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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
2Â¥2013-04-12 22:16:27
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