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1 .     5-oxo-19,20-dehydroervatamine
C21H22N2O4     ÏàËÆ¶È:61.9%
Phytochemistry          1993          32          1357-1358
5-oxo-19,20-dehydroervatamine from leaves of Tabernaemontana corymbosa
Toh-Seok Kam, Kah-Yeng Loh
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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2 .     (6S,12aR)-2-Ethyl-6-(4-chlorophenyl)-2,3,6,7,12,12a-hexahydropyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4-dione
C22H20ClN3O2     ÏàËÆ¶È:61.9%
Archiv der Pharmazie          2011          11          149-157
Design, Synthesis and Structure-Activity Relationship of Functionalized Tetrahydro-b-carboline Derivatives as Novel PDE5 Inhibitors
Nermin S. Ahmed, Bernard D. Gary, Hethar N. Tinsley, Gary A. Piazza, Stefan Laufer, and Ashraf H. Abadi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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3 .     2-(1-(2-(1H-Indol-2-yl)ethyl)indolin-2-yl)ethyl 4-methylbenzenesulfonate
C20H20N2     ÏàËÆ¶È:61.9%
Heterocycles          2011          83          2627-2633
A New Synthetic Approach to Pentacyclic Ring, 6,7,14,15-Tetrahydro[1,5]diazocino[1,2-a:6,5-a¡¯]-8-dihydrodiindole
Kittisak Sripha,* Darius Paul Zlotos, UIrike Holzgrabe, and Somsak Ruchirawat
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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4 .     2-methyl-3-[(thiomorpholin-4-yl)-methyl]-5-[4-(propyl)phenyl]-1-[4-(methylthio)phenyl]-1H-pyrrole
C26H32N2S2     ÏàËÆ¶È:61.9%
Bioorganic & Medicinal Chemistry          2010          18          8076-8084
Identification of a novel pyrrole derivative endowed with antimycobacterial activity and protection index comparable to that of the current antitubercular drugs streptomycin and rifampin
Mariangela Biava, Giulio Cesare Porretta, Giovanna Poce, Claudio Battilocchio, Salvatore Alfonso, Alessandro De Logu, Nadia Serra, Fabrizio Manetti, Maurizio Botta
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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5 .     2-methyl-3-[(thiomorpholin-4-yl)-methyl]-5-[4-(methylthio)phenyl]-1-[4-(propyl)phenyl]-1H-pyrrole
C26H32N2S2     ÏàËÆ¶È:61.9%
Bioorganic & Medicinal Chemistry          2010          18          8076-8084
Identification of a novel pyrrole derivative endowed with antimycobacterial activity and protection index comparable to that of the current antitubercular drugs streptomycin and rifampin
Mariangela Biava, Giulio Cesare Porretta, Giovanna Poce, Claudio Battilocchio, Salvatore Alfonso, Alessandro De Logu, Nadia Serra, Fabrizio Manetti, Maurizio Botta
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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