| ²é¿´: 300 | »Ø¸´: 1 | |||
xf890529ľ³æ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý3-1
|
|
ÈܼÁDMSO 31.54,35.31,66.02,115.04,115.88,117.44,136.83,148.70,161.48,205.30 |
» ²ÂÄãϲ»¶
0703»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ17È˻ظ´
¿¼Ñе÷¼Á-²ÄÁÏÀà-284
ÒѾÓÐ15È˻ظ´
Ò»Ö¾Ô¸211 0703»¯Ñ§ 346·ÖÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁϹ¤³Ì085601£¬270Çóµ÷¼Á
ÒѾÓÐ24È˻ظ´
085404 293Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
µ÷¼Á
ÒѾÓÐ21È˻ظ´
¸´ÊÔµ÷¼Á£¬Ò»Ö¾Ô¸Ö£ÖÝ´óѧ²ÄÁÏÓ뻯¹¤289·Ö
ÒѾÓÐ15È˻ظ´
08¹¤¿ÆÇóµ÷¼Á290·Ö
ÒѾÓÐ12È˻ظ´
286Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
²ÄÁÏÀà284µ÷¼Á
ÒѾÓÐ24È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÕæµÄͦ²»´íµÄ£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý3¸ö
ÒѾÓÐ3È˻ظ´
΢Æ×Ç󻯺ÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú лл¡£¡£¡£
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý3¸ö
ÒѾÓÐ6È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú ¼±¼±¼±£¡£¡£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
΢Æ×13C NMRÊý¾Ý¿â ²éδ֪»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú3¸öÓÃ΢Æ×½âÎöµÄ½á¹¹
ÒѾÓÐ8È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
ÓÐËù²»Îª
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 304 (´óѧÉú)
- ½ð±Ò: 9684.2
- É¢½ð: 16
- ºì»¨: 14
- Ìû×Ó: 1106
- ÔÚÏß: 814.3Сʱ
- ³æºÅ: 481441
- ×¢²á: 2007-12-17
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
xf890529(¶¹¸ç´ú·¢): ½ð±Ò+20, лл 2013-12-07 15:24:34
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
xf890529(¶¹¸ç´ú·¢): ½ð±Ò+20, лл 2013-12-07 15:24:34
|
²éѯ½á¹û£º¹²²éµ½71¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . regiolone ÏàËÆ¶È:100% Modern Chinese Medicine 2005 7(1) 7-8 Studies on the Chemical Constituents of Juglans Msndshurica Maxim. SHI Jianhui, WANG Jinhui, CHE Dong, SONG Yurong, LI Xian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . regiolone C10H10O3 ÏàËÆ¶È:100% Journal of Shenyang Pharmaceutical University 2013 30 342-345 Secondary metabolites from marine sponge-associated fungus Hansfordia sp. ZHAO Dan-qi, WU Ze-hong, LIU Dong, PEI Yue-hu, LIN Wen-han, BAI Jiao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . (4RS)-4,8-dihydroxy-3,4-dihydronaphthalen-1(2H)-one C10H10O3 ÏàËÆ¶È:70% Acta Crystallographica Section E 2007 63 o2713-o2714 Regiolone from the pericarps of Juglans regia L. Jun-Xi Liu, Duo-Long Di, Chen Li and Xin-Yi Huang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (4S)-4,8-dihydroxy-1-tetralone ÏàËÆ¶È:70% Chinese Traditional and Herbal Drugs 2013 44 803-807 Chemical constituents from barks of Pterocarya stenoptera GAO Shuang, YE Kai-he, ZHANG Ying, ZHOU Guang-xiong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 1-(2-allyl-3,6-dihydroxyphenyl)ethanone ÏàËÆ¶È:63.6% Tetrahedron 2012 68 7116-7121 Wacker oxidation methodology for the synthesis of the benzo-fused acetal core of marticin Adushan Pillay, Amanda L. Rousseau, Manuel A. Fernandes, Charles B. de Koning Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . DG-5 C10H10O3 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1998 46 423-429 Immunosuppressive Components from an Ascomycete, Diplogelasinospora grovesii Haruhiro FUJIMOTO,Junko NAGANO,Kentaro YAMAGUCHI and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Isosclerone ÏàËÆ¶È:60% Natural Product Research and Development 2012 24 1707-1711 Chemical Constituents and Bioactivity Studies of Diaphragma juglandis Fructus YANG Ming-zhu, TIAN Xin-yan, XIAO Chao-jiang, HAN Bing-yang, JIANG Bei* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (+ )-isoshinanolone C11H12O3 ÏàËÆ¶È:54.5% Phytochemistry 1981 20 1162-1164 (+)-Isoshinanolone and 2-methylbenzofuran-4-carbaldehyde from the fish-stunning plant Habropetalum dawei Steven W. Hanson, Malcolm Crawford, Devavaram P. J. Thanasingh Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . compound 8 C11H14O3 ÏàËÆ¶È:54.5% Bulletin of the Chemical Society of Japan 2004 77 537-541 Cytotoxic Antifeedant from Dionaea muscipula Ellis: A Defensive Mechanism of Carnivorous Plants against Predators Takashi Tokunaga, Atsushi Dohmura, Noboru Takada, Minoru Ueda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 6-(1,1-dimethylethyl)-2,3-bis(carbomethoxy)[1,4]benzoxathiin C16H18O5S ÏàËÆ¶È:53.8% Heterocycles 2002 56 471-478 [4+2] Cycloadditions of o-Thioquinones with Alkynes and Arylalkenes: a Facile Synthesis of Benzoxathiins Vijay Nair* and Bini Mathew Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . Mellein ÏàËÆ¶È:50% Journal of Natural Products 2009 72 8-13 Composition and Electrophysiological Activity of Constituents Identified in Male Wing Gland Secretion of the Bumblebee Parasite Aphomia sociella Blanka Kalinov¨¢,Jiř¨ª Kindl,Pavel Jiroš, Petr ލ¢ček, So¨¾a Vaš¨ªčkov¨¢, Miloš Budĕš¨ªnský, and Irena Valterov¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . isosclerone ÏàËÆ¶È:50% Phytochemistry 2003 779-782 Dihydroisocoumarins and a tetralone from Cytospora eucalypticola Tetsuo Kokubun, Nigel C. Veitch, Paul D. Bridge, Monique S.J. Simmonds Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 4,6,8-trihydroxy-3,4-dihydronaphthalen-1(2H)-one ÏàËÆ¶È:50% Journal of Natural Products 2008 71(6) 952-956 Ymf 1029A#E, Preussomerin Analogues from the Fresh-Water-Derived Fungus YMF 1.01029 Jin Yan Dong, Hong Chuan Song, Jian Hua Li, Yu Shu Tang, Rong Sun, Le Wang,Yong Ping Zhou, Li Mei Wang, Kai Ze Shen, Chun Ren Wang, and Ke-Qin Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . moloka'iamine C11H16Br2N2O ÏàËÆ¶È:50% Journal of Natural Products 2004 67 2117-2120 Structural Activity Relationship Studies of Zebra Mussel Antifouling and Antimicrobial Agents from Verongid Sponges Jeffrey A. Diers, Hari Kishore Pennaka, Jiangnan Peng,John J. Bowling, Stephen O. Duke, and Mark T. Hamann Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 4-ethoxy-3-hydroxymethylphenol C9H12O3 ÏàËÆ¶È:50% Acta Botanica Yunnanica 2003 25(6) 711-715 A New Lignan Glycoside from Curculigo capitulata LI Ning,TAN Ning-Hua,ZHOU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . (4RS)-3,4-Dihydro-4,8-dihydroxynaphthalen-1(2H)-one ÏàËÆ¶È:50% Chemistry & Biodiversity 2009 6 1216-1223 Colomitides A and B: Novel Ketals with an Unusual 2,7-Dioxabicyclo[3.2.1]octane Ring System from the Aquatic Fungus YMF 1.01029 Jin-Yan Dong, Li-Mei Wang, Hong-Chuang Song, Kai-Ze Shen, Yong-Ping Zhou, Le Wang, and Ke-Qin Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 2-alloyl-4,5-methylenedioxyphenol ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1983 31 2879-2883 Studies on the Constituents of the Plants of Illicium Species. II. Structures of Phenolic Components KENICHI YAKUSHIJIN,TOMOKO TOHSHIMA,RIKA SUZUKI,HIROYUKI MURATA,SHENGTEN LU and HIROSHI FURUKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 4-ethoxy-3-hydroxymethylphenol C9H12O3 ÏàËÆ¶È:50% Phytochemistry 1998 49 2133-2136 Norneolignan and phenols from Curculigo capitulata Wen-liang Chang, Shoei-sheng Lee Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-12-03 12:24:03













»Ø¸´´ËÂ¥