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²éѯ½á¹û£º¹²²éµ½1331¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ¦Â-amyrin-n-nonyl ether C39H68O ÏàËÆ¶È:82.0% Chemical & Pharmaceutical Bulletin 2010 58 1093-1095 Two New Aristolochic Acid Derivatives from the Roots of Aristolochia fangchi and Their Cytotoxicities Yu Cai and Tian-Ge Cai Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ¦Â-amyrin 3-margarate C47H82O2 ÏàËÆ¶È:76.9% Natural Product Research and Development 1998 10(3) 20-23 TWO NEW TRITERPENE ESTER FROM PRATIA BEGONIFOLIA Liu Xikui; Chiu Minghua; Li Zhongrong Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (3¦Â,11¦Á)-11-hydroxyolean-12-en-3-yl palmitate C46H80O3 ÏàËÆ¶È:75% Natural Product Research 2012 26 1869¨C1875 A new triterpene from Barringtonia asiatica Consolacion Y. Ragasa, Dinah L. Espineli & Chien-Chang Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ¦Â-amyrin 3-palmitate C46H50O2 ÏàËÆ¶È:74.3% Natural Product Research and Development 1998 10(3) 20-23 TWO NEW TRITERPENE ESTER FROM PRATIA BEGONIFOLIA Liu Xikui; Chiu Minghua; Li Zhongrong Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ¦Â-amyrin hexadecanate ÏàËÆ¶È:73.1% Chinese Traditional and Herbal Drugs 2001 32 6-9 Studies on triterpenoids and steroids from Balanophora involucrata XIA Xin zhong; HAN Hong xing; TU Peng fei Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Olean-12-en-3¦Â,16¦Â-diol-3-O-palmitate ÏàËÆ¶È:71.7% Pharmazie 2006 61 70-73 Triterpenoids from Pyrethrum tatsienense Yang Ai-Mei, Liu Xia, Lu Run-Hua and Shi Yan-Ping Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . oleanol 28-Aldehyde 3-O-¦Â-palmitate C46H78O3 ÏàËÆ¶È:71.7% Chemistry of Natural Compounds 2012 48 416-418 A new triterpenoid ester from Lobelia sessilifolia Jiaming Sun, Xiuli Wang, Hui Zhang and Junshan Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3¦Â-O-(8-Hydroxyoctanoyl)-12-oleanene C38H64O3 ÏàËÆ¶È:71.7% Journal of Agricultural and Food Chemistry 2010 58 4945-4950 New Triterpenoids and Other Constituents from a Special Microbial-Fermented Tea¡ªFuzhuan Brick Tea Tie-Jun Ling, Xiao-Chun Wan, Wei-Wei Ling, Zheng-Zhu Zhang, Tao Xia, Da-Xiang Li and Ru-Yan Hou Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3¦Â-palmitate-28-hydroxyl-¦Â-amyrin ÏàËÆ¶È:70.7% Chinese Tladitional Patent Medicine 2012 34 506-508 Chemical constituents from Gentiana farreri Ball. F. YANG Ai-mei, SUN Jing, HAN Han, SHI Xiao-long, XU Guo-qiang, ZHANG Xiao-ru Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . glut-5-ene-3¦Á-methylbutyrate C35H58O2 ÏàËÆ¶È:69.2% Planta Medica 1994 60 594-596 Biologically Active Compounds from the Euphorbiaceae; 2. Two Triterpenoids of Euphorbia cyparissias Sevil Oks¨¹z. Roberto R. Gil,Heebyung Chai,JohnM. Pezzuto, GeoffreyA. Cordell,and Ayhan Ulubelen Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 5a C30H52O3 ÏàËÆ¶È:69.2% Phytochemistry 1985 24 2359-2367 Triterpenoids from Mangifera indica V. Anjaneyulu, K. Harischandra Prasad, K. Ravi, J.D. Connolly Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 1¦Â-O-(4-Methoxy cinnamoyl)-15¦Á-hydroxy-¦Â-amyrin C40H56O4 ÏàËÆ¶È:69.2% Natural Product Research 2010 24 197-202 Triterpenoids from the stem bark of Rhizophora mucronata R. M. Rohini; Amit Kumar Das Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 3-O-oxtylmalonyl-3¦Á,25-dihydroxy-(20S,24R)-epox-ydammarane C41H70O6 ÏàËÆ¶È:68.2% Bioorganic & Medicinal Chemistry 2010 18 2964-2975 Papyriferic acid derivatives as reversal agents of multidrug resistance in cancer cells Juan Xiong, Masatoshi Taniguchi, Yoshiki Kashiwada, Michiko Sekiya, Takashi Yamagishi, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . ¦Á,¦Â-amyrin ÏàËÆ¶È:68.2% Natural Product Research and Development 2002 14(3) 1-6 STUDIES ON THE CHEMICAL CONSTITUENTS OF THE FLOWER OF CAMPSIS GRANDIFLORA (THUNB.)K.SCHUM.AND ITS CONTRACEPTIVE EFFECT ZHAO Qian; LIAO Mao chuan GUO Ji xian Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 3¦Â,24(S),25-trihydroxycycloartane and 3¦Â,24(R),25-trihydroxycycloartane ÏàËÆ¶È:68.2% Zeitschrift f¨¹r Naturforschung C 2004 59 15-18 Chemical Constituents of Euphorbia marschalliana Boiss. A. R. Jassbi, S. Zamanizadehnajari, and S. Tahara Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 1,1-dimethylethyl 6-[(2-cyano-3,12-dioxooleana-1,9(11)-dien-28-oyl)amino]hexylcarbamate C42H63N3O5 ÏàËÆ¶È:67.5% Journal of Medicinal Chemistry 2004 47 4923-4932 Design, Synthesis, and Biological Evaluation of Biotin Conjugates of 2-Cyano-3,12-dioxooleana-1,9(11)-dien-28-oic Acid for the Isolation of the Protein Targets Tadashi Honda, Tomasz Janosik, Yukiko Honda, Jie Han, Karen T. Liby, Charlotte R. Williams, Robin D. Couch, Amy C. Anderson, Michael B. Sporn, and Gordon W. Gribble Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . madhucic acid C38H60O5 ÏàËÆ¶È:66.6% Helvetica Chimica Acta 2004 Vol. 87 1194 Chemical Constituents from the Fruits of Madhuca latifolia Bina S. Siddiqui, Shazia Khan, M. Nadeem Kardar, and Huma Aslam Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 3¦Á-(E)-caffeoyloxyolean-12-en-30-oic acid C39H54O6 ÏàËÆ¶È:66.6% Journal of Natural Products 2008 71(5) 789-792 Oleanane-Type Triterpenes from the Flowers and Roots of Saussurea muliensis Chun-Mei Liu, He-Xiang Wang, Shi-Lei Wei, and Kun Gao Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 3¦Á-(E)-coumaroyloxyolean-12-en-30-oic acid C39H54O5 ÏàËÆ¶È:66.6% Journal of Natural Products 2008 71(5) 789-792 Oleanane-Type Triterpenes from the Flowers and Roots of Saussurea muliensis Chun-Mei Liu, He-Xiang Wang, Shi-Lei Wei, and Kun Gao Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . Cycloartan-3¦Â-(2-methyl butanoate) ÏàËÆ¶È:66.6% Molecules 2000 5 M163 Cycloeucalen-3¦Â-(2-methyl Butanoate). ew Cycloeucalen Isolated from the Espeletiabarclayana Cuatr (Asteraceae) Tellez Alba ohemi, Torrenegra Ruben, Pedrozo Julio and Mart¨ªnez Astrid Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 4-Butyl-5-N-cyclohexylcarboxamido-4-aza-5¦Á-cholestan-3-one C37H64N2O2 ÏàËÆ¶È:66.6% Steroids 2008 73 1270-1276 Synthesis of 4-azasteroids by an intramolecular Ugi reaction Fernando Alonso, Sof¨ªa L. Acebedo, Andrea C. Bruttomesso, Javier A. Ram¨ªrez Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 3¦Â-dodecanoyl erythrodiol C42H72O3 ÏàËÆ¶È:66.6% Acta Pharmaceutica Sinica 2009 Vol 44 1258−1261 A new erythrodiol triterpene fatty ester from Scorzonera mongolica WANG Bin; LI Guo-qiang; GUAN Hua-shi; YANG Li-ye; TONG Guo-zhong Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . compound 1a C39H51NO5 ÏàËÆ¶È:66.6% Phytochemistry 1993 32 1239-1244 Triterpenes of Poria cocos Takaaki Tai, Akira Akahori, Tetsuro Shingu Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . compound 3a C40H53NO5 ÏàËÆ¶È:66.6% Phytochemistry 1993 32 1239-1244 Triterpenes of Poria cocos Takaaki Tai, Akira Akahori, Tetsuro Shingu Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . compound 4a C40H55NO5 ÏàËÆ¶È:66.6% Phytochemistry 1993 32 1239-1244 Triterpenes of Poria cocos Takaaki Tai, Akira Akahori, Tetsuro Shingu Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . ¦Â-amyrin-3-palmitate C46H80O2 ÏàËÆ¶È:66.6% Chinese Journal of Natural Medicines 2007 5 259-262 Non-alkaline Constituents From the Leaf of Alstonia scholaris DU Guo-Shun; CAI Xiang-Hai; SHANG Jian-Hua; LUO Xiao-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 4¦Â-demethyl-24-methylenecy-cloartanyl 3¦Â-p-hydroxy-m-methoxy-trans-cinnamate C40H58O4 ÏàËÆ¶È:66.6% Journal of the Indian Chemical Society 1993 70 543-548 Jatrocurin,a New Tetracyclic Triterpene from Jatropha curcas SUNIL K.TALAPATRA.KABITA MANDAL and BANI TALAPATRA Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . compound 1d C41H62O4 ÏàËÆ¶È:66.6% Journal of the Indian Chemical Society 1991 68 88-91 Arundinol,A New Triterpene from the Orchid Arundina bambusifolia P.L.MAJUMDER and SABARI GHOSAL Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . 3¦Á-Succinyl-14-taraxeren-28-oic acid C34H52O6 ÏàËÆ¶È:66.6% Journal of Asian Natural Products Research 2013 15 515-524 Anti-HIV and NO production inhibition activities of epi-aleuritolic acid derivatives Jia-Bao Liu, Ying Zhang, Bao-Song Cui, Ying-Li Cao, Shao-Peng Yuan, Ying Guo, Qi Hou & Shuai Li Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . ¦Á-amyrin hexacosoate ÏàËÆ¶È:65.9% Journal of Chinese Pharmaceutical Sciences 2000 9 131-133 A New Triterpene from Rosemary (Rosmarinus officinalis) Zhou Qunfang, Xu Zhanhui, Tu Pengfei, Li Gansun and Chen Hongming Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . Cholesteryl-9,10-dihydroxystearate C45H80O4 ÏàËÆ¶È:65.9% Steroids 2008 73 1098-1109 Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1] Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . ¦Â-ÏãÊ÷Ö¬ËØ×Ø¸éËáõ¥ ÏàËÆ¶È:65.9% Chinese Traditional and Herbal Drugs 2006 37 338-340 Chemical constituents in Ixeridium gramineum LIU Jun-xi; WEI Xiao-ning; LU Run-hua; SHI Yan-ping Structure 13C NMR ̼Æ×Ä£Äâͼ |

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