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ÈܼÁ ë®´úÂÈ·Â 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 ²éѯ½á¹û£º ÈܼÁ:CDCl3 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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. 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²éѯ½á¹û£º¹²²éµ½5339¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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