| ²é¿´: 264 | »Ø¸´: 1 | ||
hejiangboľ³æ (ÖøÃûдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×²éѯ
|
|
ÈܼÁ£ºÂÈ·Â ÏàËÆ¶È£º90%ÒÔÉÏ ºË´ÅÊý¾Ý£º 11.5,15.3,16.5,17.9,18.6,19.0,22.4,24.9,25.7,27.8,29.0,29.0,31.0,34.2,35.3,35.5,35.8,36.136.1,36.4,45.0,49.7,50.4,50.6,50.6,50.7,72.9,125.2,130.9 |
» ²ÂÄãϲ»¶
»·¾³×¨Ë¶µ÷¼Á
ÒѾÓÐ7È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ23È˻ظ´
301Çóµ÷¼Á
ÒѾÓÐ15È˻ظ´
304Çóµ÷¼Á£¨085602£¬¹ýËļ¶£¬Ò»Ö¾Ô¸985£©
ÒѾÓÐ17È˻ظ´
302·ÖÇóµ÷¼Á Ò»Ö¾Ô¸°²»Õ´óѧ085601
ÒѾÓÐ12È˻ظ´
288»·¾³×¨Ë¶,Çóµ÷²ÄÁÏ·½Ïò
ÒѾÓÐ23È˻ظ´
22408 µ÷¼Á²ÄÁÏ
ÒѾÓÐ6È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
085600²ÄÁÏÓ뻯¹¤301·ÖÇóµ÷¼ÁԺУ
ÒѾÓÐ19È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÕæµÄͦ²»´íµÄ£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖúÒ»¸ö¿ÉÒԲ鵽¾§ÌåѧÊý¾ÝµÄÍøÕ¾
ÒѾÓÐ5È˻ظ´
Çó΢Æ×Êý¾Ý лл
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
Çó΢Æ×¼ìË÷»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻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´

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 ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
hejiangbo: ½ð±Ò+10 2013-11-19 13:35:24
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
hejiangbo: ½ð±Ò+10 2013-11-19 13:35:24
|
²éѯ½á¹û£º¹²²éµ½4018¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . compound 26 ÏàËÆ¶È:76.6% 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 -------------------------------------------------------------------------------- 2 . euphol (eupha-8,24-di-en-3¦Â-ol) C30H50O ÏàËÆ¶È:73.3% China Journal of Chinese Materia Medica 2006 31 742-744 Studies on constituents from roots of Euphorbia hylonoma RUAN Hanli, ZHANG Yue, ZHANG Yonghui, PI Huifang, WU Jizhou Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . euphol C30H50O ÏàËÆ¶È:73.3% Phytochemistry 1999 50 849-857 (20R,23E)-Eupha-8,23-diene-3¦Â,25-diol from Tripetalum cymosum Yuan-Wah Leong, Leslie J. Harrison Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . compound 2 ÏàËÆ¶È:73.3% Phytochemistry 1991 30 3822-3823 A dammarane fromStevia salicifolia Rachel Mata, Vero´nica Rodri´guez, Rogelio Pereda-Miranda, Robert Bye, Edelmira Linares Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . euphol ÏàËÆ¶È:73.3% Phytochemistry 1990 29 1625-1628 Constituents of the latex of Euphorbia antiquorum Mohan B. Gewali,Masao Hattori,Yasuhiro Tezuka,Tohru Kikuchi,Tsuneo Namba Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . inonotsudiol A C30H48O2 ÏàËÆ¶È:73.3% Phytochemistry 2010 71 1774-1779 An unusual lanostane-type triterpenoid, spiroinonotsuoxodiol, and other triterpenoids from Inonotus obliquus Noriko Handa, Takeshi Yamada, Reiko Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . euphol ÏàËÆ¶È:73.3% Chinese Traditional and Herbal Drugs 2008 39 1779-1781 Optimization of purification of Panax notoginseng extract for injection CHU Yang; SONG Hong-tao; LI Dan; YAN Lu; LIU Dan; CHEN Da-wei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . lanosterol C30H50O ÏàËÆ¶È:73.3% Chinese Traditional and Herbal Drugs 2005 36 1763-1767 Ingenane diterpene ester constituents from Tibetan medicine Euphorbia wallichii LI Yu-lin; SUO You-rui Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . euphol ÏàËÆ¶È:73.3% International Journal of Molecular Sciences 2012 13 11247-11259 Bio-Guided Isolation of the Cytotoxic Terpenoids from the Roots of Euphorbia kansui against Human Normal Cell Lines L-O2 and GES-1 Li Zhang, Lan Gao, Zhengjun Li, Xiaojing Yan, Yanjing Yang, Yuping Tang, Yudan Cao and Anwei Ding Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . euphadienol ÏàËÆ¶È:73.3% Organic Magnetic Resonance 1974 6 603-611 Carbon-13 NMR spectra of some tetra-and pentacyclic triterpenoids S. A. Knight Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . Euphol ÏàËÆ¶È:73.3% International Journal of Molecular Sciences 2012 13 11247-11259 Bio-Guided Isolation of the Cytotoxic Terpenoids from the Roots of Euphorbia kansui against Human Normal Cell Lines L-O2 and GES-1 Li Zhang, Lan Gao, Zhengjun Li, Xiaojing Yan, Yanjing Yang, Yuping Tang, Yudan Cao and Anwei Ding Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . euphol ÏàËÆ¶È:73.3% Journal of Chinese Medicinal Materials 2007 30 412-415 Study on Chemical Constituents of Euphorbia hylonoma Hand.-Mazz. GUO Zeng-jun, ZUO Jian-feng, BO Xiao-qian, SUN Qi-shi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . ¡÷8,25(27) Stigmastadiene-3¦Â-OAc ÏàËÆ¶È:72.4% Phytochemistry 1989 28 1721-1724 Acylglucosyl sterols from Momordica charantia Amelia P. Guevara,Clara Y. Lim-Sylianco,Fabian M. Dayrit,Paul Finch Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . antiquol B C30H50O ÏàËÆ¶È:70% Journal of Natural Products 2002 65 158-162 Eupha-7,9(11),24-trien-3â-ol (¡°Antiquol C¡±) and Other Triterpenes from Euphorbia antiquorum Latex and Their Inhibitory Effects on Epstein-Barr Virus Activation Toshihiro Akihisa, E. M. Kithsiri Wijeratne, Harukuni Tokuda, Fumio Enjo, Masakazu Toriumi,Yumiko Kimura, Kazuo Koike, Tamotsu Nikaido, Yasuhiro Tezuka, and Hoyoku Nishino Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . dammar-24-ene-3¦Á,12¦Â,20(S)-triol 3-O-acetate ÏàËÆ¶È:70% 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 -------------------------------------------------------------------------------- 16 . euphol ÏàËÆ¶È:70% Acta Pharmaceutica Sinica 1992 27 445-451 TRITERPENE CONSTITUENTS FROM EUPHORBIA NEMTOCYPHA HAND-MAZZ D Cao; YL Su; JS Yang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . lanosterol ÏàËÆ¶È:70% Acta Pharmaceutica Sinica 1996 31 524-529 STUDIES ON CHEMICAL CONSTITUENTS OF ROOTS OF EUPHORBIA PEKINENSIS LY Kong and ZD Min Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . euphol ÏàËÆ¶È:70% China Journal of Chinese Materia Medica 2005 30 1162-1165 Studies on chemical constitutes of green alga Chaetomorpha basiretorsa and their bioactivity Shi Dayong, HAN Lijun, SUN Jie, YANG Yongchun, SHI Jiangong, FAN Xiao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . boeticol C30H50O ÏàËÆ¶È:70% Journal of Natural Products 1995 Vol 58 275-279 Boeticol, a New Tetracyclic Triterpene from Euphorbia boetica Maria Jos¨¦ U. Ferreira, Jos¨¦ R. Ascenso, Olga S. Tavares Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . compound 3 ÏàËÆ¶È:70% Phytochemistry 1991 30 3822-3823 A dammarane fromStevia salicifolia Rachel Mata, Vero´nica Rodri´guez, Rogelio Pereda-Miranda, Robert Bye, Edelmira Linares Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . Euphol ÏàËÆ¶È:70% Records of Natural Products 2012 6 255-262 Two New Phorbol-Type Diterpene Esters from Synadenium grantii Hook F. Leaves Emad M. Hassan, Magdy M. D. Mohammed and Samy M. Mohamed Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . tirucallol ÏàËÆ¶È:70% Chinese Traditional and Herbal Drugs 2008 39 1779-1781 Optimization of purification of Panax notoginseng extract for injection CHU Yang; SONG Hong-tao; LI Dan; YAN Lu; LIU Dan; CHEN Da-wei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . lanosterol ÏàËÆ¶È:70% Journal of the Chemical Society, Perkin Transactions 1 1988 2403-2406 Penasterol, a novel antileukemic sterol from the okinawan marine sponge Penares sp. Jie-fei Cheng, Jun'ichi Kobayashi, Hideshi Nakamura, Yasushi Ohizumi, Yoshimasa Hirata and Takuma Sasaki Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . Inoterpene A C30H52O3 ÏàËÆ¶È:70% Tetrahedron 2009 65 2443-2450 Absolute stereostructures of inoterpenes A¨CF from sclerotia of Inonotus obliquus Seikou Nakamura, Junko Iwami, Hisashi Matsuda, Shuichi Mizuno, Masayuki Yoshikawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . 21-hydroxylanosterol C30H50O2 ÏàËÆ¶È:70% Indian Journal of Chemistry Section B 1987 26B 722-724 21-Hydroxylanosterol,a New Lanostane Derivative from Stem Bark of Uvariastrum zenkeri Engl. & Diels ILIAS MUHAMMAD & CHOUDHUPY M HASAN Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-11-19 12:20:27














»Ø¸´´ËÂ¥