| ²é¿´: 415 | »Ø¸´: 1 | ||
±ÉÈËÓÇÌìľ³æ (ÖøÃûдÊÖ)
|
[ÇóÖú]
Çó΢Æ×Êý¾Ý£¬Ê¹ØÈ¢Ï±¸¾£¡
|
|
ÈܼÁCDCl3£¬Êý¾ÝÈçÏ£º 18.02181£¬19.3028£¬23.4784£¬24.3429£¬28.7383£¬29.4709£¬30.5770£¬31.1118£¬31.5440£¬32.8187£¬32.8993£¬36.7673£¬37.1189£¬39.6170£¬40.1884£¬40.9722£¬45.1845£¬46.5178£¬117.7896£¬120.4781£¬122.6099£¬123.6355£¬132.9685£¬141.8838£¬145.0046£¬146.0448£¬152.0519£¬172.9009£¬182.0214£¬192.1455£¬205.1047 ÇóÏàËÆ¶È80%ÒÔÉϵÄ΢Æ×Êý¾Ý¡£ ´óÉñ³öÊÖÏàÖú£¡ [ Last edited by ±ÉÈËÓÇÌì on 2013-5-7 at 21:47 ] |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸ÎäÀí²ÄÁÏ305·ÖÇóµ÷¼Á
ÒѾÓÐ5È˻ظ´
²ÄÁÏר˶ӢһÊý¶þ306
ÒѾÓÐ3È˻ظ´
085600²ÄÁÏÓ뻯¹¤µ÷¼Á 324·Ö
ÒѾÓÐ7È˻ظ´
311Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
26µ÷¼Á/²ÄÁÏ/Ó¢Ò»Êý¶þ/×Ü·Ö289/ÒѹýAÇøÏß
ÒѾÓÐ7È˻ظ´
295Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
354Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
²ÄÁÏרҵÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Çó²ÄÁϵ÷¼Á
ÒѾÓÐ7È˻ظ´
Ò»Ö¾Ô¸Ìì´ó²ÄÁÏÓ뻯¹¤£¨085600£©×Ü·Ö338
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö΢Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
1power1
ľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 62 (³õÖÐÉú)
- ½ð±Ò: 2925.7
- É¢½ð: 23
- ºì»¨: 3
- Ìû×Ó: 461
- ÔÚÏß: 173.6Сʱ
- ³æºÅ: 1441199
- ×¢²á: 2011-10-13
- ÐÔ±ð: GG
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
±ÉÈËÓÇÌì: ½ð±Ò+5, ¡ïÓаïÖú, µÈÎÒµ÷ÕûÁËÔÙ²é²é£¬Õâ´ÎûÓÐÌ«ºÃµÄ¡¡´ò¸öÕÛߣ¬½ð±Ò²»¶àÁË 2013-05-08 20:45:50
±ÉÈËÓÇÌì(¶¹¸ç´ú·¢): ½ð±Ò+5, лл 2013-05-29 15:07:37
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
±ÉÈËÓÇÌì: ½ð±Ò+5, ¡ïÓаïÖú, µÈÎÒµ÷ÕûÁËÔÙ²é²é£¬Õâ´ÎûÓÐÌ«ºÃµÄ¡¡´ò¸öÕÛߣ¬½ð±Ò²»¶àÁË 2013-05-08 20:45:50
±ÉÈËÓÇÌì(¶¹¸ç´ú·¢): ½ð±Ò+5, лл 2013-05-29 15:07:37
|
ûÓÐ80%ÒÔÉϵġ£ ÁбíÈçÏ£º ²éѯ½á¹û£º¹²²éµ½933¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . hypoglauterpenic acid ÏàËÆ¶È:67.7% Acta Botanica Yunnanica 1993 15(1) 92-96 THE OLEANANE TYPE TRITERPENES FROM THE ROOT OF TRIPTERYGIUM HYPOGLAUCUM ZHANG Xian-Min,WU Da-Gang Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . regeol C ÏàËÆ¶È:64.5% Phytochemistry 1997 45 969-974 Triterpenoid inhibitors of interleukin-1 secretion and tumour-promotion from Tripterygium wilfordii var. regelii Yoshihisa Takaishi, Noriko Wariishi, Hideo Tateishi, Kazuyoshi Kawazoe, Kimiko Nakano, Yukihisa Ono, Haruyuki Tokuda, Hoyoku Nishino, Akio Iwashima Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . isopristimerin III ÏàËÆ¶È:64.5% Phytochemistry 1995 39 1159-1163 D:A-friedo-24-noroleanane triterpenoids from Tripterigium wilfordii Takashi Morota, Chun-Xin Yang, Tatsunori Ogino, Wan-Zhang Qin, Takao Katsuhara, Li-Hong Xu, Yasuhiro Komatsu, Kang-Li Miao, Masao Maruno, Bing-Hui Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . wilforic acid A ÏàËÆ¶È:61.2% Phytochemistry 1997 46 535-543 Di- and triterpenoids from Tripterygium hypoglaucum Hongquan Duan, Kazuyoshi Kawazoe, Masahiko Bando, Masaru Kido, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . wilforic acid A C29H42O4 ÏàËÆ¶È:61.2% Phytochemistry 1997 45 791-796 Terpenoids from Tripterygium wilfordii Kunhua Li, Hongquan Duan, Kazuyoshi Kawazoe, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . isopristimerin III ÏàËÆ¶È:61.2% Phytochemistry 1991 30 3713-3716 Triterpenes fromMaytenus ilicifolia Hideji Itokawa, Osamu Shirota, Hiroshi Ikuta, Hiroshi Morita, Koichi Takeya, Yoichi Iitaka Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . glutinol ÏàËÆ¶È:61.2% Fitoterapia 2011 82 493-496 Triterpenes and steroids from the roots of Scorzonera austriaca Quan-Xiang Wu, Yi-Bin Su, Ying Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 22-O-hexanoyl-28-al-12-en-olean-3¦Â,16¦Á-diol C36H56O5 ÏàËÆ¶È:61.1% Chinese Journal of Natural Medicines 2003 1 76-78 Chemical Constituents of Maesa indica LAI Guo Fang; WANG Yi Fen; CAO Jian Xin; LUO Shi De Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Maejaposide A Aglycon ÏàËÆ¶È:58.3% Journal of Natural Products 1999 62 228-232 New Triterpenoid Saponins from Maesa japonica Kazuo Koike, Momoe Kudo, Zhonghua Jia, Tamotsu Nikaido, Yuji Ide, and Tsuguo Sakura Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 2,3-seco-taraxer-14-ene-2,3,28-trioic acid 3-methyl ester C31H48O6 ÏàËÆ¶È:58.0% Journal of Natural Products 2008 71(2) 292-294 Seco-Terpenoids and Other Constituents from Elateriospermum tapos Duangpen Pattamadilok, and Rutt Suttisri Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound PH2 C30H48O ÏàËÆ¶È:58.0% Planta Medica 1999 65 371-374 The Anti-Inflammatory Compounds of Polygonum bistorta: IsoIaton and Characterisation Mahama Duwiejua, lsaacJ. Zeitlin, Alexander. Gray,and Peter G. Waterman Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . glut-5-ene-3-one ÏàËÆ¶È:58.0% Planta Medica 1994 60 594-596 Biologically Active Compounds from the Euphorbiaceae; 2. Two Triterpenoids of Euphorbia cyparissias Sevil Oks¨¹z. Roberto R. Gil,Heebyung Chai,JohnM. Pezzuto, GeoffreyA. Cordell,and Ayhan Ulubelen Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . glutin-5-ene ÏàËÆ¶È:58.0% Chemical & Pharmaceutical Bulletin 1995 43 198-203 NMR Spectra of Triterpenoids. III. Oleanenes and Migrated Oleanenes Hiroyuki AGETA,Yoko ARAI,Hideki SUZUKI,Tamiko KIYOTANI and Miyoe KITABAYASHI Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . longispinogenin ÏàËÆ¶È:58.0% Chemical & Pharmaceutical Bulletin 1994 42 2455-2460 Antisweet Natural Products. XI. Structures of Sitakisosides VI-X from Stephanotis lutchuensis KOIDZ. var. japonica Kazuko YOSHIKAWA,Hitomi TANINAKA,Yukiko KAN and Shigenobu ARIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . glutinone C30H48O ÏàËÆ¶È:58.0% Chemical & Pharmaceutical Bulletin 1992 40 789-791 Triterpenoid Ketones from Lingnania chungii MOCLURE : Arborinone, Friedelin and Glutinone Toshihiro AKIHISA,Kazuhiro YAMAMOTO,Toshitake TAMURA,Yumiko KIMURA,Takashi IIDA,Toshio NAMBARA and Frederic C. CHANG Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . asterogenic acid ÏàËÆ¶È:58.0% Chemical & Pharmaceutical Bulletin 1991 39 2609-2612 Saponins from Amaranthus hypochondriacus Hiroshi KOHDA,Seiji TANAKA,Yasutoshi YAMAOKA and Yoshie OHHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 6 ÏàËÆ¶È:58.0% Chemical & Pharmaceutical Bulletin 1989 37 1977-1983 Studies on the Constituents of Aster tataricus L.f. II. : Structures of Aster Saponins Isolated from the Root Tsuneatsu NAGAO,Shizuko HACHIYAMA,Hikaru OKABE and Tatsuo YAMAUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . primulagenin A ÏàËÆ¶È:58.0% Chemical & Pharmaceutical Bulletin 1985 33 4685-4690 Minor Triterpenoid Saponins from the Leaves of Bupleurum rotundifolium L. ERIKO AKAI,TADAHIRO TAKEDA,YOSHIMASA KOBAYASHI,YINGJIE CHEN and YUKIO OGIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . longispinogenin ÏàËÆ¶È:58.0% Chemical & Pharmaceutical Bulletin 1980 28 2367-2373 Isolation, Characterization, and Nuclear Magnetic Resonance Spectra of New Saponins from the Roots of Bupleurum falcatum L. HIROSHI ISHII,MIHARU NAKAMURA,SHUJIRO SEO,KAZUO TORI,TAKEHIKO TOZYO and YOHKO YOSHIMURA Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . echinocystic acid ÏàËÆ¶È:58.0% Chemical & Pharmaceutical Bulletin 1982 30 2747-2760 Legume Saponins of Gleditsia japonica MIQUEL. IV. 13C-Nuclear Magnetic Resonance Spectral Studies for Structure Elucidation of Gleditsia Saponins B and C TAKAO KONOSHIMA and TOKUNOSUKE SAWADA Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-05-08 09:39:14













»Ø¸´´ËÂ¥