| ²é¿´: 239 | »Ø¸´: 1 | |||
kengkengsee½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú£¡
|
|
ÈܼÁ£ºë®´úÂÈ·Â CÆ×Ðźţº9.34,14.86,17.61,18.59,23.81,24.39,35.27,37.56,37.94,38.73,39.38,48.25,56.40,71.88,107.75,138.83,147.93,156.28,195.20 |
» ²ÂÄãϲ»¶
336²ÄÁÏÓ뻯¹¤085600Çóµ÷¼Á
ÒѾÓÐ21È˻ظ´
²ÄÁÏÓ뻯¹¤×¨Ë¶306·ÖÕÒºÏÊʵ÷¼Á
ÒѾÓÐ17È˻ظ´
278Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
266Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
ÉúÎïѧ308·ÖÇóµ÷¼Á£¨Ò»Ö¾Ô¸»ª¶«Ê¦´ó£©×ö¹ý·Ö×ÓʵÑé
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸0703»¯Ñ§ÕÐ61×îÖÕÅÅÃû62»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
259Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
071000ÉúÎïѧ£¬Ò»Ö¾Ô¸ÉîÛÚ´óѧ296·Ö£¬Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
287Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Ц¶à»á»³ÔÐ
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1216 (½²Ê¦)
- ½ð±Ò: 9788.1
- É¢½ð: 610
- ºì»¨: 40
- ɳ·¢: 3
- Ìû×Ó: 2723
- ÔÚÏß: 1284.6Сʱ
- ³æºÅ: 2010893
- ×¢²á: 2012-09-18
- ÐÔ±ð: GG
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
kengkengsee: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-10-28 20:11:10
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
kengkengsee: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-10-28 20:11:10
|
²éѯ½á¹û£º¹²²éµ½489¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 15-nor-14-oxo-8(17),12-labdadiene-18-ol C19H30O2 ÏàËÆ¶È:100% Journal of Natural Products 1998 61 997-1000 Five New Diterpenoids from the Wood of Cunninghamia konishii Yen-Cheng Li and Yueh-Hsiung Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 15-nor-14-oxolabda-8(17),12E-diene-18-oic acid C19H28O3 ÏàËÆ¶È:78.9% Planta Medica 2008 74 449-452 Labdane-Type Diterpenes Active against Acne from Pine Cones (Pinus densiflora) Md. Zakir Sultan, Young-Min Jeon, Surk-Sik Moon Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 15-nor-14-oxolabda-8(17),12E-dien-19-ol C19H30O2 ÏàËÆ¶È:78.9% Planta Medica 2009 75 1344-1348 Terpenoids from Roots of Chloranthus henryi Xianwen Gan, LeiMa, Qigang Chen, Qiuqun Chen, Qiang Yu, Lihong Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 4S,5R,9S,10R-8(17),12,14-labdantrien-18-ol C20H32O ÏàËÆ¶È:75% Planta Medica 2001 67 542-547 Two New Bislabdane-Type Diterpenoids and Three New Diterpenoids from the Roots of Cunninghamia lanceolata Jiang Du, Ming-Lei Wang, Ruo-Yun Chen, De-Quan Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3¦Â-hydroxy-15-nor-14-oxo-8(17),12-labdadien-14-al C19H30O2 ÏàËÆ¶È:73.6% Journal of Natural Products 2012 75 694-698 Terpenoids from Chloranthus serratus and Their Anti-inflammatory Activities Mi Zhang, Munekazu Iinuma, Jun-Song Wang, Masayoshi Oyama, Tetsuro Ito, and Ling-Yi Kong Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 3R,14R,15-trihydroxy-3-oxolabd-8(17)-ene C20H35O4 ÏàËÆ¶È:65% Phytochemistry 2006 67 1455-1459 Microbiological transformation of two labdane diterpenes, the main constituents of Madia species, by two fungi Mamdouh S.A. Haridy, Ahmed A. Ahmed, Matsumi Doe Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 13-epitorreferol ÏàËÆ¶È:65% Chemical & Pharmaceutical Bulletin 1995 43 5-8 Fern Constituents : Four New Diterpenoid Glycosides from Fresh Leaflets of Gleichenia japonica Kenji SHIOJIMA,Masayoshi SUZUKI,Hiroshi AOKI and Hiroyuki AGETA Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 18-hydroxy(-)-manool ÏàËÆ¶È:65% China Journal of Chinese Materia Medica 2000 25 291-292 Chemical Constituents from Speranskia tuberculata(Bge.)Baill Li Chong, ZHANG Chengzhong, HU Fangdi, SHI Jiangong Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . excoecarin G2 C20H34O4 ÏàËÆ¶È:65% Chemical & Pharmaceutical Bulletin 1999 47 456-458 Stereostructures of New Labdane-Type Diterpenes, Excoecarins F, G1, and G4 from the Wood of Excoecaria agallocha Tenji KONISHI,Takao KONOSHIMA,Yasuhiro FUJIWARA,Shiu KIYOSAWA,Kazumoto MIYAHARA and Masatoshi NISHI Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . isoagatholal ÏàËÆ¶È:65% Phytochemistry 1980 19 2479-2481 A diterpene glycoside and lignans from seed of Thujopsis dolabrata Shinichi Hasegawa, Yoshiyuki Hirose Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-10-28 19:02:51














»Ø¸´´ËÂ¥