Publication: Biologically Active Acylthioureas and Their Ni(II) and Cu(II) Complexes: Structural, Spectroscopic, Anti-Proliferative, Nucleolytic and Antimicrobial Studies
| dc.authorscopusid | 57195963366 | |
| dc.authorscopusid | 15126857900 | |
| dc.authorscopusid | 57202354907 | |
| dc.authorscopusid | 57211029294 | |
| dc.authorscopusid | 35778838600 | |
| dc.authorscopusid | 36730742500 | |
| dc.authorscopusid | 7101827334 | |
| dc.authorwosid | Biyik, H. Halil/E-5799-2011 | |
| dc.authorwosid | Yildiz, Ufuk/A-5568-2018 | |
| dc.authorwosid | Okpareke, Obinna/Q-4193-2017 | |
| dc.authorwosid | Ayogu, Jude/Hja-3390-2022 | |
| dc.authorwosid | Özmen, Ali/Abc-4166-2021 | |
| dc.authorwosid | Özdemir, Namık/J-6434-2015 | |
| dc.authorwosid | Bilgin, Mehmet D/Aas-8164-2020 | |
| dc.contributor.author | Oyeka, Ebube E. | |
| dc.contributor.author | Babahan, Ilknur | |
| dc.contributor.author | Eboma, Bernard | |
| dc.contributor.author | Ifeanyieze, Kenechukwu J. | |
| dc.contributor.author | Okpareke, Obinna C. | |
| dc.contributor.author | Coban, Esin P. | |
| dc.contributor.author | Asegbeloyin, Jonnie N. | |
| dc.contributor.authorID | Özdemir, Namık/0000-0003-3371-9874 | |
| dc.contributor.authorID | Bilgin, Mehmet Dinçer/0000-0003-0754-0854 | |
| dc.contributor.authorID | Babahan-Bircan, Ilknur/0000-0002-1336-671X | |
| dc.contributor.authorID | Poyrazoglu, Esin/0000-0002-3921-5362 | |
| dc.contributor.authorID | Aksel, Mehran/0000-0002-3942-2257 | |
| dc.contributor.authorID | Bıyık, Hacı Halil/0000-0003-0258-054X | |
| dc.date.accessioned | 2025-12-11T01:37:34Z | |
| dc.date.issued | 2021 | |
| dc.department | Ondokuz Mayıs Üniversitesi | en_US |
| dc.department-temp | [Oyeka, Ebube E.; Eboma, Bernard; Ifeanyieze, Kenechukwu J.; Okpareke, Obinna C.; Ayogu, Jude, I; Asegbeloyin, Jonnie N.] Univ Nigeria, Dept Pure & Ind Chem, Nsukka, Enugu State, Nigeria; [Oyeka, Ebube E.] Clemson Univ, Dept Chem, Clemson, SC 29634 USA; [Babahan, Ilknur] Adnan Menderes Univ, Dept Chem, TR-09010 Aydin, Turkey; [Coban, Esin P.; Ozmen, Ali; Biyik, H. Halil] Adnan Menderes Univ, Dept Biol, TR-09010 Aydin, Turkey; [Coban, Burak; Yildiz, Ufuk] Zonguldak Bulent Ecevit Univ, Dept Chem, TR-67100 Zonguldak, Turkey; [Aksel, Mehran; Bilgin, Mehmet Dincer] Adnan Menderes Univ, Fac Med, Dept Biophys, TR-09010 Aydin, Turkey; [Ozdemir, Namik] Ondokuz Mayis Univ, Fac Educ, Dept Math & Sci Educ, TR-55139 Samsun, Turkey; [Groutso, Tatiana, V] Univ Auckland, Sch Chem Sci, Auckland, New Zealand; [Schrage, Briana R.; Ziegler, Christopher J.] Univ Akron, Dept Chem, Akron, OH 44325 USA | en_US |
| dc.description | Özdemir, Namık/0000-0003-3371-9874; Bilgin, Mehmet Dinçer/0000-0003-0754-0854; Babahan-Bircan, Ilknur/0000-0002-1336-671X; Poyrazoglu, Esin/0000-0002-3921-5362; Aksel, Mehran/0000-0002-3942-2257; Bıyık, Hacı Halil/0000-0003-0258-054X; Coban, Burak/0000-0003-1401-668X; Obinna, Okpareke/0000-0003-0815-8198; | en_US |
| dc.description.abstract | The study investigated the effects of morpholine substituent and metal complexation on in vitro anticancer and antimicrobial activities of acylthioureas using two acylthiourea molecules that differ only by the presence of morpholine oxygen; N,N-diethyl-N' -(4-chlorobenzoyl)thiourea (CBDEA) and N-morpholine-N' -(4-chlorobenzoyl) thiourea (CBMOR), and their Ni(II) and Cu(II) complexes (NiCBDEA, CuCBDEA, NiCBMOR, CuCBMOR). All compounds were synthesized and characterized by physicochemical and spectroscopic studies. CBDEA, CuCBDEA, NiCBDEA, CBMOR, and NiCBMOR were structurally elucidated by single-crystal X-ray diffraction. The metal complexes were isolated as neutral four coordinate complexes of the form, ML2 (M: Ni(II), Cu(II), H.L.: CBDEA/CBMOR) in square-planar geometry. The compounds were screened for DNA binding/cleavage, antimicrobial activity, and anti-proliferative effects on human prostate cancer PC-3 and breast cancer MCF-7 cells. DNA binding interaction studies suggest that the metal complexes bind more strongly to the DNA compared to the ligands. The morpholine derivative CBMOR shows similar activity to CBDEA against PC-3 cell lines but twice as effective against MCF-3 cells at cell death and apoptotic levels. Anticancer activities were enhanced by complexation with Cu(II), as evident in CuCBMOR, which showed the optimal anticancer activity (IC50: 1.76 mu M for MCF-7 and 1.97 mu M for PC-3), comparable to known anticancer drug paclitaxel. The CuCBMOR apoptosis results show that the cancer cells die by apoptotic mechanisms (Apoptosis rate: 91.53 % in MCF-7 and 85.95 % in PC-3). In vitro screening of the compounds against seventeen bacteria and four yeast strains confirmed antimicrobial potency against more susceptible Gram-positive bacteria strains. The results of the study suggest that some of the compounds could be developed into novel antimicrobial and anticancer agents. | en_US |
| dc.description.sponsorship | Sci-entific Research Projects Unit of Ondokuz Mays University [PYO.FEN.1906.19.001] | en_US |
| dc.description.sponsorship | The authors are grateful to the Department of Chemistry, Akron University, for assistance with X-ray crystal structure determination of CBDEA and CBMOR, School of Chemical Sciences, University of Auck-land, New Zealand for crystal data of NiCBDEA and CuCBDEA and Sci-entific Research Projects Unit of Ondokuz Mays University (Project No: PYO.FEN.1906.19.001) , Turkey for NiCBMOR. Many thanks to National Centre for Energy Research and Development, University of Nigeria, Nsukka for infrastructural support. | en_US |
| dc.description.woscitationindex | Science Citation Index Expanded | |
| dc.identifier.doi | 10.1016/j.ica.2021.120590 | |
| dc.identifier.issn | 0020-1693 | |
| dc.identifier.issn | 1873-3255 | |
| dc.identifier.scopus | 2-s2.0-85114469875 | |
| dc.identifier.scopusquality | Q2 | |
| dc.identifier.uri | https://doi.org/10.1016/j.ica.2021.120590 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/44961 | |
| dc.identifier.volume | 528 | en_US |
| dc.identifier.wos | WOS:000704368300004 | |
| dc.identifier.wosquality | Q2 | |
| dc.language.iso | en | en_US |
| dc.publisher | Elsevier Science SA | en_US |
| dc.relation.ispartof | Inorganica Chimica Acta | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Anticancer | en_US |
| dc.subject | Antimicrobial | en_US |
| dc.subject | Complexes | en_US |
| dc.subject | DNA Binding | en_US |
| dc.subject | Morpholine | en_US |
| dc.subject | Thiourea | en_US |
| dc.subject | X-Ray Diffraction | en_US |
| dc.subject | Breast Cancer (MCF-7) | en_US |
| dc.subject | Prostate Cancer (PC-3) | en_US |
| dc.title | Biologically Active Acylthioureas and Their Ni(II) and Cu(II) Complexes: Structural, Spectroscopic, Anti-Proliferative, Nucleolytic and Antimicrobial Studies | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication |
