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meitianyxsÖ÷¹ÜÇø³¤
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άÆÕÇóÖú ÒÑÓÐ1È˲ÎÓë
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| 15.3, 15.8, 16.0, 16.2, 17.9, 21.7, 22.6, 23.1, 23.9, 25.0, 27.7, 30.2, 31.9, 33.1, 37.1, 37.7, 39.0, 39.3, 39.5, 41.3, 41.5, 42.0, 44.0, 55.1, 64.4, 65.5, 73.2, 103.8, 122.0, 125.6, 138.0, 143.9, 153.1. |
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ר¼Ò¾Ñé: +726 - PhEPI: 3
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meitianyxs: ½ð±Ò+15, ¡ïÓаïÖú 2014-01-07 14:26:48
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meitianyxs: ½ð±Ò+15, ¡ïÓаïÖú 2014-01-07 14:26:48
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½7291¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 230 ÏàËÆ¶È:72.7% Phytochemistry 1994 37 1517-1575 13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features Shashi B. Mahato, Asish P. Kundu Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 255 ÏàËÆ¶È:72.7% Phytochemistry 1994 37 1517-1575 13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features Shashi B. Mahato, Asish P. Kundu Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 2¦Á,3¦Á,24-ÈýôÇ»ù-12-Ï©-28-ÎÚËÕËá(2¦Á,3¦Á,24-trihydr-oxyurs-12-en-28-oic acid) ÏàËÆ¶È:72.7% Chinese Traditional and Herbal Drugs 2011 42(5) 841-843 Chemical constituents in root of Actinidia chinensis CHEN Xiao-xiao, YANG Shang-jun, BAI Shao-yan Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . methyl 2¦Á,3¦Á,24-trihydroxyursa-12,20(30)-dien-28-oate C37H54O8 ÏàËÆ¶È:72.7% Phytochemistry 1987 26 1107-1111 Pentacyclic triterpenoids from Prunella vulgaris Hisashi Kojima,Hideo Tominaga,Shigeki Sato,Haruo Ogura Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . methyl 2¦Á,3¦Á,24-trihydroxyurs-12-en-28-oate C31H50O5 ÏàËÆ¶È:72.7% Phytochemistry 1987 26 1107-1111 Pentacyclic triterpenoids from Prunella vulgaris Hisashi Kojima,Hideo Tominaga,Shigeki Sato,Haruo Ogura Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 2 ÏàËÆ¶È:72.7% Phytochemistry 1981 20 2436-2438 13C nmr spectra of some serjanic acid derivatives M. Alvarado, M. Moreno, V. M. Rodr¨ªguez Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 5e C33H52O6 ÏàËÆ¶È:72.7% Phytochemistry 1983 22 2547-2552 Terpenoids of Rhododendron japonicum Jinsaku Sakakibara, Toyo Kaiya Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 30-chloro-3¦Â-acetoxy-22¦Á-hydroxyl-20(21)-taraxastene C32H51O3Cl ÏàËÆ¶È:72.7% Molecules 2012 17 12895-12909 Secondary Metabolites from Two Species of Tolpis and Their Biological Activities Jorge Triana, Mariana L¨®pez, Francisco Javier P¨¦rez, Milagros Rico, Aroa L¨®pez, Francisco Est¨¦vez, Mar¨ªa Teresa Marrero, Ignacio Brouard and Francisco Le¨®n Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3-Oacetyloleanolic acid ÏàËÆ¶È:72.7% Journal of Chinese Medicinal Materials 2011 34 1540-1544 Study on the Triterpenoids from the Fruits of Ligustrum lucidum FENG Jing, FENG Zhi-yi, WANG Jun-ming, CUI Ying Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 1a ÏàËÆ¶È:70.5% Journal of Natural Products 1985 Vol 48 128-131 Secondary Metabolites from Satureja Species. New Triterpenoid from Satureja acinos Javier Escudero, J. Crist¨®bal L¨®pez, Rosa Maria Rabanal, Serafi¨½ Valverde Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3¦Â-acetoxy-20-taraxasten-22¦Á-ol C32H52O3 ÏàËÆ¶È:69.6% Journal of Natural Products 2000 63 898-901 Taraxastane-Type Triterpenes from the Aerial Roots of Ficus microcarpa Y. M. Chiang and Y. H. Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 3¦Â-O-{¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-glucopyranosyl-(1¡ú4)-[¦Â-D-glucopyranosyl-(1¡ú2)]-¦Á-L-arabinopyranosyl}-28,30-dihydroxyolean-12-ene C53H88O21 ÏàËÆ¶È:69.6% Planta Medica 2009 75 70-75 Triterpenoid Saponins from Ardisia pusilla and their Cytotoxic Activity Ye Tian, Hai-Feng Tang, Feng Qiu, Xiao-JuanWang, Xiao-Li Chen, Ai-DongWen Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Oleanolic acid C30H48O3 ÏàËÆ¶È:69.6% Chemistry of Natural Compounds 2004 40 137-140 PHYTOCHEMICAL STUDIES OF Berberis vulgaris S. Saied and S. Begum Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 3¦Â,24-Dihydroxyurs-12-en-28-oic acid methyl ester C31H50O4 ÏàËÆ¶È:69.6% Journal of Natural Products 1987 Vol 50 63 Plant Anticancer Agents, XLIV. Cytotoxic Constituents from Stizophyllum riparium Chang-Yih Duh, John M. Pezzuto, A. Douglas Kinghorn, Sai L. Leung, Norman R. Farnsworth Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . soyasapogenol B ÏàËÆ¶È:69.6% Journal of Natural Products 1990 Vol 53 298 Sapogenin Structure: Analysis of the 13C- and 1H-nmr Spectra of Soyasapogenol B Robert L. Baxter, Keith R. Price, G. Roger Fenwick Structure 13C NMR ̼Æ×Ä£Äâͼ |

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