| ²é¿´: 274 | »Ø¸´: 1 | ||
°×ÃæÍõ¹«×ÓÌú³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
|
ÈܼÁ£ºDMSO C-NMR:11.23,20.53,21.60,35.86,40.93,41.23,41.47,46.57,77.07,110.38,130.35,145.92,147.51,190.69,210.73 |
» ²ÂÄãϲ»¶
0703×Ü·Ö331Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
085600£¬321·ÖÇóµ÷¼Á
ÒѾÓÐ7È˻ظ´
325Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
085600£¬320·ÖÇóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Ò»Ö¾Ô¸0817»¯Ñ§¹¤³ÌÓë¼¼Êõ£¬Çóµ÷¼Á
ÒѾÓÐ27È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤085600 310·ÖÇóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸¹þ¶û±õ¹¤Òµ´óѧ085600Ó¢Ò»Êý¶þ337·ÖÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
22408Çóµ÷¼Á 354·Ö ¿É¿çרҵ
ÒѾÓÐ3È˻ظ´
277¹¤¿ÆÇóµ÷¼Á
ÒѾÓÐ4È˻ظ´
Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á£¬326·Ö
ÒѾÓÐ3È˻ظ´

÷´º
½ð³æ (ÕýʽдÊÖ)
- Ó¦Öú: 242 (´óѧÉú)
- ½ð±Ò: 1940.6
- É¢½ð: 48
- ºì»¨: 3
- Ìû×Ó: 465
- ÔÚÏß: 121.1Сʱ
- ³æºÅ: 1536801
- ×¢²á: 2011-12-14
- ÐÔ±ð: MM
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
°×ÃæÍõ¹«×Ó: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл´óÏÀ 2015-03-03 09:32:38
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
°×ÃæÍõ¹«×Ó: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл´óÏÀ 2015-03-03 09:32:38
|
1 . 14,15-dinorguai-1,11-dien-9,10-dione C15H20O2 ÏàËÆ¶È:80% Chinese Journal of Natural Medicines 2012 10 477-480 The structural elucidation and antimicrobial activities of two new sesquiterpenes from Syringa pinnatifolia Hemsl. Wu-Li-Ji AO, Qing-Hu WANG, Si-Qin, Mu-Dan, Sa-Ren-Tu-Ya, Na-Yin-Tai DAI, Du-Ri-Si-Ha-La-Tu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 14-noreudesma-3-hydroxy-3-en-2,9-dione C15H20O3 ÏàËÆ¶È:80% Natural Product Research 2014 28 1579-1582 A new sesquiterpene from Ixeris chinensis Qinghu Wang, Nayintai Dai, Narenchaoketu Han, Rongjun Wu & Jiesi Wu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . pinnatifone A C15H20O3 ÏàËÆ¶È:80% Chemical & Pharmaceutical Bulletin 2014 62 1009-1012 Sesquiterpenoids and Lignans from the Roots of Syringa pinnatifolia Ze-Ming Zhang, Chun-Hua Wang, Xiao-Jie Zeng, Qiu Qiu, Wei Tang, Guo-Qiang Li, Yao-Lan Li, Guo-Cai Wang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 3,4-epoxy-11¦Á,13-dihydroelemen-12, 8-olide C15H22O3 ÏàËÆ¶È:66.6% Journal of Natural Products 2001 64 466-471 Sesquiterpenes and Monoterpenes from the Bark of Inula macrophylla Bao-Ning Su,Yoshihisa Takaishi, Tetsuya Yabuuchi, Takenori Kusumi, Motoo Tori,Shigeru Takaoka,Gisho Honda, Michiho Ito, Yoshio Takeda, Olimjon K. Kodzhimatov, and Ozodbek Ashurmetov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 11,13-dihydroivalin C15H22O3 ÏàËÆ¶È:66.6% Phytochemistry 1993 33 407-410 Cytotoxic and antibacterial sesquiterpenes from Inula graveolens G¨¹laçti Topçu, Sevil Öks¨¹z, Hui-Ling Shieh, Geoffrey A. Cordell, John M. Pezzuto, Candan Bozok-Johansson Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (3R,4aR,5R,6R)-6-hydroxy-4a,5-dimethyl-3-(prop-1-en-2-yl)-3,4,4a,5,6,7-hexahydronaphthalen-1(2H)-one C15H22O2 ÏàËÆ¶È:66.6% Phytochemistry 2011 72 2244-2252 Terpenoids and phenethyl glucosides from Hyssopus cuspidatus (Labiatae) Megumi Furukawa, Mitsuko Makino, Emika Ohkoshi, Taketo Uchiyama, Yasuo Fujimoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 11¦Á,13-dihydro-¦Â-cyclocostunolide C15H22O2 ÏàËÆ¶È:66.6% Phytochemistry 1990 29 541-545 Sesquiterpene lactones from Artemisia herba-alba Juan F. Sanz,Gloria Castellano,J. Alberto Marco Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 11,13-dihydroisoalantolactone ÏàËÆ¶È:66.6% Natural Product Research and Development 2009 21 616-618 Study on the Chemical Components of the Inula helenium ZHAO Yong-ming;ZHANG Man-li; HUO Chang-hong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 11¦Á H,13-dihydroisoalantolactone C15H22O2 ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 2012 48 416-418 A new triterpenoid ester from Lobelia sessilifolia Jiaming Sun, Xiuli Wang, Hui Zhang and Junshan Yang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 6-isopropenyl-1-methylbicyclo[3.3.1]nonan-3-one C13H20O ÏàËÆ¶È:66.6% European Journal of Organic Chemistry 2008 2008 4697-4705 Towards the Total Synthesis of Spirovibsanin A: Total Synthesis of (¡À)-5,14-Bis-epi-spirovibsanin A Michael J. Gallen and Craig M. Williams Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 8-Hydroxy-11-eremophilen-9-one (santalcamphor) ÏàËÆ¶È:66.6% Phytochemistry 2011 72 400-408 Chemical composition and cytotoxicity of oils and eremophilanes derived from various parts of Eremophila mitchellii Benth. (Myoporaceae) Karren D. Beattie, Peter G. Waterman, Paul I. Forster, Dion R. Thompson, David N. Leach Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 11,13-dihydroisolantolactone ÏàËÆ¶È:66.6% Chinese Pharmaceutical Journal 2011 46 1159-1162 Study on Chemical Constituents in Roots of Inula racemosa ZHANG, Ting, CHEN, Ruo-yun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 4 ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 2014 52 318-328 Unequivocal structural assignments of three cycloheptenoid intermediates for guaiane sesquiterpenes: an experimental and theoretical approach Layla R. Barbosa, Ygor W. Vieira, Valdemar Lacerda Jr., Kleber T. de Oliveira, Reginaldo B. Dos Santos, Sandro J. Greco, Alvaro C. Neto, Eustaquio V. R. de Castro and Timothy J. Brocksom Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 2¦Á-hydroxy-eudesman-4(15)-en-12,8¦Â-olide ÏàËÆ¶È:66.6% Journal of Lanzhou University (Natural Sciences) 2002 38 61-67 Chemical constituents of the aerial parts of Carpesium cernuun YANG Chao, WANG Xing, SHI Yan-ping, JIA Zhong-jian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 11,13-Dihydroisoalantolactone ÏàËÆ¶È:66.6% Journal of Chemistry 2014 2014 1−6 Mosquito Larvicidal Constituents from the Ethanol Extract of Inula racemosa Hook. f. Roots against Aedes albopictus Qing He, Xin Chao Liu, Rui Qi Sun, ZhiWei Deng, Shu Shan Du, and Zhi Long Liu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . acetate of ligucyperonol ÏàËÆ¶È:64.7% Bulletin of the Chemical Society of Japan 1990 63 2239-2245 Sesquiterpenes from the Rhizomes of Ligularia dentata Hara Keizo Naya, Tohru Okayama, Masaaki Fujiwara, Makoto Nakata, Tsutomu Ohtsuka, Seiko Kurio Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . (-)-(1R*,2R*,3R*,12S*,5Z)-1,2-Epoxy-12-isopropenyl-5-methyl-9-methylidene-7,10-dioxocyclotetra-dec-5-ene-1,3-carbolactone ÏàËÆ¶È:64.7% Helvetica Chimica Acta 1989 72 1590-1596 Novel cembranolides (Coralloidolide D and E) and a 3,7-Cyclized cembranolide (Coralloidolide C) from the mediterranean coral Alcyonium coralloides Michele D'Ambrosio, Antonio Guerriero and Francesco Pietra Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 1¦Â-hydroxy-4(15),5-eudesmadiene C15H24O ÏàËÆ¶È:60% Phytochemistry 2003 64 303-323 Terpenoids from the seeds of Artemisia annua Geoffrey D. Brown, Guang-Yi Liang, Lai-King Sy Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . macrophyllilactone D ÏàËÆ¶È:60% Phytochemistry 2001 58 1121-1128 A bis-sesquiterpene and sesquiterpenolides from Inula macrophylla Bo Fu, Bao-Ning Su, Yoshihisa Takaishi, Gisho Honda, Michiho Ito,Yoshio Takeda, Olimjon K. Kodzhimatov, Ozodbek Ashurmetov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . axinisothiocyanate N C16H25NO2S ÏàËÆ¶È:60% Journal of Natural Products 2008 71(12) 2004-2010 Sesquiterpenes from the Sponge Axinyssa isabela Eva Zub¨ªa, Mar¨ªa J. Ortega, and J. Luis Carballo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-03-03 09:16:02














»Ø¸´´ËÂ¥