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²éѯ½á¹û£º¹²²éµ½125¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 4 ÏàËÆ¶È:65.3% Chemical & Pharmaceutical Bulletin 1984 32 4653-4657 Effects of O-Methylation and O-Glucosylation on Carbon-13 Nuclear Magnetic Resonance Chemical Shifts of Matairesinol, (+)-Pinoresinol and (+)-Epipinoresinol SANSEI NISHIBE,HIROKI TSUKAMOTO and SUEO HISADA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . matairesinol 4'-O-glucoside ÏàËÆ¶È:65.3% Phytochemistry 1990 29 1971-1980 Lignans of Forsythia intermedia Maiada M.A. Rahman,Paul M. Dewick,David E. Jackson,John A. Lucas Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . N-(4-(2-(6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)ethyl)phenyl)-2-(2-aminophenoxy)acetamide C27H31N3O4 ÏàËÆ¶È:65.3% Bioorganic & Medicinal Chemistry 2009 17 2524-2535 Synthesis and biological evaluation of a small molecule library of 3rd generation multidrug resistance modulators Werner Klinkhammer, Henrik M¨¹ller, Christoph Globisch, Ilza K. Pajeva, Michael Wiese Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 2-amino-N-{4-[2-(6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl)ethyl]phenyl}benzamide C26H29N3O3 ÏàËÆ¶È:61.5% Bioorganic & Medicinal Chemistry 2009 17 2524-2535 Synthesis and biological evaluation of a small molecule library of 3rd generation multidrug resistance modulators Werner Klinkhammer, Henrik M¨¹ller, Christoph Globisch, Ilza K. Pajeva, Michael Wiese Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . silybin ÏàËÆ¶È:57.6% Planta Medica 1981 43 121-127 Structure of Silandrin and Silymonin, two New Flavanolignans from a White Blooming Silybum marianum Variety I. Szil¨¢gi, P. T¨¦t¨¦nyi, S. Antus, 0. Seligmann, V. M. Chari, M. Seitz und H. Wagner Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 7-hydroxymethyl-8,8-dimethyl-4,8-dihydrobenzol[1, 4]thiazine-3,5-dione-(2-O-caffeoyl)-¦Â-D-glucopyranoside C26H29O11NS ÏàËÆ¶È:57.6% Fitoterapia 2006 77 245-246 A new thiazinedione from Xanthium strumarium Luping Qin, Ting Han , Huiliang Li , Qiaoyan Zhang , Hanchen Zheng Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 4,5-dicaffeoylquinic acid ÏàËÆ¶È:57.6% Phytochemical Analysis 2007 18 436-440 Preparative isolation and purification of dicaffeoylquinic acids from the Ainsliaea fragrans champ by high-speed counter-current chromatography Yingfeng Wang and Bo Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . N-(4-(2-(6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)ethyl)phenyl)quinoxaline-2-carboxamide C28H28N4O3 ÏàËÆ¶È:57.6% Bioorganic & Medicinal Chemistry 2009 17 2524-2535 Synthesis and biological evaluation of a small molecule library of 3rd generation multidrug resistance modulators Werner Klinkhammer, Henrik M¨¹ller, Christoph Globisch, Ilza K. Pajeva, Michael Wiese Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 7-O-methylsilybin B C26H24O10 ÏàËÆ¶È:57.6% Bioorganic & Medicinal Chemistry 2013 21 742-747 Enhanced bioactivity of silybin B methylation products Arlene A. Sy-Cordero, Tyler N. Graf, Scott P. Runyon, Mansukh C. Wani, David J. Kroll, Rajesh Agarwal, Scott J. Brantley, Mary F. Paine, Stephen J. Polyak, Nicholas H. Oberlies Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3-((4-Hydroxy-3-methoxyphenyl)(3-methyl-5-oxo-1-phenyl-4,5-dihydro-1H-pyrazol-4-yl)methyl)chroman-2,4-dione ÏàËÆ¶È:57.6% Molecules 2012 17 14146-14158 Ultrasound-Promoted Greener Synthesis of Novel Trifurcate 3-Substituted-chroman-2,4-dione Derivatives and Their Drug-Likeness Evaluation Chengyuan Liang, Hailong Jiang, Zhiguang Zhou, Dong Lei, Yu Xue and Qizheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . N-(4-(2-(6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)ethyl)phenyl)isoquinoline-3-carboxamide C29H29N3O3 ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2009 17 2524-2535 Synthesis and biological evaluation of a small molecule library of 3rd generation multidrug resistance modulators Werner Klinkhammer, Henrik M¨¹ller, Christoph Globisch, Ilza K. Pajeva, Michael Wiese Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 8R, 8'R-matairesinol 4-O-¦Â-D-xylopyranosyl-(1¡ú2)-O-¦Â-D-glucopy- ranoside C31H40O15 ÏàËÆ¶È:54.8% Phytochemistry 2008 69 788-795 Neolignan glycosides from Symplocos caudata Changhong Huo, Hong Liang, Yuying Zhao, Bin Wang, Qingying Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . methyl-3-O-(4''-hydroxy-3'',5''-dimethoxybenzoyl)-chlorogenate C26H28O13 ÏàËÆ¶È:53.8% Phytochemistry 2007 68 1775-1780 Rare biscoumarins and a chlorogenic acid derivative from Erycibe obtusifolia Jian Liu, Ziming Feng, Jianfu Xu, Yinghong Wang, Peicheng Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . latifolian B C25H23NO6 ÏàËÆ¶È:53.8% Journal of Natural Products 2005 68 1080-1082 Latifolians A and B, Novel JNK3 Kinase Inhibitors from the Papua New Guinean Plant Gnetum latifolium Simone J. Rochfort, Leanne Towerzey, Anthony Carroll, Gordon King, Adam Michael,Greg Pierens, Topul Rali, Joanne Redburn, Jaqueline Whitmore, and Ronald J. Quinn Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . nortrachelogenin 8'-O-¦Â-D-glucopyranoside C26H32O12 ÏàËÆ¶È:53.8% Planta Medica 2005 71 93-95 Lignans from Trachelospermum jasminoides Tan, Xing-Qi; Chen, Hai-Sheng; Liu, Run-Hui; Tan, Chang-Heng; Xu, Cong-Li; Xuan, Wei-Dong; Zhang, Wei-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . orosunol C21H16O7 ÏàËÆ¶È:53.8% Planta Medica 1982 44 154-156 Two New Arylnaphthalide Lgnans from Justicia f lava Roots Ajibola A. Olaniyi Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 5 ÏàËÆ¶È:53.8% Chemical & Pharmaceutical Bulletin 1984 32 4653-4657 Effects of O-Methylation and O-Glucosylation on Carbon-13 Nuclear Magnetic Resonance Chemical Shifts of Matairesinol, (+)-Pinoresinol and (+)-Epipinoresinol SANSEI NISHIBE,HIROKI TSUKAMOTO and SUEO HISADA Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (¨C)-Lariciresinol-4-O-¦Â-D-glucopyranoside C26H34O11 ÏàËÆ¶È:53.8% Chemistry of Natural Compounds 2008 44 648-650 LIGNANS FROM Daphne giraldii Juan Su, Zhijun Wu, Yunheng Shen,Chuan Zhang, and Weidong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . lariciresinol-9-O-¦Â-D-glucopyranoside ÏàËÆ¶È:53.8% China Journal of Chinese Materia Medica 2007 32 688-691 Studies on chemical constituents in root of Isatis indigotica ZUO Li, LI Jianbei, XU Jing, YANG Jingzhi, ZHANG Dongming, TONG Yongling Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . compound 1 C26H26O11 ÏàËÆ¶È:53.8% Fitoterapia 2007 78 602-604 A new isoflavone glucoside from Astragalus membranaceus var. mongholicus Yuehu Pei , Ruifen Li, Hongwei Fu, Jing Wang, Yuzhi Zhou Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 5-O-caffeoyl-3-O-syringoylquinic acid C25H26O13 ÏàËÆ¶È:53.8% Journal of Natural Products 2010 73 177-184 Hepatoprotective Constituents from the Roots and Stems of Erycibe hainanesis Shuang Song, Yixiu Li, Ziming Feng, Jianshuang Jiang and Peicheng Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . tortoside E C27H36O12 ÏàËÆ¶È:53.8% Phytochemistry 1997 45 159-166 Lignan, phenylpropanoid and iridoid glycosides from Pedicularis torta Wang Changzeng, Jia Zhongjian Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . Marinoid B C26H32O12 ÏàËÆ¶È:53.8% Magnetic Resonance in Chemistry 2008 46 638-642 Structure elucidation of five new iridoid glucosides from the leaves of Avicennia marina (pages 638¨C642) Yu Sun, Jie Ouyang, Zhiwei Deng, Qingshan Li and Wenhan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . (+)lariciresinol 4-O-¦Â-D-glucopyranoside ÏàËÆ¶È:53.8% Chinese Journal of Natural Medicines 2003 1 199-203 Studies on Lignan Constituents of Clematis armandii Franch HUANG Wen-Wu; KONG De-Yun; YANG Pei-Ming Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 7-O-m-Coumaroyloxy-ugandoside C25H28O12 ÏàËÆ¶È:53.8% Pharmazie 1999 54 145-147 Two new terpenoid glucosides from Clerodendrum serratum J.-C. Chen, Qi-Xiu Zhu, Dong-Liang Cheng - Q.-X. Zhu - D.-L. Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . (E)-3(5)-[¦Â-(4-hydroxy-3-methoxyphenyl)-ethenyl]-5(3)-phenyl-1H-pyrazole C18H16N2O2 ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry 2009 17 1290-1296 Synthesis and biological evaluation of curcuminoid pyrazoles as new therapeutic agents in inflammatory bowel disease: Effect on matrix metalloproteinases R.M. Claramunt, L. Bouissane, M.P. Cabildo, M.P. Cornago, J. Elguero, A. Radziwon, C. Medina Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . N-(4-(2-(6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)ethyl)phenyl)-3,4-dimethoxybenzamide C28H32N2O5 ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry 2009 17 2524-2535 Synthesis and biological evaluation of a small molecule library of 3rd generation multidrug resistance modulators Werner Klinkhammer, Henrik M¨¹ller, Christoph Globisch, Ilza K. Pajeva, Michael Wiese Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . N-(4-(2-(6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)ethyl)phenyl)-2-phenoxyacetamide C27H30N2O4 ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry 2009 17 2524-2535 Synthesis and biological evaluation of a small molecule library of 3rd generation multidrug resistance modulators Werner Klinkhammer, Henrik M¨¹ller, Christoph Globisch, Ilza K. Pajeva, Michael Wiese Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . N-(4-(2-(6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)ethyl)phenyl)-2-(2-nitrophenoxy)acetamide C27H29N3O6 ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry 2009 17 2524-2535 Synthesis and biological evaluation of a small molecule library of 3rd generation multidrug resistance modulators Werner Klinkhammer, Henrik M¨¹ller, Christoph Globisch, Ilza K. Pajeva, Michael Wiese Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . tracheloside ÏàËÆ¶È:53.8% Phytotherapy Research 2012 26 722-726 Potent ¦Á-Glucosidase Inhibitors from Safflower (Carthamus tinctorius L.) Seed Toshiyuki Takahashi and Mitsuo Miyazawa Structure 13C NMR ̼Æ×Ä£Äâͼ |
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