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xuyuk(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+10 2015-06-30 17:03:12
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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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