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xuyuk(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+10 2015-06-30 17:03:12
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²éѯ½á¹û£º¹²²éµ½60¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (E)-2-(3,5-dimethoxy-4-(methoxymethoxy)benzylidene)-4,6-dimethoxybenzofuran-3(2H)-one C21H22O8 ÏàËÆ¶È:61.1% Heterocycles 1983 20 2203-2209 CARBON-13 NUCLEAR MAGNETIC RESONANCE SPECTRA OF 2-ARYLIDENE-3(2H)-BENZOFURANONES Aurora Bellino.Maria Luisa Marino, and Pietro Venturella Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 6,7-dimethoxy-2-(3,4-dimethoxy-2-nitrophenyl)-3-hydroxy-1,4-naphthoquinone C20H17NO9 ÏàËÆ¶È:57.8% Tetrahedron 2002 58 3015-3019 From phenylacetylphenylacetic acids to indoles: a simple new divergent synthesis of 6,11-dihydro-5H-benzo[a]carbazol-5,6-diones and 6,11-dihydro-5H-benzocarbazol-6,11-diones Jacobo Cruces, Elena Martı́nez, M¨®nica Treus, Luis A Martı́nez, Juan C Est¨¦vez, Ram¨®n J Est¨¦vez, Luis Castedo Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 3a ÏàËÆ¶È:57.8% Journal of Natural Products 2011 74 1188-1200 Lignans and Neolignans from Sinocalamus affinis and Their Absolute Configurations Liang Xiong, Chenggeng Zhu, Yanru Li, Ye Tian, Sheng Lin, Shaopeng Yuan, Jinfeng Hu, Qi Hou, Naihong Chen, Yongchun Yang, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 1,8-Dihydroxy-4,5,6-trimethoxyxanthone ÏàËÆ¶È:55.5% Molecules 2015 20 127−134 Xanthones from the Roots of Moutabea guianensis Aubl. Haroldo da S. Ripardo Filho, Luidi C. Pacheco, Edinaldo da S. Andrade, Marivaldo Jos¨¦ C. Correa, Railda Neyva M. Ara¨²jo, Giselle Maria S. P. Guilhon, Joyce Kelly R. da Silva and Lourivaldo S. Santos Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Gomphilactone Dimethyl Ether C14H10O6 ÏàËÆ¶È:55.5% European Journal of Organic Chemistry 2012 380-390 Coloured Artefacts Formed by Oxidation of Benzene-1,2,4-triol and ¦Â-Dopa During the Extraction of Cortinarius violaceus (Agaricales) with Alcohols Franz von Nussbaum, Matthias R¨¹th, Peter Spiteller, Tina H¨¹bscher-Weissert, Florian Löbermann, Kurt Polborn and Wolfgang Steglich Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . baculiferin O C18H9NO11S ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2010 18 5466-5474 Baculiferins A¨CO, O-sulfated pyrrole alkaloids with anti-HIV-1 activity, from the Chinese marine sponge Iotrochota baculifera Guotao Fan, Zelin Li, Shi Shen, Yi Zeng, Yishu Yang, Minjuang Xu, Torsten Bruhn, Heike Bruhn, Joachim Morschhäuser, Gerhard Bringmann, Wenhan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 5,10-dibromo-9-(bromomethyl)-2,3,6-trimethoxyphenanthrene C18H15Br3O3 ÏàËÆ¶È:55.5% European Journal of Organic Chemistry 2010 292-299 Efficient and Chirally Specific Synthesis of Phenanthro-Indolizidine Alkaloids by Parham-Type Cycloacylation Ziwen Wang, Zheng Li, Kailiang Wang and Qingmin Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Proserin B C16H14O8 ÏàËÆ¶È:55.5% Phytochemistry 2011 72 1431-1435 Phenolic compounds from the cultured mycobionts of Graphis proserpens Yukiko Takenaka, Natsuko Morimoto , Nobuo Hamada , Takao Tanahashi Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Proserin C C17H16O8 ÏàËÆ¶È:55.5% Phytochemistry 2011 72 1431-1435 Phenolic compounds from the cultured mycobionts of Graphis proserpens Yukiko Takenaka, Natsuko Morimoto , Nobuo Hamada , Takao Tanahashi Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (2E)-3-(3-nitrophenyl)-1-(2',4',5'-trimethoxyphenyl)prop-2-en-1-one C18H16O6 ÏàËÆ¶È:55.5% Medicinal Chemistry Research 2014 23 4301−4319 Apoptotic effect of synthetic 2¡ä,4¡ä,5¡ä-trimethoxychalcones in human K562 and Jurkat leukemia cells Aline Costa, Louise Domeneghini Chiaradia-Delatorre, Lorena dos Santos Bubniak, Alessandra Mascarello, Marley Aparecida Lic¨ªnio Marzarotto, Ana Carolina Rabello de Moraes, Taisa Regina Stumpf, Marlon Norberto Sechini Cordeiro, Rosendo Augusto Yunes, Ricar Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 2-methoxy-N-methyl-N-(4-(3,4,5-trimethoxyphenyl)thiazol-2-yl)benzamide C21H22N2O5S ÏàËÆ¶È:55.5% Journal of Medicinal Chemistry 2014 57 6653−6667 Modification and Biological Evaluation of Thiazole Derivatives as Novel Inhibitors of Metastatic Cancer Cell Migration and Invasion Shilong Zheng, Qiu Zhong, Yulan Xi, Madhusoodanan Mottamal, Qiang Zhang, Richard L. Schroeder, Jayalakshmi Sridhar, Ling He, Harris McFerrin, and Guangdi Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (7E)-7,8-dehydroheliobuphthalmin ÏàËÆ¶È:55% Journal of Natural Products 2014 77 2641-2650 Evaluation of Lignans from Heliopsis helianthoides var. scabra for Their Potential Antimetastatic Effects in the Brain Zsanett Hajdu, J¨¢nos Hask¨®, Istv¨¢n A. Krizbai, Imola Wilhelm, Nikoletta Jedlinszki, Csilla Fazakas, Judit Moln¨¢r, Peter Forgo, Judit Hohmann, and Dezső Csupor Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . nemerosin C22H23O7 ÏàËÆ¶È:54.5% Chemical & Pharmaceutical Bulletin 1998 46 871-874 Antiproliferative Constituents in Umbelliferae Plants. III. Constituents in the Root and the Ground Part of Anthriscus sylvestris HOFFM. Ryuji IKEDA,Tsuneatsu NAGAO,Hikaru OKABE,Yukitaka NAKANO,Hisashi MATSUNAGA,Mitsuo KATANO and Masato MORI Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . nemerosin ÏàËÆ¶È:54.5% Phytochemistry 1989 28 2863-2866 Lignans from Juniperus thurifera Arturo San Feliciano,Manuel Medarde,Jose L. Lopez,Pilar Puebla,Jose M. Miguel del Corral,Alejandro F. Barrer Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . nemerosin ÏàËÆ¶È:54.5% Biological and Pharmaceutical Bulletin 2007 30 1340-1343 Lignans and Coumarins from the Roots of Anthriscus sylvestris and Their Increase of Caspase-3 Activity in HL-60 Cells Gil-Saeng Jeong, Ok-Kyoung Kwon, Bo-Young Park, Sei-Ryang Oh, Kyung-Seop Ahn, Min-Jung Chang, Won Keun Oh, Jin-Cheol Kim, Byung-Sun Min, Youn-Chul Kim, Hyeong-Kyu Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Evelynin C19H20O7 ÏàËÆ¶È:52.6% Journal of Natural Products 2010 73 1590-1592 Evelynin, a Cytotoxic Benzoquinone-Type retro-Dihydrochalcone from Tacca chantrieri Jiangnan Peng, Evelyn M. Jackson, David J. Babinski, April L. Risinger, Gregory Helms, Doug E. Frantz, and Susan L. Mooberry Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . meliternin ÏàËÆ¶È:52.6% Organic Magnetic Resonance 1979 12 583−586 13C NMR spectra of polymethoxy- and methylenedioxyflavonols D. J. Calvert, R. C. Cambie and B. R. Davis Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . coeloginanthridin C16H16O5 ÏàËÆ¶È:50% Phytochemistry 2001 58 581-586 Phenanthrene derivatives from the orchid Coelogyne cristata P.L. Majumder, S. Sen, S. Majumder Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 7,4'-dihydroxy-2',5'-dimethoxyisoflav-3-ene C17H16O5 ÏàËÆ¶È:50% Planta Medica 2003 69 658-661 Flavonoids and Isoflavonoids with Antiplasmodial Activities from the Root Bark of Erythrina abyssinica Abiy Yenesew,Solomon Derese,Beatrice Irungu,Jacob O.Midiwo,Norman C.Waters, Pamela Liyala,Hoseah Akala,Matthias Heydenreich,Martin G.Peter Structure 13C NMR ̼Æ×Ä£Äâͼ |

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