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¶¹¸ç: ½ð±Ò+2, лл²ÎÓë½»Á÷ 2012-05-15 20:38:27
myvalerie: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ¶àлÁË£¡ 2012-05-15 21:02:37
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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 16.10,16.75,18.31,19.76,22.31,23.62,25.12,25.71,27.22,28.20,30.40,32.45,33.04,36.53,37.27,38.28,39.51,41.13,41.97,42.35,44.79,46.00,47.61,49.29,55.71,64.34,76.33,80.35,122.25,143.71 ÈܼÁÑ¡Ï È«²¿ CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O (CH3)4Si C4D8O2 CD3COOD C4D8O2 H2O D2O CF3COOD CD3OD ND3 CD3COCD3 C6D6 CD3CN ²éѯ¿ÕÖµ Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½815¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . soyasapogenol C30H50O3 ÏàËÆ¶È:96.6% Acta Pharmaceutica Sinica 1993 28 116-121 STUDIES ON THE TRITERPENOIDS FROM ROOTS OF GLYCYRRHIZA SQUAMULOSA FROANCH H Liang and RY Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . Soyasapogenol B C30H50O3 ÏàËÆ¶È:96.6% Journal of Asian Natural Products Research 2005 7 237-243 Three new isoprenylated flavonoids from the roots of Sophora flavescens PEI-LAN DING, AI-JUN HOU and DAO-FENG CHEN Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Soyasapogenol B ÏàËÆ¶È:96.6% Phytochemistry 1996 41 1573-1577 Triterpenoids from Melilotus messanensis; soyasapogenol G, the first natural carbonate derivative Francisco A. Mac¨ªas*, Ana M. Simonet, M. Dolores Esteban, Juan Carlos G. Galindo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . soyasapogenol B ÏàËÆ¶È:96.6% Phytochemistry 1992 31 1773-1777 Saponins from Trifolium repens Shiho Sakamoto, Sanae Kofuji, Masanori Kuroyanagi, Akira Ueno, Setsuko Sekita Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . soyasapogenol B ÏàËÆ¶È:96.6% China Journal of Chinese Materia Medica 2010 35 607-609 Chemical constituents in Flos Sophorae Carbonisatus LI Raorao*; WANG Caifang; LEI Peilin; HUANG Lanlan; YUAN Sitong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . Soyasapogenol B ÏàËÆ¶È:96.6% Chinese Journal of Medicinal Chemistry 2008 18 142-156 Chemical constituents of processed Astragalus membranaceus Bunge LIU Wei, WANG Zhi-cheng, LIANG Fei-fei, LI Xian, WANG Jin-hui Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 12-oleanene-3,22,24-triol ÏàËÆ¶È:96.6% Chinese Journal of Medicinal Chemistry 2010 20 201-205 Chemical constituents from themycelium of a new streptomycete ZHENG Dan, JIANG Yi, HAN Li, LOU Kai, CHEN Yun, XU Li-hua, HUANG Xue-shi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . soyasapogenol B ÏàËÆ¶È:96.6% Journal of Shenyang Pharmaceutical University 2010 27 797-802 Isolation and identification of whole plant of chemical constituents from Trifolium repens L. SUN Lin, LI Zhan-lin, PENG Jing-bo, HAN Guo-hua, HUA Hui-ming Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . soyasapogenin B ÏàËÆ¶È:96.6% Russian Chemical Bulletin 2001 50 1107-1112 Secondary metabolites of Astragalus danicus Retz. and A. inopinatus Boriss. A. S. Gromova, V. I. Lutsky, J. G. Cannon, D. Li and N. L. Owen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . soyasapogenol ÏàËÆ¶È:93.5% Chinese Pharmaceutical Sciences 2005 14 75-78 Chemical Constituents of Hedysarum gmelinii LIU Yi; MA Xiao-xia; CHEN Hu-biao; TU Guang-zhong; HE Jiu-ming; and ZHAO Yu-ying Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . soyasapogenol B ÏàËÆ¶È:93.3% 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 -------------------------------------------------------------------------------- 12 . myrioside C C42H66 ÏàËÆ¶È:86.6% Chemical & Pharmaceutical Bulletin 2002 50(8) 1097-1099 Five Triterpene Glycosides from Oxytropis myriophylla Masafumi OKAWA,Rie YAMAGUCHI, Hurlad DELGER,Ryota TSUCHIHASHI, Toshihiro NOHARA,Junei KINJO, Susumu ISODA, and Yoshiteru IDA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . myrioside D C47H74O19 ÏàËÆ¶È:86.6% Chemical & Pharmaceutical Bulletin 2002 50(8) 1097-1099 Five Triterpene Glycosides from Oxytropis myriophylla Masafumi OKAWA,Rie YAMAGUCHI, Hurlad DELGER,Ryota TSUCHIHASHI, Toshihiro NOHARA,Junei KINJO, Susumu ISODA, and Yoshiteru IDA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . soyasapogenol B ÏàËÆ¶È:86.6% 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 -------------------------------------------------------------------------------- 15 . soyasapogenol B ÏàËÆ¶È:86.6% Phytochemistry 1991 30 3389-3393 Triterpenoid saponins from Medicago hispida Sashi B. Mahato Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . azukisapogenol ÏàËÆ¶È:86.6% Chemical Research in Chinese Universities 1988 4 39-43 Studies on the Chemical Constituents of Oxytropis Glabra DC(I) Sun Rongqi,Jia Zongjian and Zhu Ziqing;Chen Nenyu and Zhao Fanzhi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 3-O-[¦Á-L-rhamnopyranosyl(1¡ú2)-¦Â-D-glucopyranosyl(1¡ú4)-¦Â-D-glucuronopyranosyl]-soyasapogenol B ÏàËÆ¶È:86.6% Acta Chimica Sinica 1987 45 145-149 Studies on the Chemical Components of Oxtropis ochrocephala Bunge II. The Structures of Two Triterpenoid Saponins Sun Rong-Qi Cheng Dong-Liang Jia Zhong-JianZhu Zi-Qing Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . soyasapogenol B ÏàËÆ¶È:83.3% Planta Medica 1991 57 94-95 Phaseoluside-A, A New Soyasapogenol B Triglucoside from Phaseolus vulgaris Seeds Dharam C. fain, PawanK Agrawal, and Raghunath S. Thakur Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . soyasapogenol A ÏàËÆ¶È:83.3% Chemical & Pharmaceutical Bulletin 1995 43 1176-1179 Oleanene-Type Triterpene Glycosides from Puerariae Radix. II. Isolation of Saponins and the Application of Tandem Mass Spectrometry to Their Structure Determination Tomonori ARAO,Junei KINJO,Toshihiro NOHARA and Ryuichi ISOBE Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . soyasapogenol A ÏàËÆ¶È:83.3% Chemical & Pharmaceutical Bulletin 1994 42 1874-1878 Five New Triterpene Glycosides from Russell Lupine Junei KINJO,Fumiko KISHIDA,Kazutaka WATANABE,Fumio HASHIMOTO and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . soyasapogenol B ÏàËÆ¶È:83.3% Chemical & Pharmaceutical Bulletin 1989 37 1550-1553 Studies on the Constituents of Leguminous Plants. XI. : The Structures of New Triterpenoids from Wistaria brachybotrys SIEB. et ZUCC. Takao KONOSHIMA,Mutsuo KOZUKA,Mitsumasa HARUNA,Kazuo ITO and Takeatsu KIMURA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . soyasapogenol A ÏàËÆ¶È:83.3% Chemical & Pharmaceutical Bulletin 1985 33 1293-1296 OLEANENE-SAPOGENOLS FROM PUERARIAE RADIX Junei Kinjo,Izumi Miyamoto,Kotaro Murakami,Kiyoshi Kida,Toshiaki Tomimatsu,Masaki Yamasaki and Toshihiro Nohara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . Soyasapogenol A ÏàËÆ¶È:83.3% Chemistry of Natural Compounds 1992 28 1-23 13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES A. I. Kalinovskii Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . 3¦Á,22¦Â-dihydroxyolean-12-ene C30H50O2 ÏàËÆ¶È:83.3% Natural Product Research 2002 16 415-418 Alysinol - A New Triterpene from Alysicarpus Monolifer Naheed Riaz; Itrat Anis; Pir Muhammad Khan; Raza Shah; Abdul Malik Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . soyasapogenol A ÏàËÆ¶È:83.3% Chemical & Pharmaceutical Bulletin 1997 45 362-366 Oleanene-Type Triterpene Glycosides from Puerariae Radix. IV. Six New Saponins from Pueraria lobata Tomonori ARAO,Junnei KINJO,Toshihiro NOHARA and Ryuichi ISOBE Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . Melilotigenin C C30H48O3 ÏàËÆ¶È:83.3% Phytochemistry 1998 49 709-717 Bioactive polar triterpenoids from Melilotus messanensis Francisco A. Mac¨ªas, Ana M. Simonet, Juan Carlos G. Galindo, Pedro C. Pacheco, Jose A. S¨¢nchez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . katonic acid ÏàËÆ¶È:83.3% Journal of Natural Products 1992 Vol 55 654 Plant Anticancer Agents, L. Cytotoxic Triterpenes from Sandoricum koetjape Stems Norito Kaneda, John M. Pezzuto, A. Douglas Kinghorn, Norman R. Farnsworth, Thawatchai Santisuk, Patoomratana Tuchinda, Jinda Udchachon, Vichai Reutrakul Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . soyasapogenol A ÏàËÆ¶È:83.3% 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 -------------------------------------------------------------------------------- 29 . olean-12-ene-1¦Â-24-diol C30H50O3 ÏàËÆ¶È:83.3% Zeitschrift f¨¹r Naturforschung B 2008 63b 101-104 Sigmoiside F and Propyloxyamyrin, Two New Triterpenoid Derivatives from Erythrina sigmoidea (Fabaceae) Jacques Kouam, Alain L. Meli, Muhammad I. Choudhary, and Zacharias T. Fomum Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . soyasapogenol B ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2010 41 187-190 Studies on chemical constituents of Oxytropis kansuensis GONG Hong-fei; YANG Ai-mei; LIU Jun-xi; DI Duo-long Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . olean-12-en-3¦Â,24-diol ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2007 38 32-34 ºì³µÖá²ÝµÄ»¯Ñ§³É·ÖÑо¿ Ë÷Ö¾ÐÂ;˹½¨ÓÂ;ÉòÁ¬¸Ö;ÍõÈ𻢠Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . compound 10a C44H62O3 ÏàËÆ¶È:81.2% Chemical & Pharmaceutical Bulletin 1997 45 877-882 Medicinal Foodstuffs. VI. Histamine Release Inhibitors from Kidney Bean, the Seeds of Phaseolus vulgaris L : Chemical Structures of Sandosaponins A and B Masayuki YOSHIKAWA,Hiromi SHIMADA,Hajime KOMATSU,Tetsuo SAKURAMA,Norihisa NISHIDA,Johji YAMAHARA,Hiroshi SHIMODA,Hisashi MATSUDA and Tadato TANI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . A-homo-4-aza-3-oxoolean-12-en-30-oic acid methyl ester C31H49O3N ÏàËÆ¶È:80.6% Chemistry of Natural Compounds 2009 45 519-521 BECKMANN REARRANGEMENT OF 11-DEOXO-GLYCYRRHETICACID 3-KETOXIME L. R. Mikhailova, M. V. Khudobko,L. A. Baltina, Jr., and L. A. Baltina Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . oleanolic aldehyde acetate ÏàËÆ¶È:80.6% Korean Journal of Pharmacognosy 2010 41 97-102 Inhibition of IL-6 Production in TNF-¦Á Stimulated MG-63 by the Triterpenoids Isolated from Aucuba japonica Qinglong Jin, Hong-Guang Jin, Ji Eun Shin, Eun Jin Choi and Eun-Rhan Woo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . myrioside B C36H56O10 ÏàËÆ¶È:80% Chemical & Pharmaceutical Bulletin 2002 50(8) 1097-1099 Five Triterpene Glycosides from Oxytropis myriophylla Masafumi OKAWA,Rie YAMAGUCHI, Hurlad DELGER,Ryota TSUCHIHASHI, Toshihiro NOHARA,Junei KINJO, Susumu ISODA, and Yoshiteru IDA Structure 13C NMR ̼Æ×Ä£Äâͼ |
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