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12.82,29.66,52.94,55.86,55.95,56.00,56.04,76.30,110.15,110.31,111.13,112.24,119.04,123.50,128.82,131.56,148.77,148.89,148.93,153.25,165.27,208.97
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1 .     magnostellin B
C22H26O8     ÏàËÆ¶È:63.6%
Chemical & Pharmaceutical Bulletin          2002          50(4)          541-543
Lignans and Sesquiterpenes from Magnolia praecocissima
Hironobu TAKAHASHI,Seiko YOSHIOKA, Shoichi KAWANO,Hiroshi AZUMA,and Yoshiyasu FUKUYAMA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     7,8-seco-holostylone B
C21H22O7     ÏàËÆ¶È:63.6%
Phytochemistry          2004          65          751-759
Aryltetralone lignans and 7,8-seco-lignans from Holostylis reniformis
Tito da Silva, Lucia M.X. Lopes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     magnone A
    ÏàËÆ¶È:63.6%
Journal of Natural Products          1998          61          808-811
Magnone A and B, Novel Anti-PAF Tetrahydrofuran Lignans from the Flower Buds of Magnolia fargesii
Keun Young Jung, Dong Seon Kim, Sei Ryang Oh, Si-Hyung Park, Im Seon Lee, Jung Joon Lee, Dong-Hyuk Shin, and Hyeong-Kyu Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (E)-2-(2-(3,4-dimethoxystyryl)-4,5-dimethoxyphenyl)ethanamine
C20H25NO4     ÏàËÆ¶È:63.6%
Heterocycles          2012          86          469-485
Catalytic Asymmetric Synthesis of (S)-Laudanosine by Hydroamination
Tokutaro Ogata, Tetsutaro Kimachi, Ken-ichi Yamada, Yasutomo Yamamoto, and Kiyoshi Tomioka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (7'R,8'S)-3,4-Methylenedioxy-3',4'-dimethoxy-7,8¨Cseco¨C7,7'¨Cepoxylignan-7,8-dione
C21H22O7     ÏàËÆ¶È:63.6%
Natural Product Communications          2009          4          1571-1574
Two New Lignans from the Fruits of Schisandra sphenanthera
Chun Ren Wang, Rong Sun, Chen Ren Ou Yang, Ye Gao Chen and Hong Chuang Song
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     7,8-Seco-holostylone
    ÏàËÆ¶È:63.6%
Natural Product Communications          2009          4          1571-1574
Two New Lignans from the Fruits of Schisandra sphenanthera
Chun Ren Wang, Rong Sun, Chen Ren Ou Yang, Ye Gao Chen and Hong Chuang Song
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     tetra-O-methylpilosidine
C27H34O11     ÏàËÆ¶È:61.5%
Phytochemistry          2000          55          411-417
Benzylbenzoate and norlignan glucosides from Curculigo pilosa: structural analysis and in vitro vascular activity
Giovanna Palazzino, Corrado Galeffi, Elena Federici, Franco Delle Monache, Maria Francesca Cometa, Maura Palmery
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Compound 3
    ÏàËÆ¶È:61.5%
Magnetic Resonance in Chemistry          2007          45          182-184
1H and 13C chemical shifts for some tetrasubstituted 2, 5-diaryl di- and tetrahydrofuran derivatives (pages 182¨C184)
S. Martinet, A. M¨¦ou and P. Brun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     6,7-dimethoxy-2-[3-[N-(3,4-dimethoxyphenethyl-2)methylamino]propyl]-1,2,3,4-tetrahydroisochinolinone
C35H34N2O5     ÏàËÆ¶È:60%
Journal of Medicinal Chemistry          1990          33          1496-1504
Specific bradycardic agents. 1. Chemistry, pharmacology, and structure-activity relationships of substituted benzazepinones, a new class of compounds exerting antiischemic properties
Manfred Reiffen, Wolfgang Eberlein, Peter Mueller, Manfred Psiorz, Klaus Noll, Joachim Heider, Christian Lillie, Walter Kobinger, Peter Luger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (-)-8'-epi-8-hydroxy-aristoligone
C22H26O6     ÏàËÆ¶È:59.0%
Phytochemistry          2006          67          929-937
Aryltetralol and aryltetralone lignans from Holostylis reniformis
Tito da Silva, Lucia M.X. Lopes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     (+)-8,8'-epi-aristoligone
C22H26O5     ÏàËÆ¶È:59.0%
Phytochemistry          2004          65          751-759
Aryltetralone lignans and 7,8-seco-lignans from Holostylis reniformis
Tito da Silva, Lucia M.X. Lopes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     saxicolaline A
C20H22O5N     ÏàËÆ¶È:59.0%
Planta Medica          2007          73          787-791
Two New Quaternary Alkaloids and Anti-Hepatitis B Virus Active Constituents from Corydalis saxicola
Ying-Rui Wu, Yun-Bao Ma, You-Xing Zhao, Shu-Ying Yao, Jun Zhou, Ying Zhou, Ji-Jun Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     Methyl 3,4-bis(3',4'-dimethoxyphenyl)-1H-pyrrole-2-carboxylate
C22H23NO6     ÏàËÆ¶È:59.0%
Molecules          2004          9          135-147
Lipid-Lowering Effects of Ethyl 2-Phenacyl-3-aryl-1H-pyrrole- 4-carboxylates in Rodents
Justin M. Holub, Kathy O'Toole-Colin, Adam Getzel, Anthony Argenti, Michael A. Evans, Daniel C. Smith, Gerard A. Dalglish, Shahzad Rifat, Donna L. Wilson, Brett M. Taylor, Ulander Miott, Josephine Glersaye, Kam S. Lam, Bryan J. McCranor, Joshua D. Berkowi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     (E)-1,3-Bis(3,4-dimethoxyphenyl)prop-2-en-1-one
C19H20O5     ÏàËÆ¶È:59.0%
Bioorganic & Medicinal Chemistry          2012          20          346-355
Investigation of chalcones and benzochalcones as inhibitors of breast cancer resistance protein
Kapil Juvale, Veronika F.S. Pape, Michael Wiese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     1-(4,7-Dimethoxy-benzothiophen-2-yl)-3-[4-(2-methoxyphenyl)piperazin-1-yl]-1-propanol
C24H30N2O4S     ÏàËÆ¶È:59.0%
Molecules          2012          17          1388-1407
Synthesis, Docking Studies and Biological Evaluation of Benzothiophen-2-yl-3-(4-arylpiperazin-1-yl)-propan-1-one Derivatives on 5-HT1A Serotonin Receptors
Hern¨¢n Pessoa-Mahana,Gonzalo Recabarren-Gajardo, Jenny Fiedler Temer ,Gerald Zapata-Torres , C. David Pessoa-Mahana, Claudio Saitz Barr¨ªa and Ramiro Araya-Maturana
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
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