| ²é¿´: 201 | »Ø¸´: 2 | ||
lmlfeixueľ³æ (ÖøÃûдÊÖ)
|
[ÇóÖú]
΢Æ×Êý¾Ý¿â¿â»¯ºÏÎï¼ìË÷
|
| 15.4,15.5,18.6,22.6,23.7,24.1,24.7,24.9,25.0,26.8,32.6,36.3,37.6,38.9,39.2,41.2,45.4,47.0,47.1,48.9,60.9,61.0,61.5,68.4,70.0,71.8.71.9,73.4,76.6,76.8,86.2,102.9,124.7,134.2,177.6. |
» ²ÂÄãϲ»¶
272·Ö²ÄÁÏ×ÓÇóµ÷¼Á
ÒѾÓÐ31È˻ظ´
297Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
²ÄÁϹ¤³ÌÈÕÓÉúÇóµ÷¼Á
ÒѾÓÐ5È˻ظ´
¹ã¶«Ê¡ 085601 329·ÖÇóµ÷¼Á
ÒѾÓÐ8È˻ظ´
¿¼Ñе÷¼Á
ÒѾÓÐ25È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ18È˻ظ´
µ÷¼Á »¯Ñ§ 307
ÒѾÓÐ17È˻ظ´
²ÄÁÏÀà284µ÷¼Á
ÒѾÓÐ45È˻ظ´
368Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
295·ÖÇóµ÷¼Á
ÒѾÓÐ5È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖúÈý¸ö»¯ºÏÎ̼Æ×£©µÄ΢Æ×Êý¾Ý¿â¼ìË÷½á¹û£¨ÏàËÆ¶Èǰ20%£©
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ3¸ö»¯ºÏÎïµÄÄ£ºý²éÕÒ£¨¡·80%£©
ÒѾÓÐ4È˻ظ´
Çó4¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý¿â²éѯ£¨50½ð±Ò£©
ÒѾÓÐ6È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â¼ìË÷Ò»»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
΢Æ×13C NMRÊý¾Ý¿â ²éδ֪»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯһ¸ö»¯ºÏÎï~¼±~£¡Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×Êý¾Ý¿â²éѯһ¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²é»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
scifinder ½á¹¹¼ìË÷£¨¼±¼±¼±£¬ÔÚÏߵȸßÊÖÇë½Ì£©
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â¼ìË÷Ò»»¯ºÏÎï
ÒѾÓÐ4È˻ظ´
΢Æ×13C NMRÊý¾Ý¿â ²éδ֪»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
Çó΢Æ×Êý¾Ý¿â¼ìË÷2¸öÎå»·ÈýÝÆ»¯ºÏÎï
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
΢Æ×13C NMRÊý¾Ý¿â ²éδ֪»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖú¡¡Î¢Æ×Êý¾Ý¿â £Ã£Î£Í£ÒÊý¾Ý²éδ֪»¯ºÏÎï½á¹¹
ÒѾÓÐ6È˻ظ´
¡¾ÇóÖú¡¿ÇâÆ×ºÍ̼Æ×¼ìË÷ºóÊý¾Ý¿âûÓиû¯ºÏÎ½ÓÏÂÀ´QCºÍBC¶¼Òª×öÒ»ÏÂÂð£¿
ÒѾÓÐ8È˻ظ´
wq0616
Ìú¸Ëľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 323 (´óѧÉú)
- ½ð±Ò: 6659.6
- ºì»¨: 8
- Ìû×Ó: 955
- ÔÚÏß: 72.9Сʱ
- ³æºÅ: 2001721
- ×¢²á: 2012-09-14
- ÐÔ±ð: MM
- רҵ: ÖÐÒ©ÅÚÖÆ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
lmlfeixue: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ¸Ðл»Ø¸´ 2013-01-03 19:29:32
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
lmlfeixue: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ¸Ðл»Ø¸´ 2013-01-03 19:29:32
|
1 . rosamultin C36H60O10 ÏàËÆ¶È:69.4% Chinese Journal of Natural Medicines 2010 8 12-15 Triterpenoids from the Roots of Rose odorata var.gigantean LIU Dai-Lin; ZHU Shan; MA Rong; ZHANG Jing-Ze; LI He-Yu; CHEN Hong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 20(S),24(R)-epoxydammarane-12¦Á,3¦Â ,25-triol 3-o-(2',3',4',6' tetra-O-acetyl-¦Â-D-glucopyranoside) C44H70O13 ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 1983 19 174-178 CATALYTIC REARRANGEMENT OF A 20(S),24(R)-EFOXYDAMMARANE-3¦Â,12¦Á,25-TRIOL (a-D-GLUCOSE 1,2-ORTHOACETATE). II. N. S. Samoshina, V. L. Novikov, V. A. Denlsenko, and N. I. Uvarova Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Ursolazuroside 1 C36H58O10 ÏàËÆ¶È:66.6% Helvetica Chimica Acta 2010 93 457-465 Four New Triterpenes from Anchusa azurea var. azurea Ayşe Kuru¨¹z¨¹m-Uz, Zuhal G¨¹venalp, Cavit Kazaz, Bekir Salih and L. Öm¨¹r Demirezer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . kaji-ichigoside F1 C36H60O10 ÏàËÆ¶È:66.6% Chinese Journal of Natural Medicines 2010 8 12-15 Triterpenoids from the Roots of Rose odorata var.gigantean LIU Dai-Lin; ZHU Shan; MA Rong; ZHANG Jing-Ze; LI He-Yu; CHEN Hong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . peracetylated 28-O-¦Â-D-glucopyranosylester of 20(S)-3¦Â,19¦Á,24-trihydroxyurs-12-ene-23,28-dioic acid ÏàËÆ¶È:63.8% Natural Product Research 2002 16 401-406 Triterpenes and Saponins from Ilex psammophila V. S. Pires; G. Gosmann; D. Guillaume; E. P. Schenkel Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . vitalboside-A C36H58O8 ÏàËÆ¶È:63.8% Fitoterapia 2001 72 140-145 A new oleanane glycoside from the stem bark of Albizia gummifera G.M. Rukunga, P.G. Waterman Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . momorcharaside B C36H60O9 ÏàËÆ¶È:63.8% Acta Pharmaceutica Sinica 1990 Vol 25 898-903 STUDIES ON THE ACTIVE CONSTITUENTS OF MOMORDICA CHARANTIA L. ZJ Zhu; ZC Zhong; ZY Luo and ZY Xiao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 24-deoxy-sericoside C36H58O10 ÏàËÆ¶È:63.8% Chinese Traditional and Herbal Drugs 2006 37 165-168 Triterpenoids from roots of Potentilla anserina HONG Xia; CAI Guang-ming; XIAO Xiao-he Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 2¦Á,3¦Á,19¦Á,23-tetrahydroxy-urs-12-en-28-oic acid-3-O-¦Â-D-glucopyranosyl ester C36H60O11 ÏàËÆ¶È:63.8% Chinese Journal of Natural Medicines 2010 8 12-15 Triterpenoids from the Roots of Rose odorata var.gigantean LIU Dai-Lin; ZHU Shan; MA Rong; ZHANG Jing-Ze; LI He-Yu; CHEN Hong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . kajiichigoside F ÏàËÆ¶È:63.8% Modern Chinese Medicine 2008 10(3) 10-12 Studies on the chemical constituents of Potentill anserine L. Chu Liang, Wang Libo, Zhang Zhe, Gao Huiyuan, Huang Jian, Sun Bohang, Wu Lijun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . hederagenin-3-O-¦Â-glucuronopyranoside ÏàËÆ¶È:63.8% Journal of Shenyang Pharmaceutical University 2005 22 181-182 Chemical constituents of the seeds of Acanthopanax senticosus(Rupr. et Maxim) Harms ZHANG Jie, LI Wen, GAO Hui-Yuan, WU Bin, WU Li-jun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . Methyl ester of ocetylated 3-O-¦Â-D-glucuronopyranosy-oleanolic acid ÏàËÆ¶È:63.1% Phytochemistry 1994 37 821-825 Triterpenoid saponins from Melanthera scandens Andr¨¦ Penders, Cl¨¦ment Delaude Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . compound 7 C37H60O8 ÏàËÆ¶È:62.1% Planta Medica 1998 64 189-191 Kalaic Acid, A New Ursane-Type Saponin from Musanga cecroploides D. Lontsi, B. L. Sondengam, B. Bodo, and M. 1. Martin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 20-monoglucoside ÏàËÆ¶È:61.1% Chemistry of Natural Compounds 1986 22 279-288 GLYCOSYLATION OF TRITERPENOIDS OF THE DAMMARANE SERIES.IV. ¦Â-D-GLUCOPYRANOSIDES OF BETULAFOLIENETRIOL AND ITS DERIVATIVES L. N. Atopkina, V. A. Denisenko V. L. Novikov, and N. I. Uvarova Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . Oleanolic acid 3-O-¦Á-L-rhamnopyranoside C36H58O7 ÏàËÆ¶È:61.1% Molecules 2008 13 1472-1486 Facile Synthesis of Oleanolic Acid Monoglycosides and Diglycosides Yu Sha, Mao-Cai Yan, Jiao Liu, Yang Liu and Mao-Sheng Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . ¦Â-D-galactopyranosyl oleanolate C36H58O8 ÏàËÆ¶È:61.1% Molecules 2008 13 1472-1486 Facile Synthesis of Oleanolic Acid Monoglycosides and Diglycosides Yu Sha, Mao-Cai Yan, Jiao Liu, Yang Liu and Mao-Sheng Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . kaji-ichigoside F1 ÏàËÆ¶È:61.1% Acta Pharmaceutica Sinica 1996 31 844-848 NEW ELLAGIC GLYCOSIDES AND KNOWN TRITERPENOIDS FROM DUCHESNEA INDICA FOCKE L Ye and JS Yang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . quillaic acid 3-O-{¦Â-D-galactopyranosyl-(1¡ú2)-¦Â-D-glucopyranosiduronic acid} C42H64O16 ÏàËÆ¶È:61.1% Phytochemistry 1998 48 175-180 Triterpenoid saponins from Quillaja saponaria Shengjun Guo, Lennart Kenne, Lennart N. Lundgren, Bengt Rönnberg, Bo G. Sundquist Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . spinogenin C3 monoglucosyl ester ÏàËÆ¶È:61.1% Phytochemistry 1997 46 1255-1259 3¦Á-hydroxy-oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus Masazumi Miyakoshi, Susumu Isoda, Hirotoshi Sato, Yasuaki Hirai, Junzo Shoji, Yoshiteru Ida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 28-O-¦Â-D-glucopyranosyl-ester-oleanolic acid ÏàËÆ¶È:61.1% Phytochemistry 1997 46 1267-1270 13C NMR analysis of monodesmosidic saponinis from Gomphrena macrocephala Maria Cl¨¢udia Marx Young, Adriana Potomati, Edison Paulo Chu, Mitsue Haraguchi, Massao Yamamoto, Toshie Kawano Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . sericoside ÏàËÆ¶È:61.1% Acta Pharmaceutica Sinica 2008 Vol 43 504-508 Triterpene saponins from Adinandra nitida WANG Ying; YE Wen-cai; YIN Zhi-qi; ZHAO Shou-xun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . 28-O-¦Â-D-glucopyranosyl oleanolic acid peracetate ÏàËÆ¶È:61.1% Phytochemistry 1994 37 1667-1670 Seco-glycosides of oleanolic acid fromBeta vulgaris Georges Massiot, Marie-Genevieve Dijoux, Catherine Lavaud, Louisette Le Men-Olivier, Joseph D. Connolly, Douglas M. Sheeley Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . 2¦Á,3¦Á,19¦Á-trihydroxy-ursa-12-en-28-oic acid-28-O-¦Â-D-glucopyranosyl ester ÏàËÆ¶È:61.1% China Journal of Chinese Materia Medica 2010 35 3297-3301 Chemical constituents from Callicarpa nudiflora and their hemostatic acitivity ZHANG Jie; LI Baoquan; FENG Feng; TANG Yuping; LIU Wenyuan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . Ursolazuroside 2 C36H56O11 ÏàËÆ¶È:61.1% Helvetica Chimica Acta 2010 93 457-465 Four New Triterpenes from Anchusa azurea var. azurea Ayşe Kuru¨¹z¨¹m-Uz, Zuhal G¨¹venalp, Cavit Kazaz, Bekir Salih and L. Öm¨¹r Demirezer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . 2-oxo-pomolic acid ¦Â-D-glucopyranosyl ester ÏàËÆ¶È:61.1% Chinese Traditional and Herbal Drugs 2006 37 165-168 Triterpenoids from roots of Potentilla anserina HONG Xia; CAI Guang-ming; XIAO Xiao-he Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . niga-ichigoside F1 C36H58O11 ÏàËÆ¶È:61.1% Chinese Journal of Natural Medicines 2005 3 17-20 Isolation and Identification of Chemical Constituents from Rubus Parvifolius L. DU Shu-Hu; FENG Fang; LIU Wen-Ying; RAO Jin-Hua; BAI Juan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . chikusetsusaponin I ÏàËÆ¶È:61.1% Chinese Pharmaceutical Journal 2007 42 178-180 Studies on Triterpenoid Saponins from Achyranthese bidentata Bl LI Juan, BI Zhi-ming, XIAO Ya-jie, LI Ping Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . kaji-ichigoside F1 ÏàËÆ¶È:61.1% Journal of China Pharmaceutical University 2002 33 184-187 Studies on the Constituents of Rosa multiflora Thunb LI Yan Fang*; HU Li Hong; LOU Feng Chang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . rosamultin ÏàËÆ¶È:61.1% Journal of China Pharmaceutical University 2002 33 184-187 Studies on the Constituents of Rosa multiflora Thunb LI Yan Fang*; HU Li Hong; LOU Feng Chang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . Cycloccidentaliside II C36H58O12 ÏàËÆ¶È:61.1% Planta Medica 2012 78 821-827 Li, Shi-Fei; Di, Ying-Tong; Luo, Rong-Hua; Zheng, Yong-Tang; Wang, Yue-Hu; Fang, Xin; Zhang, Yu; Li, Ling; He, Hong-Ping; Li, Shun-Lin; Hao, Xiao-Jiang: Cycloartane Triterpenoids from Cassia occidentalis Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-01-03 19:11:54
lmlfeixue
ľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 3825.7
- É¢½ð: 130
- ºì»¨: 2
- Ìû×Ó: 1257
- ÔÚÏß: 386.5Сʱ
- ³æºÅ: 1114683
- ×¢²á: 2010-10-06
- ÐÔ±ð: GG
- רҵ: ÖÐÒ©×ÊÔ´
3Â¥2013-01-03 19:27:40













»Ø¸´´ËÂ¥
20