2013
DOI: 10.1016/j.crci.2012.11.013
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Novel trialkylsilyl(germyl)-substituted thienyl- and furylbenzimidazoles and their N-substituted derivatives – synthesis, structure and cytotoxic activity

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Cited by 7 publications
(4 citation statements)
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“…The propargyl moiety was introduced in the 1,4-DHP molecule at position 1; better mitochondria-regulating properties were expected because this group was considered as essential in the antidepressant rasagiline molecule [20]. Moreover, N-alkylation of benzimidazole derivatives with propargyl halides led to more active compounds [25]. All 1,4-DHP derivatives were synthesised as N-H (N-unsubstituted) compounds (1, 3, 5, 7, 9, 11, 13, 15 and 17) and Npropargyl substituted compounds (2, 4, 6, 8, 10, 12, 14, 16 and 18).…”
Section: Chemistrymentioning
confidence: 99%
“…The propargyl moiety was introduced in the 1,4-DHP molecule at position 1; better mitochondria-regulating properties were expected because this group was considered as essential in the antidepressant rasagiline molecule [20]. Moreover, N-alkylation of benzimidazole derivatives with propargyl halides led to more active compounds [25]. All 1,4-DHP derivatives were synthesised as N-H (N-unsubstituted) compounds (1, 3, 5, 7, 9, 11, 13, 15 and 17) and Npropargyl substituted compounds (2, 4, 6, 8, 10, 12, 14, 16 and 18).…”
Section: Chemistrymentioning
confidence: 99%
“…Apart from the modification of natural compounds, GeR 3 moeity is introduced to various heterocyclic derivatives. Thus, a number of germylsubstituted hetarylbenzimidazoles (14) was synthesized, and showed high cytotoxicity on the cell lines MG-22A, HT-1080 and NIH 3T3 (Figure 16) [142]. A similar series of germylsubstituted pyrane-3-carbonitriles (15) also showed high cytotoxicity and the inhibition of matrix metalloproteinase (Figure 16) [143].…”
Section: Inorganic and Coordination Germanium Compoundsmentioning
confidence: 99%
“…Apart from the modification of natural compounds, GeR3 moeity is introduced into various heterocyclic derivatives. Thus, a number of germylsubstituted hetarylbenzimidazoles (14) was synthesized that showed high cytotoxicity on the cell lines MG-22A, HT-1080 and NIH 3T3 [147]. A similar series of germylsubstituted pyrane-3-carbonitriles (15) also showed high cytotoxicity and inhibition of matrix metalloproteinase [148].…”
Section: Other Germanium Compoundsmentioning
confidence: 99%