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liangtingmei: ½ð±Ò+11, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2015-04-15 19:40:52
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1 .     Pachybasin
    ÏàËÆ¶È:100%
Archives of Pharmacal Research          2012          35          461-468
Tetrahydroanthraquinone and Xanthone Derivatives from the Marine-Derived Fungus Trichoderma aureoviride PSU-F95
Nanthaphong Khamthong,Vatcharin Rukachaisirikul,Kwanruthai Tadpetch,Morakot Kaewpet,Souwalak Phongpaichit,Sita Preedanon,and Jariya Sakayaroj
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     Pachybasin
    ÏàËÆ¶È:100%
Chirality          2013          25          141-148
Structural and Stereochemical Studies of Hydroxyanthraquinone Derivatives from the Endophytic Fungus Coniothyrium sp
Peng Sun, Juan Huo, Tibor Kurt¨¢n, Attila M¨¢ndi, S¨¢ndor Antus, Hua Tang, Siegfried Draeger, Barbara Schulz, Hidayat Hussain, Karsten Krohn, Weihua Pan, Yanghua Yi and Wen Zhang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     Pachybasin
    ÏàËÆ¶È:100%
Chirality          2013          25          141-148
Structural and Stereochemical Studies of Hydroxyanthraquinone Derivatives from the Endophytic Fungus Coniothyrium sp (pages 141¨C148)
Peng Sun, Juan Huo, Tibor Kurt¨¢n, Attila M¨¢ndi, S¨¢ndor Antus, Hua Tang, Siegfried Draeger, Barbara Schulz, Hidayat Hussain, Karsten Krohn, Weihua Pan, Yanghua Yi and Wen Zhang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     1-hydroxy-6-Methyl-9,10-anthraquinone
    ÏàËÆ¶È:93.3%
Natural Product Research and Development          2014          26          159-161
A New Compound from Trichoderma sp. KK19L1
YU He, WANG Xiang-fen, JI Yan-nan, XU Yan, TIAN Sha-sha, ZHU Hua-jie*
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     1-Hydroxy-3-methoxyanthraquinone
    ÏàËÆ¶È:80%
Archives of Pharmacal Research          2012          35          461-468
Tetrahydroanthraquinone and Xanthone Derivatives from the Marine-Derived Fungus Trichoderma aureoviride PSU-F95
Nanthaphong Khamthong,Vatcharin Rukachaisirikul,Kwanruthai Tadpetch,Morakot Kaewpet,Souwalak Phongpaichit,Sita Preedanon,and Jariya Sakayaroj
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     anthraquinones chrysophanol
C15H10O4     ÏàËÆ¶È:73.3%
Acta Botanica Sinica          2003          45          1003-1007
Two New Triterpenes from Neonauclea sessilifolia
KANG Wen-Yi, LI Guo-Hong, HAO Xiao-Jiang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     1-hydroxy-anthraquinone
C14H8O3     ÏàËÆ¶È:73.3%
Acta Pharmaceutica Sinica          1992          27          358-364
ANTHRAQUINONES ISOLATED FROM MORINDA OFFICINALIS AND DAMNACANTHUS INDICUS
YJ Yang; HY Shu; ZD Min
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     1-hydroxyanthraquinone
    ÏàËÆ¶È:73.3%
Natural Product Sciences          2002          8          48-51
Antioxidant Activity of Anthraquinones from Morinda elliptica
Ismail, Nor Hadiani; Mohamad, Habsah; Mohidin, Amran; Lajis, Nordin Hj.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     Pachybasin,1-hydroxy-3-methyl-9,10-anthraquinone
    ÏàËÆ¶È:73.3%
Journal of the Brazilian Chemical Society          2006          17          929-934
Novel Anthraquinone Derivatives Produced by Phoma sorghina, an Endophyte Found in Association with the Medicinal Plant Tithonia diversifolia (Asteraceae)
Warley de Souza Borges and Mônica Tallarico Pupo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     Ýìõ«´ó»Æ·Ó
    ÏàËÆ¶È:73.3%
Journal of Chinese Medicinal Materials          2002          25          875-877
Study on the Constituents from Neonauclea sessilifolia
Kang Wenyi, Hao Xiaojiang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     2-hydroxy-9,10-anthraquinone
    ÏàËÆ¶È:73.3%
Organic Magnetic Resonance          1978          11          375-377
The carbon-13 nuclear magnetic resonance spectra of anthraquinone, eight polyhydroxyanthraquinones and eight polymethoxyanthraquinones
Y. Berger and A. Castonguay
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     2-ethyl-1(3)H-anthra[1,2-d]imidazole-6,11-dione
C17H12N2O2     ÏàËÆ¶È:70.5%
Bioorganic & Medicinal Chemistry          2009          17          7418-7428
Synthesis, cytotoxicity and human telomerase inhibition activities of a series of 1,2-heteroannelated anthraquinones and anthra[1,2-d]imidazole-6,11-dione homologues
Hsu-Shan Huang, Tsung-Chih Chen, Ruei-Huei Chen, Kuo-Feng Huang, Fong-Chun Huang, Jing-Ru Jhan, Chun-Liang Chen, Chia-Chung Lee, Yang Lo, Jing-Jer Lin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     1-hydroxy-2-hydroxymethy-3-methoxyanthraquinine
    ÏàËÆ¶È:68.7%
Journal of Shenyang Pharmaceutical University          2009          26          904-906
Chemical constituents from whole plant of Galiun verum L.
ZHAO Chun-chao, SHAO Jian-hua, ZHANG Yu-wei, CAO Dan-dan, LI Xian
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     11-methyl-6H-isoindolo[2,1-a]indol-6-one
C16H11NO     ÏàËÆ¶È:68.7%
Tetrahedron          2012          68          3112-3116
Synthesis of 6H-isoindolo[2,1-a]indol-6-ones through a sequential copper-catalyzed C-N coupling and palladium-catalyzed C¨CH activation reaction
Hua-Feng He, Sheng Dong, Yi Chen, Yang Yang, Yueqin Le, Weiliang Bao
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     barleriaquinone
C15H10O3     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1984          32          4137-4139
Chemical Examination of the Roots of Barleria buxifolia LINN. Structure of Barleriaquinone
SUBBARAYAN GOPALAKRISHNAN,STHANUSUBRAMANIA NEELAKANTAN,PATHAI VENKATESWARA RAMAN,TORU OKUYAMA and SHOJI SHIBATA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     1-hydroxy-2-methylanthraquinone
C15H10O3     ÏàËÆ¶È:66.6%
Acta Pharmaceutica Sinica          1992          27          358-364
ANTHRAQUINONES ISOLATED FROM MORINDA OFFICINALIS AND DAMNACANTHUS INDICUS
YJ Yang; HY Shu; ZD Min
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     6-(3,4-dichlorophenyl)-2-(4-methoxyphenyl)-4,5-dihydro-3(2H)-pyridazinone
C17H14Cl2N2O2     ÏàËÆ¶È:66.6%
Journal of Heterocyclic Chemistry          2005          42          131-135
A general and facile synthesis of 1,3-diaryl-4-pyrazoleacetic acid esters
David D. Xu,George T. Lee,Xinglong Jiang,Kapa Prasad,Oljan Repic and Thomas J. Blacklock
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     o-[N-(2-thiothenoyl)amino]benzyl 2-thiophencarboxylate
C17H13NO2S3     ÏàËÆ¶È:66.6%
Heterocycles          2002          58          203-212
Sulfur-containing Heterocycles Derived by Reaction of N-Thioacylamino Alcohols with Lawesson's Reagent and Saponification of N-Thioacylamino Esters
Takehiko Nishio* and Hiroshi Sekiguchi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-04-14 20:38:39
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