| ²é¿´: 342 | »Ø¸´: 1 | |||
jwdongynľ³æ (ÖøÃûдÊÖ)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
|
CDCl3 24.7,34.0,39.4,41.6,43.2,47.8,48.0,55.1,56.2,57.9,109.8,112.4,118.7,121.0,127.1,144.9,145.8,152.7,192.9 |
» ²ÂÄãϲ»¶
²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ27È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ20È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ17È˻ظ´
277 ÊýÒ»104£¬Ñ§Ë¶£¬Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
²ÄÁÏÀà284µ÷¼Á
ÒѾÓÐ44È˻ظ´
295·ÖÇóµ÷¼Á
ÒѾÓÐ4È˻ظ´
Ò»Ö¾Ô¸Î÷±±¹¤Òµ´óѧ289 085602
ÒѾÓÐ29È˻ظ´
272·Ö²ÄÁÏ×ÓÇóµ÷¼Á
ÒѾÓÐ27È˻ظ´
ÖпÆÔº×Ü·Ö315Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
²ÄÁϹ¤³Ì085601£¬270Çóµ÷¼Á
ÒѾÓÐ30È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48426.9
- ºì»¨: 52
- Ìû×Ó: 6748
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
jwdongyn: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-01-15 18:25:25
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
jwdongyn: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-01-15 18:25:25
|
1 . Sinomenine ÏàËÆ¶È:78.9% Journal of Asian Natural Products Research 2007 9 13-18 Three major urinary metabolites of sinomenine in rats W.-M. CHENG, F. QIU and X.-S. YAO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . Sinomenine ÏàËÆ¶È:73.6% Archives of Pharmacal Research 2006 29 627-632 Aporphine alkaloids and their reversal activity of multidrug resistance (MDR) from the stems and rhizomes ofSinomenium acutum Yong Deuk Min, Sang Un Choi and Kang Ro Lee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . sinomenine ÏàËÆ¶È:68.4% Chemistry of Natural Compounds 2013 49 336-337 Kaempferol-3-O-¦Á-L-arabinopyranosyl(1¡ú6)-¦Â-D-galactopyranoside from Phytolacca octandra and its antimicrobial activity R. Manivannan, S. Ilayaraja Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . sinomenine N-oxide C19H23NO5 ÏàËÆ¶È:63.1% Journal of Natural Products 2005 68 1128-1130 Morphinane Alkaloids with Cell Protective Effects from Sinomenium acutum Guan-Hu Bao, Guo-Wei Qin, Rui Wang, and Xi-Can Tang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . (R)-disinomenine C38H44N2O8 ÏàËÆ¶È:63.1% Organic Letters 2008 10 3879-3882 pH-Dependent, Stereoselective Dimerization of Sinomenine Zhang-Shuang Deng, Yu Zhao, Cui-Cui He, Jie Jin, Yun-Mian He and Jian-Xin Li Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . milonine C19H23NO4 ÏàËÆ¶È:63.1% Phytochemical Analysis 2012 23 426-432 A Validated Method for the Simultaneous Quantitation of Bioactive Alkaloid Markers in the Leaf Ethanolic Extract of Cissampelos sympodialis Eichl.: a Phenological Variation Study A. F. Marinho, J. M. Barbosa-Filho and E. J. Oliveira Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . sinomenine ÏàËÆ¶È:63.1% China Journal of Chinese Materia Medica 2013 38 574-577 Akaloids from roots of Stephania dentifolia ZUO Ai-xue, LI Li, MA Yun-shu, RAO Gao-xiong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 8,14-dihydrosalutaridine C18H21O4N ÏàËÆ¶È:63.1% Natural Product Communications 2013 8 779-780 Two New Morphinandienone Alkaloids from Croton micradenus Armando L. Payo-Hill, Daysi Sandoval-L¨®pez, Herm¨¢n T. V¨¦lez-Castro, IraidaSpengler-Salabarr¨ªa and Luca Rastrelli Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . sinomenine C19H22O4 ÏàËÆ¶È:63.1% Chemistry of Natural Compounds 2013 49 980-982 Alkaloids from Stephania macrantha Ai-Xue Zuo, Gao-Xiong Rao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . sinomenine C19H23O4N ÏàËÆ¶È:63.1% Journal of Yunnan College of Traditional Chinese Medicine 2012 35 14-19 Studies on Alkaloids from the Stephania epigaea of Dai Traditional M edicine LI Li, ZUO Ai-xue, RAO Gao-xiong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . sinomenine C19H23O4N ÏàËÆ¶È:63.1% Chinese Joumal of Experimental Traditional Medical Fomulae 2013 19 134-137 Studies on Alkaloids of Stephania micrantha ZUO Ai-xue, ZHANG Qiu-ling, LI Li, MA Yun-shu, RAO Gao-xiong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 10¦Â-Methoxysinomenine C20H25N1O5 ÏàËÆ¶È:60% Tetrahedron 2012 68 2172-2178 Regio- and stereoselective C10¦Â¨CH functionalization of sinomenine: an access to more potent immunomodulating derivatives Yang-Tong Lou, Li-Yan Ma, Meng Wang, Dongsheng Yin, Ting-Ting Zhou, Ai-Zhong Chen, Zhao Ma, Chao Bian, Shaozhong Wang, Zhen-Yu Yang, Bing Sun, Zhu-Jun Yao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 4-Hydroxy-3-methoxy-17-methyl-(2',3'-dihydro-3',6'-bis-trifluoromethyl-pyridazino)[4',5'-6,7]-morphinan C22H23F6N3O2 ÏàËÆ¶È:59.0% Archiv der Pharmazie 1997 330 163-168 Syntheses of Novel Pyridazinomorphinans by Inverse Electron Demand Cycloaddition and their Binding to ¦Ì and ¦Ê Receptors Thilo Klindert, Isabel Stroetmann, Gunther Seitz, Georg Höfner, Klaus Th. Wanner, Gerlinde Frenzen and Brigitta Eckhoff Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . sinomenine ÏàËÆ¶È:57.8% Journal of Natural Products 2004 67 1842-1849 N-Inversion-Associated Conformational Dynamics Is Unusually Rapid in Morphine Alkaloids Anatoly M. Belostotskii, Zafrir Goren, and Hugo E. Gottlieb Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 14-episinomenine C19H23NO4 ÏàËÆ¶È:57.8% Journal of Natural Products 1996 59 476-480 New Morphinane and Hasubanane Alkaloids from Stephania cepharantha Noriaki Kashiwaba, Shigeo Morooka, Michiko Kimura, Minoru Ono, Jun Toda, Hideki Suzuki, and Takehiro Sano Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . sinomenine C19H23NO4 ÏàËÆ¶È:57.8% Chemistry of Natural Compounds 1996 32 737-858 ALKALOIDS. PLANTS, STRUCTURES, PROPERTIES" Chapter 2, continued R. Shakirov, M. V. Telezhenetskaya, I. A. Bessonova,S. F. Aripova, I. A. Israilov, M. N. Sultankhodzhaev,V. I. Vinogradova, V. I. Akhmedzhanova, T. S. Tulyaganov,B. T. Salimov, and V. A. Tel'nov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . tetrahydropronuciferine C19H26NO3 ÏàËÆ¶È:57.8% Natural Product Research 2007 21 704-709 New alkaloids from Phoebe scortechinii Khalijah Awang; Mat Ropi Mukhtar; M. Rais Mustafa; Marc litaudon; Khozirah shaari; Khalit Mohamad; A. Hamid A. Hadi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 17-Demethyl sinomenine ÏàËÆ¶È:57.8% Bioorganic & Medicinal Chemistry 2011 19 3096-3104 Synthesis and biological evaluation of unique stereodimers of sinomenine analogues as potential inhibitors of NO production Peng Teng,Hai-Liang Liu, Zhang-Shuang Deng, Zhi-Bing Shi ,Yun-Mian He , Li-Li Feng,Qiang Xu ,Jian-Xin Li Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . 6-Hydroxyimino sinomenine ÏàËÆ¶È:57.8% Bioorganic & Medicinal Chemistry 2011 19 3096-3104 Synthesis and biological evaluation of unique stereodimers of sinomenine analogues as potential inhibitors of NO production Peng Teng,Hai-Liang Liu, Zhang-Shuang Deng, Zhi-Bing Shi ,Yun-Mian He , Li-Li Feng,Qiang Xu ,Jian-Xin Li Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . (S)-disinomenine ÏàËÆ¶È:57.8% Organic Letters 2008 10 3879-3882 pH-Dependent, Stereoselective Dimerization of Sinomenine Zhang-Shuang Deng, Yu Zhao, Cui-Cui He, Jie Jin, Yun-Mian He and Jian-Xin Li Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-01-15 17:02:24













»Ø¸´´ËÂ¥