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13C NMR (100 MHz) °´´ÓСµ½´ó˳ÐòÊäÈ룺
11.86,11.99,18.78,19.04,19.4,19.82,21.1,23.1,24.3,26.1,28.2,29.2,29.7,31.7,31.9,31.9,34.0,36.2,36.5,37.3,39.8,42.3,42.3,45.9,50.1,56.1,56.8,71.8,121.7,140.8
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Ñà¿Ê¸ß·É: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-09-18 19:44:30
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1 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
Phytochemistry          2004          65          2463-2470
Biosynthesis of the irregular monoterpene artemisia ketone, the sesquiterpene germacrene D and other isoprenoids in Tanacetum vulgare L. (Asteraceae)
Dirk Umlauf, Josef Zapp, Hans Becker, Klaus Peter Adam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
Planta Medica          1988          54          33-36
In vitro Fibrinolytic Phytosterols Isolated from the Roots of Spatholobus suberetus
Yoshiyasu Fukuyama, Yoshinori Nakano, Geng Pei-Wu, Wang Rui, Junko Sumitomo, Bao Jinxian,and Kazuyuki Nakagawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     sitosterol
    ÏàËÆ¶È:96.6%
Chemical & Pharmaceutical Bulletin          1979          27          38-42
Carbon-13 Nuclear Magnetic Resonance of 24-Substituted Steroids
NAOYUKI KOIZUMI,YOSHINORI FUJIMOTO,TORU TAKESHITA and NOBUO IKEKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     clionasterol
    ÏàËÆ¶È:96.6%
Chemical & Pharmaceutical Bulletin          1979          27          38-42
Carbon-13 Nuclear Magnetic Resonance of 24-Substituted Steroids
NAOYUKI KOIZUMI,YOSHINORI FUJIMOTO,TORU TAKESHITA and NOBUO IKEKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     ¦Â-Sitosterol
C29H50O     ÏàËÆ¶È:96.6%
Chemistry of Natural Compounds          2007          43          358-359
TRITERPENE GLYCOSIDES FROM Astragalus AND THEIR GENINS.LXXV. STEROLS AND TRITERPENOIDS FROM Astragalus orbiculatus
I. M. Isaev, R. P. Mamedova, M. A. Agzamova, and M. I. Isaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
Chemistry of Natural Compounds          2000          36          595-598
13C NMR SPECTRA OF FUNCTIONALLY SUBSTITUTED 3 ¦Â-CHLORODERIVATIVES OF CHOLESTEROL AND ¦Â -SITOSTEROL
N. V. Kovganko, Zh. N. Kashkan, and E. V. Borisov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
Chemistry of Natural Compounds          1999          35          672-645
I3C NMR SPECTRA OF STEROL DERIVATIVES,INTERMEDIATES IN THE SYNTHESIS OF ECDY- AND BRASSINOSTEROIDS
N. V. Kovganko, Zh. N. Kashkan,and E. V. Borisov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:96.6%
Acta Bot. Boreal. -Occident. Sin.          2004          24          1292-1294
Chemical constituents from Saussurea polycolea
LI Yu-lin, WANG Hong-lun, SUO You-rui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
Acta Bot. Boreal. -Occident. Sin.          2008          28          1246-1249
Chemical Constituents in the Leaves of Alsophila spinulosa
CHEN Feng-zheng, XIANG Qing-xiang, LI Shu-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
Acta Botanica Sinica          1999          41          107-110
Chemical constituents of the Anemone tomentosa Root
Wang Jun-Ru, Peng Shu-Lin, Wang Ming-Kui, Feng Jun-Tao, Ding Li-Sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:96.6%
Acta Botanica Sinica          2003          45          1003-1007
Two New Triterpenes from Neonauclea sessilifolia
KANG Wen-Yi, LI Guo-Hong, HAO Xiao-Jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
Journal of Chinese Pharmaceutical Sciences          1999          8          237-240
Chemical Constituents of Stelmatocrypton khasianum
Zhang Qingying; Zhao Yuying; Ma Libin; Cheng Tieming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
Journal of Chinese Pharmaceutical Sciences          2005          14          75-78
Chemical Constituents of Hedysarum gmelinii
LIU Yi; MA Xiao-xia; CHEN Hu-biao; TU Guang-zhong; HE Jiu-ming; and ZHAO Yu-ying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
Guihaia          2007          27          140-142
Chemical constituents from leaves of Livistona chinensis
LIU Zhi-Ping; CUI Jian-Guo ; LIU Hong-Xing; HUANG Chu-Sheng; ZHONG Zhen-Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     ¦Â-Sitosterol
    ÏàËÆ¶È:96.6%
Journal of Asian Natural Products Research          2008          10          281-283
Artemisterol, a new steryl ester from the whole plant of Artemisia apiacea
Sung-Jin Lee Hye Min Kim, Jeong Min Lee, Hee Seung Park and Sanghyun Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
Journal of Asian Natural Products Research          2002          4          73-79
A NEW COMPOUND FROM GASTRODIA ELATA BLUME
YONG-QING XIAO, LI LI, XIAO-LIN YOU, BAO-LIN BIAN, XIN-MIAO LIANG and YI-TAO WANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
Natural Product Research          1994          4          195-201
Isolation and Characterization of a Dihydroxysterol from Lawsonia inermis
Sarita Gupta; Mohammad Ali; M. Sarwar Alam; Masatake Niwa; Tatsuko Sakai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
Natural Product Research          2006          20          860-865
A new dihydroisocoumarin from the rhizomes of Notopterygium forbesii
Yan-Hui Li; Fan Luo; Shu-Lin Peng; Jian Liang; Li-Sheng Ding
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     stigmast-5-en-3¦Â-ol
    ÏàËÆ¶È:96.6%
Natural Product Research          2008          22          942-949
Bioactivities and chemical constituents of a Vietnamese medicinal plant Che Vang, Jasminum subtriplinerve Blume (Oleaceae)
Dai Hue Ngan; Ho Thi Cam Hoai; Le Mai Huong; Poul Erik Hansen; Ole Vang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:96.6%
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
21 .     stigmasterol
    ÏàËÆ¶È:96.6%
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
22 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
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
23 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
China Journal of Chinese Materia Medica          2002          27          843-845
Studies on Chemical Constituents in the Root of Hedysarum polybotrys
HAI Liqian, LIANG Hong, ZHAO Yuying, DU Niansheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
China Journal of Chinese Materia Medica          1997          22          293-295
Separation and Identification of the Compounds from A chyranthes biden tata Bl
W ei Song, L iang Hong, Zhao Yuying and Zhang Ruyi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
Fitoterapia          2005          76          433-438
A new dihydroxysterol from the marine phytoplankton Diacronema sp.
Am¨¦lia P. Rauter, Manuela M. Filipe, Carla Prata,João P. Noronha, Maria A.M. Sampayo,Jorge Justino,Jaime Bermejo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     sitosterol
    ÏàËÆ¶È:96.6%
Journal of Natural Products          1987          Vol 50          881
Sterols and Steryl Glycosides from Urtica dioica
Neera Chaurasia, Max Wichtl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
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
28 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
Acta Pharmaceutica Sinica          2002          Vol 37          196-198
STUDIES ON FLAVONIOD CONSTITUENTS OF HEDYSARUM MULTIJUGUM
WANG Wei; CHEN Hu-biao; WANG Wen-ming; ZHAO Yu-ying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
Natural Product Sciences          2000          6          135-138
Antioxidative Constituents from the Seeds of Cuscuta chinensis
Kwon, Yong-Soo; Chang, Bok-Sim; Kim, Chang-Min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     beta-sitosterol
    ÏàËÆ¶È:96.6%
Natural Product Sciences          2002          8          137-140
The Constituents of the Aerial Part of Gastrodia elata Blume
Liu, Xiang Qian; Baek, Wan-Sook; Ahn, Duk-Kyun; Choi, Ho-Young; Yook, Chang-Soo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
Natural Product Sciences          2004          10          306-309
Triterpenoids from Orostachys japonicus
Lee, Sang-Hyun; Paek, Sun-Ha; Kim, Seung-Ki; Kim, Bak-Kwang; Shin, Kuk-Hyun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:96.6%
Natural Product Sciences          2007          13          317-321
Phytochemical Study of Lotus ornithopodioloides L.
Abdel-Kader, Maged S.; Basudan, Omer A.; Alqasoumi, Saleh I.; Abou-Shoer, Mohamed I.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     ¦Â-Sitosterol
    ÏàËÆ¶È:96.6%
Natural Product Sciences          2007          13          332-336
Norsesquiterpene and Steroid Constituents of Humulus japonicus
Yu, Byung-Chul; Yang, Min-Cheol; Lee, Kyu-Ha; Kim, Ki-Hyun; Lee, Kang-Ro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     ¦Â-Sitosterol
    ÏàËÆ¶È:96.6%
Natural Product Sciences          2007          13          394-397
Chemical Constituents of the Moss Hylocomium splendens
Kang, Shin-Jung; Jovel, Eduardo; Hong, Seong-Su; Hwang, Bang-Yeon; Liu, Patty; Lee, Meng-Hsin; Lee, Meng-Chun; Lee, Kyung-Soon; Towers, George Hugh Neil
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     sitosterol
    ÏàËÆ¶È:96.6%
Phytochemistry          1992          31          2558-2560
24¦Â-Ethylcholest-4-en-3¦Â-ol from the roots of Lawsonia inermis
M. Sarwar Alam, Masatake Niwa, Tatsuko Sakai, Sarita Gupta, Mohd. Ali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     ¦Â-Sitosterol
C29H50O     ÏàËÆ¶È:96.6%
Korean Journal of Pharmacognosy          2008          39(4)          357-364
Chemical Constituents of Saposhnikovia divaricata
Kim, So-Jun; Chin, Young-Won; Yoon, Kee-Dong; Ryu, Min-Youl; Yang, Min-Hye; Lee, Je-Hyun; Kim, Jin-Woong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     ¦Â-Sitosterol
    ÏàËÆ¶È:96.6%
Korean Journal of Pharmacognosy          2008          39(3)          186-193
Phytochemical Studies on Astragalus Root (3);Triterpenoids and Sterols
Jung, Hye-Sil; Lee, Eun-Ju; Lee, Je-Hyun; Kim, Ju-Sun; Kang, Sam-Sik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     ¦Â-Sitosterol
    ÏàËÆ¶È:96.6%
Korean Journal of Pharmacognosy          2007          38(4)          354-357
Isolation of Two Steroids and a Triterpenoid from the Roots of Potentilla discolor
Park, Hee-Juhn; Lee, Kyung-Tae; Park, Jong-Hee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     compound 5
    ÏàËÆ¶È:96.6%
Korean Journal of Pharmacognosy          2000          31(3)          300-305
Chemical Components of Evodia daniellii
Ju, Hei-Kyoung; Hwang, Bang-Yeon; Ahn, Byong-Tae; Kim, Mi-Jeong; Choi, Woo-Hoi; Cho, Bong-Jn; Ro, Jai-Seup; Lee, Kyong-Soon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     compound 1
C29H50O     ÏàËÆ¶È:96.6%
Korean Journal of Pharmacognosy          1998          29(4)          277-282
Isolation of Anti-Herpes Simplex Virus Type 1(HSV-1) Component from Thujae orientalis Semen
Kang, Eun-Jung; Kang, Bong-Joo; Park, Kap-Joo; Ko, Byoung-Seob; Kim, Ho-Kyoung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     compound 3a
    ÏàËÆ¶È:96.6%
Korean Journal of Pharmacognosy          1996          27(4)          389-396
Constituents of Spiraea prunifolia var. simpliciflora
Lee, Eun-Hee; Chung, Soon-Ok; Kim, Chong-Won; Woo, Mi-Hee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
Korean Journal of Pharmacognosy          1981          12(1)          12-24
Revision of 13C NMR Assignments of ¦Â-sitosterol and ¦Â-sitosteryl-3-O-¦Â-D-glucopyranoside Isolated from Plantago asiatica Seed
Chang, Il-Moo; YunChoi, Hye-Sook; Yamasaki, Kazuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:96.6%
Chinese Journal of Marine Drugs          2006          25(1)          21-24
Studies on chemical constituents of the marine sponge Craniell a australiensis from the South China Sea
KUANG Xia, ZHANG Hong-jun, SUN Jing-bo, WANG Zeng-lei, LIN Hou-wen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     ¦Â-¹ÈçÞ´¼
C29H48O     ÏàËÆ¶È:96.6%
Chinese Journal of Marine Drugs          2006          25(3)          15-17
Study on the chemical constituents of Ipomoea Pescaprae( L.) Sweet(I)
WANG Qing-Ji, WANG You-Shao, HE Lei, ZHANG Si
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     (24s)-stigmast-5-en-3-ol
    ÏàËÆ¶È:96.6%
Chinese Journal of Marine Drugs          2004          23(2)          15-17
Studies on chemical constituents of the marine sponge Spheciospongia vagabunda from the South China Sea (I)
MA Wei-jie, XIAO Ding-jun, DENG Song-zhi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     (24S)-stigmast-5-en-3¦Â-ol
    ÏàËÆ¶È:96.6%
Chinese Journal of Marine Drugs          2002          21(2)          1-4
Studies on the chemical constituents of the marine sponge Clathria fasciculate from the South China Sea
XIAO Ding-jun, DENG Song-zhi, ZENG Long-mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     ¦Â-¹ÈçÞ´¼
    ÏàËÆ¶È:96.6%
Chinese Journal of Marine Drugs          2002          21(1)          1-4
Sterol con stituents from marine brown alga ishige okamurai
TANG Hai-feng, YI Yang-hua, YAO Xin-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     sitosterol
    ÏàËÆ¶È:96.6%
Phytochemistry          1990          29          2351-2355
Sterol glucosides from Prunella vulgaris
Hisashi Kojima,Noriko Sato,Akiko Hatano,Haruo Ogura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     Stosterol
    ÏàËÆ¶È:96.6%
Natural Product Research          2010          24          34-39
A new analogue of fatty alcohol from Tamarix hampeana L.
Ahmet Aykaç; Yurdanur Akg¨¹l
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     ¦Â-¹ÈçÞ´¼
    ÏàËÆ¶È:96.6%
Chinese Traditional and Herbal Drugs          2010          41          206-208
÷×»¨¶Å¾éÒ¶µÄ»¯Ñ§³É·ÖÑо¿
ÖÜÏÈÀñ; ÇØ³¤ºì; ÷Ө; »ÆË§; °¢Æ¼
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     ¦Â-¹ÈçÞ´¼
    ÏàËÆ¶È:96.6%
Chinese Traditional and Herbal Drugs          2010          41          704-707
Âúɽºì»¯Ñ§³É·ÖµÄÑо¿
¸¶ÏþÀö;ÕÅÁ¢Î°;ÁÖÎĺ²;ÀîÇàɽ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.6%
Chinese Traditional and Herbal Drugs          2009          40          1015-1018
Chemical constituents in Tridax procumbens
XU Run-sheng; YUAN Ke; YIN Ming-wen; FANG Lei-jie; MAO Nong-nong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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