| ²é¿´: 483 | »Ø¸´: 1 | |||
[ÇóÖú]
΢Æ×Êý¾ÝÇóÖú£¬¶àл ÒÑÓÐ1È˲ÎÓë
|
|
ÈܼÁ£ºCDCl3 13C-NMRÊý¾Ý:27.2,28.2,28.9,28.9,29.0,29.2,29.3,29.6,29.7,31.9,31.9,34.0,34.2,34.2,36.1,36.7,37.3,38.9,39.8,40.5,42.3,45.9,50.2,51.2,56.0,56.1,56.8,56.9,63.3,70.2,73.6,73.9,76.0,76.6,77.0,77.2,77.4,79.6,101.2,122.1,125.4,128.1,129.3,130.0,138.3,140.3,174.6 |
» ²ÂÄãϲ»¶
һ־Ըɽ¶«´óѧ£¬085600£¬344
ÒѾÓÐ5È˻ظ´
22408µ÷¼Á
ÒѾÓÐ5È˻ظ´
070300»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
»¯¹¤µ÷¼Á303·Ö£¬¹ýËļ¶
ÒѾÓÐ11È˻ظ´
260Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
266·Ö£¬Ò»Ö¾Ô¸µçÆø¹¤³Ì£¬±¾¿Æ²ÄÁÏ£¬Çó²ÄÁÏרҵµ÷¼Á
ÒѾÓÐ7È˻ظ´
349Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
ѧ˶»úе¹¤³Ì303Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
312Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
Çó½âÇâÆ×ÊÔÌ⣡
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»df12
ÒѾÓÐ5È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖúάÆ×Êý¾Ý¿â
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÈË΢Æ×²éѯ£¬¼±£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
RUSSIAN CHEMICAL BULLETIN
ÒѾÓÐ5È˻ظ´
jiandanai187
гæ (СÓÐÃûÆø)
- Ó¦Öú: 63 (³õÖÐÉú)
- ½ð±Ò: 737.6
- ºì»¨: 2
- Ìû×Ó: 83
- ÔÚÏß: 14.1Сʱ
- ³æºÅ: 3068959
- ×¢²á: 2014-03-19
- רҵ: ÖÐÒ©ÖÊÁ¿ÆÀ¼Û
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Áõ-æ: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2015-03-14 09:52:22
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Áõ-æ: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2015-03-14 09:52:22
|
1 . ¦Â-sitosteryl-3¦Â-glucopyranoside-6'-O-palmitate ÏàËÆ¶È:70.2% Chinese Traditional and Herbal Drugs 2013 44 2657-2660 Chemical constituents from Cardamine leucantha ZHENG Cong-cong, SU Yan-fang, CHEN Lei, BI Yan-ping, YANG Fan, XU Jing, YAN Shi-lun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . balanoinvolin ÏàËÆ¶È:68.6% Journal of Anhui Agricultural Sciences 2012 40 9641-9643 Study on the Chemical Constituents of Mirabilis himalaica Roots YANG Pan-pan et al Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . ¦Â-sitosteryl-3¦Â-glucopyranoside-6'-O-palmitate ÏàËÆ¶È:68.0% Fitoterapia 2004 75 500-504 Cytotoxic constituents from Plumbago zeylanica A.T. Nguyen , H. Malonne , P. Duez , R. Vanhaelen-a,b, b a anhaelen-Fastrea,M. Vanhaelen, J. Fontaine Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 1 C61H110O7 ÏàËÆ¶È:68.0% Archives of Pharmacal Research 2007 30 172-176 Isolation of constituents and anti-complement activity from Acer okamotoanum WenYi Jin, Byung-Sun Min, JongPill Lee, Phuong Thien Thuong and Hyeong-Kyu Lee, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . ¦Â-sitosteryl-3¦Â-glucopyranoside-6'-O-palmitate ÏàËÆ¶È:68.0% Pharmaceutical Chemistry Journal 2012 46 225-227 Chemical constituents of Ficus odorata P.-W. Tsai, K. A. De Castro-Cruz, C.-C. Shen, C.-T. Chiou, C. Y. Ragasa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . ¦Â-sitosteryl glucoside-6'-palmitoleoate ÏàËÆ¶È:68.0% Chinese Journal of Applied & Environmental Biology 2000 6 194-196 CHEMICAL CONSTITUENTS FROM RUBUS SETCHUENENSIS HUANG Kexin; ZHANG Xiaorong; WANG Mingkui & DING Lisheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . ¦Â-sitosteryl-D-glucoside-6'-palmitate C51H90O7 ÏàËÆ¶È:65.9% China Journal of Chinese Materia Medica 2006 31 307-308 Studies on the chemical constituents from stem of Chirta longgangensis var. hongyao WANG Manyuan, YANG Lan, TU Youyou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . ¦Â-Sitosterol glucoside 6'-O-palmitate ÏàËÆ¶È:65.9% Korean Journal of Pharmacognosy 2008 39(3) 186-193 Phytochemical Studies on Astragalus Root (3);Triterpenoids and Sterols Jung, Hye-Sil; Lee, Eun-Ju; Lee, Je-Hyun; Kim, Ju-Sun; Kang, Sam-Sik Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 6'-linoleic-¦Â-daucosterol C30H50O ÏàËÆ¶È:65.9% Natural Product Research and Development 2009 21 776-778 Chemical Constituents of the Roots of Ligularia fischeri DENG Mei-cai; JIAO Wei; DONG Wei-wei; LU Run-hua Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . ¦Â-sitosterol-3¦Â-glucopyranoside-6'-palmitate ÏàËÆ¶È:65.9% Journal of Chinese Medicinal Materials 2008 31 222-223 Studies on Chemical Constituents of the Seeds of Allium cepa YUAN Ling, JI Teng-fei, WANG Ai-guo, YANG Jian-bo, SU Ya-lun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . ¦Â-sitosteryl-3-O-¦Â-D-glucopyranoside-2'-O-palmitate C51H90O7 ÏàËÆ¶È:63.8% Phytochemistry 2008 69 2627-2633 Non-cannabinoid constituents from a high potency Cannabis sativa variety Mohamed M. Radwan, Mahmoud A. ElSohly, Desmond Slade, Safwat A. Ahmed, Lisa Wilson,Abir T. El-Alfy, Ikhlas A. Khan, Samir A. Ross Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 3 ÏàËÆ¶È:63.8% Korean Journal of Pharmacognosy 1999 30(3) 290-294 Isolation of Acylated Sterylglycosides from the Legumes of Albizzia julibrissin Kim, Young-Hee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . stigmast-5-en-3¦Â-ol-3-O-¦Â-D-(2'-n-triacontanoyl) glucopyranoside C65H118O7 ÏàËÆ¶È:63.8% Journal of Asian Natural Products Research 2012 14 301-307 New steroidal glycoside ester and aliphatic acid from the fruits of Lycium chinense Woo-Suk Jung,Ill-Min Chung,Mohd Ali and Ateeque Ahmad Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 3,7,11,19,23,27-hexamethyl-15-hydroxymethylene-n-octacos-5,8,20-triene-10¦Â,18¦Á-diol-10¦Â-D-glucopyranoside C43H78O9 ÏàËÆ¶È:63.8% Bulletin of the Korean Chemical Society 2007 28 229-234 A New Chemical Constituent from the Hairy Root Cultures of Catharanthus roseus Ill-Min Chung, Han-Young Park, Mohd Ali, Ka Yiu San, Christie A. M. Peebles, Seung-Beom Hong, Ateeque Ahmad* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . ¦Â-sitosteryl glucoside-3'-O-heptadecoicate ÏàËÆ¶È:63.8% Natural Product Research and Development 1997 9(2) 7-10 STUDIES ON THE CHEMICAL CONSTITUENTS OF THE CULTIVATED DESERTLIVING CISTANCHE (CISTANCHE DESERTICOLA) Tu Pengfei; He Yanping and Lou Zhicen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 6'-palmitoxyl-¦Â-daucosterin ÏàËÆ¶È:63.8% Journal of the Chinese Chemical Society 2008 55 863-870 Diversity of Chemical Constituents from Saxifraga montana H. Jun-Xi Liu, Duo-Long Di* and Yan-Ping Shi* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . balanoinvolin C53H90O7 ÏàËÆ¶È:63.2% Chemistry of Natural Compounds 2009 45 371-373 BALANOINVOLIN, A NEW STEROID DERIVATIVEFROM Balanophora involucrate Bing Luo, Kun Zou, Zhiyong Guo, Feijun Dan, Juizhi Wang, and Hui Wang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . Stigmast-5-en-3¦Â-ol linoleate C17H18O6 ÏàËÆ¶È:61.7% Acta Botanica Yunnanica 2001 23(3) 368-372 Chemical Constituents from Dysoxylum hainanense LUO Xiao-Dong,WU Shao-Hua,MA Yun-Bao,WU Da-Gang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . 3-O-[6'-O-stearyl-¦Â-D-glucosyl]-clerosterol ÏàËÆ¶È:61.7% Phytochemistry 1994 36 167-170 Acylglucosylsterols from two Aegiphila species Suzana G. Leitão, Maria Auxiliadora C. Kaplan, Franco Delle Monache Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . ¦Â-sitosterol linoleate ÏàËÆ¶È:61.7% Chinese Pharmaceutical Journal 2007 42 661-663 Studies on Chemical Constituents of Paeonia veitchii L. WANG Rui, CHOU Gui-xin, ZHU En-yuan, WANG Zheng-tao, BI Kai-shun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-03-13 16:52:13














»Ø¸´´ËÂ¥