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12.86,17.79,17.99,21.70,21.82,24.49,24.64,25.85,26.15,27.53,30.12,32.44,33.61,34.99,35.19,38.71,43.46,47.38,48.04,48.28,49.95,51.12,52.47,118.37,123.64,132.46,145.58,182.01




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1 .     ¶¹çÞ´¼-¦Â-D-ÆÏÌÑÌÇÜÕ
    ÏàËÆ¶È:93.3%
Chinese Traditional and Herbal Drugs          2002          33          300-303
Studies on chemical constituents in seed of Litchi chinensis
TU Peng fei; LUO Qing; ZHENG Jun hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     3-oxotirucalla-7,24-dien-21-oic acid
    ÏàËÆ¶È:90%
Journal of Natural Products          2000          63          238-242
Inhibitory Effects on HIV-1 Protease of Constituents from the Wood of Xanthoceras sorbifolia
Chao-mei Ma, Norio Nakamura,Masao Hattori, Hiroko Kakuda,Jun-chan Qiao, and Hai-lan Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     3-oxotrirucalla-7,24-dien-21-oic acid
    ÏàËÆ¶È:89.2%
Chinese Journal of Natural Medicines          2012          10          36-39
Chemical constituents of Allophylus longipes
Xiang-Yun ZHANG, Xiang-Hai CAI, Xiao-Dong LUO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     3-oxo-tirucalla-7,24-dien-21-al
C30H46O2     ÏàËÆ¶È:86.6%
Phytochemistry          1998          49          2457-2460
Triterpenoids from Owenia cepiodora
Dulcie A. Mulholland, Maria Kotsos, Hamdani A. Mahomed, David A. H. Taylor
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     3-oxotirucalla-7,24-dien-21-oic acid
    ÏàËÆ¶È:86.6%
Chinese Traditional and Herbal Drugs          2012          43          1276-1279
Chemical constituents in stems of Eurycorymbus cavaleriei
HE Yi; ZHANG Yu-mei; CHE Chun-tao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     3¦Á-hidroxi-tirucala-7,24-dien-21-¨®ico respectivamente para
    ÏàËÆ¶È:80%
Qu¨ªmica Nova          2000          23          623-626
Triterpenes from the resin of Protium heptaphyllum March (Burseraceae): characterization in binary mixtures
Maia, Robinson Magalhães; Barbosa, Pedro Rocha; Cruz, Frederico Guar¨¦; Roque, N¨ªdia Franca; Fascio, Miguel
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     3¦Á-ôÇ»ù¸ÊËì-7,24-¶þÏ©-21-Ëá
    ÏàËÆ¶È:80%
Chinese Traditional and Herbal Drugs          2011          42          1293-1296
Chemical constituents from frankincense
WANG, Feng, HUA, Hui-ming, WANG, Shu-mei, LIANG, Sheng-wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     xanthocerasic acid
C31H48O4     ÏàËÆ¶È:76.6%
Journal of Natural Products          2000          63          238-242
Inhibitory Effects on HIV-1 Protease of Constituents from the Wood of Xanthoceras sorbifolia
Chao-mei Ma, Norio Nakamura,Masao Hattori, Hiroko Kakuda,Jun-chan Qiao, and Hai-lan Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     3¦Á,29-dihydroxytirucalla-7,24-dien-21-oic acid
    ÏàËÆ¶È:76.6%
Journal of Natural Products          2000          63          238-242
Inhibitory Effects on HIV-1 Protease of Constituents from the Wood of Xanthoceras sorbifolia
Chao-mei Ma, Norio Nakamura,Masao Hattori, Hiroko Kakuda,Jun-chan Qiao, and Hai-lan Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     3¦Â,29-dihydroxytirucalla-7,24-dien-21-oic acid
    ÏàËÆ¶È:76.6%
Journal of Natural Products          2000          63          238-242
Inhibitory Effects on HIV-1 Protease of Constituents from the Wood of Xanthoceras sorbifolia
Chao-mei Ma, Norio Nakamura,Masao Hattori, Hiroko Kakuda,Jun-chan Qiao, and Hai-lan Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     3¦Á-hydroxytirucalla-7,24-dien-21-oic
    ÏàËÆ¶È:76.6%
Natural Product Communications          2010          5          1181-1182
Triterpenes from Protium hebetatum Resin
Delcio Dias Marques, Ilmar Bernardo Graebner, Telma Leda Gomes de Lemos,Luciana Lucas Machado, Jõao Carlos Costa Assunção and Francisco Jos¨¦ Queiroz Monte
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     29-O-acetyl-3-oxotirucalla-7,24-dien-21-oic acid
    ÏàËÆ¶È:75%
Journal of Natural Products          2000          63          238-242
Inhibitory Effects on HIV-1 Protease of Constituents from the Wood of Xanthoceras sorbifolia
Chao-mei Ma, Norio Nakamura,Masao Hattori, Hiroko Kakuda,Jun-chan Qiao, and Hai-lan Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     24,25,26,27-tetranortirucall-7-ene-3-oxo-23(21)-lactone
C26H38O3     ÏàËÆ¶È:75%
Acta Botanica Sinica          2004          46          1256-1260
A New Triterpenoid froMamoora dasyclada
WANG Huan, ZHANG Xiao-Feng, YANG Shu-Min, LUO Xiao-Dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     phellogine
C25H40O2     ÏàËÆ¶È:75%
Chinese Chemical Letters          2008          19          937-939
A new sesterterpenoid from the fruits of Phellodendron chinense vac glabriusculum Schneid
Chen Yan, Ye Wang , Xiao Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     3-oxo-24,25,26,27-tetranortirucall-7-ene-23(21)-lactone
C26H38O3     ÏàËÆ¶È:75%
Chinese Traditional and Herbal Drugs          2012          43          38-42
Chemical constituents from Dysoxylum lenticellatum
TANG Ting; NA Zhi; XU You-kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     21¦Á-methylmelianodiol
C31H50O5     ÏàËÆ¶È:74.1%
Chemical & Pharmaceutical Bulletin          2008          56(6)          839-842
Terpenoids and Coumarins Isolated from the Fruits of Poncirus trifoliata
Guang-Hua XU,Jeong-Ah KIM,So-Young KIM,b Jae-Chun RYU,Young-Soo KIM,d Sang-Hun JUNG,Mi-Kyeong KIM,and Seung-Ho LEE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     compound 7
C31H50O5     ÏàËÆ¶È:74.1%
Chemical & Pharmaceutical Bulletin          2007          55(10)          1442-1447
Apotirucallane and Tirucallane Triterpenoids from Cedrela sinensis
Kumiko MITSUI, Hiroaki SAITO, Ryota YAMAMURA, Haruhiko FUKAYA, Yukio HITOTSUYANAGI, and Koichi TAKEYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     21¦Á-methylmelianodiol
    ÏàËÆ¶È:74.1%
Planta Medica          2008          74          396-400
21-Methylmelianodiols from Poncirus trifoliata as Inhibitors of Interleukin-5 Bioactivity in Pro-B Cells
In Jeong Lee, Guang-Hua Xu, Jung-Hun Ju, Jeong Ah Kim, Soon-Woo Kwon, Seung Ho Lee, Sang-Bae Han,Youngsoo Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     ¦Á-methylmelianodiol
C31H50O5     ÏàËÆ¶È:74.1%
Chinese Journal of Natural Medicines          2010          8          97-100
Chemical Constituents from the Fruits of Poncirus trifoliata
YU Ping; LIANG Jing-Yu; LIU Xin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     21¦Á-methylmelianodiol
C31H50O5     ÏàËÆ¶È:74.1%
European Journal of Pharmacology          2007          572          239-248
Anti-inflammatory activity of 21(¦Á, ¦Â)-methylmelianodiols, novel compounds from Poncirus trifoliata Rafinesque
Hong Yu Zhou, Eun Myung Shin, Lian Yu Guo, Li Bo Zou, Guang Hua Xu, Seung-Ho Lee, Keum Ryon Ze, Eun-Kyung Kim, Sam Sik Kang, Yeong Shik Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     3,23-dioxotirucalla-7,24-dien-21-al
C30H44O3     ÏàËÆ¶È:73.3%
Phytochemistry          2005          66          2324-2328
Tirucallane triterpenes from the leaf extract of Entandrophragma angolense
Abayomi T. Orisadipe, Akinbobola A. Adesomoju, Michele D Ambrosio,Antonio Guerriero, Joseph I. Okogun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     3,21-dioxotirucalla-7,24-dien-21,23-oxide
    ÏàËÆ¶È:73.3%
Journal of Natural Products          2003          66          675-678
Apotirucallane and Tirucallane Triterpenoids from Luvunga sarmentosa
Christine Kamperdick, Trinh Phuong Lien, Guenter Adam, and Tran Van Sung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     3¦Â-hydroxytirucalla-7,24-dien-21-oic acid
    ÏàËÆ¶È:73.3%
Journal of Natural Products          2000          63          238-242
Inhibitory Effects on HIV-1 Protease of Constituents from the Wood of Xanthoceras sorbifolia
Chao-mei Ma, Norio Nakamura,Masao Hattori, Hiroko Kakuda,Jun-chan Qiao, and Hai-lan Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     melianodiol
C30H48O5     ÏàËÆ¶È:73.3%
Planta Medica          2000          66          740-745
Phytochemical Investigation of Aglaia andamanica
Jindaporn Puripattanavong,Sabine Weber, Volker Brecht,August Wilhelm Frahm
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     masticadienoic acid
    ÏàËÆ¶È:73.3%
Planta Medica          1981          42          268-274
Structure of Methyl Adenophorate and Triphyllol,Triterpenoids of Adenophora triphylla var. japonica Roots
Chohachi Konno,Takashi Saito, Yoshiteru Oshima, Hiroshi Hikino and Chizuko Kabuto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     24,25-Epoxy-tirucall-7-ene-3,23-dione
C30H46O3     ÏàËÆ¶È:73.3%
Acta Botanica Sinica          2004          46          1256-1260
A New Triterpenoid froMamoora dasyclada
WANG Huan, ZHANG Xiao-Feng, YANG Shu-Min, LUO Xiao-Dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     dysolenticin H
C30H44O3     ÏàËÆ¶È:73.3%
Journal of Natural Products          2011          74          2235-2242
Tirucallane-Type Triterpenoids from Dysoxylum lenticellatum
Hong-Li Huang,Chun-Ming Wang, Zhen-Hua Wang, Ming-Jun Yao, Guang-Tian Han,Ji-Cheng Yuan,Kun Gao, and Cheng-Shan Yuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     masticadienoic acid
    ÏàËÆ¶È:73.3%
Phytochemistry          1990          29          1629-1632
Lanost-7-en triterpenes from stem bark of Santiria trimera
M.F¨¢tima Das G.F. Da Silva,Regina H.P. Francisco,Alexander I. Gray,Johannes R. Lechat,Peter G. Waterman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     21,23-epoxy-21¦Á,24,25-trihy-droxytirucalla-7-en-3-one
    ÏàËÆ¶È:73.3%
Chinese Journal of Natural Medicines          2009          7          31-33
Triterpenes from the Fruits of Phellodendron chinense Schneid var. glabriusculum Schneid
YAN Chen; WANG Ye; HAO Xiao-Jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     toonapubesin A
    ÏàËÆ¶È:73.3%
Organic & Biomolecular Chemistry          2011          9          7685-7696
Protolimonoids and norlimonoids from the stem bark of Toona ciliata var. pubescens
Jian-Rong Wang, Hai-Li Liu, Tibor Kurt¨¢n, Attila M¨¢ndi, S¨¢ndor Antus, Jia Li, Hai-Yan Zhang and Yue-Wei Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     toonapubesin D
C30H50O5     ÏàËÆ¶È:73.3%
Organic & Biomolecular Chemistry          2011          9          7685-7696
Protolimonoids and norlimonoids from the stem bark of Toona ciliata var. pubescens
Jian-Rong Wang, Hai-Li Liu, Tibor Kurt¨¢n, Attila M¨¢ndi, S¨¢ndor Antus, Jia Li, Hai-Yan Zhang and Yue-Wei Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     cornusalterin L
C30H50O2     ÏàËÆ¶È:73.3%
Journal of Natural Products          2011          74          54-59
Tirucallane Triterpenoids from Cornus walteri
Ki Hyun Kim, Sang Un Choi, Young Choong Kim, and Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     Deoxyflindissone
    ÏàËÆ¶È:73.3%
Journal of Natural Products          2011          74          54-59
Tirucallane Triterpenoids from Cornus walteri
Ki Hyun Kim, Sang Un Choi, Young Choong Kim, and Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     capulin
    ÏàËÆ¶È:73.3%
Fitoterapia          2012          83          901-906
A new protolimonoid from Capuronianthus mahafalensis
Torgils Fossen, Philippe Rasoanaivo, Christian Sambany Manjovelo, Fanja Hanitriniala Raharinjato, Sviatlana Yahorava, Aleh Yahorau, Jarl Erik Sylvester Wikberg
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     3¦Â-Hydroxylanosta-9,24-dien-24-oic acid
C30H46O3     ÏàËÆ¶È:73.3%
African Journal of Pharmacy and Pharmacology          2011          5          2698-2714
Triterpenes from the stem bark of Protorhus longifolia exhibit anti-platelet aggregation activity
Rebamang A. Mosa, Adebola O. Oyedeji, Francis O. Shode, Mogie Singh and Andy R. Opoku
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     (21R,23R)-epoxy-21¦Á-ethoxy-24S, 25-dihydroxyapotirucalla-7-en-3-one
C32H52O5     ÏàËÆ¶È:71.8%
Journal of Natural Products          2009          72          685-689
Terpenoids from Toona ciliata
Hua-Dong Chen, Sheng-Ping Yang, Yan Wu, Lei Dong, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     21R,23R-epoxy-21¦Á-ethoxy,24S,25-dihydroxy-apotirucalla-7-en-3-one
C32H52O5     ÏàËÆ¶È:71.8%
Chinese Journal of Natural Medicines          2010          8          97-100
Chemical Constituents from the Fruits of Poncirus trifoliata
YU Ping; LIANG Jing-Yu; LIU Xin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     3-oxo-24,25,26,27-tetranortirucall-7-ene-23(21)- lactone
C26H38O3     ÏàËÆ¶È:71.4%
Chinese Chemical Letters          2004          15          1187-1190
Two New Tetranortriterpenoids from Amoora dasyclada
Shu Min YANG, Yun Bao MA, Xiao Dong LUO, Shao Hua WU, Da Gang WU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     compound 3
C26H40O2     ÏàËÆ¶È:71.4%
Phytochemistry          1988          27          1220-1221
Protolimonoids from Turraea nilotica
Dulcie A. Mulholland,David A.H. Taylor
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     3-oxo-21¦Á-methoxy-24,25,26,27-tetranortirucall-7-ene-23(21)-lactone
C27H40O4     ÏàËÆ¶È:71.4%
Phytochemistry          2010          71          2199-2204
Cytotoxic tirucallane C26 triterpenoids from the stem barks of Aphanamixis grandifolia
Yao Zhang, Junsong Wang, Dandan Wei, Xiaobing Wang, Jun Luo, Jianguang Luo, Lingyi Kong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     3-oxo-21¦Á-ethoxy-24,25,26,27-tetranortirucall-7-ene-23(21)-lactone
C28H42O4     ÏàËÆ¶È:71.4%
Phytochemistry          2010          71          2199-2204
Cytotoxic tirucallane C26 triterpenoids from the stem barks of Aphanamixis grandifolia
Yao Zhang, Junsong Wang, Dandan Wei, Xiaobing Wang, Jun Luo, Jianguang Luo, Lingyi Kong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     21R,23R-epoxy-21-ethoxy-24S,25-dihydroxy-apotirucalla-7-ene-3-one
    ÏàËÆ¶È:70.9%
Acta Pharmaceutica Sinica          2009          Vol 44          625−627
Triterpenes from fruits of Paliurus ramosissimus
YU Lei; YANG Jing-zhi; ZHANG Dong-ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     25-methoxy-tirucall-7-23 (trans)-diene-3-one
C31H50O2     ÏàËÆ¶È:70.9%
Phytochemistry          1995          40          1485-1487
Tirucallane triterpenes from the stem bark of Aglaia leucophylla
Abdelilah Benosman, Pascal Richomme, Thierry Sevenet, Guillaume Perromat, A. Hamid A. Hadi, Jean Bruneton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     dysolenticin I
C31H46O5     ÏàËÆ¶È:70.9%
Journal of Natural Products          2011          74          2235-2242
Tirucallane-Type Triterpenoids from Dysoxylum lenticellatum
Hong-Li Huang,Chun-Ming Wang, Zhen-Hua Wang, Ming-Jun Yao, Guang-Tian Han,Ji-Cheng Yuan,Kun Gao, and Cheng-Shan Yuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     Melianone
    ÏàËÆ¶È:70.9%
Molecules          2013          18          2589-2597
Hirtinone, a Novel Cycloartane-Type Triterpene and Other Compounds from Trichilia hirta L. (Meliaceae)
Ivo Jos¨¦ Curcino Vieira, Otoniel de Aquino Azevedo, Jucimar Jorgeane de Souza, Raimundo Braz-Filho, Milena dos Santos Gonçalves and Marcelo Francisco de Ara¨²jo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     ailexcelone
C30H50O3     ÏàËÆ¶È:70%
Chemistry & Biodiversity          2006          Vol. 3          930
Two New Tetracyclic Triterpenes from the Heartwood of Ailanthus excelsa Roxb.
Pullela V. Srinivas, R. Ranga Rao, and J. Madhusudana Rao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     25-chloro-24-hydoroxytirucall-7-en-3-one
C30H49O2Cl     ÏàËÆ¶È:70%
Phytochemistry          2002          61          93-98
Terpenoids from Tripterygium doianum (Celastraceae)
Naonobu Tanaka, Hongquan Duan, Yoshihisa Takaishi,Kazuyoshi Kawazoe, Satoru Goto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     aglaiodiol
C30H50O5     ÏàËÆ¶È:70%
Planta Medica          2000          66          740-745
Phytochemical Investigation of Aglaia andamanica
Jindaporn Puripattanavong,Sabine Weber, Volker Brecht,August Wilhelm Frahm
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     24-epi-melianodiol
C30H48O5     ÏàËÆ¶È:70%
Planta Medica          2000          66          740-745
Phytochemical Investigation of Aglaia andamanica
Jindaporn Puripattanavong,Sabine Weber, Volker Brecht,August Wilhelm Frahm
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     hispidone
    ÏàËÆ¶È:70%
Chemical & Pharmaceutical Bulletin          1992          40          1053-1055
Cytotoxic Quassinoids and Tirucallane-Type Triterpenes from the Woods of Eurycoma longifolia
Hideji ITOKAWA,Etsuko KISHI,Hiroshi MORITA and Koichi TAKEYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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1 .     ¶¹çÞ´¼-¦Â-D-ÆÏÌÑÌÇÜÕ
    ÏàËÆ¶È:93.3%
Chinese Traditional and Herbal Drugs          2002          33          300-303
Studies on chemical ...

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500MHz
11.97,12.10,12.16,12.39,18.90,19.15,19.52,19.95,21.19,23.16,24.42,28.37,31.71,31.99,32.02,36.26,36.60,37.36,39.87,42.36,42.42,45.91,50.22,56.15,56.86,71.86,121.81,129.35,138.45,140.86
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²éѯ½á¹û£º¹²²éµ½4946¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     ¡÷5,22-stigmasterol
    ÏàËÆ¶È:93.3%
Journal of Guangdong Phamaceutical University          2011          27          364-366
Studies on the anti-inflammatory chemical constituents of Hedyotis hedyotidea(DC.) Merr.
TAO Shu-hong, CHEN Yan-fen, LI Zhong, YANG Chao-yan, YAN You-shao, WU Yan-wen, XU Pei-ting
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     ¦¤5,22-¶¹çÞ´¼
    ÏàËÆ¶È:93.3%
Journal of Chinese Medicinal Materials          2005          28          1060-1062
Study on Sterols and Triterpenes from the Stems of Akebia quinata
Liu Guiyan, Zheng Jian, Yu Zhenxi, Zhang Ji, Lin Ruichao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     ¹ÈçÞ´¼
C29H48O     ÏàËÆ¶È:90%
Journal of Anhui Agricultural Sciences          2009          37          11001-11002
Study on the Chemical Components in the Roots of Anthriscus sylvestris
WANG Yue-feng et al
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     ¦Â-sitosterol
    ÏàËÆ¶È:86.6%
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
5 .     Stigmasterol
    ÏàËÆ¶È:86.6%
Acta Botanica Yunnanica          1995          17(1)          103-108
CHEMICAL CONSTITUENTS FROM CLERODENDRUM JAPONICUM
TIAN Jun, SUN Han-Dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     sitosterol
    ÏàËÆ¶È:86.6%
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
7 .     ¦Â-sitosterol
    ÏàËÆ¶È:86.6%
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
8 .     ¦Â-sitosterol
    ÏàËÆ¶È:86.6%
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
9 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:86.6%
Acta Botanica Boreali-Occidentalia Sinica          2004          24          1292-1294
Chemical constituents from Saussurea polycolea
LI Yu-lin, WANG Hong-lun, SUO You-rui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     ¦Â-sitosterol
    ÏàËÆ¶È:86.6%
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
11 .     stigmasta-5,22-dien-3-ol
    ÏàËÆ¶È:86.6%
Guihaia          2009          29          279-280
Chemical study on Brassaiopsis glomerulata
ZHAO Chao; YANG Xiao-Sheng; ZHU Hai-Yan; REN Yong-Qi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     ¦Â-sitosterol
    ÏàËÆ¶È:86.6%
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
13 .     ¦Â-sitosterol
    ÏàËÆ¶È:86.6%
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
14 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:86.6%
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
15 .     stigmasterol
    ÏàËÆ¶È:86.6%
Natural Product Research          2009          23          1218-1230
Chemical composition of the stem bark and leaves of Ficus pandurata Hance
M. A. Ramadan; A. S. Ahmad; A. M. Nafady; A. I. Mansour
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     stigmasterol
    ÏàËÆ¶È:86.6%
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
17 .     ¦Â-sitosterol
    ÏàËÆ¶È:86.6%
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
18 .     ¦Â-sitosterol
    ÏàËÆ¶È:86.6%
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
19 .     ¦Â-sitosterol
    ÏàËÆ¶È:86.6%
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
20 .     ¦Â-sitosterol
    ÏàËÆ¶È:86.6%
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
21 .     ¦Â-sitosterol
    ÏàËÆ¶È:86.6%
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
22 .     ¦Â-Sitosterol
    ÏàËÆ¶È:86.6%
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
23 .     ¦Â-Sitosterol
    ÏàËÆ¶È:86.6%
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
24 .     sitosterol
    ÏàËÆ¶È:86.6%
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
25 .     ¦Â-Sitosterol
C29H50O     ÏàËÆ¶È:86.6%
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
26 .     ¦Â-Sitosterol
    ÏàËÆ¶È:86.6%
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
27 .     ¦Â-Sitosterol
    ÏàËÆ¶È:86.6%
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
28 .     compound 5
    ÏàËÆ¶È:86.6%
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
29 .     compound 1
C29H50O     ÏàËÆ¶È:86.6%
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
30 .     compound 3a
    ÏàËÆ¶È:86.6%
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
31 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:86.6%
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
32 .     ¦Â-¹ÈçÞ´¼
C29H48O     ÏàËÆ¶È:86.6%
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
33 .     (24s)-stigmast-5-en-3-ol
    ÏàËÆ¶È:86.6%
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
34 .     (24S)-stigmast-5-en-3¦Â-ol
    ÏàËÆ¶È:86.6%
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
35 .     ¦Â-¹ÈçÞ´¼
    ÏàËÆ¶È:86.6%
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
36 .     3¦Á-hydroxylanosta-5,15-diene
C30H50O     ÏàËÆ¶È:86.6%
Natural Product Research          2012          26          654-658
Triterpenoids from Arctium lappa
S. Jeelani and M.A. Khuroo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     Stosterol
    ÏàËÆ¶È:86.6%
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
38 .     ¦Â-rosasterol
C29H50O     ÏàËÆ¶È:86.6%
Chinese Traditional and Herbal Drugs          2006          37          666-668
Å·ÑÇÐý¸²»¨ÖÐÈýÝÆºÍçÞÌ廯ºÏÎïµÄ·ÖÀëºÍ½á¹¹¼ø¶¨
ÎâÒ»±ø;ÍõÔÆÖ¾;²é½¨Åî;ÑîË«¸ï;ʯÏþΰ;ÕŵÕȺ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     ¦Â-rosasterol
C29H50O     ÏàËÆ¶È:86.6%
Chinese Traditional and Herbal Drugs          1996          27          389-391
Studies on the Chemical Constituents of Dyers Woad(Isatis tinctoria)
Li Ling; Yang Genjin; Dong Tongyi; et al(Address£ºLi Ling£®College of Pharmacy; Second Military Medical University; Sanghai);
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     ¦Â-sitosterol
    ÏàËÆ¶È:86.6%
Chinese Journal of Natural Medicines          2009          7          293-296
Chemical Constituents from Thalictrum fortunei
ZHANG Xian-Tao; ZHANG Lei-Hong; WANG Ying; LI Yan; WANG Yu-Sheng; YE Wen-Cai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     compound 3
    ÏàËÆ¶È:86.6%
Archives of Pharmacal Research          1998          21          357-360
Isolation of 3- O -(4'-Hydroxybenzyl)-¦Â-sitosterol and 4-[4'-(4¡å-Hydroxybenzyloxy)benzyloxy]benzyl methyl ether from fresh tubers of Gastrodia elata
Hye Sook Yun-Choi, Mi Kyung Pyo and Kyung Mi Park
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     ¦Â-Sitosterol
    ÏàËÆ¶È:86.6%
Archives of Pharmacal Research          2006          29          617-623
Chemical constituents of the root of Dystaenia takeshimana and their anti-inflammatory activity
Ju Sun Kim, Jin Cheul Kim, Sang Hee Shim, Eun Ju Lee and Wen Yi Jin, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     ¦Â-¹ÈçÞ´¼
    ÏàËÆ¶È:86.6%
Chinese Pharmaceutical Journal          2004          39          173-175
Studies on the chemical constituents of Caragana rosea
CUI Yi-ling, MU Qing, HU Chang-qi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     ¦Â-sitosterol
    ÏàËÆ¶È:86.6%
Chinese Pharmaceutical Journal          2006          41          1293-1295
Studies on Chemical Constituents of Mimosa pudica
YUAN Ke, L¦B Jie-li, JIA An
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     ¦Â-sitosterol
    ÏàËÆ¶È:86.6%
Chinese Pharmaceutical Journal          2011          46          341-343
Chemical Constituents of Lysimachia clethroides Duby
YUE Shu-mei, CHEN Bai-quan, YUAN Peng-fei, CUI Wei-heng, KANG Wen-yi*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     ¦Â-sitosterol
    ÏàËÆ¶È:86.6%
Chinese Journal of Medicinal Chemistry          2006          16          303-305
The constituents of Veratrum japonicum Loes. f.
ZHOU Jian-xia, KANG Lu, SHEN Zheng-wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     ¦Â-sitosterol
    ÏàËÆ¶È:86.6%
Chinese Journal of Medicinal Chemistry          2007          17          390-391
Chemical constituents of Boschniakia himalaica
JIN Yin-ping, ZHANG Guo-gang, ZHENG Hong-ting, DU Shu-shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     ¦Â-sitosterol
    ÏàËÆ¶È:86.6%
Chinese Journal of Medicinal Chemistry          2009          19          130-134
Chemical constituents of Dillenia kerrii and their activities on antitumor and anti-hypoxia in vitro
LI Xia, LI Chang-wei, CUI Cheng-bin, LIMing-ming, FAN Ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     ¦Â-¹ÈçÞ´¼
    ÏàËÆ¶È:86.6%
Journal of Shenyang Pharmaceutical University          2007          24          611-614
Chemical constituents of Duchesnea indica Focke
XU Wen-dong, LIN Hou-wen, QIU Feng, CHEN Wan-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     stigmasterol
    ÏàËÆ¶È:86.6%
Journal of Shenyang Pharmaceutical University          2007          24          619-622
Isolation and identification of non-alkaloid constituents from Gelsemium elegans Benth.
ZHAO Qing-chun, FU Yan-hui, GU O Tao, HU A Wei, WU Li-jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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