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baojingm½ð³æ (СÓÐÃûÆø)
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[ÇóÖú]
΢Æ×ÇóÖú£¬ÔÚÏßµÈ £¡£¡ ÒÑÓÐ1È˲ÎÓë
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| 13C NMR (101 MHz,Pyridine) ¦Ä 15.98,17.25,17.54,18.86,23.25,24.23,24.51,26.41,26.55,28.60,31.62,32.19,33.08,33.81,35.08,37.43,37.99,38.54,38.78,40.45,42.37,43.05,47.42,48.17,55.89,69.05, 80.90,116.18,117.27,122.68,126.59,131.10,145.40,145.49,161.88,167.66 |
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baojingm: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2015-03-14 11:39:30
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baojingm: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2015-03-14 11:39:30
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1 . 3¦Â-O-trans-coumaroyl-12-en-28-oleanolic acid ÏàËÆ¶È:89.1% Natural Product Research and Development 2014 26 1345-1349 Isolation,Structural Identification and Bioactivity of Chemical Constituents from the Bark of Eucalyptus exserta F. Muell LI Jing-jing, XU Han-hong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . erythrodiol 3¦Â-caffeate ÏàËÆ¶È:87.1% Phytochemistry 1994 37 795-799 Triterpene caffeates from bark of Betula pubescens Hefeng Pan, Lennart N. Lundgren, Rolf Andersson Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 3¦Â-O-¶ÔôÇ»ù-·´-Èâ¹ðõ£-Æë¶Õ¹ûËá(3¦Â-O-(p-hydroxy-(E)-cinnamoyl)-1-oleanen-28-oic acid) C39H54O5 ÏàËÆ¶È:84.6% Chemical Journal of Chinese Universities 2003 24 2022-2023 New Triterpenoids from Helicteres Angustifolia GUO Xin-Dong,AN Lin-Kun, XU DI, MA Lin, GU Lian-Quan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . triterpenoid A ÏàËÆ¶È:84.6% Phytochemistry 1988 27 233-235 3¦Â-(3,4-Dihydroxycinnamoyl)-erythrodiol and 3¦Â-(4-hydroxycinnamoyl)-erythrodiol from Larrea tridentata Xue Hui-Zheng,Lu Zhi-Zhen,Konno Chohachi,D.Doel Soejarto,Geoffrey A. Cordell,Harry H.S. Fong,Wendy Hodgson Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . trans-hydroxycinnamoyl ester of amyrin C39H56O3 ÏàËÆ¶È:83.7% Journal of Natural Products 1997 60 1150-1151 Triterpene Esters from Australian Acacia Marina Ali, Andrew Heaton, and David Leach Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 3¦Â-O-(p-hydroxy-(E)-cinnamoyl)-1-oleanen-28-oic acid ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2015 46 174−177 A new coumarins from residue of Glycyrrhiza uralensis LU Jing-jing, CAO Jia-qing, LI Wei, NIU Xiu-li, ZHAO Yu-qing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 3¦Â-(3,4-dihydroxycinnamoyl)-erythrodiol C39H56O5 ÏàËÆ¶È:82.0% Journal of Ethnopharmacology 2004 95 405-407 3¦Â-(3,4-Dihydroxycinnamoyl)-erythrodiol, a cytotoxic constituent of Zygophyllum geslini collected in the Algerian Sahara Dalila Smati, Arlette Longeon, Mich¨¨le Guyot Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 23-trans-p-coumaroyloxy-2¦Á,3¦Á-dihydroxy-olean-12-en-28-oic acid C39H54O7 ÏàËÆ¶È:81.0% Bioorganic & Medicinal Chemistry Letters 2010 20 1944-1947 Bioactivity-guided isolation of cytotoxic triterpenoids from the trunk of Berberis koreana Ki Hyun Kim, Sang Un Choi, Kang Ro Lee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . liensinine ÏàËÆ¶È:81.0% Chinese Traditional and Herbal Drugs 1998 29 367-369 NMR Study of 3¦Â-(p-hydroxy trans cinnamoyloxy)-2¦Á-hydroxy-oleanlic acid Wu Lijun; Xiang Ting; Liu Tiehan; et al (Shenyang Pharmaceutical University; Shenyang); Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 3¦Â-acetoxy-28-hydroxyolean-12-ene ÏàËÆ¶È:80.5% Phytotherapy Research 2008 22 1303-1306 Triterpenoids and a sterol from the stem-bark of Styrax japonica and their protein tyrosine phosphatase 1B inhibitory activities Joo-Hee Kwon, Min-Jung Chang, Hyo-Won Seo, Jeong-Hun Lee, Byung-Sun Min, MinKyun Na, Jin Cheol Kim, Mi Hee Woo, Jae Sue Choi, Hyeong Kyu Lee and KiHwan Bae Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 3¦Â-·´Ê½¶ÔôÇ»ùÈâ¹ðõ£Ñõ»ù-2¦Á-ôÇ»ùÆë¶Õ¹ûËá ÏàËÆ¶È:79.4% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 3-O-(Z)-coumaroyl erythrodiol C39H56O4 ÏàËÆ¶È:79.4% Phytochemistry 1999 51 543-550 Coumaroyl triterpenes from Casuarina equisetifolia Hironobu Takahashi, Miho Iuchi, Yoshimi Fujita, Hiroyuki Minami, Yoshiyasu Fukuyama Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 12-oleanaen-3¦Â-caffeate ÏàËÆ¶È:79.4% China Journal of Chinese Materia Medica 2010 35 323-326 Immunosuppressive triterpenes from Tetraena mongolica DING Linlin; LIU Qiang; HU Jiaxu; TANG Sheng an; DUAN Hongquan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 3-O-caffeoyl oleanolic acid ÏàËÆ¶È:79.4% Molecules 2014 19 9515-9534 Studies on Cytotoxic Constituents from the Leaves of Elaeagnus oldhamii Maxim. in Non-Small Cell Lung Cancer A549 Cells Chi-Ren Liao, Yueh-Hsiung Kuo, Yu-Ling Ho, Ching-Ying Wang, Chang -Syun Yang, Cheng-Wen Lin and Yuan-Shiun Chang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 23-trans-p-coumaroyloxy-2¦Á,3¦Â-dihydroxyolean-12-en-28-oic acid C39H54O7 ÏàËÆ¶È:78.3% Phytochemistry 2001 58 121-127 Constituents of Eugenia sandwicensis with potential cancer chemopreventive activity Jian-Qiao Gu, Eun Jung Park, Lumonadio Luyengi, Michael E.Hawthorne,Rajendra G.Mehta, Norman R.Farnsworth, John M.Pezzuto,A.Douglas Kinghorn Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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