Synthesis of bis-indolylmethanes as new potential inhibitors of β-glucuronidase and their molecular docking studies
Thirty-two (32) bis-indolylmethane-hydrazone hybrids 1–32 were synthesized and characterized by 1HNMR, 13CNNMR and HREI-MS. All compounds were evaluated in vitro for β-glucuronidase inhibitory potential. All analogs showed varying degree of β-glucuronidase inhibitory potential ranging from 0.10 ± 0....
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Veröffentlicht in: | European journal of medicinal chemistry 2018-01, Vol.143, p.1757-1767 |
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Sprache: | eng |
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