To combine in the same molecule R1-adrenoreceptor blocking and antioxidant properties, compounds 2-5 were designed and synthesized. All compounds were effective R1-adrenoreceptor antagonists and were tested in both functional and binding assays. In addition, compounds 2 and 5 also displayed significant capacity to inhibit intracellular oxidative stress, whereas 3-5 exerted potent antiproliferative activity in lymph node carcinoma of prostate cells.

Design, synthesis, and biological evaluation of prazosin-related derivatives as multipotent compounds

MARUCCI, Gabriella;
2005-01-01

Abstract

To combine in the same molecule R1-adrenoreceptor blocking and antioxidant properties, compounds 2-5 were designed and synthesized. All compounds were effective R1-adrenoreceptor antagonists and were tested in both functional and binding assays. In addition, compounds 2 and 5 also displayed significant capacity to inhibit intracellular oxidative stress, whereas 3-5 exerted potent antiproliferative activity in lymph node carcinoma of prostate cells.
2005
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11581/112931
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