Synthesis and pharmacological activity of 2-(biphenyl-4-yl)imidazo[1,2-a]benzimidazoles
An efficient method for the synthesis of novel 9 H -imidazo[1,2- a ]benzimidazole derivatives containing a biphenyl substituent at position 2 was developed. These compounds, belonging to the privileged substructures, have been tested for a wide range of pharmacological activities in the in vitro tes...
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Published in | Russian chemical bulletin Vol. 66; no. 10; pp. 1905 - 1912 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Springer US
01.10.2017
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | An efficient method for the synthesis of novel 9
H
-imidazo[1,2-
a
]benzimidazole derivatives containing a biphenyl substituent at position 2 was developed. These compounds, belonging to the privileged substructures, have been tested for a wide range of pharmacological activities in the
in vitro
test panel. It was shown that the synthesized derivatives demonstrated high antioxidant activity, some of them inhibit type 1B protein tyrosine phosphatase, activate AMP-activated protein kinase, possess antiplatelet properties, and a rare and very interesting kind of activity, the ability to break cross-links of glycated proteins. The most active compounds can be suggested for further optimization. |
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ISSN: | 1066-5285 1573-9171 |
DOI: | 10.1007/s11172-017-1965-7 |