| ²é¿´: 222 | »Ø¸´: 1 | ||
kengkengsee½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬¸Ðл£¡
|
|
ÈܼÁ£ºë®´úÂȷ ̼Æ×Ðźţº14.45,17.32,18.38,19.63,20.10,25.78,27.01,27.04,27.24,27.74,32.89,36.93,38.82,39.64,41.15,42.15,42.59,47.20,48.65,52.88,54.70,55.36,73.11,76.42,78.39,82.61,124.47,125.93,135.49,137.42 |
» ²ÂÄãϲ»¶
22408 µ÷¼Á²ÄÁÏ
ÒѾÓÐ6È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
085600²ÄÁÏÓ뻯¹¤301·ÖÇóµ÷¼ÁԺУ
ÒѾÓÐ19È˻ظ´
277¹¤¿ÆÇóµ÷¼Á
ÒѾÓÐ11È˻ظ´
277Çóµ÷¼Á ÊýÒ»104·Ö
ÒѾÓÐ13È˻ظ´
304Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
336Çóµ÷¼Á£¬Ò»Ö¾Ô¸Öпƴó
ÒѾÓÐ6È˻ظ´
071000ÉúÎïѧ£¬Ò»Ö¾Ô¸ÉîÛÚ´óѧ296·Ö£¬Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤085600 310·ÖÇóµ÷¼Á
ÒѾÓÐ19È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
2΢Æ×ÇóÖú£¬Ð»Ð»¡£
ÒѾÓÐ9È˻ظ´
8΢Æ×ÇóÖú£¬Ð»Ð»¡£
ÒѾÓÐ3È˻ظ´
΢Æ×ÕæµÄͦ²»´íµÄ£¡
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬¸Ðл£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Íò·Ö¸Ðл
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл¡£¡£¡£
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÈý¸ö»¯ºÏÎ̼Æ×£©µÄ΢Æ×Êý¾Ý¿â¼ìË÷½á¹û£¨ÏàËÆ¶Èǰ20%£©
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú ¼±¼±¼±£¡£¡£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
΢Æ×Êý¾Ý¿â²éѯһ¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
΢Æ×²é½á¹¹ лл
ÒѾÓÐ3È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
kengkengsee: ½ð±Ò+5, ¡ïÓаïÖú 2013-11-22 17:20:38
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
kengkengsee: ½ð±Ò+5, ¡ïÓаïÖú 2013-11-22 17:20:38
|
²éѯ½á¹û£º¹²²éµ½7767¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . yunganogenin E C30H44O5 ÏàËÆ¶È:73.3% Phytochemistry 1992 31 1747-1752 Oleanane glycosides from Glycyrrhiza yunnanensis roots Kazuhiro Ohtani, Katsuki Ogawa, Ryoji Kasai, Chong-Ren Yang, Kazuo Yamasaki, Jun Zhou, Osamu Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . cycloartan-23E-ene-1¦Á,2¦Á,3¦Â,25-tetrol C30H50O4 ÏàËÆ¶È:70% Journal of Natural Products 2008 71(1) 81-86 Cycloartane-Type Triterpenoids from the Resinous Exudates of Commiphora opobalsamum Tao Shen, Hui-Qing Yuan, Wen-Zhu Wan, Xiao-Ling Wang, Xiao-Ning Wang, Mei Ji, and Hong-Xiang Lou Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . macedonic acid ÏàËÆ¶È:70% 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 -------------------------------------------------------------------------------- 4 . 1¦Â,22¦Â-dihydroxyolean-11,13(18)-diene C30H48O2 ÏàËÆ¶È:70% Phytochemistry 1998 48 693-697 Saikosaponins from Taverniera aegyptiaca H. A. Hassanean Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . ursolic acid ÏàËÆ¶È:70% Chinese Traditional and Herbal Drugs 1999 30(3) 161-164 Studies on the Chemical Constituents of Shady Jerusalemsage (Phlomis umbrosa)(¢ñ) Liu Shiwang; Fu Hongzheng and Lin Wenhan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . pomolic acid C30H48O4 ÏàËÆ¶È:70% Natural Product Research and Development 2001 13(2) 11-13 THE STUDIES OF CHEMICAL COMPONENTS OF CLAUSENA DUNNIANA CUI Shu ya;CHENG Dong liang; TIAN Jun; WU Feng e Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . compound 10a ÏàËÆ¶È:70% Natural Medicines 1999 53 166-172 Studies on Index Compounds for HPLC Analysis of Glycyrrhiza macedonica SHIBANO MAKIO,NUKUI HISASHI, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 19¦Á-hydroxylursolic acid ÏàËÆ¶È:70% 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 -------------------------------------------------------------------------------- 9 . 20¦Â,28-epoxy-28¦Á-methoxytaraxasteran-3¦Â-ol C31H52O3 ÏàËÆ¶È:67.7% Journal of Natural Products 2006 69 1164-1167 Taraxasterane- and Ursane-Type Triterpenes from Nerium oleander and Their Biological Activities Ming Zhao, Shujun Zhang, Liwei Fu, Na Li, Jiao Bai, Junichi Sakai, Liyan Wang, Wanxia Tang, Toshiaki Hasegawa, Hirotsugu Ogura, Takao Kataoka, Seiko Oka, Miwa Kiuch, Katutoshi Hirose, and Masayoshi Ando Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 21-dehydro-macedonic acid methyl ester C31H46O4 ÏàËÆ¶È:67.7% Acta Pharmaceutica Sinica 1990 Vol 25 795-797 ISOLATION AND IDENTIFICATION OF YIBEINOSIDE A DM Xu; S Arihara; N Shoji; XW Yang; EX Huang and CS Li Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 1¦Â,2¦Â,3¦Â,19¦Á-tetrahydroxy-urs-12-ene-28-oate C31H50O6 ÏàËÆ¶È:67.7% Pharmaceutical Biology 1999 37 314-317 Two New Triterpenoids from Centipeda minima Rai N., Siddiqui I.R., Singh J. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 3¦Â-hydroperoxy-7¦Â,25-epoxy-D:B-friedoolean-5-ene C30H48O3 ÏàËÆ¶È:66.6% Journal of Natural Products 2009 72 1045-1048 Triterpenoids and a Lignan from the Aerial Parts of Maytenus apurimacensis Nabil E. J. Vazdekis, Haydee Ch¨¢vez, Ana Est¨¦vez-Braun, and Ángel G. Ravelo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . gamboukokoensein A C30H48O7 ÏàËÆ¶È:66.6% Phytochemistry 2003 845-849 Pentacyclic triterpenoid and saponins from Gambeya boukokoensis Jean Wandji, François Tillequin, Dulcie A. Mulholland, Jovita Chi Shirri,Nole Tsabang, ElisabethSeguin, Philippe Verite, Francine Libotb, Z.T. Fomum Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 6¦Â-hydroxybetulin C30H50O3 ÏàËÆ¶È:66.6% Journal of Natural Products 2005 68 1018-1021 Lupane Triterpenoids from Maytenus Species Marvin J. Nez, Carolina P. Reyes, Ignacio A. Jimnez, Laila Moujir, and Isabel L. Bazzocchi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . argenteanol D C30H50O3 ÏàËÆ¶È:66.6% Journal of Natural Products 1997 60 81-85 Argenteanones C-E and Argenteanols B-E, Cytotoxic Cycloartanes from Aglaia argentea K. Mohamad, M.-T. Martin, E. Leroy, C. Temp¨ºte, T. S¨¦venet, K. Awang, and M. Païs Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . pomolic acid C36H46O4 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1992 40 1990-1992 Triterpenoid Saponins of Aquifoliaceous Plants. V. Ilexosides XV-XIX from the Barks of Ilex crenata THUNB. Chieko HATA,Miho KAKUNO,Kazuko YOSHIKAWA and Shigenobu ARIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . pomolic acid C30H48O4 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1992 40 3138-3141 Triterpenoid Saponins of Aquifoliaceous Plants. VIII. Ilexosides XXIX-XXXII from the Leaves of Ilex rotunda THUNB. Kayoko AMIMOTO,Kazuko YOSHIKAWA and Shigenobu ARIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . compound 2a C30H46O6 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1992 40 3138-3141 Triterpenoid Saponins of Aquifoliaceous Plants. VIII. Ilexosides XXIX-XXXII from the Leaves of Ilex rotunda THUNB. Kayoko AMIMOTO,Kazuko YOSHIKAWA and Shigenobu ARIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . compound 11 C30H50O5 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1985 33 37-40 19¦Á-Hydroxyursane-Type Triterpene Glucosyl Esters from the Roots of Rubus suavissimus S. LEE FENG GAO,FENGHUAI CHEN,TAKASHI TANAKA,RYOJI KASAI,TAKASHI SETO and OSAMU TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . cyclomacrogenin B ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 2009 45 55-60 TRITERPENE GLYCOSIDES FROM Astragalus AND THEIR GENINS.LXXX. CYCLOMACROSIDE D, A NEW BISDESMOSIDE D. A. Iskenderov, I. M. Isaev, and M. I. Isaev Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . cyclomacrogenin B ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 2009 45 132-134 TRITERPENE GLYCOSIDES FROM Astragalus AND THEIR GENINS.LXXIX. STRUCTURE OF CYCLOMACROSIDE C D. A. Iskenderov, I. M. Isaev, and M. I. Isaev Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-11-22 17:02:31














»Ø¸´´ËÂ¥