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| 13C NMR (151 MHz, MeOD) ¦Ä 45.70, 47.24, 52.25, 61.17, 62.80, 71.64, 74.89, 77.97, 78.51, 82.39, 98.44, 100.41, 110.92, 130.23, 147.66, 154.02,170.44. |
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2Â¥2013-11-18 19:01:00
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xp¡ªfly: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-11-22 16:22:37
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²éѯ½á¹û£º¹²²éµ½327¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . scandoside methyl ester ÏàËÆ¶È:94.1% Chemical & Pharmaceutical Bulletin 1991 39 2049-2052 Isolation of 10-O-Acyl Iridoid Glucosides from a Philippine Medicinal Plant, Oldenlandia corymbosa L. (Rubiaceae) Hideaki OTSUKA,Kayoko YOSHIMURA,Kazuo YAMASAKI and Magdalena C. CANTORIA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (6¦Â)-6-hydroxygeniposide ÏàËÆ¶È:94.1% Helvetica Chimica Acta 2010 93 1751-1757 New Chemical Constituents from Borreria verticillata (Rubiaceae) Vinicius F. Moreira, Rodrigo R. Oliveira, Leda Mathias, Raimundo Braz-Filho and Ivo J. Curcino Vieira Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 6¦Â-hydroxygeniposide C17H24O11 ÏàËÆ¶È:94.1% Chinese Traditional and Herbal Drugs 1995 26 443-444 ·ãÏãÊ÷ƤÖеĻ·Ï©ÃÑÝÆ³É·Ö ½ªÖ¾ºê,ÖÜÈÙºº,ºÓÒ°¹¦ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . scandoside methyl ester C17H24O11 ÏàËÆ¶È:94.1% Turkish Journal of Chemistry 2006 30 515-523 Chemical Constituents of Galium tortumense ZÜHAL GÜVENALP, NURCAN KILIÇ, CAVİT KAZAZ, YUSUF KAYA, L. ÖMÜR DEMİREZER Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . scandoside methyl ester ÏàËÆ¶È:94.1% Journal of Chinese Medicinal Materials 2008 31 522-524 Studies on the Chemical Constituents in Herb of Hedyotis diffusa ZHANG Yong-yong, LUO Jia-bo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 6¦Â-hydroxygeniposide ÏàËÆ¶È:88.2% Planta Medica 1987 53 462-464 The Structural Transformation of Gardenoside and Its Related Iridoid Compounds by Acid and -Glucosidase Masanori Miyagoshi, Sakae Amagaya, and Yukio Ogihara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . scandoside methyl ester ÏàËÆ¶È:82.3% China Journal of Chinese Materia Medica 1999 24 Studies on Chemical Constituents of Fruits of Gardenia sootepensis Hutch Wang Gangli, Zhao Shujie and Chen Dechang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . Scandoside ÏàËÆ¶È:82.3% Heterocycles 2002 56 537-544 Studies on the Constituents of Indonesian Borreria latifolia Kohei Kamiya, Yasuhiro Fujita, Yasuhisa Saiki, Endang Hanani, Umar Mansur, and Toshiko Satake* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . scandoside ÏàËÆ¶È:76.4% Zeitschrift f¨¹r Naturforschung C 2007 62 597-602 Iridoid Glucosides with Insecticidal Activity from Galium melanantherum O. Tzakou, P. Mylonas, C. Vagias, and P. V. Petrakis Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . geniposide ÏàËÆ¶È:70.5% Chemical & Pharmaceutical Bulletin 2005 53(10) 1342-1344 Iridoid Glucosides from the Fruit of Genipa americana Masateru ONO,Masami UENO,Chikako MASUOKA,Tsuyoshi IKEDA,and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . aucubin ÏàËÆ¶È:70.5% Planta Medica 1984 50 444-445 Indoid Glucosides and an Acetophenone Glucoside from Penstemon whippleanus Peter Junior Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . aucubin ÏàËÆ¶È:70.5% Planta Medica 1982 46 33-37 Iridoids in Equatorial and Tropical Flora Part Isolation of Amareloside Armando Bianco, Pietro Passacantilli, Marcello Nicoletti and Roberto Alves de Lima Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . aucubin ÏàËÆ¶È:70.5% Planta Medica 1981 43 34-38 Iso-Scrophularioside, a New Iridoid Glucoside from Penstemon eriantherus Peter Junior Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . aucubin ÏàËÆ¶È:70.5% Planta Medica 1980 38 246-254 Scrophularioside, a New lridoid Glucoside from Scrophularia lateriflora O. Sticher, B. Meier, D. Lehmann und L. Swiatek Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . aucubin ÏàËÆ¶È:70.5% Helvetica Chimica Acta 1981 64 2401-2404 Iridoid and Aryl Glucosides from Globularia nudicaulis and Globularia nana Ratan K. Chaudhuri, Osama Salama, Otto Sticher Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . secologanol ÏàËÆ¶È:70.5% Journal of Natural Products 1989 Vol 52 1146 New Secoiridoid Glucosides from Gentiana verna E. Mpondo Mpondo, J. Garcia, J. Lestani Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . aucubin ÏàËÆ¶È:70.5% Zeitschrift f¨¹r Naturforschung B 2007 62b 1465-1470 Chemical Constituents from Pedicularis rex C. B. Clarke Hong-Biao Chu, Ning-Hua Tan, and Yu-Mei Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . geniposide ÏàËÆ¶È:70.5% Chinese Traditional and Herbal Drugs 2008 39 648-651 Chemical components from Dryopteris fragrans and their cytotoxicity ZHANG Yan-long; FU Hai-yan; ZHANG Ying-ying; SONG Qing-yu; XU Wen-hua; KUANG Hai-xue Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . aucubin ÏàËÆ¶È:70.5% Chinese Traditional and Herbal Drugs 2006 37 1637-1638+1706 ¿à²ÎÌÀÓÐЧ²¿Î»»¯Ñ§³É·ÖÑо¿(¢ñ) Áõ±ó;ʯÈαø Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . geniposide ÏàËÆ¶È:70.5% Chinese Pharmaceutical Journal 2006 41 10-12 Study on Chemical Constitutes of Codonopsis pilosula HE Qing, ZHU En-yuan, WANG Zheng-tao, CHOU Gui-xin, XU Luo-shan, HU Zhi-bi Structure 13C NMR ̼Æ×Ä£Äâͼ |
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