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1 .     hyptatic acid-A
C30H48O5     ÏàËÆ¶È:73.3%
Journal of Ethnopharmacology          2008          116          554-560
Antibacterial compounds from Planchonia careya leaf extracts
Jacqui M. McRae, Qi Yang, Russell J. Crawford, Enzo A. Palombo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Hyptatic acid-A
C30H48O5     ÏàËÆ¶È:70%
Natural Product Research          2013          27          532-536
A new triterpenoid from the rhizomes of Nelumbo nucifera
Prabir K. Chaudhuri & Deepika Singh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     3¦Á-hydroxy-5¦Â-cholan-24-amide
    ÏàËÆ¶È:67.8%
Journal of Chemical Research          2008          32          260-265
Synthesis of novel amide-linked dimers of lithocholic acid
Joachimiak, Roman; Piasecka, Monika; Paryzek, Zdzisław
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     N-phenyl-3¦Á-hydroxy-5¦Â-cholan-24-amide
C30H45NO2     ÏàËÆ¶È:67.8%
Journal of Chemical Research          2008          32          260-265
Synthesis of novel amide-linked dimers of lithocholic acid
Joachimiak, Roman; Piasecka, Monika; Paryzek, Zdzisław
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     hederagenin
    ÏàËÆ¶È:66.6%
Carbohydrate Research          2011          346          1302-1306
Fatty acid synthase inhibitors from the hulls of Nephelium lappaceum L.
You-Xing Zhao, Wen-Juan Liang, Hui-Jin Fan, Qing-Yun Ma, Wei-Xi Tian, Hao-Fu Dai, He-Zhong Jiang, Ning Li, Xiao-Feng Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     sericic acid
    ÏàËÆ¶È:66.6%
Chemistry & Biodiversity          2011          8          1301-1309
Novel 3-Oxo- and 3,24-Dinor-2,4-secooleanane-Type Triterpenes from Terminalia ivorensis A. Chev.
Beaudelaire Kemvoufo Ponou, R¨¦my Bertrand Teponno, Massimo Ricciutelli, T¨¦lesphore B¨¦noit Nguelefack, Luana Quassinti, Massimo Bramucci, Giulio Lupidi, Luciano Barboni*, and L¨¦on Azefack Tapondjou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     Hederagenin
    ÏàËÆ¶È:66.6%
Chemistry of Natural Compounds          2012          47          935-939
A new hederagenin glycoside from Nephelium lappaceum
Wen-Juan Liang, Qing-Yun Ma, He-Zhong Jiang, Jun Zhou and Jie Pang, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     scutellaric acid
C30H48O4     ÏàËÆ¶È:64.5%
Chinese Traditional and Herbal Drugs          2009          40          1036-1039
ŵÀöÇà¹û»¯Ñ§³É·ÖÑо¿
ÌÀ½¨¹ú;Èθ£²Å;Áõ¼ª¿ª
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     24¦Æ,25-¶þ¼×»ù-5-µ¨çÞÏ©-2¦Â,3¦Á-¶þ´¼
C29H50O2     ÏàËÆ¶È:64.2%
Chinese Journal of Marine Drugs          2005          24(6)          24-27
Studies on the chemical constituents of the sponge Halichondria rugosa
SUN Jing-bo, LIN Hou-wen, ZHANG Hong-jun, Wang Zeng-lei, ZHANG Heng-bi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     N-n-butyl-3¦Á-hydroxy-5¦Â-cholan-24-amide
C28H49NO2     ÏàËÆ¶È:64.2%
Journal of Chemical Research          2008          32          260-265
Synthesis of novel amide-linked dimers of lithocholic acid
Joachimiak, Roman; Piasecka, Monika; Paryzek, Zdzisław
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     Dihydroxestoproxamine C TFA Salt
C31H60N2     ÏàËÆ¶È:64.2%
Journal of Natural Products          2011          74          430-440
Xestoproxamines A−C from Neopetrosia proxima. Assignment of Absolute Stereostructure of Bis-piperidine Alkaloids by Integrated Degradation-CD Analysis
Brandon I. Morinaka and Tadeusz F. Molinski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     arjunolic acid
    ÏàËÆ¶È:63.3%
China Journal of Chinese Materia Medica          2009          34          867-870
Chemical constituents from roots of Phlamis umbrosa
LIU Pu, DENG Ruixue, DUAN Hongquan, YIN Wei ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     maslinic acid
    ÏàËÆ¶È:63.3%
China Journal of Chinese Materia Medica          2009          34          2610-2612
Chemical constituents of roots of Boehme rianivea
XU Qiongming, CHEN Guoqing, FAN Jinying, ZHANGMengjia, LIXia, YANG Shilin, LIxiaoran
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     3-oxo-olean-12-en-28-oic acid
C30H46O3     ÏàËÆ¶È:63.3%
Phytochemistry          1996          43          99-104
Ring-A cleavage of 3-oxo-olean-12-en-28-oic acid by the fungus Chaetomium longirostre
Noboru Shirane, Yutaka Hashimoto, Kazuo Ueda, Hideyuki Takenaka, Kenji Katoh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     maslinic acid
C30H48O4     ÏàËÆ¶È:63.3%
Chinese Traditional and Herbal Drugs          2007          38          1311-1313
ÉßÝ®ÖоßÓп¹°©»îÐÔµÄÈýÝÆÀà³É·Ö
ÎâÅàéª;¶ÎºêȪ;Ò¦ÖÇ;ÅËÇÚ;ÕŸ»âÙ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     compound 5
C30H52N2     ÏàËÆ¶È:63.3%
European Journal of Organic Chemistry          1999          1999          697-701
Plakinamines C and D and Three Other New Steroidal Alkaloids from the Sponge Corticium sp.
Simona De Marino, Maria Iorizzi, Franco Zollo, Christos Roussakis and C¨¦cile Debitus
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     2¦Á,3¦Â,23-trihydroxyolean-12-en-28-oic acid
    ÏàËÆ¶È:63.3%
China Journal of Chinese Materia Medica          2011          36          162-165
Triterpenoids and triterpenoid saponins of Viscum liquidambaricolum
YANG Yanjun, CHEN Meiguo, SHA Congwei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     Pseuderanic Acid
C30H48O6     ÏàËÆ¶È:63.3%
Chemical & Pharmaceutical Bulletin          2012          60          1125-1133
Lignans and Triterpenes from the Root of Pseuderanthemum carruthersii var. atropurpureum
Thi Nga Vo, Phi Linh Nguyen, Lam Truong Tuong, Lawrence Michael Pratt, Phung Nguyen Vo, Kim Phi Phung Nguyen, Ngoc Suong Nguyen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     hederagenin
    ÏàËÆ¶È:62.0%
Phytochemistry          1995          40          891-897
Hederagenin glycosides from Pometia eximia
Lalith Jayasinghe, Hiroyasu Shimada, Noriyuki Hara, Yoshinori Fujimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     N-benzyl-3¦Á-hydroxy-5¦Â-cholan-24-amide
C31H47NO2     ÏàËÆ¶È:62.0%
Journal of Chemical Research          2008          32          260-265
Synthesis of novel amide-linked dimers of lithocholic acid
Joachimiak, Roman; Piasecka, Monika; Paryzek, Zdzisław
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     sitost-4-en-3-one
    ÏàËÆ¶È:62.0%
Chemistry Central Journal          2013          7          24
Discovery and antitumor activities of constituentsfrom Cyrtomium fortumei (J.) Smith rhizomes
Shengjie Yang, Mingchuan Liu, Na Liang, Qi Zhao, Yuping Zhang, Wei Xue, and Song Yang,
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     stigmastane-3,6-diol
C29H52O2     ÏàËÆ¶È:62.0%
Journal of Tropical and Subtropical Botany          2009          17          156-159
Studies on Chemical Constituents of Excoecaria cochinchinensis Lour .
WANG, Yunsong, HUANG, Rong, ZHANG, Hongbin, LI, Liang, YANG, Jinghua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     hederagenin
    ÏàËÆ¶È:62.0%
Chinese Traditional and Herbal Drugs          2013          44          1872-1876
Chemical constituents of Quercus pannosa
OU Ying-bao, WEI Ming-jie, LI He-ran
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     Tetrahydroxestoproxamine C Bis-methiodide Salt
C33H64N2     ÏàËÆ¶È:61.2%
Journal of Natural Products          2011          74          430-440
Xestoproxamines A−C from Neopetrosia proxima. Assignment of Absolute Stereostructure of Bis-piperidine Alkaloids by Integrated Degradation-CD Analysis
Brandon I. Morinaka and Tadeusz F. Molinski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     lycochinine A
C28H49N3     ÏàËÆ¶È:60.7%
Tetrahedron Letters          2009          50          4816-4819
Lycochinines A¨CC, novel C27N3 alkaloids from Lycopodium chinense
Yusuke Hirasawa, Tomoyuki Tanaka, Koichiro Koyama, Hiroshi Morita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     5¦Â-steroid disulphate
    ÏàËÆ¶È:60.7%
Tetrahedron Letters          1992          33          4641-4644
Isolation, structure characterization and conformational analysis of a unique 4¦Á, 9¦Á-epoxysteroid sulphate from the okinawan ophiuroid Ophiomastix annulosa
M.Valeria D'Auria, Luigi Gomez Paloma, Luigi Minale, Raffaele Riccio, Angela Zampella, Jun-ichi Tanaka, Tatsuo Higa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     (24S)24-methylcholestane-3¦Â,5¦Â,6¦Á,25-tetrol
C28H50O4     ÏàËÆ¶È:60.7%
Natural Product Research and Development          2001          13(1)          30-32
STUDIES ON THE CHEMICAL CONSTITUENTS OF THE SOFT CORAL LOBOPHYTUM SP.FROM SOUTH CHINA SEA
LIANG Li yan; DENG Song zhi and WU Hou ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     coscinolactam A
C27H41NO7S     ÏàËÆ¶È:60.7%
Tetrahedron          2009          65          2905-2909
Coscinolactams A and B: new nitrogen-containing sesterterpenoids from the marine sponge Coscinoderma mathewsi exerting anti-inflammatory properties
Simona De Marino, Carmen Festa, Maria Valeria D'Auria, Marie-Lise Bourguet-Kondracki, Sylvain Petek, Cecile Debitus, Rosa Mar¨ªa Andr¨¦s, Maria Carmen Terencio, Miguel Pay¨¢, Angela Zampella
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     24-amino-5¦Â-cholan-3¦Á-ol
    ÏàËÆ¶È:60.7%
Journal of Chemical Research          2008          32          260-265
Synthesis of novel amide-linked dimers of lithocholic acid
Joachimiak, Roman; Piasecka, Monika; Paryzek, Zdzisław
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     24-n-butylamino-5¦Â-cholan-3¦Á-ol
C28H51NO     ÏàËÆ¶È:60.7%
Journal of Chemical Research          2008          32          260-265
Synthesis of novel amide-linked dimers of lithocholic acid
Joachimiak, Roman; Piasecka, Monika; Paryzek, Zdzisław
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     N,N'-bis(3¦Á-acetoxy-5¦Â-cholan-24-oyl)-p-phenylenediamine
C58H88N2O6     ÏàËÆ¶È:60.7%
Journal of Chemical Research          2008          32          260-265
Synthesis of novel amide-linked dimers of lithocholic acid
Joachimiak, Roman; Piasecka, Monika; Paryzek, Zdzisław
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     N,N'-bis(3¦Á-acetoxy-5¦Â-cholan-24-oyl)-ethylenediamine
C54H88N2O6     ÏàËÆ¶È:60.7%
Journal of Chemical Research          2008          32          260-265
Synthesis of novel amide-linked dimers of lithocholic acid
Joachimiak, Roman; Piasecka, Monika; Paryzek, Zdzisław
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     3¦Â,27-dihydroxyolean-12-en-28-oic acid
C30H48O7S     ÏàËÆ¶È:60%
Journal of Natural Products          2007          70          584-588
Sulfated Triterpene Derivatives from Fagonia arabica
Angela Perrone,Milena Masullo, Carla Bassarello, Arafa I. Hamed, Maria Antonietta Belisario, Cosimo Pizza, and Sonia Piacente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     compound 11a
    ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1988          36          1646-1663
Tannins and Related Compounds. LXVII. : Isolation and Characterization of Castanopsinins A-H, Novel Ellagitannins Containing a Triterpenoid Glycoside Core, from Castanopsis cuspidata var. sieboldii NAKAI. (3)
MASAYUKI AGETA,GEN-ICHIRO NONAKA and ITSUO NISHIOKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     2¦Á-ôÇ»ùÆë¶Õ¹ûËá
    ÏàËÆ¶È:60%
Acta Botanica Sinica          1998          40          83-87
Chemical Constituents from Fruits of Ligustrum lucidum
WU Li-Jun, XIANG Ting, HOU Bai-Ling, LIANG Wei, Yin Shuang, ZHOU Xiao-Chuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     3¦Á-hydroxy-D-friedoolean-5-ene
C30H50O     ÏàËÆ¶È:60%
Natural Product Research          1997          10          249-256
Phytochemical Studies on Adhatoda Vasica Nees
Atta-Ur-Rahman; Nighat Sultana; Farzana Akhter; Farzana Nighat; M. Iqbal Choudhary
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     1¦Â,3¦Â,23-trihydroxyolean-12-en-28-oic acid
C30H48O5     ÏàËÆ¶È:60%
Natural Product Research          2003          17          247-251
Emodinol, ß-Glucuronidase Inhibiting Triterpene from Paeonia Emodi
Naheed Riaz; Itrat Anis; Aziz-ur-Rehman; Abdul Malik; Zaheer Ahmed; Pir Muhammad; Shahida Shujaat; Atta-ur-Rahman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     corosolic acid
    ÏàËÆ¶È:60%
China Journal of Chinese Materia Medica          2009          34          867-870
Chemical constituents from roots of Phlamis umbrosa
LIU Pu, DENG Ruixue, DUAN Hongquan, YIN Wei ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     hederagenin
    ÏàËÆ¶È:60%
China Journal of Chinese Materia Medica          2009          34          867-870
Chemical constituents from roots of Phlamis umbrosa
LIU Pu, DENG Ruixue, DUAN Hongquan, YIN Wei ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     belleric acid
    ÏàËÆ¶È:60%
China Journal of Chinese Materia Medica          2009          34          867-870
Chemical constituents from roots of Phlamis umbrosa
LIU Pu, DENG Ruixue, DUAN Hongquan, YIN Wei ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     maslinic acid
C30H48O4     ÏàËÆ¶È:60%
China Journal of Chinese Materia Medica          2006          31          1875-1879
Triterpenes from herb of Potentilla chinesis
LIU Pu, DUAN Hongquan, PAN Qin, ZHANG Yanwen, YAO Zhi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     2¦Á,3¦Á-dihydroxyolean-12-en-28-oic acid
C30H48O4     ÏàËÆ¶È:60%
China Journal of Chinese Materia Medica          2006          31          1875-1879
Triterpenes from herb of Potentilla chinesis
LIU Pu, DUAN Hongquan, PAN Qin, ZHANG Yanwen, YAO Zhi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     oleanolic acid
    ÏàËÆ¶È:60%
China Journal of Chinese Materia Medica          2004          29          237-239
Studies on chemical constitutents in roots of Jasminum sambac
ZHANG Zhengfu, BIAN Baolin, YANG Jian, TIAN Xiufeng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     cycloartan-3,23,29-triol 3,29-disodium sulfate
C30H50O9S2Na2     ÏàËÆ¶È:60%
Journal of Natural Products          1994          Vol 57          74
New Cycloartanol Sulfates from the Alga Tydemania expeditionis: Inhibitors of the Protein Tyrosine Kinase pp60v-src
Meledath Govindan, Syed A. Abbas, Francis J. Schmitz, Rita H. Lee, Jacqueline S. Papkoff, Doris L. Slate
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     28-hydroxy-olean-12-en-3,11-dione
    ÏàËÆ¶È:60%
China Journal of Chinese Materia Medica          2010          35          1001-1003
Chemical constituents from Sinacalia davidii
LAN Xiaocong; WU Haibo; WANG Wenshu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     compound 1a
    ÏàËÆ¶È:60%
Steroids          1984          43          639-649
24¦Î-Methyl-5¦Á-cholestane-3¦Â,5,6¦Â.22r.24-pentol 6-acetate: New polyhydroxylated sterol from the soft coral asterospicularia randalli.
Mohamad B. Ksebati, Francis J. Schmitz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     2¦Á,3¦Â,23-trihydroxy olean-12-en-28-oic acid
    ÏàËÆ¶È:60%
Chinese Traditional and Herbal Drugs          2010          41          11-14
Studies on constituents from pericarps of Juglans mandshurica with anti-tumor activity
ZHOU Yuan-yuan; WANG Dong; NIU Feng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     2¦Á,3¦Â-23-trihydroxyolean-12-en-28-oic acid
    ÏàËÆ¶È:60%
Chinese Traditional and Herbal Drugs          2010          41          1612-1615
Studies on chemcial constituents in Patrinia scabiosaefolia
XIA Ming-wen; TAN Jing-jing; YANG Ling; SHANG Zhen-ping; ZHAO Qing-chun; SHI Guo-bing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     arjunolic acid
C30H50O5     ÏàËÆ¶È:60%
Chinese Traditional and Herbal Drugs          2009          40          1696-1700
Chemical constituents in roots of Myrica nana
WANG Jun-feng; ZHONG Hui-mi; CHENG Yong-xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     2¦Á-ôÇ»ùÆë¶Õ¹ûËá
C30H48O4     ÏàËÆ¶È:60%
Chinese Traditional and Herbal Drugs          2008          39          978-981
ÈÕ±¾Â·±ßÇàµÄ»¯Ñ§³É·ÖÑо¿
ÕÔ¾§;¸ßÎÄÔ¶;¶ÎºêȪ;ëø½Ü;¸ßʯϲ¾Ã
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     cycloart-23-ene-3¦Â,25-diol
    ÏàËÆ¶È:60%
Chinese Traditional and Herbal Drugs          2005          36          669-671
ÌÙ¿à²Î»¯Ñ§³É·ÖÑо¿(¢ò)
ÕÅÁÕ,ÐìÀöÕä,ÑîÊÀÁÖ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     Salvin B
    ÏàËÆ¶È:60%
Archives of Pharmacal Research          2006          29          195-198
New butyrylcholinesterase inhibitory triterpenes from Salvia santolinifolia
Sajid Mehmood, Naheed Riaz, Sarfraz Ahmed Nawaz, Nighat Afza and Abdul Malik, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     compound 6
C30H48O3     ÏàËÆ¶È:60%
Chemistry of Natural Compounds          2010          46          686-691
Constituents of fruit pulp of Maytenus salicifolia and complete 1D/2D NMR data of 3¦Â-hydroxy-D:B-friedo-olean-5-ene
Frederico N. Valladao, Roqueline R. S. de Miranda, Gabriela S. de Oliveira, Gracia D. F. Silva and Lucienir P. Duarte, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
54 .     oleanolic acid
    ÏàËÆ¶È:60%
Natural Product Research and Development          2007          19          807-808
Chemical Constituents of Incarvillea arguta
ZHOU Da-ying;YANG Xiao-sheng; YANG Bo; ZHU Hai-yan; HAO Xiao-jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
55 .     compound 3
C30H50O4     ÏàËÆ¶È:60%
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