| ²é¿´: 245 | »Ø¸´: 1 | ||
ѼÀæÄ¾³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú лл£¡51d ÒÑÓÐ1È˲ÎÓë
|
|
̼Æ×Êý¾Ý 15.86, 20.30, 20.61, 25.83, 37.48, 39.85, 41.51, 75.56, 82.34, 121.79, 127.59, 138.63, 140.86, 167.23, 169.22, 214.66 |
» ²ÂÄãϲ»¶
085602µ÷¼Á ³õÊÔ×Ü·Ö335
ÒѾÓÐ7È˻ظ´
»¯Ñ§357·Ö£¬¿¼Ñе÷¼Á
ÒѾÓÐ7È˻ظ´
278Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
085400µç×ÓÐÅÏ¢319Çóµ÷¼Á£¨½ÓÊÜ¿çרҵµ÷¼Á£©
ÒѾÓÐ6È˻ظ´
323Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
Ò»Ö¾Ô¸±±¾©2£¬²ÄÁÏÓ뻯¹¤308Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
26¿¼Ñе÷¼Á0710 0860
ÒѾÓÐ13È˻ظ´
296²ÄÁÏר˶Çóµ÷¼Á
ÒѾÓÐ22È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ12È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬Ð»Ð»~~
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
̼Æ×ÇóÖú ¼±ÓÃ
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¡¼±£¡Ð»Ð»£¡
ÒѾÓÐ5È˻ظ´
άÆÕÇóÖú£¬Ð»Ð»£¡£¡
ÒѾÓÐ3È˻ظ´
JYN-33 ΢Æ×ÇóÖú£¬¼±Çó£¬Ð»Ð»£¬×·¼Ó½ð±Ò¡£¡£¡£
ÒѾÓÐ6È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
΢Æ× Ç󻯺ÏÎï
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â¼ìË÷Ò»»¯ºÏÎï
ÒѾÓÐ4È˻ظ´
ÇóÖú13C΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖúÒ»»¯ºÏÎï΢Æ×Êý¾Ý½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
Çó´óϺ²é΢Æ×£¬Íò·Ö¸Ðл°¡£¡£¡£¡
ÒѾÓÐ3È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
·çÐÐÕß007
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1309 (½²Ê¦)
- ½ð±Ò: 12672.8
- ºì»¨: 15
- Ìû×Ó: 1490
- ÔÚÏß: 299.5Сʱ
- ³æºÅ: 2542465
- ×¢²á: 2013-07-12
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
²éѯ½á¹û£º¹²²éµ½172¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . carpelipine A C20H28O5 ÏàËÆ¶È:80% Planta Medica 1999 65 94-96 Germacranolides from Carpesium Iipskyi Yan-Ping Shi, Wei Guo, and ZhongJianJia Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . germacranolide(3-oxo-9¦Â-angeloyl-6(¦ÂH),7(¦ÁH)-germacra-11(13)-ene-6,12-olide) C20H28O5 ÏàËÆ¶È:80% Chemical Research in Chinese Universities 1998 14 337¡«339 New Sesquiterpene Lactones from Carpesium Lipskyi SHI Yan-ping, YANG Chao and JIA Zhong-jian Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ineupatorolide B ÏàËÆ¶È:60% Chinese Traditional and Herbal Drugs 2011 42 1083-1086 Chemical constituents of Inula cappa flowers YANG, Yan, WANG, Yu-fang, ZHAO, Lei, DONG, Mei, HUO, Chang-hong, GU, Yu-cheng, SHI, Qing-wen Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 2-hydroxy-3-(1,2,2-trimethylcyclopentyl)-6-methylphenyl acetate C17H24O3 ÏàËÆ¶È:58.8% Tetrahedron 2006 62 9393-9402 Structure revision of HM-3, an aromatic sesquiterpene isolated from the phytopathogenic fungus Helicobasidium mompa. First total syntheses of HM-3 and HM-4 A. Srikrishna, P.C. Ravikumar Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . blepharostol C15H26O ÏàËÆ¶È:56.2% Phytochemistry 2004 65 2357-2362 Terpenoids from the liverwort Blepharostoma trichophyllum Hildegard Feld, Josef Zapp, Joseph D. Connolly, Hans Becker Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 9b ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 1994 42 265-270 Marine Natural Products. XXXII. Absolute Configurations of C-4 of the Manoalide Family, Biologically Active Sesterterpenes from the Marine Sponge Hyrtions erecta Motomasa KOBAYASHI,Takumi OKAMOTO,Kozo HAYASHI,Norio YOKOYAMA,Takuma SASAKI and Isao KITAGAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 2,6-dimethyl-2E,6E-octadienoic acid 1,6'-lactone 8-¦Â-D-glucopyranoside ÏàËÆ¶È:56.2% Chinese Chemical Letters 2000 11 709-710 A New Monoterpene Glycoside from Swertia punicea Xin MING, Ming Hua QIU, Rui Lin NI',Guo Lin ZHANG Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . encelin ÏàËÆ¶È:56.2% Journal of Natural Products 1982 Vol 45 749-753 Molecular Structure of Irazunolide, A New Eudesmanolide From Hieracium irazuensis Carlos Hasbun, Marco A. Calvo, Luis J. Poveda, Arcelio Malcolm, Terry J. Delord, Steven F. Watkins, Frank R. Fronczek, Nikolaus H. Fischer Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 2b ÏàËÆ¶È:56.2% Phytochemistry 1994 36 637-641 Cadinanes from Artemisia annua that may be intermediates in the biosynthesis of artemisinin Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . eudesmanolide ÏàËÆ¶È:56.2% Phytochemistry 1991 30 3293-3295 Hydroxy-bis-dihydroencelin, a dimeric eudesmanolide and other eudesmanolides from Montanoa speciosa Leovigildo Quijano, Federico G¨®mez-Garibay, I.B.Trejo RuthI. B., Tirso Rios Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Norsubspicatin A C16H24O3 ÏàËÆ¶È:56.2% Tetrahedron Letters 2011 52 6388-6391 Five new subspicatins and noreremophilane from Parasenecio petasitoides collected in China Yoshinori Saito, Mayu Ichihara , Yasuko Okamoto , Xun Gong, Chiaki Kuroda , Motoo Tori Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Subvellerolactones D C15H20O5 ÏàËÆ¶È:56.2% Bioorganic & Medicinal Chemistry Letters 2010 20 5385-5388 Lactarane sesquiterpenoids from Lactarius subvellereus and their cytotoxicity Ki Hyun Kim, Hyung Jun Noh, Sang Un Choi, Ki Moon Park, Soon-Ja Seok, Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Subvellerolactones E C15H20O5 ÏàËÆ¶È:56.2% Bioorganic & Medicinal Chemistry Letters 2010 20 5385-5388 Lactarane sesquiterpenoids from Lactarius subvellereus and their cytotoxicity Ki Hyun Kim, Hyung Jun Noh, Sang Un Choi, Ki Moon Park, Soon-Ja Seok, Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . gigantene ÏàËÆ¶È:56.2% Natural Product Research 2010 24 391-397 Secondary metabolites from Eryngium species B. Muckensturm; A. Boulanger; M. Farahi; J. P. Reduron Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 1 C15H20O3 ÏàËÆ¶È:56.2% Journal of the Chemical Society, Perkin Transactions 1 1988 157-160 A new eudesmenolide and 2-hydroxycostic acid from Sphaeranthus indicus linn. X-Ray molecular structure of 4¦Á,5¦Á-epoxy-7¦Á-hydroxyeudesmanolide Jayant S. Sohoni, Supada R. Rojatkar, Mandakini M. Kulkarni, Narayandatta N. Dhaneshwar, Sudam S. Tavale, Tayur N. Gururow and Bhimsen A. Nagasampagi Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 1,3-bis[5-fluoro-1-(¦Â-2'-deoxy-3',5'-di-O-acetylribofuranosyl)-2,4-dioxopyrimidinyl]propane C29H34F2N4O14 ÏàËÆ¶È:56.2% Bioorganic & Medicinal Chemistry 2012 20 5164-5168 Synthesis and one-electron reduction characteristics of radiation-activated prodrugs possessing two 5-fluorodeoxyuridine units Kazuhito Tanabe, Masaaki Sugiura, Takeo Ito, Sei-ichi Nishimoto Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 2-(R)-(1S,4R,5-methoxy-7-methyl-1,2,3,4-tetrahydronaphthalen-1-yl)-propan-1-ol C16H24O2 ÏàËÆ¶È:56.2% Tetrahedron 2013 69 6468-6473 Total synthesis and structural confirmation of the antibacterial diterpene leubethanol Jessica M.H. Lu, Michael V. Perkins, Hans J. Griesser Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . N3-butyl-N1-(1-methylethyl)-N1-[(1Z)-2-phenylprop-1-en-1-yl]propanediamide C19H28N2O2 ÏàËÆ¶È:56.2% Helvetica Chimica Acta 2013 96 2081-2091 Synthesis of 3-Carbamoyl ¦Â-Lactams via Manganese(III)-Promoted Cyclization of N-Alkenylmalonamides Paweł Punda, Łukasz Ponikiewski and Sławomir Makowiec Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 9-Oxo-11¦Â,13-dihydrotournefortiolide C15H20O3 ÏàËÆ¶È:56.2% European Journal of Organic Chemistry 1990 1990 541-545 New eudesmane derivatives from Artemisia tournefortiana Juan Francisco Sanz and Juan Alberto Marco Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . philippinlin C C15H22O3 ÏàËÆ¶È:56.2% Marine Drugs 2014 12 4495-4503 Oxygenated Eremophilane- and Neolemnane-Derived Sesquiterpenoids from the Soft Coral Lemnalia philippinensis Yun-Jie Xio, Jui-Hsin Su, Yen-Ju Tseng, Bo-Wei Chen, Wangta Liu and Jyh-Horng SheuMar. Drugs Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-10-20 23:17:04














»Ø¸´´ËÂ¥