| ²é¿´: 465 | »Ø¸´: 1 | ||
×ÏÒÂÇáÆïľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖú»¯ºÏÎï ÒÑÓÐ1È˲ÎÓë
|
|
ÈܼÁDMSO Êý¾ÝÈçÏ£º 16.8,17.3,18.3,18.4,23.1,23.5,23.8,26.1,27.6,28.9,30.9,32.6,32.7,33.3,33.8,38.0,39.3,40.6,41.3,41.8,45.9,46.1,47.4,47.9,54.9,65.2,84.0,115.6,116.2,121.8,125.7,130.6,144.5,160.1,167.1,179.1 |
» ²ÂÄãϲ»¶
308Çóµ÷¼Á
ÒѾÓÐ20È˻ظ´
ÖпÆÔº×Ü·Ö315Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á ²ÄÁÏÓ빤³Ì 324·Ö ר˶
ÒѾÓÐ3È˻ظ´
»¯Ñ§¹¤³ÌÓë¼¼Êõ324µ÷¼Á
ÒѾÓÐ15È˻ظ´
Ò»Ö¾Ô¸¿ó´ó£¬²ÄÁϹ¤³Ìר˶314·Ö£¬0856¿Éµ÷¶¼¿ÉÒÔ
ÒѾÓÐ12È˻ظ´
»·Ñõ¹à·â½º ¿¹³Á¼Á
ÒѾÓÐ4È˻ظ´
268·Ö085602»¯Ñ§¹¤³Ìµ÷¼Á
ÒѾÓÐ22È˻ظ´
¿¼Ñе÷¼Á
ÒѾÓÐ18È˻ظ´
»¹Óл¯¹¤¶þÂÖµ÷¼ÁµÄѧУÂð
ÒѾÓÐ39È˻ظ´
277 ÊýÒ»104£¬Ñ§Ë¶£¬Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
÷´º
½ð³æ (ÕýʽдÊÖ)
- Ó¦Öú: 242 (´óѧÉú)
- ½ð±Ò: 1940.6
- É¢½ð: 48
- ºì»¨: 3
- Ìû×Ó: 465
- ÔÚÏß: 121.1Сʱ
- ³æºÅ: 1536801
- ×¢²á: 2011-12-14
- ÐÔ±ð: MM
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
×ÏÒÂÇáÆï: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-09 21:10:01
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
×ÏÒÂÇáÆï: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-09 21:10:01
|
1 . liensinine ÏàËÆ¶È:97.2% 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 2 . 3-O-trans-p-coumaroyl maslinic acid ÏàËÆ¶È:97.2% Journal of Shenyang Pharmaceutical University 2013 30 851-857 Isolation and identification of triterpenes of fruit of Rosa laevigata Michx£® LIU Xue-gui, ZHANG Wen-chao, JIN Mei, WU Zhi-yu, MU Xiao-kun, GAO Pin-yi* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 3-O-cis-p-coumaroyl maslinic acid ÏàËÆ¶È:97.2% Journal of Shenyang Pharmaceutical University 2013 30 851-857 Isolation and identification of triterpenes of fruit of Rosa laevigata Michx£® LIU Xue-gui, ZHANG Wen-chao, JIN Mei, WU Zhi-yu, MU Xiao-kun, GAO Pin-yi* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 3¦Â-·´Ê½¶ÔôÇ»ùÈâ¹ðõ£Ñõ»ù-2¦Á-ôÇ»ùÆë¶Õ¹ûËá ÏàËÆ¶È:92.3% 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 5 . 3¦Â-O-trans-p-coumaroyl-2¦Á-hydroxy-olean-12-en-28-oic acid ÏàËÆ¶È:92.3% Journal of Shenyang Pharmaceutical University 1997 14 111-114 A Study on the Chemical Constituents of Ligustrum Lucidum Ait. Tian Yan, Wu Lijun, Yang Wuxi, Wu Haiou, Huang Qi, Dai Xiaobing, Tai Yongshan, Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 3¦Â-trans-p-coumaroyloxy-2¦Á-hydroxy oleanolic acid ÏàËÆ¶È:92.1% Lishizhen Medicine and Materia Medica Research 2012 23 1568-1569 Å®ÕêÒ¶ÈýÝÆÀ໯ѧ³É·ÖÑо¿ ʯ¾²; ÐìÔÆÁá; Äô¾§ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . p-methoxybenzyl(2¦Á,3¦Â)2,3-dihydroxy-olean-12-en-28-oate C38H56O5 ÏàËÆ¶È:91.6% Bioorganic & Medicinal Chemistry 2014 22 594-615 Towards cytotoxic and selective derivatives of maslinic acid Bianka Siewert, Elke Pianowski, Anja Obernauer, Ren¨¦ Csuk Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 3-O-trans-pcoumaroylmaslinic acid ÏàËÆ¶È:89.7% Planta Medica 1997 63 47-50 Isolation and Structural Elucidation of Acylated Pentacyclic Triterpenoids from the Leaves of Eucalyptus camaldulensis var. obtusa Bina S. Siddiqui, Farhat, Sabira Begum, and Salimuzzaman Siddiqui Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 3¦Â-(p-hydroxy-trans-cinnamoyloxy)olean-12-en-28-oic acid C39H54O5 ÏàËÆ¶È:89.1% Planta Medica 1993 59 369-372 A New Oleanolic Acid Derivative from Securinega tinctoria LuisM. Carvalho and J. Seita Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 3¦Â-hydroxy-27-p-(Z)-coumaroyloxyolean-12-en-28-oic acid ÏàËÆ¶È:89.1% Natural Product Research and Development 2009 21 593-599 Chemical Constituents of Osmanthus yunnanensis MA Xiao-li;LIN Wen-bing; ZHANG Guo-lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . (4-oxa-4-phenyl)-butyl(2¦Á,3¦Â)2,3-dihydroxy-olean-12-en-28-oate C39H58O5 ÏàËÆ¶È:89.1% Bioorganic & Medicinal Chemistry 2014 22 594-615 Towards cytotoxic and selective derivatives of maslinic acid Bianka Siewert, Elke Pianowski, Anja Obernauer, Ren¨¦ Csuk Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 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 13 . ¹³ÌÙËá E ÏàËÆ¶È:88.8% Chinese Journal of Medicinal Chemistry 2007 17 108-110 Chemical constituents of Gelsemium elegans Benth. HUA Wei, GUO Tao, ZHANG Lin, WU Li-jun, ZHAO Qing-chun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . p-fluorobenzyl(2¦Á,3¦Â)2,3-dihydroxy-olean-12-en-28-oate C37H53FO4 ÏàËÆ¶È:88.8% Bioorganic & Medicinal Chemistry 2014 22 594-615 Towards cytotoxic and selective derivatives of maslinic acid Bianka Siewert, Elke Pianowski, Anja Obernauer, Ren¨¦ Csuk Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . p-nitrobenzyl(2¦Á,3¦Â)2,3-dihydroxy-olean-12-en-28-oate C37H53NO6 ÏàËÆ¶È:88.8% Bioorganic & Medicinal Chemistry 2014 22 594-615 Towards cytotoxic and selective derivatives of maslinic acid Bianka Siewert, Elke Pianowski, Anja Obernauer, Ren¨¦ Csuk Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . ¨¢cido 3-O-trans-p-cumaroil-masl¨ªnico C39H54O6 ÏàËÆ¶È:87.1% Qu¨ªmica Nova 2002 25 349-352 Triterpenes from Styrax camporum (styracaceae) Pauletti, Patr¨ªcia Mendonça; Ara¨²jo, Angela Regina; Bolzani, Vanderlan da Silva; Young, Maria Claudia Marx Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 3¦Â-O-(trans-p-Coumaroyl)-2¦Á-hydroxy oleanolic acid C39H54O6 ÏàËÆ¶È:86.8% China Pharmacy 2011 22 2931-2933 Chemical Constituents of Ligustrum lucidum ZHANG Ting-fang, DAI Yi, YAO Xin-sheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . diospyrosooleanolide C39H54O6 ÏàËÆ¶È:86.4% Phytochemistry 2004 65 2153-2158 Coumaroyl triterpene lactone, phenolic and naphthalene glycoside from stem bark of Diospyros angustifolia Arunendra Pathak, Dinesh K. Kulshreshtha, Rakesh Maurya Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . 3¦Â-cis-p-coumaroyloxy-2¦Á,23-dihydroxyolean-12-en-28-oic acid C39H54O7 ÏàËÆ¶È:86.4% 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 20 . 3¦Â-trans-p-coumaroyloxy-2¦Á,23-dihydroxyolean-12-en-28-oic acid C39H54O7 ÏàËÆ¶È:86.4% 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 |
2Â¥2015-03-09 15:57:18













»Ø¸´´ËÂ¥