Isolation of potassium salt of oxadiazole-2-thione and anticancer activities of its Cu() and Zn() complexes against MDA-MB-231 human breast carcinoma cells

A potassium 4-(pyridyl)-1,3,4-oxadiazole-2-thione was isolated in a basic medium, and its complexes [Cu(en) 2 (pot) 2 ] ( 1 ) and [Zn(en) 2 (pot) 2 ]HBr·CH 3 OH ( 2 ) containing ethylenediamine (en) as secondary ligand were synthesized and fully characterized. Upon changing the reaction conditions,...

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Veröffentlicht in:Dalton transactions : an international journal of inorganic chemistry 2023-07, Vol.52 (29), p.1213-1221
Hauptverfasser: Gond, M. K, Rai, Nilesh, Chandra, Brijesh, Gautam, Vibhav, Garai, Somenath, Butcher, R. J, Bharty, M. K
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container_end_page 1221
container_issue 29
container_start_page 1213
container_title Dalton transactions : an international journal of inorganic chemistry
container_volume 52
creator Gond, M. K
Rai, Nilesh
Chandra, Brijesh
Gautam, Vibhav
Garai, Somenath
Butcher, R. J
Bharty, M. K
description A potassium 4-(pyridyl)-1,3,4-oxadiazole-2-thione was isolated in a basic medium, and its complexes [Cu(en) 2 (pot) 2 ] ( 1 ) and [Zn(en) 2 (pot) 2 ]HBr·CH 3 OH ( 2 ) containing ethylenediamine (en) as secondary ligand were synthesized and fully characterized. Upon changing the reaction conditions, the Cu( ii ) complex ( 1 ) adopts an octahedral geometry around the metal center. The cytotoxic activity of ligand (Kpot·H 2 O) along with complexes 1 and 2 was tested, and their anticancer activity against MDA-MB-231 human breast cancer cells was demonstrated, with complex 1 exhibiting superior cytotoxicity against these cells as compared to Kpot·H 2 O and complex 2 . According to the DNA nicking assay, the ligand (Kpot·H 2 O) was found to be more potent to scavenge hydroxyl radicals even at a lower concentration (50 μg mL −1 ) than that of both complexes. The wound healing assay revealed that ligand Kpot·H 2 O and its complexes 1 and 2 attenuated the migration of the above-mentioned cell line. The loss of cellular and nuclear integrity and induction in the activity of Caspase-3 suggest the anticancer potential of ligand Kpot·H 2 O and its complexes 1 and 2 against MDA-MB-231 cells. A potassium 4-(pyridyl)-1,3,4-oxadiazole-2-thione was isolated in a basic medium, and its complexes [Cu(en) 2 (pot) 2 ] ( 1 ) and [Zn(en) 2 (pot) 2 ]HBr·CH 3 OH ( 2 ) containing ethylenediamine (en) as secondary ligands were synthesized and fully characterized.
doi_str_mv 10.1039/d3dt01388j
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K ; Rai, Nilesh ; Chandra, Brijesh ; Gautam, Vibhav ; Garai, Somenath ; Butcher, R. J ; Bharty, M. K</creator><creatorcontrib>Gond, M. K ; Rai, Nilesh ; Chandra, Brijesh ; Gautam, Vibhav ; Garai, Somenath ; Butcher, R. J ; Bharty, M. K</creatorcontrib><description>A potassium 4-(pyridyl)-1,3,4-oxadiazole-2-thione was isolated in a basic medium, and its complexes [Cu(en) 2 (pot) 2 ] ( 1 ) and [Zn(en) 2 (pot) 2 ]HBr·CH 3 OH ( 2 ) containing ethylenediamine (en) as secondary ligand were synthesized and fully characterized. Upon changing the reaction conditions, the Cu( ii ) complex ( 1 ) adopts an octahedral geometry around the metal center. The cytotoxic activity of ligand (Kpot·H 2 O) along with complexes 1 and 2 was tested, and their anticancer activity against MDA-MB-231 human breast cancer cells was demonstrated, with complex 1 exhibiting superior cytotoxicity against these cells as compared to Kpot·H 2 O and complex 2 . According to the DNA nicking assay, the ligand (Kpot·H 2 O) was found to be more potent to scavenge hydroxyl radicals even at a lower concentration (50 μg mL −1 ) than that of both complexes. The wound healing assay revealed that ligand Kpot·H 2 O and its complexes 1 and 2 attenuated the migration of the above-mentioned cell line. The loss of cellular and nuclear integrity and induction in the activity of Caspase-3 suggest the anticancer potential of ligand Kpot·H 2 O and its complexes 1 and 2 against MDA-MB-231 cells. A potassium 4-(pyridyl)-1,3,4-oxadiazole-2-thione was isolated in a basic medium, and its complexes [Cu(en) 2 (pot) 2 ] ( 1 ) and [Zn(en) 2 (pot) 2 ]HBr·CH 3 OH ( 2 ) containing ethylenediamine (en) as secondary ligands were synthesized and fully characterized.</description><identifier>ISSN: 1477-9226</identifier><identifier>EISSN: 1477-9234</identifier><identifier>DOI: 10.1039/d3dt01388j</identifier><ispartof>Dalton transactions : an international journal of inorganic chemistry, 2023-07, Vol.52 (29), p.1213-1221</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Gond, M. 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The cytotoxic activity of ligand (Kpot·H 2 O) along with complexes 1 and 2 was tested, and their anticancer activity against MDA-MB-231 human breast cancer cells was demonstrated, with complex 1 exhibiting superior cytotoxicity against these cells as compared to Kpot·H 2 O and complex 2 . According to the DNA nicking assay, the ligand (Kpot·H 2 O) was found to be more potent to scavenge hydroxyl radicals even at a lower concentration (50 μg mL −1 ) than that of both complexes. The wound healing assay revealed that ligand Kpot·H 2 O and its complexes 1 and 2 attenuated the migration of the above-mentioned cell line. The loss of cellular and nuclear integrity and induction in the activity of Caspase-3 suggest the anticancer potential of ligand Kpot·H 2 O and its complexes 1 and 2 against MDA-MB-231 cells. A potassium 4-(pyridyl)-1,3,4-oxadiazole-2-thione was isolated in a basic medium, and its complexes [Cu(en) 2 (pot) 2 ] ( 1 ) and [Zn(en) 2 (pot) 2 ]HBr·CH 3 OH ( 2 ) containing ethylenediamine (en) as secondary ligands were synthesized and fully characterized.</abstract><doi>10.1039/d3dt01388j</doi><tpages>9</tpages></addata></record>
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title Isolation of potassium salt of oxadiazole-2-thione and anticancer activities of its Cu() and Zn() complexes against MDA-MB-231 human breast carcinoma cells
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