| ²é¿´: 765 | »Ø¸´: 3 | ||
weiwei_lľ³æ (Ö°Òµ×÷¼Ò)
ÓÐÀíÏëµÄÈË
|
[ÇóÖú]
ÇóÖú [color=Red]΢Æ×[/color] Êý¾Ý²éѯ
|
| MeOD ¦Ä 162.28, 159.64, 159.58, 141.69, 112.83, 112.09, 111.73, 110.58, 104.23, 103.09, 55.72, 21.64, 21.54. |
» ±¾ÌûÒÑ»ñµÃµÄºì»¨£¨×îÐÂ10¶ä£©
» ²ÂÄãϲ»¶
287·ÖÇóµ÷¼Á ÓÐרÀû¹ú½±Ò»Ö¾Ô¸¹þ¹¤´ó085406
ÒѾÓÐ4È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
085405Èí¼þ¹¤³Ì301·ÖÇóµ÷¼Á£¬×¨Ë¶¿É¿çרҵ£¬ËÄÁù¼¶Òѹý
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
274Çóµ÷¼ÁÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Áµ½²ÄÁÏ
ÒѾÓÐ5È˻ظ´
²ÄÁÏ¿¼ÑÐÇóµ÷¼Á×Ü·Ö280
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸Ö£ÖÝ´óѧ²ÄÁÏÓ뻯¹¤085600£¬Çóµ÷¼Á
ÒѾÓÐ27È˻ظ´
»¯¹¤Çóµ÷¼Á£¡
ÒѾÓÐ11È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
΢Æ×Êý¾ÝÇóÖú²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´

jasminelw
Ìú¸Ëľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 269 (´óѧÉú)
- ½ð±Ò: 8813.7
- É¢½ð: 80
- ºì»¨: 6
- Ìû×Ó: 972
- ÔÚÏß: 604.2Сʱ
- ³æºÅ: 1858727
- ×¢²á: 2012-06-13
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡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
weiwei_l: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ÎÒ¶ÔËýµÄ»Ø¸´ºÜÂúÒâ 2013-08-10 12:22:14
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
weiwei_l: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ÎÒ¶ÔËýµÄ»Ø¸´ºÜÂúÒâ 2013-08-10 12:22:14
|
ÒÔºó¼ÇµÃ´ÓСµ½´óÅÅÊý¾Ý£¬Êý¾Ý¼ä²»ÒªÓпոñ¡£¡£¡£¡£ ²éѯ½á¹û£º¹²²éµ½551¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . cordyol E C15H16O3 ÏàËÆ¶È:86.6% Journal of Natural Products 2013 76 547-553 Bioactive Indole Alkaloids and Phenyl Ether Derivatives from a Marine-Derived Aspergillus sp. Fungus Min Chen, Chang-Lun Shao, Xiu-Mei Fu, Ru-Fang Xu, Juan-Juan Zheng, Dong-Lin Zhao, Zhi-Gang She, and Chang-Yun Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . produce 3-O-methyldiorcinol ÏàËÆ¶È:85.7% Planta Medica 2012 78 1861-1866 Cytotoxic Polyphenols from the Fungus Penicillium expansum 091 006 Endogenous with the Mangrove Plant Excoecaria agallocha Wang, Junfeng; Lu, Zhenyu; Liu, Peipei; Wang, Yi; Li, Jing; Hong, Kui; Zhu, Weiming: Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3-hydroxy-5-methylphenyl 2,4-dihydroxy-6-methylbenzoate C15H14O5 ÏàËÆ¶È:80% Planta Medica 2012 78 1767-1776 Secondary Metabolites from a Culture of the Fungus Neosartorya pseudofischeri and Their In Vitro Cytostatic Activity in Human Cancer Cells Eamvijarn, Amnat; Kijjoa, Anake; Bruy¨¨re, C¨¦line; Mathieu, V¨¦ronique; Manoch, Leka; Lefranc, Florence; Silva, Artur; Kiss, Robert; Herz, Werner: Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . cordyol C C14H14O4 ÏàËÆ¶È:71.4% Chemical & Pharmaceutical Bulletin 2007 55(2) 304-307 New Diphenyl Ethers from the Insect Pathogenic Fungus Cordyceps sp.BCC 1861 Taridaporn BUNYAPAIBOONSRI,Seangaroon YOIPROMMARAT, Kamolphan INTEREYA, and Kanokarn KOCHARIN Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . isohaplopine C13H11NO4 ÏàËÆ¶È:69.2% Phytochemistry 1988 27 959-960 Quinoline alkaloids from the leaves of Teclea simplicifolia Assefa Wondimu,Ermias Dagne,Peter G. Waterman Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 2-acetyl-7-methoxybenzofuran ÏàËÆ¶È:69.2% Chemistry of Natural Compounds 2010 46 363-365 A new griseofulvin derivative from the mangrove endophytic fungus Sporothrix SP. Lu Wen, Zhiyong Guo, Qing Li, Dezhi Zhang and Zhigang She, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 7-Methyl-benzofuran-2-carboxylate ÏàËÆ¶È:69.2% Chemistry of Natural Compounds 2013 49 137-140 Chemical constituents from the mangrove endophytic fungus Sporothrix sp. Lu Wen, Qiqiu Wei, Gang Chen, Juanni Cai, Zhigang She Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . lecanorin ÏàËÆ¶È:66.6% Journal of Natural Products 2000 63 1396-1399 Effect of Lichen Metabolites on Thylakoid Electron Transport and Photophosphorylation in Isolated Spinach Chloroplasts1 Irma S. Rojas,Blas Lotina-Hennsen, and Rachel Mata Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . thamnoliadepside B C18H18O7 ÏàËÆ¶È:66.6% Planta Medica 2011 77 2042-2046 Three New Phenolic Compounds from the Lichen Thamnolia vermicularis and Their Antiproliferative Effects in Prostate Cancer Cells Guo, Jia; Li, Zhan-lin; Wang, Ao-li; Liu, Xiao-qiu; Wang, Jian; Guo, Xin; Jing, Yong-kui; Hua, Hui-ming: Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3-O-propyldiorcinol C17H20O3 ÏàËÆ¶È:64.7% Journal of Natural Products 2013 76 547-553 Bioactive Indole Alkaloids and Phenyl Ether Derivatives from a Marine-Derived Aspergillus sp. Fungus Min Chen, Chang-Lun Shao, Xiu-Mei Fu, Ru-Fang Xu, Juan-Juan Zheng, Dong-Lin Zhao, Zhi-Gang She, and Chang-Yun Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3,6,7-tri-hydroxy-1-methoxy-xanthone C14H10O6 ÏàËÆ¶È:64.2% Natural Product Research 2006 20 1237-1240 Two new xanthones from Hypericum japonicum P. Fu; W. -D. Zhang; R. H. Liu; T. -Z. Li; Y. -H. Shen; H. -L. Li; W. Zhang; H. -S. Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Gerfelin C15H14O6 ÏàËÆ¶È:64.2% Bioscience, Biotechnology, and Biochemistry 2006 70 2523-2528 Synthesis of Gerfelin and Related Analogous Compounds Md. Sadequl ISLAM, Mitsuhiro KITAGAWA, Masaya IMOTO, Takeshi KITAHARA and Hidenori WATANABE Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Tetraorcinol A C28H26O5 ÏàËÆ¶È:64.2% Tetrahedron 2011 67 7085-7089 Cyclopeptides and polyketides from coral-associated fungus, Aspergillus versicolor LCJ-5-4 Yibin Zhuang, Xiancun Teng, Yi Wang, Peipei Liu, Hui Wang, Jing Li, Guoqiang Li, Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Orcinoside H C28H40O14 ÏàËÆ¶È:64.2% Fitoterapia 2013 86 64-69 Phenolic glycosides from Curculigo orchioides Gaertn. Zhen-Hui Wang, Jian Huang, Xiao-Ci Ma, Guo-Yu Li, Yue-Ping Ma, Ning Li, Jin-Hui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . lespeflorin I3 C21H18O6 ÏàËÆ¶È:62.5% Journal of Natural Products 2009 72 194-203 Melanin Synthesis Inhibitors from Lespedeza floribunda Maya Mori-Hongo,Hiroyuki Takimoto, Takayuki Katagiri, Makoto Kimura, Yu Ikeda, and Toshio Miyase Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . penicillocitrin A C16H12O6 ÏàËÆ¶È:62.5% Natural Product Communications 2013 8 587-588 A New Metabolite from the Endophytic Fungus Penicillium citrinum Xinlan Li, Liang Zhang, Yanhui Liu, Zhiyong Guo, Zhangshuang Deng, Jianfeng Chen, XuanTu and Kun Zou Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 6,8,5',6'-Tetrahydroxy-3'-methylflavone C16H12O6 ÏàËÆ¶È:62.5% The Journal of Antibiotics 2013 66 219-223 Antifouling and antibacterial polyketides from marine gorgonian coral-associated fungus Penicillium sp. SCSGAF 0023 Jie Bao, Yu-Lin Sun, Xiao-Yong Zhang, Zhuang Han, Hai-Chun Gao, Fei He, Pei-Yuan Qian and Shu-Hua Qi Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 6-hydroxymethyleugenin ÏàËÆ¶È:61.5% Journal of Natural Products 2002 65 1681-1682 The Isolation of Two New Chromone Derivatives from the New Zealand Fungus Tolypocladium extinguens Yunjiang Feng, John W. Blunt, Anthony L. J. Cole, and Murray H. G. Munro Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . meridianin B C12H9N4OBr ÏàËÆ¶È:61.5% Journal of Natural Products 1998 61 1130-1132 Indole Alkaloids from the Tunicate Aplidium meridianum Laura Hern¨¢ndez Franco, Elisa Bal de Kier Joff¨¦, Lydia Puricelli, Marcos Tatian, Alicia M. Seldes, and Jorge A. Palermo Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . orcinol glucoside C13H18O7 ÏàËÆ¶È:61.5% 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 21 . 6H-dibenzo[b,d]pyran-3,9-dihydroxy-6-one ÏàËÆ¶È:61.5% Biochemical Systematics and Ecology 2009 37 535-537 Chemical constituents of Duabanga grandiflora (Lythraceae) Wanida Auamcharoen, Angsumarn Chandrapatya, Anake Kijjoa, Artur M.S. Silva, Werner Herz Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . orcinol-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:61.5% China Journal of Chinese Materia Medica 2008 33 269-272 Chemical constituents in roots of Hemerocallis fulva YANG Zhongduo, LI Tao, LI Yuanchao Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . anacardoside ÏàËÆ¶È:61.5% Chemical Research in Chinese Universities 199 15 294-299 Synthesis of Analogs of Anacardoside from Semecarpus Anacardium WANG Yu-lan and CAI Meng-shen Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . Meridianin B ÏàËÆ¶È:61.5% Marine drugs 2010 8 1526-1549 Halogenated Indole Alkaloids from Marine Invertebrates Patr¨ªcia Mendonça Pauletti,Lucas Silva Cintra,Caio Guedes Braguine,Ademar Alves da Silva Filho,M¨¢rcio Lu¨ªs Andrade e Silva,Wilson Roberto Cunha and Ana Helena Janu¨¢rio Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 4-(4-fluoro-1H-indol-3-yl)-2-pyrimidinamine C12H9FN4 ÏàËÆ¶È:61.5% Journal of Heterocyclic Chemistry 2007 44 793-801 Dimethylformamide dimethyl acetal in heterocyclic synthesis: Synthesis of polyfunctionally substituted pyridine derivatives as precursors to bicycles and polycycles Fathi A. Abu-Shanab,A. M. Hessen and S. A. S. Mousa Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . compound 8b C13H12O4 ÏàËÆ¶È:61.5% Journal of Heterocyclic Chemistry 2000 37 751-755 The birch reduction of heterocyclic compounds V Birch reduction of 2- and 5-acylfuran-3-carboxylic acids and reductive elimination of 2-(arylmethoxymethyl)furan-3-carboxylic acids Yasuo Ohta, Matsumi Doe, Yoshiki Morimoto and Takamasa Kinoshita Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . isobergapten ÏàËÆ¶È:61.5% China Journal of Chinese Materia Medica 2010 35 58-62 Chemical constituents of Incarvillea younghusbandii FU Yu; BAI Yang; DAWA Zhuoma; BAI Bingru; DING Lisheng Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . 3-hydroxy-7,8,9,10-tetrahydro-6H-benzo[c]chromen-6-one C13H12O3 ÏàËÆ¶È:61.5% Heterocycles 2007 71 2721-2733 Al2O3/MeSO3H (AMA) as a Novel Heterogeneous System for Synthesis of Coumarins under Mild Conditions Hashem Sharghi and Mahboubeh Jokar Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . compound 3c ÏàËÆ¶È:61.5% Heterocycles 2004 63 505-508 Dodecasubstituted Porphyrins ¡ª An Easily Accessible Type of Dendritic Porphyrins with Tunable Properties Claudia Ryppa and Mathias O. Senge* Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . 7-Hydroxy-3-(3',5'-dihydroxyphenyl)coumarin C15H10O5 ÏàËÆ¶È:61.5% Bioorganic & Medicinal Chemistry Letters 2006 16 257-261 Design, synthesis, and vasorelaxant and platelet antiaggregatory activities of coumarin¨Cresveratrol hybrids Santiago Vilar, El¨ªas Quezada, Lourdes Santana, Eugenio Uriarte, Matilde Y¨¢nez, Nuria Fraiz, Carlos Alcaide, Ernesto Cano, Francisco Orallo Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-08-10 09:56:14
weiwei_l
ľ³æ (Ö°Òµ×÷¼Ò)
ÓÐÀíÏëµÄÈË
- Ó¦Öú: 2 (Ó×¶ùÔ°)
- ½ð±Ò: 3909.1
- ºì»¨: 9
- Ìû×Ó: 3128
- ÔÚÏß: 249.8Сʱ
- ³æºÅ: 1770327
- ×¢²á: 2012-04-21
- רҵ: º£ÑóÒ©Îï

3Â¥2013-08-10 11:41:10
Ëͺ컨һ¶ä
|
4Â¥2013-08-10 11:44:01














»Ø¸´´ËÂ¥