Regarding the efficacy of each compound, assessed comparing the maximal antiproliferative effect observed at 3 mM, all active biguanides (Q42, Q48, Q49, Q50, Q53 and Q54) caused a highly significant inhibition of GSC viability, showing efficacy ranging between − 71 and − 83%.
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Chloride intracellular channel 1 activity is not required for glioblastoma development but its inhibition dictates glioma stem cell responsivity to novel biguanide derivatives.
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