| ²é¿´: 307 | »Ø¸´: 1 | ||
haoyumomoÒø³æ (СÓÐÃûÆø)
|
[ÇóÖú]
άÆÕÇóÖú
|
| 8.3,10.8,17.7,25.9,39.7,100.3,105.2,109.5,113.9,142.2,161.1,170.8 |
» ²ÂÄãϲ»¶
331Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
081200-11408-276ѧ˶Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
336²ÄÁÏÓ뻯¹¤085600Çóµ÷¼Á
ÒѾÓÐ19È˻ظ´
274Çóµ÷¼ÁÇóµ÷¼Á
ÒѾÓÐ9È˻ظ´
277¡¢Ñ§Ë¶£¬Çóµ÷¼Á ÊýÒ»104£¬
ÒѾÓÐ9È˻ظ´
Ò»Ö¾Ô¸Ö£ÖÝ´óѧ²ÄÁÏÓ뻯¹¤085600£¬Çóµ÷¼Á
ÒѾÓÐ33È˻ظ´
0854µç×ÓÐÅÏ¢319Çóµ÷¼Á£¨½ÓÊÜ¿çרҵµ÷¼Á£©
ÒѾÓÐ5È˻ظ´
388µ÷¼Á
ÒѾÓÐ3È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
388Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
¶«Éý¶«Âä
гæ (СÓÐÃûÆø)
- Ó¦Öú: 12 (СѧÉú)
- ½ð±Ò: 1340.2
- É¢½ð: 100
- ºì»¨: 6
- Ìû×Ó: 184
- ÔÚÏß: 60.9Сʱ
- ³æºÅ: 2070083
- ×¢²á: 2012-10-18
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
haoyumomo: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-09-10 18:10:01
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
haoyumomo: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-09-10 18:10:01
|
1 . sclerotinin A ÏàËÆ¶È:92.3% Journal of Chinese Medicinal Materials 2009 32 1843-1845 Secondary Metabolites of Mangrove Endophytic Fungus SK5 in the South China Sea XIAO Na-na, GAO Jun-ping, CAI Xiao-ling, SHE Zhi-gang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . Agropyrenone C11H12O4 ÏàËÆ¶È:75% Phytochemistry 2012 79 102-108 Agropyrenol and agropyrenal, phytotoxins from Ascochyta agropyrina var. nana, a fungal pathogen of Elitrigia repens Anna Andolfi, Alessio Cimmino, Maurizio Vurro, Alexander Berestetskiy, Ciro Troise, Maria Chiara Zonno, Andrea Motta, Antonio Evidente Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . citrinin H2 C12H16O4 ÏàËÆ¶È:58.3% Bioscience, Biotechnology, and Biochemistry 2003 66 206-210 A Major Decomposition Product, Citrinin H2, from Citrinin on Heating with Moisture Mitsuru HIROTA, Alka MENTA, Keiko YONEYAMA and Naofumi KITABATAKE Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . taurodispacamide A C13H16Br2N6O4S ÏàËÆ¶È:53.8% Tetrahedron Letters 2000 41 9917-9922 Two novel pyrrole-imidazole alkaloids from the Mediterranean sponge Agelas oroides Ernesto Fattorusso, Orazio Taglialatela-Scafati Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . butyl 2,4-dihydroxy-6-methylbenzoate C12H16O4 ÏàËÆ¶È:50% Chemistry & Biodiversity 2006 Vol. 3 210 The Chemical Constituents of the Fungus Stereum sp. Guo-Hong Li, Lei Li, Meng Duan, and Ke-Qin Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (S)-3-(3',5'-dihydroxy-2',4'-methylphenyl) butan-2-one ÏàËÆ¶È:50% Chemistry of Natural Compounds 2009 45 805-807 A NEW CYTOTOXIC ISOCOUMARIN FROM ENDOPHYTIC FUNGUS Penicillium SP. 091402 OF THE MANGROVE PLANTBruguiera sexangula Zhuang Han, Wenli Mei, Youxing Zhao,Yuanyuan Deng,and Haofu Dai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 4-(2'-methyl-4'hydroxyphenyl)azodenzenesalicylic acid ÏàËÆ¶È:50% Chinese Chemical Letters 2008 19 419-422 Synthesis of phenol-class azo derivatives of 4-aminosalicylic acid Shi Fei Sheng, Hui Xia Zheng, Jiang Liu, Zheng Bao Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 3,6-Diethyl-4-hydroxy-5-methyl-2H-pyran-2-one C10H14O3 ÏàËÆ¶È:50% Journal of Natural Products 2010 73 472-475 Modified Phenazines from an Indonesian Streptomyces sp. Serge Fotso, Dwi Andreas Santosa, Rasti Saraswati, Jongtae Yang, Taifo Mahmud, T. Mark Zabriskie and Philip J. Proteau Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (¡À)-5,5'-Bis-(t-butyldimethylsilyloxymethyl)-2-methyl-hepta-1,6-dien-3-ol C22H46O3Si2 ÏàËÆ¶È:50% Archiv der Pharmazie 2004 337 457-463 Synthesis and Antiviral Activities of Novel 2',4'-or 3',4'-Doubly Branched Carbocyclic Nucleosides as Potential Antiviral Agents Chang Hyun Oh and Joon Hee Hong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . compound 21 C11H16O4 ÏàËÆ¶È:50% The Journal of Organic Chemistry 1997 62 1691-1701 Total Synthesis of (− -Ircinianin and (+)-WistarinJun'ichi Uenishi, Reiko Kawahama, and Osamu Yonemitsu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . N'-(3-cyano-4,5-dimethyl-2-furyl)-N,N-dimethyleth-animidamide C11H15N3O ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2009 17 4406-4419 Synthesis and cytotoxic activity of 5,6-heteroaromatically annulated pyridine-2,4-diamines C. Willemann, R. Gr¨¹nert, P.J. Bednarski, R. Trosch¨¹tz Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 6-(2-(furan-2-yl)ethyl)-2,2-dimethyl-4H-1,3-dioxin-4-one C12H14O4 ÏàËÆ¶È:50% Tetrahedron 2013 69 5588-5603 Studies toward welwitindolinones: formal syntheses of N-methylwelwitindolinone C isothiocyanate and related natural products Tsung-hao Fu, William T. McElroy, Mariam Shamszad, Richard W. Heidebrecht Jr., Brian Gulledge, Stephen F. Martin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . altechromone A C11H10O3 ÏàËÆ¶È:50% World Journal of Microbiology and Biotechnology 2009 25 1677-1683 Bioactive metabolites from Alternaria brassicicola ML-P08, an endophytic fungus residing in Malus halliana Wen Gu Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-09-10 13:40:40














»Ø¸´´ËÂ¥
-Ircinianin and (+)-Wistarin