| ²é¿´: 364 | »Ø¸´: 1 | |||
fangfuhu123гæ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖú»¯ºÏÎïs-3-17 ÒÑÓÐ1È˲ÎÓë
|
| 13C NMR (101 MHz, CDCl3) ¦Ä 23.50,23.67,27.17,27.91,36.51,47.47,55.42,68.39,125.92,126.66,138.47,161.75,199.04, |
» ²ÂÄãϲ»¶
290µ÷¼ÁÉúÎï0860
ÒѾÓÐ5È˻ظ´
359Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á£¬985²ÄÁÏÓ뻯¹¤348·Ö
ÒѾÓÐ5È˻ظ´
211±¾¿Æ²ÄÁÏ»¯¹¤Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
²ÄÁÏ¿¼Ñе÷¼Á
ÒѾÓÐ24È˻ظ´
366Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
Çóµ÷¼Á£¬Ò»Ö¾Ô¸´óÁ¬Àí¹¤´óѧ354·Ö
ÒѾÓÐ5È˻ظ´
308Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
266Çóµ÷¼Á£¬Ò»Ö¾Ô¸¹þ¹¤³Ìµç×ÓÐÅÏ¢£¬±¾¿Æ»ñ¶àÏî¹ú½±ºÍÊ¡½±
ÒѾÓÐ7È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÖØ½ðÇóÖúÒ»¸ö»¯ºÏÎïµÄÀí»¯ÐÔÖʵȸ÷ÏîÊý¾Ý¡£
ÒѾÓÐ3È˻ظ´
ÇóÖú°ïæÓÃscifinder²éÕÒÏÂÃæÁ½¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
¡¾ÇóÖú¡¿ ÔõÑùÈ·¶¨Ò»¸ö»¯ºÏÎïÊÇ·ñÊÇл¯ºÏÎï
ÒѾÓÐ7È˻ظ´
ÇóÖú¼¸¸ö»¯ºÏÎï΢Æ×Êý¾Ý£¬¼±¼±£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖúÒ»»¯ºÏÎ£¡
ÒѾÓÐ5È˻ظ´
»ÆÍªÀ໯ºÏÎïpKaÇóÖú
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿ÈçºÎÅжÏÈý¸ö»¯ºÏÎïµÄ¹âѧ»îÐÔ
ÒѾÓÐ8È˻ظ´
ÇóÖú¹ØÓÚ»¯ºÏÎïÀí»¯ÐÔÖʲéѯµÄÍøÕ¾ºÍÊý¾Ý¿â
ÒѾÓÐ9È˻ظ´
¡¾ÇóÖú¡¿Î´Öª»¯ºÏÎïµÄ¼ì²â·½·¨
ÒѾÓÐ13È˻ظ´
¡¾ÇóÖú¡¿¸÷λºÃ£¬ÇëÎÒ¿´Ò»¸ö¼òµ¥»¯ºÏÎïµÄHNMRÆ×ͼ¡£
ÒѾÓÐ20È˻ظ´
¡¾ÇóÖú¡¿Õæ³ÏÇóÖúÒ©Æ·»¯ºÏÎïÔʼרÀûÔõô²éÕÒ£¿
ÒѾÓÐ50È˻ظ´
¡¾ÇóÖú¡¿ÓлúÎý»¯ºÏÎïÔõô´¦Àí
ÒѾÓÐ19È˻ظ´
¡¾ÇóÖú¡¿ÒÑÖª»¯ºÏÎï·Ö×ÓÁ¿£¬¿ÉÒÔÔÚSCIENCE-FINDERÉϲéÕÒÏà¹Ø½á¹¹Ê½Âð£¿
ÒѾÓÐ10È˻ظ´
¡¾ÇóÖú¡¿°ïæÃèÊöÒ»ÏÂÈý¸öС·Ö×Ó»¯ºÏÎֻÓÐһάºË´Åͼ£¡
ÒѾÓÐ7È˻ظ´
¡¾ÇóÖú¡¿ÈçºÎ·ÖÀëÓлúÀë×Ó»¯ºÏÎï
ÒѾÓÐ6È˻ظ´
¡¾ÇóÖú¡¿±È½ÏÁ©»¯ºÏÎKÐÔ´óС
ÒѾÓÐ19È˻ظ´
¡¾ÇóÖú¡¿ÇóÖú»¯ºÏÎïÎȶ¨ÐÔ
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿ÒºÌ廯ºÏÎïÈçºÎ²âºìÍâ
ÒѾÓÐ15È˻ظ´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
fangfuhu123: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-04-01 22:08:49
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
fangfuhu123: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-04-01 22:08:49
|
²éѯ½á¹û£º¹²²éµ½36¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (6R,7E,9R) - 9 - hydroxy - 4,7 - megastigmadien-3-one C13H20O2 ÏàËÆ¶È:100% Phytochemistry 2004 65 497-505 Structure elucidation and phytotoxicity of C13 nor-isoprenoids from Cestrum parqui Brigida D¡¯Abrosca, Marina DellaGreca, Antonio Fiorentino, Pietro Monaco,Palma Oriano, Fabio Temussi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . (6R,7E,9S)-9-hydroxy-4,7-megastigmadien-3-one ÏàËÆ¶È:100% Natural Product Research 2005 19 99-103 C13 Norisoprenoids from Brassica Fruticulosa Francesca Cutillo; Marina Dellagreca; Lucio Previtera; Armando Zarrelli Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . (6R,7E)-9-hydroxy-4,7-megastigmadien-3-one ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2014 39 83-88 Anti-inflammatory constituents from Inula japonica ZHU Hong, TANG Sheng-an, QIN Nan, DUAN Hong-quan, JIN Mei-hua Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 9-hydroxymegastigma-4,7-dlen-3-one ÏàËÆ¶È:100% Australian Journal of Chemistry 1989 42 2071-2084 Norisoprenoids in Vitis vinifera White Wine Grapes and the Identification of a Precursor of Damascenone in These Fruits MA Sefton, GK Skouroumounis, RA Massywestropp and PJ Williams Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 4-[(1E)-3-hydroxy-1-buten-1-yl]-3,5,5-trimethyl-2-cyclohexen-1-one ÏàËÆ¶È:92.3% Journal of Chinese Medicinal Materials 2013 36 1267-1270 Non-taxoid Chemical Constituents from Needles of Taxus cuspidata SU Jian, ZHANG Man-li, HUO Chang-hong, SHI Qing-wen, WU Yi-bing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 9-hydroxy-4,7-magastimadiene-3-one-3-oxo-¦Á-ionol C13H20O2 ÏàËÆ¶È:92.3% Journal of the Chemical Society of Pakistan 2003 25 337−340 Chemical constituents of Taxus wallichiana Zucc. HABIB-UR-REHMAN, M.ARFAN, ATTA-UR-RAHMAN, M.I.CHOUDHARY AND A.M.KHAN Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 6R,9R-3-oxo-¦Á-ionol ÏàËÆ¶È:84.6% Acta Pharmaceutica Sinica 2006 Vol 41 431-434 Chemical constituents of Glechoma longituba YANG Nian-yun; DUAN Jin-ao; LI Ping; QIAN Shi-hui Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . (6R,7E,9S)-9-hydroxy-4,7-megastigmadien-3-one ÏàËÆ¶È:84.6% Acta Chemica Scandinavica 1978 32B 391-394 Tobacco Chemistry. 47. (3S,6R,7E,9R)- and (3S*,6R*,7E,9S*)-4,7-Megastigmadiene-3,9-diol. Two New Nor-carotenoids of Greek Tobacco. Behr, Dan; Wahlberg, Inger; Nishida, Toshiaki; Enzell, Curt R. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . compound ÏàËÆ¶È:84.6% Acta Chemica Scandinavica 1978 32B 391-394 Tobacco Chemistry. 47. (3S,6R,7E,9R)- and (3S*,6R*,7E,9S*)-4,7-Megastigmadiene-3,9-diol. Two New Nor-carotenoids of Greek Tobacco. Behr, Dan; Wahlberg, Inger; Nishida, Toshiaki; Enzell, Curt R. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . (6R,9R) 9-hydroxy-4-megastigmen-3-one C13H22O2 ÏàËÆ¶È:69.2% Phytochemistry 2004 65 497-505 Structure elucidation and phytotoxicity of C13 nor-isoprenoids from Cestrum parqui Brigida D¡¯Abrosca, Marina DellaGreca, Antonio Fiorentino, Pietro Monaco,Palma Oriano, Fabio Temussi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . blumenol C ÏàËÆ¶È:69.2% Acta Botanica Yunnanica 2003 25(4) 503-506 An Ionone Derivative from Isodon leucophyllus ZHAO Ai-Hua,PENGLi-Yan,WANG Zong-Yu,SUN Han-Dong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 6a ÏàËÆ¶È:69.2% Chemical & Pharmaceutical Bulletin 1988 36 2475-2484 Studies on the Glycosides of Epimedium grandiflorum MORR. var. thunbergianum (MIQ.) NAKAI. III TOSHIO MIYASE,AKIRA UENO,NOBUO TAKIZAWA,HIROMI KOBAYASHI and HIROKO OGUCHI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 3-oxo-¦Á-ionol(3,4-dehydro-blumenol C) ÏàËÆ¶È:69.2% Phytochemistry 1995 39 617-619 Nor-sesquiterpenes from Teucrium heterophyllum Braulio M. Fraga, Melchor G. Hern¨¢ndez, Teresa Mestres, David Terrero, Jos¨¦M. Arteaga Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 2 ÏàËÆ¶È:69.2% Phytochemistry 1992 31 1649-1652 Two diastereomeric 3-oxo-¦Á-ionol ¦Â-d-glucosides from raspberry fruit Anni Pabst, Denis Barron, Etienne S¨¦mon, Peter Schreier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 4 ÏàËÆ¶È:69.2% Phytochemistry 1992 31 1649-1652 Two diastereomeric 3-oxo-¦Á-ionol ¦Â-d-glucosides from raspberry fruit Anni Pabst, Denis Barron, Etienne S¨¦mon, Peter Schreier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-04-01 12:30:29













»Ø¸´´ËÂ¥