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1 .     6-ketostearoyluvidin A
    ÏàËÆ¶È:56.2%
Journal of Natural Products          1994          Vol 57          905
New Fatty Acid Esters of Drimane Sesquiterpenes from Lactarius uvidus
Luigi Garlaschelli, Giorgio Mellerio, Giovanni Vidari, Paola Vita-Finzi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (2R,3S,5¦Á,22S,23E)-6,6-ethylenedioxy-2,3-isopropylidenedioxy-26,27-dinorcholest-23-en-22-ol
C30H48O5     ÏàËÆ¶È:54.8%
Canadian Journal of Chemistry          1993          71          156-163
A new synthesis of castasterone and brassinolide from stigmasterol. A concise and stereoselective elaboration of the side chain from a C-22 aldehyde
Thomas G. Back, Peter G. Blazecka, M. Vijaya Krishna
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     2,3-Dihydro-21-hydroxytrechonolide A
C28H38O8     ÏàËÆ¶È:54.8%
Phytochemistry          2014          98          232-235
Withanolides from Jaborosa caulescens var. bipinnatifida
Huaping Zhang, Cong-Mei Cao, Robert J. Gallagher, Victor W. Day, Gloria Montenegro, Barbara N. Timmermann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     N-[1-cyano-19¦Â,28-epoxy-2,3-seco-2-nor-18¦ÁH-olean-3-oyl]-2-aminopropane-1,3-diol
    ÏàËÆ¶È:54.5%
Chemistry of Natural Compounds          2014          49          1050-1058
Synthesis and antiviral activity of C-3(C-28)-substituted 2,3-seco-triterpenoids
I. A. Tolmacheva, E. V. Igosheva, O. V. Savinova, E. I. Boreko, V. V. Grishko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     K-Trap
C34H47N5O8     ÏàËÆ¶È:53.1%
Journal of the American Chemical Society          1996          118          10412-10422
Synthesis of Natural and Modified Trapoxins, Useful Reagents for Exploring Histone Deacetylase Function
Jack Taunton, Jon L. Collins, and Stuart L. Schreiber
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     3¦Â-hydroxy-21-oxo-11,13(18)-oleanadien-28-oic acid methyl ester
C31H46O4     ÏàËÆ¶È:51.6%
Phytochemistry          2007          68          631-635
Oleanane-type triterpenes from the flowers, pith, leaves, and fruit of Tetrapanax papyriferus
Jiau-Ching Ho, Chiu-Ming Chen, Lie-Ching Row
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     2-ethoxycarbonyl-24-ethyl-2¦Â-hydroxy-A-nor-cholesta-5-en-4-one
C31H50O4     ÏàËÆ¶È:51.6%
Journal of Natural Products          2006          69          1330-1334
Oculatol, Oculatolide, and A-nor Sterols from the Sponge Haliclona oculata
Shanjiang Yu, Zhiwei Deng, Peter Proksch, and Wenhan Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     3¦Á-hydroxy-24S,25R-epoxylanost-9(11)-en-27-oic Acid
    ÏàËÆ¶È:51.6%
Chemistry of Natural Compounds          1990          26          545-548
STRUCTURE OF A NEW TRITERPENOID FROM THE BARK OF THE SIBERIAN LARCH
G. F. Chernenko, I. Yu. Bagryanskaya,and E. N. Shmidt
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (5Z)-(7R,8R,10S)-7,8;10,19-Diepoxy-9,10-secoergosta-5,22-dien-3¦Â-yl acetate
C30H46O4     ÏàËÆ¶È:51.6%
Steroids          2006          71          565-577
Regio and stereoselective oxidations of unsaturated steroidal compounds with H2O2 mediated by CH3ReO3
Francesco P. Ballistreri, Rosa Chillemi, Sebastiano Sciuto, Gaetano A. Tomaselli, Rosa M. Toscano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     24S-ethyl-2¦Â-hydroxy-4,7-diketo-Anorcholest-5-en-2-oic acid
C31H48O5     ÏàËÆ¶È:51.6%
Steroids          2008          73          1500-1504
New A-nor steroids and their antifouling activity from the Chinese marine sponge Acanthella cavernosa
Yan Qiu, Zhi Wei Deng, Minjuan Xu, Qingshan Li, Wen Han Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     2¦Â-hydroxy-4,7-diketo-24R-methyl-Anorcholest-5,22(E)-diene-2-oic acid
C30H44O5     ÏàËÆ¶È:51.6%
Steroids          2008          73          1500-1504
New A-nor steroids and their antifouling activity from the Chinese marine sponge Acanthella cavernosa
Yan Qiu, Zhi Wei Deng, Minjuan Xu, Qingshan Li, Wen Han Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     24,25-dihydrowithacnistine
    ÏàËÆ¶È:51.6%
Phytochemistry          1993          34          517-521
Withanolides from Iochroma coccineum
Doroth¨¦e Alfonso, G¨¦rald Bernardinelli, Ilias Kapetanidis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     petuniolide E
C29H42O6     ÏàËÆ¶È:51.6%
Phytochemistry          1990          29          2853-2863
Ergostanoids from Petunia parodii
Carl A. Elliger,Anthony C. Waiss Jr,Mabry Benson,Rosalind Y. Wong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     24-hydroxytormentic acid
    ÏàËÆ¶È:51.6%
Phytochemistry          1986          25          1939-1944
Triterpenoids from Desfontainia spinosa
Peter J. Houghton, Lu Ming Lian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     compound 19
C31H49O3I     ÏàËÆ¶È:51.6%
Natural Product Research          2010          24          177-196
Different pathways for the deoxygenation of the A-ring of natural triterpene compounds
Andres Parra; Pilar E. Lopez; Andres Garcia-Granados
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     compound 4
    ÏàËÆ¶È:51.6%
Archives of Pharmacal Research          1992          15          374-375
A steroselective synthesis of (22R, 23R)-methylenecholesterol
Deukjoon Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (22S,23Z)-6-(1,3-Dioxolan-2-yl)-3¦Á,5-cyclo-26,27-bisnor-5¦Ácholest-23-en-22-ol
    ÏàËÆ¶È:51.6%
Steroids          2012          77          780-790
A new approach to the side chain formation of 24-alkyl-22-hydroxy steroids: Application to the preparation of early brassinolide biosynthetic precursors
Alaksiej L. Hurski, Vladimir N. Zhabinskii, Vladimir A. Khripach
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     triptolidyl 2-(1-methylpiperidine-1-yl) acetate
C27H35O7N1     ÏàËÆ¶È:51.6%
Bioorganic & Medicinal Chemistry          2010          18          1806-1815
Design, synthesis, and biological evaluation of novel water-soluble triptolide derivatives: Antineoplastic activity against imatinib-resistant CML cells bearing T315I mutant Bcr-Abl
Fang Xu, Xianping Shi, Shichang Li, Jieshun Cui, Zhongzheng Lu, Yanli Jin, Yongcheng Lin, Jiyan Pang, Jingxuan Pan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     triptolidyl 2-(diethylamine-1-yl) acetate
C26H35O7N1     ÏàËÆ¶È:51.6%
Bioorganic & Medicinal Chemistry          2010          18          1806-1815
Design, synthesis, and biological evaluation of novel water-soluble triptolide derivatives: Antineoplastic activity against imatinib-resistant CML cells bearing T315I mutant Bcr-Abl
Fang Xu, Xianping Shi, Shichang Li, Jieshun Cui, Zhongzheng Lu, Yanli Jin, Yongcheng Lin, Jiyan Pang, Jingxuan Pan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     VM 54159
    ÏàËÆ¶È:51.6%
The Journal of Antibiotics          1991          44          492-497
NEW PARAHERQUAMIDE ANTIBIOTICS WITH ANTHELMINTIC ACTIVITY
SIMON E. BLANCHFLOWER, RHONA M. BANKS, JEREMY R. EVERETT, BRIAN R. MANGER, CHRISTOPHER READING
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     phenyl 3,4,6-tri-O-hexanoyl-2-O-octanoyl-1-thio-¦Á-D-mannopyranoside S-oxide
C38H60O10S     ÏàËÆ¶È:51.6%
Tetrahedron          2013          69          9917-9930
Stereoselective total synthesis of acremomannolipin A and its anomer, the potent calcium signal modulators with a novel glycolipid structure: role of the stereochemistry at the anomeric center on the activity
Nozomi Tsutsui, Genzoh Tanabe, Genki Gotoh, Ayako Kita, Reiko Sugiura, Osamu Muraoka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     (22R)-6¦Â-methoxy-3¦Á,5-cyclo-5¦Á-cholest-23-yn-22-ol
    ÏàËÆ¶È:51.6%
Magnetic Resonance in Chemistry          1993          31          605-608
Synthesis and configurational assignment of epimeric 22-hydroxy-, 23, 24-acetylenic, olefinic or epoxy steroids using carbon-13 NMR Spectroscopy
Braja G. Hazra, Vandana S. Pore, Padmakar L. Joshi, Sharmila N. Padalkar, Shubhada A Deshpande and Pattuparambil R. Rajamohanan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     (22R,23S,24R)-6¦Â-methoxy-3¦Á,5-cyclo-5¦Á-cholest-23,24-epoxy-22-ol
C28H46O3     ÏàËÆ¶È:51.6%
Magnetic Resonance in Chemistry          1993          31          605-608
Synthesis and configurational assignment of epimeric 22-hydroxy-, 23, 24-acetylenic, olefinic or epoxy steroids using carbon-13 NMR Spectroscopy
Braja G. Hazra, Vandana S. Pore, Padmakar L. Joshi, Sharmila N. Padalkar, Shubhada A Deshpande and Pattuparambil R. Rajamohanan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     compound 1A
C30H46O5     ÏàËÆ¶È:51.6%
Natural Product Research          2013          27          711-718
Cytotoxicity of semisynthetic acetal triterpenes from one-pot vicinal diol cleavage following by lactolization: Reaction promoted by NaIO4/SiO2 gel in THF
Louis Pergaud Sandjo, Aurelie Vigee Barry Songfack Djoumessi, Vincent Rincheval, Herv¨¦ Martial Poumale Poumale, Berhanu M. Abegaz & Bonaventure T. Ngadjui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     Davinvolunic acid C
C31H50O7     ÏàËÆ¶È:51.6%
Molecules          2014          19          4897-4906
Three New Ring-A Modified Ursane Triterpenes from Davidia involucrata
Qing-Wei Tan, Ming-An Ouyang and Bo Gao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     3-(4'-methoxy-4'-oxosuccinyloxy)-1-cyano-19¦Â,28-epoxy-2,3-seco-2-nor-18¦ÁH-oleanane
    ÏàËÆ¶È:51.4%
Chemistry of Natural Compounds          2014          49          1050-1058
Synthesis and antiviral activity of C-3(C-28)-substituted 2,3-seco-triterpenoids
I. A. Tolmacheva, E. V. Igosheva, O. V. Savinova, E. I. Boreko, V. V. Grishko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     12¦Á-acetoxy-16¦Á-(3'-hydroxypentanoyloxy)-20,24-dimethyl-24-oxoscalaran-25¦Â-oic acid
C34H54O8     ÏàËÆ¶È:50%
Journal of Natural Products          2007          70          802-807
Additional Scalarane Sesterterpenes from the Sponge Phyllospongia papyracea
Hou-Jin Li,Taro Amagata, Karen Tenney, and Phillip Crews
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     amphidinolide B6
C32H54O8     ÏàËÆ¶È:50%
Journal of Natural Products          2007          70          1676-1679
Amphidinolides B6 and B7, Cytotoxic Macrolides from a Symbiotic Dinoflagellate Amphidinium Species
Keiko Oguchi, Masashi Tsuda, Rie Iwamoto, Yumiko Okamoto, Taeko Endo,Jun¡¯ichi Kobayashi, Tomoko Ozawa, and Atsunori Masuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     acidissiminin epoxide
    ÏàËÆ¶È:50%
Journal of Natural Products          1991          Vol 54          1389
Tyramine Derivatives from the Fruit of Limonia acidissima
Parthasarathi Ghosh, Prabal Sil, Srabani Das, Swapnadip Thakur, W. C. M. C. Kokke, Toshihiro Akihisa, Naoto Shimizu, Toshitake Tamura, Taro Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     ethyl (1R,6R,7S)-1,5,5,6-tetramethylbicyclo[4.3.0]-nonane-[8.2']-spirooxirane-7-carboxylates
    ÏàËÆ¶È:50%
Indian Journal of Chemistry Section B          2009          48B          413-422
Enantiospecific total synthesis of ent-10,11-thapsan-10-ol
Srikrishna,A; Anebouselvy,K
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     23,24-Diacetoxy-19-hydroxy-3-oxo-urs-12-en-28-oic acid
    ÏàËÆ¶È:50%
Phytochemistry          1984          23          627-630
Triterpenoids from enkianthus campanulatus
Jinsaku Sakakibara, Toyo Kaiya, Haruyo Fukuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     N-Boc-Sta-Thr-Ala-N¦Á-Me-D-Phe-L-Pro-OMe
C36H57N5O10     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2012          20          4774-4780
Total synthesis of grassystatin A, a probe for cathepsin E function
Siming Yang, Wei Zhang, Ning Ding, Jeannette Lo, Yanxia Liu, Michael J. Clare-Salzler, Hendrik Luesch, Yingxia Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     2¦Â-bromo-3-oxo-28-O-acetylbetulin
C32H48Br2O3     ÏàËÆ¶È:50%
Journal of Natural Products          2014          77          863-872
Antineoplastic Agents. 595. Structural Modifications of Betulin and the X-ray Crystal Structure of an Unusual Betulin Amine Dimer1
George R. Pettit, Noeleen Melody, Frank Hempenstall, Jean-Charles Chapuis, Thomas L. Groy, and Lee Williams
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     2¦Á-Acetyl tormentic acid
    ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2007          15          7355-7360
Natural triterpenoids from Cecropia lyratiloba are cytotoxic to both sensitive and multidrug resistant leukemia cell lines
Gleice da Graça Rocha, Marisol Simões, Kelly Araujo L¨²cio, Rodrigo Rodrigues Oliveira, Maria Auxiliadora Coelho Kaplan, Cerli Rocha Gattass
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     Methyl (4S)-4-({[(2S)-1-({(2R)-1-[(1R,2S,3R,4R)-3-(tert-Butyl)-2-isopropyl-4-nitrocyclobutyl]pyrrolidin-2-yl}carbonyl)pyrrolidin-2-yl]carbonyl}amino)-5-(dodecylamino)-5-oxopentanoate
C39H70N5O7     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2013          96          799-852
Stoichiometric Reactions of Enamines Derived from Diphenylprolinol Silyl Ethers with Nitro Olefins and Lessons for the Corresponding Organocatalytic Conversions ¨C a Survey
Dieter Seebach, Xiaoyu Sun, Marc-Olivier Ebert, W. Bernd Schweizer, Nirupam Purkayastha, Albert K. Beck, Jörg Duschmal¨¦, Helma Wennemers, Takasuke Mukaiyama, Meryem Benohoud, Yujiro Hayashi and Markus Reiher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     6¦Á-Hydroxy-5¦Á-cholestan-3¦Â-yl N,N-bis(2-hydroxyethyl) carbamate
C32H57NO5     ÏàËÆ¶È:50%
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   Ì¼Æ×Ä£Äâͼ
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