| ²é¿´: 252 | »Ø¸´: 2 | ||
lqm19890117Òø³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬Ê®·Ö¸Ðл£¡
|
| ̼Æ×Êý¾Ý£º172.5, 150.8, 137.8£¬ 135.2£¬ 129.3£¬ 122.3£¬ 108.9£¬ 68.9£¬ 63.4£¬ 56.1£¬ 43.5£¬ 42.1£¬ 40.4£¬ 37.9£¬ 34.6£¬ 34.1£¬ 24.6£¬ 22.4£¬ 20.2£¬ 15.6 |
» ²ÂÄãϲ»¶
288»·¾³×¨Ë¶,Çóµ÷²ÄÁÏ·½Ïò
ÒѾÓÐ39È˻ظ´
353Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
Ò»Ö¾Ô¸211µç×ÓÐÅÏ¢347Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
323Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
22408 266Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
313Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
305Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×½á¹¹Ò»¸ö£¡Ê®·Ö¸Ðл£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×½á¹¹Ò»¸ö
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×½á¹¹Ò»¸ö£¡£¡
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¡¼±£¡£¡£¡ÏÈлл°¡£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú ¸ÐлÍò·Ö
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¡¼±¼±¼±£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿¼±¼±¼±£¡£¡ÇëÎÊÓÐûÓÐרÃŲ黯ºÏÎï±ê×¼¹âÆ×µÄÍøÕ¾ÄØ£¿
ÒѾÓÐ3È˻ظ´
danil1288
½ð³æ (ÕýʽдÊÖ)
- Ó¦Öú: 96 (³õÖÐÉú)
- ½ð±Ò: 4099.5
- É¢½ð: 14
- ºì»¨: 2
- Ìû×Ó: 405
- ÔÚÏß: 109.3Сʱ
- ³æºÅ: 779961
- ×¢²á: 2009-05-26
- ÐÔ±ð: GG
- רҵ: ÖÐÒ©Ò©ÐÔÀíÂÛ
ÒÔºóд»¯Ñ§Î»ÒÆÓðë½Ç¶ººÅ¸ô¿ªÖмäÎÞ¿Õ¸ñ![]() ²éѯ½á¹û£º¹²²éµ½631¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 8¦Á-Hydroxy-11E,13Z-labdadiene-15-al C20H32O2 ÏàËÆ¶È:65% Chemical & Pharmaceutical Bulletin 2002 50(4) 498-500 Labdane-Type Diterpenoids from the Wood of Cunninghamia konishii Yen-Cheng LI and Yueh-Hsiung KUO Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 12(S)-15,16-epoxy-13(16),14-labdaiene-8,12-diol C20H30O2 ÏàËÆ¶È:65% Acta Chemica Scandinavica 1978 32 203-215 Tobacco Chemistry. 50. (3S,5R,8S,9xi)-5,8-Epoxy-6-megastigmene-3,9-diol and (3S*,5R*,6R*,7E,9xi)-3,6-Epoxy-7-megastigmene-5,9-diol. Two New Nor-carotenoids of Greek Tobacco. Behr, Dan; Wahlberg, Inger; Nishida, Toshiaki; Enzell, Curt R. Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 15-isopimaren-8¦Â,20-diol ÏàËÆ¶È:65% Journal of the Brazilian Chemical Society 1991 2 25-30 Diterpenes from Vellozia bicolor. Angelo C. Pinto, Pedro P.S. Queiroz and Walmir S. Garcez. Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 16 ÏàËÆ¶È:65% Natural Product Communications 2008 3 399-412 Structural Elucidation of Pimarane and IsopimaraneDiterpenoids: The 13C NMR Contribution Ana M. L. Seca, Diana C. G. A. Pinto and Artur M. S. Silva Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-[(2-hydroxy-2,5,5,8¦Á-tetramethyldecahydro-1-naphthalenyl)methyl]-4-hydroxybenzoicacid C22H32O4 ÏàËÆ¶È:63.6% Chinese Chemical Letters 2004 15 316-318 A New Sesquiterpene-substituted Benzoic Acid from the Brown Alga Dictyopteris divaricata Fu Hang SONG, Xiao FAN , Xiu Li XU, Jie Lu ZHAO, Li Jun HAN,Jian Gong SHI Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Dictyvaric acid C22H32O4 ÏàËÆ¶È:63.6% Journal of Asian Natural Products Research 2005 7 777-781 Chemical constituents of the brown alga Dictyopteris divaricata F.-H. SONG, X. FAN, X.-L. XU, J.-L. ZHAO, L.-J. HAN and J.-G. SHI Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . cryptoporic acid A ÏàËÆ¶È:61.9% Phytochemistry 1991 30 1555-1559 Cryptoporic acids H and I, drimane sesquiterpenes from Ganoderma neo-japonicum and Cryptoporus volvatus Masao Hirotani, Tsutomu Furuya, Motoo Shiro Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . zonarol C21H30O2 ÏàËÆ¶È:61.9% Tetrahedron Letters 2000 41 5469-5473 Total synthesis of the marine sesquiterpene hydroquinones zonarol and isozonarol and the sesquiterpene quinones zonarone and isozonarone Jörg Schröder, Christine Magg, Karlheinz Seifert Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . hamiltonin A C21H31O3Cl ÏàËÆ¶È:61.9% Tetrahedron 1995 51 8189-8198 Unusual chlorinated homo-diterpenes from the South African nudibranch Chromodoris hamiltoni Jana Pika, D. John Faulkner Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (1S,3R,4R)-ent-3,4-Epoxyverticilla-7,12(18)-dien-1-ol C20H32O2 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2008 56(8) 1184-1188 New ent-Verticillane Diterpenoids from the Japanese Liverwort Jackiella javanica Fumihiro NAGASHIMA,Kozue WAKAYAMA, Yuki IOKA, and Yoshinori ASAKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 15-hydroxy-11¦Î,14¦Î-peroxylabda-8(17),12-dien-16-al ÏàËÆ¶È:60% Journal of Natural Products 1997 60 904-908 Labdane Diterpenoids from Alpinia chinensis Lai-King Sy and Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . peronemin B2 C20H24O5 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1994 42 1050-1055 Indonesian Medicinal Plants. VII. Seven New Clerodane-Type Diterpenoids, Peronemins A2, A3, B1, B2, B3, C1, and D1, from the Leaves of Peronema canescens (Verbenaceae) Isao KITAGAWA,Partomuan SIMANJUNTAK,Kazuyuki HORI,Nobumasa NAGAMI,Taifo MAHMUD,Hirotaka SHIBUYA and Motomasa KOBAYASHI Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . peronemin B1 C20H24O4 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1994 42 1050-1055 Indonesian Medicinal Plants. VII. Seven New Clerodane-Type Diterpenoids, Peronemins A2, A3, B1, B2, B3, C1, and D1, from the Leaves of Peronema canescens (Verbenaceae) Isao KITAGAWA,Partomuan SIMANJUNTAK,Kazuyuki HORI,Nobumasa NAGAMI,Taifo MAHMUD,Hirotaka SHIBUYA and Motomasa KOBAYASHI Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . isopimara-7,15-dien ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1982 30 3912-3921 Studies on the Constituents of the Crude Drug "Fritillariae Bulbus." III. On the Diterpenoid Constituents of Fresh Bulbs of Fritillaria thunbergii MIQ. JUNICHI KITAJIMA,TETSUYA KOMORI and TOSHIO KAWASAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (E)15-nor-16-oxo-8 (17),12-labdadiene C19H30O ÏàËÆ¶È:60% Journal of Asian Natural Products Research 2004 6 199-204 CHEMICAL CONSTITUENTS FROM ALPINIA TONKINENSIS JIAN ZHANG and LING-YI KONG Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . villosin C20H28O2 ÏàËÆ¶È:60% Fitoterapia 2001 72 837-838 New diterpene from Hedychium villosum Peng Xiao, Cuirong Sun, Muhammad Zahid,Omar Ishrud, Yuanjiang Pan |
» ±¾ÌûÒÑ»ñµÃµÄºì»¨£¨×îÐÂ10¶ä£©

2Â¥2013-08-24 11:32:00
lqm19890117
Òø³æ (СÓÐÃûÆø)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 327.5
- ºì»¨: 15
- Ìû×Ó: 131
- ÔÚÏß: 69.7Сʱ
- ³æºÅ: 1102613
- ×¢²á: 2010-09-18
- ÐÔ±ð: GG
- רҵ: ÌìȻҩÎﻯѧ
3Â¥2013-08-24 11:58:49














»Ø¸´´ËÂ¥
lqm19890117