Title of article :
Antitumor agents 251: Synthesis, cytotoxic evaluation, and structure–activity relationship studies of phenanthrene-based tylophorine derivatives (PBTs) as a new class of antitumor agents Original Research Article
Author/Authors :
Linyi Wei، نويسنده , , Arnold Brossi، نويسنده , , Ross Kendall، نويسنده , , Kenneth F. Bastow، نويسنده , , Susan L. Morris-Natschke، نويسنده , , Rong-qian Shi، نويسنده , , Kuo-Hsiung Lee، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2006
Pages :
10
From page :
6560
To page :
6569
Abstract :
Polar phenanthrene-based tylophorine derivatives (PBTs) were designed, synthesized and evaluated as potential antitumor agents. These compounds contain a core phenanthrene structure and can be synthesized efficiently in excellent yield. The newly synthesized PBTs were evaluated for cytotoxic activity against the A549 human cancer cell line. Among them, N-(2,3-methylenedioxy-6-methoxy-phenanthr-9-ylmethyl)-l-2-piperidinemethanol (34) and N-(2,3-methylenedioxy-6-methoxy-phenanthr-9-ylmethyl)-5-aminopentanol (28) showed the highest potency with IC50 values of 0.16 and 0.27 μM, respectively, which are comparable to those of currently used antitumor drugs. A structure–activity relationship (SAR) study was also explored to facilitate the further development of this new compound class.
Keywords :
Archaea , Inhibitor , Reaction mechanism , Type 2 isopentenyl diphosphate isomerase
Journal title :
Bioorganic and Medicinal Chemistry
Serial Year :
2006
Journal title :
Bioorganic and Medicinal Chemistry
Record number :
1305121
Link To Document :
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