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CÆ×Êý¾Ý£º13.78,16.80,16.88,17.47,18.52,19.17,23.12,23.41,25.68,27.21,30.38,31.66,31.82,32.82,33.28,37.40,40.79,41.41,42.56,44.20,45.97,46.06,46.83,47.15,48.89,
               60.72,63.91,67.50,69.58,72.40,75.56,76.69,77.76,94.12,114.60,121.66,143.62,175.31
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1 .     arjunglucoside
    ÏàËÆ¶È:86.8%
Phytochemistry          1996          41          591-594
Pentacyclic triterpenes from Combretum nigricans
Akino Jossang, Mannan Seuleiman, Eric Maidou, Bernard Bodo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     2¦Á,3¦Á,23-Trihydroxyolean-12-en-28-oic acid O-¦Â-D-glucopyranosyl ester
C36H58O10     ÏàËÆ¶È:86.8%
Natural Product Communications          2007          2          895-900
Flavonoids and Triterpenoid Saponins from Pimenta dioica(Merr.) L.
Fatma A. Moharram, Mona A Mohamed, Mohamed SA Marzouk and Elsayed A Aboutabl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     arjunglucoside I
C36H58O11     ÏàËÆ¶È:86.8%
Chromatographia          2006          64          695-699
Preparative Droplet Counter-Current Chromatography for the Separation of the New Nor-Seco-Triterpene and Pentacyclic Triterpenoids from Qualea Parviflora
A. L. M. Nasser, L. P. Mazzolin, C. A. Hiruma-Lima, L. S. Santos, M. N. Eberlin, A. R. Monteiro de Souza Brito, W. Vilegas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     bellericaside B
C36H58O12     ÏàËÆ¶È:84.2%
Chromatographia          2006          64          695-699
Preparative Droplet Counter-Current Chromatography for the Separation of the New Nor-Seco-Triterpene and Pentacyclic Triterpenoids from Qualea Parviflora
A. L. M. Nasser, L. P. Mazzolin, C. A. Hiruma-Lima, L. S. Santos, M. N. Eberlin, A. R. Monteiro de Souza Brito, W. Vilegas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     21-O-¦Â-D-Glucopyranosyl-2¦Á,3¦Â,21¦Â,23-tetrahydroxyolean-12-en-28-oic acid
C36H58O11     ÏàËÆ¶È:81.5%
Chemical Research in Chinese Universities          2009          25          404-406
Triterpene Acids from Cynoglossum amabile
XU Qing-jun, ZHANG De-zhi*, DANG Li-juan and LI Kun-ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Hederagenic acid-28-O-¦Â-D-glucopyranoside
C36H56O9     ÏàËÆ¶È:81.5%
Biochemical Systematics and Ecology          2012          42          14-17
Triterpenoids and their saponins from the roots of Kalopanax septemlobus
Huankai Yao, Jingyu Duan, Jianhui Wang, Yan Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     2¦Á,3¦Á,23-Trihydroxyolean-13(18)-en-28-oic acidO-¦Â-D-glucopyranosyl ester
C36H58O10     ÏàËÆ¶È:81.5%
Natural Product Communications          2007          2          895-900
Flavonoids and Triterpenoid Saponins from Pimenta dioica(Merr.) L.
Fatma A. Moharram, Mona A Mohamed, Mohamed SA Marzouk and Elsayed A Aboutabl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     prosapogenin B
    ÏàËÆ¶È:80.4%
Planta Medica          1987          53          62-65
Triterpenoid Glycosides from the Roots of Patrinia scab iosaefolia
Jae Sue Choi and Won Sick Woo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     gamboukokoenside A
C35H56O11     ÏàËÆ¶È:78.9%
Phytochemistry          2003                   845-849
Pentacyclic triterpenoid and saponins from Gambeya boukokoensis
Jean Wandji, François Tillequin, Dulcie A. Mulholland, Jovita Chi Shirri,Nole Tsabang, ElisabethSeguin, Philippe Verite, Francine Libotb, Z.T. Fomum
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     glinoside B
C35H58O8     ÏàËÆ¶È:78.9%
Planta Medica          2000          66          368-371
Structure and Antiprotozoal Activity of Triterpenoid Saponins from Glinus oppositifolius
Fanta Traore,Robert Faure,Evelyne Ollivier,Monique Gasquet,Nadine Azas,Laurent Debrauwer,Arouna Keita,Pierre Timon-David,Guy Balansard
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     sericoside
    ÏàËÆ¶È:78.9%
Chinese Pharmaceutical Journal          2003          38          336-338
Studies on the constituents of Rosa multiflora
LI Yan fang, HU Li hong, LOU Feng chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     hederagenin-3-O-¦Â-glucuronopyranoside
    ÏàËÆ¶È:78.9%
Journal of Shenyang Pharmaceutical University          2005          22          181-182
Chemical constituents of the seeds of Acanthopanax senticosus(Rupr. et Maxim) Harms
ZHANG Jie, LI Wen, GAO Hui-Yuan, WU Bin, WU Li-jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     2¦Á,19¦Á-dihydroxy-3-oxo-olean-12-en-oic acid 28-¦Â-D-glucopyranoside
C36H56O10     ÏàËÆ¶È:78.9%
Indian Journal of Chemistry Section B          2001          40B          354-356
New constituent from the roots of Terminalia arjuna: antifungal agent
B K Chouksey, S K Srivastava
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     PJS-1
    ÏàËÆ¶È:78.9%
Jiangsu Pharmacertical and Clinical Research          2004          12          18-19
Studies on the Chemical Constituents of Achyranthes bidentata
Hu An-ming, Bi Zhi-ming, Li Ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     oleanolic acid 28-O-¦Â-D-glucopyranosyl ester
C36H58O8     ÏàËÆ¶È:78.9%
Chinese Joumal of Experimental Traditional Medical Fomulae          2012          18          83-85
Studies on Chemical Constituents of Lycopus lucidus Turcz.var.hirtus Regel.
WANG Tao, LI Chao, PU She-ban, QIAN Shi-hui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     collinsonidin
C41H66O13     ÏàËÆ¶È:78.0%
Journal of Natural Products          1992          Vol 55          1468
Saponins from Collinsonia canadensis
Balawant S. Joshi, Kristi M. Moore, S. William Pelletier, Mohindar S. Puar, B. N. Pramanik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     hederagenin 3-O-¦Á-L-arabinopyranosyl(1e¡ú2)-¦Á-L-arabinopyranoside
    ÏàËÆ¶È:78.0%
Korean Journal of Pharmacognosy          1997          28(2)          93-98
Studies on Components of Patrinia scabiosaefolia
Kim, Young-Hee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     hederagenin-3-O-¦Â-D-glucopyranosyl-(1¡ú2)-¦Á-L-arabinopyranoside
C41H66O13     ÏàËÆ¶È:78.0%
Journal of Anhui Agricultural Sciences          2012          40          745-747
Study on the Chemical Constitutes of C. robustum root
MA Yang-min et al
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     chikusetsusaponin IVa methyl ester
    ÏàËÆ¶È:78.0%
Chemistry of Natural Compounds          2012          48          258-261
A new triterpenoid saponin and other saponins from Salicornia europaea
Min Yin, Xiangyun Wang, Ming Wang, Yu Chen and Yunfa Dong, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     cauloside C
C41H66O13     ÏàËÆ¶È:78.0%
Journal of Agricultural and Food Chemistry          2001          49          5969-5974
Characterization of the Triterpene Saponins of the Roots and Rhizomes of Blue Cohosh (Caulophyllum Thalictroides)
Jin-Woo Jhoo, Shengmin Sang, Kan He, Xiaofang Cheng, Nanqun Zhu, Ruth E. Stark, Qun Yi Zheng, Robert T. Rosen, and Chi-Tang Ho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     prosapogenin A
    ÏàËÆ¶È:76.3%
Planta Medica          1987          53          62-65
Triterpenoid Glycosides from the Roots of Patrinia scab iosaefolia
Jae Sue Choi and Won Sick Woo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     sigmoiside A
C36H60O7     ÏàËÆ¶È:76.3%
Journal of Natural Products          1991          Vol 54          1288
Two New Triterpenoid Saponins from Erythrina sigmoidea
J. Kouam, A. Ephrem Nkengfack, Z. Tanee Fomum, Rosa Ubillas, Michael S. Tempesta, Mich¨¨le Meyer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     sigmoiside B
    ÏàËÆ¶È:76.3%
Journal of Natural Products          1991          Vol 54          1288
Two New Triterpenoid Saponins from Erythrina sigmoidea
J. Kouam, A. Ephrem Nkengfack, Z. Tanee Fomum, Rosa Ubillas, Michael S. Tempesta, Mich¨¨le Meyer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     trachelosperoside D-1
    ÏàËÆ¶È:76.3%
Chinese Traditional and Herbal Drugs          2006          37          171-174
Triterpenoids from canes with leaves of Trachelospermum jasminoides
TAN Xing-qi; CHEN Hai-sheng; ZHOU Mi; ZHANG Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     niga-ichigoside F1
C36H58O11     ÏàËÆ¶È:76.3%
Chinese Journal of Natural Medicines          2005          3          17-20
Isolation and Identification of Chemical Constituents from Rubus Parvifolius L.
DU Shu-Hu; FENG Fang; LIU Wen-Ying; RAO Jin-Hua; BAI Juan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     niga-ichigosideF1
    ÏàËÆ¶È:76.3%
Natural Product Research and Development          2014          26          215-217
Chemical Constituents from the Water-soluble Fraction of Rabdosia excisa
TANG Jian, MA Rui-li, LIU Hong-chuan, OUYANG Zhen, CHEN Hai-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     3¦Â,21¦Á-dihydroxyl-ursolic acid-28-O-¦Â-D-glucopyranoside
C36H58O9     ÏàËÆ¶È:76.3%
Chinese Traditional and Herbal Drugs          2014          45          1043-1046
Microbial transformation of ursolic acid by Penicillium adametzi
WANG Zhi-ping, LIU Dai-lin, YAN Hui-jun, MA Wei-jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     pulsatilla saponin A
    ÏàËÆ¶È:75.6%
Chinese Traditional and Herbal Drugs          2013          44          1086-1090
Chemical constituents from berries of Physalis pubescens
JIA Yuan-min, CHEN Zhong, XU Qiong-ming, LI Xiao-ran, YANG Shi-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     bidentatoside II
C40H62O13     ÏàËÆ¶È:75%
Chemical & Pharmaceutical Bulletin          2001          49(11)          1492-1494
Two Triterpene Saponins from Achyranthes bidentata
Anne-Claire MITAINE-OFFER, Abderrazak MAROUF,Bernard HANQUET,Nicolas BIRLIRAKIS,and Marie-Aleth LACAILLE-DUBOIS
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     [¦Á-L-rhamnopyranosyl(1¡ú4)-¦Â-D-glucopyranosyl(1¡ú3)]-3,23¦Â-di-hydroxy-olean-12-en-28-oic acid
    ÏàËÆ¶È:73.8%
Phytochemistry          1992          31          1427-1428
Triterpenoid saponins from roots of Clematis grata
Sudhir K Uniyal, O.P Sati
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     gamboukokoenside B
C35H54O10     ÏàËÆ¶È:73.6%
Phytochemistry          2003                   845-849
Pentacyclic triterpenoid and saponins from Gambeya boukokoensis
Jean Wandji, François Tillequin, Dulcie A. Mulholland, Jovita Chi Shirri,Nole Tsabang, ElisabethSeguin, Philippe Verite, Francine Libotb, Z.T. Fomum
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     compound 2a
    ÏàËÆ¶È:73.6%
Journal of Natural Products          2000          63          1497-1502
Two New Biologically Active Triterpene Saponins from Acanthophyllum squarrosum
Ghezala Gaidi,Tomofumi Miyamoto, Abdolhossein Rustaiyan, V¨¦ronique Laurens,and Marie-Aleth Lacaille-Dubois
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     glinoside A
C35H58O9     ÏàËÆ¶È:73.6%
Planta Medica          2000          66          368-371
Structure and Antiprotozoal Activity of Triterpenoid Saponins from Glinus oppositifolius
Fanta Traore,Robert Faure,Evelyne Ollivier,Monique Gasquet,Nadine Azas,Laurent Debrauwer,Arouna Keita,Pierre Timon-David,Guy Balansard
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     ¦Â-amyrin-3-O-(2'-acetyl(glucoside))
    ÏàËÆ¶È:73.6%
Natural Product Research          2012          26          619-629
Chemical and biological study of the seeds of Eragrostis tef (Zucc.) Trotter
Taha S. El-Alfy, Shahira M. Ezzat and Amani A. Sleem
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     22¦Á-hydroxyolean-12-en-3¦Â-yl-¦Â-D-galactopyra-noside
C36H60O7     ÏàËÆ¶È:73.6%
Chemical & Pharmaceutical Bulletin          2010          58          1093-1095
Two New Aristolochic Acid Derivatives from the Roots of Aristolochia fangchi and Their Cytotoxicities
Yu Cai and Tian-Ge Cai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     compound 9
    ÏàËÆ¶È:73.6%
Phytochemistry          1984          23          2893-2898
Further triterpenoids and 13C NMR spectra of oleanane derivatives from Phytolacca acinosa
S. Harkar, T.K. Razdan, E.S. Waight
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     Junceoside D
    ÏàËÆ¶È:73.6%
Pharmazie          2005          60          635-637
An unusual new sulfated triterpene saponin from Arenaria juncea
G. Gaidi, T. Miyamoto and M. A. Lacaille-Dubois
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     9¦Â,25-cyclo 3¦Â-O-(¦Â-D-glucopyranosyl)echynocystic acid
C36H56O9     ÏàËÆ¶È:73.6%
Journal of Ethnopharmacology          2011          135          78-87
Chemical constituents from the stem bark of Symplocos paniculata Thunb. with antimicrobial, analgesic and anti-inflammatory activities
Ruchi Badoni Semwal, Deepak Kumar Semwal, Ravindra Semwal, Randhir Singh, Mohan Singh Maniyari Rawat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     3¦Â,19¦Á-hydroxyolean-12-en-28-oic acid 28-¦Â-D-glucopyranoside
C36H58O9     ÏàËÆ¶È:73.6%
Molecules          2012          17          7629-7636
Terpene Glycosides from the Roots of Sanguisorba officinalis L. and Their Hemostatic Activities
Wei Sun, Zi-Long Zhang, Xin Liu, Shuang Zhang, Lu He, Zhe Wang and Guang-Shu Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     16¦Á,23,28-trihydroxy-olean-12-en-3-O-¦Á-L-arabinopyranoside
C35H58O8     ÏàËÆ¶È:73.6%
Journal of Anhui Agricultural Sciences          2012          40          745-747
Study on the Chemical Constitutes of C. robustum root
MA Yang-min et al
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     hederagenin-3-O-¦Á-L-arabinopyranoside
C35H56O8     ÏàËÆ¶È:73.6%
Journal of Anhui Agricultural Sciences          2012          40          745-747
Study on the Chemical Constitutes of C. robustum root
MA Yang-min et al
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     caulophyllogenin-3-O-¦Á-L-arabinopyranoside
C35H56O9     ÏàËÆ¶È:73.6%
Journal of Anhui Agricultural Sciences          2012          40          745-747
Study on the Chemical Constitutes of C. robustum root
MA Yang-min et al
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     eclalbatin
C41H66O12     ÏàËÆ¶È:73.1%
Journal of Asian Natural Products Research          2001          3          213-217
Eclalbatin, a Triterpene Saponin from Eclipta Alba
R. K. UPADHYAY, M. B. PANDEY, R. N. JHA and V. B. PANDEY
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     3¦Â-[(¦Á-L-arabinopyranosyl)oxy]-19¦Á-hydroxyolean-12-en-28-oic acid 28-¦Â-D-glucopyranoside
C41H66O13     ÏàËÆ¶È:73.1%
Molecules          2012          17          7629-7636
Terpene Glycosides from the Roots of Sanguisorba officinalis L. and Their Hemostatic Activities
Wei Sun, Zi-Long Zhang, Xin Liu, Shuang Zhang, Lu He, Zhe Wang and Guang-Shu Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     3-O-(methyl-¦Â-D-glucuronopyranosiduronoate)-28-O-¦Â-D-glucopyranosyl oleanolate
C43H68O14     ÏàËÆ¶È:72.0%
Phytochemistry          2001          56          93-97
Bioactive oleanolic acid saponins and other constituents from the roots of Viguiera decurrens
Silvia Marquina, Nora Maldonado, Marı́a Luisa Garduño-Ramı́rez, Eduardo Aranda, Marı́a Luisa Villarreal, Vı́ctor Navarro, Robert Bye, Guillermo Delgado, Laura Alvarez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     hederagenin-3-O-¦Á-L-rhamnopyranosyl(1¡ú4)-¦Â-D-glucopyranosyl
    ÏàËÆ¶È:71.4%
Natural Product Research and Development          2014          26          864-867
Chemical Constituents of Clematis tangutica
NIU Jiang-jin, ZHANG Ben-yin, WANG Ying, ZHANG Lin, SHAO Yun, MEI Li-juan, TAO Yan-duo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     Oleanolic acid 3-O-¦Â-D-galactopyranoside
C36H58O8     ÏàËÆ¶È:71.0%
Molecules          2008          13          1472-1486
Facile Synthesis of Oleanolic Acid Monoglycosides and Diglycosides
Yu Sha, Mao-Cai Yan, Jiao Liu, Yang Liu and Mao-Sheng Cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     compound 10
    ÏàËÆ¶È:71.0%
Acta Pharmaceutica Sinica          1995          30          27-33
NEW TRTEKPENOIDAL SAPOGENINS FROM THE ROOTS OF GLYCYRRHIZA YUNNANENSIS
JF Hu; ZL Ye and FJ Shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     Terminoside A
C36H58O10     ÏàËÆ¶È:71.0%
Journal of Asian Natural Products Research          2003          5          137-142
TERMINOSIDE A, A NEW TRITERPENE GLYCOSIDE FROM THE BARK OF TERMINALIA ARJUNA INHIBITS NITRIC OXIDE PRODUCTION IN MURINE MACROPHAGES
ASIF ALI, GURPREET KAUR, HINNA HAMID, TARIQUE ABDULLAH,MOHAMMED ALI, M. NIWAd and M.S. ALAM
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     termiarjunoside I
C36H58O11     ÏàËÆ¶È:71.0%
Natural Product Research          2008          22          1279-1288
Two new bioactive oleanane triterpene glycosides from Terminalia arjuna
M. Sarwar Alam; Gurpreet Kaur; Asif Ali; Hinna Hamid; Mohammad Ali; Mohammad Athar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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