| ²é¿´: 214 | »Ø¸´: 1 | ||
willkuangͳæ (³õÈëÎÄ̳)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý²éѯ
|
| 23.6,27.6,30.9,31.5,41.5,46.7,53.9,55.8,55.8,60.3,65.3,89.9,110.6,121.9,128.1,136.2,144.1,145.9 ÂÈ·Â×öÈܼÁ |
» ²ÂÄãϲ»¶
295·ÖÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
ɽ¶«¸ßУ½Ìʦ¿¼ºË³¬¼¶ÎÞµ×Ïߣ¬Ô±¹¤¹ý²»ÏÂÈ¥À²
ÒѾÓÐ4È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
µ÷¼Á
ÒѾÓÐ19È˻ظ´
²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ10È˻ظ´
307Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
303Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁÏÓ뻯¹¤300Çóµ÷¼Á
ÒѾÓÐ35È˻ظ´
²ÄÁÏרҵ344Çóµ÷¼Á
ÒѾÓÐ21È˻ظ´
Ò»Ö¾Ô¸±±Àí¹¤298Ó¢Ò»Êý¶þÇóµ÷¼Á
ÒѾÓÐ15È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
½¨ÒéȺÖ÷¿ªÒ»¸ö΢Æ×ÇóÖúרÀ¸°É
ÒѾÓÐ14È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
ÇóÖú3¸öÓÃ΢Æ×½âÎöµÄ½á¹¹
ÒѾÓÐ8È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú/½»Á÷¡¿ÈçºÎ´ÓGENBANKÉϲéѯ¾úÖêµÄµÄAcession No
ÒѾÓÐ5È˻ظ´
¡¾ÇóÖú¡¿Î¢·´-É«Æ× ÔõôʹÓ𡣿
ÒѾÓÐ8È˻ظ´
¡¾ÇóÖú¡¿ôȼ׻ù¿Ç¾ÛÌÇ ¼«À仯Äý½º¼¼Êõ ΢Çò É«Æ×¹Ì¶¨Ïà
ÒѾÓÐ3È˻ظ´
wq0616
Ìú¸Ëľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 323 (´óѧÉú)
- ½ð±Ò: 6659.6
- ºì»¨: 8
- Ìû×Ó: 955
- ÔÚÏß: 72.9Сʱ
- ³æºÅ: 2001721
- ×¢²á: 2012-09-14
- ÐÔ±ð: MM
- רҵ: ÖÐÒ©ÅÚÖÆ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
willkuang: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-01-21 22:22:05
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
willkuang: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-01-21 22:22:05
|
1 . lycoramine ÏàËÆ¶È:94.4% Planta Medica 1987 53 259-261 Alkaloids of Lycoris guangxiensis Hui-Yin Li, Guang-En Ma, Yin Xu and Shan-Hai Hong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . lycoramine C16H19NO4 ÏàËÆ¶È:94.4% Phytochemistry 1991 30 675-677 Alkaloid N-oxides from Lycoris sanguinea Shigeru Kobayashi, Kimihito Satoh, Atsushi Numata, Tetsuro Shingu, Masaru Kihara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . lycoramine ÏàËÆ¶È:94.4% Phytochemistry 1990 29 2685-2687 A heterodimer alkaloid from Narcissus pallidiflorus Carles Codina,Francesc Viladomat,Jaume Bastida,Mario Rubiralta,Jean-Charles Quirion Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . O-demethyllycoramine ÏàËÆ¶È:77.7% Heterocycles 2009 77 1389-1396 Two New Alkaloids from Bulbs of Lycoris squamigera Mariko Kitajima, Eri Kinoshita, Noriyuki Kogure, and Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . epinorlycoramine C16H21NO3 ÏàËÆ¶È:72.2% Phytochemistry 1993 34 1656-1658 Alkaloids from Narcissus leonensis Jaume Bastida, Francesc Viladomat, Salvador Bergoñon, Juan Marcos Fernandez, Carles Codina, Mario Rubiralta, Jean-Charles Quirion Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . acetyllycoramine C19H25NO4 ÏàËÆ¶È:63.1% Pharmazie 1999 54 535-537 Further alkaloids from the flowers of Pancratium maritimum D.T.A. Youssef Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (¨C)-(4¦Á ¦Á,6¦Á)-6-Chloro-4¦Á,5,9,10,11,12-Hexahydro-3-methoxy-11-methyl-6 H-benzofuro [3¦Á,3,2-e,f] [2] benzazepin C17H20ClNO2 ÏàËÆ¶È:61.1% Pharmazie 2007 62 403-405 Synthesis of 6¦Â-d-glucosyl and 6-nitroxy (− -galanthamine derivatives as acetylcholinesterase inhibitorsE. Perissutti, F. Fiorino, B. Severino, F. Frecentese, P. Massarelli, C. Nencini, V. Santagada and G. Caliedno Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . equatorial 8-hydroxy-saraine-1 ÏàËÆ¶È:61.1% Tetrahedron 1996 52 14961-14974 Further studies of alkaloids from Reniera sarai: Structures of saraine-3 and isosaraine-3; absolute stereochemistry of saraine-1 and saraine-2 Yuewei Guo, Anna Madaio, Enrico Trivellone, Gennaro Scognamiglio, Guido Cimino Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . tubotaiwine C20H24N2O2 ÏàËÆ¶È:60% Phytochemistry 1990 29 3321-3325 Alkaloids from leaves and bark ofAlstonia scholaris in the Philippines Tatsuo Yamauchi,Fumiko Abe,William G. Padolina,Fabian M. Dayrit Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . Tubotaiwine ÏàËÆ¶È:60% Phytochemistry 1984 23 1771-1778 Antimicrobially active alkaloids from Tabernaemontana pachysiphon T. A. van Beek, F. L. C. Kuijlaars, P. H. A. M. Thomassen, R. Verpoorte, A. Baerheim Svendsen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . reticuline C19H23NO4 ÏàËÆ¶È:57.8% Biochemical Systematics and Ecology 2011 39 872-875 Chemical constituents from the bark of Annona salzmannii (Annonaceae) Pedro Ernesto Oliveira da Cruz, Emmanoel Vilaça Costa, Val¨¦ria Regina de Souza Moraes, Paulo Cesar de Lima Nogueira, Mayara Evelyn Vendramin, Andersson Barison, Antonio Gilberto Ferreira, Ana Paula do Nascimento Prata Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . isolariciresinol-4'-Me ether C21H26O6 ÏàËÆ¶È:57.8% Phytochemistry 1978 17 499-502 13C NMR spectral analysis of lignans from Araucaria angustifolia Sebastião Ferreira Fonseca, Jayr de Paiva Campello, Lauro E.S. Barata, Edmundo A. R¨²veda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . corymotine ÏàËÆ¶È:55.5% Journal of Natural Products 1988 Vol 51 262 Alkaloids from Corydalis remota Xiaoyong Fu, Wenzao Liang, Guoshi Tu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . (S)-17-Demethyl disinomenine C36H40N2O8 ÏàËÆ¶È:55.5% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . (+)-galanthamine C17H19NO4 ÏàËÆ¶È:55.5% Heterocycles 2010 82 563-579 Total Synthesis of (+)- and (-)-Galanthamine Tomoaki Kato, Hiroki Tanimoto, Hisako Yamada, and Noritaka Chida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . carinol ÏàËÆ¶È:55.5% Phytochemistry 1983 22 749-753 Lignans and other constituents from Carissa edulis Hans Achenbach, Reiner Waibel, Ivan Addae-Mensah Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . (1S,3S,4R)-1-Cyclohexyl-3-(hydroxymethyl)-6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-ol C19H29NO4 ÏàËÆ¶È:55.5% Tetrahedron 2012 68 883-893 Chiral aziridine-2-carboxylates: versatile precursors for functionalized tetrahydroisoquinoline (THIQ) containing heterocycles Kyu Myung Lee, Jong Chan Kim, Philjun Kang, Won Koo Lee, Heesung Eum, Hyun-Joon Ha Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . compound 12S ÏàËÆ¶È:55.5% Tetrahedron 1996 52 14961-14974 Further studies of alkaloids from Reniera sarai: Structures of saraine-3 and isosaraine-3; absolute stereochemistry of saraine-1 and saraine-2 Yuewei Guo, Anna Madaio, Enrico Trivellone, Gennaro Scognamiglio, Guido Cimino Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . compound 12R ÏàËÆ¶È:55.5% Tetrahedron 1996 52 14961-14974 Further studies of alkaloids from Reniera sarai: Structures of saraine-3 and isosaraine-3; absolute stereochemistry of saraine-1 and saraine-2 Yuewei Guo, Anna Madaio, Enrico Trivellone, Gennaro Scognamiglio, Guido Cimino Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 6-shogaol C17H24O3 ÏàËÆ¶È:55.5% Food Chemistry 2011 128 778-782 Phenolic compounds isolated from Zingiber officinale roots inhibit cell adhesion Seung Woong Lee, Ju-Hwan Lim, Min Seok Kim, Ji-Hak Jeong, Gyu-Yong Song, Woo Song Lee, Mun-Chual Rho Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . 8-hydroxy-3,9-dimethoxy-1,2-methylenedioxyaporphine C20H21NO5 ÏàËÆ¶È:55.5% Natural Product Research 2012 26 1296-1302 Cytotoxic and antimicrobial aporphine alkaloids from Fissistigma poilanei (Annonaceae) collected in Vietnam Tran Thi Thanh Thuy, Tran Duc Quan, Nguyen Thi Hoang Anh & Tran Van Sung Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-01-21 18:53:07













»Ø¸´´ËÂ¥
-galanthamine derivatives as acetylcholinesterase inhibitors