| ²é¿´: 502 | »Ø¸´: 2 | |||
250350663ľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
12 ÒÑÓÐ1È˲ÎÓë
|
| 13C NMR (100 MHz, CDCl3) ¦Ä26.0, 27.3, 29.4, 33.2, 35.2, 39.2, 39.3, 48.4, 50.7, 52.2, 53.0, 57.1,65.2, 66.2, 66.3, 70.1 , 93.2, 96.4, 97.7, 119.0, 134.9, 136.2,145.5 |
» ²ÂÄãϲ»¶
071000ÉúÎïѧµ÷¼ÁÇóÖú
ÒѾÓÐ14È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ9È˻ظ´
277Çóµ÷¼Á
ÒѾÓÐ19È˻ظ´
344Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
»¯¹¤µ÷¼ÁÇóµ¼Ê¦ÊÕÁô£¡Ò»Ö¾Ô¸Ê§Àû£¬Ì¤Êµ¿Ï¸É£¬ÓÐÖ²ÎïÌáÈ¡¿ÆÑоÀú
ÒѾÓÐ13È˻ظ´
Ò»Ö¾Ô¸Î÷½»»úеר˶Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
277 ÊýÒ»104£¬Ñ§Ë¶£¬Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
Çóµ÷¼Á ²ÄÁÏÓ빤³Ì 324·Ö ר˶
ÒѾÓÐ17È˻ظ´
342µç×ÓÐÅϢר˶Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
0835ѧ˶299Çóµ÷¼Á 08´óÀà¿É½ÓÊÜ
ÒѾÓÐ7È˻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 ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
250350663: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-02-04 14:43:29
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
250350663: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-02-04 14:43:29
|
1 . 17-hydroxydaphnigraciline C23H35NO5 ÏàËÆ¶È:56.5% Journal of Natural Products 2009 72 1669-1672 Alkaloids from the Leaves of Daphniphyllum subverticillatum Chuan-Rui Zhang, Hong-Bing Liu, Teng Feng, Jian-Yong Zhu, Mei-Yu Geng, and Jian-Min Yue Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . napelline ÏàËÆ¶È:56.5% Planta Medica 1988 54 318-320 Structures of Flavamine and Flavadine from Aconitum flavum Zhi-gang Chen, Ai-na Lao, Hong-cheng Wang, and Shan-hai Hong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . napelline C22H33NO3 ÏàËÆ¶È:56.5% Chemistry of Natural Compounds 1996 32 596-675 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 4 . Napelline ÏàËÆ¶È:56.5% Chemistry of Natural Compounds 1993 29 791-794 12-EPINAPELLINE AND ITS N-OXIDE FROM Aconitum baicalense Ts. Zhapova and A. A. Semenov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . luciculine ÏàËÆ¶È:56.5% Heterocycles 1989 29 2141-2148 Studies on Aconitum Species. XI. Two New Diterpenoid Alkaloids from Aconitum yesoense var. Macroyesoense (Nakai) Tamura V Koji Wada, Hideo Bando, Takashi Amiya, and Norio Kawahara Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . napelline ÏàËÆ¶È:56.5% Heterocycles 1987 26 1455-1460 Studies on the Active Principles from Aconitum flavum Hand-Mazz. The Structures of Five New Deterpenoid Alkaloids Zhi-gang Chen, Ai-na Lao, Hong-chemg Wang, and Shan-hai Hong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . yuzurimine E C25H35NO5 ÏàËÆ¶È:56% Journal of Natural Products 2004 67 1094-1099 New Alkaloids from Daphniphyllum calycinum Hoda El Bitar, Van Hung Nguyen, Anthony Gramain, Thierry Svenet, and Bernard Bodo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . N1,N5-Bis{4-[(6-methoxyquinolin-8-yl)amino]pentyl}-L-glutamamide 3HCl ÏàËÆ¶È:56% Bioorganic & Medicinal Chemistry 2011 19 197-210 Synthesis, antiprotozoal, antimicrobial, b-hematin inhibition, cytotoxicity and methemoglobin (MetHb) formation activities of bis(8-aminoquinolines) Kirandeep Kaur, Meenakshi Jain, Shabana I. Khan, Melissa R. Jacob, Babu L. Tekwani, Savita Singh,Prati Pal Singh, Rahul Jain Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . daphnioldhanine K C23H33NO4 ÏàËÆ¶È:52.1% Journal of Natural Products 2008 71(4) 564-569 Alkaloids from Daphniphyllum oldhami Shu-Zhen Mu, Jun-Song Wang, Xiao-Sheng Yang, Hong-Ping He, Chun-Shun Li,Ying-Tong Di, Ye Wang, Yu Zhang, Xin Fang, Lie-Jun Huang, and Xiao-Jiang Hao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . daphnioldhanin A C23H35NO4 ÏàËÆ¶È:52.1% Journal of Natural Products 2006 69 1065-1069 Daphnioldhanins A−C, Alkaloids from Daphniphyllum oldhami Shu-Zhen Mu, Ye Wang, Hong-Ping He, Xian-Wen Yang, Yue-Hu Wang, Ying-Tong Di, Yang Lu, Ying Chang, and Xiao-Jiang Hao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . pordamacrine B C23H31NO4 ÏàËÆ¶È:52.1% Journal of Natural Products 2007 70 1516-1518 Pordamacrines A and B, Alkaloids from Daphniphyllum macropodum Yosuke Matsuno, Mariko Okamoto,Yusuke Hirasawa, Nobuo Kawahara,Yukihiro Goda, Motoo Shiro, and Hiroshi Morita Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . deacetylyuzurimine ÏàËÆ¶È:52.1% Acta Botanica Yunnanica 1993 15(2) 205-207 CALYCININE A,A NEW ALKALOID FROM THE SEED OF DAPHNIPHYLLUM CALYCINUM HAO Xiao-Jiang,ZHOU Jun,Node Mamanbu ,Fuji Kaoru Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . Napelline ÏàËÆ¶È:52.1% Chemistry of Natural Compounds 1993 29 658-661 ALKALOIDS OF THE FLORA OF MONGOLIA V. TURPELLINE -- A NEW ALKALOID FROM Aconitum turczaninowii N. Batbaryar, D. Batsuren, A. A. Semenov,and M. N. Sultankhodzhaev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . methyl ent-11¦Á-acetoxy-17-mesyloxy-20-nor-16-epi-gibberellan-7-oate 19,10-lactone C23H32O9S ÏàËÆ¶È:52.1% Phytochemistry 1992 31 2519-2521 Confirmation of structure for the new 11¦Â-hydroxy gibberellin GA84 Petra Kraft-Klaunzer, Lewis N. Mander Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . yuzurimine derivative(compound 10) ÏàËÆ¶È:52.1% Bulletin of the Chemical Society of Japan 1975 48 2120-2123 The structure of Yuzurimine-C Shosuke Yamamura, Hajime Irikawa, Yasuaki Okumura, Yoshimasa Hirata Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . compound compound C15H23NO5 ÏàËÆ¶È:52.1% Heterocycles 2004 62 407-422 An Improved Synthesis of the Tricyclic Core of Sarains by a 3-Oxidopyridinium Betaine Cycloaddition Hyoung Ik Lee, Moo Je Sung, Hee Bong Lee, and Jin Kun Cha* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . Calyciphylline L C23H35NO2 ÏàËÆ¶È:52.1% Tetrahedron 2008 64 1901-1908 Calyciphyllines H¨CM, new Daphniphyllum alkaloids from Daphniphyllum calycinum Shizuka Saito, Hiroko Yahata, Takaaki Kubota, Yutaro Obara, Norimichi Nakahata, Jun'ichi Kobayashi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . N-(7-{[6-chloro-2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-ylidene]amino}butyl)-5-(1,2-dithiolan-3-yl)-pentanamide 23H31ClN4OS2 ÏàËÆ¶È:52.1% Bioorganic & Medicinal Chemistry 2008 16 4252-4261 Design, synthesis and pharmacological evaluation of hybrid molecules out of quinazolinimines and lipoic acid lead to highly potent and selective butyrylcholinesterase inhibitors with antioxidant properties Michael Decker, Birgit Kraus, Jörg Heilmann Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . karakomine C22H33NO3 ÏàËÆ¶È:52.1% Heterocycles 1991 32 2429-2432 Studies on the Alkaloids from Aconitum karakolicum Rap. Baoshan Huang, Hongcheng Wang, Aina Lao, Yasuo Fujimoto, and Makoto Kirisawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . trinervine C19H22N2O2 ÏàËÆ¶È:52.1% Heterocycles 1990 31 1819-1822 Trinervine, a New Indole Alkaloid from Strychnos trinervis Rabindranath Mukherjee, Margareth de F. F. Melo, Cid A. de M. Santos, Eric Guittet, and Bhupesh C. Das Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . ethylene ketal of cis-8a-[[(benzyloxy)methoxy]methyl]-1¦Á-hydroxy-3¦Â-methyl-1,4,4a,5,6,8a-hexahydronaphthalene-8(2H,7H)-one ÏàËÆ¶È:52.1% Canadian Journal of Chemistry 1993 71 1184-1199 Spruce budworm (Choristoneura fumiferana) antifeedants 3. Structure¨Cactivity relationship among some angularly functionalized decalin compounds A.E. Schwerdtfeger, T.H. Chan, A.W. Thomas, G.M. Strunz, A. Salonius, M. Chiasson Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . 20(R)-dammarane-3,12,20,25-tetrol ÏàËÆ¶È:52.1% Asia-Pacific Traditional Medicine 2008 4 41-43 Studies on the Rare Anticancer Compounds of the Hydrolysate of the Saponins from Gynostemma pentaphfllum(Thunb)Makino Xu Zhi-chao, Han Ling, Zhao Yu-qing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . Puberunine C23H35NO7 ÏàËÆ¶È:52.1% Organic Letters 2012 14 2758-2761 Puberunine and Puberudine, Two New C18-Diterpenoid Alkaloids from Aconitum barbatum var. puberulum Zhen-Qiang Mu, Hao Gao, Zhi-Yun Huang, Xiao-Lin Feng, and Xin-Sheng Yao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-02-04 12:52:16
|
3Â¥2015-02-04 14:43:25













»Ø¸´´ËÂ¥