Znn3bq.jpeg
²é¿´: 482  |  »Ø¸´: 2

yetta_he

½ð³æ (СÓÐÃûÆø)

[ÇóÖú] ÇóÖú ÒÑÓÐ1È˲ÎÓë

»¯ºÏÎï1:
CDCL3
12.07,12.20,18.99,19.25,19.61,20.04,21.30,23.28,24.52,31.85,32.11,36.36,36.72,37.46,39.99,42.53,46.04,50.34,56.98,72.03,121,94,140.96

»¯ºÏÎï2:
CDCL3
11.74,11.87,18.66,18.93,19.30,19.71,20.93,24.16,29.00,31.44,31.77,35.99,36.40,37.19,39.64,42.15,42.17,45.66,50.00,56.62,71.14,121.18,141.01
»Ø¸´´ËÂ¥
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

lifeliuyan

ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
²éѯ½á¹û£º¹²²éµ½602¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:81.4%
Chemical & Pharmaceutical Bulletin          1993          41          2007-2009
Constituents of Prunus zippeliana Leaves and Branches
Junichi KITAJIMA and Yasuko TANAKA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:81.4%
Steroids          2005          70          886-895
Gram-scale chromatographic purification of ¦Â-sitosterol: Synthesis and characterization of ¦Â-sitosterol oxides
Xin Zhang, Philippe Geoffroy, Michel Miesch, Diane Julien-David, Francis Raul, Dalal Aoud¨¦-Werner, Eric Marchioni
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     ¦Â-sitosterol
    ÏàËÆ¶È:81.4%
Korean Journal of Pharmacognosy          2005          36(2)          145-150
Phytochemical Constituents of Cirsium nipponicum (MAX.) Makino
Lee, Jong-Hwa; Lee, Kang-Ro
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     ¦Â-sitosterol
    ÏàËÆ¶È:81.4%
Korean Journal of Pharmacognosy          2010          41          238-244
Constituents of Cynanchum auriculatum and their Inhibitory Effect on Melanogenesis in B16 Mouse Melanoma Cell Lines
Choi, Hyun-Gyu; Jiang, Yanfu; Roh, Eun-Mi-Ri; Kim, Young-Soo; Xu, Guang-Hua; Na, Min-Kyun; Lee, Seung-Ho
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     ¦Â-sitosterol
    ÏàËÆ¶È:81.4%
Journal of Agricultural and Food Chemistry          2002          50          4709-4712
Sphingolipid and Other Constituents from Almond Nuts (Prunus amygdalus Batsch)
Shengmin Sang, Hiroe Kikuzaki, Karen Lapsley, Robert T. Rosen, Nobuji Nakatani, and Chi-Tang Ho
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     ¦Â-sitosterol
C29H58O     ÏàËÆ¶È:81.4%
Journal of Agricultural and Food Chemistry          1989          37          1363-1367
Isolation of compounds with antimutagenic activity from Savoy Chieftain cabbage
Terence Lawson, Janet Nunnally, Betty Walker, Edward Bresnick, Desmond Wheeler, Maureen Wheeler
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     ¦Â-sitosterol
    ÏàËÆ¶È:81.4%
Journal of Wood Science          2013          59          155-159
Antibacterial compounds from shoot skins of moso bamboo (Phyllostachys pubescens)
Akinobu Tanaka, Kuniyoshi Shimizu, Ryuichiro Kondo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     sitosterol
C29H50O     ÏàËÆ¶È:81.4%
Asian Journal of Chemistry          2014          26          8019-8021
Constituents from the Root of Lantana camara
AMMAR A. AL-FADHLI, * and JAMAL A. NASSER
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:80.7%
Chemical & Pharmaceutical Bulletin          1993          41          1238-1243
Two New 2-Arylbenzofuran Derivatives from Hypoglycemic Activity-Bearing Fractions of Morus insignis
Purusotam BASNET,Shigetoshi KADOTA,Satoshi TERASHIMA,Mineo SHIMIZU and Tsuneo NAMBA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     ¦Â-Sitosterol
    ÏàËÆ¶È:80.7%
Korean Journal of Pharmacognosy          2007          38(1)          67-70
Isolation of Isoprenoidal Compounds from the Stems of Acer tegmentosum Max
Hur, Jong-Moon; Jun, Mi-Ra; Yang, Eun-Ju; Choi, Sun-Ha; Park, Jong-Cheol; Song, Kyung-Sik
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     ¦Â-sitosterol
    ÏàËÆ¶È:80.7%
Korean Journal of Pharmacognosy          2004          35(1)          80-87
The Chemical Structures and Their Antioxidant Activity of the Components Isolated from the Heartwood of Hemiptelea davidii
Chang, Bok-Sim; Kwon, Yong-Soo; Kim, Chang-Min
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     sitosterol
C29H50O     ÏàËÆ¶È:80.7%
Phytochemistry          1987          26          753-754
Iridoid glycosides from Penstemon richardsonii
Birgit Gering,Peter Junior,Max Wichtl
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     ¦Â-sitosterol
    ÏàËÆ¶È:80%
Industrial Crops and Products          2014          59          189−196
Antimicrobial and cytotoxic activities of Alnus rugosa L. aerial parts and identification of the bioactive components
Khaled Rashed, Ana Ćirić, Jasmina Glamočlija, Ricardo C. Calhelha, Isabel C.F.R. Ferreira, Marina Soković
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     5¦Á-stigmast-9(11)-en-3¦Â-ol
C29H50O     ÏàËÆ¶È:78.5%
China Journal of Chinese Materia Medica          1996          21          666-667
Studies on Chemical Components of Cynomorium songaricum Rupr.
Xu Xiuzhi, Zhang Chengzhong and Li Chong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     ¦Â-sistosterol
C29H50O     ÏàËÆ¶È:78.5%
Natural Product Sciences          2007          13          220-224
Antioxidant Activity of Cholesterol Derived from Silkworm Pupae
Heo, Jung-Eun; Ryu, Jae-Ha; Jeong, Hye-Kyoung; Chung, Wan-Tae; Ahn, Mi-Young
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     ¦Â-sitosterol
    ÏàËÆ¶È:78.5%
Chinese Pharmaceutical Journal          2009          44          1372-1374
Chemical Constituents of the Roots of Uritca fissa E.Pritz.
JI Bao-quan, FENG Bao-min, SHI Li-ying, TANG Ling, WANG Yong-qi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     ¦Â-sitosterol
    ÏàËÆ¶È:78.5%
Modern Chinese Medicine          2007          9(12)          11-13
Studies on the chemical Constituents of Ampelopsis grossedentata
He Guixia, Pei Gang, Du Fanglu, OU Yangwen, Li Bin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     ¦Â-sitosterol
    ÏàËÆ¶È:78.5%
Journal of Shenyang Pharmaceutical University          2011          28          364-367
Isolation and identification of chemical constituents of root of Girardinia suborbiculata C. J. Chen subsp. Triloba
FENG Bao-min, LIU Jing-yan, WANG Hui-guo, SHI Li-ying, TANG Ling, WANG Yong-qi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     ¦Â-sitosterol
    ÏàËÆ¶È:78.5%
Natural Product Research and Development          2004          16          213-214
STUDIES ON LIPOSOLUBLE CONSTITUENTS OF HUPERZIA CRISPATE CHING
PEI Gang;; ZHOU Pu-hua; HE Gui-xia; DU Fang-lu; JIANG Dao-song
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     ¦Â-sitosterol
    ÏàËÆ¶È:78.5%
Zeitschrift f¨¹r Naturforschung C          2003          58          441-445
Feeding Stimulative Activity of Steroidal and Secoiridoid Glucosides and Their Hydrolysed Derivatives toward the Olive Weevil (Dyscerus perforatus)
E. Kadowaki, Y. Yoshida, N. Baba, and S. Nakajima
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
21 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:78.5%
Molecules          2013          18          1325-1336
Chemical Constituents of Caesalpinia decapetala (Roth) Alston
Xiao-Hua Wei, Sheng-Jie Yang, Na Liang, De-Yu Hu, Lin-Hong Jin, Wei Xue and Song Yang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
22 .     ¦Â-sitosterol
    ÏàËÆ¶È:78.5%
Chemistry and Industry of Forest Products          2013          33          133-136
Chemical Constituents from the Branch of Litsea cubeba ( Lour. ) Pers.
CHEN Zhan-juan, BI He-ping, FAN Chao-jun, BAO Chang-yu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
23 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:78.5%
Natural Product Research and Development          2013          25          1367-1369
Study on the Chemical Constituents of Fruticosa potentilla L.
XU Xiao-jie, WANG Wei, WANG Yu-hua
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
24 .     ¦Â-Sitosterol
    ÏàËÆ¶È:78.5%
Guihaia          2014          34          155-159
Study on the chemical constituents of Peristrophe roxburghiana
GE Li, LAN Liu-Feng, BAO Hui-Bin, YANG Ke-Di
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-04-02 19:57:37
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

lifeliuyan

ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
yetta_he: ½ð±Ò+20, ¡ïÓаïÖú 2015-04-02 20:15:44
²éѯ½á¹û£º¹²²éµ½785¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     ¦Â-sitosterol
C29H58O     ÏàËÆ¶È:85.1%
Journal of Agricultural and Food Chemistry          1989          37          1363-1367
Isolation of compounds with antimutagenic activity from Savoy Chieftain cabbage
Terence Lawson, Janet Nunnally, Betty Walker, Edward Bresnick, Desmond Wheeler, Maureen Wheeler
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     24-oxochol-5-en-3¦Â-ol
C27H44O2     ÏàËÆ¶È:83.3%
Steroids          2009          74          81-87
A facile synthesis of C-24 and C-25 oxysterols by in situ generated ethyl(trifluoromethyl)dioxirane
Shoujiro Ogawa, Genta Kakiyama, Akina Muto, Atsuko Hosoda, Kuniko Mitamura, Shigeo Ikegawa, Alan F. Hofmann, Takashi Iida
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     23-Iodo-24-norchol-5-en-3¦Â-ol
C23H37OI     ÏàËÆ¶È:82.6%
Steroids          2005          70          551-562
Preparation of (25R)- and (25S)-26-functionalized steroids as tools for biosynthetic studies of cholic acids
Vladimir A. Khripach, Vladimir N. Zhabinskii, Olga V. Konstantinova, Natalya B. Khripach, Alexey V. Antonchick, Andrey P. Antonchick, Bernd Schneider
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     N-Methyl-3¦Â-hydroxy-¡÷5-cholenamide
C25H41NO2     ÏàËÆ¶È:82.6%
Bioorganic & Medicinal Chemistry          2013          21          5297-5309
Structure¨Cactivity relationship studies of Niemann-Pick type C1-like 1 (NPC1L1) ligands identified by screening assay monitoring pharmacological chaperone effect
Fumika Karaki, Kenji Ohgane, Kosuke Dodo, Yuichi Hashimoto
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     ¦Â-sistosterol
C29H50O     ÏàËÆ¶È:82.1%
Natural Product Sciences          2007          13          220-224
Antioxidant Activity of Cholesterol Derived from Silkworm Pupae
Heo, Jung-Eun; Ryu, Jae-Ha; Jeong, Hye-Kyoung; Chung, Wan-Tae; Ahn, Mi-Young
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     [28-pro-R-2H]-clionasterol
    ÏàËÆ¶È:82.1%
Tetrahedron Letters          2002          43          5479-5481
Mechanism of clerosterol biosynthesis in Ajuga hairy roots: stereochemistry of C-28 methylation of 24-methylene sterol
Takeshi Koami, Kiyoshi Ohyama, Yoshinori Fujimoto
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     [28-pro-S-2H]-clionasterol
    ÏàËÆ¶È:82.1%
Tetrahedron Letters          2002          43          5479-5481
Mechanism of clerosterol biosynthesis in Ajuga hairy roots: stereochemistry of C-28 methylation of 24-methylene sterol
Takeshi Koami, Kiyoshi Ohyama, Yoshinori Fujimoto
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     ¦Â-sitosterol
    ÏàËÆ¶È:82.1%
Zeitschrift f¨¹r Naturforschung C          2003          58          441-445
Feeding Stimulative Activity of Steroidal and Secoiridoid Glucosides and Their Hydrolysed Derivatives toward the Olive Weevil (Dyscerus perforatus)
E. Kadowaki, Y. Yoshida, N. Baba, and S. Nakajima
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:82.1%
Molecules          2013          18          1325-1336
Chemical Constituents of Caesalpinia decapetala (Roth) Alston
Xiao-Hua Wei, Sheng-Jie Yang, Na Liang, De-Yu Hu, Lin-Hong Jin, Wei Xue and Song Yang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     ¦Â-sitosterol
    ÏàËÆ¶È:82.1%
Chemistry and Industry of Forest Products          2013          33          133-136
Chemical Constituents from the Branch of Litsea cubeba ( Lour. ) Pers.
CHEN Zhan-juan, BI He-ping, FAN Chao-jun, BAO Chang-yu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     ¦Â-Sitosterol
    ÏàËÆ¶È:82.1%
Guihaia          2014          34          155-159
Study on the chemical constituents of Peristrophe roxburghiana
GE Li, LAN Liu-Feng, BAO Hui-Bin, YANG Ke-Di
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     ¦Â-sitosterol
    ÏàËÆ¶È:82.1%
Chinese Journal of Modern Applied Pharmacy          2009          26          460-462
Studies on the Chemical Constituents in Ranunculus muricatus L
WANG Ling-jie, GAO Xiao-zhong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     campesterol
    ÏàËÆ¶È:82.1%
Chinese Pharmaceutical Journal          2012          47          500-503
Study on Chemical Constituents of Rosa chinensis Jacq. Flower
WANG Xiao-yan; WANG Wen-wen; ZHOU Yong-hui; JIANG Xin-ke; JING Lin-lin; JIA Lu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     ¦Â-sitosterol
    ÏàËÆ¶È:82.1%
Korean Journal of Pharmacognosy          2013          44          1-5
Isolation of Compounds having Inhibitory Activity toward Tyrosinase from Receptaculum Nelumbinis
Hyun Woo Cho, Won Seok Jung, Byeong Gwan An, Jung Hee Cho and Su Young Jung
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     ¦Â-sitosterol
    ÏàËÆ¶È:82.1%
Northwest Pharmaceutical Journal          2013          28          241-244
Study on chemical constituents of Arenaria kansuensis Maxim. ¢ô
LEI Ning, L¨¹ Yali, DU Shushan, DENG Zhiwei, MA Ping
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     ¦Â-sitosterol
    ÏàËÆ¶È:82.1%
Chinese Joumal of Experimental Traditional Medical Fomulae          2011          17          118-120
Research on Chemical Constituents of Ethyl Acetate Fraction from Li Nationality Medicine Elaeagnus gonyanthes Caulis et Folium
WEI Na, WANG Yong, LI Pei-pei, LI Hong-fu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:81.4%
Chemical & Pharmaceutical Bulletin          1993          41          2007-2009
Constituents of Prunus zippeliana Leaves and Branches
Junichi KITAJIMA and Yasuko TANAKA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     ¦Â-sitosterol
    ÏàËÆ¶È:81.4%
Acta Botanica Boreali-Occidentalia Sinica          2004          24          1093-1095
Studies on chemical constituents from tibetan medioine Elsholtzia ianthina
DNG Chen-xu, ZHOU Ling-yun, JILAN-JU, JIWEN-he, MA Yu-hua
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:81.4%
Steroids          2005          70          886-895
Gram-scale chromatographic purification of ¦Â-sitosterol: Synthesis and characterization of ¦Â-sitosterol oxides
Xin Zhang, Philippe Geoffroy, Michel Miesch, Diane Julien-David, Francis Raul, Dalal Aoud¨¦-Werner, Eric Marchioni
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     ¦Â-sitosterol
    ÏàËÆ¶È:81.4%
China Journal of Chinese Materia Medica          2003          28          237-239
Studies on Chemical Constituents in the Peels of Citrus changshan-huyou (I)
ZHAO Xxuemei, YE Xingqian, XI Yufang, ZHU Dayuan, JIANG Shanhao
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
21 .     ¦Â-sitosterol
    ÏàËÆ¶È:81.4%
Korean Journal of Pharmacognosy          2005          36(2)          145-150
Phytochemical Constituents of Cirsium nipponicum (MAX.) Makino
Lee, Jong-Hwa; Lee, Kang-Ro
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3Â¥2015-04-02 20:01:29
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ yetta_he µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] 086000µ÷¼Á +4 Ê®Æßsa 2026-04-07 4/200 2026-04-09 09:27 by Ò¼ÍùŸoǰ
[¿¼ÑÐ] ²ÄÁϵ÷¼Á +14 Ò»ÑùYWY 2026-04-06 14/700 2026-04-08 23:00 by Öí»á·É
[¿¼ÑÐ] Èí¼þ¹¤³ÌÇóµ÷¼Á22Èí¹¤296·ÖÇóµ÷¼Á£¬½ÓÊÜ¿çµ÷ +4 yangchen2017 2026-04-08 5/250 2026-04-08 21:56 by ÍÁľ˶ʿÕÐÉú
[¿¼ÑÐ] ÉúÎïѧ328·ÖÇóµ÷¼Á +9 ÉÁµçkkl 2026-04-08 10/500 2026-04-08 21:42 by liuhuiying09
[¿¼ÑÐ] ²ÄÁÏ¿ÆÑ§Ó빤³Ì320Çóµ÷¼Á£¬080500 +12 »Æ¹ÏζÊíÆ¬ 2026-04-06 12/600 2026-04-08 16:26 by luoyongfeng
[¿¼ÑÐ] ²ÄÁÏר˶(0856) 339·ÖÇóµ÷¼Á +16 ¹þ¹þ¹þ¶ì¹þ¹þ¹þ 2026-04-05 16/800 2026-04-08 16:02 by luoyongfeng
[¿¼²©] É격 +8 IQwQl 2026-04-04 8/400 2026-04-08 09:43 by 0608104024
[¿¼ÑÐ] µ÷¼Á +3 µçÆø300Çóµ÷¼Á²» 2026-04-08 6/300 2026-04-08 09:39 by µçÆø300Çóµ÷¼Á²»
[¿¼ÑÐ] 085602µ÷¼Á ³õÊÔ×Ü·Ö335 +3 19123253302 2026-04-06 3/150 2026-04-07 18:00 by jp9609
[¿¼ÑÐ] 277Çóµ÷¼Á ÊýÒ»104·Ö +9 Æ¿×ÓPZ 2026-04-05 14/700 2026-04-07 17:52 by À¶ÔÆË¼Óê
[¿¼ÑÐ] Ò»Ö¾Ô¸»ªÖÐũҵ´óѧ0710£¨A£©³õÊÔ329·Ö Çóµ÷¼Á +5 Ò»Ãû26¿¼ÑÐÉú 2026-04-04 5/250 2026-04-07 08:54 by 18828373951
[¿¼ÑÐ] 22408 331·ÖÇóµ÷¼Á +4 y__1 2026-04-06 4/200 2026-04-06 17:26 by ÍÁľ˶ʿÕÐÉú
[¿¼ÑÐ] ÉúÎïѧ308·ÖÇóµ÷¼Á£¨Ò»Ö¾Ô¸»ª¶«Ê¦´ó£© +8 ÏàÐűػá¹ââÍòÕ 2026-04-05 10/500 2026-04-05 12:19 by Hdyxbekcb
[¿¼ÑÐ] Çóµ÷¼Á +4 êɹ¦? 2026-04-03 4/200 2026-04-04 21:58 by hemengdong
[¿¼ÑÐ] 331Çóµ÷¼Á +3 niby 2026-04-02 3/150 2026-04-04 19:56 by À¶ÔÆË¼Óê
[¿¼ÑÐ] Çóµ÷¼Á +3 ffyyu 2026-04-02 3/150 2026-04-04 19:03 by À¶ÔÆË¼Óê
[¿¼ÑÐ] ²ÄÁÏרҵ383Çóµ÷¼Á +8 ¹ùÑôÑôÑô³É 2026-04-03 8/400 2026-04-04 10:29 by Rednal.
[¿¼ÑÐ] 085601Ò»Ö¾Ô¸±±Àí325·ÖÇóµ÷¼Á +6 ÕÒµ÷¼Á£¬£¬ 2026-04-02 6/300 2026-04-03 22:20 by –¹Æ?
[¿¼ÑÐ] 294Çóµ÷¼Á +6 Grey_Ey 2026-04-03 6/300 2026-04-03 20:46 by ÐÀϲ777
[¿¼ÑÐ] 366Çóµ÷¼Á +7 sbdnd 2026-04-03 7/350 2026-04-03 12:40 by cymywx
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û