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2,4-Bis(2,4-dimethoxyphenyl)-1,3-dithia-2,4-diphosphetane 2,4-disulfide and its derivatives: Syntheses, structural characterizations, anticancer activities, and theoretical studies on some dithiophosphonato Ni(II) complex

dc.contributor.authorSAĞLAM, ERTUĞRUL GAZİ
dc.contributor.authorsSağlam E. G. , Bulat E., Zeyrek C. T. , Akkoç S., Zorlu Y., Yılmaz H.
dc.date.accessioned2022-10-11T16:59:55Z
dc.date.accessioned2026-01-10T19:16:22Z
dc.date.available2022-10-11T16:59:55Z
dc.date.issued2022-10-01
dc.description.abstractNew 2,4- bis (2,4-dimethoxyphenyl)-1,3-dithia-2,4-diphosphetane 2,4-disulfide, (SAV-A2), was synthesized from the reaction P 4 S 10 and 1,3-dimethoxybenzene. SAV-A2 was reacted with alcohols to form dithiophos- phonic acid monoesters (HLn, HS 2 P((2,4-CH 3 O) 2 C 6 H 3 )(ORn); n = 1–3, R1 = 2–butyl–; R2 = n -pentyl-; R3 = 4–tert –but-benzyl-). The acids were converted to the ammonium salts ([NH 4 L n ]) to serve as the source of the ligands (Ln), to obtain Ni(II) complexes, ([N i (L n ) 2 ]). [Ni(L2) 2 ] crystal structure was elucidated by single-crystal X-ray diffraction analysis. In addition, Density Functional Theory (DFT) calculations of [Ni(L2) 2 ] was performed. The molecular docking studies of the complex with liver cancer protein, PDB ID: 3WZE and colon cancer antigen proteins, ID 2HQ6 were done compare with experimental and the- oretical results. All compounds were tested on liver- and colon cancer cell lines. Among the complexes tested, [Ni(L3) 2 ] showed an activity closer to that of cisplatin against the colon cancer cell line. The other compounds were found to be have less active.
dc.identifier.citationSağlam E. G. , Bulat E., Zeyrek C. T. , Akkoç S., Zorlu Y., Yılmaz H., "2,4-Bis(2,4-dimethoxyphenyl)-1,3-dithia-2,4-diphosphetane 2,4-disulfide and its derivatives: Syntheses, structural characterizations, anticancer activities, and theoretical studies on some dithiophosphonato Ni(II) complex", JOURNAL OF MOLECULAR STRUCTURE, cilt.1272, sa.134197, ss.1-15, 2022
dc.identifier.doi10.1016/j.molstruc.2022.13419
dc.identifier.endpage15
dc.identifier.issn0022-2860
dc.identifier.issue134197
dc.identifier.startpage1
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0022286022018488?via%3Dihub
dc.identifier.urihttps://hdl.handle.net/11424/282265
dc.identifier.volume1272
dc.language.isoeng
dc.relation.ispartofJOURNAL OF MOLECULAR STRUCTURE
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectKimya
dc.subjectİnorganik Kimya
dc.subjectTemel Bilimler
dc.subjectChemistry
dc.subjectInorganic Chemistry
dc.subjectNatural Sciences
dc.subjectTemel Bilimler (SCI)
dc.subjectDoğa Bilimleri Genel
dc.subjectÇOK DİSİPLİNLİ BİLİMLER
dc.subjectKİMYA, İNORGANİK VE NÜKLEER
dc.subjectNatural Sciences (SCI)
dc.subjectNATURAL SCIENCES, GENERAL
dc.subjectCHEMISTRY
dc.subjectMULTIDISCIPLINARY SCIENCES
dc.subjectCHEMISTRY, INORGANIC & NUCLEAR
dc.subjectİnorganik kimya
dc.subjectKimya (çeşitli)
dc.subjectGenel Kimya
dc.subjectMultidisipliner
dc.subjectFizik Bilimleri
dc.subjectChemistry (miscellaneous)
dc.subjectGeneral Chemistry
dc.subjectMultidisciplinary
dc.subjectPhysical Sciences
dc.subjectPerthiophosphonic acid anhydrides 2
dc.subject4-diorganyl-1
dc.subject3
dc.subject2
dc.subject4-dithiadiphosphetan- 2
dc.subject4-disulfide Phosphonodithioates Dithiophosphonates Organodithiophosphorus compounds Single crystal X-ray analysis Density functional theory Molecular docking Antiproliferative activity Anticancer
dc.title2,4-Bis(2,4-dimethoxyphenyl)-1,3-dithia-2,4-diphosphetane 2,4-disulfide and its derivatives: Syntheses, structural characterizations, anticancer activities, and theoretical studies on some dithiophosphonato Ni(II) complex
dc.typearticle
dspace.entity.typePublication

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