| ²é¿´: 533 | »Ø¸´: 1 | ||
Èç¹ûÔÆÖªµÀ@гæ (³õÈëÎÄ̳)
|
[ÇóÖú]
whj-7΢Æ×ÇóÖú£¡¼±¼±¼±£¡¶àл£¡ ÒÑÓÐ1È˲ÎÓë
|
|
ë®´ú¼×´¼ 15.6,17.9,23.8,24.9,25.2,26.1,26.4,41.5,42.2,45.6,55.4,75.6,82.1,126.0,131.9 |
» ²ÂÄãϲ»¶
ÓжàÉÙÈËÊǽñÌì²éϵͳ֪µÀ½á¹ûµÄ£¿
ÒѾÓÐ18È˻ظ´
2026ÄêÒ¶ÆóËï»ù½ð
ÒѾÓÐ5È˻ظ´
¹ú×ÔÈ»ÃæÉϸ´ÅÌ~»¶ÓÌÖÂÛ
ÒѾÓÐ13È˻ظ´
»ù½ðϵͳʲôÄÚÈÝҲûÓÐ
ÒѾÓÐ9È˻ظ´
Ϊʲô×ÊÖúÊý¸÷´ó¸ßУ¶¼´´Ð¸ߣ¬×Ô¼ºÉêÇëÔõô¾ÍÕâôÄÑ
ÒѾÓÐ11È˻ظ´
Ôõô²é°¡
ÒѾÓÐ6È˻ظ´
ÄÄλ¸ßÈËÖÐÁË£¬°Ñ²éѯµ½µÄ½ØÍ¼Ìù³öÀ´ÈÃÎÒ¿´¿´£¬ÈÃÎÒ³¤³¤¼ûʶ
ÒѾÓÐ6È˻ظ´
ÃæÉϺÏ×÷µ¥Î»¸ÇÕÂ
ÒѾÓÐ5È˻ظ´
µ¼Ê¦Í²ۣºÎÒÔõô̯ÉÏÁËÕâô¸ö¼«Æ·Ñо¿Éú£¡
ÒѾÓÐ7È˻ظ´
ÉêÇëɾ³ý±¾Ìû
ÒѾÓÐ7È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÒѾÅÅÐòºÃµÄ̼»¯Ñ§Î»ÒÆÖµ£¬°ïæ΢Æ×²é»¯ºÏÎ¶àлÁË
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬¶àлÁË
ÒѾÓÐ3È˻ظ´
ÇóÖú±±¾©ÄÄÀïÓÐ FLS920 Ó«¹â¹âÆ×ÒÇ£¬ ¶àл£¡
ÒѾÓÐ12È˻ظ´
΢Æ×ÇóÖú£¡¼±¼±¼±£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú ¼±¼±¼±£¡£¡£¡
ÒѾÓÐ4È˻ظ´
¼±¼±¼±¡£¡£¡£¡£ÇóÖú΢Æ×Êý¾Ý£¨50%ÏàËÆ¶È¾ÍOKÁË£©£¬²»Ê¤¸Ðл£¡
ÒѾÓÐ8È˻ظ´

yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1566 (½²Ê¦)
- ½ð±Ò: 15048.4
- ºì»¨: 21
- Ìû×Ó: 2773
- ÔÚÏß: 261.2Сʱ
- ³æºÅ: 942922
- ×¢²á: 2010-01-15
- ÐÔ±ð: MM
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Èç¹ûÔÆÖªµÀ@: ½ð±Ò+8 2015-01-21 18:52:07
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Èç¹ûÔÆÖªµÀ@: ½ð±Ò+8 2015-01-21 18:52:07
|
1 . cyclonerodiol ÏàËÆ¶È:100% Magnetic Resonance in Chemistry 1990 28 662-664 Characterization of cyclonerodiol isolated from corn infested by fusarium moniliforme sheld.: One- and two-dimensional 1H and 13C NMR study D. Laurent, N. Goasdoue, F. Kohler, F. Pellegrin and N. Platzer Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . cyclonerotriol C15H28O3 ÏàËÆ¶È:80% Journal of the Chemical Society, Perkin Transactions 1 1975 1586-1590 Cyclonerotriol [6-(3-hydroxy-2,3-dimethylcyclopentyl)-2-methylhept-2-ene-1,6-diol], a new sesquiterpenoid metabolite of Fusarium culmorum James R. Hanson, Peter B. Hitchcock and Robert Nyfeler Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 10,11-dihydrocyclonerotriol C15H30O3 ÏàËÆ¶È:80% Natural Product Communications 2014 9 313-314 Cyclonerol Derivatives from Trichoderma longibrachiatum YM311505 Qi-Cun Xuan, Rong Huang, You-Wei Chen, Cui-Ping Miao, Kai-Xia Ma, Tang Wang and Shao-Hua Wu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . Trichoderiol A C15H26O2 ÏàËÆ¶È:73.3% Fitoterapia 2011 82 1035-1038 Sesquiterpenoids from Trichoderma atroviride, an endophytic fungus in Cephalotaxus fortunei Cheng-Jian Zheng, Pei-Xin Sun, Gui-Lin Jin, Lu-Ping Qin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . compound 2 C15H26O ÏàËÆ¶È:66.6% Canadian Journal of Chemistry 1997 75 634-640 Isolation, structure, and synthesis of chenopodanol and the absolute configuration of chenopodene and chenopodanol Motoo Tori, Tomonobu Hamaguchi, Mamiko Aoki, Masakazu Sono, Yoshinori Asakawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . cyclonerodiol C15H28O3 ÏàËÆ¶È:66.6% Journal of Shenyang Pharmaceutical University 2013 30 342-345 Secondary metabolites from marine sponge-associated fungus Hansfordia sp. ZHAO Dan-qi, WU Ze-hong, LIU Dong, PEI Yue-hu, LIN Wen-han, BAI Jiao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Deacetyllycoclavine ÏàËÆ¶È:62.5% Chinese Journal of Natural Medicines 2014 12 373-376 A new Lycopodium alkaloid from Phlegmariurus fargesii Ke PAN, Jian-Guang LUO, Ling-Yi KONG Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-01-07 18:31:34









»Ø¸´´ËÂ¥