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µÚÒ»¸ö15.171,19.398,19.575,21.119,23.869,24.324,26.206,27.361,28.250,29.695,31.730,31.948,32.714,34.017,34.857,36.171,37.307,37.679,42.369,43.086,56.825,71.839,78.942,109.605
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12.499,12.679,19.538,19.751,19.938,20.477,21.817,23.950,25.029,26.997,29.048,30.048,30.796,32.609,32.706,34.769,36.908,37.466,38.024,39.888,40.499,43.025,46.610,50.907,56.811,57.378,63.414,72.289,75.867,78.691,78.964,79.136,103.130,141.478
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xiaoxiao270: ½ð±Ò+4 2013-02-25 19:41:33
wenjuan9716: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-02-25 20:49:00
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1 .     compound 21
    ÏàËÆ¶È:76%
Organic Magnetic Resonance          1983          21          305-309
Carbon-13 NMR spectra of hydroxylated bile acid stereoisomers
Takashi Iida, Toshitake Tamura, Taro Matsumoto and Frederic C. Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     compound 29
    ÏàËÆ¶È:76%
Organic Magnetic Resonance          1983          21          305-309
Carbon-13 NMR spectra of hydroxylated bile acid stereoisomers
Takashi Iida, Toshitake Tamura, Taro Matsumoto and Frederic C. Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (20R)-25-thia-27-norcholest-5-en-3¦Â-ol
C28H50OSiS     ÏàËÆ¶È:72%
Bioorganic & Medicinal Chemistry          2012          20          4064-4081
Substrate analog studies of the ¦Ø-regiospecificity of Mycobacterium tuberculosis cholesterol metabolizing cytochrome P450 enzymes CYP124A1, CYP125A1 and CYP142A1
Jonathan B. Johnston, Arti A. Singh, Anaelle A. Clary, Chiung-Kuan Chen, Patricia Y. Hayes, Sharon Chow, James J. De Voss, Paul R. Ortiz de Montellano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     compound 26
    ÏàËÆ¶È:72%
Organic Magnetic Resonance          1983          21          305-309
Carbon-13 NMR spectra of hydroxylated bile acid stereoisomers
Takashi Iida, Toshitake Tamura, Taro Matsumoto and Frederic C. Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound II
    ÏàËÆ¶È:70.8%
Russian Journal of Organic Chemistry          2009          45          78-86
Synthesis of nitrogen- and oxygen-containing macrocycles by palladium-catalyzed amination of 3,24-bis(6-chloropyridin-2-yloxy)cholane
A. D. Averin, E. R. Ranyuk, N. V. Lukashev, A. K. Buryak and I. P. Beletskaya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (20R)-24-bromochol-5-en-3¦Â-ol
C24H39BrO     ÏàËÆ¶È:70.8%
Bioorganic & Medicinal Chemistry          2012          20          4064-4081
Substrate analog studies of the ¦Ø-regiospecificity of Mycobacterium tuberculosis cholesterol metabolizing cytochrome P450 enzymes CYP124A1, CYP125A1 and CYP142A1
Jonathan B. Johnston, Arti A. Singh, Anaelle A. Clary, Chiung-Kuan Chen, Patricia Y. Hayes, Sharon Chow, James J. De Voss, Paul R. Ortiz de Montellano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     3¦Á-Hydroxy-5¦Â-cholan-24-oic acid lithocholic acid
C24H40O3     ÏàËÆ¶È:70.8%
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
8 .     (20R)-3¦Â-(tert-butyldimethylsilyloxy)-24-bromochol-5-ene
C30H53BrOSi     ÏàËÆ¶È:70.3%
Bioorganic & Medicinal Chemistry          2012          20          4064-4081
Substrate analog studies of the ¦Ø-regiospecificity of Mycobacterium tuberculosis cholesterol metabolizing cytochrome P450 enzymes CYP124A1, CYP125A1 and CYP142A1
Jonathan B. Johnston, Arti A. Singh, Anaelle A. Clary, Chiung-Kuan Chen, Patricia Y. Hayes, Sharon Chow, James J. De Voss, Paul R. Ortiz de Montellano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     ¡÷ 9(11),22-24-norchlolest-3¦Â-ol
    ÏàËÆ¶È:69.2%
Steroids          2010          75          834-847
Synthesis of cytotoxic novel 9,11-secosterol analogs: Structure/activity studies
Boonsong Kongkathip, Anuch Hasakunpaisarn, Suthinee Boonananwong, Ngampong Kongkathip
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     N-(2-thioethyl)-3¦Á-hydroxy-5¦Â-cholan-24-amide
C26H45NO2S     ÏàËÆ¶È:69.2%
Steroids          2012          77          193-203
Bile acid¨Ccysteamine conjugates: Structural properties, gelation, and toxicity evaluation
Virpi Noponen, Heini Belt, Manu Lahtinen, Arto Valkonen, Hannu Salo, Jitka Ulrichov¨¢, Ad¨¦la Galand¨¢kov¨¢, Elina Sievänen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     stigmast-5-ene-3¦Â,17¦Á-diol
C29H50O2     ÏàËÆ¶È:68.9%
Journal of Asian Natural products Research          2010          12          424-428
New cytotoxic steroids from the fruits of Syzygium siamense
Parinuch Chumkaew; Shigeru Kato; Kan Chantrapromma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     nitidasin
C25H40O3     ÏàËÆ¶È:68%
Chemical & Pharmaceutical Bulletin          1997          45          1717-1719
NITIDASIN, A NOVEL SESTERTERPENOID, FROM THE PERUVIAN FOLK MEDICINE "HERCAMPURI" (GENTIANELLA NITIDA)
Nobuo KAWAHARA,Masato NOZAWA,Diana FLORES,Pablo BONILLA,Setsuko SEKITA,Motoyoshi SATAKE and Ken-ichi KAWAI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     Sodium 3¦Á-hydroxy-5¦Â-cholan-24-ol sulfate
C24H41SO5     ÏàËÆ¶È:68%
Steroids          2011          76          291-300
Synthesis and olfactory activity of unnatural, sulfated 5-bile acid derivatives in the sea lamprey (Petromyzon marinus)
Aaron C. Burns, Peter W. Sorensen, Thomas R. Hoye
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     compound 8
    ÏàËÆ¶È:68%
Organic Magnetic Resonance          1983          21          305-309
Carbon-13 NMR spectra of hydroxylated bile acid stereoisomers
Takashi Iida, Toshitake Tamura, Taro Matsumoto and Frederic C. Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     (24S)-24-methylcholest-5-ene-3¦Â,25-diol
    ÏàËÆ¶È:67.8%
Chemical & Pharmaceutical Bulletin          1983          31          1848-1855
Marine Sterols. XI. Polyhydroxysterols of the Soft Coral Sarcophyton glaucum : Isolation and Synthesis of 5¦Á-Cholestane-1¦Â, 3¦Â, 5, 6¦Â-tetrol
MASARU KOBAYASHI,TAKAAKI HAYASHI,KOJI HAYASHI,MASATO TANABE,TAKASHI NAKAGAWA and HIROSHI MITSUHASHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     daucosterol
    ÏàËÆ¶È:67.8%
China Journal of Chinese Materia Medica          2002          27          752-754
Studies on the Chemical Constituents in Radix Astilbes Chinensis
SUN Hongxiang, YE Yiping, YANG Ke
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (24S)-24¦Á-¼×»ùµ¨çÞ-5-Ï©-3¦Â,25-¶þ´¼((24S)-24¦Á-methylcholest-5-en-3¦Â,25-diol)
C28H48O2     ÏàËÆ¶È:67.8%
Chinese Journal of Marine Drugs          2002          21(1)          5-7,57
Chemical studies on the soft coral lobophytum j aeckel Tix. -Dur.
WANG Ming-yan, ZENG Long-mei, SU Jing-yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     Alkesterol A
C28H44O2     ÏàËÆ¶È:67.8%
Journal of Asian Natural products Research          2010          12          752-759
C28 sterols with a cyclopentane ring at C-22 and 26 from cape gooseberry (berries of Physalis pubeacens L.)
Qiong-Ming Xu; Yan-Li Liu; Yu-Lin Feng; Xiao-Ran Li; Shi-Lin Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     (24R)-[26-2H3]-24-methylcholestan-3¦Â-ol 12/[26-2H3]campestanol
    ÏàËÆ¶È:67.8%
Chemistry of Natural Compounds          2012          48          606-609
Synthesis of [26-2H3]-campesterin and [26-2H3]-campestanol, deuterated analogs of biosynthetic precursors of 28C-brassinosteroids
V. A. Khripach, V. N. Zhabinskii, Yu. V. Ermolovich and O. V. Gulyakevich
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     cholesterol
    ÏàËÆ¶È:66.6%
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
21 .     pythocholic lactone
C24H38O4     ÏàËÆ¶È:66.6%
Acta Pharmaceutica Sinica          1992          27          674-678
STUDIES ON CHEMICAL CONSTITUENTS OF THE GALL OF PYTHON MOLURUS BIVITTATUS SCHLEGEL
YJ You; JG Lin; LF Ji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     3-Oxo-5¦Â-cholan-24-oic acid
    ÏàËÆ¶È:66.6%
Steroids          2003          68          1157-1161
Synthesis of ester-linked lithocholic acid dimers
Lutfun Nahar, Alan B. Turner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-02-25 19:24:47
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tianhenlanqi

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¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
wenjuan9716: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-02-25 20:48:38
»¯ºÏÎï2
²éѯ½á¹û£º¹²²éµ½6741¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     Daucosterol
C35H60O6     ÏàËÆ¶È:97.1%
Acta Botanica Yunnanica          1997          19(1)          92-96
STUDY ON CHEMICAL CONSTITUENTS OF SAUSSUREA LAPPA ¢ò
Yang Hui, ¡¡Xie J inlun,¡¡Sun Handong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     ¦Â-Sitosterol ¦Â-D-glucopyranoside
C35H60O6     ÏàËÆ¶È:97.1%
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
3 .     ¦Â-Sitosterol Glucoside
    ÏàËÆ¶È:97.1%
Chemistry of Natural Compounds          1991          27          603-606
TRITERPENE GLYCOSIDES OF Hedera taurica VII. STRUCTURES OF TAUEOSIDES A AND D 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
4 .     daucosterol
    ÏàËÆ¶È:97.1%
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
5 .     daucosterol
    ÏàËÆ¶È:97.1%
China Journal of Chinese Materia Medica          2005          30          1340-1342
Studies on chemical constituents from flowers of Apocynum venetum
CHEN Long, DU Lijun, DING Yi, XISNG Dongming , WANG Wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     ºúÂܲ·ÜÕ
    ÏàËÆ¶È:97.1%
China Journal of Chinese Materia Medica          2005          30          153-154
²ØÒ©¶ÌËëÍöú²Ý»¯Ñ§³É·ÖÑо¿
ÑîÔÆÉÑ, ºÎ Àó, Ñ÷, Ê·¸ß·å, ³Èó»ª
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     daucosterol
    ÏàËÆ¶È:97.1%
China Journal of Chinese Materia Medica          2004          29          741-758
Studies on chemical constituents in root of Paeonia sinjiangensis
SONG Zhaohui, WANG Baode, BA Hang, TONG Xiaotian, ZHU Dayuan, JIANG Fuxiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     ¦Â-sitosterol-3-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:97.1%
China Journal of Chinese Materia Medica          2001          26          43-47
Studies on Chemical Constituents from Buddleja lindleyana Fert
LU Jianghai, ZHAO Yuying, QIAO Liang, FANG Yiou, HUANG Qinan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     daucosterol
    ÏàËÆ¶È:97.1%
China Journal of Chinese Materia Medica          2001          26          45-46
Chemical Constituents of Gymnotheca involucrata Pei
YANG Weili, TIAN Jun, DING Lisheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     ¦Â-sitosterol
    ÏàËÆ¶È:97.1%
China Journal of Chinese Materia Medica          1996          21          104-105
Chemical Constituents of Coleus carnosifolius Dunn.
Mu Qing, Li Chaoming and Sun Handong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     daucosterol
C35H60O6     ÏàËÆ¶È:97.1%
China Journal of Chinese Materia Medica          1992          17          36-38
Studies on the Chemical Constituents of Actinidia arguta(Sieb.et Zuce.)Planch.ex Miquel
Shi Yue and Wang Huili, Ma Bingru
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     daucosterol
    ÏàËÆ¶È:97.1%
China Journal of Chinese Materia Medica          1992          17          737-739
Studies on the Chemical Constituents of Drynotria propinqua(Wall)J.Sm
Liu Songqiang and Xiao Zhuoyin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     ¦Â-sitosteryl-3-O-¦Â-glucopiranoside
    ÏàËÆ¶È:97.1%
Phytochemistry          2000          53          417-422
Steroidal alkaloids from Cryptolepis obtusa
Alexandra Paulo, M. Luisa Jimeno, Elsa T. Gomes, Peter J. Houghton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     ¦Â-sitosterol-3-O-glucoside
    ÏàËÆ¶È:97.1%
Natural Product Sciences          1998          4          263-267
Constituents from Syzygium aromaticum Merr. et Perry
Son, Kun-Ho; Kwon, Soon-Youl; Kim, Hyun-Pyo; Chang, Hyeun-Wook; Kang, Sam-Sik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     ¦Â-sitosterol-3-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:97.1%
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
16 .     Daucosterol
    ÏàËÆ¶È:97.1%
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
17 .     3-O-¦Â-Glucosylsitosterol
    ÏàËÆ¶È:97.1%
Phytochemistry          1994          36          221-223
Furocoumarins from the rhizomes of Dorstenia brasiliensis
Ricardo M. Kuster, Robson R. Bernardo, Antonio J.R. Da Silva, Jos¨¦ P. Parente, Walter B. Mors
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     3-O-¦Â-D-glucopyranosylsitosterol
    ÏàËÆ¶È:97.1%
Phytochemistry          1992          31          1317-1320
Pomolic acid derivatives from the rootof Sanguisorba officinalis
Cheng, D. and Cao, X.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     ¦Â-Sitosterol-3-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:97.1%
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   Ì¼Æ×Ä£Äâͼ
20 .     ¦Â-Sitosterol 3-O-¦Â-glucoside
    ÏàËÆ¶È:97.1%
Korean Journal of Pharmacognosy          2007          38(1)          76-83
Triterpenoids and Flavonoids Isolated from the Leaves of Alnus firma
Yu, Young-Beob; Nakamura, Norio; Miyashiro, Hirotsugu; Hattori, Masao; Park, Jong-Cheol
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3Â¥2013-02-25 19:27:29
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