| ²é¿´: 388 | »Ø¸´: 1 | |||
bb864448334ľ³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬Ð»Ð» ÒÑÓÐ1È˲ÎÓë
|
|
ÈܼÁ£ºë®´úÂȷ ̼Æ×Êý¾Ý£º15.89,17.43,17.57,19.21,23.71,25.34,25.95,28.22,28.53,30.22,31.22,34.55,37.92,39.25,46.53,50.99,51.79,52.05,52.76,70.91,78.92,139.86,163.70,198.77 |
» ²ÂÄãϲ»¶
²ÄÁϸ´ÊÔÇóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸0703»¯Ñ§ÕÐ61×îÖÕÅÅÃû62»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ17È˻ظ´
¿¼Ñе÷¼Á
ÒѾÓÐ5È˻ظ´
085600²ÄÁÏÓ뻯¹¤301·ÖÇóµ÷¼ÁԺУ
ÒѾÓÐ33È˻ظ´
284Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
269Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
283Çóµ÷¼Á
ÒѾÓÐ17È˻ظ´
292Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
070300»¯Ñ§ Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
30½ð±Ò¼±Ðè3¸ö»¯ºÏÎïµÄ΢Æ×£¬Çó°ï棬лл~~~~~~
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
΢Æ×Êý¾ÝÇóÖúлл
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
Çó´óϺ²é΢Æ×£¬Íò·Ö¸Ðл°¡£¡£¡£¡
ÒѾÓÐ3È˻ظ´
׿Խ_ÏÈ·æ
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
ºýÍ¿³æ
- Ó¦Öú: 990 (²©ºó)
- ¹ó±ö: 2.955
- ½ð±Ò: 6796.4
- É¢½ð: 12161
- ºì»¨: 82
- ɳ·¢: 17
- Ìû×Ó: 3017
- ÔÚÏß: 2457Сʱ
- ³æºÅ: 1713223
- ×¢²á: 2012-03-24
- ÐÔ±ð: GG
- רҵ: ÁÙ´²Ò©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
bb864448334: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, 3ks 2015-05-14 12:04:12
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
bb864448334: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, 3ks 2015-05-14 12:04:12
|
²éѯ½á¹û£º¹²²éµ½1630¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 17(R)-3¦Â-hydroxyhexanordammaran-20-one ÏàËÆ¶È:79.1% Chinese Journal of Natural Medicines 2004 2 20-24 Chemical Studies on the Herb of Ocimum basilicum L. YIN Feng; HU Li Hong; LOU Feng Chang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . lanosterol ÏàËÆ¶È:76% Phytochemistry 1984 23 1721-1723 23,24,25,26,27-Pentanorlanost-8-en-3¦Â,22-diol from Verticillium lecanii John Frederick Grove Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . lanostenol ÏàËÆ¶È:76% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 3¦Â,12¦Â-dihydroxy-23,24,25,26,27-pentanordammarane-22-carbaldehyde C25H42O3 ÏàËÆ¶È:76% Helvetica Chimica Acta 2015 98 273−278 Nordammarane Triterpenoids from Sanguisorba officinalis (pages 273¨C278) Jiang Hu, Hui Li, Ben-Shou Yang, Xia Mao and Xiao-Dong Shi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . cylindrictone E C24H38O3 ÏàËÆ¶È:75% Helvetica Chimica Acta 2008 Vol. 91 1578 Six New Dammarane Triterpenoids from Viburnum cylindricum Lin Tu, Yu Zhao, Zu-Yin Yu, Yu-Wen Cong, Gang Xu, Li-Yan Peng, Peng-Tao Zhang, Xiao Cheng, and Qin-Shi Zhao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . Aglaiabbreviatin C C24H40O2 ÏàËÆ¶È:75% Journal of Natural Products 2010 73 2042-2046 Triterpenoids from Aglaia abbreviata and Their Cytotoxic Activities Feng Zhang, Jun-Song Wang, Yu-Cheng Gu, and Ling-Yi Kong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 20,20-trimethylenedithio-5,15-pregnadien-3¦Â,17¦Â-diol ÏàËÆ¶È:75% Steroids 1996 61 74-81 15¦Â-Hydroxysteroids(Part I). Steroids of the human perinatal period: The synthesis of 3¦Â,15¦Â,17¦Á-trihydroxy-5-pregnen-20-one Anthony Y. Reeder, George E. Joannou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 3¦Â-hydroxyhexanordammaran-20-one ÏàËÆ¶È:75% Chinese Journal of Natural Medicines 2004 2 20-24 Chemical Studies on the Herb of Ocimum basilicum L. YIN Feng; HU Li Hong; LOU Feng Chang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 3¦Â-hydroxy-22,23,24,25,26,27-hexanordammarane-20-one C24H40O2 ÏàËÆ¶È:75% The Journal of Organic Chemistry 1999 64 9587-9595 The Fluorine Atom as a Cation-Stabilizing Auxiliary in Biomimetic Polyene Cyclizations: Total Synthesis of dl-Dammarenediol1 William S. Johnson, William R. Bartlett, Boris A. Czeskis, Arnaud Gautier, Cheol H. Lee, R¨¦my Lemoine, Eric J. Leopold, Gregory R. Luedtke, and Katherine J. Bancroft Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . Sch 38512 C23H45N2O5 ÏàËÆ¶È:75% The Journal of Antibiotics 1992 45 633-638 MACROLACTAMS: TWO NOVEL HOMOLOGOUS SERIES OF COMPOUNDS PRODUCED BY Actinomadura sp. SCC 1778 R. COOPER, I. TRUUMEES, R. YARBOROUGH, D. LOEBENBERG, J. MARQUEZ, A. HORAN, M. PATEL, V. GULLO, M. PUAR, B. PRAMANIK Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 20' C31H53NO4Si ÏàËÆ¶È:75% Journal of the American Chemical Society 2003 125 1498-1500 Total Synthesis of Ingenol Keiji Tanino, Kei Onuki, Kohei Asano, Masaaki Miyashita, Tsuyoshi Nakamura, Yoshinori Takahashi, and Isao Kuwajima Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 21 C29H48O4Si ÏàËÆ¶È:75% Journal of the American Chemical Society 2003 125 1498-1500 Total Synthesis of Ingenol Keiji Tanino, Kei Onuki, Kohei Asano, Masaaki Miyashita, Tsuyoshi Nakamura, Yoshinori Takahashi, and Isao Kuwajima Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 20(R)-dammarane-3,12,20,25-tetrol ÏàËÆ¶È:75% Asia-Pacific Traditional Medicine 2008 4 41-43 Studies on the Rare Anticancer Compounds of the Hydrolysate of the Saponins from Gynostemma pentaphfllum(Thunb)Makino Xu Zhi-chao, Han Ling, Zhao Yu-qing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 2 ÏàËÆ¶È:73.0% Phytochemistry 1987 26 3365-3366 3¦Â-Hydroxyhexanordammaran-20-one from Euphorbia supina Reiko Tanaka (ne¨¦ Morita),Minako Matsuda,Shunyo Matsunaga Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . sphaerophysone A ÏàËÆ¶È:73.0% Journal of Shenyang Pharmaceutical University 2003 20 252-254 Cycloartane triterpenoids from the pericarp of Sphaerophysa salsula DC. LI Guo-yu, WANG Jin-hui, LI Ning, LI Xian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . cladosporide A C25H40O3 ÏàËÆ¶È:72% Chemical & Pharmaceutical Bulletin 2000 48(10) 1422-1426 A New Pentanorlanostane Derivative, Cladosporide A, as a Characteristic Antifungal Agent against Aspergillus fumigatus, Isolated form Cladosporium sp. Tomoo HOSOE,Hideaki OKADA,Takeshi ITABASHI,Koohei NOZAWA,Kaoru OKADA,Galba Maria de CAMPOS TAKAKI,Kazutaka FUKUSHIMA,Makoto MIYAJI and Ken-ichi KAWAI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 23,24,25,26,27-pentanorlanost-8-ene-3¦Â,22,diol ÏàËÆ¶È:72% Chemical & Pharmaceutical Bulletin 2000 48(10) 1422-1426 A New Pentanorlanostane Derivative, Cladosporide A, as a Characteristic Antifungal Agent against Aspergillus fumigatus, Isolated form Cladosporium sp. Tomoo HOSOE,Hideaki OKADA,Takeshi ITABASHI,Koohei NOZAWA,Kaoru OKADA,Galba Maria de CAMPOS TAKAKI,Kazutaka FUKUSHIMA,Makoto MIYAJI and Ken-ichi KAWAI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 23,24,25,26,27-pentanorlanost-8-en-3¦Â,22-diol C25H42O2 ÏàËÆ¶È:72% Phytochemistry 1984 23 1721-1723 23,24,25,26,27-Pentanorlanost-8-en-3¦Â,22-diol from Verticillium lecanii John Frederick Grove Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . 3¦Â-isopropylsulfonamido-5¦Â,17¦Á-pregnane-21,17-carbolactone C25H41NO4S ÏàËÆ¶È:72% Steroids 1998 63 464-469 Partial synthetic derivatization of canrenone and characterization of its impact on the inhibitory effect on Na1/K1-ATPase activity in human heart muscle J¨¹rgen Weiland,Rudolf Megges,Bernd Undeutsch,Rudolf Schön,Horst B¨¹chting,and Kurt R.H.Repke Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . ÎÚËÕËá ÏàËÆ¶È:72% Chinese Traditional and Herbal Drugs 2006 37 989-990 ºÚ³áÍÁ°×ÒϵĻ¯Ñ§³É·ÖÑо¿ ѦµÂ¾û;ÍõÐãÀö Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . 2,3-dihydroxy-9(11)-fernen-23-oic acid ÏàËÆ¶È:72% Natural Product Research and Development 2010 22 940-944 Chemical Constituents from Melastoma dodecandrum YANG Dan;MA Qing-yun; LIU Yu-qing; DING Zhong-tao; ZHOU Jun; ZHAO You-xing; Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . cladosporide A C25H40O3 ÏàËÆ¶È:72% The Journal of Antibiotics 2001 54 747-750 New Pentanorlanostane Derivatives, Cladosporide B-D, as Characteristic Antifungal Agents Against Aspergillus fumigatus, Isolated from Cladosporium sp. TOMOO HOSOE,SHIGERU OKAMOTO,KOOHEI NOZAWA,KEN-ICHI KAWAI,KAORU OKADA,GALBA MARIA DE CAMPOS TAKAKI,KAZUTAKA FUKUSHIMA and MAKOTO MIYAJI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . 20(S)-panaxadiol ÏàËÆ¶È:72% Asia-Pacific Traditional Medicine 2008 4 41-43 Studies on the Rare Anticancer Compounds of the Hydrolysate of the Saponins from Gynostemma pentaphfllum(Thunb)Makino Xu Zhi-chao, Han Ling, Zhao Yu-qing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 24 . methyl lucidenate C C28H42O7 ÏàËÆ¶È:71.4% Chinese Traditional and Herbal Drugs 2005 36 502-504 ËÉɼÁéÖ¥µÄ»¯Ñ§³É·ÖÑо¿ ÆÕÇí»Ý,³Âºç,³ÂÈôÜ¿ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 25 . 13S-hydroxy-9-oxo-9,10-seco-abiet-8(14)-en-18,10¦Á-olide C20H30O4 ÏàËÆ¶È:70.8% Planta Medica 2004 70 877-880 A New seco-Abietane-Type Diterpene from the Stem Bark of Picea glehni Reiko Tanaka,Shun-ichi Wada, Yoshitaka Kinouchi , Harukuni Tokuda , Shunyo Matsunaga Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 26 . vitetrifolin A C20H32O3 ÏàËÆ¶È:70.8% Phytochemistry 2000 55 873-877 Diterpenoids from the fruits of Vitex trifolia Masateru Ono, Hiromi Sawamura, Yasuyuki Ito, Koichi Mizuki , Toshihiro Nohara Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 27 . ursolic acid C30H48O3 ÏàËÆ¶È:70.8% Chemical & Pharmaceutical Bulletin 1985 33 5355-5357 Studies on Bioactive Substances in Crude Drugs Used for Arthritic Diseases in Traditional Chinese Medicine. III. Isolation and Identification of Anti-inflammatory and Analgesic Principles from the Whole Herb of Pyrola rotundifolia L. TAKUO KOSUGE,MASAMI YOKOTA,KIYOSHI SUGIYAMA,TAKAK |

2Â¥2015-05-14 11:08:21













»Ø¸´´ËÂ¥