Synthesis and anticancer activity of novel 2-substituted pyranopyridine derivatives
A novel series of 2-aminopyranopyridine derivatives ( 3 – 19 ) were synthesized utilizing 2-chloro-4-(thiophen-2-yl)-7,8-dihydro-5 H -pyrano[4,3- b ]pyridine-3-carbonitrile ( 2 ) as a key starting compound. The structures of the newly synthesized compounds were confirmed on the basis of elemental an...
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Veröffentlicht in: | Research on chemical intermediates 2017, Vol.43 (1), p.437-456 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A novel series of 2-aminopyranopyridine derivatives (
3
–
19
) were synthesized utilizing 2-chloro-4-(thiophen-2-yl)-7,8-dihydro-5
H
-pyrano[4,3-
b
]pyridine-3-carbonitrile (
2
) as a key starting compound. The structures of the newly synthesized compounds were confirmed on the basis of elemental analyses and infrared (IR),
1
H,
13
C-nuclear magnetic resonance (NMR) and mass spectra. Anticancer evaluation was carried out for the new derivatives against Hep-G2 (human liver carcinoma), MCF-7 (human breast carcinoma), Caco-2 (human colorectal adenocarcinoma) and HCT116 (human colorectal carcinoma) cell lines using doxorubicin as a reference drug. The biological results revealed that the compounds
12
and
14
exhibited more potent anticancer activity than the reference drug. |
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ISSN: | 0922-6168 1568-5675 |
DOI: | 10.1007/s11164-016-2633-5 |