19          106-111
Saponins from Zhuang-medicine Gocaekmbaw before and after Heat-processing
LIU Hui-min, CHEN Dao-jin, PIAO Xiang-lan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     lanost-5,24-dien-3¦Â-ol-3-O-¦Â-D-glucopyranosyl-(6'¡ú1'')-¦Â-D-glucopyranosyl-(6''¡ú1''')-¦Â-D-glucopyranoside
C48H80O16     ÏàËÆ¶È:72.9%
Bioorganic & Medicinal Chemistry Letters          2014          24          4203-4208
Triterpene glycosides from red ginseng marc and their anti-inflammatory activities
Ill-Min Chung, Young-Ock Kim, Mohammed Ali, Seung-Hyun Kim, Inmyoung Park, Eun-Hye Kim, Ye-Sul Yang, Hye-Ran Park, Eun-Suk Son, Ateeque Ahmad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     ginsenoside Rg5
    ÏàËÆ¶È:72.7%
Archives of Pharmacal Research          1996          19          551-553
High performance liquid chromatographic assay of a new fluoroquinolone, LB20304, in the plasma of rats and dogs
Mi-Kyeong Seo, Yi-Na Jeong, Hoon-Joo Kim, In-Chull Kim and Yong-Hee Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     ginsenoside Rf
    ÏàËÆ¶È:72.7%
Chinese Joumal of Experimental Traditional Medical Fomulae          2012          18          78-81
Study of Chemical Components from Qili Qiangxin Capsule (¢ò)
QIAO Li, WANG Zong-quan, MENG Zuo-huan, JIANG Xin-gang, JIA Ji-ming, SONG Jian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (25R)-26-O-¦Â-D-glucopyranosyl-5¦Â-furostan-3¦Â,22¦Á,26-triol 3-O-[¦Â-D-glucopyranosyl-(1¡ú2)-O-¦Â-D-glucopyranoside]
C45H76O19     ÏàËÆ¶È:71.1%
Biochemical Systematics and Ecology          2006          34          809-814
Furostanol saponins from Yucca gloriosa L. rhizomes
Alexandre Skhirtladze, Alberto Plaza, Paola Montoro, Mariam Benidze, Ether Kemertelidze, Cosimo Pizza, Sonia Piacente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     ecliptasaponin B
C48H47O19     ÏàËÆ¶È:70.8%
Journal of Chinese Pharmaceutical Sciences          1996          5          177-181
Isolation and Identification of Ecliptasaponin A and Ecliptasaponin B from Eclipta alba (L.) Hasssk
Mei Zhang and Ya-Yan Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     ecliptasaponin B
    ÏàËÆ¶È:70.8%
Acta Pharmaceutica Sinica          1996          31          196-199
ISOLATION AND IDENTIFICATION OF ECLIPTASAPONIN A AND ECLIPTASAPONIN B FROM ECLIPTA ALBA(L.)HASSK
M Zhang and YY Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     ginsenoside Re
    ÏàËÆ¶È:70.8%
Chinese Joumal of Experimental Traditional Medical Fomulae          2012          18          78-81
Study of Chemical Components from Qili Qiangxin Capsule (¢ò)
QIAO Li, WANG Zong-quan, MENG Zuo-huan, JIANG Xin-gang, JIA Ji-ming, SONG Jian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     damulin B
C42H70O13     ÏàËÆ¶È:70.4%
Bioorganic & Medicinal Chemistry          2011          19          6254-6260
New dammarane-type glucosides as potential activators of AMP-activated protein kinase (AMPK) from Gynostemma pentaphyllum
Phi Hung Nguyen, Rehman Gauhar, Seung Lark Hwang, Trong Tuan Dao, Dong Chan Park, Ji Eun Kim, Hebok Song, Tae Lin Huh, Won Keun Oh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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